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G H Travis

Showing results (31-40 of 41) with videos related to

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Neuropharmacology|July 1, 1987
Subtractive cloning of complementary DNAs and analysis of messenger RNAs with regional heterogeneous distributions in primate cortexG H Travis, C G Naus, J H Morrison, et al.
Nature|December 12, 1991
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosaK Kajiwara, L B Hahn, S Mukai, et al.
Investigative Ophthalmology & Visual Science|June 30, 2001
Delayed dark-adaptation and lipofuscin accumulation in abcr+/- mice: implications for involvement of ABCR in age-related macular degenerationN L Mata, R T Tzekov, X Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2001
Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosaW Kedzierski, S Nusinowitz, D Birch, et al.
Cell|July 21, 1999
Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout miceJ Weng, N L Mata, S M Azarian, et al.
Experimental Eye Research|February 16, 2002
Visual function in patients with cone-rod dystrophy (CRD) associated with mutations in the ABCA4(ABCR) geneD G Birch, A Y Peters, K L Locke, et al.
Journal of Cell Science|October 1, 1996
Three homologs of rds/peripherin in Xenopus laevis photoreceptors that exhibit covalent and non-covalent interactionsW Kedzierski, W N Moghrabi, A C Allen, et al.
Genomics|July 1, 1991
The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNAG H Travis, L Christerson, P E Danielson, et al.
Genomics|July 20, 1995
Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon IIJ Ma, J C Norton, A C Allen, et al.
Epilepsy Research. Supplement|January 1, 1991
Molecular approaches to genes of the CNSJ G Sutcliffe, G H Travis, P E Danielson, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Neuropharmacology|July 1, 1987
Subtractive cloning of complementary DNAs and analysis of messenger RNAs with regional heterogeneous distributions in primate cortexG H Travis, C G Naus, J H Morrison, et al.
Nature|December 12, 1991
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosaK Kajiwara, L B Hahn, S Mukai, et al.
Investigative Ophthalmology & Visual Science|June 30, 2001
Delayed dark-adaptation and lipofuscin accumulation in abcr+/- mice: implications for involvement of ABCR in age-related macular degenerationN L Mata, R T Tzekov, X Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2001
Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosaW Kedzierski, S Nusinowitz, D Birch, et al.
Cell|July 21, 1999
Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout miceJ Weng, N L Mata, S M Azarian, et al.
Experimental Eye Research|February 16, 2002
Visual function in patients with cone-rod dystrophy (CRD) associated with mutations in the ABCA4(ABCR) geneD G Birch, A Y Peters, K L Locke, et al.
Journal of Cell Science|October 1, 1996
Three homologs of rds/peripherin in Xenopus laevis photoreceptors that exhibit covalent and non-covalent interactionsW Kedzierski, W N Moghrabi, A C Allen, et al.
Genomics|July 1, 1991
The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNAG H Travis, L Christerson, P E Danielson, et al.
Genomics|July 20, 1995
Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon IIJ Ma, J C Norton, A C Allen, et al.
Epilepsy Research. Supplement|January 1, 1991
Molecular approaches to genes of the CNSJ G Sutcliffe, G H Travis, P E Danielson, et al.
Pageof 5