Zhou Q - Search Results

1

YTHDC1 aggravates high glucose-induced retinal vascular endothelial cell injury via m6A modification of CDK6.

Zhou Q, Tian M, Cao Y, Tang M, Xiang X, Guo L, Lv H. Zhou Q, et al. Biol Direct. 2024 Jul 8;19(1):54. doi: 10.1186/s13062-024-00498-7. Biol Direct. 2024. PMID: 38978074 Free PMC article.

2

Identification of a novel heterozygous missense mutation in the CACNA1F gene in a chinese family with retinitis pigmentosa by next generation sequencing.

Zhou Q, Cheng J, Yang W, Tania M, Wang H, Khan MA, Duan C, Zhu L, Chen R, Lv H, Fu J. Zhou Q, et al. Biomed Res Int. 2015;2015:907827. doi: 10.1155/2015/907827. Epub 2015 May 17. Biomed Res Int. 2015. PMID: 26075273 Free PMC article. Clinical Trial.

3

A Novel Variant of the FZD4 Gene in a Chinese Family Causes Autosomal Dominant Familial Exudative Vitreoretinopathy.

Yang L, Fu J, Cheng J, Wei C, Zhou Q, Ijaz I, Lv H, Fu J. Yang L, et al. Among authors: zhou q. Cell Physiol Biochem. 2018;51(5):2445-2455. doi: 10.1159/000495901. Epub 2018 Dec 11. Cell Physiol Biochem. 2018. PMID: 30537745 Free article.

4

A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree.

Cheng J, Fu J, Zhou Q, Xiang X, Wei C, Yang L, Fu S, Khan MA, Lv H, Fu J. Cheng J, et al. Among authors: zhou q. J Cell Mol Med. 2019 May;23(5):3776-3780. doi: 10.1111/jcmm.14278. Epub 2019 Mar 20. J Cell Mol Med. 2019. PMID: 30892800 Free PMC article. No abstract available.

5

A novel missense variant c.G644A (p.G215E) of the RPGR gene in a Chinese family causes X-linked retinitis pigmentosa.

Fu J, Cheng J, Zhou Q, Wei C, Chen H, Lv H, Fu J. Fu J, et al. Among authors: zhou q. Biosci Rep. 2019 Oct 30;39(10):BSR20192235. doi: 10.1042/BSR20192235. Biosci Rep. 2019. PMID: 31652454 Free PMC article.

6

Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the CDH23 Gene Causing Usher Syndrome Type ID in a Chinese Patient.

Zhang L, Cheng J, Zhou Q, Khan MA, Fu J, Duan C, Sun S, Lv H, Fu J. Zhang L, et al. Among authors: zhou q. Front Genet. 2020 Apr 30;11:422. doi: 10.3389/fgene.2020.00422. eCollection 2020. Front Genet. 2020. PMID: 32425987 Free PMC article.

7

Novel compound heterozygous EYS variants may be associated with arRP in a large Chinese pedigree.

Wei C, Xiao T, Cheng J, Fu J, Zhou Q, Yang L, Lv H, Fu J. Wei C, et al. Among authors: zhou q. Biosci Rep. 2020 Jun 26;40(6):BSR20193443. doi: 10.1042/BSR20193443. Biosci Rep. 2020. PMID: 32436957 Free PMC article.

8

Novel compound heterozygous nonsense variants, p.L150* and p.Y3565*, of the USH2A gene in a Chinese pedigree are associated with Usher syndrome type IIA.

Fu J, Cheng J, Zhou Q, Khan MA, Duan C, Peng J, Lv H, Fu J. Fu J, et al. Among authors: zhou q. Mol Med Rep. 2020 Oct;22(4):3464-3472. doi: 10.3892/mmr.2020.11400. Epub 2020 Aug 3. Mol Med Rep. 2020. PMID: 32945453 Free PMC article.

9

Novel compound heterozygous missense variants (c.G955A and c.A1822C) of CACNA2D4 likely causing autosomal recessive retinitis pigmentosa in a Chinese patient.

Cheng J, Zhou Q, Fu J, Wei C, Zhang L, Khan MSS, Lv H, Anuchapreeda S, Fu J. Cheng J, et al. Among authors: zhou q. 3 Biotech. 2021 May;11(5):208. doi: 10.1007/s13205-021-02761-4. Epub 2021 Apr 10. 3 Biotech. 2021. PMID: 33927996 Free PMC article.

10

Identification and validation of tumor microenvironment-related lncRNA prognostic signature for uveal melanoma.

Liao CL, Hu N, Sun XY, Zhou Q, Tian M, Cao Y, Lyu HB. Liao CL, et al. Among authors: zhou q. Int J Ophthalmol. 2021 Aug 18;14(8):1151-1159. doi: 10.18240/ijo.2021.08.03. eCollection 2021. Int J Ophthalmol. 2021. PMID: 34414077 Free PMC article.

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