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Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Fan S, Jiao Y, Khan R, Jiang X, Javed AR, Ali A, Zhang H, Zhou J, Naeem M, Murtaza G, Li Y, Yang G, Zaman Q, Zubair M, Guan H, Zhang X, Ma H, Jiang H, Ali H, Dil S, Shah W, Ahmad N, Zhang Y, Shi Q. Fan S, et al. Among authors: yang g. Am J Hum Genet. 2021 Feb 4;108(2):324-336. doi: 10.1016/j.ajhg.2021.01.010. Epub 2021 Jan 27. Am J Hum Genet. 2021. PMID: 33508233 Free PMC article.
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Fan S, Jiao Y, Khan R, Jiang X, Javed AR, Ali A, Zhang H, Zhou J, Naeem M, Murtaza G, Li Y, Yang G, Zaman Q, Zubair M, Guan H, Zhang X, Ma H, Jiang H, Ali H, Dil S, Shah W, Ahmad N, Zhang Y, Shi Q. Fan S, et al. Among authors: yang g. Am J Hum Genet. 2022 Jul 7;109(7):1343. doi: 10.1016/j.ajhg.2022.06.006. Am J Hum Genet. 2022. PMID: 35803236 Free PMC article. No abstract available.
Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans.
Liu J, Rahim F, Zhou J, Fan S, Jiang H, Yu C, Chen J, Xu J, Yang G, Shah W, Zubair M, Khan A, Li Y, Shah B, Zhao D, Iqbal F, Jiang X, Guo T, Xu P, Xu B, Wu L, Ma H, Zhang Y, Zhang H, Shi Q. Liu J, et al. Among authors: yang g. iScience. 2023 Jun 28;26(7):107193. doi: 10.1016/j.isci.2023.107193. eCollection 2023 Jul 21. iScience. 2023. PMID: 37485353 Free PMC article.
Eimeria: Navigating complex intestinal ecosystems.
Weng S, Tian E, Gao M, Zhang S, Yang G, Zhou B. Weng S, et al. Among authors: yang g. PLoS Pathog. 2024 Nov 22;20(11):e1012689. doi: 10.1371/journal.ppat.1012689. eCollection 2024 Nov. PLoS Pathog. 2024. PMID: 39576763 Review.
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