Wang L - Search Results

1

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: wang x, wang 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

2

A pharmacogenetic study of risperidone on histamine H3 receptor gene (HRH3) in Chinese Han schizophrenia patients.

Wei Z, Wang L, Zhang M, Xuan J, Wang Y, Liu B, Shao L, Li J, Zeng Z, Li T, Liu J, Wang T, Zhang M, Qin S, Xu Y, Feng G, He L, Xing Q. Wei Z, et al. Among authors: wang l, wang y, wang t. J Psychopharmacol. 2012 Jun;26(6):813-8. doi: 10.1177/0269881111405358. Epub 2011 Jun 7. J Psychopharmacol. 2012. PMID: 21652606

3

Analysis of JAG1 gene variant in Chinese patients with Alagille syndrome.

Wang H, Wang X, Li Q, Chen S, Liu L, Wei Z, Wang L, Liu Y, Zhao X, He L, Wang J, Xing Q. Wang H, et al. Among authors: wang x, wang l, wang j. Gene. 2012 May 10;499(1):191-3. doi: 10.1016/j.gene.2012.02.038. Epub 2012 Mar 2. Gene. 2012. PMID: 22405927

4

Lack of support for association between the copy number variants in the FCGR locus and schizophrenia: a case control study.

Zhao A, Xiang Y, Xu J, Li Q, Wang L, Xing Q, Zhang Z, Liu Y, Feng G, He L, Zhao X. Zhao A, et al. Among authors: wang l. Neurosci Lett. 2012 Aug 1;522(2):85-91. doi: 10.1016/j.neulet.2012.04.037. Epub 2012 May 1. Neurosci Lett. 2012. PMID: 22580203

5

Association between a COMT polymorphism and clinical response to risperidone treatment: a pharmacogenetic study.

Zhao QZ, Liu BC, Zhang J, Wang L, Li XW, Wang Y, Ji J, Yang FP, Wan CL, Xu YF, Feng GY, He L, He G. Zhao QZ, et al. Among authors: wang l, wang y. Psychiatr Genet. 2012 Dec;22(6):298-9. doi: 10.1097/YPG.0b013e328358629a. Psychiatr Genet. 2012. PMID: 22935916

6

Promoter hypomethylation of TIMP3 is associated with pre-eclampsia in a Chinese population.

Xiang Y, Zhang X, Li Q, Xu J, Zhou X, Wang T, Xing Q, Liu Y, Wang L, He L, Zhao X. Xiang Y, et al. Among authors: wang l, wang t. Mol Hum Reprod. 2013 Mar;19(3):153-9. doi: 10.1093/molehr/gas054. Epub 2012 Nov 19. Mol Hum Reprod. 2013. PMID: 23172037

7

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: wang h, wang 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

8

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: wang h, wang 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

9

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: wang h, wang 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.

10

Association of Interleukin 6 gene polymorphisms with genetic susceptibilities to spastic tetraplegia in males: a case-control study.

Chen M, Li T, Lin S, Bi D, Zhu D, Shang Q, Ma C, Wang H, Wang L, Zhang Y, He L, Zhu C, Xing Q. Chen M, et al. Among authors: wang h, wang l. Cytokine. 2013 Mar;61(3):826-30. doi: 10.1016/j.cyto.2013.01.011. Epub 2013 Feb 13. Cytokine. 2013. PMID: 23415255

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