Sun K - Search Results

1

Deletion of Emc1 in photoreceptor cells causes retinal degeneration in mice.

Li X, Jiang Z, Su Y, Wang K, Jiang X, Sun K, Yang Y, Zhou Y, Zhu X, Zhang L. Li X, et al. Among authors: sun k. FEBS J. 2023 Sep;290(17):4356-4370. doi: 10.1111/febs.16807. Epub 2023 May 19. FEBS J. 2023. PMID: 37098815 Free article.

2

Targeted Next Generation Sequencing Revealed Novel PRPF31 Mutations in Autosomal Dominant Retinitis Pigmentosa.

Xie D, Peng K, Yi Q, Liu W, Yang Y, Sun K, Zhu X, Lu F. Xie D, et al. Among authors: sun k. Genet Test Mol Biomarkers. 2018 Jul;22(7):425-432. doi: 10.1089/gtmb.2018.0036. Epub 2018 Jun 29. Genet Test Mol Biomarkers. 2018. PMID: 29957067

3

Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells.

Yang Y, Sun K, Liu W, Zhang L, Peng K, Zhang S, Li S, Yang M, Jiang Z, Lu F, Zhu X. Yang Y, et al. Among authors: sun k. Cell Death Dis. 2018 Sep 5;9(9):899. doi: 10.1038/s41419-018-0938-6. Cell Death Dis. 2018. PMID: 30185775 Free PMC article.

4

Tmem30a deficiency leads to retinal rod bipolar cell degeneration.

Yang Y, Liu W, Sun K, Jiang L, Zhu X. Yang Y, et al. Among authors: sun k. J Neurochem. 2019 Feb;148(3):400-412. doi: 10.1111/jnc.14643. Epub 2019 Jan 15. J Neurochem. 2019. PMID: 30548540 Free article.

5

TMEM30A deficiency in endothelial cells impairs cell proliferation and angiogenesis.

Zhang S, Liu W, Yang Y, Sun K, Li S, Xu H, Yang M, Zhang L, Zhu X. Zhang S, et al. Among authors: sun k. J Cell Sci. 2019 Apr 3;132(7):jcs225052. doi: 10.1242/jcs.225052. J Cell Sci. 2019. PMID: 30814335

6

Identification of Novel Mutations in the FZD4 and NDP Genes in Patients with Familial Exudative Vitreoretinopathy in South India.

Zhu X, Sun K, Huang L, Ma S, Hao F, Yang Z, Sundaresan P, Zhu X. Zhu X, et al. Among authors: sun k. Genet Test Mol Biomarkers. 2020 Feb;24(2):92-98. doi: 10.1089/gtmb.2019.0212. Genet Test Mol Biomarkers. 2020. PMID: 31999491 Clinical Trial.

7

Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice.

Xu H, Qu C, Gan L, Sun K, Tan J, Liu X, Jiang Z, Tian W, Liu W, Zhang S, Yang Y, Jiang L, Zhu X, Zhang L. Xu H, et al. Among authors: sun k. Hum Mol Genet. 2020 Jun 27;29(10):1624-1634. doi: 10.1093/hmg/ddaa062. Hum Mol Genet. 2020. PMID: 32242237

8

Identification of novel USH2A mutations in patients with autosomal recessive retinitis pigmentosa via targeted next‑generation sequencing.

Zhu X, Li X, Tian W, Yang Y, Sun K, Li S, Zhu X. Zhu X, et al. Among authors: sun k. Mol Med Rep. 2020 Jul;22(1):193-200. doi: 10.3892/mmr.2020.11087. Epub 2020 Apr 22. Mol Med Rep. 2020. PMID: 32319668 Free PMC article.

9

Disease Mutation Study Identifies Critical Residues for Phosphatidylserine Flippase ATP11A.

Sun K, Tian W, Li X, Liu W, Yang Y, Zhu X. Sun K, et al. Biomed Res Int. 2020 Jun 2;2020:7342817. doi: 10.1155/2020/7342817. eCollection 2020. Biomed Res Int. 2020. PMID: 32596364 Free PMC article.

10

Identification of Novel EYS Mutations by Targeted Sequencing Analysis.

Tian W, Li X, Li Y, Wang L, Yang Y, Sun K, Liu W, Zhou B, Lei B, Zhu X. Tian W, et al. Among authors: sun k. Genet Test Mol Biomarkers. 2020 Nov;24(11):745-753. doi: 10.1089/gtmb.2020.0186. Epub 2020 Oct 15. Genet Test Mol Biomarkers. 2020. PMID: 33058741

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