Search research articles
Contact Us
Filters
Showing results (151-160 of 175) with videos related to
Page
of 18
Sort By:
Investigative Ophthalmology & Visual Science
|
January 27, 2005
Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype
Sharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science
|
March 2, 2026
Combined Expression of hRdCVF and hRdCVFL Through AAV-Mediated Delivery for the Treatment of Retinitis Pigmentosa
Emmanuelle Clérin, Ying Yang, Delphine Pagan, et al.
Molecular Genetics and Metabolism
|
February 8, 2014
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder
Shandi Hiebler, Tomohiro Masuda, Joseph G Hacia, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 20, 2005
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success
Samuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Plos One
|
May 14, 2013
AAV-mediated gene therapy for choroideremia: preclinical studies in personalized models
Vidyullatha Vasireddy, Jason A Mills, Rajashekhar Gaddameedi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 5, 2004
In utero gene therapy rescues vision in a murine model of congenital blindness
Nadine S Dejneka, Enrico M Surace, Tomas S Aleman, et al.
Plos One
|
June 20, 2015
Correction: AAV-Mediated Gene Therapy for Choroideremia: Preclinical Studies in Personalized Models
Vidyullatha Vasireddy, Jason A Mills, Rajashekhar Gaddameedi, et al.
Experimental Eye Research
|
May 17, 2002
Macular pigment and lutein supplementation in choroideremia
Jacque L Duncan, Tomas S Aleman, Leigh M Gardner, et al.
Ophthalmology
|
August 25, 2019
Efficacy, Safety, and Durability of Voretigene Neparvovec-rzyl in RPE65 Mutation-Associated Inherited Retinal Dystrophy: Results of Phase 1 and 3 Trials
Albert M Maguire, Stephen Russell, Jennifer A Wellman, et al.
Human Molecular Genetics
|
February 21, 2012
Nxnl2 splicing results in dual functions in neuronal cell survival and maintenance of cell integrity
Céline Jaillard, Aurélie Mouret, Marie-Laure Niepon, et al.
Page
of 18
Search research articles
Search
Showing results (151-160 of 175) with videos related to
Sort By:
Page
of 18
Investigative Ophthalmology & Visual Science
|
January 27, 2005
Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype
Sharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science
|
March 2, 2026
Combined Expression of hRdCVF and hRdCVFL Through AAV-Mediated Delivery for the Treatment of Retinitis Pigmentosa
Emmanuelle Clérin, Ying Yang, Delphine Pagan, et al.
Molecular Genetics and Metabolism
|
February 8, 2014
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder
Shandi Hiebler, Tomohiro Masuda, Joseph G Hacia, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 20, 2005
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success
Samuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Plos One
|
May 14, 2013
AAV-mediated gene therapy for choroideremia: preclinical studies in personalized models
Vidyullatha Vasireddy, Jason A Mills, Rajashekhar Gaddameedi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 5, 2004
In utero gene therapy rescues vision in a murine model of congenital blindness
Nadine S Dejneka, Enrico M Surace, Tomas S Aleman, et al.
Plos One
|
June 20, 2015
Correction: AAV-Mediated Gene Therapy for Choroideremia: Preclinical Studies in Personalized Models
Vidyullatha Vasireddy, Jason A Mills, Rajashekhar Gaddameedi, et al.
Experimental Eye Research
|
May 17, 2002
Macular pigment and lutein supplementation in choroideremia
Jacque L Duncan, Tomas S Aleman, Leigh M Gardner, et al.
Ophthalmology
|
August 25, 2019
Efficacy, Safety, and Durability of Voretigene Neparvovec-rzyl in RPE65 Mutation-Associated Inherited Retinal Dystrophy: Results of Phase 1 and 3 Trials
Albert M Maguire, Stephen Russell, Jennifer A Wellman, et al.
Human Molecular Genetics
|
February 21, 2012
Nxnl2 splicing results in dual functions in neuronal cell survival and maintenance of cell integrity
Céline Jaillard, Aurélie Mouret, Marie-Laure Niepon, et al.
Page
of 18