<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu R</submitter><funding>International S&amp;amp;T Cooperation Program</funding><pagination>924105</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4151485</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2014</volume><pubmed_abstract>Coronary artery disease is the leading cause of mortality and morbidity in the world. Left main coronary artery disease (LMCAD) is a particularly severe phenotypic form of CAD and has a genetic basis. We hypothesized that some inflammation- and hyperhomocysteinemia-related gene polymorphisms may contribute to LMCAD susceptibility in a Chinese population. We studied the association between polymorphisms in the genes hepatocyte nuclear factor 1 alpha (HNF1A; rs7310409, G/A), C-reactive protein (rs1800947 and rs3093059 T/C), methylenetetrahydrofolate reductase (rs1801133, C/T), and methylenetetrahydrofolate dehydrogenase (rs1076991, A/G) in 402 LMCAD and 804 more peripheral CAD patients in a Chinese population. Genotyping was performed using the matrix-assisted laser desorption/ionization tim</pubmed_abstract><journal>Biochemistry research international</journal><pubmed_title>A Polymorphism in Hepatocyte Nuclear Factor 1 Alpha, rs7310409, Is Associated with Left Main Coronary Artery Disease.</pubmed_title><pmcid>PMC4151485</pmcid><funding_grant_id>2011BAI11B02</funding_grant_id><funding_grant_id>2010DFB33140</funding_grant_id><funding_grant_id>2011BAI11B21</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Zheng Z</pubmed_authors><pubmed_authors>Hu S</pubmed_authors><pubmed_authors>Gu H</pubmed_authors><pubmed_authors>Liu R</pubmed_authors><pubmed_authors>Teng X</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Nie Y</pubmed_authors><pubmed_authors>Zhou Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Polymorphism in Hepatocyte Nuclear Factor 1 Alpha, rs7310409, Is Associated with Left Main Coronary Artery Disease.</name><description>Coronary artery disease is the leading cause of mortality and morbidity in the world. Left main coronary artery disease (LMCAD) is a particularly severe phenotypic form of CAD and has a genetic basis. We hypothesized that some inflammation- and hyperhomocysteinemia-related gene polymorphisms may contribute to LMCAD susceptibility in a Chinese population. We studied the association between polymorphisms in the genes hepatocyte nuclear factor 1 alpha (HNF1A; rs7310409, G/A), C-reactive protein (rs1800947 and rs3093059 T/C), methylenetetrahydrofolate reductase (rs1801133, C/T), and methylenetetrahydrofolate dehydrogenase (rs1076991, A/G) in 402 LMCAD and 804 more peripheral CAD patients in a Chinese population. Genotyping was performed using the matrix-assisted laser desorption/ionization tim</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2025-04-04T12:24:35.447Z</modification><creation>2019-03-27T01:35:01Z</creation></dates><accession>S-EPMC4151485</accession><cross_references><pubmed>25202455</pubmed><doi>10.1155/2014/924105</doi></cross_references></HashMap>