Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy

This publication has 42 references indexed in Scilit:

• Dissection of the Mammalian Midbody Proteome Reveals Conserved Cytokinesis Mechanisms
  Science, 2004
• Nuclear Reorganization of Mammalian DNA Synthesis Prior to Cell Cycle Exit
  Molecular and Cellular Biology, 2004
• Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo
  Journal of Cell Science, 2003
• Effects of expressing lamin A mutant protein causing Emery-Dreifuss muscular dystrophy and familial partial lipodystrophy in Hela cells
  Experimental Cell Research, 2003
• A progeroid syndrome in mice is caused by defects in A-type lamins
  Nature, 2003
• Nuclear lamins: building blocks of nuclear architecture
  Genes & Development, 2002
• Direct Interaction between Emerin and Lamin A
  Biochemical and Biophysical Research Communications, 2000
• Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease
  New England Journal of Medicine, 1999
• Distribution of emerin and lamins in the heart and implications for Emery-Dreifuss muscular dystrophy
  Human Molecular Genetics, 1999
• Emery-Dreifuss syndrome.
  Journal of Medical Genetics, 1989