Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies

Hutchinson–Gilford progeria syndrome (HGPS) is a rare genetic disease that causes premature aging symptoms, such as vascular diseases, lipodystrophy, loss of bone mineral density, and alopecia. HGPS is mostly linked to a heterozygous and de novo mutation in the LMNA gene (c.1824 C > T; p.G608G),...

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Detalles Bibliográficos
Autores principales: Hartinger, Ramona, Lederer, Eva-Maria, Schena, Elisa, Lattanzi, Giovanna, Djabali, Karima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216179/
https://www.ncbi.nlm.nih.gov/pubmed/37408186
http://dx.doi.org/10.3390/cells12101350

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216179/
https://www.ncbi.nlm.nih.gov/pubmed/37408186
http://dx.doi.org/10.3390/cells12101350

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