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Jean Bennett

Showing results (131-140 of 175) with videos related to

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Ophthalmology|April 2, 2021
Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease: Phase 3 Results at 3 and 4 YearsAlbert 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 functionManzar 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 TherapyUnikora Yang, Susan Gentleman, Xiaowu Gai, et al.
Investigative Ophthalmology & Visual Science|May 20, 2020
Treatment Potential for LCA5-Associated Leber Congenital AmaurosisKatherine 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 RetinaPavitra S Ramachandran, Vivian Lee, Zhangyong Wei, et al.
Biology of Reproduction|December 31, 2005
Deficiency of SPAG16L causes male infertility associated with impaired sperm motilityZhibing 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 DegenerationsJean 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 amaurosisManzar 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 amaurosisTomas 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 disorderCatherine Argyriou, Anna Polosa, Ji Yun Song, et al.
Pageof 18

Showing results (131-140 of 175) with videos related to

Sort By:
Pageof 18
Ophthalmology|April 2, 2021
Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease: Phase 3 Results at 3 and 4 YearsAlbert 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 functionManzar 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 TherapyUnikora Yang, Susan Gentleman, Xiaowu Gai, et al.
Investigative Ophthalmology & Visual Science|May 20, 2020
Treatment Potential for LCA5-Associated Leber Congenital AmaurosisKatherine 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 RetinaPavitra S Ramachandran, Vivian Lee, Zhangyong Wei, et al.
Biology of Reproduction|December 31, 2005
Deficiency of SPAG16L causes male infertility associated with impaired sperm motilityZhibing 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 DegenerationsJean 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 amaurosisManzar 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 amaurosisTomas 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 disorderCatherine Argyriou, Anna Polosa, Ji Yun Song, et al.
Pageof 18