Edwin C. Oh

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 66	2013

Other Publications

Article	Year
Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors. Human molecular genetics\| PubMed ID: 15190009	2004
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\| PubMed ID: 16505381	2006
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\| PubMed ID: 17242361	2007
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\| PubMed ID: 17392470	2007
Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors. Brain research\| PubMed ID: 18294621	2008
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\| PubMed ID: 19805139	2009
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\| PubMed ID: 20385826	2010
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\| PubMed ID: 20498079	2010
Planar cell polarity acts through septins to control collective cell movement and ciliogenesis. Science (New York, N.Y.)\| PubMed ID: 20671153	2010
Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry. Nature cell biology\| PubMed ID: 21394081	2011
DISC1-dependent switch from progenitor proliferation to migration in the developing cortex. Nature\| PubMed ID: 21471969	2011
Neuroscience: Imprinting in the brain. Nature\| PubMed ID: 21776070	2011
Cilia in vertebrate development and disease. Development (Cambridge, England)\| PubMed ID: 22223675	2012
Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy. American journal of human genetics\| PubMed ID: 22341973	2012
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant. Nature\| PubMed ID: 22596160	2012
Context-dependent regulation of Wnt signaling through the primary cilium. Journal of the American Society of Nephrology : JASN\| PubMed ID: 23123400	2013
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome. American journal of human genetics\| PubMed ID: 23159249	2012