Zhao X - 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: zhao x. 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

Promoter hypomethylation of COMT in human placenta is not associated with the development of pre-eclampsia.

Zhao A, Cheng Y, Li X, Li Q, Wang L, Xu J, Xiang Y, Xing Q, He L, Zhao X. Zhao A, et al. Among authors: zhao x. Mol Hum Reprod. 2011 Mar;17(3):199-206. doi: 10.1093/molehr/gaq092. Epub 2010 Nov 3. Mol Hum Reprod. 2011. PMID: 21047975

3

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: zhao x. Hum Genet. 2011 May;129(5):553-61. doi: 10.1007/s00439-011-0954-4. Epub 2011 Jan 28. Hum Genet. 2011. PMID: 21274726

4

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: zhao x. Mol Hum Reprod. 2013 Mar;19(3):153-9. doi: 10.1093/molehr/gas054. Epub 2012 Nov 19. Mol Hum Reprod. 2013. PMID: 23172037

5

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

6

DNA methylome profiling of maternal peripheral blood and placentas reveal potential fetal DNA markers for non-invasive prenatal testing.

Xiang Y, Zhang J, Li Q, Zhou X, Wang T, Xu M, Xia S, Xing Q, Wang L, He L, Zhao X. Xiang Y, et al. Among authors: zhao x. Mol Hum Reprod. 2014 Sep;20(9):875-84. doi: 10.1093/molehr/gau048. Epub 2014 Jul 4. Mol Hum Reprod. 2014. PMID: 24996894

7

Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8.

Chen WY, Shi YY, Zheng YL, Zhao XZ, Zhang GJ, Chen SQ, Yang PD, He L. Chen WY, et al. Hum Mol Genet. 2004 Dec 1;13(23):2991-5. doi: 10.1093/hmg/ddh322. Epub 2004 Oct 15. Hum Mol Genet. 2004. PMID: 15489219

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: zhao x. 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

Up-regulated expression and aberrant DNA methylation of LEP and SH3PXD2A in pre-eclampsia.

Xiang Y, Cheng Y, Li X, Li Q, Xu J, Zhang J, Liu Y, Xing Q, Wang L, He L, Zhao X. Xiang Y, et al. Among authors: zhao x. PLoS One. 2013;8(3):e59753. doi: 10.1371/journal.pone.0059753. Epub 2013 Mar 27. PLoS One. 2013. PMID: 23544093 Free PMC article.

10

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: zhao x. 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

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