<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0034-8376</journal-id>
<journal-title><![CDATA[Revista de investigación clínica]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. invest. clín.]]></abbrev-journal-title>
<issn>0034-8376</issn>
<publisher>
<publisher-name><![CDATA[Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0034-83762005000500009</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Efecto de la biotina sobre la expresión genética y el metabolismo]]></article-title>
<article-title xml:lang="en"><![CDATA[Effect of biotin upon gene expression and metabolism]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vilches-Flores]]></surname>
<given-names><![CDATA[Alonso]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fernández-Mejía]]></surname>
<given-names><![CDATA[Cristina]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,UNAM Instituto de Investigaciones Biomédicas ]]></institution>
<addr-line><![CDATA[México D.F.]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>10</month>
<year>2005</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>10</month>
<year>2005</year>
</pub-date>
<volume>57</volume>
<numero>5</numero>
<fpage>716</fpage>
<lpage>724</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0034-83762005000500009&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0034-83762005000500009&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0034-83762005000500009&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[During the last few decades, an increasing number of vitamin-mediated effects has been discovered at the level of gene expression in addition to their well-known roles as substrates and cofactors; the best recognized examples are the lipophilic vitamins A and D. Although little is known about water-soluble vitamins as genetic modulators, there are increasing examples of their effect on gene expression. Biotin is a hydro soluble vitamin that acts as a prosthetic group of carboxylases. Besides its role as carboxylase cofactor, biotin affects several systemic functions such as development, immunity and metabolism. In recent years, significant progress has been made in the identification of genes that are affected by biotin at the transcriptional and post-transcriptional levels as well as in the elucidation of mechanisms that mediate the effects of biotin on the gene expression. These studies bring new insights into biotin mediated gene expression and will lead to a better under-standing of biotin roles in the metabolism and in systemic functions.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[En décadas recientes, diversas investigaciones han demostrado que las vitaminas afectan la expresión genética. Los casos mejor estudiados son los de las vitaminas A y D. Existe menos información para las vitaminas hidrosolubles sobre su efecto en la expresión de los genes, sin embargo, se sabe que éstas también los modifican. La biotina es una vitamina hidrosoluble que actúa como grupo prostético de las carboxilasas. Además de su función como cofactor de enzimas, participa en el desarrollo embrionario, en la proliferación celular, en funciones inmunológicas y en el metabolismo. Ha habido un notable avance en la identificación de genes cuya expresión está regulada por la biotina. Asimismo, se han investigado los mecanismos moleculares a través de los cuales la biotina efectúa estas acciones. Estos estudios brindan nuevas claves para entender el papel de la biotina en la expresión genética, en el metabolismo, y en otras funciones biológicas de esta vitamina.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Biotin]]></kwd>
<kwd lng="en"><![CDATA[Metabolism]]></kwd>
<kwd lng="en"><![CDATA[Gene expression]]></kwd>
<kwd lng="es"><![CDATA[Biotina]]></kwd>
<kwd lng="es"><![CDATA[Metabolismo]]></kwd>
<kwd lng="es"><![CDATA[Expresión genética]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="justify"><font face="verdana" size="4">Rinc&oacute;n del residente</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="4"><b>Efecto de la biotina sobre la expresi&oacute;n gen&eacute;tica y el metabolismo</b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="3"><b>Effect of biotin upon gene expression and metabolism</b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>*Alonso Vilches&#150;Flores, "Cristina Fern&aacute;ndez&#150;Mej&iacute;a</b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i>* Unidad de Gen&eacute;tica de la Nutrici&oacute;n. Instituto Nacional de Pediatr&iacute;a.</i></font></p>     <p align="justify"><font face="verdana" size="2"><i>** Instituto de Investigaciones Biom&eacute;dicas, UNAM.</i></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Reimpresos:</b><i>    <br>   </i><i>Biol. Alonso Vilches&#150;Flores<b>    <br>   </b>Instituto de Investigaciones Biom&eacute;dicas, UNAM.    <br>   Unidad de Gen&eacute;tica de la Nutrici&oacute;n.     <br>   Instituto Nacional de Pediatr&iacute;a.    <br>   Torre de Investigaci&oacute;n, 4o. piso    <br>   Av. IM&Aacute;N No.1 Col. Insurgentes Cuicuilco    <br>   04530&#150;M&eacute;xico, D.F.    <br>   Fax: 5606&#150;3489</i>    ]]></body>
<body><![CDATA[<br>   Correo electr&oacute;nico: <a href="mailto:crisfer@biomedicas.unam.mx">crisfer@biomedicas.unam.mx</a></font></p>     <p align="justify"><font face="verdana" size="2">Recibido el 18 de octubre de 2004.     <br>   Aceptado el 5 de julio de 2005.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b><i>ABSTRACT</i></b></font></p>     <p align="justify"><font face="verdana" size="2"><i>During the last few decades, an increasing number of vitamin&#150;mediated effects has been discovered at the level of gene expression in addition to their well&#150;known roles as substrates and cofactors; the best recognized examples are the lipophilic vitamins A and D. Although little is known about water&#150;soluble vitamins as genetic modulators, there are increasing examples of their effect on gene expression. Biotin is a hydro soluble vitamin that acts as a prosthetic group of carboxylases. Besides its role as carboxylase cofactor, biotin affects several systemic functions such as development, immunity and metabolism. In recent years, significant progress has been made in the identification of genes that are affected by biotin at the transcriptional and post&#150;transcriptional levels as well as in the elucidation of mechanisms that mediate the effects of biotin on the gene expression. These studies bring new insights into biotin mediated gene expression and will lead to a better under&#150;standing of biotin roles in the metabolism and in systemic functions.</i></font></p>     <p align="justify"><font face="verdana" size="2"><b><i>Key words. </i></b><i>Biotin. Metabolism. Gene expression.</i></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>RESUMEN</b></font></p>     <p align="justify"><font face="verdana" size="2">En d&eacute;cadas recientes, diversas investigaciones han demostrado que las vitaminas afectan la expresi&oacute;n gen&eacute;tica. Los casos mejor estudiados son los de las vitaminas A y D. Existe menos informaci&oacute;n para las vitaminas hidrosolubles sobre su efecto en la expresi&oacute;n de los genes, sin embargo, se sabe que &eacute;stas tambi&eacute;n los modifican. La biotina es una vitamina hidrosoluble que act&uacute;a como grupo prost&eacute;tico de las carboxilasas. Adem&aacute;s de su funci&oacute;n como cofactor de enzimas, participa en el desarrollo embrionario, en la proliferaci&oacute;n celular, en funciones inmunol&oacute;gicas y en el metabolismo. Ha habido un notable avance en la identificaci&oacute;n de genes cuya expresi&oacute;n est&aacute; regulada por la biotina. Asimismo, se han investigado los mecanismos moleculares a trav&eacute;s de los cuales la biotina efect&uacute;a estas acciones. Estos estudios brindan nuevas claves para entender el papel de la biotina en la expresi&oacute;n gen&eacute;tica, en el metabolismo, y en otras funciones biol&oacute;gicas de esta vitamina.</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><b>Palabras clave. </b>Biotina. Metabolismo. Expresi&oacute;n gen&eacute;tica.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>INTRODUCCI&Oacute;N</b></font></p>     <p align="justify"><font face="verdana" size="2">La biotina es una vitamina hidrosoluble del complejo B cuya funci&oacute;n m&aacute;s conocida en los organismos eucariontes es la de participar como grupo prost&eacute;tico de las enzimas acetil&#150;CoA Carboxilasa (ACC)(E.C. 6.4.1.2), tanto de la isoforma citos&oacute;lica (ACC1) como de la mitocondrial (ACC2); y de las enzimas mitocondriales piruvato carboxilasa (PC)(E.C. 6.4.1.1); propionil&#150;CoA carboxilasa (PCC)(E.C. 6.4.1.3) y metilcrotonil&#150;CoA carboxilasa (MCC)(E.C.6.4.1.4).<sup>1</sup> Estas enzimas participan en diversos procesos metab&oacute;licos tales como la gluconeog&eacute;nesis, la lipog&eacute;nesis y el catabolismo de amino&aacute;cidos.</font></p>     <p align="justify"><font face="verdana" size="2">Adem&aacute;s de la participaci&oacute;n de la biotina en procesos metab&oacute;licos como grupo prost&eacute;tico, la biotina modifica funciones biol&oacute;gicas como la proliferaci&oacute;n celular, el desarrollo embrionario, funciones inmunol&oacute;gicas y el metabolismo a trav&eacute;s de un efecto sobre la expresi&oacute;n gen&eacute;tica.<sup>2,3</sup> En este art&iacute;culo se revisa el conocimiento actual de las acciones moleculares de esta vitamina sobre la expresi&oacute;n de genes, lo cual sirve como base en el entendimiento de la participaci&oacute;n de la biotina en el metabolismo y en diversas funciones biol&oacute;gicas.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>METABOLISMO DE LA BIOTINA EN MAM&Iacute;FEROS</b></font></p>     <p align="justify"><font face="verdana" size="2">Los mam&iacute;feros no pueden sintetizar la biotina, por lo que es necesario su consumo en la dieta diaria. La biotina se encuentra en los alimentos, en la mayor&iacute;a de ellos unida al grupo &epsilon;&#150;amino de una lisina formando el d&iacute;mero conocido como biocitina, p&eacute;ptidos biotinilados, o bien en forma libre.<sup>4</sup> Para su absorci&oacute;n se requiere romper este enlace semipept&iacute;dico por acci&oacute;n de la biotinidasa pancre&aacute;tica.<sup>5</sup> La biotina libre se absorbe por los enterocitos de la porci&oacute;n distal del duodeno y proximal del yeyuno, y posteriormente pasa al torrente sangu&iacute;neo. La entrada a las c&eacute;lulas se lleva a cabo a trav&eacute;s de un transportador m&uacute;ltiple de vitaminas dependiente de sodio (SMVT) que reconoce principalmente la porci&oacute;n del &aacute;cido val&eacute;rico de la biotina.<sup>6,7</sup> El SMVT es una prote&iacute;na transmembranal que funciona como simportador electroneutro, introduciendo a la biotina y al &aacute;cido pantot&eacute;nico junto con el sodio, a favor de un gradiente de concentraci&oacute;n.</font></p>     <p align="justify"><font face="verdana" size="2">Las carboxilasas son sintetizadas como apocarboxilasas, sin actividad enzim&aacute;tica, en el citoplasma. Al un&iacute;rseles la biotina covalentemente por acci&oacute;n de la holocarboxilasa sintetasa, se forma la prote&iacute;na activa u holoenzima.<sup>8</sup> Esta reacci&oacute;n se lleva a cabo en dos etapas: en la primera la biotina se activa al reaccionar con una mol&eacute;cula de ATP, formando el intermediario biotinil&#150;5'&#150;adenilato. En la segunda etapa el grupo biotinilo se transfiere a la apoenzima form&aacute;ndose un enlace semipept&iacute;dico con un residuo de lisina, localizada dentro de una secuencia Met&#150;Lys&#150;Met altamente conservada en todas las apocarboxilasas.<sup>9</sup> La biotina, como grupo prost&eacute;tico de las carboxilasas, participa en el mecanismo de transferencia de un grupo carboxilo activado al sustrato correspondiente.<sup>10</sup></font></p>     <p align="justify"><font face="verdana" size="2">Posteriormente, la prote&oacute;lisis de las holocarboxila&#150;sas libera residuos de lisina unidos covalentemente a la biotina (biocitina). Este enlace se rompe por acci&oacute;n de la biotinidasa, y de este modo la biotina puede ser reciclada e integrarse como grupo prost&eacute;tico a nuevas carboxilasas sintetizadas, o bien puede catabolizarse formando otros productos derivados y excretarse. La s&iacute;ntesis de las holocarboxilasas y su catabolismo se denomina ciclo de la biotina.</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>EFECTO DE LA BIOTINA SOBRE LA EXPRESI&Oacute;N GEN&Eacute;TICA</b></font></p>     <p align="justify"><font face="verdana" size="2">Observaciones que se realizaron en la d&eacute;cada de 1960 suger&iacute;an que la biotina interven&iacute;a en diversas funciones biol&oacute;gicas independientemente de su acci&oacute;n como grupo prost&eacute;tico de las carboxilasas.<sup>11&#150;</sup><sup>13 </sup>En la actualidad se ha establecido que, adem&aacute;s de su funci&oacute;n cl&aacute;sica como grupo prost&eacute;tico, la biotina modifica la expresi&oacute;n g&eacute;nica, tanto a nivel de la transcripci&oacute;n como de la traducci&oacute;n. Este efecto es an&aacute;logo al de otras vitaminas que, aparte de sus funciones como sustratos y cofactores, regulan la expresi&oacute;n gen&eacute;tica. Los ejemplos mejor estudiados son los de las vitaminas A y D, que act&uacute;an como ligandos de receptores nucleares de la superfamilia de receptores hormonales y de esta manera, afectan diversas funciones como la morfog&eacute;nesis, inmunidad, diferenciaci&oacute;n y metabolismo.<sup>14</sup></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>EFECTOS DE LA BIOTINA SOBRE LA TRANSCRIPCI&Oacute;N</b></font></p>     <p align="justify"><font face="verdana" size="2">La biotina participa en la regulaci&oacute;n de la transcripci&oacute;n de diversos genes. Esto se ha demostrado tanto para las enzimas que requieren de la vitamina como grupo prost&eacute;tico y sustrato, como son la holocarboxilasa sintetasa (HCS),<sup>1516</sup> la acetil coenzima A carboxilasa &#150;1 (ACC&#150;1), la propionil coenzima A carboxilasa &#150;A (PCCA),<sup>16</sup> como para prote&iacute;nas que no la requieren como cofactor; entre estas &uacute;ltimas se han identificado a la glucocinasa hep&aacute;tica,<sup>17</sup> la fosfoenol&#150;piruvato carboxicinasa hep&aacute;tica,<sup>18</sup> la glucocinasa pancre&aacute;tica,<sup>19,20</sup> la insulina,<sup>20,21</sup> el factor transcripcional PDX&#150;1,<sup>21</sup> la interleucina 2 y el receptor de interleucina 2,<sup>22,23</sup> los factores transcripcionales NF&#150;kB,<sup>2</sup> N&#150;myc, c&#150;myb, N&#150;ras y raf.<sup>24</sup> La acci&oacute;n de la biotina sobre la expresi&oacute;n gen&eacute;tica parece ser muy amplia: en un estudio de microarreglos en c&eacute;lulas mononucleadas de sangre perif&eacute;rica humana, se encontr&oacute; que la biotina afecta positivamente la expresi&oacute;n de 139 genes, mientras que disminuye la de otros 131.<sup>25</sup> Los mecanismos moleculares a trav&eacute;s de los cuales la biotina produce su acci&oacute;n sobre la expresi&oacute;n de algunas de estas prote&iacute;nas han sido estudiados, y se describen en secciones posteriores de esta revisi&oacute;n.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Efectos de la biotina sobre la traducci&oacute;n</b></font></p>     <p align="justify"><font face="verdana" size="2">La biotina afecta la expresi&oacute;n de genes a nivel pos&#150;transcripcional. Investigaciones efectuadas por el grupo de Stacker,<sup>26&#150;</sup><sup>30</sup> encontraron que la vitamina modifica la expresi&oacute;n del receptor de asialoglicoproteinas a trav&eacute;s de una v&iacute;a que requiere de GMPc y de la prote&iacute;na cinasa G (PKG),<sup>26,27</sup> lo cual conduce a un aumento en la fosforilaci&oacute;n<sup>28,</sup><sup>29</sup> y activaci&oacute;n de la subunidad a&#150;COP,<sup>30</sup> una prote&iacute;na coatom&eacute;rica de 140kDa asociada a un complejo de traducci&oacute;n en la regi&oacute;n <i>trans </i>de la membrana del Golgi. Esta subunidad se une a elementos <i>cis </i>localizados en un fragmento de 187 nucle&oacute;tidos de la regi&oacute;n no traducida 5' del ARN mensajero del receptor, repercutiendo de manera positiva sobre la traducci&oacute;n de esta prote&iacute;na (<a href="/img/revistas/ric/v57n5/a9f1.jpg" target="_blank">Figura 1</a>). Por un mecanismo postranscripcional que requiere de la activaci&oacute;n de la PKG, la biotina tambi&eacute;n regula la expresi&oacute;n del receptor de insulina.<sup>31</sup></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><b>Mecanismos moleculares de la biotina</b></font></p>     <p align="justify"><font face="verdana" size="2">En los &uacute;ltimos a&ntilde;os han comenzado a delinearse los mecanismos moleculares a trav&eacute;s de los cuales la biotina modifica la expresi&oacute;n de genes. Se han identificado diferentes v&iacute;as, no necesariamente excluyentes, que podr&iacute;an participar en la acci&oacute;n gen&eacute;tica de la vitamina:</font></p>     <p align="justify"><font face="verdana" size="2">1. Activaci&oacute;n de la guanilato ciclasa soluble.</font></p>     <p align="justify"><font face="verdana" size="2">2. Biotinilaci&oacute;n de histonas.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Activaci&oacute;n de la guanilato ciclasa soluble</b></font></p>     <p align="justify"><font face="verdana" size="2">Estudios pioneros de Vesely,<sup>32</sup> en 1982, descubrieron que la adici&oacute;n de biotina a extractos celulares aumentaba la actividad de la guanilato ciclasa soluble. Posteriormente, Spence y Koudel ka,<sup>33</sup>encontraron que el aumento producido por la biotina en la actividad de la glucocinasa hep&aacute;tica estaba precedido por un incremento en las concentraciones intracelulares de GMPc, lo que suger&iacute;a que la biotina ejerc&iacute;a su efecto g&eacute;nico a trav&eacute;s de este segundo mensajero. A partir de entonces, diversos estudios han identificado que un denominador com&uacute;n en el efecto de la biotina sobre la expresi&oacute;n gen&eacute;tica involucra el incremento en la actividad de la guanilato ciclasa soluble (GCs), la elevaci&oacute;n de las concentraciones de guanosil monofosfato c&iacute;clico (GMPc) intracelular, y la participaci&oacute;n de la prote&iacute;nacinasa G (PKG).<sup>16,27,31</sup></font></p>     <p align="justify"><font face="verdana" size="2">Sol&oacute;rzano <i>et al. </i>han propuesto que el compuesto biotinil&#150;AMP es el v&iacute;nculo en la cascada de fosforilaciones involucradas en la regulaci&oacute;n de la expresi&oacute;n gen&eacute;tica por la biotina. Este compuesto est&aacute; formado por la holocarboxilasa sintetasa en la primera etapa de su acci&oacute;n catal&iacute;tica (ver secci&oacute;n Metabolismo de la biotina en mam&iacute;feros). Estos investigadores encontraron que la regulaci&oacute;n de la expresi&oacute;n de la acetyl&#150;CoA carboxilasa 1, la propionilCoA carboxilasa y de la propia holocarboxilasa sintetasa requiere de la actividad enzim&aacute;tica de la holocarboxilasa sintetasa. Con base en sus resultados proponen que el biotinil&#150;AMP, por un mecanismo a&uacute;n no conocido, activa la guanilato ciclasa soluble, y que, de esta manera, se incrementa el contenido de GMPc, que a su vez activa a la PKG, favoreciendo as&iacute; una serie de fosforilaciones que modifican la expresi&oacute;n de los genes (<a href="/img/revistas/ric/v57n5/a9f2.jpg" target="_blank">Figura 2</a>).</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Biotinilaci&oacute;n de histonas</b></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">Otro mecanismo molecular que podr&iacute;a estar involucrado en el efecto de la vitamina sobre la expresi&oacute;n gen&eacute;tica es la biotinilaci&oacute;n de histonas. Diversas observaciones en las d&eacute;cadas de los 60's y 70's suger&iacute;an acciones nucleares de la biotina: la presencia de biotina en el n&uacute;cleo,<sup>34</sup> las alteraciones en animales deficientes en biotina en la fosforilaci&oacute;n, metilaci&oacute;n y ace&#150;tilaci&oacute;n de las histonas, y en la asociaci&oacute;n de estas &uacute;ltimas con el DNA<sup>35</sup> indicaban un posible efecto de la vitamina sobre la cromatina. Posteriormente, estudios <i>in vitro </i>demostraron que las histonas son susceptibles a ser biotiniladas,<sup>36</sup> lo que otorgaba una explicaci&oacute;n a la presencia de biotina en el n&uacute;cleo y a la relaci&oacute;n entre biotina e histonas. En a&ntilde;os recientes se ha encontrado que, efectivamente, las histonas en las c&eacute;lulas se encuentran biotiniladas<sup>37&#150;</sup><sup>39</sup> y se ha propuesto que esta modificaci&oacute;n covalente, similar a modificaciones covalentes como la metilaci&oacute;n y/o acetilaci&oacute;n de las histonas, podr&iacute;an ser parte de los mecanismos a trav&eacute;s de los cuales la biotina modifica la expresi&oacute;n gen&eacute;tica. La presencia en el n&uacute;cleo de dos enzimas claves en el metabolismo de la biotina, la biotinidasa y la holocarboxilasa sintetasa,<sup>40,41</sup> as&iacute; como su demostrada capacidad de biotinilar histonas,<sup>42</sup> apoyan igualmente esta hip&oacute;tesis. Recientemente, Narang, <i>et al.</i><sup>43</sup> encontraron que la holocarboxilasa sintetasa est&aacute; asociada con la cromatina y la l&aacute;mina nuclear, y que durante la mitosis se encuentra distribuida en estructuras en forma de anillo. Adem&aacute;s, los fibroblastos de pacientes con deficiencia en la enzima presentan menos histonas biotiniladas que los fibroblastos de individuos no deficientes. Entre las funciones relacionadas con la biotinilaci&oacute;n de histonas se encuentran el incremento en la abundancia de &eacute;stas durante la proliferaci&oacute;n celular de linfocitos polimorfonucleares,<sup>42</sup> los cambios en la biotinilaci&oacute;n de histonas durante el ciclo celular<sup>41</sup> y el incremento en la biotinilaci&oacute;n de histonas producidas por da&ntilde;o al DNA causado por luz ultravioleta.<sup>39</sup> Estas funciones sugieren que la biotinilaci&oacute;n de histonas podr&iacute;a estar ligada a la reparaci&oacute;n y/o replicaci&oacute;n del DNA.</font></p>     <p align="justify"><font face="verdana" size="2">En resumen, hasta el momento las piezas que forman parte de los mecanismos involucrados en las acciones gen&eacute;ticas de la biotina son: la formaci&oacute;n de biotinil&#150;AMPc por la holocarboxilasa sintetasa, las modificaciones en el contenido de GMPc y la biotinilaci&oacute;n de histonas. En la actualidad se ha establecido que las hormonas modifican la expresi&oacute;n de genes,<sup>44 </sup>y ha sido precisamente el estudio de la acci&oacute;n hormonal lo que ha contribuido a la comprensi&oacute;n del efecto de los nutrimentos en la regulaci&oacute;n gen&eacute;tica. Se sabe que los efectos de las hormonas esteroides ocurren con diferentes latencias y duraci&oacute;n variable, y que las hormonas pueden ejercer m&aacute;s de un efecto a trav&eacute;s de varios mecanismos que involucran la participaci&oacute;n de diferentes mol&eacute;culas en distintos compartimentos celulares.<sup>44</sup> Al igual que lo observado en la acci&oacute;n gen&eacute;tica de la biotina: el metabolismo del efector, la presencia de prote&iacute;nas de uni&oacute;n en el n&uacute;cleo, as&iacute; como la modificaci&oacute;n de la cromatina son componentes de la regulaci&oacute;n de las hormonas esteroides sobre la expresi&oacute;n gen&eacute;tica.<sup>45</sup></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>ACCI&Oacute;N DE LA BIOTINA SOBRE DIVERSAS FUNCIONES BIOL&Oacute;GICAS</b></font></p>     <p align="justify"><font face="verdana" size="2">La proliferaci&oacute;n celular,<sup>42,46</sup> la funci&oacute;n inmunol&oacute;gica,<sup>47,</sup><sup>48</sup> el desarrollo embrionario,<sup>49&#150;</sup><sup>52</sup> y el metabolismo de carbohidratos y de l&iacute;pidos se ven afectados por la biotina. Estos efectos parecen estar mediados por la acci&oacute;n de la vitamina sobre la expresi&oacute;n de genes. Resulta interesante se&ntilde;alar que fueron los estudios de la biotina sobre el metabolismo de los carbohidratos los que sentaron las bases para el descubrimiento del efecto de la biotina sobre la expresi&oacute;n gen&eacute;tica y que muchos de los genes regulados por la biotina participan a su vez en la regulaci&oacute;n del metabolismo de los carbohidratos.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Efectos de la biotina sobre el metabolismo de los carbohidratos</b></font></p>     <p align="justify"><font face="verdana" size="2">Los efectos de la biotina sobre el metabolismo han sido puestos de manifiesto tanto <i>in vivo </i>como <i>in vitro </i>en diferentes condiciones fisiol&oacute;gicas:</font></p>     <p align="justify"><font face="verdana" size="2">&bull; De deficiencia de biotina.</font></p>     <p align="justify"><font face="verdana" size="2">&bull; En condiciones fisiol&oacute;gicas normales.</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&bull; En estado diab&eacute;tico.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Efecto de la deficiencia de biotina</b></font></p>     <p align="justify"><font face="verdana" size="2">Las primeras evidencias que sugirieron que la biotina interven&iacute;a en el metabolismo de los carbohidratos y permitieron el descubrimiento del efecto de la biotina sobre la expresi&oacute;n gen&eacute;tica fueron reportadas por Dakshinamurti, <i>et al.</i><sup>53</sup> Este grupo encontr&oacute; que las ratas deficientes en biotina presentaban curvas de tolerancia significativamente m&aacute;s elevadas que los animales control, y que el contenido de gluc&oacute;geno hep&aacute;tico y la fosforilaci&oacute;n de la glucosa eran menores en los animales deficientes de biotina.<sup>54</sup> Estudios posteriores mostraron que las anomal&iacute;as en el metabolismo de carbohidratos en ratas deficientes de la vitamina se deb&iacute;an a una disminuci&oacute;n en la actividad de la glucocinasa hep&aacute;tica,<sup>55</sup> enzima clave en la captaci&oacute;n posprandial de glucosa por el h&iacute;gado. El desarrollo de nuevas tecnolog&iacute;as de biolog&iacute;a molecular permiti&oacute; que Chauhan y Dakshinamurti,<sup>17</sup> demostraran que el efecto de la biotina sobre la glucocinasa hep&aacute;tica se produce a trav&eacute;s de un aumento en la transcripci&oacute;n del gen. La deficiencia de biotina igualmente sirvi&oacute; como herramienta para revelar que la biotina participa en la traducci&oacute;n del receptor de la insulina: En la l&iacute;nea celular HuH7 derivada de hepatocitos humanos cultivadas en ausencia de biotina se encontr&oacute; que la vitamina regula la expresi&oacute;n del receptor de insulina;<sup>31</sup> el mecanismo de acci&oacute;n indica que se requiere la activaci&oacute;n de la PKG, a trav&eacute;s de una elevaci&oacute;n del GMPc.</font></p>     <p align="justify"><font face="verdana" size="2">La deficiencia de biotina afecta el metabolismo del islote pancre&aacute;tico. Estudios realizados en nuestro laboratorio con ratas deficientes de biotina mostraron que la carencia de la vitamina produce una disminuci&oacute;n tanto de la actividad como de la abundancia de ARN mensajero de la glucocinasa pancre&aacute;tica, enzima clave en el proceso que permite a la c&eacute;lula beta secretar insulina en respuesta a la glucosa.<sup>20</sup> Nuestros estudios igualmente encontraron que los islotes pancre&aacute;ticos aislados de ratas deficientes de biotina, presentan una secreci&oacute;n disminuida de la insulina en respuesta a la glucosa. Este detrimento en la secreci&oacute;n de la hormona en respuesta a la glucosa se observ&oacute; igualmente en la perfusi&oacute;n <i>in vivo </i>de islotes pancre&aacute;ticos aislados de ratas deficientes de biotina.<sup>56</sup> Tambi&eacute;n se ha reportado que la deficiencia de biotina en pollos afecta las concentraciones de glucag&oacute;n s&eacute;rico.<sup>57</sup></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Efectos de la biotina sobre </b><b>el metabolismo de los carbohidratos </b><b>en diferentes estados fisiol&oacute;gicos</b></font></p>     <p align="justify"><font face="verdana" size="2">La administraci&oacute;n de biotina es capaz de modificar el metabolismo de los carbohidratos en condiciones no deficientes de la vitamina. Estudios efectuados en ratas demostraron que la administraci&oacute;n de dosis farmacol&oacute;gicas de vitamina (1 mg/kg) incrementa la actividad de la glucocinasa hep&aacute;tica. Este efecto se observ&oacute; tanto en condiciones posprandiales, situaci&oacute;n metab&oacute;lica en la que la glucocinasa se encuentra normalmente aumentada, como en condiciones metab&oacute;licas en las que la actividad de la enzima hep&aacute;tica se encuentra normalmente disminuida como lo es el ayuno o la dieta rica en grasas.<sup>54,</sup><sup>55,58 </sup>La administraci&oacute;n de biotina a dosis de 1 mg/kg produce un incremento prematuro en la s&iacute;ntesis de la glucocinasa hep&aacute;tica en ratas lactantes, periodo en el cual esta enzima no se encuentra presente.<sup>55</sup> En ratas pre&ntilde;adas la administraci&oacute;n de altas dosis de biotina disminuye la cantidad de gluc&oacute;geno en &uacute;tero y placenta, as&iacute; como la actividad de la glucosa&#150;6&#150;fosfato deshidrogenasa en ovario, &uacute;tero e h&iacute;gado.<sup>49</sup></font></p>     <p align="justify"><font face="verdana" size="2">En cultivos <i>in vitro </i>de c&eacute;lulas aisladas de animales no deficientes de la vitamina tambi&eacute;n se ha encontrado que la biotina tiene la facultad de regular la expresi&oacute;n gen&eacute;tica. Spence y Kodelka<sup>33</sup> encontraron que en hepatocitos aislados de ratas normales la biotina incrementa la actividad de la glucocinasa y este aumento se encuentra precedido por un incremento en las concentraciones intracelulares de GMPc. Estudios en nuestro laboratorio encontraron que en cultivos primarios de islotes de ratas normales, el tratamiento con biotina aumenta la actividad y la expresi&oacute;n de la glucocinasa pancre&aacute;tica.<sup>20</sup> Este efecto tambi&eacute;n se observa en la l&iacute;nea celular pancre&aacute;tica RIN1046&#150;38.<sup>19</sup> Nuestros estudios y los de otros investigadores encontraron que la expresi&oacute;n del gen de la insulina y la secreci&oacute;n de esta hormona en respuesta a la glucosa se incrementan con el tratamiento con biotina.<sup>59</sup> Recientemente se report&oacute; que la biotina aumenta la expresi&oacute;n del factor transcripcional PDX&#150;1, el cual es determinante en el desarrollo pancre&aacute;tico<sup>21</sup> y en la expresi&oacute;n de genes que participan en funciones espec&iacute;ficas del islote de Langerhans.</font></p>     <p align="justify"><font face="verdana" size="2">El efecto de la biotina sobre el metabolismo de los carbohidratos se ha observado en levaduras. En cultivos de <i>Saccharomyces cerevisiae </i>se encontr&oacute; que en un medio con alto contenido de biotina se aumentan las actividades de la piruvato carboxilasa y de la isocitrato liasa mientras que disminuye el contenido de gluc&oacute;geno,<sup>60</sup> lo que sugiere que el efecto de la biotina sobre el metabolismo apareci&oacute; desde etapas tempranas de la evoluci&oacute;n.</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Efectos de la biotina en modelos diab&eacute;ticos</b></font></p>     <p align="justify"><font face="verdana" size="2">Diversos estudios han encontrado que la administraci&oacute;n de dosis farmacol&oacute;gicas de biotina disminuyen la hiperglucemia: pacientes con diabetes tipo 1 tratados durante una semana con biotina (sin recibir insulina ex&oacute;gena), disminuyeron sus concentraciones de glucosa en ayuno.<sup>61</sup> En un estudio en pacientes japoneses diab&eacute;ticos tipo 2,<sup>62</sup> se encontr&oacute; que la administraci&oacute;n oral de 9 mg de biotina diariamente durante un mes disminuy&oacute; las concentraciones sangu&iacute;neas en ayuno de glucosa, piruvato y lactato; al suspender la administraci&oacute;n de la vitamina se produjo un retorno a las concentraciones hipergluc&eacute;micas observadas antes del inicio del tratamiento. Nuestro grupo ha encontrado que en pacientes diab&eacute;ticos tipo 2, el tratamiento con 15 mg/d&iacute;a de biotina durante 28 d&iacute;as disminuye el &aacute;rea de las curvas de tolerancia a la glucosa.<sup>63</sup></font></p>     <p align="justify"><font face="verdana" size="2">En modelos animales con diabetes tipo 2 tambi&eacute;n se ha reportado que la biotina disminuye la hiperglucemia. En ratones de la cepa KK no obesos y en las ratas OLETF que presentan obesidad espont&aacute;nea, se observ&oacute; una disminuci&oacute;n de la hiperglucemia y en la curva de tolerancia a la glucosa en respuesta al tratamiento con dosis farmacol&oacute;gicas de la vitamina.<sup>27,</sup><sup>28</sup> Estudios en modelos experimentales con ratas diab&eacute;ticas generadas por el tratamiento con alloxana o con estreptozotocina encontraron que la biotina aumenta significativamente la actividad de laglucocinasahep&aacute;tica.<sup>64,65</sup> El tratamiento con la vitamina igualmente increment&oacute; las actividades de las enzimas glucol&iacute;ticas fosfofructocinasa y piruvato cinasa. En otros estudios en ratas cuya diabetes fue inducida por estreptozotocina, la biotina disminuy&oacute; en m&aacute;s de 50% la transcripci&oacute;n de la fosfoenolpiruvato carboxicinasa, enzima limitante de la gluconeog&eacute;nesis.<sup>66</sup></font></p>     <p align="justify"><font face="verdana" size="2">En resumen, el estado nutricional de biotina afecta el metabolismo de los carbohidratos; la deficiencia de biotina produce un efecto hiperglucemiante en tanto que dosis farmacol&oacute;gicas de biotina revierten la hiperglucemia. Este efecto concuerda con la acci&oacute;n de la biotina sobre la expresi&oacute;n de genes que favorecen la captaci&oacute;n y el catabolismo de la glucosa, ejemplo de ellos son la glucocinasa hep&aacute;tica y pancre&aacute;tica, la insulina y el receptor de insulina; en tanto que disminuye la expresi&oacute;n de la enzima fosfoenolpiruvato carboxicinasa, enzima de acci&oacute;n hiperglucemiante que regula la gluconeog&eacute;nesis.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>La biotina en el metabolismo de l&iacute;pidos</b></font></p>     <p align="justify"><font face="verdana" size="2">Existen menos conocimientos del efecto de la biotina sobre el metabolismo de l&iacute;pidos. Dado que la biotina interviene directamente como cofactor de la ACC (1 y 2), enzima crucial en la s&iacute;ntesis y oxidaci&oacute;n de &aacute;cidos grasos, existe una relaci&oacute;n directa entre la deficiencia de biotina y el metabolismo de l&iacute;pidos<sup>67,68</sup> a trav&eacute;s de su funci&oacute;n como grupo prost&eacute;tico. Sin embargo, en condiciones no deficientes de la vitamina, se han descrito efectos de la biotina que podr&iacute;an estar mediados a trav&eacute;s de su acci&oacute;n en la regulaci&oacute;n de genes.</font></p>     <p align="justify"><font face="verdana" size="2">En condiciones normales de biotina, se ha observado que el tratamiento con dosis farmacol&oacute;gicas de la vitamina puede modificar las concentraciones de triglic&eacute;ridos y colesterol. En pacientes con ateroesclerosis e hipercolesterolemia la administraci&oacute;n de 5 mg de biotina durante cuatro semanas produjo un decremento significativo sobre las concentraciones de colesterol total; tambi&eacute;n se observ&oacute; una disminuci&oacute;n, aunque no significativa, de las concentraciones de LDL.<sup>69</sup> Estudios en voluntarios sanos muestran que la administraci&oacute;n de 0.9 mg/d&iacute;a de biotina durante 71 d&iacute;as redujo las concentraciones de l&iacute;pidos plasm&aacute;ticos.<sup>70</sup> En nuestro laboratorio se encontr&oacute; que el tratamiento con 5 mg de biotina tres veces al d&iacute;a disminuye las concentraciones de triglic&eacute;ridos plasm&aacute;ticos en pacientes con hipertrigliceridemia.<sup>63</sup> En estudios con modelos animales tambi&eacute;n se ha observado que la biotina modifica la hiperlipidemia. En la cepa de ratas BHE con predisposici&oacute;n gen&eacute;tica para desarrollar elevadas concentraciones sangu&iacute;neas de glucosa y de l&iacute;pidos, el tratamiento con biotina disminuy&oacute; las concentraciones plasm&aacute;ticas de l&iacute;pidos.<sup>71,72</sup></font></p>     <p align="justify"><font face="verdana" size="2">Se conoce poco sobre la regulaci&oacute;n gen&eacute;tica de las enzimas participantes en el metabolismo de l&iacute;pidos por la biotina. Sin embargo, recientemente, Levert, <i>et al.</i><sup>73</sup> encontraron que en la l&iacute;nea celular de adipocitos 3T3&#150;L1 un an&aacute;logo cloroacetilado de biotina (CABI), adem&aacute;s de inhibir la actividad de la acetil&#150;CoA&#150;carboxilasa, reduce la expresi&oacute;n de los factores de diferenciaci&oacute;n STAT 1 y STAT 5a y de PPARy, factores transcripcionales que juegan un papel muy importante en el metabolismo de l&iacute;pidos. Estas primeras evidencias sugieren que el mecanismo de acci&oacute;n a trav&eacute;s del cual la biotina afecta al metabolismo de los l&iacute;pidos podr&iacute;a realizarse sobre la transcripci&oacute;n de estos genes.</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>CONCLUSI&Oacute;N</b></font></p>     <p align="justify"><font face="verdana" size="2">El papel de la biotina en la regulaci&oacute;n gen&eacute;tica se ha confirmado en diversos estudios, demostrando que esta vitamina hidrosoluble tiene otras funciones biol&oacute;gicas adem&aacute;s de su tradicional papel como grupo prost&eacute;tico de las enzimas carboxilasas. El avance de las t&eacute;cnicas en las &aacute;reas de biolog&iacute;a molecular y celular ha permitido conocer las bases moleculares de los efectos de la biotina sobre el metabolismo, la reproducci&oacute;n y la funci&oacute;n inmunol&oacute;gica; sin embargo, en la actualidad todav&iacute;a quedan muchos interrogantes pendientes: &iquest;por qu&eacute; mecanismo el biotinil&#150;AMP activa a la guanilato ciclasa soluble?, &iquest;qu&eacute; factores existen entre la cascada de se&ntilde;ales del GMPc y la regulaci&oacute;n de la expresi&oacute;n gen&eacute;tica?, &iquest;c&oacute;mo participa la biotinilaci&oacute;n de histonas en la reparaci&oacute;n y replicaci&oacute;n del DNA?, &iquest;interviene la biotinilaci&oacute;n de histonas en la expresi&oacute;n de genes?, &iquest;hay otros intermediarios moleculares que participan en el mecanismo de acci&oacute;n de la biotina?, &iquest;cu&aacute;ntos genes m&aacute;s y qu&eacute; otras funciones biol&oacute;gicas son afectados por la presencia o ausencia de biotina? Estas preguntas y otras que seguramente saldr&aacute;n de la investigaci&oacute;n de estas inc&oacute;gnitas, hacen del estudio de la biotina como efector de la expresi&oacute;n gen&eacute;tica un &aacute;rea excitante a descubrir.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>REFERENCIAS</b></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">1. Chapman   A,   Cronan   J.   Molecular  biology  of attachment  to proteins. <i>J Nutr </i>1999;  129: 447S&#150;484S.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765879&pid=S0034-8376200500050000900001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">2. Rodriguez&#150;Melendez  R,  Zempleni  J.   Regulation  of gene  expression by biotin (review). <i>J Nutr Biochem </i>2003;   14:  680&#150;90.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765880&pid=S0034-8376200500050000900002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">3. Pacheco&#150;Alvarez  D,  Solorzano  S,  Le&oacute;n  del  Rio  A.  Biotin in metabolism  and  its  relationship to  human  disease. <i>Arch Med Res </i>2002; 33: 439&#150;47.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765881&pid=S0034-8376200500050000900003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">4. Dakshinamurti  K,  Chauhan J.  Biotin&#150;binding proteins.  In:  Vitamin  receptors:   vitamins   as   ligands   in   cell   communication. EEUU: Cambridge University Press;  1994, p. 200&#150;49.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765882&pid=S0034-8376200500050000900004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">5. Hymes J, Wolf B.  Biotinidase and its roles in biotin metabolism. <i>Clin Chim Acta </i>1996; 225: 1&#150;11.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765883&pid=S0034-8376200500050000900005&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">6. Cohen N, Thomas M.  Biotin transport into fully differentiated 3T3&#150;L1    cells. <i>Biochim   Biophys   Res   Comm    </i>1982;    108(4): 1508&#150;16.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765884&pid=S0034-8376200500050000900006&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">7. Chatterjee N, Kumar C, Ortiz A, Rubin S,  Said H.  Molecular mechanism of the intestinal biotin transport process. <i>Am J Physiol  </i>1999;  277(46):  C605&#150;C613.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765885&pid=S0034-8376200500050000900007&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">8. Chapman&#150;Smith A,  Cronan JE  Jr.  The  enzimatic biotinylation of proteins: a post&#150;traslational modification of exceptional specificy. <i>Trends Biochem Sci </i>1999; 24: 359&#150;63.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765886&pid=S0034-8376200500050000900008&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">9. Lamhonwah   AM,   Quan   F,   Gravel   RA.   Secuence   homology around  the  biotin&#150;binding  site   of human  propionyl&#150;CoA  carboxylase   and   pyruvate   carboxilase. <i>Arch   Biochem   Biophys </i>1987;  254:  631&#150;6.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765887&pid=S0034-8376200500050000900009&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">10. Jitrapakdee S, Wallace JC.  The biotin enzyme family: conserved structural motifs and domain rearrangements. <i>Curr Protein Pept Sci </i>2003; 4(3): 217&#150;29.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765888&pid=S0034-8376200500050000900010&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">11. Dakshinamurti   K,   Cheah&#150;Tan  C.   Biotin&#150;mediated  syntesis   of hepatic  glucokinase  in the  rat. <i>Arch Biochem Biophys   </i>1968; 127:   17&#150;21.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765889&pid=S0034-8376200500050000900011&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">12. Dakshinamurti K, Modi VV, Mistry SP.  Some aspects of carbohydrates  metabolism  in biotin&#150;deficient rats. <i>Proc Soc Exp Biol Med </i>1968;   127(2):  396&#150;400.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765890&pid=S0034-8376200500050000900012&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">13. Deodhar AD, Mistry SP. Gluconeogenesis in biotin deficiency: In vivo  synthesis  of pyruvate holocarboxylase  in biotin  deficient rat  liver. <i>Biochem Biophys Res  Comm   </i>1969;  34(6): 755&#150;9.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765891&pid=S0034-8376200500050000900013&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">14. Balmer  JE,  Blomhoff R.   Gene  expression regulation by retinoic acid, (review). <i>J Lipid Res. </i>2002; 43(11):  1773&#150;808.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765892&pid=S0034-8376200500050000900014&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">15. Rodriguez&#150;Melendez   R,   Cano   S,   M&eacute;ndez   ST,   Velazquez   A. Biotin regulates the genetic expression of holocarboxylase synthetase  and  mitochondrial  carboxylases  in rats. <i>J Nutr </i>2001; 131:    1909&#150;13.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765893&pid=S0034-8376200500050000900015&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">16. Solorzano&#150;Vargas S, Pacheco&#150;Alvarez D, Le&oacute;n&#150;Del&#150;R&iacute;o A. Holocarboxylase  synthetase   is   an  obligate  participant  in  biotin&#150;mediated  regulation  of its   own  expression  and  of biotin&#150;depend  carboxylases   mRNA  levels   in  human   cells. <i>Proc Natl Acad Sci </i>2002;  99(8):  5325&#150;30.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765894&pid=S0034-8376200500050000900016&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">17. Chauhan   J,   Dakshinamurti   KC.   Transcriptional  regulation  of the  glucokinase  gene  by biotin  in  starved rats. <i>J Biol Chem </i>1991;   266:   10035&#150;8.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765895&pid=S0034-8376200500050000900017&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">18. Dakshinamurti   K,   Li   W.   Transcriptional   regulation   of  liver phosphoenolpyruvate  carboxykinase by biotin in diabetic rats. <i>Mol Cell Biochem </i>1994;  132:  127&#150;32.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765896&pid=S0034-8376200500050000900018&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">19. Borboni P, Magnaterra R, Rabini RA, Staffolanni R, Porzio O, Sesti G, Fusco A, Mazzanti L, Lauro R, Marlier JNJL. Effect of biotin  on  glucokinase   activity,   mRNA  expression  and insulin release in cultured 6&#150;cell. <i>Acta Diabetol  </i>1996;  33: 154&#150;8.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765897&pid=S0034-8376200500050000900019&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">20. Romero&#150;Navarro G, Cabrera&#150;Valladares G, German MS, Matschinsky FM, Wang J, Fernandez&#150;Mejia C. Biotin regulation of pancreatic glucokinase and insulin in primary cultured rat islets and in biotin deficient rats. <i>Endocrinology </i>1999;  140: 4595&#150;4600.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765898&pid=S0034-8376200500050000900020&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">21. Yoshikawa   H,   Tajiri   Y,   Sako   Y,   Hashimoto   T,   Umeda   F, Nawata H. Effects of biotin on glucotoxycity of lipotoxicity in rat pancreatic islets. <i>Metabolism </i>2002; 51(2):  163&#150;8.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765899&pid=S0034-8376200500050000900021&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">22. Rodriguez&#150;Melendez R, Camporeale G, Griffin JB, Zempleni J. Interleukin&#150;2   receptor   y&#150;dependent   endocytosis    depends    on biotin  in Jurkat cells. <i>Am J Physiol Cell Physiol </i>2003;  284: C415&#150;C421.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765900&pid=S0034-8376200500050000900022&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">23. Manthey KC, Griffin JB, Zampleni J. Biotin supply affects expression   of  biotin  transporters,   biotinylation   of  carboxilases and metabolism of interleukin&#150;2 in Jurkat cells. <i>J Nutr </i>2002; 132(5):    887&#150;92.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765901&pid=S0034-8376200500050000900023&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">24. Scheerger  SB,  Zempleni  J.   Expression  of oncogenes  depends on biotin in human small cell lung cancer cells NCI&#150;H69. <i>Int J Vitam Nutr Res </i>2003; 73(6): 461&#150;7.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765902&pid=S0034-8376200500050000900024&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">25. Wiedmann  S,  Rodriguez&#150;Melendez  R,  Ortega&#150;Cuellar  D,  Zempleni J. Clusters of biotin&#150;responsive genes in human peripheral blood mononuclear cells. <i>J Nutr Biochem </i>2004;  15(7): 433&#150;9.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765903&pid=S0034-8376200500050000900025&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">26. Collins JC, Paietta E, Green R, Morell AG, Stockert RJ. Biotin&#150;dependent   expression   of  the   asialoglycoprotein   receptor   in HepG2 cells. <i>J Biol Chem </i>1988; 263:  11280&#150;3.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765904&pid=S0034-8376200500050000900026&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">27. Stockert  RJ,  Morell  A.   Second messanger modulation  of the asialogycoprotein receptor. <i>J Biol Chem  </i>1990; 265(4):  1841&#150;6.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765905&pid=S0034-8376200500050000900027&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">28. Stockert RJ, Paietta E, Racevskis J, Morell AG. Posttranscriptional regulation of the asialoglycoprotein receptor by cGMP. <i>J Biol Chem  </i>1992; 267(1):  56&#150;9.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765906&pid=S0034-8376200500050000900028&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">29. Stockert RJ,  Ren  Q.  Cytoplasmic  protein mRNA interaction mediates  cGMP&#150;modulated translational  control  of the  asialoglycoprotein receptor. <i>J Biol Chem  </i>1997; 272(14): 9161&#150;5.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765907&pid=S0034-8376200500050000900029&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">30. De la Vega L, Stockert RJ. The cytoplasmic coatomer protein COPI&#150;A potential  translational  regulator. <i>J Biol  Chem   </i>1999; 247(44):    31135&#150;8.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765908&pid=S0034-8376200500050000900030&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">31. De la Vega L, Stockert R. Regulation of the insulin and asialoglycoprotein   receptors   via   cGMP&#150;dependent   protein   kinase. <i>Am J Phisiol&#150; Cell Physiol </i>2000; 279(6): C2037&#150;C2042.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765909&pid=S0034-8376200500050000900031&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">32. Vesely D.  Biotin enhances guanylate cyclase activity. <i>Science </i>1982;   216:   1329&#150;30.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765910&pid=S0034-8376200500050000900032&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">33. Spence JT, Koudelka AP. Effects of biotin upon the intracellular level of cGMP and the activity of glucokinase in cultured rat hepatocytes. <i>J Biol Chem </i>1984; 259(10): 6393&#150;6.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765911&pid=S0034-8376200500050000900033&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">34. Dakshinamurti K, Mistry SP.  Tissue and intracellular distribution of biotin&#150;C<sup>14</sup>OOH in rats and chicks. <i>J Biol Chem   </i>1963; 266:   294&#150;6.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765912&pid=S0034-8376200500050000900034&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">35. Petrelli F, Coderoni S, Moretti P, Paparelli M. Effect of biotin on phosphorylation, acetylation, methylation of rat liver histones. <i>Mol Biol Rep </i>1978;  16; 4(2): 87&#150;92.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765913&pid=S0034-8376200500050000900035&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">36. Hymes J, Fleischhauer K, Wolf B. Biotinylation of histones by human serum biotinidase: assessment of biotinyl&#150;transferase activity in sera from normal individuals and children with biotinidase deficiency. <i>Biochem Mol Med </i>1995; 56: 76&#150;83.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765914&pid=S0034-8376200500050000900036&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">37. Crisp  SE, Griffin JB, White BR, Toombs CF, Camporeale G, Said HM, Zempleni J. Biotin supply affects rates of cell proliferation, biotinylation of carboxylases and histones, and expression of the gene encoding the sodium&#150;dependent multivitamin transporter   in   JAr   choriocarcinoma  cells. <i>Eur J Nutr  </i>2004; 43(1):   23&#150;31.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765915&pid=S0034-8376200500050000900037&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">38. Stanley JS, Griffin JB, Zempleni J. Biotinylation of histones in human cells: effects of cell proliferation. <i>Eur J Biochem </i>2001; 268:   5424&#150;9.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765916&pid=S0034-8376200500050000900038&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">39. Peters DM, Griffin JB, Stanley JS, Beck MM, Zempleni J. Exposure to UV light causes increased biotinylation of histones in Jurkat cells. <i>Am J Physiol Cell Physiol </i>2002;  283(3):  C878&#150;C884.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765917&pid=S0034-8376200500050000900039&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">40. Hymes  J,  Wolf B.  Human biotinidase  isn't just for recycling biotin. Review. <i>J Nutr </i>1999;  129(2S Suppl.): 485S&#150;489S.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765918&pid=S0034-8376200500050000900040&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">41. Stanley JS, Griffin JB, Zempleni J. Biotinylation of histones in human cells. Effects of cell proliferation. <i>Eur J Biochem </i>2001; 268(20):    5424&#150;9.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765919&pid=S0034-8376200500050000900041&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">42. Zempleni J, Helm RM, Mock DM. <i>In vivo </i>biotin supplementation  at a pharmacologic  dose  decreases  proliferation rates  of human peripheral blood mononuclear cells and cytokine release. <i>J Nutr </i>2001;  131(5):  1479&#150;84.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765920&pid=S0034-8376200500050000900042&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">43. Narang MA, Dumas R, Ayer LM, Gravel RA. Reduced histone biotinylation in multiple carboxylase deficiency patients: a nuclear   role   for   holocarboxylase   synthetase. <i>Hum   Mol   Genet </i>2004;   1,  13(1):   15&#150;23.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765921&pid=S0034-8376200500050000900043&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">44. Fernandez&#150;Mejia C,  German M.  Regulation of glucokinase by vitamins  and hormones.   In:  Matschinsky FM,  Magnuson  MA (Eds.): Glucokinase disease: from basics to novel therapeutics. <i>Basel Karger </i>2004;  16: 225&#150;45.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765922&pid=S0034-8376200500050000900044&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">45. Foretz  M,  Guichard C,  Ferre  P,  Foufelle  F.  Sterol regulatory element binding protein&#150;1c is a major mediator of insulin action on the hepatic expression on the hepatic expression of glucokinase and lipogenesis&#150;related genes. <i>Proc Nati Acad of Sci </i>1999;   96:   12737&#150;42.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765923&pid=S0034-8376200500050000900045&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">46. Bhullar RP, Dakshinamurti K. The effect of biotin on cellular functions in HeLa cells. <i>J Cell Physiol </i>1985;  123(3): 425&#150;30.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765924&pid=S0034-8376200500050000900046&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">47. Rabin BS.  Inhibition of experimentally induced autoimmunity in rats by biotin deficiency. <i>J Nutr </i>1983;  113(11): 2316&#150;22.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765925&pid=S0034-8376200500050000900047&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">48. Baez&#150;Saldana A,  Diaz  G,  Espinoza B,  Ortega E.  Biotin deficiency  induces  changes   in  subpopulations  of spleen  lymphocytes in mice. <i>Am J Clin Nutr </i>1998; 67(3): 431&#150;7.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765926&pid=S0034-8376200500050000900048&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">49. Paul PK, Duttagupta PN. The effect of an acute dose of biotin at a post&#150;implantation stage and its relation with female sex steriods in the rat. <i>J Nutr Sci Vitaminol </i>1976; 22(3):  181&#150;6.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765927&pid=S0034-8376200500050000900049&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">50. Watanabe T, Endo A.  Species and strain differences in teratogenic   effects   of biotin   deficiency   in  rodents. <i>J Nutr   </i>1989; 119(2):    255&#150;61.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765928&pid=S0034-8376200500050000900050&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">51. Watanabe  T,  Endo  A.   Teratogenic  effects  of maternal  biotin deficiency on mouse embryos examined at midgestation. <i>Teratology   </i>1990;  42(3):   295&#150;300.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765929&pid=S0034-8376200500050000900051&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">52. Watanabe T.  Morphological and biochemical effects of excessive amounts of biotin on embryonic development in mice. <i>Experientia  </i>1996;  15;  52(2):  149&#150;54.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765930&pid=S0034-8376200500050000900052&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">53. Mistry SP, Dakshinamurti K, Modi VV. Impairment of glucose utilization  in  biotin  deficiency. <i>Arch Biochem Biophys   </i>1962; 96:   674&#150;5.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765931&pid=S0034-8376200500050000900053&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">54. Dakshinamurti K, Cheah&#150;Tan C.  Liver glucokinase of the biotin deficient rat. <i>Can J Biochem </i>1968; 46(1): 75&#150;80.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765932&pid=S0034-8376200500050000900054&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">55. Dakshinamurti K, Ho Chong Hong. Regulation of key hepatic glycolytic enzymes. <i>Enzymol Biol Clin </i>1970;  11(5): 423&#150;8.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765933&pid=S0034-8376200500050000900055&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">56. Son&eacute; H, Ito M, Shimizu M, Sasaki Y, Komai M, Furukawa Y. Characteristics   of the  biotin  enhancement  of glucose&#150;induced insulin secretion in pancreatic  islets  of rat. <i>Biosci Biotechnol Biochem  </i>2000;  64(3):   550&#150;4.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765934&pid=S0034-8376200500050000900056&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">57. Klandorf H,  Clarke  L,  Brown J.  Altered glucogen release  in biotin   deficiency.   Ger   of  medicine. <i>Gerl   Comp  Endocrinol </i>1987;  65:   133&#150;40.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765935&pid=S0034-8376200500050000900057&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">58. Dakshinamurti K, Tarrago&#150;Litvak L, Hong HC. Biotin and glucose metabolism. <i>Can J Biochem </i>1970; 48(4): 493&#150;500.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765936&pid=S0034-8376200500050000900058&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">59. Furukawa Y, Ohinata K, Ikai M, Maebashi M, Zhang H, Kimura S. Biotin&#150;stimulated insulin secretion in biotin&#150;deficient rats. <i>J Clin Biochem Nutr </i>1995; 18: 35&#150;42.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765937&pid=S0034-8376200500050000900059&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">60. Pejin D, Razmovski R. Continuous cultivation of Saccharomyces cerevisiae at different biotin concentrations in nutrient media. <i>J Appl Bacterial </i>1996; 80(1):  53&#150;5.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765938&pid=S0034-8376200500050000900060&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">61. Coggeshal JC, Heggers JP, Robson MC, Beker H. Biotin status and plasma glucose in diabetes. <i>Ann NY Acad Sci  </i>1985; 447: 389&#150;92.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765939&pid=S0034-8376200500050000900061&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">62. Maebashi M,  Makino Y,  Furukawa Y,  Ohinata K,  Kimura S, Takao S. Therapeutic evaluation of the effect of biotin on hyperglycemia  in  patients  with  non&#150;insulin  diabetes  mellitus. <i>J Clin Biochem Nutr </i>1993;  14: 211&#150;18.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765940&pid=S0034-8376200500050000900062&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">63. Baez&#150;Saldana A,  Zendejas&#150;Ruiz  I,   Revilla&#150;Monsalve  C,  Islas&#150;Andrade  S,  Cardenas  A,  Rojas&#150;Ochoa A,  Vilches  A,  Fernandez&#150;Mejia C. Effects of biotin on pyruvate carboxylase, acetyl&#150;CoA   carboxylase,   propionyl&#150;CoA   carboxylase,   and   markers for glucose  and lipid homeostasis  in type  2  diabetic  patients and nondiabetic subjects. <i>Am J Clin Nutr </i>2004; 79(2): 238&#150;43.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765941&pid=S0034-8376200500050000900063&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">64. Reddi A, DeAngelis B, Frank O, lasker N, Baker H. Biotin suplementation improves glucose and insulin tolerances in genetically diabetic KK mice. <i>Life Sci </i>1988; 42:  1323&#150;30.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765942&pid=S0034-8376200500050000900064&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">65. Zhang H, Osada K, Maebashi M, Ito M, Komai M, Furukawa Y. A high biotin diet improves the impaired glucose tolerance of long&#150;term spontaneously hyperglycemic rats with non&#150;insulin&#150;dependent   diabetes   mellitus. <i>J Nutr  Sci   Vitaminol   </i>1996; 42(6):    517&#150;26.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765943&pid=S0034-8376200500050000900065&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">66. Zhang H, Osada K, Son&eacute; H, Furukawa Y. Biotin administration improves the  impaired glucose tolerance  of streptozotocin&#150;induced diabetic Wistar rats. <i>J Nutr Sci Vitaminol </i>1997; 43(3): 271&#150;80.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765944&pid=S0034-8376200500050000900066&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">67. Dakshinamurti  K,   Desjardins  PR.   Lipogenesis   in biotin  deficiency. <i>Can J Biochem  </i>1968; 46(10):  1261&#150;7.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765945&pid=S0034-8376200500050000900067&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">68. Suchy SF, Wolf B. Effect of biotin deficiency and supplementation on lipid metabolism in rats: cholesterol and lipoproteins. <i>Am J Clin Nutr </i>1986; 43(5): 831&#150;8.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765946&pid=S0034-8376200500050000900068&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">69. Dokusova OK, Krivoruchenko IV.  The effect of biotin on the level of cholesterol in the blood of patients with atherosclerosis and essential hyperlipidemia. <i>Kardiologiia </i>1972;   12(12):   113.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765947&pid=S0034-8376200500050000900069&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">70. Marshall   MW,   Kliman   PG,   Washington   VA,   Mackin   JF, Weinland  BT.   Effects  of biotin  on  lipids  and  other  constituents  of plasma  of healthy  men  and  women. <i>Artery   </i>1980; 7(4):   330&#150;51.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765948&pid=S0034-8376200500050000900070&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">71. Marshall MW, Knox VA, Trout DL, Durand AMA, Benton DA. Biotin status and lipid metabolism in young inbred rats. <i>Nutr Rep Inter </i>1972;  5(3): 201&#150;12.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765949&pid=S0034-8376200500050000900071&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">72. Marshall   MW,   Haubrich   M,   Washington   VA,   Chang   MW, Young CW, Wheeler MA. Biotin status and lipid metabolism in adult   obese   hypercholesterolemic    inbred   rats. <i>Nutr   Metab </i>1976;   20(1):   41&#150;61.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765950&pid=S0034-8376200500050000900072&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">73. Levert KL, Waldrop GL, Stephens JM. A biotin analog inhibits acetyl&#150;CoA carboxylase activity and adipogenesis. <i>J Biol Chem </i>2002;   277(19):   16347&#150;50.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=6765951&pid=S0034-8376200500050000900073&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --> ]]></body><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Chapman]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Cronan]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Molecular biology of attachment to proteins]]></article-title>
<source><![CDATA[J Nutr]]></source>
<year>1999</year>
<volume>129</volume>
<page-range>447S-484S</page-range></nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rodriguez-Melendez]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Zempleni]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Regulation of gene expression by biotin (review)]]></article-title>
<source><![CDATA[J Nutr Biochem]]></source>
<year>2003</year>
<volume>14</volume>
<page-range>680-90</page-range></nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pacheco-Alvarez]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Solorzano]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[León del Rio]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin in metabolism and its relationship to human disease]]></article-title>
<source><![CDATA[Arch Med Res]]></source>
<year>2002</year>
<volume>33</volume>
<page-range>439-47</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Chauhan]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin-binding proteins]]></article-title>
<source><![CDATA[Vitamin receptors: vitamins as ligands in cell communication]]></source>
<year>1994</year>
<page-range>200-49</page-range><publisher-name><![CDATA[Cambridge University Press]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B5">
<label>5</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hymes]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Wolf]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotinidase and its roles in biotin metabolism]]></article-title>
<source><![CDATA[Clin Chim Acta]]></source>
<year>1996</year>
<volume>225</volume>
<page-range>1-11</page-range></nlm-citation>
</ref>
<ref id="B6">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cohen]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Thomas]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin transport into fully differentiated 3T3-L1 cells]]></article-title>
<source><![CDATA[Biochim Biophys Res Comm]]></source>
<year>1982</year>
<volume>108</volume>
<numero>4</numero>
<issue>4</issue>
<page-range>1508-16</page-range></nlm-citation>
</ref>
<ref id="B7">
<label>7</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Chatterjee]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Kumar]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Ortiz]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Rubin]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Said]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Molecular mechanism of the intestinal biotin transport process]]></article-title>
<source><![CDATA[Am J Physiol]]></source>
<year>1999</year>
<volume>277</volume>
<numero>46</numero>
<issue>46</issue>
<page-range>C605-C613</page-range></nlm-citation>
</ref>
<ref id="B8">
<label>8</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Chapman-Smith]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Cronan]]></surname>
<given-names><![CDATA[JE Jr]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The enzimatic biotinylation of proteins: a post-traslational modification of exceptional specificy]]></article-title>
<source><![CDATA[Trends Biochem Sci]]></source>
<year>1999</year>
<volume>24</volume>
<page-range>359-63</page-range></nlm-citation>
</ref>
<ref id="B9">
<label>9</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Lamhonwah]]></surname>
<given-names><![CDATA[AM]]></given-names>
</name>
<name>
<surname><![CDATA[Quan]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Gravel]]></surname>
<given-names><![CDATA[RA]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Secuence homology around the biotin-binding site of human propionyl-CoA carboxylase and pyruvate carboxilase]]></article-title>
<source><![CDATA[Arch Biochem Biophys]]></source>
<year>1987</year>
<volume>254</volume>
<page-range>631-6</page-range></nlm-citation>
</ref>
<ref id="B10">
<label>10</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Jitrapakdee]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Wallace]]></surname>
<given-names><![CDATA[JC]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The biotin enzyme family: conserved structural motifs and domain rearrangements]]></article-title>
<source><![CDATA[Curr Protein Pept Sci]]></source>
<year>2003</year>
<volume>4</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>217-29</page-range></nlm-citation>
</ref>
<ref id="B11">
<label>11</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Cheah-Tan]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin-mediated syntesis of hepatic glucokinase in the rat]]></article-title>
<source><![CDATA[Arch Biochem Biophys]]></source>
<year>1968</year>
<volume>127</volume>
<page-range>17-21</page-range></nlm-citation>
</ref>
<ref id="B12">
<label>12</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Modi]]></surname>
<given-names><![CDATA[VV]]></given-names>
</name>
<name>
<surname><![CDATA[Mistry]]></surname>
<given-names><![CDATA[SP]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Some aspects of carbohydrates metabolism in biotin-deficient rats]]></article-title>
<source><![CDATA[Proc Soc Exp Biol Med]]></source>
<year>1968</year>
<volume>127</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>396-400</page-range></nlm-citation>
</ref>
<ref id="B13">
<label>13</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Deodhar]]></surname>
<given-names><![CDATA[AD]]></given-names>
</name>
<name>
<surname><![CDATA[Mistry]]></surname>
<given-names><![CDATA[SP]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Gluconeogenesis in biotin deficiency: In vivo synthesis of pyruvate holocarboxylase in biotin deficient rat liver]]></article-title>
<source><![CDATA[Biochem Biophys Res Comm]]></source>
<year>1969</year>
<volume>34</volume>
<numero>6</numero>
<issue>6</issue>
<page-range>755-9</page-range></nlm-citation>
</ref>
<ref id="B14">
<label>14</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Balmer]]></surname>
<given-names><![CDATA[JE]]></given-names>
</name>
<name>
<surname><![CDATA[Blomhoff]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Gene expression regulation by retinoic acid, (review)]]></article-title>
<source><![CDATA[J Lipid Res]]></source>
<year>2002</year>
<volume>43</volume>
<numero>11</numero>
<issue>11</issue>
<page-range>1773-808</page-range></nlm-citation>
</ref>
<ref id="B15">
<label>15</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rodriguez-Melendez]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Cano]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Méndez]]></surname>
<given-names><![CDATA[ST]]></given-names>
</name>
<name>
<surname><![CDATA[Velazquez]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin regulates the genetic expression of holocarboxylase synthetase and mitochondrial carboxylases in rats]]></article-title>
<source><![CDATA[J Nutr]]></source>
<year>2001</year>
<volume>131</volume>
<page-range>1909-13</page-range></nlm-citation>
</ref>
<ref id="B16">
<label>16</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Solorzano-Vargas]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Pacheco-Alvarez]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[León-Del-Río]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Holocarboxylase synthetase is an obligate participant in biotin-mediated regulation of its own expression and of biotin-depend carboxylases mRNA levels in human cells]]></article-title>
<source><![CDATA[Proc Natl Acad Sci]]></source>
<year>2002</year>
<volume>99</volume>
<numero>8</numero>
<issue>8</issue>
<page-range>5325-30</page-range></nlm-citation>
</ref>
<ref id="B17">
<label>17</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Chauhan]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[KC]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Transcriptional regulation of the glucokinase gene by biotin in starved rats]]></article-title>
<source><![CDATA[J Biol Chem]]></source>
<year>1991</year>
<volume>266</volume>
<page-range>10035-8</page-range></nlm-citation>
</ref>
<ref id="B18">
<label>18</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Li]]></surname>
<given-names><![CDATA[W]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Transcriptional regulation of liver phosphoenolpyruvate carboxykinase by biotin in diabetic rats]]></article-title>
<source><![CDATA[Mol Cell Biochem]]></source>
<year>1994</year>
<volume>132</volume>
<page-range>127-32</page-range></nlm-citation>
</ref>
<ref id="B19">
<label>19</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Borboni]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Magnaterra]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Rabini]]></surname>
<given-names><![CDATA[RA]]></given-names>
</name>
<name>
<surname><![CDATA[Staffolanni]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Porzio]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
<name>
<surname><![CDATA[Sesti]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Fusco]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Mazzanti]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Lauro]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Marlier]]></surname>
<given-names><![CDATA[JNJL]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Effect of biotin on glucokinase activity, mRNA expression and insulin release in cultured 6-cell]]></article-title>
<source><![CDATA[Acta Diabetol]]></source>
<year>1996</year>
<volume>33</volume>
<page-range>154-8</page-range></nlm-citation>
</ref>
<ref id="B20">
<label>20</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Romero-Navarro]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Cabrera-Valladares]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[German]]></surname>
<given-names><![CDATA[MS]]></given-names>
</name>
<name>
<surname><![CDATA[Matschinsky]]></surname>
<given-names><![CDATA[FM]]></given-names>
</name>
<name>
<surname><![CDATA[Wang]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Fernandez-Mejia]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin regulation of pancreatic glucokinase and insulin in primary cultured rat islets and in biotin deficient rats]]></article-title>
<source><![CDATA[Endocrinology]]></source>
<year>1999</year>
<volume>140</volume>
<page-range>4595-4600</page-range></nlm-citation>
</ref>
<ref id="B21">
<label>21</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Yoshikawa]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Tajiri]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
<name>
<surname><![CDATA[Sako]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
<name>
<surname><![CDATA[Hashimoto]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Umeda]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Nawata]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Effects of biotin on glucotoxycity of lipotoxicity in rat pancreatic islets]]></article-title>
<source><![CDATA[Metabolism]]></source>
<year>2002</year>
<volume>51</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>163-8</page-range></nlm-citation>
</ref>
<ref id="B22">
<label>22</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rodriguez-Melendez]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Camporeale]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Griffin]]></surname>
<given-names><![CDATA[JB]]></given-names>
</name>
<name>
<surname><![CDATA[Zempleni]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Interleukin-2 receptor y-dependent endocytosis depends on biotin in Jurkat cells]]></article-title>
<source><![CDATA[Am J Physiol Cell Physiol]]></source>
<year>2003</year>
<volume>284</volume>
<page-range>C415-C421</page-range></nlm-citation>
</ref>
<ref id="B23">
<label>23</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Manthey]]></surname>
<given-names><![CDATA[KC]]></given-names>
</name>
<name>
<surname><![CDATA[Griffin]]></surname>
<given-names><![CDATA[JB]]></given-names>
</name>
<name>
<surname><![CDATA[Zampleni]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin supply affects expression of biotin transporters, biotinylation of carboxilases and metabolism of interleukin-2 in Jurkat cells]]></article-title>
<source><![CDATA[J Nutr]]></source>
<year>2002</year>
<volume>132</volume>
<numero>5</numero>
<issue>5</issue>
<page-range>887-92</page-range></nlm-citation>
</ref>
<ref id="B24">
<label>24</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Scheerger]]></surname>
<given-names><![CDATA[SB]]></given-names>
</name>
<name>
<surname><![CDATA[Zempleni]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Expression of oncogenes depends on biotin in human small cell lung cancer cells NCI-H69]]></article-title>
<source><![CDATA[Int J Vitam Nutr Res]]></source>
<year>2003</year>
<volume>73</volume>
<numero>6</numero>
<issue>6</issue>
<page-range>461-7</page-range></nlm-citation>
</ref>
<ref id="B25">
<label>25</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Wiedmann]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Rodriguez-Melendez]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Ortega-Cuellar]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Zempleni]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Clusters of biotin-responsive genes in human peripheral blood mononuclear cells]]></article-title>
<source><![CDATA[J Nutr Biochem]]></source>
<year>2004</year>
<volume>15</volume>
<numero>7</numero>
<issue>7</issue>
<page-range>433-9</page-range></nlm-citation>
</ref>
<ref id="B26">
<label>26</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Collins]]></surname>
<given-names><![CDATA[JC]]></given-names>
</name>
<name>
<surname><![CDATA[Paietta]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Green]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Morell]]></surname>
<given-names><![CDATA[AG]]></given-names>
</name>
<name>
<surname><![CDATA[Stockert]]></surname>
<given-names><![CDATA[RJ]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin-dependent expression of the asialoglycoprotein receptor in HepG2 cells]]></article-title>
<source><![CDATA[J Biol Chem]]></source>
<year>1988</year>
<volume>263</volume>
<page-range>11280-3</page-range></nlm-citation>
</ref>
<ref id="B27">
<label>27</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Stockert]]></surname>
<given-names><![CDATA[RJ]]></given-names>
</name>
<name>
<surname><![CDATA[Morell]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Second messanger modulation of the asialogycoprotein receptor]]></article-title>
<source><![CDATA[J Biol Chem]]></source>
<year>1990</year>
<volume>265</volume>
<numero>4</numero>
<issue>4</issue>
<page-range>1841-6</page-range></nlm-citation>
</ref>
<ref id="B28">
<label>28</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Stockert]]></surname>
<given-names><![CDATA[RJ]]></given-names>
</name>
<name>
<surname><![CDATA[Paietta]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Racevskis]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Morell]]></surname>
<given-names><![CDATA[AG]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Posttranscriptional regulation of the asialoglycoprotein receptor by cGMP]]></article-title>
<source><![CDATA[J Biol Chem]]></source>
<year>1992</year>
<volume>267</volume>
<numero>1</numero>
<issue>1</issue>
<page-range>56-9</page-range></nlm-citation>
</ref>
<ref id="B29">
<label>29</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Stockert]]></surname>
<given-names><![CDATA[RJ]]></given-names>
</name>
<name>
<surname><![CDATA[Ren]]></surname>
<given-names><![CDATA[Q]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Cytoplasmic protein mRNA interaction mediates cGMP-modulated translational control of the asialoglycoprotein receptor]]></article-title>
<source><![CDATA[J Biol Chem]]></source>
<year>1997</year>
<volume>272</volume>
<numero>14</numero>
<issue>14</issue>
<page-range>9161-5</page-range></nlm-citation>
</ref>
<ref id="B30">
<label>30</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[De la Vega]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Stockert]]></surname>
<given-names><![CDATA[RJ]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The cytoplasmic coatomer protein COPI-A potential translational regulator]]></article-title>
<source><![CDATA[J Biol Chem]]></source>
<year>1999</year>
<volume>247</volume>
<numero>44</numero>
<issue>44</issue>
<page-range>31135-8</page-range></nlm-citation>
</ref>
<ref id="B31">
<label>31</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[De la Vega]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Stockert]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Regulation of the insulin and asialoglycoprotein receptors via cGMP-dependent protein kinase]]></article-title>
<source><![CDATA[Am J Phisiol- Cell Physiol]]></source>
<year>2000</year>
<volume>279</volume>
<numero>6</numero>
<issue>6</issue>
<page-range>C2037-C2042</page-range></nlm-citation>
</ref>
<ref id="B32">
<label>32</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Vesely]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin enhances guanylate cyclase activity]]></article-title>
<source><![CDATA[Science]]></source>
<year>1982</year>
<volume>216</volume>
<page-range>1329-30</page-range></nlm-citation>
</ref>
<ref id="B33">
<label>33</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Spence]]></surname>
<given-names><![CDATA[JT]]></given-names>
</name>
<name>
<surname><![CDATA[Koudelka]]></surname>
<given-names><![CDATA[AP]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Effects of biotin upon the intracellular level of cGMP and the activity of glucokinase in cultured rat hepatocytes]]></article-title>
<source><![CDATA[J Biol Chem]]></source>
<year>1984</year>
<volume>259</volume>
<numero>10</numero>
<issue>10</issue>
<page-range>6393-6</page-range></nlm-citation>
</ref>
<ref id="B34">
<label>34</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Mistry]]></surname>
<given-names><![CDATA[SP]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Tissue and intracellular distribution of biotin-C14OOH in rats and chicks]]></article-title>
<source><![CDATA[J Biol Chem]]></source>
<year>1963</year>
<volume>266</volume>
<page-range>294-6</page-range></nlm-citation>
</ref>
<ref id="B35">
<label>35</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Petrelli]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Coderoni]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Moretti]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Paparelli]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Effect of biotin on phosphorylation, acetylation, methylation of rat liver histones]]></article-title>
<source><![CDATA[Mol Biol Rep]]></source>
<year>1978</year>
<volume>4</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>87-92</page-range></nlm-citation>
</ref>
<ref id="B36">
<label>36</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hymes]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Fleischhauer]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Wolf]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotinylation of histones by human serum biotinidase: assessment of biotinyl-transferase activity in sera from normal individuals and children with biotinidase deficiency]]></article-title>
<source><![CDATA[Biochem Mol Med]]></source>
<year>1995</year>
<volume>56</volume>
<page-range>76-83</page-range></nlm-citation>
</ref>
<ref id="B37">
<label>37</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Crisp]]></surname>
<given-names><![CDATA[SE]]></given-names>
</name>
<name>
<surname><![CDATA[Griffin]]></surname>
<given-names><![CDATA[JB]]></given-names>
</name>
<name>
<surname><![CDATA[White]]></surname>
<given-names><![CDATA[BR]]></given-names>
</name>
<name>
<surname><![CDATA[Toombs]]></surname>
<given-names><![CDATA[CF]]></given-names>
</name>
<name>
<surname><![CDATA[Camporeale]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Said]]></surname>
<given-names><![CDATA[HM]]></given-names>
</name>
<name>
<surname><![CDATA[Zempleni]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin supply affects rates of cell proliferation, biotinylation of carboxylases and histones, and expression of the gene encoding the sodium-dependent multivitamin transporter in JAr choriocarcinoma cells]]></article-title>
<source><![CDATA[Eur J Nutr]]></source>
<year>2004</year>
<volume>43</volume>
<numero>1</numero>
<issue>1</issue>
<page-range>23-31</page-range></nlm-citation>
</ref>
<ref id="B38">
<label>38</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Stanley]]></surname>
<given-names><![CDATA[JS]]></given-names>
</name>
<name>
<surname><![CDATA[Griffin]]></surname>
<given-names><![CDATA[JB]]></given-names>
</name>
<name>
<surname><![CDATA[Zempleni]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotinylation of histones in human cells: effects of cell proliferation]]></article-title>
<source><![CDATA[Eur J Biochem]]></source>
<year>2001</year>
<volume>268</volume>
<page-range>5424-9</page-range></nlm-citation>
</ref>
<ref id="B39">
<label>39</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Peters]]></surname>
<given-names><![CDATA[DM]]></given-names>
</name>
<name>
<surname><![CDATA[Griffin]]></surname>
<given-names><![CDATA[JB]]></given-names>
</name>
<name>
<surname><![CDATA[Stanley]]></surname>
<given-names><![CDATA[JS]]></given-names>
</name>
<name>
<surname><![CDATA[Beck]]></surname>
<given-names><![CDATA[MM]]></given-names>
</name>
<name>
<surname><![CDATA[Zempleni]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Exposure to UV light causes increased biotinylation of histones in Jurkat cells]]></article-title>
<source><![CDATA[Am J Physiol Cell Physiol]]></source>
<year>2002</year>
<volume>283</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>C878-C884</page-range></nlm-citation>
</ref>
<ref id="B40">
<label>40</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hymes]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Wolf]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Human biotinidase isn't just for recycling biotin: Review]]></article-title>
<source><![CDATA[J Nutr]]></source>
<year>1999</year>
<volume>129</volume>
<numero>^s2S</numero>
<issue>^s2S</issue>
<supplement>2S</supplement>
<page-range>485S-489S</page-range></nlm-citation>
</ref>
<ref id="B41">
<label>41</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Stanley]]></surname>
<given-names><![CDATA[JS]]></given-names>
</name>
<name>
<surname><![CDATA[Griffin]]></surname>
<given-names><![CDATA[JB]]></given-names>
</name>
<name>
<surname><![CDATA[Zempleni]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotinylation of histones in human cells: Effects of cell proliferation]]></article-title>
<source><![CDATA[Eur J Biochem]]></source>
<year>2001</year>
<volume>268</volume>
<numero>20</numero>
<issue>20</issue>
<page-range>5424-9</page-range></nlm-citation>
</ref>
<ref id="B42">
<label>42</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zempleni]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Helm]]></surname>
<given-names><![CDATA[RM]]></given-names>
</name>
<name>
<surname><![CDATA[Mock]]></surname>
<given-names><![CDATA[DM]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[In vivo biotin supplementation at a pharmacologic dose decreases proliferation rates of human peripheral blood mononuclear cells and cytokine release]]></article-title>
<source><![CDATA[J Nutr]]></source>
<year>2001</year>
<volume>131</volume>
<numero>5</numero>
<issue>5</issue>
<page-range>1479-84</page-range></nlm-citation>
</ref>
<ref id="B43">
<label>43</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Narang]]></surname>
<given-names><![CDATA[MA]]></given-names>
</name>
<name>
<surname><![CDATA[Dumas]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Ayer]]></surname>
<given-names><![CDATA[LM]]></given-names>
</name>
<name>
<surname><![CDATA[Gravel]]></surname>
<given-names><![CDATA[RA]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Reduced histone biotinylation in multiple carboxylase deficiency patients: a nuclear role for holocarboxylase synthetase]]></article-title>
<source><![CDATA[Hum Mol Genet]]></source>
<year>2004</year>
<volume>13</volume>
<numero>1</numero>
<issue>1</issue>
<page-range>15-23</page-range></nlm-citation>
</ref>
<ref id="B44">
<label>44</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Fernandez-Mejia]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[German]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Regulation of glucokinase by vitamins and hormones]]></article-title>
<person-group person-group-type="editor">
<name>
<surname><![CDATA[Matschinsky]]></surname>
<given-names><![CDATA[FM]]></given-names>
</name>
<name>
<surname><![CDATA[Magnuson]]></surname>
<given-names><![CDATA[MA]]></given-names>
</name>
</person-group>
<source><![CDATA[Glucokinase disease: from basics to novel therapeutics]]></source>
<year>2004</year>
<page-range>225-45</page-range><publisher-name><![CDATA[Basel Karger]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B45">
<label>45</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Foretz]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Guichard]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Ferre]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Foufelle]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Sterol regulatory element binding protein-1c is a major mediator of insulin action on the hepatic expression on the hepatic expression of glucokinase and lipogenesis-related genes]]></article-title>
<source><![CDATA[Proc Nati Acad of Sci]]></source>
<year>1999</year>
<volume>96</volume>
<page-range>12737-42</page-range></nlm-citation>
</ref>
<ref id="B46">
<label>46</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bhullar]]></surname>
<given-names><![CDATA[RP]]></given-names>
</name>
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The effect of biotin on cellular functions in HeLa cells]]></article-title>
<source><![CDATA[J Cell Physiol]]></source>
<year>1985</year>
<volume>123</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>425-30</page-range></nlm-citation>
</ref>
<ref id="B47">
<label>47</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rabin]]></surname>
<given-names><![CDATA[BS]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Inhibition of experimentally induced autoimmunity in rats by biotin deficiency]]></article-title>
<source><![CDATA[J Nutr]]></source>
<year>1983</year>
<volume>113</volume>
<numero>11</numero>
<issue>11</issue>
<page-range>2316-22</page-range></nlm-citation>
</ref>
<ref id="B48">
<label>48</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Baez-Saldana]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Diaz]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Espinoza]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
<name>
<surname><![CDATA[Ortega]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin deficiency induces changes in subpopulations of spleen lymphocytes in mice]]></article-title>
<source><![CDATA[Am J Clin Nutr]]></source>
<year>1998</year>
<volume>67</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>431-7</page-range></nlm-citation>
</ref>
<ref id="B49">
<label>49</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Paul]]></surname>
<given-names><![CDATA[PK]]></given-names>
</name>
<name>
<surname><![CDATA[Duttagupta]]></surname>
<given-names><![CDATA[PN]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The effect of an acute dose of biotin at a post-implantation stage and its relation with female sex steriods in the rat]]></article-title>
<source><![CDATA[J Nutr Sci Vitaminol]]></source>
<year>1976</year>
<volume>22</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>181-6</page-range></nlm-citation>
</ref>
<ref id="B50">
<label>50</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Watanabe]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Endo]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Species and strain differences in teratogenic effects of biotin deficiency in rodents]]></article-title>
<source><![CDATA[J Nutr]]></source>
<year>1989</year>
<volume>119</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>255-61</page-range></nlm-citation>
</ref>
<ref id="B51">
<label>51</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Watanabe]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Endo]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Teratogenic effects of maternal biotin deficiency on mouse embryos examined at midgestation]]></article-title>
<source><![CDATA[Teratology]]></source>
<year>1990</year>
<volume>42</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>295-300</page-range></nlm-citation>
</ref>
<ref id="B52">
<label>52</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Watanabe]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Morphological and biochemical effects of excessive amounts of biotin on embryonic development in mice]]></article-title>
<source><![CDATA[Experientia]]></source>
<year>1996</year>
<volume>52</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>149-54</page-range></nlm-citation>
</ref>
<ref id="B53">
<label>53</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Mistry]]></surname>
<given-names><![CDATA[SP]]></given-names>
</name>
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Modi]]></surname>
<given-names><![CDATA[VV]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Impairment of glucose utilization in biotin deficiency]]></article-title>
<source><![CDATA[Arch Biochem Biophys]]></source>
<year>1962</year>
<volume>96</volume>
<page-range>674-5</page-range></nlm-citation>
</ref>
<ref id="B54">
<label>54</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Cheah-Tan]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Liver glucokinase of the biotin deficient rat]]></article-title>
<source><![CDATA[Can J Biochem]]></source>
<year>1968</year>
<volume>46</volume>
<numero>1</numero>
<issue>1</issue>
<page-range>75-80</page-range></nlm-citation>
</ref>
<ref id="B55">
<label>55</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Ho Chong]]></surname>
<given-names><![CDATA[Hong]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Regulation of key hepatic glycolytic enzymes]]></article-title>
<source><![CDATA[Enzymol Biol Clin]]></source>
<year>1970</year>
<volume>11</volume>
<numero>5</numero>
<issue>5</issue>
<page-range>423-8</page-range></nlm-citation>
</ref>
<ref id="B56">
<label>56</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Soné]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Ito]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Shimizu]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Sasaki]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
<name>
<surname><![CDATA[Komai]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Furukawa]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Characteristics of the biotin enhancement of glucose-induced insulin secretion in pancreatic islets of rat]]></article-title>
<source><![CDATA[Biosci Biotechnol Biochem]]></source>
<year>2000</year>
<volume>64</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>550-4</page-range></nlm-citation>
</ref>
<ref id="B57">
<label>57</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Klandorf]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Clarke]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Brown]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Altered glucogen release in biotin deficiency]]></article-title>
<source><![CDATA[Gerl Comp Endocrinol]]></source>
<year>1987</year>
<volume>65</volume>
<page-range>133-40</page-range></nlm-citation>
</ref>
<ref id="B58">
<label>58</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Tarrago-Litvak]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Hong]]></surname>
<given-names><![CDATA[HC]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin and glucose metabolism]]></article-title>
<source><![CDATA[Can J Biochem]]></source>
<year>1970</year>
<volume>48</volume>
<numero>4</numero>
<issue>4</issue>
<page-range>493-500</page-range></nlm-citation>
</ref>
<ref id="B59">
<label>59</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Furukawa]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
<name>
<surname><![CDATA[Ohinata]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Ikai]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Maebashi]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Zhang]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Kimura]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin-stimulated insulin secretion in biotin-deficient rats]]></article-title>
<source><![CDATA[J Clin Biochem Nutr]]></source>
<year>1995</year>
<volume>18</volume>
<page-range>35-42</page-range></nlm-citation>
</ref>
<ref id="B60">
<label>60</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pejin]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Razmovski]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Continuous cultivation of Saccharomyces cerevisiae at different biotin concentrations in nutrient media]]></article-title>
<source><![CDATA[J Appl Bacterial]]></source>
<year>1996</year>
<volume>80</volume>
<numero>1</numero>
<issue>1</issue>
<page-range>53-5</page-range></nlm-citation>
</ref>
<ref id="B61">
<label>61</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Coggeshal]]></surname>
<given-names><![CDATA[JC]]></given-names>
</name>
<name>
<surname><![CDATA[Heggers]]></surname>
<given-names><![CDATA[JP]]></given-names>
</name>
<name>
<surname><![CDATA[Robson]]></surname>
<given-names><![CDATA[MC]]></given-names>
</name>
<name>
<surname><![CDATA[Beker]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin status and plasma glucose in diabetes]]></article-title>
<source><![CDATA[Ann NY Acad Sci]]></source>
<year>1985</year>
<volume>447</volume>
<page-range>389-92</page-range></nlm-citation>
</ref>
<ref id="B62">
<label>62</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Maebashi]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Makino]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
<name>
<surname><![CDATA[Furukawa]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
<name>
<surname><![CDATA[Ohinata]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Kimura]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Takao]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Therapeutic evaluation of the effect of biotin on hyperglycemia in patients with non-insulin diabetes mellitus]]></article-title>
<source><![CDATA[J Clin Biochem Nutr]]></source>
<year>1993</year>
<volume>14</volume>
<page-range>211-18</page-range></nlm-citation>
</ref>
<ref id="B63">
<label>63</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Baez-Saldana]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Zendejas-Ruiz]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
<name>
<surname><![CDATA[Revilla-Monsalve]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Islas-Andrade]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Cardenas]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Rojas-Ochoa]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Vilches]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Fernandez-Mejia]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Effects of biotin on pyruvate carboxylase, acetyl-CoA carboxylase, propionyl-CoA carboxylase, and markers for glucose and lipid homeostasis in type 2 diabetic patients and nondiabetic subjects]]></article-title>
<source><![CDATA[Am J Clin Nutr]]></source>
<year>2004</year>
<volume>79</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>238-43</page-range></nlm-citation>
</ref>
<ref id="B64">
<label>64</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Reddi]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[DeAngelis]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
<name>
<surname><![CDATA[Frank]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
<name>
<surname><![CDATA[lasker]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Baker]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin suplementation improves glucose and insulin tolerances in genetically diabetic KK mice]]></article-title>
<source><![CDATA[Life Sci]]></source>
<year>1988</year>
<volume>42</volume>
<page-range>1323-30</page-range></nlm-citation>
</ref>
<ref id="B65">
<label>65</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zhang]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Osada]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Maebashi]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Ito]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Komai]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Furukawa]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[A high biotin diet improves the impaired glucose tolerance of long-term spontaneously hyperglycemic rats with non-insulin-dependent diabetes mellitus]]></article-title>
<source><![CDATA[J Nutr Sci Vitaminol]]></source>
<year>1996</year>
<volume>42</volume>
<numero>6</numero>
<issue>6</issue>
<page-range>517-26</page-range></nlm-citation>
</ref>
<ref id="B66">
<label>66</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zhang]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Osada]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Soné]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Furukawa]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin administration improves the impaired glucose tolerance of streptozotocin-induced diabetic Wistar rats]]></article-title>
<source><![CDATA[J Nutr Sci Vitaminol]]></source>
<year>1997</year>
<volume>43</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>271-80</page-range></nlm-citation>
</ref>
<ref id="B67">
<label>67</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dakshinamurti]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Desjardins]]></surname>
<given-names><![CDATA[PR]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Lipogenesis in biotin deficiency]]></article-title>
<source><![CDATA[Can J Biochem]]></source>
<year>1968</year>
<volume>46</volume>
<numero>10</numero>
<issue>10</issue>
<page-range>1261-7</page-range></nlm-citation>
</ref>
<ref id="B68">
<label>68</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Suchy]]></surname>
<given-names><![CDATA[SF]]></given-names>
</name>
<name>
<surname><![CDATA[Wolf]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Effect of biotin deficiency and supplementation on lipid metabolism in rats: cholesterol and lipoproteins]]></article-title>
<source><![CDATA[Am J Clin Nutr]]></source>
<year>1986</year>
<volume>43</volume>
<numero>5</numero>
<issue>5</issue>
<page-range>831-8</page-range></nlm-citation>
</ref>
<ref id="B69">
<label>69</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dokusova]]></surname>
<given-names><![CDATA[OK]]></given-names>
</name>
<name>
<surname><![CDATA[Krivoruchenko]]></surname>
<given-names><![CDATA[IV]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The effect of biotin on the level of cholesterol in the blood of patients with atherosclerosis and essential hyperlipidemia]]></article-title>
<source><![CDATA[Kardiologiia]]></source>
<year>1972</year>
<volume>12</volume>
<numero>12</numero>
<issue>12</issue>
<page-range>113</page-range></nlm-citation>
</ref>
<ref id="B70">
<label>70</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Marshall]]></surname>
<given-names><![CDATA[MW]]></given-names>
</name>
<name>
<surname><![CDATA[Kliman]]></surname>
<given-names><![CDATA[PG]]></given-names>
</name>
<name>
<surname><![CDATA[Washington]]></surname>
<given-names><![CDATA[VA]]></given-names>
</name>
<name>
<surname><![CDATA[Mackin]]></surname>
<given-names><![CDATA[JF]]></given-names>
</name>
<name>
<surname><![CDATA[Weinland]]></surname>
<given-names><![CDATA[BT]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Effects of biotin on lipids and other constituents of plasma of healthy men and women]]></article-title>
<source><![CDATA[Artery]]></source>
<year>1980</year>
<volume>7</volume>
<numero>4</numero>
<issue>4</issue>
<page-range>330-51</page-range></nlm-citation>
</ref>
<ref id="B71">
<label>71</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Marshall]]></surname>
<given-names><![CDATA[MW]]></given-names>
</name>
<name>
<surname><![CDATA[Knox]]></surname>
<given-names><![CDATA[VA]]></given-names>
</name>
<name>
<surname><![CDATA[Trout]]></surname>
<given-names><![CDATA[DL]]></given-names>
</name>
<name>
<surname><![CDATA[Durand]]></surname>
<given-names><![CDATA[AMA]]></given-names>
</name>
<name>
<surname><![CDATA[Benton]]></surname>
<given-names><![CDATA[DA]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin status and lipid metabolism in young inbred rats]]></article-title>
<source><![CDATA[Nutr Rep Inter]]></source>
<year>1972</year>
<volume>5</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>201-12</page-range></nlm-citation>
</ref>
<ref id="B72">
<label>72</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Marshall]]></surname>
<given-names><![CDATA[MW]]></given-names>
</name>
<name>
<surname><![CDATA[Haubrich]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Washington]]></surname>
<given-names><![CDATA[VA]]></given-names>
</name>
<name>
<surname><![CDATA[Chang]]></surname>
<given-names><![CDATA[MW]]></given-names>
</name>
<name>
<surname><![CDATA[Young]]></surname>
<given-names><![CDATA[CW]]></given-names>
</name>
<name>
<surname><![CDATA[Wheeler]]></surname>
<given-names><![CDATA[MA]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Biotin status and lipid metabolism in adult obese hypercholesterolemic inbred rats]]></article-title>
<source><![CDATA[Nutr Metab]]></source>
<year>1976</year>
<volume>20</volume>
<numero>1</numero>
<issue>1</issue>
<page-range>41-61</page-range></nlm-citation>
</ref>
<ref id="B73">
<label>73</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Levert]]></surname>
<given-names><![CDATA[KL]]></given-names>
</name>
<name>
<surname><![CDATA[Waldrop]]></surname>
<given-names><![CDATA[GL]]></given-names>
</name>
<name>
<surname><![CDATA[Stephens]]></surname>
<given-names><![CDATA[JM]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[A biotin analog inhibits acetyl-CoA carboxylase activity and adipogenesis]]></article-title>
<source><![CDATA[J Biol Chem]]></source>
<year>2002</year>
<volume>277</volume>
<numero>19</numero>
<issue>19</issue>
<page-range>16347-50</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
