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Nuclear localization signal deletion mutants of lamin A and progerin reveal insights into lamin A processing and emerin targeting
Lamin A is a major component of the lamina, which creates a dynamic network underneath the nuclear envelope. Mutations in the lamin A gene (LMNA) cause severe genetic disorders, one of which is Hutchinson-Gilford progeria syndrome (HGPS), a disease triggered by a dominant mutant named progerin. Unli...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Landes Bioscience
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4028357/ https://ncbi.nlm.nih.gov/pubmed/24637396 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/nucl.28068 |
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