Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: SLC7A1[original query] |
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Identification of a novel polymorphism in the 3'UTR of the L-arginine transporter gene SLC7A1: contribution to hypertension and endothelial dysfunction. Circulation 2007 Mar 115 (10): 1269-74. Yang Zhiyong, Venardos Kylie, Jones Emma, Morris Brian J, Chin-Dusting Jaye, Kaye David |
Contribution of SLC7A1 genetic variant to hypertension, the TAMRISK study. BMC medical genetics 2013 14 (1): 69. Määttä Kirsi, Kunnas Tarja, Nikkari Seppo |
Genome-wide association study analysis of disease severity in Acne reveals novel biological insights. medRxiv : the preprint server for health sciences 2023 11 . Zhaohui Du, Tejaswi Iyyanki, Samuel Lessard, Michael Chao, , Christian Asbrand, Dany Nassar, Katherine Klinger, Emanuele de Rinaldis, Shameer Khader, Clément Chatela |
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- Page last updated:Apr 29, 2024
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