Molecular mechanisms of ataxia telangiectasia /

Ataxia telangiectasia (AT) is an incurable, rare autosomal recessive genetic disorder which affects approximately one in 40,000-100,000 and the carrier frequency is estimated to be 1:100-200. In the United Kingdom it affects 1 in 300,000 live births amounting to about 5 or 6 cases per year. Although...

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Bibliographic Details
Main Author:	Ahmad, Shamim I. (Author)
Corporate Author:	Taylor and Francis
Format:	Electronic eBook
Language:	English
Published:	Boca Raton, FL : CRC Press, an imprint of Taylor and Francis, 2009.
Edition:	First edition.
Subjects:	Ataxia telangiectasia > Molecular aspects. Ataxia Telangiectasia > physiopathology. Ataxia Telangiectasia > genetics.
Online Access:	Full text (WIT users only)

Table of Contents:

chapter 1 Clinical Features of AtaxiaTelangiectasia
chapter 2 Mutations in the Ataxia Telangiectasia Mutated (ATM ) G ene
chapter 3 Cell Signaling in Ataxia Telangiectasia
chapter 4 DNA Damage and Repair in Ataxia Telangiectasia
chapter 5 Protein-Protein Interactions in Ataxia Telangiectasia
chapter 6 Chromosomal Instability in Ataxia Telangiectasia
chapter 7 Cell Cycle Defects and Apoptosis in Ataxia Telangiectasia
chapter 8 Ataxia Telangiectasia: An Oxidative Stress-Related Disease
chapter 9 Oncogenesis in Ataxia Telangectasia: Roles of ATM, p53, NF-kB and DDE Recombination Pathogenesis
chapter 10 Ataxia Telangiectasia and Its Overlap with Nijmegen Breakage Syndrome and Ataxia-Like Disorders
chapter 11 Animal Models for Ataxia Telangiectasia.

Molecular mechanisms of ataxia telangiectasia /

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