Huang T - Search Results

1

Diagnostic role of microRNA expression profile in the serum of pregnant women with fetuses with neural tube defects.

Gu H, Li H, Zhang L, Luan H, Huang T, Wang L, Fan Y, Zhang Y, Liu X, Wang W, Yuan Z. Gu H, et al. Among authors: huang t. J Neurochem. 2012 Aug;122(3):641-9. doi: 10.1111/j.1471-4159.2012.07812.x. Epub 2012 Jun 27. J Neurochem. 2012. PMID: 22642222 Free article.

2

Identification of PCSK9 as a novel serum biomarker for the prenatal diagnosis of neural tube defects using iTRAQ quantitative proteomics.

An D, Wei X, Li H, Gu H, Huang T, Zhao G, Liu B, Wang W, Chen L, Ma W, Zhang H, Cao S, Yuan Z. An D, et al. Among authors: huang t. Sci Rep. 2015 Dec 22;5:17559. doi: 10.1038/srep17559. Sci Rep. 2015. PMID: 26691006 Free PMC article.

3

Expression profile of maternal circulating microRNAs as non-invasive biomarkers for prenatal diagnosis of congenital heart defects.

Gu H, Chen L, Xue J, Huang T, Wei X, Liu D, Ma W, Cao S, Yuan Z. Gu H, et al. Among authors: huang t. Biomed Pharmacother. 2019 Jan;109:823-830. doi: 10.1016/j.biopha.2018.10.110. Epub 2018 Nov 5. Biomed Pharmacother. 2019. PMID: 30551536 Free article.

4

Comparative proteomics of Hirschsprung's disease.

Fan Y, Wang L, Zhang Y, Huang T, Li H, Gu H, Wang W, Yuan Z. Fan Y, et al. Among authors: huang t. J Proteomics. 2013 Jun 12;84:176-84. doi: 10.1016/j.jprot.2013.03.024. Epub 2013 Apr 3. J Proteomics. 2013. PMID: 23563203 Clinical Trial.

5

Sensory neuron differentiation potential of in utero mesenchymal stem cell transplantation in rat fetuses with spina bifida aperta.

Ma W, Wei X, Gu H, Li H, Guan K, Liu D, Chen L, Cao S, An D, Zhang H, Huang T, Miao J, Zhao G, Wu D, Liu B, Wang W, Yuan Z. Ma W, et al. Among authors: huang t. Birth Defects Res A Clin Mol Teratol. 2015 Sep;103(9):772-9. doi: 10.1002/bdra.23401. Epub 2015 Jul 14. Birth Defects Res A Clin Mol Teratol. 2015. PMID: 26172505

6

Comprehensive maternal serum proteomics identifies the cytoskeletal proteins as non-invasive biomarkers in prenatal diagnosis of congenital heart defects.

Chen L, Gu H, Li J, Yang ZY, Sun X, Zhang L, Shan L, Wu L, Wei X, Zhao Y, Ma W, Zhang H, Cao S, Huang T, Miao J, Yuan Z. Chen L, et al. Among authors: huang t. Sci Rep. 2016 Jan 11;6:19248. doi: 10.1038/srep19248. Sci Rep. 2016. PMID: 26750556 Free PMC article.

7

Complement factors and alpha-fetoprotein as biomarkers for noninvasive prenatal diagnosis of neural tube defects.

Dong N, Gu H, Liu D, Wei X, Ma W, Ma L, Liu Y, Wang Y, Jia S, Huang J, Wang C, He X, Huang T, He Y, Zhang Q, An D, Bai Y, Yuan Z. Dong N, et al. Among authors: huang t, huang j. Ann N Y Acad Sci. 2020 Oct;1478(1):75-91. doi: 10.1111/nyas.14443. Epub 2020 Aug 5. Ann N Y Acad Sci. 2020. PMID: 32761624

8

Nuclear factor I-C disrupts cellular homeostasis between autophagy and apoptosis via miR-200b-Ambra1 in neural tube defects.

Huang W, Huang T, Liu Y, Fu J, Wei X, Liu D, Ma W, Gu H, Yuan Z. Huang W, et al. Among authors: huang t. Cell Death Dis. 2021 Dec 20;13(1):17. doi: 10.1038/s41419-021-04473-2. Cell Death Dis. 2021. PMID: 34930914 Free PMC article.

9

Semaphorin 3A expression in the colon of Hirschsprung disease.

Wang LL, Fan Y, Zhou FH, Li H, Zhang Y, Miao JN, Gu H, Huang TC, Yuan ZW. Wang LL, et al. Birth Defects Res A Clin Mol Teratol. 2011 Sep;91(9):842-7. doi: 10.1002/bdra.20837. Epub 2011 Jun 8. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21656899

10

SEMA3A rs7804122 polymorphism is associated with Hirschsprung disease in the Northeastern region of China.

Wang LL, Zhang Y, Fan Y, Li H, Zhou FH, Miao JN, Gu H, Huang TC, Yuan ZW. Wang LL, et al. Birth Defects Res A Clin Mol Teratol. 2012 Feb;94(2):91-5. doi: 10.1002/bdra.22866. Epub 2011 Dec 20. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 22184102

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