Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and FMO3[original query] |
---|
Genetic polymorphism of the flavin-containing monooxygenase 3 (FMO3) associated with trimethylaminuria (fish odor syndrome): observations from Japanese patients. Current drug metabolism 2007 Jun 8 (5): 487-91. Yamazaki Hiroshi, Shimizu Maki |
A common FMO3 polymorphism may amplify the effect of nicotine exposure in sudden infant death syndrome (SIDS). International journal of legal medicine 2010 Jul 124 (4): 301-6. Poetsch Micaela, Czerwinski Marco, Wingenfeld Lisa, Vennemann Mechtild, Bajanowski Thom |
FMO3 allelic variants in Sicilian and Sardinian populations: trimethylaminuria and absence of fish-like body odor. Gene 2012 Dec . D'Angelo R, Esposito T, Calabrò M, Rinaldi C, Robledo R, Varriale B, Sidoti A |
Genetic Variant in Flavin-Containing Monooxygenase 3 Alters Lipid Metabolism in Laying Hens in a Diet-Specific Manner. International journal of biological sciences 2016 12 (11): 1382-1393. Wang Jing, Long Cheng, Zhang Haijun, Zhang Yanan, Wang Hao, Yue Hongyuan, Wang Xiaocui, Wu Shugeng, Qi Guangh |
Associations of the T329S Polymorphism in Flavin-Containing Monooxygenase 3 With Atherosclerosis and Fatty Liver Syndrome in 90-Week-Old Hens. Frontiers in veterinary science 2022 4 9 868602. Song Jianlou, Shi Xuefeng, Li Xianyu, Liang Qianni, Zeng Lingsen, Li Guangqi, Yan Yiyuan, Xu Guiyun, Zheng Jiangx |
- Page last reviewed:Feb 1, 2024
- Content source: