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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
    </authors>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2018</year>
    <pub-dates>
     <date>2020-09-11</date>
    </pub-dates>
   </dates>
   <doi>10.1007/s11033-018-4257-x</doi>
   <abstract>Essential arterial hypertension is a disease with distinct yet unexplored inflammatory component. Our aim was to assess&#13;
the role of chemokine genes and their interaction in its development. Genotyping of polymorphic markers in six chemokine&#13;
genes (CXCL13, CCL8, CCL16, CCL17, CCL18, and CCL23) was performed in the group of 522 men of Tatar ethnic origin&#13;
from the Republic of Bashkortostan, Russia (213 patients with essential hypertension and 309 healthy individuals without&#13;
history of cardiovascular disease). We found a strong association of CXCL13 rs355689*C allele with essential hypertension&#13;
under additive (OR 0.56, PFDR=0.008) and dominant (OR 0.41, PFDR 4.38×10−4&#13;
) genetic model. The analysis of gene–gene&#13;
interactions revealed 12 allele/genotype combinations that remained significantly associated with essential hypertension after&#13;
correction for multiple testing was applied, and each of these combinations included CXCL13 rs355689 polymorphism. Our&#13;
results indicate that CXCL13 rs355689 polymorphism is strongly associated with essential hypertension in the ethnic group&#13;
of Tatars, alone and in combination with polymorphic markers in other chemokine genes.</abstract>
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     <url>https://repo.bashgmu.ru/files/2</url>
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