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Ophthalmology
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April 2, 2021
Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease: Phase 3 Results at 3 and 4 Years
Albert M Maguire, Stephen Russell, Daniel C Chung, et al.
The Journal of Clinical Investigation
|
May 25, 2011
The human visual cortex responds to gene therapy-mediated recovery of retinal function
Manzar Ashtari, Laura L Cyckowski, Justin F Monroe, et al.
JAMA Ophthalmology
|
October 4, 2019
Utility of In Vitro Mutagenesis of RPE65 Protein for Verification of Mutational Pathogenicity Before Gene Therapy
Unikora Yang, Susan Gentleman, Xiaowu Gai, et al.
Investigative Ophthalmology & Visual Science
|
May 20, 2020
Treatment Potential for LCA5-Associated Leber Congenital Amaurosis
Katherine E Uyhazi, Puya Aravand, Brent A Bell, et al.
Human Gene Therapy
|
October 19, 2016
Evaluation of Dose and Safety of AAV7m8 and AAV8BP2 in the Non-Human Primate Retina
Pavitra S Ramachandran, Vivian Lee, Zhangyong Wei, et al.
Biology of Reproduction
|
December 31, 2005
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
Zhibing Zhang, Igor Kostetskii, Waixing Tang, et al.
Translational Vision Science & Technology
|
January 30, 2023
Optimization and Validation of a Virtual Reality Orientation and Mobility Test for Inherited Retinal Degenerations
Jean Bennett, Elena M Aleman, Katherine H Maguire, et al.
Science Translational Medicine
|
July 17, 2015
Plasticity of the human visual system after retinal gene therapy in patients with Leber's congenital amaurosis
Manzar Ashtari, Hui Zhang, Philip A Cook, et al.
Investigative Ophthalmology & Visual Science
|
March 24, 2004
Impairment of the transient pupillary light reflex in Rpe65(-/-) mice and humans with leber congenital amaurosis
Tomas S Aleman, Samuel G Jacobson, John D Chico, et al.
Molecular Therapy. Methods & Clinical Development
|
October 27, 2021
AAV-mediated <i>PEX1</i> gene augmentation improves visual function in the PEX1-Gly844Asp mouse model for mild Zellweger spectrum disorder
Catherine Argyriou, Anna Polosa, Ji Yun Song, et al.
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of 18
Search research articles
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Showing results (131-140 of 175) with videos related to
Sort By:
Page
of 18
Ophthalmology
|
April 2, 2021
Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease: Phase 3 Results at 3 and 4 Years
Albert M Maguire, Stephen Russell, Daniel C Chung, et al.
The Journal of Clinical Investigation
|
May 25, 2011
The human visual cortex responds to gene therapy-mediated recovery of retinal function
Manzar Ashtari, Laura L Cyckowski, Justin F Monroe, et al.
JAMA Ophthalmology
|
October 4, 2019
Utility of In Vitro Mutagenesis of RPE65 Protein for Verification of Mutational Pathogenicity Before Gene Therapy
Unikora Yang, Susan Gentleman, Xiaowu Gai, et al.
Investigative Ophthalmology & Visual Science
|
May 20, 2020
Treatment Potential for LCA5-Associated Leber Congenital Amaurosis
Katherine E Uyhazi, Puya Aravand, Brent A Bell, et al.
Human Gene Therapy
|
October 19, 2016
Evaluation of Dose and Safety of AAV7m8 and AAV8BP2 in the Non-Human Primate Retina
Pavitra S Ramachandran, Vivian Lee, Zhangyong Wei, et al.
Biology of Reproduction
|
December 31, 2005
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
Zhibing Zhang, Igor Kostetskii, Waixing Tang, et al.
Translational Vision Science & Technology
|
January 30, 2023
Optimization and Validation of a Virtual Reality Orientation and Mobility Test for Inherited Retinal Degenerations
Jean Bennett, Elena M Aleman, Katherine H Maguire, et al.
Science Translational Medicine
|
July 17, 2015
Plasticity of the human visual system after retinal gene therapy in patients with Leber's congenital amaurosis
Manzar Ashtari, Hui Zhang, Philip A Cook, et al.
Investigative Ophthalmology & Visual Science
|
March 24, 2004
Impairment of the transient pupillary light reflex in Rpe65(-/-) mice and humans with leber congenital amaurosis
Tomas S Aleman, Samuel G Jacobson, John D Chico, et al.
Molecular Therapy. Methods & Clinical Development
|
October 27, 2021
AAV-mediated <i>PEX1</i> gene augmentation improves visual function in the PEX1-Gly844Asp mouse model for mild Zellweger spectrum disorder
Catherine Argyriou, Anna Polosa, Ji Yun Song, et al.
Page
of 18