Morphological, physiological, and biochemical changes in rhodopsin knockout mice
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference30 articles.
1. Rhodopsin mutations in inherited retinal dystrophies and dysfunctions
2. Mechanisms of Rhodopsin Inactivation in Vivo as Revealed by a COOH-Terminal Truncation Mutant
3. Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degeneration.
4. Transgenic mice carrying the dominant rhodopsin mutation P347S: Evidence for defective vectorial transport of rhodopsin to the outer segments
5. A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment
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