Tang YP - Search Results

1

Proteomic Analysis of Zika Virus Infected Primary Human Fetal Neural Progenitors Suggests a Role for Doublecortin in the Pathological Consequences of Infection in the Cortex.

Jiang X, Dong X, Li SH, Zhou YP, Rayner S, Xia HM, Gao GF, Yuan H, Tang YP, Luo MH. Jiang X, et al. Among authors: tang yp. Front Microbiol. 2018 Jun 5;9:1067. doi: 10.3389/fmicb.2018.01067. eCollection 2018. Front Microbiol. 2018. PMID: 29922247 Free PMC article.

2

Human cytomegalovirus infection perturbs neural progenitor cell fate via the expression of viral microRNAs.

Jiang X, Liu S, Fu YR, Liu XJ, Li XJ, Yang B, Jiang HF, Shen ZZ, Alemu EA, Vazquez P, Tang Y, Kaarbø M, McVoy MA, Rayner S, Luo MH. Jiang X, et al. J Med Virol. 2023 Feb;95(2):e28574. doi: 10.1002/jmv.28574. J Med Virol. 2023. PMID: 36772841

3

Selective targeting of MD2 attenuates intestinal inflammation and prevents neonatal necrotizing enterocolitis by suppressing TLR4 signaling.

Huang D, Wang P, Chen J, Li Y, Zhu M, Tang Y, Zhou W. Huang D, et al. Front Immunol. 2022 Nov 1;13:995791. doi: 10.3389/fimmu.2022.995791. eCollection 2022. Front Immunol. 2022. PMID: 36389716 Free PMC article.

4

Demographic and Clinical Features of Small-for-Gestational-Age Infants Born to Mothers With Gestational Diabetes Mellitus.

Chen J, Xiao H, Yang Y, Tang Y, Yang X, Zhang Z, Lu W, Yao J, Huang L, Liu X, Zhou W. Chen J, et al. Front Pediatr. 2021 Oct 1;9:741793. doi: 10.3389/fped.2021.741793. eCollection 2021. Front Pediatr. 2021. PMID: 34660493 Free PMC article.

5

Maternal exposure to triclosan constitutes a yet unrecognized risk factor for autism spectrum disorders.

Hao Z, Wu Q, Li Z, Li Y, Li Q, Lai X, Liu H, Zhang M, Yang T, Chen J, Tang Y, Miao J, Xu H, Li T, Hu R. Hao Z, et al. Cell Res. 2019 Oct;29(10):866-869. doi: 10.1038/s41422-019-0220-1. Epub 2019 Aug 28. Cell Res. 2019. PMID: 31462724 Free PMC article. No abstract available.

6

Cataract-causing Y204X mutation of crystallin protein CRYβB1 promotes its C-terminal degradation and higher-order oligomerization.

Jing X, Zhu M, Lu X, Wei P, Shi L, Zhang BY, Xu Y, Tang YP, Xiang DM, Gong P. Jing X, et al. Among authors: tang yp. J Biol Chem. 2023 Aug;299(8):104953. doi: 10.1016/j.jbc.2023.104953. Epub 2023 Jun 24. J Biol Chem. 2023. PMID: 37356717 Free PMC article.

7

A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report.

Shang L, Shi W, Xu Y, Nong T, Li X, Li Z, Liu Y, Li J, Tang YP, Zhu M, Xu H. Shang L, et al. Among authors: tang yp. Heliyon. 2024 Mar 22;10(7):e28680. doi: 10.1016/j.heliyon.2024.e28680. eCollection 2024 Apr 15. Heliyon. 2024. PMID: 38590901 Free PMC article.

8

A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate.

Xian C, Zhu M, Nong T, Li Y, Xie X, Li X, Li J, Li J, Wu J, Shi W, Wei P, Xu H, Tang YP. Xian C, et al. Among authors: tang yp. Genet Mol Biol. 2021 May 21;44(2):e20200334. doi: 10.1590/1678-4685-GMB-2020-0334. eCollection 2021. Genet Mol Biol. 2021. PMID: 34042151 Free PMC article.

9

The mucolipidosis III-causing mutation in GNPTAB, c.1760G>C, disrupts the development of somites in rats.

Nong T, Li J, Li X, Li Y, Li Z, Shi W, Zhou Q, Xu H, Zhu M, Tang YP. Nong T, et al. Among authors: tang yp. Genes Dis. 2023 Nov 17;11(6):101172. doi: 10.1016/j.gendis.2023.101172. eCollection 2024 Nov. Genes Dis. 2023. PMID: 39157455 Free PMC article. No abstract available.

10

[Role of NRXN-NLGN-SHANK pathway gene variations in the pathogenesis of autism spectrum disorders].

He L, Liu X, Song Y, Tang Y. He L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Oct 10;35(5):753-756. doi: 10.3760/cma.j.issn.1003-9406.2018.05.031. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30298512 Review. Chinese.

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