Tian T - Search Results

1

Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defects.

Tian T, Lai X, Xiang K, Han X, Yin S, Cabrera RM, Steele JW, Lei Y, Cao X, Finnell RH, Wang L, Ren A. Tian T, et al. Epigenetics. 2022 Jan-Feb;17(2):133-146. doi: 10.1080/15592294.2021.1878725. Epub 2021 Feb 17. Epigenetics. 2022. PMID: 33491544 Free PMC article.

2

Fetal DNA hypermethylation in tight junction pathway is associated with neural tube defects: A genome-wide DNA methylation analysis.

Wang L, Lin S, Zhang J, Tian T, Jin L, Ren A. Wang L, et al. Among authors: tian t. Epigenetics. 2017 Feb;12(2):157-165. doi: 10.1080/15592294.2016.1277298. Epub 2017 Jan 6. Epigenetics. 2017. PMID: 28059605 Free PMC article.

3

Relationship of Methylation within Upper Stream Region of Transcription Starts Site of HOXA5 Gene with Neural Tube Defects.

Zhang J, Tian T, Yi Q, Wang LL, Ren AG. Zhang J, et al. Among authors: tian t. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2017 Dec 20;39(6):785-791. doi: 10.3881/j.issn.1000-503X.2017.06.009. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2017. PMID: 29338823 English.

4

Digenic variants of planar cell polarity genes in human neural tube defect patients.

Wang L, Xiao Y, Tian T, Jin L, Lei Y, Finnell RH, Ren A. Wang L, et al. Among authors: tian t. Mol Genet Metab. 2018 May;124(1):94-100. doi: 10.1016/j.ymgme.2018.03.005. Epub 2018 Mar 18. Mol Genet Metab. 2018. PMID: 29573971 Free PMC article.

5

Hypomethylation of GRHL3 gene is associated with the occurrence of neural tube defects.

Tian T, Wang L, Shen Y, Zhang B, Finnell RH, Ren A. Tian T, et al. Epigenomics. 2018 Jul;10(7):891-901. doi: 10.2217/epi-2018-0016. Epub 2018 Mar 28. Epigenomics. 2018. PMID: 29587534 Free PMC article.

6

Maternal periconceptional consumption of sprouted potato and risks of neural tube defects and orofacial clefts.

Ni W, Tian T, Zhang L, Li Z, Wang L, Ren A. Ni W, et al. Among authors: tian t. Nutr J. 2018 Nov 28;17(1):112. doi: 10.1186/s12937-018-0420-4. Nutr J. 2018. PMID: 30486846 Free PMC article.

7

Maternal hypertensive disorders in pregnancy and risk of hypoxic-ischemia encephalopathy.

Yang W, Wang L, Tian T, Liu L, Jin L, Liu J, Ren A. Yang W, et al. Among authors: tian t. J Matern Fetal Neonatal Med. 2021 Jun;34(11):1754-1762. doi: 10.1080/14767058.2019.1647529. Epub 2019 Aug 4. J Matern Fetal Neonatal Med. 2021. PMID: 31331218

8

Genetic variants in GRHL3 and risk for neural tube defects: A case-control and case-parent triad/control study.

Yang W, Xiao Y, Tian T, Jin L, Wang L, Ren A. Yang W, et al. Among authors: tian t. Birth Defects Res. 2019 Nov 15;111(19):1468-1478. doi: 10.1002/bdr2.1556. Epub 2019 Jul 22. Birth Defects Res. 2019. PMID: 31332962

9

Whole-Exome Sequencing Identifies Damaging de novo Variants in Anencephalic Cases.

Wang L, Ren A, Tian T, Li N, Cao X, Zhang P, Jin L, Li Z, Shen Y, Zhang B, Finnell RH, Lei Y. Wang L, et al. Among authors: tian t. Front Neurosci. 2019 Nov 29;13:1285. doi: 10.3389/fnins.2019.01285. eCollection 2019. Front Neurosci. 2019. PMID: 31849593 Free PMC article.

10

Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida.

Cao X, Tian T, Steele JW, Cabrera RM, Aguiar-Pulido V, Wadhwa S, Bhavani N, Bi P, Gargurevich NH, Hoffman EN, Cai CQ, Marini NJ, Yang W, Shaw GM, Ross ME, Finnell RH, Lei Y. Cao X, et al. Among authors: tian t. Hum Mutat. 2020 Apr;41(4):786-799. doi: 10.1002/humu.23969. Epub 2020 Jan 16. Hum Mutat. 2020. PMID: 31898828 Free PMC article.

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