Lamin A to Z in normal aging

Almost since the discovery that mutations in the LMNA gene, encoding the nuclear structure components lamin A and C, lead to Hutchinson-Gilford progeria syndrome, people have speculated that lamins may have a role in normal aging. The most common HPGS mutation creates a splice variant of lamin A, pr...

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Detalles Bibliográficos
Autores principales: Primmer, Stanley R., Liao, Chen-Yu, Kummert, Oona M.P., Kennedy, Brian K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2022
Materias:
Research Perspective
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648802/
https://www.ncbi.nlm.nih.gov/pubmed/36260869
http://dx.doi.org/10.18632/aging.204342

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648802/
https://www.ncbi.nlm.nih.gov/pubmed/36260869
http://dx.doi.org/10.18632/aging.204342

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