<?xml version='1.0' encoding='UTF-8'?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
  <responseDate>2026-06-27T08:59:43Z</responseDate>
  <request verb="GetRecord" identifier="oai:meral.edu.mm:recid/3194" metadataPrefix="oai_dc">https://meral.edu.mm/oai</request>
  <GetRecord>
    <record>
      <header>
        <identifier>oai:meral.edu.mm:recid/3194</identifier>
        <datestamp>2021-12-13T02:50:33Z</datestamp>
        <setSpec>1582963366982:1596631786153</setSpec>
        <setSpec>user-um1</setSpec>
      </header>
      <metadata>
        <oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns="http://www.w3.org/2001/XMLSchema" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Insulin Receptor Substrate-1 Gene (G972R) Polymorphism and Insulin Resistance in Overweight and Obese Type 2 Diabetes Mellitus Patients</dc:title>
          <dc:creator>Thae Nu Htwe</dc:creator>
          <dc:creator>Myat Mon Oo</dc:creator>
          <dc:creator>Saw Wut Hmon</dc:creator>
          <dc:creator>Moh Moh Htun</dc:creator>
          <dc:creator>Ohnmar Myint Thein</dc:creator>
          <dc:creator>Myat Thandar</dc:creator>
          <dc:description>&lt;p&gt;The insulin receptor substrate-1 gene (IRS-1) gene has been considered a candidate for insulin resistance in type-2 diabetes and coronary artery disease. The most common IRS-1 variant, a glycine to arginine change at codon 972(G972R) is more prevalent among subjects who have features of insulin resistance syndrome associated with type 2 diabetes patients. The aim of the present study was to determine the insulin receptor substrate-1 gene (G972R) polymorphism and insulin resistance in overweight and obese type 2 diabetes mellitus patients. The genomic DNA of the subjects was amplified by polymerase chain reaction (PCR) and digested by restriction fragment length polymorphism (RFLP) with BstN1 used for codon 972.&lt;/p&gt;</dc:description>
          <dc:date>2015-12-24</dc:date>
          <dc:identifier>http://hdl.handle.net/20.500.12678/0000003194</dc:identifier>
          <dc:identifier>https://meral.edu.mm/records/3194</dc:identifier>
        </oai_dc:dc>
      </metadata>
    </record>
  </GetRecord>
</OAI-PMH>
