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Department of Pathology and Immunology
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Doublecortin is required in mice for lamination of the hippocampus but not the neocortex.
The Journal of neuroscience : the official journal of the Society for Neuroscience Sep, 2002 | Pubmed ID: 12196578
Colchicine myopathy in a patient with familial Mediterranean fever and normal renal function.
Arthritis and rheumatism Aug, 2003 | Pubmed ID: 12910572
A hybrid photoreceptor expressing both rod and cone genes in a mouse model of enhanced S-cone syndrome.
PLoS genetics Aug, 2005 | Pubmed ID: 16110338
Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowth.
Neuron Jan, 2006 | Pubmed ID: 16387638
A typology of photoreceptor gene expression patterns in the mouse.
Proceedings of the National Academy of Sciences of the United States of America Jul, 2007 | Pubmed ID: 17620597
A familial form of pallidoluysionigral degeneration and amyotrophic lateral sclerosis with divergent clinical presentations.
Journal of neuropathology and experimental neurology Jul, 2007 | Pubmed ID: 17620990
The cis-regulatory logic of the mammalian photoreceptor transcriptional network.
PloS one , 2007 | Pubmed ID: 17653270
Inherited diseases of photoreceptors and prospects for gene therapy.
Pharmacogenomics Mar, 2008 | Pubmed ID: 18303969
The role of cis-regulatory elements in the design of gene therapy vectors for inherited blindness.
Expert opinion on biological therapy May, 2008 | Pubmed ID: 18407764
Avian cone photoreceptors tile the retina as five independent, self-organizing mosaics.
PloS one , 2010 | Pubmed ID: 20126550
CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors.
Genome research Nov, 2010 | Pubmed ID: 20693478
Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa.
American journal of human genetics Sep, 2010 | Pubmed ID: 20705278
Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency.
Human molecular genetics Apr, 2011 | Pubmed ID: 21252205
Notch1 loss of heterozygosity causes vascular tumors and lethal hemorrhage in mice.
The Journal of clinical investigation Feb, 2011 | Pubmed ID: 21266774
Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa.
American journal of human genetics Aug, 2011 | Pubmed ID: 21835304
Transcriptional regulation of neural retina leucine zipper (Nrl), a photoreceptor cell fate determinant.
The Journal of biological chemistry Oct, 2011 | Pubmed ID: 21865162
Combing the globe for terrorism.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society Mar, 2012 | Pubmed ID: 22330854
Washington University School of Medicine
Cynthia L. Montana1,
Connie A. Myers1,
Joseph C. Corbo1
1Department of Pathology and Immunology, Washington University School of Medicine
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