PRKCG wt Allele

Known as: MGC57564, PKCC, Protein Kinase C, Gamma wt Allele 
Human PRKCG wild-type allele is located in the vicinity of 19q13.4 and is approximately 28 kb in length. This allele, which encodes Protein kinase C… (More)
National Institutes of Health

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Topic mentions per year

1988-2018
024619882018

Papers overview

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2007
2007
Several causal missense mutations in protein kinase C gamma (gamma PKC) gene have been found in spinocerebellar ataxia type 14… (More)
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2006
2006
Spinocerebellar ataxia type 14 (SCA14) is an autosomal dominant neurodegenerative disorder characterized by cerebellar ataxia and… (More)
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2006
2006
Sirs: In contrast to the repeat expansion mutations causing the autosomal dominantly inherited spinocerebellar ataxias SCA1, 2, 3… (More)
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2005
2005
Spinocerebellar ataxia type 14 (SCA14) is an autosomal dominant neurodegenerative disease characterized by various symptoms… (More)
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2005
2005
BACKGROUND Dominantly inherited spinocerebellar ataxia (SCA) is a clinically and genetically heterogeneous group of… (More)
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2005
2005
Spinocerebellar ataxia type 14 (SCA14) is an autosomal dominant neurodegenerative disorder, first described in a Japanese family… (More)
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2004
2004
BACKGROUND Autosomal dominant cerebellar ataxias comprise a clinically, neuropathologically, and genetically heterogeneous group… (More)
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2003
2003
BACKGROUND We previously discovered spinocerebellar ataxia type 14 (SCA14) in a single Japanese family with an autosomal dominant… (More)
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2003
2003
The autosomal dominant cerebellar ataxias (ADCA) are a clinically, pathologically and genetically heterogeneous group of… (More)
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1999
1999
The hypothesis that protein kinase C (PKC) is able to regulate the whole cell Ca-activated K (KCa) current independently of PKC… (More)
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