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ATR promotes cilia signalling: links to developmental impacts
Mutations in ATR (ataxia telangiectasia and RAD3-related) cause Seckel syndrome (ATR-SS), a microcephalic primordial dwarfism disorder. Hitherto, the clinical manifestation of ATR deficiency has been attributed to its canonical role in DNA damage response signalling following replication fork stalli...
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| 發表在: | Hum Mol Genet |
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| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Oxford University Press
2016
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4805311/ https://ncbi.nlm.nih.gov/pubmed/26908596 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw034 |
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