Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: SLC26A8[original query] |
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Mutational analysis of the human SLC26A8 gene: exclusion as a candidate for male infertility due to primary spermatogenic failure. Molecular human reproduction 2005 Feb 11 (2): 129-32. Mäkelä S, Eklund R, Lähdetie J, Mikkola M, Hovatta O, Kere |
Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia. American journal of human genetics 2013 May 92 (5): 760-6. Dirami Thassadite, Rode Baptiste, Jollivet Mathilde, Da Silva Nathalie, Escalier Denise, Gaitch Natacha, Norez Caroline, Tuffery Pierre, Wolf Jean-Philippe, Becq Frédéric, Ray Pierre F, Dulioust Emmanuel, Gacon Gérard, Bienvenu Thierry, Touré Amina |
A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12. PloS one 2015 10 (8): e0134720. Bianchi Matteo, Dahlgren Stina, Massey Jonathan, Dietschi Elisabeth, Kierczak Marcin, Lund-Ziener Martine, Sundberg Katarina, Thoresen Stein Istre, Kämpe Olle, Andersson Göran, Ollier William E R, Hedhammar Åke, Leeb Tosso, Lindblad-Toh Kerstin, Kennedy Lorna J, Lingaas Frode, Rosengren Pielberg Ger |
Screening for susceptibility genes in hereditary non-polyposis colorectal cancer. Oncology letters 2018 Jun 15 (6): 9413-9419. Yu Li, Yin Bo, Qu Kaiying, Li Jingjing, Jin Qiao, Liu Ling, Liu Chunlan, Zhu Yuxing, Wang Qi, Peng Xiaowei, Zhou Jianda, Cao Peiguo, Cao |
Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease. Human mutation 2021 12 43 (3): 434-443. Gao Yang, Wu Huan, Xu Yuping, Shen Qunshan, Xu Chuan, Geng Hao, Lv Mingrong, Tan Qing, Li Kuokuo, Tang Dongdong, Song Bing, Zhou Ping, Wei Zhaolian, He Xiaojin, Cao Yunx |
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- Page last updated:Apr 29, 2024
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