Wang T - Search Results

1

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: wang l, wang y, wang t. Mol Hum Reprod. 2011 Jun;17(6):386-91. doi: 10.1093/molehr/gar007. Epub 2011 Jan 31. Mol Hum Reprod. 2011. PMID: 21282199

2

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

3

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: wang l, wang t. Mol Hum Reprod. 2014 Sep;20(9):875-84. doi: 10.1093/molehr/gau048. Epub 2014 Jul 4. Mol Hum Reprod. 2014. PMID: 24996894

4

SASH1 regulates melanocyte transepithelial migration through a novel Gαs-SASH1-IQGAP1-E-Cadherin dependent pathway.

Zhou D, Wei Z, Deng S, Wang T, Zai M, Wang H, Guo L, Zhang J, Zhong H, He L, Xing Q. Zhou D, et al. Among authors: wang h, wang t. Cell Signal. 2013 Jun;25(6):1526-38. doi: 10.1016/j.cellsig.2012.12.025. Epub 2013 Jan 16. Cell Signal. 2013. PMID: 23333244

5

Experimental validation of candidate schizophrenia gene CALN1 as a target for microRNA-137.

Xia S, Zhou X, Wang T, Zhang Q, Li Q, Liu Y, Xing Q, Wang L, He L, Zhao X. Xia S, et al. Among authors: wang l, wang t. Neurosci Lett. 2015 Aug 18;602:110-4. doi: 10.1016/j.neulet.2015.07.001. Epub 2015 Jul 7. Neurosci Lett. 2015. PMID: 26163462

6

Opioid Exposure is Associated with Aberrant DNA Methylation of OPRM1 Promoter Region in a Chinese Han Population.

Xu J, Wang T, Su Z, Zhou X, Xiang Y, He L, Li C, Yang Z, Zhao X. Xu J, et al. Among authors: wang t. Biochem Genet. 2018 Oct;56(5):451-458. doi: 10.1007/s10528-018-9852-y. Epub 2018 Mar 21. Biochem Genet. 2018. PMID: 29564682

7

The aberrantly expressed miR-193b-3p contributes to preeclampsia through regulating transforming growth factor-β signaling.

Zhou X, Li Q, Xu J, Zhang X, Zhang H, Xiang Y, Fang C, Wang T, Xia S, Zhang Q, Xing Q, He L, Wang L, Xu M, Zhao X. Zhou X, et al. Among authors: wang l, wang t. Sci Rep. 2016 Jan 29;6:19910. doi: 10.1038/srep19910. Sci Rep. 2016. PMID: 26822621 Free PMC article.

8

A novel insertional mutation in the connexin 46 (gap junction alpha 3) gene associated with autosomal dominant congenital cataract in a Chinese family.

Zhou D, Ji H, Wei Z, Guo L, Li Y, Wang T, Zhu Y, Dong X, Wang Y, He L, Xing Q, Zhang L. Zhou D, et al. Among authors: wang y, wang t. Mol Vis. 2013 Apr 5;19:789-95. Print 2013. Mol Vis. 2013. PMID: 23592915 Free PMC article.

9

Prenatal nutritional deficiency reprogrammed postnatal gene expression in mammal brains: implications for schizophrenia.

Xu J, He G, Zhu J, Zhou X, St Clair D, Wang T, Xiang Y, Zhao Q, Xing Q, Liu Y, Wang L, Li Q, He L, Zhao X. Xu J, et al. Among authors: wang l, wang t. Int J Neuropsychopharmacol. 2014 Oct 31;18(4):pyu054. doi: 10.1093/ijnp/pyu054. Int J Neuropsychopharmacol. 2014. PMID: 25522397 Free PMC article.

10

Detection of Turner syndrome using X-chromosome inactivation specific differentially methylated CpG sites: A pilot study.

Zhang Q, Guo X, Tian T, Wang T, Li Q, Wang L, Liu Y, Xing Q, He L, Zhao X. Zhang Q, et al. Among authors: wang l, wang t. Clin Chim Acta. 2017 May;468:174-179. doi: 10.1016/j.cca.2017.03.008. Epub 2017 Mar 8. Clin Chim Acta. 2017. PMID: 28284085

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