Investigation of troponin I mutations causing familial hypertrophic cardiomyopathy

Samankaltaisia teoksia

• Comparison of the functional effects of mutations in troponin T which cause dilated and hypertrophic cardiomyopathies
  Tekijä: Robinson, P, et al.
  Julkaistu: (2002)
• Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility.
  Tekijä: Burton, D, et al.
  Julkaistu: (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.
  Tekijä: Robinson, P, et al.
  Julkaistu: (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.
  Tekijä: Redwood, C, et al.
  Julkaistu: (2000)
• Functional effects of mutations in troponin T and tropomyosin which cause dilated cardiomyopathy
  Tekijä: Robinson, P, et al.
  Julkaistu: (2003)