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The controlling role of ATM in homologous recombinational repair of DNA damage
The human genetic disorder ataxia telangiectasia (A–T), caused by mutation in the ATM gene, is characterized by chromosomal instability, radiosensitivity and defective cell cycle checkpoint activation. DNA double-strand breaks (dsbs) persist in A–T cells after irradiation, but the underlying defect...
保存先:
| 出版年: | EMBO J |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group
2000
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC305583/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10654944/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/emboj/19.3.463 |
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