Characterization of cardiac metabolism in iPSC-derived cardiomyocytes: lessons from maturation and disease modeling
S Vučković, R Dinani, EE Nollet, DWD Kuster… - Stem cell research & …, 2022 - Springer
Background Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) have
emerged as a powerful tool for disease modeling, though their immature nature currently …
emerged as a powerful tool for disease modeling, though their immature nature currently …
Pharmacological management of hypertrophic cardiomyopathy: from bench to bedside
C Palandri, L Santini, A Argirò, F Margara, R Doste… - Drugs, 2022 - Springer
Hypertrophic cardiomyopathy (HCM), the most common inherited heart disease, is still
orphan of a specific drug treatment. The erroneous consideration of HCM as a rare disease …
orphan of a specific drug treatment. The erroneous consideration of HCM as a rare disease …
Inflammation across the spectrum of hypertrophic cardiac phenotypes
R Lillo, F Graziani, F Franceschi, G Iannaccone… - Heart Failure …, 2023 - Springer
The hypertrophic cardiomyopathy phenotype encompasses a heterogeneous spectrum of
genetic and acquired diseases characterized by the presence of left ventricular hypertrophy …
genetic and acquired diseases characterized by the presence of left ventricular hypertrophy …
Deep learning detects cardiotoxicity in a high-content screen with induced pluripotent stem cell-derived cardiomyocytes
Drug-induced cardiotoxicity and hepatotoxicity are major causes of drug attrition. To
decrease late-stage drug attrition, pharmaceutical and biotechnology industries need to …
decrease late-stage drug attrition, pharmaceutical and biotechnology industries need to …
[HTML][HTML] Complex II ambiguities—FADH2 in the electron transfer system
E Gnaiger - Journal of Biological Chemistry, 2024 - Elsevier
The prevailing notion that reduced cofactors NADH and FADH 2 transfer electrons from the
tricarboxylic acid cycle to the mitochondrial electron transfer system creates ambiguities …
tricarboxylic acid cycle to the mitochondrial electron transfer system creates ambiguities …
Cardiometabolism as an interlocking puzzle between the healthy and diseased heart: new frontiers in therapeutic applications
Cardiac metabolism represents a crucial and essential connecting bridge between the
healthy and diseased heart. The cardiac muscle, which may be considered an omnivore …
healthy and diseased heart. The cardiac muscle, which may be considered an omnivore …
Nitric oxide and mechano-electrical transduction in cardiomyocytes
HE Boycott, MN Nguyen, B Vrellaku… - Frontiers in …, 2020 - frontiersin.org
The ability § of the heart to adapt to changes in the mechanical environment is critical for
normal cardiac physiology. The role of nitric oxide is increasingly recognized as a mediator …
normal cardiac physiology. The role of nitric oxide is increasingly recognized as a mediator …
Clinical Trials in Hypertrophic Cardiomyopathy Therapy: A Comprehensive Analysis of Trials Registered in Global Clinical Databases
H Zhang, C Yu, Y Cheng, Z Chen, M Chen… - Drug Design …, 2023 - Taylor & Francis
Background With the disappointing results associated with the use of cardiac myosin
inhibitors in the treatment of hypertrophic cardiomyopathy (HCM), the development of new …
inhibitors in the treatment of hypertrophic cardiomyopathy (HCM), the development of new …
Transcriptome data analysis of primary cardiomyopathies reveals perturbations in arachidonic acid metabolism
PK Chauhan, R Sowdhamini - Frontiers in Cardiovascular Medicine, 2023 - frontiersin.org
Introduction Cardiomyopathies are complex heart diseases with significant prevalence
around the world. Among these, primary forms are the major contributors to heart failure and …
around the world. Among these, primary forms are the major contributors to heart failure and …
[HTML][HTML] Definitional Challenges in Understanding Hypertrophic Cardiomyopathy
JM Federspiel, J Pfeifer, F Ramsthaler, JC Reil… - Diagnostics, 2024 - mdpi.com
Hypertrophic cardiomyopathy (HCM) is the most common hereditary cardiomyopathy. It is
often caused by mutations of genes encoding for sarcomeric or sarcomere-associated …
often caused by mutations of genes encoding for sarcomeric or sarcomere-associated …