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G Locke

Showing results (81-90 of 97) with videos related to

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Molecular and Cellular Biology|March 31, 2005
PKR and GCN2 kinases and guanine nucleotide exchange factor eukaryotic translation initiation factor 2B (eIF2B) recognize overlapping surfaces on eIF2alphaMadhusudan Dey, Bruce Trieselmann, Emily G Locke, et al.
Investigative Ophthalmology & Visual Science|February 26, 2003
Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3Artur V Cideciyan, Samuel G Jacobson, Nisha Gupta, et al.
JAMA Ophthalmology|May 9, 2014
Four-year placebo-controlled trial of docosahexaenoic acid in X-linked retinitis pigmentosa (DHAX trial): a randomized clinical trialDennis R Hoffman, Dianna K Hughbanks-Wheaton, N Shirlene Pearson, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2011
Phenotypic characterization of 3 families with autosomal dominant retinitis pigmentosa due to mutations in KLHL7Yuquan Wen, Kirsten G Locke, Martin Klein, et al.
Investigative Ophthalmology & Visual Science|October 16, 2015
Docosahexaenoic Acid Slows Visual Field Progression in X-Linked Retinitis Pigmentosa: Ancillary Outcomes of the DHAX TrialDennis R Hoffman, Dianna K Hughbanks-Wheaton, Rand Spencer, et al.
The Journal of Biological Chemistry|March 26, 2005
Functional characterization of mouse RDH11 as a retinol dehydrogenase involved in dark adaptation in vivoAnne Kasus-Jacobi, Jiafu Ou, David G Birch, et al.
American Journal of Ophthalmology|October 11, 2005
Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 genePetra Kozma, Dianna K Hughbanks-Wheaton, Kirsten G Locke, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 8, 2005
Lipofuscin accumulation, abnormal electrophysiology, and photoreceptor degeneration in mutant ELOVL4 transgenic mice: a model for macular degenerationG Karan, C Lillo, Z Yang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 16, 2006
The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundlesJoann McGee, Richard J Goodyear, D Randy McMillan, et al.
Molecular Vision|October 26, 2016
North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the <i>PRDM13</i> geneSara J Bowne, Lori S Sullivan, Dianna K Wheaton, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
Molecular and Cellular Biology|March 31, 2005
PKR and GCN2 kinases and guanine nucleotide exchange factor eukaryotic translation initiation factor 2B (eIF2B) recognize overlapping surfaces on eIF2alphaMadhusudan Dey, Bruce Trieselmann, Emily G Locke, et al.
Investigative Ophthalmology & Visual Science|February 26, 2003
Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3Artur V Cideciyan, Samuel G Jacobson, Nisha Gupta, et al.
JAMA Ophthalmology|May 9, 2014
Four-year placebo-controlled trial of docosahexaenoic acid in X-linked retinitis pigmentosa (DHAX trial): a randomized clinical trialDennis R Hoffman, Dianna K Hughbanks-Wheaton, N Shirlene Pearson, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2011
Phenotypic characterization of 3 families with autosomal dominant retinitis pigmentosa due to mutations in KLHL7Yuquan Wen, Kirsten G Locke, Martin Klein, et al.
Investigative Ophthalmology & Visual Science|October 16, 2015
Docosahexaenoic Acid Slows Visual Field Progression in X-Linked Retinitis Pigmentosa: Ancillary Outcomes of the DHAX TrialDennis R Hoffman, Dianna K Hughbanks-Wheaton, Rand Spencer, et al.
The Journal of Biological Chemistry|March 26, 2005
Functional characterization of mouse RDH11 as a retinol dehydrogenase involved in dark adaptation in vivoAnne Kasus-Jacobi, Jiafu Ou, David G Birch, et al.
American Journal of Ophthalmology|October 11, 2005
Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 genePetra Kozma, Dianna K Hughbanks-Wheaton, Kirsten G Locke, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 8, 2005
Lipofuscin accumulation, abnormal electrophysiology, and photoreceptor degeneration in mutant ELOVL4 transgenic mice: a model for macular degenerationG Karan, C Lillo, Z Yang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 16, 2006
The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundlesJoann McGee, Richard J Goodyear, D Randy McMillan, et al.
Molecular Vision|October 26, 2016
North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the <i>PRDM13</i> geneSara J Bowne, Lori S Sullivan, Dianna K Wheaton, et al.
Pageof 10