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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… Expand
National Institutes of Health

Papers overview

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2010
2010
Objective: Our objective was to study the role of protein kinase C delta (PKC&dgr;) in the progression of human pancreatic… Expand
2010
2010
Several causal missense mutations in the protein kinase Cγ (γPKC) gene have been found in spinocerebellar ataxia type 14 (SCA14… Expand
2006
2006
Spinocerebellar ataxia type 14 (SCA14) is an autosomal dominant neurodegenerative disorder characterized by cerebellar ataxia and… Expand
Review
2006
Review
2006
  • H. Ueda
  • Nihon yakurigaku zasshi. Folia pharmacologica…
  • 2006
  • Corpus ID: 8434568
The injury-induced intense stimulation of spinal cord neurons causes lysophosphatidic acid (LPA) biosynthesis. LPA(1) receptor… Expand
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2005
2005
Missense mutations in the PRKCG gene have recently been identified in spinocerebellar ataxia 14 (SCA14) patients; these include… Expand
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Highly Cited
2004
Highly Cited
2004
BACKGROUND Autosomal dominant cerebellar ataxias comprise a clinically, neuropathologically, and genetically heterogeneous group… Expand
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Highly Cited
2003
Highly Cited
2003
Background We previously discovered spinocerebellar ataxia type 14 (SCA14) in a single Japanese family with an autosomal dominant… Expand
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Highly Cited
2003
Highly Cited
2003
The autosomal dominant cerebellar ataxias (ADCA) are a clinically, pathologically and genetically heterogeneous group of… Expand
Highly Cited
2003
Highly Cited
2003
BACKGROUND We previously discovered spinocerebellar ataxia type 14 (SCA14) in a single Japanese family with an autosomal dominant… Expand
Highly Cited
1999
Highly Cited
1999
The hypothesis that protein kinase C (PKC) is able to regulate the whole cell Ca-activated K (KCa) current independently of PKC… Expand