Overexpression of Lamin B Receptor Results in Impaired Skin Differentiation

Hutchinson-Gilford progeria syndrome (HGPS) is a rare segmental progeroid disorder commonly caused by a point mutation in the LMNA gene that results in the increased activation of an intra-exonic splice site and the production of a truncated lamin A protein, named progerin. In our previous work, ind...

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Detalles Bibliográficos
Autores principales: Sola Carvajal, Agustín, McKenna, Tomás, Wallén Arzt, Emelie, Eriksson, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459694/
https://www.ncbi.nlm.nih.gov/pubmed/26053873
http://dx.doi.org/10.1371/journal.pone.0128917

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459694/
https://www.ncbi.nlm.nih.gov/pubmed/26053873
http://dx.doi.org/10.1371/journal.pone.0128917

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