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Peter Gouras

Showing results (31-40 of 38) with videos related to

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JAMA Ophthalmology|September 14, 2013
Novel compound heterozygous mutations resulting in cone dystrophy with supernormal rod responseTamara Lee Lenis, Elona Dhrami-Gavazi, Winston Lee, et al.
The Journal of Biological Chemistry|June 6, 2002
Muscle expression of human retinol-binding protein (RBP). Suppression of the visual defect of RBP knockout miceLoredana Quadro, William S Blaner, Leora Hamberger, et al.
Cold Spring Harbor Molecular Case Studies|June 1, 2018
Extremely hypomorphic and severe deep intronic variants in the <i>ABCA4</i> locus result in varying Stargardt disease phenotypesJana Zernant, Winston Lee, Takayuki Nagasaki, et al.
Investigative Ophthalmology & Visual Science|September 14, 2011
Analysis of the ABCA4 gene by next-generation sequencingJana Zernant, Carl Schubert, Kate M Im, et al.
Human Mutation|November 14, 2008
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same familyPascal Escher, Peter Gouras, Raphaël Roduit, et al.
Investigative Ophthalmology & Visual Science|April 27, 2013
Transduction of photoreceptors with equine infectious anemia virus lentiviral vectors: safety and biodistribution of StarGen for Stargardt diseaseKatie Binley, Peter Widdowson, Julie Loader, et al.
Human Molecular Genetics|August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt diseaseJana Zernant, Yajing Angela Xie, Carmen Ayuso, et al.
Human Molecular Genetics|November 5, 2005
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycleDebra A Thompson, Andreas R Janecke, Jessica Lange, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
JAMA Ophthalmology|September 14, 2013
Novel compound heterozygous mutations resulting in cone dystrophy with supernormal rod responseTamara Lee Lenis, Elona Dhrami-Gavazi, Winston Lee, et al.
The Journal of Biological Chemistry|June 6, 2002
Muscle expression of human retinol-binding protein (RBP). Suppression of the visual defect of RBP knockout miceLoredana Quadro, William S Blaner, Leora Hamberger, et al.
Cold Spring Harbor Molecular Case Studies|June 1, 2018
Extremely hypomorphic and severe deep intronic variants in the <i>ABCA4</i> locus result in varying Stargardt disease phenotypesJana Zernant, Winston Lee, Takayuki Nagasaki, et al.
Investigative Ophthalmology & Visual Science|September 14, 2011
Analysis of the ABCA4 gene by next-generation sequencingJana Zernant, Carl Schubert, Kate M Im, et al.
Human Mutation|November 14, 2008
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same familyPascal Escher, Peter Gouras, Raphaël Roduit, et al.
Investigative Ophthalmology & Visual Science|April 27, 2013
Transduction of photoreceptors with equine infectious anemia virus lentiviral vectors: safety and biodistribution of StarGen for Stargardt diseaseKatie Binley, Peter Widdowson, Julie Loader, et al.
Human Molecular Genetics|August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt diseaseJana Zernant, Yajing Angela Xie, Carmen Ayuso, et al.
Human Molecular Genetics|November 5, 2005
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycleDebra A Thompson, Andreas R Janecke, Jessica Lange, et al.
Pageof 4