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S G Jacobson

Showing results (101-110 of 139) with videos related to

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Molecular Vision|September 22, 1998
Exon screening of the genes encoding the beta- and gamma-subunits of cone transducin in patients with inherited retinal diseaseY Q Gao, M Danciger, N B Akhmedov, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2000
Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindnessJ P Van Hooser, T S Aleman, Y G He, et al.
Clinical Genetics|March 18, 2004
Mutational spectrum in Usher syndrome type IIX M Ouyang, D Yan, J F Hejtmancik, et al.
Experimental Eye Research|February 3, 2000
Optical coherence tomography (OCT) abnormalities in rhodopsin mutant transgenic swine with retinal degenerationY Huang, A V Cideciyan, T S Alemán, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Rhodopsin mutations in autosomal dominant retinitis pigmentosaC H Sung, C M Davenport, J C Hennessey, et al.
American Journal of Human Genetics|July 1, 1993
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsinJ P Macke, C M Davenport, S G Jacobson, et al.
Eye (London, England)|August 16, 2008
Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic waveletsT S Aleman, B L Lam, A V Cideciyan, et al.
American Journal of Human Genetics|September 29, 2000
Pitfalls in homozygosity mappingM G Miano, S G Jacobson, A Carothers, et al.
Ophthalmology|November 30, 2000
Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degenerationA H Milam, C A Curcio, A V Cideciyan, et al.
Genomics|April 2, 1998
Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3P Banerjee, C A Lewis, P W Kleyn, et al.
Pageof 14

Showing results (101-110 of 139) with videos related to

Sort By:
Pageof 14
Molecular Vision|September 22, 1998
Exon screening of the genes encoding the beta- and gamma-subunits of cone transducin in patients with inherited retinal diseaseY Q Gao, M Danciger, N B Akhmedov, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2000
Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindnessJ P Van Hooser, T S Aleman, Y G He, et al.
Clinical Genetics|March 18, 2004
Mutational spectrum in Usher syndrome type IIX M Ouyang, D Yan, J F Hejtmancik, et al.
Experimental Eye Research|February 3, 2000
Optical coherence tomography (OCT) abnormalities in rhodopsin mutant transgenic swine with retinal degenerationY Huang, A V Cideciyan, T S Alemán, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Rhodopsin mutations in autosomal dominant retinitis pigmentosaC H Sung, C M Davenport, J C Hennessey, et al.
American Journal of Human Genetics|July 1, 1993
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsinJ P Macke, C M Davenport, S G Jacobson, et al.
Eye (London, England)|August 16, 2008
Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic waveletsT S Aleman, B L Lam, A V Cideciyan, et al.
American Journal of Human Genetics|September 29, 2000
Pitfalls in homozygosity mappingM G Miano, S G Jacobson, A Carothers, et al.
Ophthalmology|November 30, 2000
Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degenerationA H Milam, C A Curcio, A V Cideciyan, et al.
Genomics|April 2, 1998
Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3P Banerjee, C A Lewis, P W Kleyn, et al.
Pageof 14