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B Haider

Showing results (101-110 of 111) with videos related to

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Human Molecular Genetics|August 14, 2003
CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retinaAdrienne K Mehalow, Shuhei Kameya, Richard S Smith, et al.
Plos One|September 5, 2014
Characterization of a spontaneous retinal neovascular mouse modelEiichi Hasegawa, Harry Sweigard, Deeba Husain, et al.
Gene Therapy|May 16, 2024
Retinoic acid related orphan receptor α is a genetic modifier that rescues retinal degeneration in a mouse model of Stargardt disease and Dry AMDM Akula, S M McNamee, Z Love, et al.
Nature Genetics|February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fateN B Haider, S G Jacobson, A V Cideciyan, et al.
Nature Genetics|May 31, 2001
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4K Mykytyn, T Braun, R Carmi, et al.
Plos One|October 15, 2011
Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiologyGyungah Jun, Michael Nicolaou, Margaux A Morrison, et al.
Vision Research|September 30, 2009
Convergence of linkage, gene expression and association data demonstrates the influence of the RAR-related orphan receptor alpha (RORA) gene on neovascular AMD: a systems biology based approachAlexandra C Silveira, Margaux A Morrison, Fei Ji, et al.
Investigative Ophthalmology & Visual Science|May 10, 2014
FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expressionLeah A Owen, Margaux A Morrison, Jeeyun Ahn, et al.
Human Molecular Genetics|April 4, 2001
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)D Y Nishimura, C C Searby, R Carmi, et al.
Human Genomics|December 14, 2011
Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degenerationMargaux A Morrison, Alexandra C Silveira, Nancy Huynh, et al.
Pageof 12

Showing results (101-110 of 111) with videos related to

Sort By:
Pageof 12
Human Molecular Genetics|August 14, 2003
CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retinaAdrienne K Mehalow, Shuhei Kameya, Richard S Smith, et al.
Plos One|September 5, 2014
Characterization of a spontaneous retinal neovascular mouse modelEiichi Hasegawa, Harry Sweigard, Deeba Husain, et al.
Gene Therapy|May 16, 2024
Retinoic acid related orphan receptor α is a genetic modifier that rescues retinal degeneration in a mouse model of Stargardt disease and Dry AMDM Akula, S M McNamee, Z Love, et al.
Nature Genetics|February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fateN B Haider, S G Jacobson, A V Cideciyan, et al.
Nature Genetics|May 31, 2001
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4K Mykytyn, T Braun, R Carmi, et al.
Plos One|October 15, 2011
Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiologyGyungah Jun, Michael Nicolaou, Margaux A Morrison, et al.
Vision Research|September 30, 2009
Convergence of linkage, gene expression and association data demonstrates the influence of the RAR-related orphan receptor alpha (RORA) gene on neovascular AMD: a systems biology based approachAlexandra C Silveira, Margaux A Morrison, Fei Ji, et al.
Investigative Ophthalmology & Visual Science|May 10, 2014
FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expressionLeah A Owen, Margaux A Morrison, Jeeyun Ahn, et al.
Human Molecular Genetics|April 4, 2001
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)D Y Nishimura, C C Searby, R Carmi, et al.
Human Genomics|December 14, 2011
Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degenerationMargaux A Morrison, Alexandra C Silveira, Nancy Huynh, et al.
Pageof 12