Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: UBR2[original query] |
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Single nucleotide polymorphism in the UBR2 gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest. Journal of assisted reproduction and genetics 2011 Aug 28 (8): 743-6. Miyamoto Toshinobu, Tsujimura Akira, Miyagawa Yasushi, Koh Eitetsu, Namiki Mikio, Horikawa Michiharu, Saijo Yasuaki, Sengoku Kaz |
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 |
Association of single nucleotide polymorphisms in UBR2 gene with idiopathic aspermia or oligospermia in Sichuan, China. Andrologia 2016 Mar . Ma T-J, Zhang X-J, Ding X-P, Chen H-H, Zhang Y-W, Ding |
Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency. PloS one 2020 10 15 (10): e0240795. França Monica M, Funari Mariana F A, Lerario Antonio M, Santos Mariza G, Nishi Mirian Y, Domenice Sorahia, Moraes Daniela R, Costalonga Everlayny F, Maciel Gustavo A R, Maciel-Guerra Andrea T, Guerra-Junior Gil, Mendonca Berenice |
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis. Journal of neuroimmunology 2021 12 362 577760. Mascia E, Clarelli F, Zauli A, Guaschino C, Sorosina M, Barizzone N, Basagni C, Santoro S, Ferrè L, Bonfiglio S, Biancolini D, Pozzato M, Guerini F R, Protti A, Liguori M, Moiola L, Vecchio D, Bresolin N, Comi G, Filippi M, Esposito F, D'Alfonso S, Martinelli-Boneschi |
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