Are There Common Mechanisms Between the Hutchinson–Gilford Progeria Syndrome and Natural Aging?

The Hutchinson–Gilford progeria syndrome (HGPS) is a premature aging disease caused by mutations of the LMNA gene leading to increased production of a partially processed form of the nuclear fibrillar protein lamin A – progerin. Progerin acts as a dominant factor that leads to multiple morphological...

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Detalles Bibliográficos
Autores principales: Ashapkin, Vasily V., Kutueva, Lyudmila I., Kurchashova, Svetlana Y., Kireev, Igor I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529819/
https://www.ncbi.nlm.nih.gov/pubmed/31156709
http://dx.doi.org/10.3389/fgene.2019.00455

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529819/
https://www.ncbi.nlm.nih.gov/pubmed/31156709
http://dx.doi.org/10.3389/fgene.2019.00455

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