Mouse models of the laminopathies
- 10 June 2007
- journal article
- review article
- Published by Elsevier BV in Experimental Cell Research
- Vol. 313 (10), 2144-2156
- https://doi.org/10.1016/j.yexcr.2007.03.026
Abstract
No abstract availableKeywords
This publication has 87 references indexed in Scilit:
- A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutationJCI Insight, 2006
- Sequencing of the Reannotated LMNB2 Gene Reveals Novel Mutations in Patients with Acquired Partial LipodystrophyAmerican Journal of Human Genetics, 2006
- Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathyHuman Mutation, 2005
- Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in miceHuman Molecular Genetics, 2005
- Reduced adiponectin and HDL cholesterol without elevated C-reactive protein: Clues to the biology of premature atherosclerosis in Hutchinson-Gilford Progeria SyndromeThe Journal of Pediatrics, 2005
- A progeroid syndrome in mice is caused by defects in A-type laminsNature, 2003
- Characterization of Adiposity and Metabolism in Lmna-Deficient MiceBiochemical and Biophysical Research Communications, 2002
- Hutchinson-Guilford progeria syndromePostgraduate Medical Journal, 2001
- 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
- Genetic modulation of the senescent phenotype in Homo sapiensGenome, 1989