Tang YP - Search Results

1

Real-world investigation of the efficacy and safety of secukinumab for psoriasis treatment in a Chinese population.

Zeng JX, Luo Q, Wen J, Tian X, Zhou X, Li W, Tang YP, Zhang SQ, Liu WY, Zhu HL, Zhang XB. Zeng JX, et al. Among authors: tang yp. Chin Med J (Engl). 2020 Oct 26;134(1):117-119. doi: 10.1097/CM9.0000000000001179. Chin Med J (Engl). 2020. PMID: 33109951 Free PMC article. No abstract available.

2

[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.

3

HOXA9 rs3801776 G>A polymorphism increases congenital talipes equinovarus risk in a Chinese population.

Li J, Wu J, Liu Y, Li Y, Xiao Z, Jiang X, Tang Y, Xu H. Li J, et al. J Gene Med. 2019 Oct;21(10):e3119. doi: 10.1002/jgm.3119. Epub 2019 Aug 30. J Gene Med. 2019. PMID: 31424148

4

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

5

De novo mutations within metabolism networks of amino acid/protein/energy in Chinese autistic children with intellectual disability.

Chen WX, Liu B, Zhou L, Xiong X, Fu J, Huang ZF, Tan T, Tang M, Wang J, Tang YP. Chen WX, et al. Among authors: tang yp, tang m. Hum Genomics. 2022 Nov 1;16(1):52. doi: 10.1186/s40246-022-00427-7. Hum Genomics. 2022. PMID: 36320054 Free PMC article.

6

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.

7

Drug repositioning based on network-specific core genes identifies potential drugs for the treatment of autism spectrum disorder in children.

Gao H, Ni Y, Mo X, Li D, Teng S, Huang Q, Huang S, Liu G, Zhang S, Tang Y, Lu L, Liang H. Gao H, et al. Comput Struct Biotechnol J. 2021 Jul 1;19:3908-3921. doi: 10.1016/j.csbj.2021.06.046. eCollection 2021. Comput Struct Biotechnol J. 2021. PMID: 34306572 Free PMC article.

8

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.

9

Iron overload facilitates neonatal hypoxic-ischemic brain damage via SLC7A11-mediated ferroptosis.

Tan X, Zhang T, Ding X, Zhao X, Liu Q, Xia Z, Cao Q, Yan F, Chen L, Zhu M, Tang Y, Song Y. Tan X, et al. J Neurosci Res. 2023 Jul;101(7):1107-1124. doi: 10.1002/jnr.25184. Epub 2023 Mar 16. J Neurosci Res. 2023. PMID: 36929608

10

MCM8-mediated mitophagy protects vascular health in response to nitric oxide signaling in a mouse model of Kawasaki disease.

Lin M, Xian H, Chen Z, Wang S, Liu M, Liang W, Tang Q, Liu Y, Huang W, Che D, Guo C, Idiiatullina E, Fang R, Al-Azab M, Chang J, Wang R, Li X, Zuo X, Zhang Y, Zhao J, Tang Y, Jin S, He Z, Feng D, Lu L, Zhang K, Wu Y, Bai F, Lew AM, Cui J, Wu Y, Gu X, Zhang Y. Lin M, et al. Nat Cardiovasc Res. 2023 Aug;2(8):778-792. doi: 10.1038/s44161-023-00314-x. Epub 2023 Aug 11. Nat Cardiovasc Res. 2023. PMID: 39195969

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