Jin L - Search Results

1

A pannexin 1 channelopathy causes human oocyte death.

Sang Q, Zhang Z, Shi J, Sun X, Li B, Yan Z, Xue S, Ai A, Lyu Q, Li W, Zhang J, Wu L, Mao X, Chen B, Mu J, Li Q, Du J, Sun Q, Jin L, He L, Zhu S, Kuang Y, Wang L. Sang Q, et al. Among authors: jin l. Sci Transl Med. 2019 Mar 27;11(485):eaav8731. doi: 10.1126/scitranslmed.aav8731. Sci Transl Med. 2019. PMID: 30918116

2

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. Among authors: jin l. 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

3

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: jin l. 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

4

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. Among authors: jin l. PLoS One. 2013;8(1):e55178. doi: 10.1371/journal.pone.0055178. Epub 2013 Jan 29. PLoS One. 2013. PMID: 23383098 Free PMC article.

5

Identification of microRNAs in human follicular fluid: characterization of microRNAs that govern steroidogenesis in vitro and are associated with polycystic ovary syndrome in vivo.

Sang Q, Yao Z, Wang H, Feng R, Wang H, Zhao X, Xing Q, Jin L, He L, Wu L, Wang L. Sang Q, et al. Among authors: jin l. J Clin Endocrinol Metab. 2013 Jul;98(7):3068-79. doi: 10.1210/jc.2013-1715. Epub 2013 May 10. J Clin Endocrinol Metab. 2013. PMID: 23666971

6

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: jin l. 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

7

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. Among authors: jin l. 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.

8

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: jin l. 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

9

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. Among authors: jin l. 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

10

Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment.

Sang Q, Mei H, Kuermanhan A, Feng R, Guo L, Qu R, Xu Y, Li H, Jin L, He L, Wang L. Sang Q, et al. Among authors: jin l. Mol Genet Genomics. 2015 Jun;290(3):1135-9. doi: 10.1007/s00438-014-0979-1. Epub 2015 Jan 4. Mol Genet Genomics. 2015. PMID: 25557914

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