【摘 要】
:
Ataxia-telangiectasia (AT) is an inherited autosomal recessive disorder caused by mutations in the ATM (ataxia-telangiectasia mutated) gene.In spite of prog
【机 构】
:
Children's Memorial Health Institute,Poland
【出 处】
:
The 16th Ataxia-Telangiectasia Workshop (ATW-2015)6th Intern
论文部分内容阅读
Ataxia-telangiectasia (AT) is an inherited autosomal recessive disorder caused by mutations in the ATM (ataxia-telangiectasia mutated) gene.In spite of progressive neurological dysfunction, especially in the cerebellum, and ocular and cutaneous telangiectasias, it has a broad spectrum of other serious clinical symptoms including recurrent infections of the respiratory tract, chronic lung diseases, granulomatous infiltrations, autoimmune diseases and lymphomas.
其他文献
Introduction: Somatic mutations in the Ataxia-telangiectasia mutated (ATM) gene have been identified in a range of cancer types, including non-small cell lu
Activation of the DNA-damage response (DDR) can enable cancer cells to resist the lethal effects of genotoxic cancer therapy.However, cancer cells frequentl
53BP 1 has been reported to have multiple roles in mammalian DNA damage response (DDR), specifically for repair of DNA double-strand breaks (DSBs) in an ATM
Homologous recombination (HR) repairs double-strand breaks (DSBs) generated by radiotherapy and anti-cancer agents such as camptothecin and cisplatin.HR is
DNA double-strand break (DSB) is considered most critical lesion among those induced by ionizing radiation (IR).In eukaryotic cells DSB is repaired mainly t
Cerebellar atrophy is the major, most devastating clinical feature of A-T,characterized by gradual relentless loss of Purkinje and granular neurons.Most ATM
Introduction: Ataxia Telangiectasia (A-T) is a rare genetic disorder with symptoms including ataxia and involuntary movements, telangiectasia, higher risk o
Introduction: Ataxia Telangiectasia (A-T) is a rare genetic disorder with symptoms including ataxia and involuntary movements, higher risk of infections, an