Why choose 9-cis retinal for therapy of congenital stationary night blindness caused by G90D rhodopsin?
Author:
Funder
National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s00214-016-2039-x.pdf
Reference42 articles.
1. Zeitz C (2007) Molecular genetics and protein function involved in nocturnal vision. Expert Rev Ophthalmol 2(3):467–485
2. Zeitz C, Robson AG, Audo I (2015) Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms. Pro Retin Eye Res 45:58–110
3. Hubbell WL, Bownds MD (1979) Visual transduction in vertebrate photoreceptors. Annu Rev Neurosci 2:17–34
4. Filipek S, Stenkamp RE, Teller DC, Palczewski K (2003) G protein-coupled receptor rhodopsin: a prospectus. Annu Rev Physiol 65:851–879
5. Rao VR, Cohen GB, Oprian DD (1994) Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. Nature 367(6464):639–642
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