Cryo-EM structure of shutdown human non-muscle myosin 2A
Casas-Mao D, Carrington G, Peckham M.
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A mutation that prevents myosin from overcoming its inhibitions. [PDF]
Short B.
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The MYH7 c.2770G > A (p.Glu924Lys) mutation exhibits phenotypic heterogeneity in hypertrophic cardiomyopathy (HCM) and restrictive cardiomyopathy (RCM): a case report. [PDF]
Han Y +5 more
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Clinical characteristics of 41 children with hypertrophic cardiomyopathy: A single-center retrospective study. [PDF]
Li SG +6 more
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Homologous mutations in human β, embryonic, and perinatal muscle myosins have divergent effects on molecular power generation. [PDF]
Liu C +8 more
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Myosin Mayhem: Losing (or Gaining) Its Chill in Hypertrophic Cardiomyopathy. [PDF]
Colson BA.
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Cardiac Myosin Inhibitors in the Treatment of Hypertrophic Cardiomyopathy: Clinical Trials and Future Challenges. [PDF]
Kukowka A, Droździk M.
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A Unique Case of a Child with Two Rare Hereditary Diseases: Familial Dilated Cardiomyopathy and Arterial Calcification. [PDF]
Burykina Y +12 more
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Heart Morphogenesis Requires Smyd1b for Proper Incorporation of the Second Heart Field in Zebrafish. [PDF]
Prill K, Windsor Reid P, Pilgrim D.
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