Prelamin A Farnesylation and Progeroid Syndromes
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference58 articles.
1. Nuclear Lamins: Laminopathies and Their Role in Premature Ageing
2. Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C
3. Loss of a-Type Lamin Expression Compromises Nuclear Envelope Integrity Leading to Muscular Dystrophy
4. Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse
5. Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction
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