Found: 14
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The relation between sarcomere energetics and the rate of isometric tension relaxation in healthy and diseased cardiac muscle.
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- Journal of Muscle Research & Cell Motility, 2021, v. 42, n. 1, p. 47, doi. 10.1007/s10974-019-09566-2
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- Article
Thin filament Ca<sup>2+</sup> binding properties and regulatory unit interactions alter kinetics of tension development and relaxation in rabbit skeletal muscle.
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- Journal of Physiology, 2008, v. 586, n. 15, p. 3683, doi. 10.1113/jphysiol.2008.152181
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- Article
The familial hypertrophic cardiomyopathy-associated myosin mutation R403Q accelerates tension generation and relaxation of human cardiac myofibrils.
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- Journal of Physiology, 2008, v. 586, n. 15, p. 3639, doi. 10.1113/jphysiol.2008.155952
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- Article
Susceptibility of isolated myofibrils to in vitro glutathionylation: Potential relevance to muscle functions.
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- Cytoskeleton, 2010, v. 67, n. 2, p. 81, doi. 10.1002/cm.20425
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- Article
Myopalladin knockout mice develop cardiac dilation and show a maladaptive response to mechanical pressure overload.
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- eLife, 2021, p. 1, doi. 10.7554/eLife.58313
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- Article
Corrigendum: Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: the impact of full-length dystrophin deficiency.
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- Frontiers in Physiology, 2023, p. 1, doi. 10.3389/fphys.2023.1222400
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- Article
Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiency.
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- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.1030920
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- Article
Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathy.
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- Cardiovascular Research, 2013, v. 99, n. 3, p. 432, doi. 10.1093/cvr/cvt119
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- Article
Tension generation and relaxation in single myofibrils from human atrial and ventricular myocardium.
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- Pflügers Archiv: European Journal of Physiology, 2007, v. 454, n. 1, p. 63, doi. 10.1007/s00424-006-0181-3
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- Article
Myocardial overexpression of ANKRD1 causes sinus venosus defects and progressive diastolic dysfunction.
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- Cardiovascular Research, 2020, v. 116, n. 8, p. 1458, doi. 10.1093/cvr/cvz291
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- Article
Pathogenesis of Hypertrophic Cardiomyopathy is Mutation Rather Than Disease Specific: A Comparison of the Cardiac Troponin T E163R and R92Q Mouse Models.
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- Journal of the American Heart Association, 2017, v. 6, n. 7, p. 1, doi. 10.1161/JAHA.116.005407
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- Article
Faster cross-bridge detachment and increased tension cost in human hypertrophic cardiomyopathy with the R403Q MYH7 mutation.
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- Journal of Physiology, 2014, v. 592, n. 15, p. 3257, doi. 10.1113/jphysiol.2014.274571
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- Article
Genotype-Driven Pathogenesis of Atrial Fibrillation in Hypertrophic Cardiomyopathy: The Case of Different TNNT2 Mutations.
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- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.864547
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- Article
Myosin Isoform-Dependent Effect of Omecamtiv Mecarbil on the Regulation of Force Generation in Human Cardiac Muscle.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 18, p. 9784, doi. 10.3390/ijms25189784
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- Article