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MicroRNAs in hereditary and sporadic premature aging syndromes and other laminopathies

Hereditary and sporadic laminopathies are caused by mutations in genes encoding lamins, their partners, or the metalloprotease ZMPSTE24/FACE1. Depending on the clinical phenotype, they are classified as tissue‐specific or systemic diseases. The latter mostly manifest with several accelerated aging f...

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Détails bibliographiques
Publié dans:Aging Cell
Auteurs principaux: Frankel, Diane, Delecourt, Valérie, Harhouri, Karim, De Sandre‐Giovannoli, Annachiara, Lévy, Nicolas, Kaspi, Elise, Roll, Patrice
Format: Artigo
Langue:Inglês
Publié: John Wiley and Sons Inc. 2018
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6052405/
https://ncbi.nlm.nih.gov/pubmed/29696758
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/acel.12766
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