Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Syndrome and ABCC2[original query] |
---|
Urinary elimination of coproporphyrins is dependent on ABCC2 polymorphisms and represents a potential biomarker of MRP2 activity in humans. Journal of biomedicine & biotechnology 2011 2011 . Benz-de Bretagne I, Respaud R, Vourc'h P, Halimi JM, Caille A, Hulot JS, Andres CR, Le Guellec C |
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 |
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 |
A pharmacogenetic candidate gene study of tenofovir-associated Fanconi syndrome. Pharmacogenetics and genomics 2015 Feb 25 (2): 82-92. Dahlin Amber, Wittwer Matthias, de la Cruz Melanie, Woo Jonathan M, Bam Rujuta, Scharen-Guivel Valeska, Flaherty John, Ray Adrian S, Cihlar Tomas, Gupta Samir K, Giacomini Kathleen |
Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2. European journal of human genetics : EJHG 2015 Sep . Slachtova Lenka, Seda Ondrej, Behunova Jana, Mistrik Martin, Martasek Pav |
Germline TYMS genotype is highly predictive in patients with metastatic gastrointestinal malignancies receiving capecitabine-based chemotherapy. Cancer chemotherapy and pharmacology 2015 Apr 75 (4): 763-72. Joerger M, Huitema A D R, Boot H, Cats A, Doodeman V D, Smits P H M, Vainchtein L, Rosing H, Meijerman I, Zueger M, Meulendijks D, Cerny T D, Beijnen J H, Schellens J H |
A Prediction Algorithm for Drug Response in Patients with Mesial Temporal Lobe Epilepsy Based on Clinical and Genetic Information. PloS one 2017 12 (1): e0169214. Silva-Alves Mariana S, Secolin Rodrigo, Carvalho Benilton S, Yasuda Clarissa L, Bilevicius Elizabeth, Alvim Marina K M, Santos Renato O, Maurer-Morelli Claudia V, Cendes Fernando, Lopes-Cendes Isc |
Genetic contribution of ABCC2 to Dubin-Johnson syndrome and inherited cholestatic disorders. Liver international : official journal of the International Association for the Study of the Liver 2019 9 40 (1): 163-174. Corpechot Christophe, Barbu Véronique, Chazouillères Olivier, Broué Pierre, Girard Muriel, Roquelaure Bertrand, Chrétien Yves, Dong Catherine, Lascols Olivier, Housset Chantal, Jéru Isabel |
Influence of CYP3A4/5 and ABC transporter polymorphisms on lenvatinib plasma trough concentrations in Japanese patients with thyroid cancer. Scientific reports 2019 Apr 9 (1): 5404. Ozeki Tomoko, Nagahama Mitsuji, Fujita Kazuma, Suzuki Akifumi, Sugino Kiminori, Ito Koichi, Miura Masato |
[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 |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: