Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa
Authors
Keywords
-
Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 109, Issue 6, Pages 2132-2137
Publisher
Proceedings of the National Academy of Sciences
Online
2012-01-24
DOI
10.1073/pnas.1118847109
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Gene Therapy for Leber Congenital Amaurosis Caused by RPE65 Mutations
- (2011) Samuel G. Jacobson ARCHIVES OF OPHTHALMOLOGY
- Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy
- (2011) L. S. Carvalho et al. HUMAN MOLECULAR GENETICS
- Allelic Heterogeneity and Genetic Modifier Loci Contribute to Clinical Variation in Males with X-Linked Retinitis Pigmentosa Due to RPGR Mutations
- (2011) Abigail T. Fahim et al. PLoS One
- Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis
- (2011) T. Zhang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Gene therapy prevents photoreceptor death and preserves retinal function in a Bardet-Biedl syndrome mouse model
- (2011) D. L. Simons et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The Genomic, Biochemical, and Cellular Responses of the Retina in Inherited Photoreceptor Degenerations and Prospects for the Treatment of These Disorders
- (2010) Alexa N. Bramall et al. Annual Review of Neuroscience
- Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration
- (2010) C. A. Murga-Zamalloa et al. HUMAN MOLECULAR GENETICS
- Gene therapy rescues cone function in congenital achromatopsia
- (2010) András M. Komáromy et al. HUMAN MOLECULAR GENETICS
- Restoration of Cone Vision in the CNGA3−/− Mouse Model of Congenital Complete Lack of Cone Photoreceptor Function
- (2010) Stylianos Michalakis et al. MOLECULAR THERAPY
- Novel Properties of Tyrosine-mutant AAV2 Vectors in the Mouse Retina
- (2010) Hilda Petrs-Silva et al. MOLECULAR THERAPY
- Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait
- (2010) Alan F. Wright et al. NATURE REVIEWS GENETICS
- Treatment Possibilities for Retinitis Pigmentosa
- (2010) Samuel G. Jacobson et al. NEW ENGLAND JOURNAL OF MEDICINE
- Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy
- (2010) Artur V. Cideciyan PROGRESS IN RETINAL AND EYE RESEARCH
- RPGR ORF15 genotype and clinical variability of retinal degeneration in an Australian population
- (2009) J B Ruddle et al. BRITISH JOURNAL OF OPHTHALMOLOGY
- Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development
- (2009) Amiya K. Ghosh et al. HUMAN MOLECULAR GENETICS
- Discordant Phenotypes in Fraternal Twins Having an Identical Mutation in Exon ORF15 of the RPGR Gene
- (2008) Saloni Walia ARCHIVES OF OPHTHALMOLOGY
- Retinitis Pigmentosa GTPase Regulator (RPGR) protein isoforms in mammalian retina: Insights into X-linked Retinitis Pigmentosa and associated ciliopathies
- (2007) Shirley He et al. VISION RESEARCH
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started