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Brian Rossmiller

Showing results (1-10 of 8) with videos related to

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Molecular Vision|October 19, 2012
Gene therapy in animal models of autosomal dominant retinitis pigmentosaBrian Rossmiller, Haoyu Mao, Alfred S Lewin
Cold Spring Harbor Perspectives in Medicine|July 20, 2014
Gene augmentation for adRP mutations in RHOAlfred S Lewin, Brian Rossmiller, Haoyu Mao
Human Gene Therapy|February 1, 2012
Long-term rescue of retinal structure and function by rhodopsin RNA replacement with a single adeno-associated viral vector in P23H RHO transgenic miceHaoyu Mao, Marina S Gorbatyuk, Brian Rossmiller, et al.
Acta Ophthalmologica|February 9, 2016
Four-port bimanual 23-gauge vitrectomy for diabetic tractional retinal detachmentZhao-Yang Wang, Ke-Ke Zhao, Jia-Kai Li, et al.
Plos One|February 13, 2014
Systematic review and meta-analysis of the association between complement factor H I62V polymorphism and risk of polypoidal choroidal vasculopathy in Asian populationsZhao-Yang Wang, Keke Zhao, Jingwei Zheng, et al.
Brain : a Journal of Neurology|January 24, 2026
Targeting UCHL3 attenuates pathological markers in neuronal models of Huntington's diseaseHasan Ishtayeh, Elena Battistoni, Sharon Pochtar, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 22, 2018
Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vectorArtur V Cideciyan, Raghavi Sudharsan, Valérie L Dufour, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 31, 2026
Modification of the VP1u region boosts transduction of adeno-associated virus vectors for ocular gene therapyMengtian Cui, Shun-Yun Cheng, Jialing Liang, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Molecular Vision|October 19, 2012
Gene therapy in animal models of autosomal dominant retinitis pigmentosaBrian Rossmiller, Haoyu Mao, Alfred S Lewin
Cold Spring Harbor Perspectives in Medicine|July 20, 2014
Gene augmentation for adRP mutations in RHOAlfred S Lewin, Brian Rossmiller, Haoyu Mao
Human Gene Therapy|February 1, 2012
Long-term rescue of retinal structure and function by rhodopsin RNA replacement with a single adeno-associated viral vector in P23H RHO transgenic miceHaoyu Mao, Marina S Gorbatyuk, Brian Rossmiller, et al.
Acta Ophthalmologica|February 9, 2016
Four-port bimanual 23-gauge vitrectomy for diabetic tractional retinal detachmentZhao-Yang Wang, Ke-Ke Zhao, Jia-Kai Li, et al.
Plos One|February 13, 2014
Systematic review and meta-analysis of the association between complement factor H I62V polymorphism and risk of polypoidal choroidal vasculopathy in Asian populationsZhao-Yang Wang, Keke Zhao, Jingwei Zheng, et al.
Brain : a Journal of Neurology|January 24, 2026
Targeting UCHL3 attenuates pathological markers in neuronal models of Huntington's diseaseHasan Ishtayeh, Elena Battistoni, Sharon Pochtar, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 22, 2018
Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vectorArtur V Cideciyan, Raghavi Sudharsan, Valérie L Dufour, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 31, 2026
Modification of the VP1u region boosts transduction of adeno-associated virus vectors for ocular gene therapyMengtian Cui, Shun-Yun Cheng, Jialing Liang, et al.
Pageof 1