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G Jacobson

Showing results (551-560 of 677) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|March 30, 2021
Gene therapy reforms photoreceptor structure and restores vision in NPHP5-associated Leber congenital amaurosisGustavo D Aguirre, Artur V Cideciyan, Valérie L Dufour, et al.
Human Mutation|June 8, 2007
Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosisArtur V Cideciyan, Tomas S Aleman, Samuel G Jacobson, et al.
American Journal of Human Genetics|February 8, 2011
A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi JewsLina Zelinger, Eyal Banin, Alexey Obolensky, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 29, 2021
Gene therapy reforms photoreceptor structure and restores vision in NPHP5-associated Leber congenital amaurosisGustavo D Aguirre, Artur V Cideciyan, Valérie L Dufour, et al.
Human Molecular Genetics|February 26, 2015
Protein misfolding and the pathogenesis of ABCA4-associated retinal degenerationsNing Zhang, Yaroslav Tsybovsky, Alexander V Kolesnikov, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutationsTomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Mutation|May 12, 2009
Predicting the pathogenicity of RPE65 mutationsA R Philp, M Jin, S Li, et al.
Vision Research|November 30, 2022
Photoreceptor function and structure in retinal degenerations caused by biallelic BEST1 mutationsArtur V Cideciyan, Samuel G Jacobson, Alexander Sumaroka, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2013
Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvementArtur V Cideciyan, Samuel G Jacobson, William A Beltran, et al.
Nature Genetics|February 14, 1998
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosaP Banerjee, P W Kleyn, J A Knowles, et al.
Pageof 68

Showing results (551-560 of 677) with videos related to

Sort By:
Pageof 68
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 30, 2021
Gene therapy reforms photoreceptor structure and restores vision in NPHP5-associated Leber congenital amaurosisGustavo D Aguirre, Artur V Cideciyan, Valérie L Dufour, et al.
Human Mutation|June 8, 2007
Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosisArtur V Cideciyan, Tomas S Aleman, Samuel G Jacobson, et al.
American Journal of Human Genetics|February 8, 2011
A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi JewsLina Zelinger, Eyal Banin, Alexey Obolensky, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 29, 2021
Gene therapy reforms photoreceptor structure and restores vision in NPHP5-associated Leber congenital amaurosisGustavo D Aguirre, Artur V Cideciyan, Valérie L Dufour, et al.
Human Molecular Genetics|February 26, 2015
Protein misfolding and the pathogenesis of ABCA4-associated retinal degenerationsNing Zhang, Yaroslav Tsybovsky, Alexander V Kolesnikov, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutationsTomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Mutation|May 12, 2009
Predicting the pathogenicity of RPE65 mutationsA R Philp, M Jin, S Li, et al.
Vision Research|November 30, 2022
Photoreceptor function and structure in retinal degenerations caused by biallelic BEST1 mutationsArtur V Cideciyan, Samuel G Jacobson, Alexander Sumaroka, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2013
Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvementArtur V Cideciyan, Samuel G Jacobson, William A Beltran, et al.
Nature Genetics|February 14, 1998
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosaP Banerjee, P W Kleyn, J A Knowles, et al.
Pageof 68