Characterization of Adiposity and Metabolism in Lmna-Deficient Mice
- 1 March 2002
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 291 (3), 522-527
- https://doi.org/10.1006/bbrc.2002.6466
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Review: The Dynamics of the Nuclear Lamins during the Cell Cycle— Relationship between Structure and FunctionJournal of Structural Biology, 2000
- Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular DystrophyAmerican Journal of Human Genetics, 2000
- Mutational and Haplotype Analyses of Families with Familial Partial Lipodystrophy (Dunnigan Variety) Reveal Recurrent Missense Mutations in the Globular C-Terminal Domain of Lamin A/CAmerican Journal of Human Genetics, 2000
- Review: Nuclear Lamins—Structural Proteins with Fundamental FunctionsJournal of Structural Biology, 2000
- LMNA, encoding lamin A/C, is mutated in partial lipodystrophyNature Genetics, 2000
- Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophyHuman Molecular Genetics, 2000
- 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
- Emery-Dreifuss Muscular DystrophySeminars in Neurology, 1999
- Nuclear Lamins: Their Structure, Assembly, and InteractionsJournal of Structural Biology, 1998
- Familial partial lipodystrophy: two types of an X linked dominant syndrome, lethal in the hemizygous state.Journal of Medical Genetics, 1986