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Samuel G Jacobson

Showing results (141-150 of 224) with videos related to

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Elife|March 28, 2023
Reserpine maintains photoreceptor survival in retinal ciliopathy by resolving proteostasis imbalance and ciliogenesis defectsHolly Y Chen, Manju Swaroop, Samantha Papal, et al.
Human Molecular Genetics|November 1, 2016
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
The New England Journal of Medicine|August 14, 2009
Vision 1 year after gene therapy for Leber's congenital amaurosisArtur V Cideciyan, William W Hauswirth, Tomas S Aleman, et al.
Ophthalmology|January 19, 2010
Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosaSaloni Walia, Gerald A Fishman, Samuel G Jacobson, et al.
Human Genetics|January 22, 2005
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationXiao Mei Ouyang, Denise Yan, Li Lin Du, et al.
Plos One|March 7, 2014
Canine retina has a primate fovea-like bouquet of cone photoreceptors which is affected by inherited macular degenerationsWilliam A Beltran, Artur V Cideciyan, Karina E Guziewicz, et al.
Plos One|April 25, 2015
Blue cone monochromacy: visual function and efficacy outcome measures for clinical trialsXunda Luo, Artur V Cideciyan, Alessandro Iannaccone, et al.
Investigative Ophthalmology & Visual Science|July 19, 2012
RPGR-associated retinal degeneration in human X-linked RP and a murine modelWei Chieh Huang, Alan F Wright, Alejandro J Roman, et al.
Iscience|November 14, 2024
Erratum: Safety and improved efficacy signals following gene therapy in childhood blindness caused by <i>GUCY2D</i> mutationsSamuel G Jacobson, Artur V Cideciyan, Allen C Ho, et al.
Ophthalmology|January 25, 2015
Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene TherapyLina Zelinger, Artur V Cideciyan, Susanne Kohl, et al.
Pageof 23

Showing results (141-150 of 224) with videos related to

Sort By:
Pageof 23
Elife|March 28, 2023
Reserpine maintains photoreceptor survival in retinal ciliopathy by resolving proteostasis imbalance and ciliogenesis defectsHolly Y Chen, Manju Swaroop, Samantha Papal, et al.
Human Molecular Genetics|November 1, 2016
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
The New England Journal of Medicine|August 14, 2009
Vision 1 year after gene therapy for Leber's congenital amaurosisArtur V Cideciyan, William W Hauswirth, Tomas S Aleman, et al.
Ophthalmology|January 19, 2010
Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosaSaloni Walia, Gerald A Fishman, Samuel G Jacobson, et al.
Human Genetics|January 22, 2005
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationXiao Mei Ouyang, Denise Yan, Li Lin Du, et al.
Plos One|March 7, 2014
Canine retina has a primate fovea-like bouquet of cone photoreceptors which is affected by inherited macular degenerationsWilliam A Beltran, Artur V Cideciyan, Karina E Guziewicz, et al.
Plos One|April 25, 2015
Blue cone monochromacy: visual function and efficacy outcome measures for clinical trialsXunda Luo, Artur V Cideciyan, Alessandro Iannaccone, et al.
Investigative Ophthalmology & Visual Science|July 19, 2012
RPGR-associated retinal degeneration in human X-linked RP and a murine modelWei Chieh Huang, Alan F Wright, Alejandro J Roman, et al.
Iscience|November 14, 2024
Erratum: Safety and improved efficacy signals following gene therapy in childhood blindness caused by <i>GUCY2D</i> mutationsSamuel G Jacobson, Artur V Cideciyan, Allen C Ho, et al.
Ophthalmology|January 25, 2015
Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene TherapyLina Zelinger, Artur V Cideciyan, Susanne Kohl, et al.
Pageof 23