Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Syndrome and SLCO1B3[original query] |
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| Serum bilirubin concentration in healthy adult North-Europeans is strictly controlled by the UGT1A1 TA-repeat variants. PloS one 2014 9 (2): e90248. Kringen Marianne K, Piehler Armin P, Grimholt Runa M, Opdal Mimi S, Haug Kari Bente F, Urdal Pett |
| Diltiazem on tacrolimus exposure and dose sparing in Chinese pediatric primary nephrotic syndrome: impact of CYP3A4, CYP3A5, ABCB1, and SLCO1B3 polymorphisms. European journal of clinical pharmacology 2020 Aug . Wang Junyan, Huang Lingfei, Gao Peng, Hu Yan, Ni Yinghua, Zhu Zhengyi, Zhang Liwen, Yang Jufei, Zhang Huifen, Fang L |
| Intronic LINE-1 insertion in SLCO1B3 as a highly prevalent cause of rotor syndrome in East Asian population. Journal of human genetics 2021 Aug . Kim Young-Gon, Sung Hobin, Shin Ho Seob, Kim Man Jin, Lee Jee-Soo, Park Sung-Sup, Seong Moon-W |
| [Clinical characteristics and genetic analysis of four children with Rotor syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 5 41 (6): 715-719. Yanfang Tan, Wenxian Ouyang, Tao Jiang, Lian Tang, Hui Zhang, Ying Yu, Xiaomei Qin, Shuangjie |
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