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Experimental Eye Research
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January 19, 2012
Iodoacetic acid, but not sodium iodate, creates an inducible swine model of photoreceptor damage
Jennifer M Noel, Juan P Fernandez de Castro, Paul J Demarco, et al.
Plos Biology
|
September 13, 2019
Nystagmus in patients with congenital stationary night blindness (CSNB) originates from synchronously firing retinal ganglion cells
Beerend H J Winkelman, Marcus H C Howlett, Maj-Britt Hölzel, et al.
American Journal of Human Genetics
|
November 10, 2009
Mutations in TRPM1 are a common cause of complete congenital stationary night blindness
Maria M van Genderen, Mieke M C Bijveld, Yvonne B Claassen, et al.
Journal of Neurophysiology
|
August 17, 2012
Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation
Neal S Peachey, Jillian N Pearring, Pasano Bojang, et al.
Human Molecular Genetics
|
August 28, 2015
Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness
Miranda L Scalabrino, Sanford L Boye, Kathryn M H Fransen, et al.
Investigative Ophthalmology & Visual Science
|
January 17, 2012
Generation of an inbred miniature pig model of retinitis pigmentosa
Jason W Ross, Juan P Fernandez de Castro, Jianguo Zhao, et al.
Visual Neuroscience
|
April 7, 2006
The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses
Bo Chang, John R Heckenlively, Philippa R Bayley, et al.
The Journal of Physiology
|
August 9, 2008
Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses
Dennis M Maddox, Kirstan A Vessey, Gary L Yarbrough, et al.
Visual Neuroscience
|
April 14, 2007
Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouse
Lawrence H Pinto, Martha H Vitaterna, Kazuhiro Shimomura, et al.
American Journal of Human Genetics
|
February 14, 2012
GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness
Neal S Peachey, Thomas A Ray, Ralph Florijn, et al.
Page
of 7
Search research articles
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Showing results (51-60 of 62) with videos related to
Sort By:
Page
of 7
Experimental Eye Research
|
January 19, 2012
Iodoacetic acid, but not sodium iodate, creates an inducible swine model of photoreceptor damage
Jennifer M Noel, Juan P Fernandez de Castro, Paul J Demarco, et al.
Plos Biology
|
September 13, 2019
Nystagmus in patients with congenital stationary night blindness (CSNB) originates from synchronously firing retinal ganglion cells
Beerend H J Winkelman, Marcus H C Howlett, Maj-Britt Hölzel, et al.
American Journal of Human Genetics
|
November 10, 2009
Mutations in TRPM1 are a common cause of complete congenital stationary night blindness
Maria M van Genderen, Mieke M C Bijveld, Yvonne B Claassen, et al.
Journal of Neurophysiology
|
August 17, 2012
Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation
Neal S Peachey, Jillian N Pearring, Pasano Bojang, et al.
Human Molecular Genetics
|
August 28, 2015
Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness
Miranda L Scalabrino, Sanford L Boye, Kathryn M H Fransen, et al.
Investigative Ophthalmology & Visual Science
|
January 17, 2012
Generation of an inbred miniature pig model of retinitis pigmentosa
Jason W Ross, Juan P Fernandez de Castro, Jianguo Zhao, et al.
Visual Neuroscience
|
April 7, 2006
The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses
Bo Chang, John R Heckenlively, Philippa R Bayley, et al.
The Journal of Physiology
|
August 9, 2008
Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses
Dennis M Maddox, Kirstan A Vessey, Gary L Yarbrough, et al.
Visual Neuroscience
|
April 14, 2007
Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouse
Lawrence H Pinto, Martha H Vitaterna, Kazuhiro Shimomura, et al.
American Journal of Human Genetics
|
February 14, 2012
GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness
Neal S Peachey, Thomas A Ray, Ralph Florijn, et al.
Page
of 7