Sang Q - Search Results

1

Bi-allelic variants in KCNU1 cause impaired acrosome reactions and male infertility.

Liu R, Yan Z, Fan Y, Qu R, Chen B, Li B, Wu L, Wu H, Mu J, Zhao L, Wang W, Dong J, Zeng Y, Li Q, Wang L, Sang Q, Zhang Z, Kuang Y. Liu R, et al. Among authors: sang q. Hum Reprod. 2022 Jun 30;37(7):1394-1405. doi: 10.1093/humrep/deac102. Hum Reprod. 2022. PMID: 35551387

2

Common genetic variation in the 3'-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well as insulin sensitivity in polycystic ovary syndrome patients.

Li Q, Yang G, Wang Y, Zhang X, Sang Q, Wang H, Zhao X, Xing Q, He L, Wang L. Li Q, et al. Among authors: sang q. Hum Genet. 2011 May;129(5):553-61. doi: 10.1007/s00439-011-0954-4. Epub 2011 Jan 28. Hum Genet. 2011. PMID: 21274726

3

A common polymorphism in the human aromatase gene alters the risk for polycystic ovary syndrome and modifies aromatase activity in vitro.

Wang H, Li Q, Wang T, Yang G, Wang Y, Zhang X, Sang Q, Wang H, Zhao X, Xing Q, Shi J, He L, Wang L. Wang H, et al. Among authors: sang q. Mol Hum Reprod. 2011 Jun;17(6):386-91. doi: 10.1093/molehr/gar007. Epub 2011 Jan 31. Mol Hum Reprod. 2011. PMID: 21282199

4

Quantitative analysis of follistatin (FST) promoter methylation in peripheral blood of patients with polycystic ovary syndrome.

Sang Q, Zhang S, Zou S, Wang H, Feng R, Li Q, Jin L, He L, Xing Q, Wang L. Sang Q, et al. Reprod Biomed Online. 2013 Feb;26(2):157-63. doi: 10.1016/j.rbmo.2012.10.011. Epub 2012 Oct 23. Reprod Biomed Online. 2013. PMID: 23265961

5

Common genetic variation in CYP1B1 is associated with concentrations of T₄, FT₃ and FT₄ in the sera of polycystic ovary syndrome patients.

Zou S, Sang Q, Wang H, Feng R, Li Q, Zhao X, Xing Q, Jin L, He L, Wang L. Zou S, et al. Among authors: sang q. Mol Biol Rep. 2013 Apr;40(4):3315-20. doi: 10.1007/s11033-012-2406-1. Epub 2013 Jan 3. Mol Biol Rep. 2013. PMID: 23283740

6

Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).

Sang Q, Yan X, Wang H, Feng R, Fei X, Ma D, Xing Q, Li Q, Zhao X, Jin L, He L, Li H, Wang L. Sang Q, et al. PLoS One. 2013;8(1):e55178. doi: 10.1371/journal.pone.0055178. Epub 2013 Jan 29. PLoS One. 2013. PMID: 23383098 Free PMC article.

7

A possible new mechanism in the pathophysiology of polycystic ovary syndrome (PCOS): the discovery that leukocyte telomere length is strongly associated with PCOS.

Li Q, Du J, Feng R, Xu Y, Wang H, Sang Q, Xing Q, Zhao X, Jin L, He L, Wang L. Li Q, et al. Among authors: sang q. J Clin Endocrinol Metab. 2014 Feb;99(2):E234-40. doi: 10.1210/jc.2013-3685. Epub 2013 Dec 3. J Clin Endocrinol Metab. 2014. PMID: 24302747

8

Quantitative methylation level of the EPHX1 promoter in peripheral blood DNA is associated with polycystic ovary syndrome.

Sang Q, Li X, Wang H, Wang H, Zhang S, Feng R, Xu Y, Li Q, Zhao X, Xing Q, Jin L, He L, Wang L. Sang Q, et al. PLoS One. 2014 Feb 5;9(2):e88013. doi: 10.1371/journal.pone.0088013. eCollection 2014. PLoS One. 2014. PMID: 24505354 Free PMC article. Clinical Trial.

9

Polymorphisms of pentanucleotide repeats (tttta)n in the promoter of CYP11A1 and their relationships to polycystic ovary syndrome (PCOS) risk: a meta-analysis.

Yu M, Feng R, Sun X, Wang H, Wang H, Sang Q, Jin L, He L, Wang L. Yu M, et al. Among authors: sang q. Mol Biol Rep. 2014 Jul;41(7):4435-45. doi: 10.1007/s11033-014-3314-3. Epub 2014 Mar 9. Mol Biol Rep. 2014. PMID: 24610422

10

Ildr1b is essential for semicircular canal development, migration of the posterior lateral line primordium and hearing ability in zebrafish: implications for a role in the recessive hearing impairment DFNB42.

Sang Q, Zhang J, Feng R, Wang X, Li Q, Zhao X, Xing Q, Chen W, Du J, Sun S, Chai R, Liu D, Jin L, He L, Li H, Wang L. Sang Q, et al. Hum Mol Genet. 2014 Dec 1;23(23):6201-11. doi: 10.1093/hmg/ddu340. Epub 2014 Jul 2. Hum Mol Genet. 2014. PMID: 24990150

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