Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: CYP2U1[original query] |
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Genetic polymorphism of CYP2U1, a cytochrome P450 involved in fatty acids hydroxylation. Prostaglandins, leukotrienes, and essential fatty acids 2010 Aug 83 (2): 105-10. Devos Aurore, Lino Cardenas Christian Lacks, Glowacki François, Engels Anne, Lo-Guidice Jean-Marc, Chevalier Dany, Allorge Delphine, Broly Franck, Cauffiez Christel |
Genetic variants associated with lung function: the long life family study. Respiratory research 2014 15 134. Thyagarajan Bharat, Wojczynski Mary, Minster Ryan L, Sanders Jason, Barral Sandra, Christiansen Lene, Barr R Graham, Newman Anne, |
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease. Brain : a journal of neurology 2015 Nov . Montecchiani Celeste, Pedace Lucia, Lo Giudice Temistocle, Casella Antonella, Mearini Marzia, Gaudiello Fabrizio, Pedroso José L, Terracciano Chiara, Caltagirone Carlo, Massa Roberto, St George-Hyslop Peter H, Barsottini Orlando G P, Kawarai Toshitaka, Orlacchio Anton |
Genomic analysis identifies masqueraders of full-term cerebral palsy. Annals of clinical and translational neurology 2018 May 5 (5): 538-551. Takezawa Yusuke, Kikuchi Atsuo, Haginoya Kazuhiro, Niihori Tetsuya, Numata-Uematsu Yurika, Inui Takehiko, Yamamura-Suzuki Saeko, Miyabayashi Takuya, Anzai Mai, Suzuki-Muromoto Sato, Okubo Yukimune, Endo Wakaba, Togashi Noriko, Kobayashi Yasuko, Onuma Akira, Funayama Ryo, Shirota Matsuyuki, Nakayama Keiko, Aoki Yoko, Kure Shig |
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