<?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>1870-199X</journal-id>
<journal-title><![CDATA[Revista odontológica mexicana]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Odont. Mex]]></abbrev-journal-title>
<issn>1870-199X</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional Autónoma de México, Facultad de Odontología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1870-199X2017000400245</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Evaluación de dos métodos para extracción de ARN en saliva en niños]]></article-title>
<article-title xml:lang="en"><![CDATA[Evaluation of two RNA extraction methods in children's saliva]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Madera Anaya]]></surname>
<given-names><![CDATA[Meisser Vidal]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Suárez Causado]]></surname>
<given-names><![CDATA[Amileth]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de Cartagena Facultad de Odontología ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad de Cartagena Facultad de Medicina ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2017</year>
</pub-date>
<volume>21</volume>
<numero>4</numero>
<fpage>245</fpage>
<lpage>252</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-199X2017000400245&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-199X2017000400245&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-199X2017000400245&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Objetivo: Estandarizar un protocolo de extracción de ARN en muestras de saliva de niños.  Material y métodos: A partir de muestras de saliva provenientes de 60 niños que participaron previa autorización de sus padres. Se compararon dos métodos para extracción de ARN, evaluando concentración, calidad y rendimiento; además se realizó la expresión génica del gen G USB a través de la técnica RT-PCR (transcriptase reversa-reacción en cadena de la polimerasa). Los datos fueron analizados mediante medidas de tendencia central y dispersión, frecuencias y porcentajes, para establecer diferencias se utilizaron las pruebas t-Student y &#967;2 (&#961; &lt; 0.05).  Resultados: Al analizar la cantidad de células por mL de saliva se encontró una media de 564,977.8 (DE = 246,678.6); se logró estandarizar un método de extracción de ARN en saliva de niños, específicamente el que utilizó RNeasy® Protect Saliva Mini Kit-Qiagen mostró mejores características de concentración de ARN (p = 0.0000) y rendimiento (p = 0.0000) al compararlo con el que uso QlAzol®; no existieron diferencias en la calidad del ARN (p = 0.146).  Conclusión: El ARN pudo extraerse de muestras salivales de niños, por lo cual se sugiere el uso de la saliva para análisis molecular de diferentes enfermedades sistémicas y de la cavidad bucal.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Objective: To standardize an RNA (ribonucleic acid) extraction protocol in children's saliva specimens.  Methods: The study was conducted on saliva specimens from 60 children who participated in the study with their parents' authorization. Comparison of two RNA extraction methods was established; methods assessed concentration, quality and yield. Moreover, genie expression of GUSB gene was achieved with RT-PCR (reverse transcriptase-polymerase chain reaction). Data were analyzed through measurements of central tendency and dispersion, frequencies and percentages. &#1058;-Student and &#967;2 tests were used in order to differentiate between both methods (p &lt; 0.05).  Results: Analysis of cell amounts per saliva ml revealed a mean of 564,977.8 (SD = 246,678.6); a RNA in children's saliva extraction method was standardized, specifically the method using RNeasy® Protect Saliva Mini Kit Qiagen exhibited better characteristics of RNA concentration (p = 0.0000) and yield (p = 0.0000) when compared to the method using QIAzór®; no RNA (p = 0.146) quality differences were found.  Conclusions: RNA could be extracted from children's saliva specimens, therefore, it is suggested to use saliva for the molecular analysis of different oral and systemic diseases.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Saliva]]></kwd>
<kwd lng="es"><![CDATA[ARN]]></kwd>
<kwd lng="es"><![CDATA[transcriptoma]]></kwd>
<kwd lng="es"><![CDATA[biomarcadores]]></kwd>
<kwd lng="en"><![CDATA[Saliva]]></kwd>
<kwd lng="en"><![CDATA[RNA]]></kwd>
<kwd lng="en"><![CDATA[transcriptome]]></kwd>
<kwd lng="en"><![CDATA[biomarkers]]></kwd>
</kwd-group>
</article-meta>
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