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Alpha and beta myosin isoforms and human atrial and ventricular contraction

Cellular and molecular life sciences : CMLS, 2021-12, Vol.78 (23), p.7309-7337

2021

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Late Sodium Current Inhibition Reverses Electromechanical Dysfunction in Human Hypertrophic Cardiomyopathy

Circulation (New York, N.Y.), 2013-02, Vol.127 (5), p.575-584

2013

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Mavacamten has a differential impact on force generation in myofibrils from rabbit psoas and human cardiac muscle

The Journal of general physiology, 2021-07, Vol.153 (7), p.1

2021

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Kinetic coupling of phosphate release, force generation and rate-limiting steps in the cross-bridge cycle

Journal of muscle research and cell motility, 2017-08, Vol.38 (3-4), p.275-289

2017

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Infectious disease in asylums: a fact-finding investigation to prevent tuberculosis contagion in the early twentieth century in Italy

Neurological sciences, 2021-03, Vol.42 (3), p.1185-1188

2021

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Development of Light-Responsive Liquid Crystalline Elastomers to Assist Cardiac Contraction

Circulation research, 2019-04, Vol.124 (8), p.e44-e54

2019

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Absence of full-length dystrophin impairs normal maturation and contraction of cardiomyocytes derived from human-induced pluripotent stem cells

Cardiovascular research, 2020-02, Vol.116 (2), p.368-382

2020

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Defects in T-tubular electrical activity underlie local alterations of calcium release in heart failure

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (42), p.15196-15201

2014

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The relation between sarcomere energetics and the rate of isometric tension relaxation in healthy and diseased cardiac muscle

Journal of muscle research and cell motility, 2021-03, Vol.42 (1), p.47-57

2021

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Ranolazine Prevents Phenotype Development in a Mouse Model of Hypertrophic Cardiomyopathy

Circulation. Heart failure, 2017-03, Vol.10 (3)

2017

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T-tubule remodeling in human hypertrophic cardiomyopathy

Journal of muscle research and cell motility, 2021-06, Vol.42 (2), p.305-322

2021

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Optical Investigation of Action Potential and Calcium Handling Maturation of hiPSC-Cardiomyocytes on Biomimetic Substrates

International journal of molecular sciences, 2019-08, Vol.20 (15), p.3799

2019

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Action potential propagation in transverse-axial tubular system is impaired in heart failure

Proceedings of the National Academy of Sciences - PNAS, 2012-04, Vol.109 (15), p.5815-5819

2012

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Tourism in the Time of Coronavirus. Fruition of the “Minor Heritage” through the Development of Bioarchaeological Sites—A Proposal

Heritage, 2021-06, Vol.4 (2), p.759-774

2021

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Genotype-Driven Pathogenesis of Atrial Fibrillation in Hypertrophic Cardiomyopathy: The Case of Different TNNT2 Mutations

Frontiers in physiology, 2022-04, Vol.13, p.864547-864547

2022

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Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathy

Cardiovascular research, 2013-08, Vol.99 (3), p.432-441

2013

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Sarcomeric determinants of striated muscle relaxation kinetics

Pflügers Archiv, 2005-03, Vol.449 (6), p.505-517

2005

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Nebulette knockout mice have normal cardiac function, but show Z-line widening and up-regulation of cardiac stress markers

Cardiovascular research, 2015-07, Vol.107 (2), p.216-225

2015

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Pathogenesis of Hypertrophic Cardiomyopathy is Mutation Rather Than Disease Specific: A Comparison of the Cardiac Troponin T E163R and R92Q Mouse Models

Journal of the American Heart Association, 2017-07, Vol.6 (7), p.n/a

2017

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Isolation and Mechanical Measurements of Myofibrils from Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes

Stem cell reports, 2016-06, Vol.6 (6), p.885-896

2016

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The familial hypertrophic cardiomyopathy-associated myosin mutation R403Q accelerates tension generation and relaxation of human cardiac myofibrils

The Journal of physiology, 2008-08, Vol.586 (15), p.3639-3644

2008

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Alpha and beta myosin isoforms and human atrial and ventricular contraction

Late Sodium Current Inhibition Reverses Electromechanical Dysfunction in Human Hypertrophic Cardiomyopathy

Mavacamten has a differential impact on force generation in myofibrils from rabbit psoas and human cardiac muscle

Kinetic coupling of phosphate release, force generation and rate-limiting steps in the cross-bridge cycle

Infectious disease in asylums: a fact-finding investigation to prevent tuberculosis contagion in the early twentieth century in Italy

Development of Light-Responsive Liquid Crystalline Elastomers to Assist Cardiac Contraction

Absence of full-length dystrophin impairs normal maturation and contraction of cardiomyocytes derived from human-induced pluripotent stem cells

Myopalladin knockout mice develop cardiac dilation and show a maladaptive response to mechanical pressure overload

Defects in T-tubular electrical activity underlie local alterations of calcium release in heart failure

The relation between sarcomere energetics and the rate of isometric tension relaxation in healthy and diseased cardiac muscle

Ranolazine Prevents Phenotype Development in a Mouse Model of Hypertrophic Cardiomyopathy

T-tubule remodeling in human hypertrophic cardiomyopathy

Optical Investigation of Action Potential and Calcium Handling Maturation of hiPSC-Cardiomyocytes on Biomimetic Substrates

Action potential propagation in transverse-axial tubular system is impaired in heart failure

Tourism in the Time of Coronavirus. Fruition of the “Minor Heritage” through the Development of Bioarchaeological Sites—A Proposal

Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiency

Genotype-Driven Pathogenesis of Atrial Fibrillation in Hypertrophic Cardiomyopathy: The Case of Different TNNT2 Mutations

Corrigendum: Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: the impact of full-length dystrophin deficiency

Ablation of palladin in adult heart causes dilated cardiomyopathy associated with intercalated disc abnormalities

Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathy

Sarcomeric determinants of striated muscle relaxation kinetics

Nebulette knockout mice have normal cardiac function, but show Z-line widening and up-regulation of cardiac stress markers

Pathogenesis of Hypertrophic Cardiomyopathy is Mutation Rather Than Disease Specific: A Comparison of the Cardiac Troponin T E163R and R92Q Mouse Models

Isolation and Mechanical Measurements of Myofibrils from Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes

The familial hypertrophic cardiomyopathy-associated myosin mutation R403Q accelerates tension generation and relaxation of human cardiac myofibrils

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