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David M Hunt

Showing results (61-70 of 102) with videos related to

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The Journal of Biological Chemistry|November 2, 2012
Functional analysis of missense mutations in Kv8.2 causing cone dystrophy with supernormal rod electroretinogramKatie E Smith, Susan E Wilkie, Joseph T Tebbs-Warner, et al.
Molecular Vision|April 24, 2008
Disease mechanism for retinitis pigmentosa (RP11) caused by missense mutations in the splicing factor gene PRPF31Susan E Wilkie, Veronika Vaclavik, Huimin Wu, et al.
Plos One|March 22, 2013
Retinal amino acid neurochemistry of the southern hemisphere lamprey, Geotria australisLisa Nivison-Smith, Shaun P Collin, Yuan Zhu, et al.
Ophthalmology|June 15, 2005
X-linked cone dysfunction syndrome with myopia and protanopiaMichel Michaelides, Samantha Johnson, Keith Bradshaw, et al.
Investigative Ophthalmology & Visual Science|January 17, 2013
Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacyMichelle McClements, Wayne I L Davies, Michel Michaelides, et al.
The Journal of Comparative Neurology|December 18, 2020
Visual opsin expression and morphological characterization of retinal photoreceptors in the pouched lamprey (Geotria australis, Gray)Rachael E Warrington, Wayne I L Davies, Jan M Hemmi, et al.
Photochemistry and Photobiology|June 20, 2007
Spectral tuning of shortwave-sensitive visual pigments in vertebratesDavid M Hunt, Lívia S Carvalho, Jill A Cowing, et al.
Translational Vision Science & Technology|September 4, 2020
Validating Fluorescent Chrnb4.EGFP Mouse Models for the Study of Cone Photoreceptor DegenerationAlicia A Brunet, Paula I Fuller-Carter, Annie L Miller, et al.
Eneuro|March 2, 2019
The Role of the Voltage-Gated Potassium Channel Proteins Kv8.2 and Kv2.1 in Vision and Retinal Disease: Insights from the Study of Mouse Gene Knock-Out MutationsNathan S Hart, Jessica K Mountford, Valentina Voigt, et al.
Investigative Ophthalmology & Visual Science|May 27, 2004
Progressive cone dystrophy associated with mutation in CNGB3Michel Michaelides, Irene A Aligianis, John R Ainsworth, et al.
Pageof 11

Showing results (61-70 of 102) with videos related to

Sort By:
Pageof 11
The Journal of Biological Chemistry|November 2, 2012
Functional analysis of missense mutations in Kv8.2 causing cone dystrophy with supernormal rod electroretinogramKatie E Smith, Susan E Wilkie, Joseph T Tebbs-Warner, et al.
Molecular Vision|April 24, 2008
Disease mechanism for retinitis pigmentosa (RP11) caused by missense mutations in the splicing factor gene PRPF31Susan E Wilkie, Veronika Vaclavik, Huimin Wu, et al.
Plos One|March 22, 2013
Retinal amino acid neurochemistry of the southern hemisphere lamprey, Geotria australisLisa Nivison-Smith, Shaun P Collin, Yuan Zhu, et al.
Ophthalmology|June 15, 2005
X-linked cone dysfunction syndrome with myopia and protanopiaMichel Michaelides, Samantha Johnson, Keith Bradshaw, et al.
Investigative Ophthalmology & Visual Science|January 17, 2013
Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacyMichelle McClements, Wayne I L Davies, Michel Michaelides, et al.
The Journal of Comparative Neurology|December 18, 2020
Visual opsin expression and morphological characterization of retinal photoreceptors in the pouched lamprey (Geotria australis, Gray)Rachael E Warrington, Wayne I L Davies, Jan M Hemmi, et al.
Photochemistry and Photobiology|June 20, 2007
Spectral tuning of shortwave-sensitive visual pigments in vertebratesDavid M Hunt, Lívia S Carvalho, Jill A Cowing, et al.
Translational Vision Science & Technology|September 4, 2020
Validating Fluorescent Chrnb4.EGFP Mouse Models for the Study of Cone Photoreceptor DegenerationAlicia A Brunet, Paula I Fuller-Carter, Annie L Miller, et al.
Eneuro|March 2, 2019
The Role of the Voltage-Gated Potassium Channel Proteins Kv8.2 and Kv2.1 in Vision and Retinal Disease: Insights from the Study of Mouse Gene Knock-Out MutationsNathan S Hart, Jessica K Mountford, Valentina Voigt, et al.
Investigative Ophthalmology & Visual Science|May 27, 2004
Progressive cone dystrophy associated with mutation in CNGB3Michel Michaelides, Irene A Aligianis, John R Ainsworth, et al.
Pageof 11