Investigation of troponin I mutations causing familial hypertrophic cardiomyopathy

مواد مشابهة

• Comparison of the functional effects of mutations in troponin T which cause dilated and hypertrophic cardiomyopathies
  حسب: Robinson, P, وآخرون
  منشور في: (2002)
• Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility.
  حسب: Burton, D, وآخرون
  منشور في: (2002)
• 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.
  حسب: Robinson, P, وآخرون
  منشور في: (2002)
• Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein.
  حسب: Redwood, C, وآخرون
  منشور في: (2000)
• Functional effects of mutations in troponin T and tropomyosin which cause dilated cardiomyopathy
  حسب: Robinson, P, وآخرون
  منشور في: (2003)