Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.

Gelijkaardige items

• Effects of DCM mutations in thin filament regulatory proteins on contractile function
  door: Robinson, P, et al.
  Gepubliceerd in: (2005)
• Structure-function relationships of eight mutations in troponin and tropomyosin that cause dilated cardiomyopathy
  door: Mirza, M, et al.
  Gepubliceerd in: (2004)
• Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy.
  door: Robinson, P, et al.
  Gepubliceerd in: (2002)
• Dilated cardiomyopathy causing mutations in cardiac troponin T (TNT), cardiac troponin C (TNC), and alpha tropomyosin (TM) reduce CA(2+) sensitivity and maximum calcium activation
  door: Redwood, C, et al.
  Gepubliceerd in: (2004)
• The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments.
  door: Mirza, M, et al.
  Gepubliceerd in: (2007)