Impact of familial hypertrophic cardiomyopathy-linked mutations in the NH(2) terminus of the RLC on β-myosin cross-bridge mechanics

Ítems similars

• The effect of myosin RLC phosphorylation in normal and cardiomyopathic mouse hearts
  per: Muthu, Priya, et al.
  Publicat: (2012)
• Myosin regulatory light chain mutation found in hypertrophic cardiomyopathy patients increases isometric force production in transgenic mice
  per: Kazmierczak, Katarzyna, et al.
  Publicat: (2012)
• Hypertrophic Cardiomyopathy Associated Lys104Glu Mutation in the Myosin Regulatory Light Chain Causes Diastolic Disturbance in Mice
  per: Huang, Wenrui, et al.
  Publicat: (2014)
• Cardiomyopathy-linked myosin regulatory light chain mutations disrupt myosin strain-dependent biochemistry
  per: Greenberg, Michael J., et al.
  Publicat: (2010)
• In Vitro Rescue Study of a Malignant Familial Hypertrophic Cardiomyopathy Phenotype by Pseudo-Phosphorylation of Myosin Regulatory Light Chain
  per: Muthu, Priya, et al.
  Publicat: (2013)