Zhang W - Search Results

1

Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment.

Yang Y, Ma M, Li L, Zhang W, Chen P, Ma Y, Liu Y, Tao D, Lin L, Zhang S. Yang Y, et al. Among authors: zhang s, zhang w. Hum Reprod. 2008 Sep;23(9):2167-72. doi: 10.1093/humrep/den229. Epub 2008 Jun 25. Hum Reprod. 2008. PMID: 18579508

2

Single nucleotide polymorphisms of the gonadotrophin-regulated testicular helicase (GRTH) gene may be associated with the human spermatogenesis impairment.

A Z, Zhang S, Yang Y, Ma Y, Lin L, Zhang W. A Z, et al. Among authors: zhang s, zhang w. Hum Reprod. 2006 Mar;21(3):755-9. doi: 10.1093/humrep/dei388. Epub 2005 Nov 17. Hum Reprod. 2006. PMID: 16293649

3

Chromosomal abnormality and Y chromosome microdeletion in Chinese patients with azoospermia or severe oligozoospermia.

Zhou-Cun A, Yang Y, Zhang SZ, Zhang W, Lin L. Zhou-Cun A, et al. Among authors: zhang sz, zhang w. Yi Chuan Xue Bao. 2006 Feb;33(2):111-6. doi: 10.1016/s0379-4172(06)60029-2. Yi Chuan Xue Bao. 2006. PMID: 16529294

4

Mutation screening of the FKBP6 gene and its association study with spermatogenic impairment in idiopathic infertile men.

Zhang W, Zhang S, Xiao C, Yang Y, Zhoucun A. Zhang W, et al. Among authors: zhang s. Reproduction. 2007 Feb;133(2):511-6. doi: 10.1530/REP-06-0125. Reproduction. 2007. PMID: 17307919

5

Some single nucleotide polymorphisms of MSY2 gene might contribute to susceptibility to spermatogenic impairment in idiopathic infertile men.

Deng Y, Zhang W, Su D, Yang Y, Ma Y, Zhang H, Zhang S. Deng Y, et al. Among authors: zhang s, zhang w, zhang h. Urology. 2008 May;71(5):878-82. doi: 10.1016/j.urology.2007.12.055. Epub 2008 Apr 18. Urology. 2008. PMID: 18372033

6

Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment.

Zhang W, Yang Y, Su D, Ma Y, Zhang S. Zhang W, et al. Among authors: zhang s. Syst Biol Reprod Med. 2008 Mar-Apr;54(2):93-5. doi: 10.1080/19396360701883266. Syst Biol Reprod Med. 2008. PMID: 18536151

7

Some single-nucleotide polymorphisms of the TSSK2 gene may be associated with human spermatogenesis impairment.

Zhang H, Su D, Yang Y, Zhang W, Liu Y, Bai G, Ma M, Ma Y, Zhang S. Zhang H, et al. Among authors: zhang s, zhang w. J Androl. 2010 Jul-Aug;31(4):388-92. doi: 10.2164/jandrol.109.008466. Epub 2009 Nov 19. J Androl. 2010. PMID: 19926886 Free article.

8

[Possible association between 278C/A single nucleotide polymorphism of FKBP6 and idiopathic azoospermia].

Zhang W, Zhang SZ, Xiao CY, Yang Y, Ma YX, Cheng L, A ZC, He GP, Shi JJ. Zhang W, et al. Among authors: zhang sz. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):10-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15696470 Chinese.

9

The common variant N372H in BRCA2 gene may be associated with idiopathic male infertility with azoospermia or severe oligozoospermia.

Zhoucun A, Zhang S, Yang Y, Ma Y, Zhang W, Lin L. Zhoucun A, et al. Among authors: zhang s, zhang w. Eur J Obstet Gynecol Reprod Biol. 2006 Jan 1;124(1):61-4. doi: 10.1016/j.ejogrb.2005.09.001. Epub 2005 Oct 27. Eur J Obstet Gynecol Reprod Biol. 2006. PMID: 16257105

10

Single nucleotide polymorphism C677T in the methylenetetrahydrofolate reductase gene might be a genetic risk factor for infertility for Chinese men with azoospermia or severe oligozoospermia.

A ZC, Yang Y, Zhang SZ, Li N, Zhang W. A ZC, et al. Among authors: zhang sz, zhang w. Asian J Androl. 2007 Jan;9(1):57-62. doi: 10.1111/j.1745-7262.2007.00225.x. Epub 2006 Aug 4. Asian J Androl. 2007. PMID: 16888682

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