Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Liver Diseases and UGT1A1[original query] |
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Gilbert syndrome redefined: a complex genetic haplotype influences the regulation of glucuronidation. Hepatology (Baltimore, Md.) 2012 Jun 55 (6): 1912-21. Ehmer Ursula, Kalthoff Sandra, Fakundiny Bastian, Pabst Brigitte, Freiberg Nicole, Naumann Ronald, Manns Michael P, Strassburg Christian |
Association between inherited monogenic liver disorders and chronic hepatitis C. World journal of hepatology 2014 Feb 6 (2): 92-7. Piekuse Linda, Kreile Madara, Zarina Agnese, Steinberga Zane, Sondore Valentina, Keiss Jazeps, Lace Baiba, Krumina Astri |
"Gilbert's-like" syndrome as part of a spectrum of persistent unconjugated hyperbilirubinemia in post-chronic hepatitis patients. Scientific reports 2018 Jan 8 (1): 2008. Ye Jin, Cui Lianlian, Zhou Yingqiao, Huang Ying, Banafa Omar, Hou Xiaohua, Ding Zhen, Lin Ro |
Compound heterozygous UGT1A1*28 and UGT1A1*6 or single homozygous UGT1A1*28 are major genotypes associated with Gilbert's syndrome in Chinese Han people. Gene 2021 2 781 145526. Zhang Meng, Wang Hongwu, Huang Yuancheng, Xu Xin, Liu Wei, Ning Qin, Chen Tao, Qi Junyi |
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