Characterization of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa. Mutations on the cytoplasmic surface affect transducin activation
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference40 articles.
1. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
2. Autosomal dominant retinitis pigmentosa: Linkage to rhodopsin and evidence for genetic heterogeneity
3. Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.
4. Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa
5. On the Molecular Genetics of Retinitis Pigmentosa
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1. Dimeric Rhodopsin R135L Mutant-Transducin-like Complex Sheds Light on Retinitis Pigmentosa Misfunctions;The Journal of Physical Chemistry B;2021-11-18
2. Coupling of Human Rhodopsin to a Yeast Signaling Pathway Enables Characterization of Mutations Associated with Retinal Disease;Genetics;2018-12-04
3. The arrestin-1 finger loop interacts with two distinct conformations of active rhodopsin;Journal of Biological Chemistry;2018-03
4. Retinitis Pigmentosa Mutants Provide Insight into the Role of the N-terminal Cap in Rhodopsin Folding, Structure, and Function;Journal of Biological Chemistry;2013-11
5. Thermal Stability of Rhodopsin and Progression of Retinitis Pigmentosa;Journal of Biological Chemistry;2013-06
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