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S G Jacobson

Showing results (81-90 of 139) with videos related to

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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.
Investigative Ophthalmology & Visual Science|August 1, 1996
Sub-retinal pigment epithelial deposits in a dominant late-onset retinal degenerationC A Kuntz, S G Jacobson, A V Cideciyan, 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.
Ophthalmology|August 1, 1995
Pattern of retinal dysfunction in acute zonal occult outer retinopathyS G Jacobson, D S Morales, X K Sun, 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.
Proceedings of the National Academy of Sciences of the United States of America|June 17, 1998
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in manA V Cideciyan, D C Hood, Y Huang, et al.
Vision Research|October 6, 2001
Augmented rod bipolar cell function in partial receptor loss: an ERG study in P23H rhodopsin transgenic and aging normal ratsT S Aleman, M M LaVail, R Montemayor, et al.
Pageof 14

Showing results (81-90 of 139) with videos related to

Sort By:
Pageof 14
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.
Investigative Ophthalmology & Visual Science|August 1, 1996
Sub-retinal pigment epithelial deposits in a dominant late-onset retinal degenerationC A Kuntz, S G Jacobson, A V Cideciyan, 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.
Ophthalmology|August 1, 1995
Pattern of retinal dysfunction in acute zonal occult outer retinopathyS G Jacobson, D S Morales, X K Sun, 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.
Proceedings of the National Academy of Sciences of the United States of America|June 17, 1998
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in manA V Cideciyan, D C Hood, Y Huang, et al.
Vision Research|October 6, 2001
Augmented rod bipolar cell function in partial receptor loss: an ERG study in P23H rhodopsin transgenic and aging normal ratsT S Aleman, M M LaVail, R Montemayor, et al.
Pageof 14