Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and EPHX1[original query] |
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Genetic variation in genes for the xenobiotic-metabolizing enzymes CYP1A1, EPHX1, GSTM1, GSTT1, and GSTP1 and susceptibility to colorectal cancer in Lynch syndrome. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008 Sep 17 (9): 2393-401. Pande Mala, Amos Christopher I, Osterwisch Daniel R, Chen Jinyun, Lynch Patrick M, Broaddus Russell, Frazier Marsha |
eNOSI4 and EPHX1 polymorphisms affect maternal susceptibility to preeclampsia: analysis of five polymorphisms predisposing to cardiovascular disease in 279 Caucasian and 241 African women. Archives of gynecology and obstetrics 2014 Mar 289 (3): 581-93. Groten T, Schleussner E, Lehmann T, Reister F, Holzer B, Danso K A, Zeillinger |
Association of ABCB1, CYP3A4, EPHX1, FAS, SCN1A, MICA, and BAG6 polymorphisms with the risk of carbamazepine-induced Stevens-Johnson syndrome/toxic epidermal necrolysis in Chinese Han patients with epilepsy. Epilepsia 2014 Aug 55 (8): 1301-6. He Xiao-Jing, Jian Ling-Yan, He Xiao-Lin, Tang Man, Wu Yan, Xu Yuan-Yuan, Sun Xiao-Jie, Zhao Li-M |
Genetic variants associated with severe cutaneous adverse drug reactions induced by carbamazepine. British journal of clinical pharmacology 2021 Aug . Nakkam Nontaya, Konyoung Parinya, Amornpinyo Warayuwadee, Saksit Niwat, Tiamkao Somsak, Khunarkornsiri Usanee, Khaeso Kanyarat, Pattanacheewapull Oranuch, Jorns Teekayu Plangkoon, Chumworathayi Pansu, Tassaneeyakul Wichitt |
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