High-Throughput Screen Detects Calcium Signaling Dysfunction in Hutchinson-Gilford Progeria Syndrome

Hutchinson–Gilford progeria syndrome (HGPS) is a deadly childhood disorder, which is considered a very rare disease. It is caused by an autosomal dominant mutation on the LMNA gene, and it is characterized by accelerated aging. Human cell lines from HGPS patients and healthy parental controls were s...

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Detalles Bibliográficos
Autores principales: Fafián-Labora, Juan A., Morente-López, Miriam, de Toro, Fco. Javier, Arufe, María C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305791/
https://www.ncbi.nlm.nih.gov/pubmed/34298947
http://dx.doi.org/10.3390/ijms22147327

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305791/
https://www.ncbi.nlm.nih.gov/pubmed/34298947
http://dx.doi.org/10.3390/ijms22147327

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