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Impact of Progerin Expression on Adipogenesis in Hutchinson—Gilford Progeria Skin-Derived Precursor Cells

Hutchinson–Gilford progeria syndrome (HGPS) is a segmental premature aging disease caused by a mutation in LMNA. The mutation generates a truncated and farnesylated form of prelamin A, called progerin. Affected individuals develop several features of normal aging, including lipodystrophy caused by t...

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Detalhes bibliográficos
Publicado no:Cells
Main Authors: Najdi, Farah, Krüger, Peter, Djabali, Karima
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8306773/
https://ncbi.nlm.nih.gov/pubmed/34202258
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells10071598
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