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S G Jacobson

Showing results (71-80 of 139) with videos related to

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Investigative Ophthalmology & Visual Science|July 1, 1994
RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor functionC M Kemp, S G Jacobson, A V Cideciyan, et al.
Human Molecular Genetics|August 1, 1994
Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6pJ A Knowles, Y Shugart, P Banerjee, et al.
Nature Genetics|November 4, 2000
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosaA Gal, Y Li, D A Thompson, et al.
Neuron|August 5, 1999
Retinal rod photoreceptor-specific gene mutation perturbs cone pathway developmentE Banin, A V Cideciyan, T S Alemán, et al.
Genomics|November 1, 1995
Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosaM Danciger, J Blaney, Y Q Gao, et al.
Human Molecular Genetics|July 13, 1999
A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locusX Guillonneau, N I Piriev, M Danciger, et al.
Nature Genetics|September 1, 1995
Night blindness in Sorsby's fundus dystrophy reversed by vitamin AS G Jacobson, A V Cideciyan, G Regunath, et al.
Human Mutation|December 29, 1999
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humansD J Orten, M D Weston, P M Kelley, et al.
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.
Investigative Ophthalmology & Visual Science|November 6, 1998
Relation of optical coherence tomography to microanatomy in normal and rd chickensY Huang, A V Cideciyan, G I Papastergiou, et al.
Pageof 14

Showing results (71-80 of 139) with videos related to

Sort By:
Pageof 14
Investigative Ophthalmology & Visual Science|July 1, 1994
RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor functionC M Kemp, S G Jacobson, A V Cideciyan, et al.
Human Molecular Genetics|August 1, 1994
Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6pJ A Knowles, Y Shugart, P Banerjee, et al.
Nature Genetics|November 4, 2000
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosaA Gal, Y Li, D A Thompson, et al.
Neuron|August 5, 1999
Retinal rod photoreceptor-specific gene mutation perturbs cone pathway developmentE Banin, A V Cideciyan, T S Alemán, et al.
Genomics|November 1, 1995
Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosaM Danciger, J Blaney, Y Q Gao, et al.
Human Molecular Genetics|July 13, 1999
A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locusX Guillonneau, N I Piriev, M Danciger, et al.
Nature Genetics|September 1, 1995
Night blindness in Sorsby's fundus dystrophy reversed by vitamin AS G Jacobson, A V Cideciyan, G Regunath, et al.
Human Mutation|December 29, 1999
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humansD J Orten, M D Weston, P M Kelley, et al.
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.
Investigative Ophthalmology & Visual Science|November 6, 1998
Relation of optical coherence tomography to microanatomy in normal and rd chickensY Huang, A V Cideciyan, G I Papastergiou, et al.
Pageof 14