Abnormal heart rate regulation in murine hearts with familial hypertrophic cardiomyopathy-related cardiac troponin T mutations

Podobne zapisy

• Computational Characterization of Mutations in Cardiac Troponin T Known to Cause Familial Hypertrophic Cardiomyopathy
  od: Guinto, Pia J., i wsp.
  Wydane: (2007)
• Myosin-driven rescue of contractile reserve and energetics in mouse hearts bearing familial hypertrophic cardiomyopathy-associated mutant troponin T is mutation-specific
  od: He, Huamei, i wsp.
  Wydane: (2012)
• Allosteric effects of cardiac troponin TNT1 mutations on actomyosin binding: A novel pathogenic mechanism for hypertrophic cardiomyopathy
  od: Moore, Rachel K., i wsp.
  Wydane: (2014)
• Decreased energetics in murine hearts bearing the R92Q mutation in cardiac troponin T
  od: Javadpour, Maryam M., i wsp.
  Wydane: (2003)
• Correlation of Molecular and Functional Effects of Mutations in Cardiac Troponin T Linked to Familial Hypertrophic Cardiomyopathy: AN INTEGRATIVE IN SILICO/IN VITRO APPROACH
  od: Manning, Edward P., i wsp.
  Wydane: (2012)