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Showing results (81-90 of 91) with videos related to

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American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, et al.
Visual Neuroscience|August 11, 2001
Comparative structural and functional analysis of photoreceptor neurons of Rho-/- mice reveal increased survival on C57BL/6J in comparison to 129Sv genetic backgroundM M Humphries, S Kiang, N McNally, et al.
American Journal of Human Genetics|July 1, 1996
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3R Fujita, E Bingham, P Forsythe, et al.
Genomics|May 20, 1999
Bestrophin gene mutations in patients with Best vitelliform macular dystrophyG M Caldwell, L E Kakuk, I B Griesinger, 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.
Human Mutation|October 26, 1999
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence changeK T Hiriyanna, E L Bingham, B M Yashar, et al.
Neuron|January 14, 1998
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degenerationP K Swain, S Chen, Q L Wang, et al.
Nature Genetics|February 1, 1997
Retinopathy induced in mice by targeted disruption of the rhodopsin geneM M Humphries, D Rancourt, G J Farrar, et al.
American Journal of Human Genetics|December 18, 1997
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosaM Buraczynska, W Wu, R Fujita, et al.
Ophthalmic Genetics|January 23, 2002
Evaluation of the ELOVL4 gene in patients with age-related macular degenerationR Ayyagari, K Zhang, A Hutchinson, et al.
Pageof 10

Showing results (81-90 of 91) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, et al.
Visual Neuroscience|August 11, 2001
Comparative structural and functional analysis of photoreceptor neurons of Rho-/- mice reveal increased survival on C57BL/6J in comparison to 129Sv genetic backgroundM M Humphries, S Kiang, N McNally, et al.
American Journal of Human Genetics|July 1, 1996
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3R Fujita, E Bingham, P Forsythe, et al.
Genomics|May 20, 1999
Bestrophin gene mutations in patients with Best vitelliform macular dystrophyG M Caldwell, L E Kakuk, I B Griesinger, 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.
Human Mutation|October 26, 1999
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence changeK T Hiriyanna, E L Bingham, B M Yashar, et al.
Neuron|January 14, 1998
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degenerationP K Swain, S Chen, Q L Wang, et al.
Nature Genetics|February 1, 1997
Retinopathy induced in mice by targeted disruption of the rhodopsin geneM M Humphries, D Rancourt, G J Farrar, et al.
American Journal of Human Genetics|December 18, 1997
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosaM Buraczynska, W Wu, R Fujita, et al.
Ophthalmic Genetics|January 23, 2002
Evaluation of the ELOVL4 gene in patients with age-related macular degenerationR Ayyagari, K Zhang, A Hutchinson, et al.
Pageof 10