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Circulation. Heart Failure|December 20, 2011
Contractile dysfunction irrespective of the mutant protein in human hypertrophic cardiomyopathy with normal systolic functionSabine J van Dijk, E Rosalie Paalberends, Aref Najafi, et al.
The Journal of Biological Chemistry|April 9, 2013
Nicotinic acid adenine dinucleotide phosphate (NAADP)-mediated calcium signaling and arrhythmias in the heart evoked by β-adrenergic stimulationMerle Nebel, Alexander P Schwoerer, Dominik Warszta, et al.
Scientific Reports|June 22, 2016
The embryological basis of subclinical hypertrophic cardiomyopathyGabriella Captur, Carolyn Y Ho, Saskia Schlossarek, et al.
Circulation Research|September 16, 2024
Chronic Activation of Tubulin Tyrosination Improves Heart FunctionNiels Pietsch, Christina Y Chen, Svenja Kupsch, et al.
Journal of Molecular and Cellular Cardiology|May 6, 2021
Translational investigation of electrophysiology in hypertrophic cardiomyopathyFrederik Flenner, Christiane Jungen, Nadine Küpker, et al.
Human Molecular Genetics|April 24, 2012
Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathyFelix W Friedrich, Brendan R Wilding, Silke Reischmann, et al.
Circulation. Heart Failure|January 12, 2021
Proteomic and Functional Studies Reveal Detyrosinated Tubulin as Treatment Target in Sarcomere Mutation-Induced Hypertrophic CardiomyopathyMaike Schuldt, Jiayi Pei, Magdalena Harakalova, et al.
Nature Communications|September 27, 2012
The miRNA-212/132 family regulates both cardiac hypertrophy and cardiomyocyte autophagyAhmet Ucar, Shashi K Gupta, Jan Fiedler, et al.
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