HuGE Literature Finder
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| Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes. Human molecular genetics 2020 May . Chen Shitao, Wang Guishuan, Zheng Xiaoguo, Ge Shunna, Dai Yubing, Ping Ping, Chen Xiangfeng, Liu Guihua, Zhang Jing, Yang Yang, Zhang Xinzong, Zhong An, Zhu Yongtong, Chu Qingjun, Huang Yonghan, Zhang Yong, Shen Changli, Yuan Yiming, Yuan Qilong, Pei Xiuying, Cheng C Yan, Sun F |
| Genetic association study of RNF8 and BRDT variants with non-obstructive azoospermia in the Chinese Han population. Systems biology in reproductive medicine 2015 Jan 61 (1): 26-31. Zhang Yan, Song Bing, Du Wei-Dong, He Xiao-Jin, Ruan Jian, Zhou Fu-Sheng, Zuo Xian-Bo, Ye Lei, Xie Xu-Shi, Cao Yun-X |
| Excess of rare variants in genes that are key epigenetic regulators of spermatogenesis in the patients with non-obstructive azoospermia. Scientific reports 2015 5 8785. Li Zesong, Huang Yi, Li Honggang, Hu Jingchu, Liu Xiao, Jiang Tao, Sun Guangqing, Tang Aifa, Sun Xiaojuan, Qian Weiping, Zeng Yong, Xie Jun, Zhao Wei, Xu Yu, He Tingting, Dong Chengliang, Liu Qunlong, Mou Lisha, Lu Jingxiao, Lin Zheguang, Wu Song, Gao Shengjie, Guo Guangwu, Feng Qiang, Li Yingrui, Zhang Xiuqing, Wang Jun, Yang Huanming, Wang Jian, Xiong Chengliang, Cai Zhiming, Gui Yaoti |
| BRDT gene sequence in human testicular pathologies and the implication of its single nucleotide polymorphism (rs3088232) on fertility. Andrology 2014 Jul 2 (4): 641-7. Barda S, Yogev L, Paz G, Yavetz H, Lehavi O, Hauser R, Doniger T, Breitbart H, Kleiman S |
| Association study of single-nucleotide polymorphisms in FASLG, JMJDIA, LOC203413, TEX15, BRDT, OR2W3, INSR, and TAS2R38 genes with male infertility. Journal of andrology 0 33 (4): 675-83. Plaseski Toso, Noveski Predrag, Popeska Zaneta, Efremov Georgi D, Plaseska-Karanfilska Dija |
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