An abnormal Ca(2+) response in mutant sarcomere protein–mediated familial hypertrophic cardiomyopathy

समान संसाधन

• Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene
  द्वारा: Fatkin, Diane, और अन्य
  प्रकाशित: (1999)
• Investigations into the Sarcomeric Protein and Ca(2+)-Regulation Abnormalities Underlying Hypertrophic Cardiomyopathy in Cats (Felix catus)
  द्वारा: Messer, Andrew E., और अन्य
  प्रकाशित: (2017)
• Hypertrophic cardiomyopathy: Translating cellular cross talk into therapeutics
  द्वारा: Teekakirikul, Polakit, और अन्य
  प्रकाशित: (2012)
• The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model
  द्वारा: Semsarian, Christopher, और अन्य
  प्रकाशित: (2002)
• A small-molecule inhibitor of sarcomere contractility suppresses hypertrophic cardiomyopathy in mice
  द्वारा: Green, Eric M., और अन्य
  प्रकाशित: (2016)