Probing Mechanisms of Photoreceptor Degeneration in a New Mouse Model of the Common Form of Autosomal Dominant Retinitis Pigmentosa due to P23H Opsin Mutations-Reference-Cited by-同舟云学术

Probing Mechanisms of Photoreceptor Degeneration in a New Mouse Model of the Common Form of Autosomal Dominant Retinitis Pigmentosa due to P23H Opsin Mutations

Published:2011-03 Issue:12 Volume:286 Page:10551-10567
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Sakami Sanae,Maeda Tadao,Bereta Grzegorz,Okano Kiichiro,Golczak Marcin,Sumaroka Alexander,Roman Alejandro J.,Cideciyan Artur V.,Jacobson Samuel G.,Palczewski Krzysztof

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference92 articles.

1. NEW EMBO MEMBER'S REVIEW: On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention

2. G Protein–Coupled Receptor Rhodopsin

3. Molecular Genetics of Human Retinal Disease

4. Molecular genetics of retinitis pigmentosa

5. Retinitis pigmentosa

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