A V Cideciyan|S G Jacobson - JoVE Visualize

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Ophthalmology|December 17, 1998

X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60G A Fishman, S Grover, S G Jacobson, et al.

Human Mutation|September 30, 1999

Analysis of DNA elements that modulate myosin VIIA expression in humansD J Orten, M D Weston, P M Kelley, et al.

Ophthalmology|December 1, 1986

Automated light- and dark-adapted perimetry for evaluating retinitis pigmentosaS G Jacobson, W J Voigt, J M Parel, et al.

Molecular Vision|March 10, 2001

Calcium channel blocker D-cis-diltiazem does not slow retinal degeneration in the PDE6B mutant rcd1 canine model of retinitis pigmentosaS E Pearce-Kelling, T S Aleman, A Nickle, et al.

Nature Genetics|July 14, 1998

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channelS Kohl, T Marx, I Giddings, et al.

Molecular Therapy : the Journal of the American Society of Gene Therapy|November 16, 2001

Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosaF Q Liang, T S Aleman, N S Dejneka, et al.

Human Mutation|July 20, 2001

Four novel mutations in the RPE65 gene in patients with Leber congenital amaurosisM J Simovich, B Miller, H Ezzeldin, et al.

American Journal of Human Genetics|October 27, 1997

Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, et al.

Investigative Ophthalmology & Visual Science|October 3, 2001

CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate geneM Danciger, J Hendrickson, J Lyon, et al.

Ophthalmology|February 1, 1995

A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degenerationM B Gorin, K E Jackson, R E Ferrell, et al.

Pageof 13

Showing results (91-100 of 126) with videos related to

Sort By:

Pageof 13

Ophthalmology|December 17, 1998

X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60G A Fishman, S Grover, S G Jacobson, et al.

Human Mutation|September 30, 1999

Analysis of DNA elements that modulate myosin VIIA expression in humansD J Orten, M D Weston, P M Kelley, et al.

Ophthalmology|December 1, 1986

Automated light- and dark-adapted perimetry for evaluating retinitis pigmentosaS G Jacobson, W J Voigt, J M Parel, et al.

Molecular Vision|March 10, 2001

Calcium channel blocker D-cis-diltiazem does not slow retinal degeneration in the PDE6B mutant rcd1 canine model of retinitis pigmentosaS E Pearce-Kelling, T S Aleman, A Nickle, et al.

Nature Genetics|July 14, 1998

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channelS Kohl, T Marx, I Giddings, et al.

Molecular Therapy : the Journal of the American Society of Gene Therapy|November 16, 2001

Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosaF Q Liang, T S Aleman, N S Dejneka, et al.

Human Mutation|July 20, 2001

Four novel mutations in the RPE65 gene in patients with Leber congenital amaurosisM J Simovich, B Miller, H Ezzeldin, et al.

American Journal of Human Genetics|October 27, 1997

Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, et al.

Investigative Ophthalmology & Visual Science|October 3, 2001

CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate geneM Danciger, J Hendrickson, J Lyon, et al.

Ophthalmology|February 1, 1995

A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degenerationM B Gorin, K E Jackson, R E Ferrell, et al.

Pageof 13