Myofibre Hyper-Contractility in Horses Expressing the Myosin Heavy Chain Myopathy Mutation, MYH1E321G

MYH1 is a candidate gene for recurrent rhabdomyolysis in humans

(2021) Hessa S. Alsaif et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic Cardiomyopathy

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Candidate gene expression and coding sequence variants in Warmblood horses with myofibrillar myopathy

(2020) Zoë J. Williams et al.   EQUINE VETERINARY JOURNAL

Prevalence of the E321G MYH1 variant for immune-mediated myositis and nonexertional rhabdomyolysis in performance subgroups of American Quarter Horses

(2019) Giuliana M. Gianino et al.   JOURNAL OF VETERINARY INTERNAL MEDICINE

Hypertrophic cardiomyopathy mutations in MYBPC3 dysregulate myosin

(2019) Christopher N. Toepfer et al.   Science Translational Medicine

Altered force generation and cell-to-cell contractile imbalance in hypertrophic cardiomyopathy

(2019) Theresia Kraft et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

SIRT1 regulates nuclear number and domain size in skeletal muscle fibers

(2018) Jacob A. Ross et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Burst-Like Transcription of Mutant and Wildtype MYH7-Alleles as Possible Origin of Cell-to-Cell Contractile Imbalance in Hypertrophic Cardiomyopathy

(2018) Judith Montag et al.   Frontiers in Physiology

A missense mutation in MYH1 is associated with susceptibility to immune-mediated myositis in Quarter Horses

(2018) Carrie J. Finno et al.   Skeletal Muscle

An E321G MYH1 mutation is strongly associated with nonexertional rhabdomyolysis in Quarter Horses

(2018) Stephanie J. Valberg et al.   JOURNAL OF VETERINARY INTERNAL MEDICINE

Clinical Implications and Hospital Outcome of Immune-Mediated Myositis in Horses

(2017) L. Hunyadi et al.   JOURNAL OF VETERINARY INTERNAL MEDICINE

Effects of myosin variants on interacting-heads motif explain distinct hypertrophic and dilated cardiomyopathy phenotypes

(2017) Lorenzo Alamo et al.   eLife

Modulating myosin restores muscle function in a mouse model of nemaline myopathy

(2016) Johan Lindqvist et al.   ANNALS OF NEUROLOGY

Major Histocompatibility Complex I and II Expression and Lymphocytic Subtypes in Muscle of Horses with Immune-Mediated Myositis

(2016) S.A. Durward-Akhurst et al.   JOURNAL OF VETERINARY INTERNAL MEDICINE

Distinct Underlying Mechanisms of Limb and Respiratory Muscle Fiber Weaknesses in Nemaline Myopathy

(2013) Johan Lindqvist et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Myosinopathies: pathology and mechanisms

(2012) Homa Tajsharghi et al.   ACTA NEUROPATHOLOGICA

Nemaline Myopathy-Related Skeletal Muscle α-Actin (ACTA1) Mutation, Asp286Gly, Prevents Proper Strong Myosin Binding and Triggers Muscle Weakness

(2012) Julien Ochala et al.   PLoS One

Myosin ATP turnover rate is a mechanism involved in thermogenesis in resting skeletal muscle fibers

(2009) M. A. Stewart et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Effects of a preferential myosin loss on Ca2+activation of force generation in single human skeletal muscle fibres

(2008) Julien Ochala et al.   EXPERIMENTAL PHYSIOLOGY