Characterization of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa. Mutations on the cytoplasmic surface affect transducin activation
Open Access
- 1 May 1993
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 268 (13) , 9400-9404
- https://doi.org/10.1016/s0021-9258(18)98364-x
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Constitutively active mutants of rhodopsinNeuron, 1992
- Rhodopsin: structure, function, and geneticsBiochemistry, 1992
- Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosaGenomics, 1991
- Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment siteGenomics, 1991
- Effect of Carboxylic Acid Side Chains on the Absorption Maximum of Visual PigmentsScience, 1989
- Octopus rhodopsin Amino acid sequence deduced from cDNAFEBS Letters, 1988
- Molecular Genetics of Human Color Vision: The Genes Encoding Blue, Green, and Red PigmentsScience, 1986
- An opsin gene expressed in only one photoreceptor cell type of the Drosophila eyeCell, 1986
- Isolation, sequence analysis, and intron-exon arrangement of the gene encoding bovine rhodopsinCell, 1983
- The structure of rhodopsin and the rod outer segment disk membraneTrends in Biochemical Sciences, 1983