Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy-Reference-Cited by-同舟云学术

Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy

Published:2000-07 Issue:3 Volume:25 Page:306-310
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Ali Robin R.,Sarra Gian-Marco,Stephens Clare,Alwis Mahesh de,Bainbridge James W.B.,Munro Peter M.,Fauser Sascha,Reichel Martin B.,Kinnon Christine,Hunt David M.,Bhattacharya Shomi S.,Thrasher Adrian J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0700_306.pdf

Reference18 articles.

1. Travis, G.H., Brennan, M.B., Danielson, P.E., Kozak, C.A. & Sutcliffe, J.G. Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds ). Nature 338, 70–73 (1989).

2. Bascom, R.A. et al. Cloning of the cDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies . Neuron 8, 1171–1184 (1992).

3. Molday, R.S. Peripherin/rds and rom-1: molecular properties and role in photoreceptor cell degeneration. Prog. Ret. Eye Res. 13, 271 –299 (1994).

4. Gregory-Evans, K. & Bhattacharya, S.S. Genetic blindness: current concepts in the pathogenesis of human outer retinal dystophies . Trends Genet. 14, 103– 108 (1998).

5. Sanyal, S. & Jansen, H. Absence of receptor outer segments in the retina of rds mutant mice. Neurosci. Lett. 21, 23–26 (1981).

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