Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Liver Diseases and ABCC2[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 |
| STAT3 signaling pathway plays importantly genetic and functional roles in HCV infection. Molecular genetics & genomic medicine 2019 Jun e821. Song Yuzhu, Yang Xianyao, Shen Yunsong, Wang Yiqian, Xia Xueshan, Zhang A-M |
| Wilson disease, ABCC2 c.3972C > T polymorphism and primary liver cancers: suggestions from a familial cluster. BMC medical genetics 2020 11 21 (1): 225. Brandi Giovanni, Rizzo Alessandro, Deserti Marzia, Relli Valeria, Indio Valentina, Bin Sofia, Pariali Milena, Palloni Andrea, De Lorenzo Stefania, Tovoli Francesco, Tavolari Simo |
| [Genetic analysis of a case with Dubin-Johnson syndrome due to two novel variants of ABCC2 gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 9 39 (9): 974-978. Zhao Ganye, Zhao Xuechao, Liu Li'na, Wang Conghui, Li Qianqian, Kong Xiangdo |
| Population-based meta-analysis and gene-set enrichment identifies FXR/RXR pathway as common to fatty liver disease and serum lipids. Hepatology communications 2022 Sep . Handelman Samuel K, Puentes Yindra M, Kuppa Annapurna, Chen Yanhua, Du Xiaomeng, Feitosa Mary F, Palmer Nicholette D, Speliotes Elizabeth |
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