Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy

समान संसाधन

• A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy.
  द्वारा: Tardiff, J C, और अन्य
  प्रकाशित: (1998)
• Allosteric effects of cardiac troponin TNT1 mutations on actomyosin binding: A novel pathogenic mechanism for hypertrophic cardiomyopathy
  द्वारा: Moore, Rachel K., और अन्य
  प्रकाशित: (2014)
• Abnormal heart rate regulation in murine hearts with familial hypertrophic cardiomyopathy-related cardiac troponin T mutations
  द्वारा: Jimenez, Jesus, और अन्य
  प्रकाशित: (2011)
• Computational Characterization of Mutations in Cardiac Troponin T Known to Cause Familial Hypertrophic Cardiomyopathy
  द्वारा: Guinto, Pia J., और अन्य
  प्रकाशित: (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
  द्वारा: Manning, Edward P., और अन्य
  प्रकाशित: (2012)