Guanylate Cyclase-Activating Protein 1

Known as: Guanylyl Cyclase-Activating Protein 1, GCAP1 Protein, Guanylate Cyclase Activating Protein 1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2015
012319992015

Papers overview

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2015
2015
One-fifth of all cases of Leber congenital amaurosis are type 1 (LCA1). LCA1 is a severe form of retinal dystrophy caused by loss… (More)
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2013
2013
Guanylyl cyclase activating protein 1 (GCAP1), a member of the neuronal calcium sensor (NCS) subclass of the calmodulin… (More)
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2011
2011
Cone dystrophy 3 (COD3) is a severe dominantly inherited retinal degeneration caused by missense mutations in GUCA1A, the gene… (More)
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2009
2009
The GUCA1A gene encodes the guanylate cyclase activating protein 1 (GCAP1) of mammalian rod and cone photoreceptor cells, which… (More)
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2009
2009
Guanylate cyclase activating protein 1 (GCAP1) is a neuronal Ca2+ sensor (NCS) that regulates the activation of rod outer segment… (More)
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2009
2009
Guanylyl cyclase activating protein 1 (GCAP1), a member of the neuronal calcium sensor (NCS) subclass of the calmodulin… (More)
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2008
2008
Guanylyl cyclase activating protein 1 (GCAP1), after substitution of Ca(2+) by Mg(2+) in its EF-hands, stimulates photoreceptor… (More)
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2005
2005
PURPOSE To describe the clinical features and genetic analysis of a family with an autosomal dominant cone dystrophy (adCD… (More)
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Review
2002
Review
2002
A range of cone and cone-rod dystrophies (CORD) have been observed in man, caused by mutations in retinal guanylate cyclase 1… (More)
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1999
1999
Mutations in the photoreceptor membrane guanylyl cyclase RetGC-1 have been linked to autosomal dominant cone-rod dystrophy. Three… (More)
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