Cellular Metabolism and Bioenergetic Function in Human Fibroblasts and Preadipocytes of Type 2 Familial Partial Lipodystrophy

LMNA mutation is associated with type-2 familial partial lipodystrophy (FPLD2). The disease causes a disorder characterized by anomalous accumulation of body fat in humans. The dysfunction at the molecular level is triggered by a lamin A/C mutation, impairing the cell metabolism. In human fibroblast...

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Detalles Bibliográficos
Autores principales: Algieri, Cristina, Bernardini, Chiara, Trombetti, Fabiana, Schena, Elisa, Zannoni, Augusta, Forni, Monica, Nesci, Salvatore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368940/
https://www.ncbi.nlm.nih.gov/pubmed/35955791
http://dx.doi.org/10.3390/ijms23158659

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368940/
https://www.ncbi.nlm.nih.gov/pubmed/35955791
http://dx.doi.org/10.3390/ijms23158659

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