Related references
Note: Only part of the references are listed.The Influence of Genotype on the Phenotype, Clinical Course, and Risk of Adverse Events in Children with Hypertrophic Cardiomyopathy
Francesca Girolami et al.
HEART FAILURE CLINICS (2022)
Human iPSC model reveals a central role for NOX4 and oxidative stress in Duchenne cardiomyopathy
Robin Duelen et al.
STEM CELL REPORTS (2022)
Diagnosis and Management of Rare Cardiomyopathies in Adult and Paediatric Patients. A Position Paper of the Italian Society of Cardiology (SIC) and Italian Society of Paediatric Cardiology (SICP)
Giuseppe Limongelli et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2022)
The harder the climb the better the view: The impact of substrate stiffness on cardiomyocyte fate
Silvia Querceto et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2022)
A humanized knockin mouse model of Duchenne muscular dystrophy and its correction by CRISPR-Cas9 therapeutic gene editing
Yu Zhang et al.
MOLECULAR THERAPY-NUCLEIC ACIDS (2022)
Full-length dystrophin deficiency leads to contractile and calcium transient defects in human engineered heart tissues
Samantha B. Bremner et al.
JOURNAL OF TISSUE ENGINEERING (2022)
Sequential Defects in Cardiac Lineage Commitment and Maturation Cause Hypoplastic Left Heart Syndrome
Markus Krane et al.
CIRCULATION (2021)
Skeletal Ryanodine Receptors Are Involved in Impaired Myogenic Differentiation in Duchenne Muscular Dystrophy Patients
Pierre Meyer et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2021)
A detailed characterization of the hyperpolarization-activated funny current (If) in human-induced pluripotent stem cell (iPSC)-derived cardiomyocytes with pacemaker activity
Federica Giannetti et al.
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2021)
Increased tissue stiffness triggers contractile dysfunction and telomere shortening in dystrophic cardiomyocytes
Alex C. Y. Chang et al.
STEM CELL REPORTS (2021)
Absence of full-length dystrophin impairs normal maturation and contraction of cardiomyocytes derived from human-induced pluripotent stem cells
J. Manuel Pioner et al.
CARDIOVASCULAR RESEARCH (2020)
Somatic gene editing ameliorates skeletal and cardiac muscle failure in pig and human models of Duchenne muscular dystrophy
A. Moretti et al.
NATURE MEDICINE (2020)
A cardiomyocyte show of force: A fluorescent alpha-actinin reporter line sheds light on human cardiomyocyte contractility versus substrate stiffness
Marcelo C. Ribeiro et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2020)
Advances in Stem Cell Modeling of Dystrophin-Associated Disease: Implications for the Wider World of Dilated Cardiomyopathy
Jose Manuel Pioner et al.
FRONTIERS IN PHYSIOLOGY (2020)
DMD Pluripotent Stem Cell Derived Cardiac Cells Recapitulatein vitroHuman Cardiac Pathophysiology
Sarka Jelinkova et al.
FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY (2020)
Isogenic models of hypertrophic cardiomyopathy unveil differential phenotypes and mechanism-driven therapeutics
Jamie R. Bhagwan et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2020)
Unchain My Heart: Integrins at the Basis of iPSC Cardiomyocyte Differentiation
Rosaria Santoro et al.
STEM CELLS INTERNATIONAL (2019)
Optical Investigation of Action Potential and Calcium Handling Maturation of hiPSC-Cardiomyocytes on Biomimetic Substrates
Jose Manuel Pioner et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2019)
Learn from Your Elders: Developmental Biology Lessons to Guide Maturation of Stem Cell-Derived Cardiomyocytes
Silvia Marchiano et al.
PEDIATRIC CARDIOLOGY (2019)
Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients
Binyamin Eisen et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2019)
Dystrophin Deficiency Leads to Genomic Instability in Human Pluripotent Stem Cells via NO Synthase-Induced Oxidative Stress
Sarka Jelinkova et al.
CELLS (2019)
Non-Glycanated Biglycan and LTBP4: Leveraging the extracellular matrix for Duchenne Muscular Dystrophy therapeutics
Justin R. Fallon et al.
MATRIX BIOLOGY (2018)
Pathogenesis of Hypertrophic Cardiomyopathy is Mutation Rather Than Disease Specific: A Comparison of the Cardiac Troponin T E163R and R92Q Mouse Models
Cecilia Ferrantini et al.
JOURNAL OF THE AMERICAN HEART ASSOCIATION (2017)
Functional correction of dystrophin actin binding domain mutations by genome editing
Viktoriia Kyrychenko et al.
JCI INSIGHT (2017)
Nanotopography-Induced Structural Anisotropy and Sarcomere Development in Human Cardiomyocytes Derived from Induced Pluripotent Stem Cells
Daniel Carson et al.
ACS APPLIED MATERIALS & INTERFACES (2016)
Time-dependent evolution of functional vs. remodeling signaling in induced pluripotent stem cell-derived cardiomyocytes and induced maturation with biomechanical stimulation
Gwanghyun Jung et al.
FASEB JOURNAL (2016)
Deficient cMyBP-C protein expression during cardiomyocyte differentiation underlies human hypertrophic cardiomyopathy cellular phenotypes in disease specific human ES cell derived cardiomyocytes
Andre Monteiro da Rocha et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2016)
Nanopatterned Human iPSC-Based Model of a Dystrophin-Null Cardiomyopathic Phenotype
Jesse Macadangdang et al.
CELLULAR AND MOLECULAR BIOENGINEERING (2015)
Crosstalk between RyR2 oxidation and phosphorylation contributes to cardiac dysfunction in mice with Duchenne muscular dystrophy
Qiongling Wang et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2015)
Contractility of single cardiomyocytes differentiated from pluripotent stem cells depends on physiological shape and substrate stiffness
Alexandre J. S. Ribeiro et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Dystrophin-deficient cardiomyocytes derived from human urine: New biologic reagents for drug discovery
Xuan Guan et al.
STEM CELL RESEARCH (2014)
In vivo single-molecule imaging identifies altered dynamics of calcium channels in dystrophin-mutant C. elegans
Hong Zhan et al.
NATURE COMMUNICATIONS (2014)
Role of Extracellular Matrix Signaling Cues in Modulating Cell Fate Commitment for Cardiovascular Tissue Engineering
Karina H. Nakayama et al.
ADVANCED HEALTHCARE MATERIALS (2014)
Hierarchical accumulation of RyR post-translational modifications drives disease progression in dystrophic cardiomyopathy
Sergii Kyrychenko et al.
CARDIOVASCULAR RESEARCH (2013)
Inhibition of CaMKII phosphorylation of RyR2 prevents inducible ventricular arrhythmias in mice with Duchenne muscular dystrophy
Sameer Ather et al.
HEART RHYTHM (2013)
Cellular and molecular mechanisms underlying muscular dystrophy
Fedik Rahimov et al.
JOURNAL OF CELL BIOLOGY (2013)
Structural and Functional Maturation of Cardiomyocytes Derived from Human Pluripotent Stem Cells
Scott D. Lundy et al.
STEM CELLS AND DEVELOPMENT (2013)
Substrate Stiffness Increases Twitch Power of Neonatal Cardiomyocytes in Correlation with Changes in Myofibril Structure and Intracellular Calcium
Anthony G. Rodriguez et al.
BIOPHYSICAL JOURNAL (2011)
Leaky RyR2 trigger ventricular arrhythmias in Duchenne muscular dystrophy
Jeremy Fauconnier et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Hypersensitivity of excitation-contraction coupling in dystrophic cardiomyocytes
Nina D. Ullrich et al.
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY (2009)
Pathways of abnormal stress-induced Ca2+ influx into dystrophic mdx cardiomyocytes
M. Fanchaouy et al.
CELL CALCIUM (2009)
Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle
Andrew M. Bellinger et al.
NATURE MEDICINE (2009)
Developmental origins of hypertrophic cardiomyopathy phenotypes: a unifying hypothesis
Iacopo Olivotto et al.
NATURE REVIEWS CARDIOLOGY (2009)
The Many Faces of Hypertrophic Cardiomyopathy: From Developmental Biology to Clinical Practice
Iacopo Olivotto et al.
JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH (2009)
Matrix elasticity directs stem cell lineage specification
Adam J. Engler et al.
CELL (2006)
Costameres: The Achilles' heel of herculean muscle
JM Ervasti
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Share Paper
