<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang Y</submitter><funding>NIAAA NIH HHS</funding><pagination>46490</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5399367</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7</volume><pubmed_abstract>The sodium taurocholate cotransporting polypeptide (NTCP) encoded by SLC10A1 was recently demonstrated to be a functional receptor for hepatitis B virus (HBV). The role of SLC10A1 polymorphisms, particularly the Ser267Phe variant (rs2296651) in exon 4, has been frequently investigated in regard to risk of persistent HBV infection. However, these investigations have generated conflicting results. To examine whether common genetic variation at the SLC10A1 locus is associated with risk of persistent HBV infection, haplotype-tagging and imputed single nucleotide polymorphisms (SNPs) were assessed in two case-control sample sets, totally including 2,550 cases (persistently HBV infected subjects, PIs) and 2,124 controls (spontaneously recovered subjects, SRs) of Southern Chinese ancestry. To tes</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Comprehensive assessment showed no associations of variants at the SLC10A1 locus with susceptibility to persistent HBV infection among Southern Chinese.</pubmed_title><pmcid>PMC5399367</pmcid><funding_grant_id>U24 AA022002</funding_grant_id><pubmed_authors>Bei J</pubmed_authors><pubmed_authors>He F</pubmed_authors><pubmed_authors>Wu M</pubmed_authors><pubmed_authors>Ping J</pubmed_authors><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Hu Z</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Shen H</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Zhai Y</pubmed_authors><pubmed_authors>Lu H</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Cui Y</pubmed_authors><pubmed_authors>Mo Z</pubmed_authors><pubmed_authors>Zhou G</pubmed_authors><pubmed_authors>Cao P</pubmed_authors><pubmed_authors>Guo B</pubmed_authors><pubmed_authors>Zeng YX</pubmed_authors><pubmed_authors>Ren Q</pubmed_authors><pubmed_authors>Xie B</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors><pubmed_authors>Liu G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comprehensive assessment showed no associations of variants at the SLC10A1 locus with susceptibility to persistent HBV infection among Southern Chinese.</name><description>The sodium taurocholate cotransporting polypeptide (NTCP) encoded by SLC10A1 was recently demonstrated to be a functional receptor for hepatitis B virus (HBV). The role of SLC10A1 polymorphisms, particularly the Ser267Phe variant (rs2296651) in exon 4, has been frequently investigated in regard to risk of persistent HBV infection. However, these investigations have generated conflicting results. To examine whether common genetic variation at the SLC10A1 locus is associated with risk of persistent HBV infection, haplotype-tagging and imputed single nucleotide polymorphisms (SNPs) were assessed in two case-control sample sets, totally including 2,550 cases (persistently HBV infected subjects, PIs) and 2,124 controls (spontaneously recovered subjects, SRs) of Southern Chinese ancestry. To tes</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Apr</publication><modification>2026-05-30T00:00:34.102Z</modification><creation>2019-03-27T02:41:46Z</creation></dates><accession>S-EPMC5399367</accession><cross_references><pubmed>28429786</pubmed><doi>10.1038/srep46490</doi></cross_references></HashMap>