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G Jacobson

Showing results (421-430 of 677) with videos related to

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International Journal of Molecular Sciences|March 6, 2021
Leber Congenital Amaurosis Due to <i>GUCY2D</i> Mutations: Longitudinal Analysis of Retinal Structure and Visual FunctionSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 24, 2005
In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosaArtur V Cideciyan, Samuel G Jacobson, Tomas S Aleman, et al.
American Journal of Human Genetics|December 1, 2001
Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectivelyDebra A Thompson, Christina L McHenry, Yun Li, et al.
Journal of Occupational and Environmental Medicine|June 12, 2012
Prospective assessment of chronic multisymptom illness reporting possibly associated with open-air burn pit smoke exposure in IraqTeresa M Powell, Tyler C Smith, Isabel G Jacobson, et al.
American Journal of Human Genetics|March 3, 1999
Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosaA J Mears, L Gieser, D Yan, et al.
Progress in Retinal and Eye Research|January 4, 2020
Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiativesAlexandra V Garafalo, Artur V Cideciyan, Elise Héon, et al.
Investigative Ophthalmology & Visual Science|October 23, 1997
Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR geneS G Jacobson, M Buraczynska, A H Milam, et al.
Investigative Ophthalmology & Visual Science|July 5, 2018
Cone Vision Changes in the Enhanced S-Cone Syndrome Caused by NR2E3 Gene MutationsAlexandra V Garafalo, Giacomo Calzetti, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|June 30, 2017
Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion CellsJason Charng, Samuel G Jacobson, Elise Heon, et al.
Sleep|July 2, 2013
Predeployment Sleep Duration and Insomnia Symptoms as Risk Factors for New-Onset Mental Health Disorders Following Military DeploymentPhilip Gehrman, Amber D Seelig, Isabel G Jacobson, et al.
Pageof 68

Showing results (421-430 of 677) with videos related to

Sort By:
Pageof 68
International Journal of Molecular Sciences|March 6, 2021
Leber Congenital Amaurosis Due to <i>GUCY2D</i> Mutations: Longitudinal Analysis of Retinal Structure and Visual FunctionSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 24, 2005
In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosaArtur V Cideciyan, Samuel G Jacobson, Tomas S Aleman, et al.
American Journal of Human Genetics|December 1, 2001
Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectivelyDebra A Thompson, Christina L McHenry, Yun Li, et al.
Journal of Occupational and Environmental Medicine|June 12, 2012
Prospective assessment of chronic multisymptom illness reporting possibly associated with open-air burn pit smoke exposure in IraqTeresa M Powell, Tyler C Smith, Isabel G Jacobson, et al.
American Journal of Human Genetics|March 3, 1999
Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosaA J Mears, L Gieser, D Yan, et al.
Progress in Retinal and Eye Research|January 4, 2020
Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiativesAlexandra V Garafalo, Artur V Cideciyan, Elise Héon, et al.
Investigative Ophthalmology & Visual Science|October 23, 1997
Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR geneS G Jacobson, M Buraczynska, A H Milam, et al.
Investigative Ophthalmology & Visual Science|July 5, 2018
Cone Vision Changes in the Enhanced S-Cone Syndrome Caused by NR2E3 Gene MutationsAlexandra V Garafalo, Giacomo Calzetti, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|June 30, 2017
Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion CellsJason Charng, Samuel G Jacobson, Elise Heon, et al.
Sleep|July 2, 2013
Predeployment Sleep Duration and Insomnia Symptoms as Risk Factors for New-Onset Mental Health Disorders Following Military DeploymentPhilip Gehrman, Amber D Seelig, Isabel G Jacobson, et al.
Pageof 68