CDHR1 gene

Known as: CORD15, KIAA1775, PROTOCADHERIN 21 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2001-2016
02420012016

Papers overview

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2016
2016
Inherited retinal dystrophies (IRDs) are Mendelian diseases with tremendous genetic and phenotypic heterogeneity. Identification… (More)
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2012
2012
PURPOSE To investigate the genetic basis for autosomal recessive cone-rod dystrophy in a consanguineous Israeli Christian Arab… (More)
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2010
2010
BACKGROUND Cone-rod dystrophy is a retinal dystrophy with early loss of cone photoreceptors and a parallel or subsequent loss of… (More)
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2010
2010
PURPOSE To describe the clinical findings and mutations in affected members of two families with an autosomal recessive retinal… (More)
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2010
2010
PURPOSE To report the clinical phenotype in patients with a retinal dystrophy associated with novel mutations in the MER tyrosine… (More)
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2010
2010
The cadherin superfamily encodes more than 100 receptors with diverse functions in tissue development and homeostasis. Classical… (More)
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Review
2009
Review
2009
In vertebrate sensory cells of the eye and the inner ear a group of nonclassical cadherins, namely cadherin 23 (CDH23… (More)
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Highly Cited
2008
Highly Cited
2008
Familial macular degeneration is a clinically and genetically heterogeneous group of disorders characterized by progressive… (More)
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2005
2005
PURPOSE It has been demonstrated that mice lacking a functional copy of prCAD, the gene encoding protocadherin-21, show… (More)
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2001
2001
The terminal sequences of long cDNAs from human brains were subjected to an improved method of motif-trap screening. This process… (More)
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