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CDHR1 gene

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

Papers overview

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2015
2015
Inherited retinal dystrophies present extensive phenotypic and genetic heterogeneity, posing a challenge for patients’ molecular… Expand
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2012
2012
Purpose To investigate the genetic basis for autosomal recessive cone-rod dystrophy in a consanguineous Israeli Christian Arab… Expand
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2011
2011
Purpose The aim of the study was to elucidate the genetic background of retinitis pigmentosa (RP) in a Faroe Islands population… Expand
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Review
2011
Review
2011
Cadherin family is classified into classical cadherins, desmosomal cadherins and protocadherins (PCDHs). Genomic structures… Expand
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Highly Cited
2010
Highly Cited
2010
Purpose To report the clinical phenotype in patients with a retinal dystrophy associated with novel mutations in the MER tyrosine… Expand
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Highly Cited
2010
Highly Cited
2010
The cadherin superfamily encodes more than 100 receptors with diverse functions in tissue development and homeostasis. Classical… Expand
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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… Expand
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Highly Cited
2005
Highly Cited
2005
Olfactory information is conveyed from the periphery to the olfactory cortices through mitral and tufted (M/T) cells in the… Expand
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2004
2004
Photoreceptor cadherin (prCAD) is a distinctive cadherin family member that is concentrated at the base of rod and cone outer… Expand
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Highly Cited
2001
Highly Cited
2001
A cadherin family member, prCAD, was identified in retina cDNA by subtractive hybridization and high throughput sequencing. prCAD… Expand
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