Q34973567 | Altered Ca2+ kinetics associated with α-actinin-3 deficiency may explain positive selection for ACTN3 null allele in human evolution |
Q46271408 | Apoptosis precedes necrosis of dystrophin-deficient muscle |
Q73070067 | Calcium homeostasis in dystrophic muscle |
Q37054632 | Ca²⁺-pumping impairment during repetitive fatiguing contractions in single myofibers: role of cross-bridge cycling |
Q33644573 | Characteristics of skeletal muscle in mdx mutant mice |
Q48415548 | Cortical and brainstem neurons containing calcium-binding proteins in a murine model of Duchenne's muscular dystrophy: selective changes in the sensorimotor cortex. |
Q44777446 | Decreased expression of ryanodine receptors alters calcium-induced calcium release mechanism in mdx duodenal myocytes |
Q39762830 | Defective excitation-contraction coupling is partially responsible for impaired contractility in hindlimb muscles of Stac3 knockout mice. |
Q42027727 | Doublet stimulation increases Ca2+ binding to troponin C to ensure rapid force development in skeletal muscle. |
Q60533862 | Dystrophin is not essential for the integrity of the cytoskeleton |
Q44873416 | Effect of creatine supplementation on skeletal muscle of mdx mice |
Q74517077 | Effect of hydrogen peroxide and dithiothreitol on contractile function of single skeletal muscle fibres from the mouse |
Q42435407 | Excitation-contraction coupling of cultured human skeletal muscle cells and the relation between basal cytosolic Ca2+ and excitability |
Q40474236 | Extraocular muscles: Basic and clinical aspects of structure and function |
Q36757538 | Heterokaryon myotubes with normal mouse and Duchenne nuclei exhibit sarcolemmal dystrophin staining and efficient intracellular free calcium control. |
Q40542404 | Improvement of calcium handling and changes in calcium-release properties after mini- or full-length dystrophin forced expression in cultured skeletal myotubes |
Q74583809 | Increased calcium entry into dystrophin-deficient muscle fibres of MDX and ADR-MDX mice is reduced by ion channel blockers |
Q36033118 | Increased resting intracellular calcium modulates NF-κB-dependent inducible nitric-oxide synthase gene expression in dystrophic mdx skeletal myotubes |
Q90199324 | Incubation with sodium nitrite attenuates fatigue development in intact single mouse fibres at physiological PO2 |
Q33907241 | Indo-1 fluorescence signals elicited by membrane depolarization in enzymatically isolated mouse skeletal muscle fibers |
Q28366903 | Inhibition of creatine kinase reduces the rate of fatigue-induced decrease in tetanic [Ca(2+)](i) in mouse skeletal muscle |
Q72111438 | Intracellular Ca2+ concentrations are not elevated in resting cultured muscle from Duchenne (DMD) patients and in MDX mouse muscle fibres |
Q74271245 | Intracellular calcium and Na+-Ca2+ exchange current in isolated toad pacemaker cells |
Q73326255 | Intracellular calcium during fatigue of cane toad skeletal muscle in the absence of glucose |
Q73087615 | Intracellular calcium signals measured with indo-1 in isolated skeletal muscle fibres from control and mdx mice |
Q34040361 | Intracellular calibration of the calcium indicator indo-1 in isolated fibers of Xenopus muscle |
Q30813768 | Large-scale analysis of differential gene expression in the hindlimb muscles and diaphragm of mdx mouse |
Q34469185 | Long-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscle |
Q71502165 | Measurement of membrane potential and myoplasmic [Ca2+] in developing rat myotubes at rest and in response to stimulation |
Q34168716 | Measurements of intracellular Mg2+ concentration in mouse skeletal muscle fibers with the fluorescent indicator mag-indo-1 |
Q46326458 | Mechanical isolation, and measurement of force and myoplasmic free [Ca2+] in fully intact single skeletal muscle fibers |
Q72681998 | Membrane potential, resting calcium and calcium transients in isolated muscle fibres from normal and dystrophic mice |
Q44640506 | Mini-dystrophin restores L-type calcium currents in skeletal muscle of transgenic mdx mice. |
Q28588083 | Myotonic dystrophy protein kinase is involved in the modulation of the Ca2+ homeostasis in skeletal muscle cells |
Q34445717 | Myotubes from transgenic mdx mice expressing full-length dystrophin show normal calcium regulation |
Q47812772 | Neurological and Motor Disorders: TRPC in the Skeletal Muscle |
Q36560597 | New insights in the regulation of calcium transfers by muscle dystrophin-based cytoskeleton: implications in DMD. |
Q73778888 | Oxidative stress as a potential pathogenic mechanism in an animal model of Duchenne muscular dystrophy |
Q35178696 | Properties of single FDB fibers following a collagenase digestion for studying contractility, fatigue, and pCa-sarcomere shortening relationship |
Q42509275 | Quantitative Ratiometric Ca2+ Imaging to Assess Cell Viability. |
Q45271630 | Reactive oxygen species reduce myofibrillar Ca2+ sensitivity in fatiguing mouse skeletal muscle at 37 degrees C. |
Q44278240 | Reduced contraction strength with increased intracellular [Ca2+] in left ventricular trabeculae from failing rat hearts |
Q35873884 | Regulation of cytosolic calcium in skeletal muscle cells of the mdx mouse under conditions of stress |
Q88404622 | Role of Ca2+ in changing active force during intermittent submaximal stimulation in intact, single mouse muscle fibers |
Q35893242 | The decrease of expression of ryanodine receptor sub-type 2 is reversed by gentamycin sulphate in vascular myocytes from mdx mice |
Q41701568 | The oculomotor periphery: the clinician's focus is no longer a basic science stepchild |
Q78083462 | The role of calcium stores in fatigue of isolated single muscle fibres from the cane toad |
Q73396317 | Time course of calcium transients derived from Fura-2 fluorescence measurements in single fast twitch fibres of adult mice and rat myotubes developing in primary culture |
Q71471001 | Total and sarcoplasmic reticulum calcium contents of skinned fibres from rat skeletal muscle |
Q33836366 | Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse |
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