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- W2010335932 startingPage "131" @default.
- W2010335932 abstract "Lamins are intermediate filament proteins that form a scaffold, termed nuclear lamina, at the nuclear periphery. A small fraction of lamins also localize throughout the nucleoplasm. Lamins bind to a growing number of nuclear protein complexes and are implicated in both nuclear and cytoskeletal organization, mechanical stability, chromatin organization, gene regulation, genome stability, differentiation, and tissue-specific functions. The lamin-based complexes and their specific functions also provide insights into possible disease mechanisms for human laminopathies, ranging from muscular dystrophy to accelerated aging, as observed in Hutchinson–Gilford progeria and atypical Werner syndromes." @default.
- W2010335932 created "2016-06-24" @default.
- W2010335932 creator A5046228251 @default.
- W2010335932 creator A5081263278 @default.
- W2010335932 date "2015-06-02" @default.
- W2010335932 modified "2023-10-18" @default.
- W2010335932 title "Lamins: Nuclear Intermediate Filament Proteins with Fundamental Functions in Nuclear Mechanics and Genome Regulation" @default.
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