Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy-Reference-Cited by-同舟云学术

Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy

Published:2017-04-05 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Lu Zhaojing,Hu Xuebin,Liu Fei,Soares Dinesh C.,Liu Xiliang,Yu Shanshan,Gao Meng,Han Shanshan,Qin Yayun,Li Chang,Jiang Tao,Luo Daji,Guo An-Yuan,Tang Zhaohui,Liu Mugen

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep46098.pdf

Reference46 articles.

1. Wright, A. F., Chakarova, C. F., Abd EI-Aziz, M. M. & Bhattacharya, S. S. Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait. Nat. Rev. Genet. 11, 273–284 (2010).

2. Abd EI-Aziz, M. M. et al. EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa. Nat. Genet. 40, 1285–1287 (2008).

3. Collin, R. W. et al. Identification of a 2Mb human ortholog of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosa. Am. J. Hum. Genet. 83, 594–603 (2008).

4. Barragan, I. et al. Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa. Hum. Mutat. 31, 1772–1800 (2010).

5. Huang, Y. et al. Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa. BMC. Med. Genet. 11, 121 (2010).

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