Tang YP - Search Results

1

A novel GTPCH deficiency mouse model exhibiting tetrahydrobiopterin-related metabolic disturbance and infancy-onset motor impairments.

Jiang X, Liu H, Shao Y, Peng M, Zhang W, Li D, Li X, Cai Y, Tan T, Lu X, Xu J, Su X, Lin Y, Liu Z, Huang Y, Zeng C, Tang YP, Liu L. Jiang X, et al. Among authors: tang yp. Metabolism. 2019 May;94:96-104. doi: 10.1016/j.metabol.2019.02.001. Epub 2019 Feb 10. Metabolism. 2019. PMID: 30742839

2

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

3

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.

4

A novel mutation in intron 1 of Wnt1 causes developmental loss of dopaminergic neurons in midbrain and ASD-like behaviors in rats.

Li Y, Zhu M, Chen WX, Luo J, Li X, Cao Y, Zheng M, Ma S, Xiao Z, Zhang Y, Jiang L, Wang X, Tan T, Li X, Gong Q, Xiong X, Wang J, Tang M, Li M, Tang YP. Li Y, et al. Among authors: tang yp, tang m. Mol Psychiatry. 2023 Sep;28(9):3795-3805. doi: 10.1038/s41380-023-02223-8. Epub 2023 Sep 1. Mol Psychiatry. 2023. PMID: 37658228 Free PMC article.

5

NR1 Splicing Variant NR1a in Cerebellar Granule Neurons Constitutes a Better Motor Learning in the Mouse.

Tan T, Jiang L, He Z, Ding X, Xiong X, Tang M, Chen Y, Tang Y. Tan T, et al. Cerebellum. 2024 Jun;23(3):1112-1120. doi: 10.1007/s12311-023-01614-5. Epub 2023 Oct 25. Cerebellum. 2024. PMID: 37880519 Free PMC article.

6

[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.

7

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.

8

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.

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

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.

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