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S G Jacobson

Showing results (111-120 of 139) with videos related to

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Genomics|August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11B Wissinger, H Jägle, S Kohl, et al.
Experimental Eye Research|February 5, 2002
Concentric retinitis pigmentosa: clinicopathologic correlationsA H Milam, E B De Castro, J E Smith, et al.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.
Clinical Genetics|March 13, 2003
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian alleleX M Ouyang, J F Hejtmancik, S G Jacobson, et al.
Investigative Ophthalmology & Visual Science|June 30, 2001
Macular pigment and lutein supplementation in retinitis pigmentosa and Usher syndromeT S Aleman, J L Duncan, M L Bieber, et al.
Investigative Ophthalmology & Visual Science|May 8, 2000
Allelic variation in the VMD2 gene in best disease and age-related macular degenerationA J Lotery, F L Munier, G A Fishman, et al.
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Investigative Ophthalmology & Visual Science|August 10, 1999
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degenerationC A Lewis, I R Batlle, K G Batlle, et al.
Investigative Ophthalmology & Visual Science|November 30, 2000
Genetics and phenotypes of RPE65 mutations in inherited retinal degenerationD A Thompson, P Gyürüs, L L Fleischer, et al.
Pageof 14

Showing results (111-120 of 139) with videos related to

Sort By:
Pageof 14
Genomics|August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11B Wissinger, H Jägle, S Kohl, et al.
Experimental Eye Research|February 5, 2002
Concentric retinitis pigmentosa: clinicopathologic correlationsA H Milam, E B De Castro, J E Smith, et al.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.
Clinical Genetics|March 13, 2003
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian alleleX M Ouyang, J F Hejtmancik, S G Jacobson, et al.
Investigative Ophthalmology & Visual Science|June 30, 2001
Macular pigment and lutein supplementation in retinitis pigmentosa and Usher syndromeT S Aleman, J L Duncan, M L Bieber, et al.
Investigative Ophthalmology & Visual Science|May 8, 2000
Allelic variation in the VMD2 gene in best disease and age-related macular degenerationA J Lotery, F L Munier, G A Fishman, et al.
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Investigative Ophthalmology & Visual Science|August 10, 1999
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degenerationC A Lewis, I R Batlle, K G Batlle, et al.
Investigative Ophthalmology & Visual Science|November 30, 2000
Genetics and phenotypes of RPE65 mutations in inherited retinal degenerationD A Thompson, P Gyürüs, L L Fleischer, et al.
Pageof 14