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Increased remodeling and impaired adaption to endurance exercise in desminopathy

Biomedicines, Vol. 10, Pages 1473: Role of Oxidative Stress in Cardiac Dysfunction and Subcellular Defects Due to Ischemia-Reperfusion Injury

Sarcolemma Wounding Activates Dynamin-Dependent Endocytosis in Striated Muscle.

Cells, Vol. 9, Pages 1936: Tsg101 Is Involved in the Sorting and Re-Distribution of Glucose Transporter-4 to the Sarcolemma Membrane of Cardiac Myocytes

Cells, Vol. 9, Pages 1936: Tsg101 Is Involved in the Sorting and Re-Distribution of Glucose Transporter-4 to the Sarcolemma Membrane of Cardiac Myocytes

Effects of myofiber isolation technique on sarcolemma biomechanics.

The Z-disc proteins myotilin and FATZ-1 interact with each other and are connected to the sarcolemma via muscle-specific filamins.

Massage increases satellite cell number independent of the age-associated alterations in sarcolemma permeability.

Evaluating Therapeutic Activity of Galectin-1 in Sarcolemma Repair of Skeletal Muscle

β-adrenergic control of sarcolemmal CaV1.2 abundance by small GTPase Rab proteins

Membranes, Vol. 12, Pages 153: Trafficking of Annexins during Membrane Repair in Human Skeletal Muscle Cells

Intracellular localization of dysferlin and its association with the dihydropyridine receptor.

Biomolecules, Vol. 10, Pages 1206: Caveolin-3: A Causative Process of Chicken Muscular Dystrophy

Biomolecules, Vol. 10, Pages 1206: Caveolin-3: A Causative Process of Chicken Muscular Dystrophy

Regulated sarcolemmal localization of the muscle-specific ClC-1 chloride channel

Pathological evaluation of rats carrying in-frame mutations in the dystrophin gene: a new model of Becker muscular dystrophy [RESEARCH ARTICLE]

Cells, Vol. 9, Pages 2524: Perlecan Facilitates Neuronal Nitric Oxide Synthase Delocalization in Denervation-Induced Muscle Atrophy

Location and function of transient receptor potential canonical channel 1 in ventricular myocytes.

Muscle follistatin gene delivery increases muscle protein synthesis independent of periodical physical inactivity and fasting

Muscle follistatin gene delivery increases muscle protein synthesis independent of periodical physical inactivity and fasting

IJMS, Vol. 22, Pages 5276: Annexins and Membrane Repair Dysfunctions in Muscular Dystrophies

Diagnostics, Vol. 11, Pages 1879: The ERG1A K+ Channel Is More Abundant in Rectus abdominis Muscle from Cancer Patients Than that from Healthy Humans

KATP channel knockout worsens myocardial calcium stress load in vivo and impairs recovery in stunned heart

X-linked myopathy with excessive autophagy: a failure of self-eating.

Pain in SCN4A mutated p.A1156T muscle sodium channelopathy - a postal survey.

A Simulation Study on Selective Stimulation of C-Fiber Nerves for Chronic Pain Relief

Delayed afterdepolarization-induced triggered activity in cardiac purkinje cells mediated through cytosolic calcium diffusion waves.

Endogenous Galectin-3 is Required for Skeletal Muscle Repair

Lack of Desmin in Mice Causes Structural and Functional Disorders of Neuromuscular Junctions

Microutrophin expression in dystrophic mice displays myofiber type differences in therapeutic effects

Comparative study of calcium and calcium-related enzymes with differentiation markers in different ages and muscle types in mdx mice.

An interaction of heart disease-associated proteins POPDC1/2 with XIRP1 in transverse tubules and intercalated discs

Cells, Vol. 10, Pages 61: Master Regulators of Muscle Atrophy: Role of Costamere Components

Cells, Vol. 10, Pages 61: Master Regulators of Muscle Atrophy: Role of Costamere Components

Nox2 signaling and muscle fiber remodeling are attenuated by losartan administration during skeletal muscle unloading.

Role of Oxidative Stress in Metabolic and Subcellular Abnormalities in Diabetic Cardiomyopathy.

RyR2 regulates Cx43 hemichannel intracellular Ca2+-dependent activation in cardiomyocytes

Persistent mdx diaphragm alterations are accompanied by increased expression and activity of calcium and muscle-specific proteins

Evaluation of the Lipid-binding Properties of Recombinant Dystrophin Spectrin-like Repeat Domains R1-3

X-linked myopathy with excessive autophagy: a failure of self-eating

Improved Bone Quality and Bone Healing of Dystrophic Mice by Parabiosis

Long-term effect of human mini-dystrophin in transgenic mdx mice improves muscle physiological function

The multifaceted view of heart problem in Duchenne muscular dystrophy

Cells, Vol. 10, Pages 1515: Does TBC1D4 (AS160) or TBC1D1 Deficiency Affect the Expression of Fatty Acid Handling Proteins in the Adipocytes Differentiated from Human Adipose-Derived Mesenchymal Stem Cells (ADMSCs) Obtained from Subcutaneous and Visc

Cells, Vol. 10, Pages 1515: Does TBC1D4 (AS160) or TBC1D1 Deficiency Affect the Expression of Fatty Acid Handling Proteins in the Adipocytes Differentiated from Human Adipose-Derived Mesenchymal Stem Cells (ADMSCs) Obtained from Subcutaneous and Visc

Dual Dysfunction of Kir2.1 Underlies Conduction and Excitation-Contraction Coupling Defects Promoting Arrhythmias in a Mouse Model of Andersen-Tawil Syndrome Type 1

The More, the Merrier? Multiple Myoglobin Genes in Fish Species, Especially in Gray Bichir (Polypterus senegalus) and Reedfish (Erpetoichthys calabaricus)

A mutation in desmin makes skeletal muscle less vulnerable to acute muscle damage after eccentric loading in rats

Fish Oil for Healthy Aging: Potential Application to Master Athletes

Cardiac contractility of the African sharptooth catfish, Clarias gariepinus: role of extracellular Ca2+, sarcoplasmic reticulum, andβ-adrenergic stimulation