Structural aspects of rod opsin and their implication in genetic diseases
Author:
Funder
UNIMORE
Fondazione Telethon
Publisher
Springer Science and Business Media LLC
Subject
Physiology (medical),Clinical Biochemistry,Physiology
Link
https://link.springer.com/content/pdf/10.1007/s00424-021-02546-x.pdf
Reference171 articles.
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2. Andres A, Garriga P, Manyosa J (2003) Altered functionality in rhodopsin point mutants associated with retinitis pigmentosa. Biochem Biophys Res Commun 303:294–301
3. Arnis S, Hofmann KP (1993) Two different forms of metarhodopsin II: Schiff base deprotonation precedes proton uptake and signaling state. Proc Natl Acad Sci U S A 90:7849–7853
4. Arvanitakis L, Geras-Raaka E, Gershengorn MC (1998) Constitutively signaling G-protein coupled receptor and human disease. Trends Endocrinol Metab 9:27–31
5. Athanasiou D, Aguila M, Bellingham J, Li WW, McCulley C, Reeves PJ, Cheetham ME (2018) The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy. Prog Retin Eye Res 62:1–23. https://doi.org/10.1016/j.preteyeres.2017.10.002
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