Zhang X - Search Results

1

Generation of the induced pluripotent stem cell line SFMUi001-A from a patient with usher syndrome type 2 caused by biallelic variants in the USH2A gene.

Qiu S, Zhang X, Zhang L, Liu Z, Wang L, Jin ZB, Xiao P. Qiu S, et al. Among authors: zhang l, zhang x. Stem Cell Res. 2023 Jun;69:103101. doi: 10.1016/j.scr.2023.103101. Epub 2023 Apr 20. Stem Cell Res. 2023. PMID: 37126974 Free article.

2

Patient iPSC-derived retinal organoids: Observable retinal diseases in-a-dish.

Zhang XH, Jin ZB. Zhang XH, et al. Histol Histopathol. 2021 Jul;36(7):705-710. doi: 10.14670/HH-18-307. Epub 2021 Jan 22. Histol Histopathol. 2021. PMID: 33491763 Review.

3

Variant Profiling of a Large Cohort of 138 Chinese Families With Autosomal Dominant Retinitis Pigmentosa.

Xiao T, Xie Y, Zhang X, Xu K, Zhang X, Jin ZB, Li Y. Xiao T, et al. Among authors: zhang x. Front Cell Dev Biol. 2021 Feb 1;8:629994. doi: 10.3389/fcell.2020.629994. eCollection 2020. Front Cell Dev Biol. 2021. PMID: 33598457 Free PMC article.

4

Generation of an induced pluripotent stem cell line BIOi002-A from a patient with autosomal dominant optic atrophy.

Zhang XH, Xie Y, Xu K, Li Y. Zhang XH, et al. Stem Cell Res. 2021 May;53:102278. doi: 10.1016/j.scr.2021.102278. Epub 2021 Mar 13. Stem Cell Res. 2021. PMID: 33752025 Free article.

5

Genotype Profile of Global EYS-Associated Inherited Retinal Dystrophy and Clinical Findings in a Large Chinese Cohort.

Xu K, Chen DF, Chang H, Shen RJ, Gao H, Wang XF, Feng ZK, Zhang X, Xie Y, Li Y, Jin ZB. Xu K, et al. Among authors: zhang x. Front Cell Dev Biol. 2021 Jun 11;9:634220. doi: 10.3389/fcell.2021.634220. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34178978 Free PMC article.

6

Mitochondrial Mutations in Ethambutol-Induced Optic Neuropathy.

Zhang XH, Xie Y, Xu QG, Cao K, Xu K, Jin ZB, Li Y, Wei SH. Zhang XH, et al. Front Cell Dev Biol. 2021 Oct 5;9:754676. doi: 10.3389/fcell.2021.754676. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34676220 Free PMC article.

7

Clinical Features and Natural History in a Cohort of Chinese Patients with RPE65-Associated Inherited Retinal Dystrophy.

Shi J, Xu K, Hu JP, Xie Y, Zhang X, Zhang XH, Jin ZB, Li Y. Shi J, et al. Among authors: zhang x, zhang xh. J Clin Med. 2021 Nov 10;10(22):5229. doi: 10.3390/jcm10225229. J Clin Med. 2021. PMID: 34830511 Free PMC article.

8

Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4-Related Retinopathy: Deep Intronic Variants and Copy Number Variations.

Tian L, Chen C, Song Y, Zhang X, Xu K, Xie Y, Jin ZB, Li Y. Tian L, et al. Among authors: zhang x. Invest Ophthalmol Vis Sci. 2022 Jun 1;63(6):5. doi: 10.1167/iovs.63.6.5. Invest Ophthalmol Vis Sci. 2022. PMID: 35657619 Free PMC article.

9

Induced pluripotent stem cell line BIOi003-A from a patient with ABCA4-associated retinal dystrophy carrying compound heterozygous c.(1222C>T;2919-884G>T) variants in ABCA4.

Tian L, Zhang XH, Xu K, Li Y. Tian L, et al. Stem Cell Res. 2022 Oct;64:102894. doi: 10.1016/j.scr.2022.102894. Epub 2022 Aug 10. Stem Cell Res. 2022. PMID: 35973334 Free article.

10

Comprehensive genetic analysis reveals the mutational landscape of ABCA4-associated retinal dystrophy in a Chinese cohort.

Tian L, Chen CJ, Song YN, Xu K, Li NE, Zhang XH, Xie Y, Jin ZB, Li Y. Tian L, et al. Gene. 2024 Jan 15;891:147832. doi: 10.1016/j.gene.2023.147832. Epub 2023 Sep 27. Gene. 2024. PMID: 37774808

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