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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Shaymardanova, E.Kh.</author>
     <author>Nurgalieva, A.Kh.</author>
     <author>Khidiyatova, I.M.</author>
     <author>Gabbasova, L.V.</author>
     <author>Kuramshina, O.A.</author>
     <author>Kryukova, A.Ya.</author>
     <author>Sagitov, R.B.</author>
     <author>Munasipov, F.R.</author>
     <author>Khusnutdinova, E.Kh.</author>
    </authors>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2016</year>
    <pub-dates>
     <date>2018-03-06</date>
    </pub-dates>
   </dates>
   <doi>10.1134/S1022795416020113</doi>
   <abstract>Abstract—Peptic ulcer disease is a chronic disease of the gastrointestinal tract, mainly manifesting itself in&#13;
the formation of the fairly persistent ulcer defect of the mucous membrane of the stomach and/or duodenum.&#13;
Association analysis of common polymorphisms of matrix metalloproteinases genes MMP1 (rs1799750,&#13;
rs494379), MMP2 (rs2285052), MMP3 (rs3025058), MMP9 (rs3918242, rs17576), and MMP12&#13;
(rs2276109) and their tissue inhibitors TIMP2 (rs8179090) and TIMP3 (rs9619311) was carried out in 353&#13;
patients with a gastric ulcer or duodenal ulcer and in 325 unrelated healthy individuals from the Republic of&#13;
Bashkortostan. Associations of polymorphic variants rs1799750 and rs494379 of gene MMP1, rs3025058 of&#13;
gene MMP3, rs3918242 and rs17576 of gene MMP9, and rs9619311 of gene TIMP3 with the risk of peptic&#13;
ulcer disease in Russians and Tatars were revealed.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/1044</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/1194</url>
    </pdf-urls>
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