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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Detalles Bibliográficos
Autores principales: Burla, Romina, La Torre, Mattia, Merigliano, Chiara, Vernì, Fiammetta, Saggio, Isabella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Special Issue on Laminopathies
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000143/
https://www.ncbi.nlm.nih.gov/pubmed/29936894
http://dx.doi.org/10.1080/19491034.2018.1476793

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000143/
https://www.ncbi.nlm.nih.gov/pubmed/29936894
http://dx.doi.org/10.1080/19491034.2018.1476793

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