Caricamento...

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...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Wu, Di, Flannery, Andrew R, Cai, Helen, Ko, Eunae, Cao, Kan
Natura: Artigo
Lingua:Inglês
Pubblicazione: Landes Bioscience 2014
Soggetti:
Accesso online: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
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !