網(wǎng)站首頁
醫(yī)師
藥師
護士
衛(wèi)生資格
高級職稱
住院醫(yī)師
畜牧獸醫(yī)
醫(yī)學(xué)考研
醫(yī)學(xué)論文
醫(yī)學(xué)會議
考試寶典
網(wǎng)校
論壇
招聘
最新更新
網(wǎng)站地圖
您現(xiàn)在的位置: 醫(yī)學(xué)全在線 > 考研院校 > 西北西南 > 四川大學(xué)華西醫(yī)學(xué)院 > 導(dǎo)師信息 > 正文:四川大學(xué)華西醫(yī)學(xué)院博導(dǎo)張思仲簡介
    

四川大學(xué)華西醫(yī)學(xué)院遺傳學(xué)博士生導(dǎo)師張思仲信息介紹



1.Yang Y, Ma M, Zhang S.Massive deletion in AZFb/b+c and azoospermia with Sertoli cell only and/or maturation arrest. Int J Androl. 2008,31(6):573-8.
2.Deng Y, Zhang W, Zhang S. Some single nucleotide polymorphisms of MSY2 gene might contribute to susceptibility to spermatogenic impairment in idiopathic infertile men. Urology. 2008, 71(5):878-82.
3.Yang Y, Ma M, Zhang S.Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment. Hum Reprod. 2008,23(9):2167-72.
4.Yang Y, Ma M, Zhang S. Evidence for the association of Y-chromosome haplogroups with susceptibility to spermatogenic failure in a Chinese Han population. J Med Genet, 2008, 45(4):210-5.
5.Song H, Su D, Zhang S. Expression and localization of the spermatogenesis-related gene, Znf230, in mouse testis and spermatozoa during postnatal development. BMB Rep. 2008, 41(9):664-9.
6. Zhang W, Yang Y, Zhang S. Absence of the H2AX mutations in idiopathic infertile men with spermatogenic gydjdsj.org.cn impairment. Syst Biol Reprod Med, 2008,54(2):93-5.
7.Xu W, Zhang S, Qiu W. Spermatogenesis-related ring finger gene ZNF230 promoter: identification and functional analysis. Mol Biol Rep. 2009, 36(5):1187-93.
8.Liu YQ, Bai G, Zhang SZ. Human RING finger protein ZNF645 is a novel testis-specific E3 ubiquitin ligase. Asian J Androl. 2010 ,12(5):658-66.
9.Bai G, Liu Y, Zhang S. Promoter demethylation mediates the expression of ZNF645, a novel cancer/testis gene. BMB Rep,2010,43(6):400-6.
10. Yang Y, Ma M, Zhang S. Differential effect of specific gr/gr deletion subtypes on spermatogenesis in the Chinese Han population. Int J Androl. 2010,33(5):745-54.
11.Ma M, Yang Y, Zhang S. Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population. J Neurol Sci. 2010, 298(1-2):57-60.
12.Li J, Yu C, Zhang S. Putative mutation of PKD1 gene responsible for autosomal dominant polycystic kidney disease in a Chinese family. Int J Urol.2011, 18(3):240-2.
聯(lián)系方式:
電話: 028-85164009    郵箱:Szzhang@mcwcums.com

上一頁  [1] [2] [3]  下一頁

關(guān)于我們 - 聯(lián)系我們 -版權(quán)申明 -誠聘英才 - 網(wǎng)站地圖 - 醫(yī)學(xué)論壇 - 醫(yī)學(xué)博客 - 網(wǎng)絡(luò)課程 - 幫助
醫(yī)學(xué)全在線 版權(quán)所有© CopyRight 2006-2010, MED126.COM, All Rights Reserved
浙ICP備12017320號 
百度大聯(lián)盟認證綠色會員