“Laminopathies”: A wide spectrum of human diseases

This publication has 153 references indexed in Scilit:

• Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins
  Biochemical and Biophysical Research Communications, 2006
• Sequencing of the Reannotated LMNB2 Gene Reveals Novel Mutations in Patients with Acquired Partial Lipodystrophy
  American Journal of Human Genetics, 2006
• Distinct structural and mechanical properties of the nuclear lamina in Hutchinson–Gilford progeria syndrome
  Proceedings of the National Academy of Sciences, 2006
• Structure of the Globular Tail of Nuclear Lamin
  Journal of Biological Chemistry, 2002
• Characterization of Adiposity and Metabolism in Lmna-Deficient Mice
  Biochemical and Biophysical Research Communications, 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
• The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
  Nature Genetics, 1997
• Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins
  Nature, 1986
• The Hutchinson-Gilford progeria syndrome
  The Journal of Pediatrics, 1972