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David M Hunt

Showing results (91-100 of 102) with videos related to

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Molecular Biology and Evolution|August 19, 2016
Visual Pigments, Ocular Filters and the Evolution of Snake VisionBruno F Simões, Filipa L Sampaio, Ronald H Douglas, et al.
Molecular Biology and Evolution|November 27, 2019
Visual Opsin Diversity in Sharks and RaysNathan S Hart, Trevor D Lamb, Hardip R Patel, et al.
The Journal of Experimental Biology|April 22, 2008
The influence of ontogeny and light environment on the expression of visual pigment opsins in the retina of the black bream, Acanthopagrus butcheriJulia Shand, Wayne L Davies, Nicole Thomas, et al.
Ophthalmic Genetics|June 22, 2017
Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalitiesValentina Cipriani, Ambreen Kalhoro, Gavin Arno, et al.
American Journal of Human Genetics|August 16, 2006
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humansHuimin Wu, Jill A Cowing, Michel Michaelides, et al.
Investigative Ophthalmology & Visual Science|April 26, 2008
Phenotypic variation in enhanced S-cone syndromeIsabelle Audo, Michel Michaelides, Anthony G Robson, et al.
European Journal of Human Genetics : EJHG|September 23, 2010
Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophyFrancesca I Arrigoni, Mar Matarin, Pamela J Thompson, et al.
Current Biology : CB|May 30, 2020
Spectral Diversification and Trans-Species Allelic Polymorphism during the Land-to-Sea Transition in SnakesBruno F Simões, David J Gower, Arne R Rasmussen, et al.
Investigative Ophthalmology & Visual Science|April 16, 2010
The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophyMichel Michaelides, Marie-Claire Gaillard, Pascal Escher, et al.
Journal of Medical Genetics|January 24, 2007
Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutationSanjay M Sisodiya, Pamela J Thompson, Anna Need, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
Molecular Biology and Evolution|August 19, 2016
Visual Pigments, Ocular Filters and the Evolution of Snake VisionBruno F Simões, Filipa L Sampaio, Ronald H Douglas, et al.
Molecular Biology and Evolution|November 27, 2019
Visual Opsin Diversity in Sharks and RaysNathan S Hart, Trevor D Lamb, Hardip R Patel, et al.
The Journal of Experimental Biology|April 22, 2008
The influence of ontogeny and light environment on the expression of visual pigment opsins in the retina of the black bream, Acanthopagrus butcheriJulia Shand, Wayne L Davies, Nicole Thomas, et al.
Ophthalmic Genetics|June 22, 2017
Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalitiesValentina Cipriani, Ambreen Kalhoro, Gavin Arno, et al.
American Journal of Human Genetics|August 16, 2006
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humansHuimin Wu, Jill A Cowing, Michel Michaelides, et al.
Investigative Ophthalmology & Visual Science|April 26, 2008
Phenotypic variation in enhanced S-cone syndromeIsabelle Audo, Michel Michaelides, Anthony G Robson, et al.
European Journal of Human Genetics : EJHG|September 23, 2010
Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophyFrancesca I Arrigoni, Mar Matarin, Pamela J Thompson, et al.
Current Biology : CB|May 30, 2020
Spectral Diversification and Trans-Species Allelic Polymorphism during the Land-to-Sea Transition in SnakesBruno F Simões, David J Gower, Arne R Rasmussen, et al.
Investigative Ophthalmology & Visual Science|April 16, 2010
The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophyMichel Michaelides, Marie-Claire Gaillard, Pascal Escher, et al.
Journal of Medical Genetics|January 24, 2007
Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutationSanjay M Sisodiya, Pamela J Thompson, Anna Need, et al.
Pageof 11