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David M Hunt

Showing results (71-80 of 102) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 28, 2007
Functional characterization, tuning, and regulation of visual pigment gene expression in an anadromous lampreyWayne L Davies, Jill A Cowing, Livia S Carvalho, et al.
Molecular Biology and Evolution|May 19, 2016
Evolution of Vertebrate Phototransduction: Cascade ActivationTrevor D Lamb, Hardip Patel, Aaron Chuah, et al.
Retina (Philadelphia, Pa.)|December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiologyAnthony G Robson, Andrew R Webster, Michel Michaelides, et al.
Brain, Behavior and Evolution|March 14, 2015
Spectral tuning in the eyes of deep-sea lanternfishes (Myctophidae): a novel sexually dimorphic intra-ocular filterFanny de Busserolles, Nathan S Hart, David M Hunt, et al.
Biochimica Et Biophysica Acta|October 8, 2004
Purification, characterisation and intracellular localisation of aryl hydrocarbon interacting protein-like 1 (AIPL1) and effects of mutations associated with inherited retinal dystrophiesVictoria A Gallon, Susan E Wilkie, Evelyne C Deery, et al.
Gene|July 19, 2005
Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2Suzanne L Inglis-Broadgate, Louise Ocaka, Ruby Banerjee, et al.
Genomics|March 28, 2003
Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7)Samantha Johnson, Stephanie Halford, Alex G Morris, et al.
The Journal of Experimental Biology|June 9, 2005
Adaptations to an extreme environment: retinal organisation and spectral properties of photoreceptors in Antarctic notothenioid fishMarie A Pointer, Chi-Hing Christina Cheng, James K Bowmaker, et al.
Human Molecular Genetics|November 22, 2002
Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31Evelyne C Deery, Eranga N Vithana, Richard J Newbold, et al.
Investigative Ophthalmology & Visual Science|September 26, 2003
Expression of PRPF31 mRNA in patients with autosomal dominant retinitis pigmentosa: a molecular clue for incomplete penetrance?Eranga N Vithana, Leen Abu-Safieh, Lucia Pelosini, et al.
Pageof 11

Showing results (71-80 of 102) with videos related to

Sort By:
Pageof 11
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 28, 2007
Functional characterization, tuning, and regulation of visual pigment gene expression in an anadromous lampreyWayne L Davies, Jill A Cowing, Livia S Carvalho, et al.
Molecular Biology and Evolution|May 19, 2016
Evolution of Vertebrate Phototransduction: Cascade ActivationTrevor D Lamb, Hardip Patel, Aaron Chuah, et al.
Retina (Philadelphia, Pa.)|December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiologyAnthony G Robson, Andrew R Webster, Michel Michaelides, et al.
Brain, Behavior and Evolution|March 14, 2015
Spectral tuning in the eyes of deep-sea lanternfishes (Myctophidae): a novel sexually dimorphic intra-ocular filterFanny de Busserolles, Nathan S Hart, David M Hunt, et al.
Biochimica Et Biophysica Acta|October 8, 2004
Purification, characterisation and intracellular localisation of aryl hydrocarbon interacting protein-like 1 (AIPL1) and effects of mutations associated with inherited retinal dystrophiesVictoria A Gallon, Susan E Wilkie, Evelyne C Deery, et al.
Gene|July 19, 2005
Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2Suzanne L Inglis-Broadgate, Louise Ocaka, Ruby Banerjee, et al.
Genomics|March 28, 2003
Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7)Samantha Johnson, Stephanie Halford, Alex G Morris, et al.
The Journal of Experimental Biology|June 9, 2005
Adaptations to an extreme environment: retinal organisation and spectral properties of photoreceptors in Antarctic notothenioid fishMarie A Pointer, Chi-Hing Christina Cheng, James K Bowmaker, et al.
Human Molecular Genetics|November 22, 2002
Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31Evelyne C Deery, Eranga N Vithana, Richard J Newbold, et al.
Investigative Ophthalmology & Visual Science|September 26, 2003
Expression of PRPF31 mRNA in patients with autosomal dominant retinitis pigmentosa: a molecular clue for incomplete penetrance?Eranga N Vithana, Leen Abu-Safieh, Lucia Pelosini, et al.
Pageof 11