Molecular Effects of Familial Hypertrophic Cardiomyopathy-Related Mutations in the TNT1 Domain of cTnT

Podobne zapisy

• Computational Characterization of Mutations in Cardiac Troponin T Known to Cause Familial Hypertrophic Cardiomyopathy
  od: Guinto, Pia J., i wsp.
  Wydane: (2007)
• 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)
• Temporal and mutation-specific alterations in Ca(2+) homeostasis differentially determine the progression of cTnT-related cardiomyopathies in murine models
  od: Guinto, Pia J., i wsp.
  Wydane: (2009)
• 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)
• Abnormal heart rate regulation in murine hearts with familial hypertrophic cardiomyopathy-related cardiac troponin T mutations
  od: Jimenez, Jesus, i wsp.
  Wydane: (2011)