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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Patsy M Nishina

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Journal of Neurophysiology|August 17, 2012

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutationNeal S Peachey, Jillian N Pearring, Pasano Bojang, et al.

Human Mutation|June 28, 2007

Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alström syndromeJan D Marshall, Elizabeth G Hinman, Gayle B Collin, et al.

Archives of Internal Medicine|March 30, 2005

New Alström syndrome phenotypes based on the evaluation of 182 casesJan D Marshall, Roderick T Bronson, Gayle B Collin, et al.

Plos Genetics|September 29, 2025

Identifying genetic determinants of outer retinal function in mice using a large-scale gene-targeted screenJanine M Wotton, Mark P Krebs, Riccardo Sangermano, et al.

The Journal of Clinical Investigation|May 25, 2011

Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and miceKarsten Boldt, Dorus A Mans, Jungyeon Won, 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 responsesDennis M Maddox, Kirstan A Vessey, Gary L Yarbrough, et al.

Nature Genetics|December 23, 2015

Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrityNicole T M Saksens, Mark P Krebs, Frederieke E Schoenmaker-Koller, 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 blindnessNeal S Peachey, Thomas A Ray, Ralph Florijn, et al.

Communications Biology|December 28, 2018

Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.

Communications Biology|March 12, 2019

Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.

Pageof 8

Search research articles

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

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 80 results.

Journal of Neurophysiology|August 17, 2012

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutationNeal S Peachey, Jillian N Pearring, Pasano Bojang, et al.

Human Mutation|June 28, 2007

Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alström syndromeJan D Marshall, Elizabeth G Hinman, Gayle B Collin, et al.

Archives of Internal Medicine|March 30, 2005

New Alström syndrome phenotypes based on the evaluation of 182 casesJan D Marshall, Roderick T Bronson, Gayle B Collin, et al.

Plos Genetics|September 29, 2025

Identifying genetic determinants of outer retinal function in mice using a large-scale gene-targeted screenJanine M Wotton, Mark P Krebs, Riccardo Sangermano, et al.

The Journal of Clinical Investigation|May 25, 2011

Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and miceKarsten Boldt, Dorus A Mans, Jungyeon Won, 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 responsesDennis M Maddox, Kirstan A Vessey, Gary L Yarbrough, et al.

Nature Genetics|December 23, 2015

Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrityNicole T M Saksens, Mark P Krebs, Frederieke E Schoenmaker-Koller, 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 blindnessNeal S Peachey, Thomas A Ray, Ralph Florijn, et al.

Communications Biology|December 28, 2018

Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.

Communications Biology|March 12, 2019

Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.

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