Accelerated telomere shortening and replicative senescence in human fibroblasts overexpressing mutant and wild-type lamin A
Author:
Publisher
Elsevier BV
Subject
Cell Biology
Reference62 articles.
1. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery–Dreifuss muscular dystrophy;Bonne;Nat. Genet.,1999
2. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease;Fatkin;N. Engl. J. Med.,1999
3. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B);Muchir;Hum. Mol. Genet.,2000
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;De Sandre-Giovannoli;Am. J. Hum. Genet.,2002
5. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy;Shackleton;Nat. Genet.,2000
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