Results 171 to 180 of about 51,825 (261)

The Baraitser–Winter Cerebrofrontofacial Syndrome Recurrent R196H Variant in Cytoplasmic β‐Actin Impairs Its Cellular Polymerization and Stability

open access: yesThe FASEB Journal, Volume 40, Issue 1, 15 January 2026.
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]

open access: yesArch Med Sci Atheroscler Dis
Hazique M   +8 more
europepmc   +1 more source

Non-muscle myosin II is a promising therapeutic target. [PDF]

open access: yesTrends Pharmacol Sci
Miller CA   +2 more
europepmc   +1 more source

Biogenesis of Organelles and Membrane Proteins. [PDF]

open access: yes, 1988
Harmey, Matthew A.   +3 more
core   +1 more source

Cardiac myosin inhibitors: a silver lining for an old disease

open access: yesOpen Heart
Satyavir Yadav   +2 more
openaire   +2 more sources

Long-Term Real-World Outcomes of Mavacamten in Symptomatic Obstructive Hypertrophic Cardiomyopathy up to 108 Weeks. [PDF]

open access: yesJ Clin Med
Reza N   +12 more
europepmc   +1 more source

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