Center for Human Disease Modeling,
Department of Cell Biology,
Center for Human Disease Modeling, Department of Cell Biology
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Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors.
Human molecular genetics Aug, 2004 | Pubmed ID: 15190009
Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors.
Proceedings of the National Academy of Sciences of the United States of America Mar, 2006 | Pubmed ID: 16505381
Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL.
Proceedings of the National Academy of Sciences of the United States of America Jan, 2007 | Pubmed ID: 17242361
Afferent control of horizontal cell morphology revealed by genetic respecification of rods and cones.
The Journal of neuroscience : the official journal of the Society for Neuroscience Mar, 2007 | Pubmed ID: 17392470
Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors.
Brain research Oct, 2008 | Pubmed ID: 18294621
Retinoid-related orphan nuclear receptor RORbeta is an early-acting factor in rod photoreceptor development.
Proceedings of the National Academy of Sciences of the United States of America Oct, 2009 | Pubmed ID: 19805139
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).
Proceedings of the National Academy of Sciences of the United States of America Apr, 2010 | Pubmed ID: 20385826
Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome.
Proceedings of the National Academy of Sciences of the United States of America Jun, 2010 | Pubmed ID: 20498079
Planar cell polarity acts through septins to control collective cell movement and ciliogenesis.
Science (New York, N.Y.) Sep, 2010 | Pubmed ID: 20671153
Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry.
Nature cell biology Apr, 2011 | Pubmed ID: 21394081
DISC1-dependent switch from progenitor proliferation to migration in the developing cortex.
Nature May, 2011 | Pubmed ID: 21471969
Neuroscience: Imprinting in the brain.
Nature Jul, 2011 | Pubmed ID: 21776070
Cilia in vertebrate development and disease.
Development (Cambridge, England) Feb, 2012 | Pubmed ID: 22223675
Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy.
American journal of human genetics Mar, 2012 | Pubmed ID: 22341973
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.
Nature May, 2012 | Pubmed ID: 22596160
Context-dependent regulation of Wnt signaling through the primary cilium.
Journal of the American Society of Nephrology : JASN Jan, 2013 | Pubmed ID: 23123400
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome.
American journal of human genetics Dec, 2012 | Pubmed ID: 23159249
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