The product of the ataxia-telangiectasia group D complementing gene, ATDC, interacts with a protein kinase C substrate and inhibitor.

Ataxia-telangiectasia (AT) is an autosomal recessive human genetic disease characterized by immunological, neurological, and developmental defects and an increased risk of cancer. Cells from individuals with AT show sensitivity to ionizing radiation, elevated recombination, cell cycle abnormalities,...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Brzoska, P M, Chen, H, Zhu, Y, Levin, N A, Disatnik, M H, Mochly-Rosen, D, Murnane, J P, Christman, M F
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1995
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC41238/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7644499/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.92.17.7824
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