Jin ZB - Search Results

1

Nonhuman Primate Model of Oculocutaneous Albinism with TYR and OCA2 Mutations.

Wu KC, Lv JN, Yang H, Yang FM, Lin R, Lin Q, Shen RJ, Wang JB, Duan WH, Hu M, Zhang J, He ZL, Jin ZB. Wu KC, et al. Among authors: jin zb. Research (Wash D C). 2020 Mar 11;2020:1658678. doi: 10.34133/2020/1658678. eCollection 2020. Research (Wash D C). 2020. PMID: 32259106 Free PMC article.

2

Identification of a novel GJA8 (Cx50) point mutation causes human dominant congenital cataracts.

Ge XL, Zhang Y, Wu Y, Lv J, Zhang W, Jin ZB, Qu J, Gu F. Ge XL, et al. Among authors: jin zb. Sci Rep. 2014 Feb 18;4:4121. doi: 10.1038/srep04121. Sci Rep. 2014. PMID: 24535056 Free PMC article.

3

Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing.

Xing DJ, Zhang HX, Huang N, Wu KC, Huang XF, Huang F, Tong Y, Pang CP, Qu J, Jin ZB. Xing DJ, et al. Among authors: jin zb. PLoS One. 2014 Mar 7;9(3):e90599. doi: 10.1371/journal.pone.0090599. eCollection 2014. PLoS One. 2014. PMID: 24608809 Free PMC article.

4

SLC7A14 linked to autosomal recessive retinitis pigmentosa.

Jin ZB, Huang XF, Lv JN, Xiang L, Li DQ, Chen J, Huang C, Wu J, Lu F, Qu J. Jin ZB, et al. Nat Commun. 2014 Mar 27;5:3517. doi: 10.1038/ncomms4517. Nat Commun. 2014. PMID: 24670872 Free PMC article.

5

A novel Bruch's membrane-mimetic electrospun substrate scaffold for human retinal pigment epithelium cells.

Xiang P, Wu KC, Zhu Y, Xiang L, Li C, Chen DL, Chen F, Xu G, Wang A, Li M, Jin ZB. Xiang P, et al. Among authors: jin zb. Biomaterials. 2014 Dec;35(37):9777-9788. doi: 10.1016/j.biomaterials.2014.08.040. Epub 2014 Sep 15. Biomaterials. 2014. PMID: 25220295 Free article.

6

Genotype-phenotype correlation and mutation spectrum in a large cohort of patients with inherited retinal dystrophy revealed by next-generation sequencing.

Huang XF, Huang F, Wu KC, Wu J, Chen J, Pang CP, Lu F, Qu J, Jin ZB. Huang XF, et al. Among authors: jin zb. Genet Med. 2015 Apr;17(4):271-8. doi: 10.1038/gim.2014.138. Epub 2014 Nov 6. Genet Med. 2015. PMID: 25356976 Free article.

7

Identification of false-negative mutations missed by next-generation sequencing in retinitis pigmentosa patients: a complementary approach to clinical genetic diagnostic testing.

Huang XF, Wu J, Lv JN, Zhang X, Jin ZB. Huang XF, et al. Among authors: jin zb. Genet Med. 2015 Apr;17(4):307-11. doi: 10.1038/gim.2014.193. Epub 2015 Jan 8. Genet Med. 2015. PMID: 25569437 Free article.

8

Toll-Like Receptor 3 Activation Initiates Photoreceptor Cell Death In Vivo and In Vitro.

Gao ML, Wu KC, Deng WL, Lei XL, Xiang L, Zhou GH, Feng CY, Cheng XW, Zhang CJ, Gu F, Wu RH, Jin ZB. Gao ML, et al. Among authors: jin zb. Invest Ophthalmol Vis Sci. 2017 Feb 1;58(2):801-811. doi: 10.1167/iovs.16-20692. Invest Ophthalmol Vis Sci. 2017. PMID: 28152141

9

Targeted RP9 ablation and mutagenesis in mouse photoreceptor cells by CRISPR-Cas9.

Lv JN, Zhou GH, Chen X, Chen H, Wu KC, Xiang L, Lei XL, Zhang X, Wu RH, Jin ZB. Lv JN, et al. Among authors: jin zb. Sci Rep. 2017 Feb 20;7:43062. doi: 10.1038/srep43062. Sci Rep. 2017. PMID: 28216641 Free PMC article.

10

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia.

Jin ZB, Wu J, Huang XF, Feng CY, Cai XB, Mao JY, Xiang L, Wu KC, Xiao X, Kloss BA, Li Z, Liu Z, Huang S, Shen M, Cheng FF, Cheng XW, Zheng ZL, Chen X, Zhuang W, Zhang Q, Young TL, Xie T, Lu F, Qu J. Jin ZB, et al. Proc Natl Acad Sci U S A. 2017 Apr 18;114(16):4219-4224. doi: 10.1073/pnas.1615970114. Epub 2017 Apr 3. Proc Natl Acad Sci U S A. 2017. PMID: 28373534 Free PMC article.

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