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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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| Publicado no: | PLoS One |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4459694/ https://ncbi.nlm.nih.gov/pubmed/26053873 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0128917 |
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