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Proteomics|June 23, 2006
Myosin binding protein C is differentially phosphorylated upon myocardial stunning in canine and rat hearts-- evidence for novel phosphorylation sitesChao Yuan, Yurong Guo, Rajashree Ravi, et al.
Circulation Research|January 17, 2004
Frequency- and afterload-dependent cardiac modulation in vivo by troponin I with constitutively active protein kinase A phosphorylation sitesEiki Takimoto, David G Soergel, Paul M L Janssen, et al.
The Journal of Physiology|March 3, 2007
Nitroxyl increases force development in rat cardiac muscleTieying Dai, Ye Tian, Carlo Gabriele Tocchetti, et al.
Circulation|September 14, 2012
Multiple reaction monitoring to identify site-specific troponin I phosphorylated residues in the failing human heartPingbo Zhang, Jonathan A Kirk, Weihua Ji, et al.
European Journal of Nuclear Medicine and Molecular Imaging|May 2, 2003
125I-BMIPP and 18F-FDG uptake in a transgenic mouse model of stunned myocardiumHein J Verberne, Gerrit W Sloof, Arnold L Beets, et al.
Circulation Research|December 26, 2009
The C terminus of cardiac troponin I stabilizes the Ca2+-activated state of tropomyosin on actin filamentsAgnieszka Galińska, Victoria Hatch, Roger Craig, et al.
Cardiology in the Young|June 15, 2019
Genetic aetiologies should be considered in paediatric cases of acute heart failure presumed to be myocarditisEmily E Brown, Kristen Nelson McMilllan, Marc K Halushka, et al.
Biorxiv : the Preprint Server for Biology|July 28, 2023
The HCM - Linked Mutation Arg92Leu in TNNT2 Allosterically Alters the cTnC - cTnI Interface and Disrupts the PKA-mediated Regulation of Myofilament RelaxationMelissa L Lynn, Jesus Jimenez, Romi L Castillo, et al.
Circulation Research|November 8, 2008
O-linked GlcNAc modification of cardiac myofilament proteins: a novel regulator of myocardial contractile functionGenaro A Ramirez-Correa, Wenhai Jin, Zihao Wang, et al.
American Journal of Medical Genetics. Part A|May 16, 2012
A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with a PTPN11 mutation and a novel variant in SOS1Jill A Fahrner, Aisha Frazier, Suha Bachir, et al.
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