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PMID: 8794004 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Ataxia-telangiectasia: a multifaceted genetic disorder associated with defective signal transduction.

Current opinion in immunology ·Vol. 8 ·No. 4 ·1996-08-00 ·Pages 459-64

Lavin MF, Shiloh Y

Abstract

The gene responsible for the defect in the human genetic disorder ataxia-telangiectasia, ATM, was cloned recently. The part of the gene coding for a phosphatidylinositol 3-kinase domain showed it to be related to a family of genes involved in signal transduction, cell cycle control and the response to DNA damage. The elucidation of the role of the ATM gene product will provide valuable insight into the radiosensitivity, cancer predisposition, immunodeficiency and neuropathology that characterize this syndrome.

MeSH Terms
Ataxia Telangiectasia/genetics,radiotherapy Ataxia Telangiectasia Mutated Proteins Cell Cycle Proteins Cloning, Molecular DNA-Binding Proteins Humans Leucine Zippers/genetics Polymorphism, Genetic/genetics Protein Serine-Threonine Kinases Proteins/genetics Radiation Tolerance/physiology Signal Transduction/genetics Tumor Suppressor Proteins
Chemicals
Cell Cycle Proteins DNA-Binding Proteins Proteins Tumor Suppressor Proteins ATM protein, human Ataxia Telangiectasia Mutated Proteins Protein Serine-Threonine Kinases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lavin M F
Queensland Institute of Medical Research, The Bancroft Centre and Department of Surgery, University of Queensland, Post Office, Royal Brisbane Hospital, Herston, Australia. [email protected]
Shiloh Y
Article Info
Journal
Current opinion in immunology
Abbr.
Curr Opin Immunol
ISSN
0952-7915
Published
1996-08-00
Pages
459-64
Language
English
Region
England
NLM ID
8900118
Subset
IM
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