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JAMA Ophthalmology
|
September 14, 2013
Novel compound heterozygous mutations resulting in cone dystrophy with supernormal rod response
Tamara 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 mice
Loredana 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 phenotypes
Jana Zernant, Winston Lee, Takayuki Nagasaki, et al.
Investigative Ophthalmology & Visual Science
|
September 14, 2011
Analysis of the ABCA4 gene by next-generation sequencing
Jana 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 family
Pascal 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 disease
Katie Binley, Peter Widdowson, Julie Loader, et al.
Human Molecular Genetics
|
August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt disease
Jana 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 cycle
Debra A Thompson, Andreas R Janecke, Jessica Lange, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 38) with videos related to
Sort By:
Page
of 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 response
Tamara 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 mice
Loredana 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 phenotypes
Jana Zernant, Winston Lee, Takayuki Nagasaki, et al.
Investigative Ophthalmology & Visual Science
|
September 14, 2011
Analysis of the ABCA4 gene by next-generation sequencing
Jana 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 family
Pascal 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 disease
Katie Binley, Peter Widdowson, Julie Loader, et al.
Human Molecular Genetics
|
August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt disease
Jana 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 cycle
Debra A Thompson, Andreas R Janecke, Jessica Lange, et al.
Page
of 4