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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: jiao y. 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.
Reprogramming of Meiotic Chromatin Architecture during Spermatogenesis.
Wang Y, Wang H, Zhang Y, Du Z, Si W, Fan S, Qin D, Wang M, Duan Y, Li L, Jiao Y, Li Y, Wang Q, Shi Q, Wu X, Xie W. Wang Y, et al. Among authors: jiao y. Mol Cell. 2019 Feb 7;73(3):547-561.e6. doi: 10.1016/j.molcel.2018.11.019. Mol Cell. 2019. PMID: 30735655 Free 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: jiao y. 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.
A TOP6BL mutation abolishes meiotic DNA double-strand break formation and causes human infertility.
Jiao Y, Fan S, Jabeen N, Zhang H, Khan R, Murtaza G, Jiang H, Ali A, Li Y, Bao J, Zhang B, Xu J, Xu B, Hussain HMJ, Zaman Q, Khan I, Bukhari I, Iqbal F, Yousaf A, Dil S, Khan M, Ahmad N, Ma H, Jiang X, Zhang Y, Shi Q. Jiao Y, et al. Sci Bull (Beijing). 2020 Dec 30;65(24):2120-2129. doi: 10.1016/j.scib.2020.08.026. Epub 2020 Aug 20. Sci Bull (Beijing). 2020. PMID: 36732965
14 results