Citations for
1CMH13, TNNC1
A mutation in TNNC1-encoded cardiac troponin C, TNNC1-A31S, predisposes to hypertrophic cardiomyopathy and ventricular fibrillation.
Parvatiyar MS, Landstrom AP, Figueiredo-Freitas C, Potter JD, Ackerman MJ, Pinto JR.
J Biol Chem 287(38):31845-55. doi: 10.1074/jbc.M112.377713. 2012
2CMH13, TNNC1
Hypertrophic cardiomyopathy-linked mutation D145E drastically alters calcium binding by the C-domain of cardiac troponin C.
Swindle N, Tikunova SB.
Biochemistry 49(23):4813-20.PMID: 20459070 2010
3CMH13, TNN1C
A dilated cardiomyopathy troponin C mutation lowers contractile force by reducing strong myosin-actin binding.
Dweck D, Reynaldo DP, Pinto JR, Potter JD.
J Biol Chem 285(23):17371-9. Epub 2010 Apr 6.PMID: 20371872 2010
4CMH13, TNNC1
Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy.
van Spaendonck-Zwarts KY, van Tintelen JP, van Veldhuisen DJ, van der Werf R, Jongbloed JD, Paulus WJ, Dooijes D, van den Berg MP.
Circulation 121(20):2169-75. Epub 2010 May 10.PMID: 20458010 2010
5CMH13, TNNC1
A functional and structural study of troponin C mutations related to hypertrophic cardiomyopathy.
Pinto JR, Parvatiyar MS, Jones MA, Liang J, Ackerman MJ, Potter JD.
J Biol Chem 284(28):19090-100. Epub 2009 May 12. 2009
6CMH13, TNNC1, TNNI3
Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy.
Carballo S, Robinson P, Otway R, Fatkin D, Jongbloed JD, de Jonge N, Blair E, van Tintelen JP, Redwood C, Watkins H.
Circ Res 105(4):375-82. Epub 2009 Jul 9. 2009
7CMH13, TNNC1
Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin C.
Landstrom AP, Parvatiyar MS, Pinto JR, Marquardt ML, Bos JM, Tester DJ, Ommen SR, Potter JD, Ackerman MJ.
J Mol Cell Cardiol 45(2):281-8. Epub 2008 May 11.PMID: 18572189 2008
8CMH13, TNNC1
Cardiac troponin C-L29Q, related to hypertrophic cardiomyopathy, hinders the transduction of the protein kinase A dependent phosphorylation signal from cardiac troponin I to C.
Schmidtmann A, Lindow C, Villard S, Heuser A, Mugge A, Gessner R, Granier C, Jaquet K.
FEBS J 272(23):6087-97. 2005
9CMH13, TNNC1
Mutations in human cardiac troponin I that are associated with restrictive cardiomyopathy affect basal ATPase activity and the calcium sensitivity of force development.
Gomes AV, Liang J, Potter JD.
J Biol Chem 280(35):30909-15. Epub 2005 Jun 15.PMID: 15961398 2005