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G Jacobson

Showing results (581-590 of 677) with videos related to

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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.
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.
Human Molecular Genetics|August 29, 2003
Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degenerationCaroline Hayward, Xinhua Shu, Artur V Cideciyan, et al.
American Journal of Human Genetics|December 18, 1997
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosaM Buraczynska, W Wu, R Fujita, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degenerationAmir A Azari, Tomas S Aleman, Artur V Cideciyan, et al.
BMC Public Health|February 2, 2011
Health impact of US military service in a large population-based military cohort: findings of the Millennium Cohort Study, 2001-2008Tyler C Smith, Isabel G Jacobson, Tomoko I Hooper, et al.
Scientific Reports|September 24, 2017
Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degenerationChloe M Stanton, Shyamanga Borooah, Camilla Drake, et al.
Human Molecular Genetics|December 23, 2020
RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP)Laura Moreno-Leon, Emma L West, Michelle O'Hara-Wright, et al.
Pageof 68

Showing results (581-590 of 677) with videos related to

Sort By:
Pageof 68
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.
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.
Human Molecular Genetics|August 29, 2003
Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degenerationCaroline Hayward, Xinhua Shu, Artur V Cideciyan, et al.
American Journal of Human Genetics|December 18, 1997
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosaM Buraczynska, W Wu, R Fujita, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degenerationAmir A Azari, Tomas S Aleman, Artur V Cideciyan, et al.
BMC Public Health|February 2, 2011
Health impact of US military service in a large population-based military cohort: findings of the Millennium Cohort Study, 2001-2008Tyler C Smith, Isabel G Jacobson, Tomoko I Hooper, et al.
Scientific Reports|September 24, 2017
Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degenerationChloe M Stanton, Shyamanga Borooah, Camilla Drake, et al.
Human Molecular Genetics|December 23, 2020
RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP)Laura Moreno-Leon, Emma L West, Michelle O'Hara-Wright, et al.
Pageof 68