Serum amyloid A protein in patients with ataxia-telangiectasia:biomarker of disease progression? A p

来源 :The 16th Ataxia-Telangiectasia Workshop (ATW-2015)6th Intern | 被引量 : 0次 | 上传用户:st_daivd
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
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
会议
  Introduction: Somatic mutations in the Ataxia-telangiectasia mutated (ATM) gene have been identified in a range of cancer types, including non-small cell lu
会议
  Activation of the DNA-damage response (DDR) can enable cancer cells to resist the lethal effects of genotoxic cancer therapy.However, cancer cells frequentl
会议
  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
会议
  Homologous recombination (HR) repairs double-strand breaks (DSBs) generated by radiotherapy and anti-cancer agents such as camptothecin and cisplatin.HR is
会议
会议
  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
会议
  Cerebellar atrophy is the major, most devastating clinical feature of A-T,characterized by gradual relentless loss of Purkinje and granular neurons.Most ATM
会议
  Introduction: Ataxia Telangiectasia (A-T) is a rare genetic disorder with symptoms including ataxia and involuntary movements, telangiectasia, higher risk o
会议
  Introduction: Ataxia Telangiectasia (A-T) is a rare genetic disorder with symptoms including ataxia and involuntary movements, higher risk of infections, an
会议