BWCFF, a severe disease with neurological symptoms, is caused by mutations in the cytoskeletal actin genes. Patient‐derived fibroblasts carrying the R196H β‐actin mutation were compared to wild type cells. The mutant cells displayed slower proliferation and migration and a lower F‐actin content, which correlated with reduced cell stiffness ...
Éva Gráczer +12 more
wiley +1 more source
Efficacy and safety of myosin inhibitors for symptomatic hypertrophic cardiomyopathy: systematic review and meta-analysis. [PDF]
Hazique M +8 more
europepmc +1 more source
Non-muscle myosin II is a promising therapeutic target. [PDF]
Miller CA +2 more
europepmc +1 more source
Biogenesis of Organelles and Membrane Proteins. [PDF]
Harmey, Matthew A. +3 more
core +1 more source
Mavacamten for Obstructive Hypertrophic Cardiomyopathy: Targeting Sarcomeric Hypercontractility with Demonstrated Long-Term Safety and Efficacy-A Narrative Review. [PDF]
Mansour GK +5 more
europepmc +1 more source
Cardiac myosin inhibitors: a silver lining for an old disease
Satyavir Yadav +2 more
openaire +2 more sources
PTUPB, a soluble epoxide hydrolase/cyclooxygenase‑2 dual inhibitor, reduces endothelial‑to‑mesenchymal transition and improves doxorubicin‑induced vascular and cardiac toxicity. [PDF]
Dhulkifle H +6 more
europepmc +1 more source
Cellular and Molecular Mechanisms of Heart Failure and Sudden Cardiac Death in Hypertrophic Cardiomyopathy and Methods Used for Their Pathogenetic Correction. [PDF]
Kakturskiy L +6 more
europepmc +1 more source
Myosin Mayhem: Losing (or Gaining) Its Chill in Hypertrophic Cardiomyopathy. [PDF]
Colson BA.
europepmc +1 more source
Long-Term Real-World Outcomes of Mavacamten in Symptomatic Obstructive Hypertrophic Cardiomyopathy up to 108 Weeks. [PDF]
Reza N +12 more
europepmc +1 more source

