Laminopathies: multiple disorders arising from defects in nuclear architecture.
Open Access
- 1 September 2006
- journal article
- review article
- Published by Springer Nature in Journal of Biosciences
- Vol. 31 (3) , 405-421
- https://doi.org/10.1007/bf02704113
Abstract
No abstract availableKeywords
This publication has 134 references indexed in Scilit:
- Lamina-associated polypeptide 2α regulates cell cycle progression and differentiation via the retinoblastoma–E2F pathwayThe Journal of cell biology, 2006
- Deficient DNA repair in the human progeroid disorder, Werner syndromeMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 2005
- Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organizationExperimental Cell Research, 2005
- The nuclear lamina comes of ageNature Reviews Molecular Cell Biology, 2005
- p.S143F mutation in lamin A/C: A new phenotype combining myopathy and progeriaAnnals of Neurology, 2004
- Effects of expressing lamin A mutant protein causing Emery-Dreifuss muscular dystrophy and familial partial lipodystrophy in Hela cellsExperimental Cell Research, 2003
- A progeroid syndrome in mice is caused by defects in A-type laminsNature, 2003
- Structure of the Globular Tail of Nuclear LaminJournal of Biological Chemistry, 2002
- Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System DiseaseNew England Journal of Medicine, 1999
- Purification and biochemical characterization of interchromatin granule clustersThe EMBO Journal, 1999