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Genomic instability and DNA replication defects in progeroid syndromes
Progeroid syndromes induced by mutations in lamin A or in its interactors – named progeroid laminopathies – are model systems for the dissection of the molecular pathways causing physiological and premature aging. A large amount of data, based mainly on the Hutchinson Gilford Progeria syndrome (HGPS...
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| Vydáno v: | Nucleus |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Taylor & Francis
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7000143/ https://ncbi.nlm.nih.gov/pubmed/29936894 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19491034.2018.1476793 |
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