| scholarly article | Q13442814 |
| P2093 | author name string | Turner PR | |
| Steinhardt RA | |||
| Fong PY | |||
| Denetclaw WF | |||
| P2860 | cites work | Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches | Q22337395 |
| The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle | Q24297845 | ||
| A new generation of Ca2+ indicators with greatly improved fluorescence properties | Q27860793 | ||
| X chromosome-linked muscular dystrophy (mdx) in the mouse | Q28589078 | ||
| Simultaneous recording of calcium transients in skeletal muscle using high- and low-affinity calcium indicators | Q34260376 | ||
| Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse | Q35009267 | ||
| Regulation of cortical vesicle exocytosis in sea urchin eggs by inositol 1,4,5-trisphosphate and GTP-binding protein | Q36214084 | ||
| Calcium gradients in single smooth muscle cells revealed by the digital imaging microscope using Fura-2. | Q36491669 | ||
| Parvalbumin, molecular and functional aspects | Q37931708 | ||
| Assessment of Fura-2 for measurements of cytosolic free calcium | Q37932223 | ||
| Calcium regulation in muscle diseases; the influence of innervation and activity | Q38630177 | ||
| Cytosolic Ca2+ gradients triggering unidirectional fluid secretion from exocrine pancreas | Q39243929 | ||
| Fluorescence measurements of cytosolic free Na concentration, influx and efflux in gastric cells | Q39244153 | ||
| Role of intracellular calcium in promoting muscle damage: A strategy for controlling the dystrophic condition | Q39782584 | ||
| The selectivity of ion channels in nerve and muscle | Q40131210 | ||
| Multiple conductance levels of the dihydropyridine-sensitive calcium channel in GH3 cells | Q41717271 | ||
| Stretch-sensitive channels in developing muscle cells from a mouse cell line | Q41726414 | ||
| Simultaneous monitoring of changes in magnesium and calcium concentrations in frog cut twitch fibers containing antipyrylazo III. | Q41889015 | ||
| Fluorescence ratio imaging of cytosolic free Na+ in individual fibroblasts and lymphocytes | Q42490771 | ||
| Satellite cells from dystrophic (mdx) mouse muscle are stimulated by fibroblast growth factor in vitro | Q42515527 | ||
| Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma | Q43107646 | ||
| [3H]nitrendipine receptors as markers of a class of putative voltage-sensitive Ca2+ channels in normal human skeletal muscle and in muscle from Duchenne muscular dystrophy patients | Q44109181 | ||
| Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin | Q44177784 | ||
| Fluorescent indicators for cytosolic sodium. | Q45932889 | ||
| Fluorescent indicators for cytosolic calcium based on rhodamine and fluorescein chromophores | Q46089769 | ||
| Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice | Q46266620 | ||
| Calcium entry through stretch-inactivated ion channels in mdx myotubes | Q46603395 | ||
| Photochemically generated cytosolic calcium pulses and their detection by fluo-3. | Q46892671 | ||
| The use of Fura-2 to estimate myoplasmic [Ca2+] in human skeletal muscle. | Q51754798 | ||
| Association of dystrophin and an integral membrane glycoprotein. | Q52485843 | ||
| Barium- and calcium-permeable channels open at negative membrane potentials in rat ventricular myocytes. | Q54105106 | ||
| Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells | Q59073603 | ||
| Fura-2 calcium transients in frog skeletal muscle fibres | Q68105485 | ||
| Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patients | Q68278618 | ||
| Resting calcium concentrations in isolated skeletal muscle fibres of dystrophic mice | Q68589242 | ||
| Voltage-dependent channels of human muscle cultures | Q68958939 | ||
| Altered regulation of airway epithelial cell chloride channels in cystic fibrosis | Q68967044 | ||
| Intracellular sodium-activity at rest and after tetanic stimulation in muscles of normal and dystrophic (dy2J/dy2J) C57BL/6J mice | Q69568623 | ||
| Relations between chronic stimulation-induced changes in contractile properties and the Ca2+-sequestering system of rat and rabbit fast-twitch muscles | Q69794393 | ||
| Neutral carrier ion-selective microelectrodes for measurement of intracellular free calcium | Q71289916 | ||
| Muscle calcium and magnesium content in Duchenne muscular dystrophy | Q71840156 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 12 | |
| P304 | page(s) | 1701-1712 | |
| P577 | publication date | 1991-12-01 | |
| P1433 | published in | Journal of Cell Biology | Q1524550 |
| P1476 | title | Increased calcium influx in dystrophic muscle | |
| P478 | volume | 115 |
| Q41078211 | 23Na MRI and myometry to compare eplerenone vs. glucocorticoid treatment in Duchenne dystrophy |
| Q36232550 | A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. |
| Q28297222 | Absence of alpha 7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy |
| Q92932547 | Adenylosuccinic acid therapy ameliorates murine Duchenne Muscular Dystrophy |
| Q28354192 | Alteration of excitation-contraction coupling mechanism in extensor digitorum longus muscle fibres of dystrophic mdx mouse and potential efficacy of taurine |
| Q34106079 | Alterations in the expression of leukemia inhibitory factor following exercise: comparisons between wild-type and mdx muscles |
| Q36878041 | Altered calcium pump and secondary deficiency of gamma-sarcoglycan and microspan in sarcoplasmic reticulum membranes isolated from delta-sarcoglycan knockout mice. |
| Q36915922 | Animal models of muscular dystrophy |
| Q46271408 | Apoptosis precedes necrosis of dystrophin-deficient muscle |
| Q28511114 | Apoptosis repressor with a CARD domain (ARC) restrains Bax-mediated pathogenesis in dystrophic skeletal muscle |
| Q24795418 | Brain dystrophin-glycoprotein complex: persistent expression of beta-dystroglycan, impaired oligomerization of Dp71 and up-regulation of utrophins in animal models of muscular dystrophy |
| Q34178063 | Ca(2+) influx and opening of Ca(2+)-activated K(+) channels in muscle fibers from control and mdx mice |
| Q24241080 | Calcium antagonists for Duchenne muscular dystrophy |
| Q24247587 | Calcium antagonists for Duchenne muscular dystrophy |
| Q34283184 | Calcium indicators and calcium signalling in skeletal muscle fibres during excitation-contraction coupling |
| Q37419160 | Calcium influx is sufficient to induce muscular dystrophy through a TRPC-dependent mechanism |
| Q38103213 | Cardiac and respiratory dysfunction in Duchenne muscular dystrophy and the role of second messengers. |
| Q36691646 | Cardiomyopathy of Duchenne muscular dystrophy: pathogenesis and prospect of membrane sealants as a new therapeutic approach |
| Q42641718 | Cationic channels in normal and dystrophic human myotubes |
| Q54519217 | Cellular mechanism underlying the facilitation of contractile response of vas deferens smooth muscle by sodium orthovanadate. |
| Q35660362 | Chronic administration of a leupeptin-derived calpain inhibitor fails to ameliorate severe muscle pathology in a canine model of duchenne muscular dystrophy |
| Q46388856 | Comparison of the myoplasmic calcium transient elicited by an action potential in intact fibres of mdx and normal mice |
| Q39314141 | Constitutive calcium entry and cancer: updated views and insights. |
| Q48415548 | Cortical and brainstem neurons containing calcium-binding proteins in a murine model of Duchenne's muscular dystrophy: selective changes in the sensorimotor cortex. |
| Q42522517 | Cultured rat skeletal muscle cells treated with cytochalasin exhibit normal dystrophin expression and intracellular free calcium control |
| Q72565069 | Decreased rates of Ca(2+)-dependent heat production in slow- and fast-twitch muscles from the dystrophic (mdx) mouse |
| Q42494294 | Defective regulation of energy metabolism in mdx-mouse skeletal muscles |
| Q70915847 | Dihydropyridine receptors in transverse tubules from normal and dystrophic chicken skeletal muscle |
| Q35169510 | Distinct pathophysiological mechanisms of cardiomyopathy in hearts lacking dystrophin or the sarcoglycan complex |
| Q46604988 | Dystrophic heart failure blocked by membrane sealant poloxamer |
| Q40883565 | Dystrophin and the membrane skeleton |
| Q42755001 | Dystrophin deficiency is associated with myotendinous junction defects in prenecrotic and fully regenerated skeletal muscle. |
| Q39205845 | Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretion |
| Q70765933 | Dystrophin expression in the human retina is required for normal function as defined by electroretinography |
| Q60533862 | Dystrophin is not essential for the integrity of the cytoskeleton |
| Q35700706 | Elevated subsarcolemmal Ca2+ in mdx mouse skeletal muscle fibers detected with Ca2+-activated K+ channels. |
| Q38111711 | Exercise and muscular dystrophy: implications and analysis of effects on musculoskeletal and cardiovascular systems |
| Q73851362 | Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice |
| Q40474236 | Extraocular muscles: Basic and clinical aspects of structure and function |
| Q48261529 | Failure to make normal alpha ryanodine receptor is an early event associated with the crooked neck dwarf (cn) mutation in chicken |
| Q79171939 | Gadolinium reduces short-term stretch-induced muscle damage in isolated mdx mouse muscle fibres |
| Q52909513 | Gender differences in skeletal muscle fibre damage after eccentrically biased downhill running in rats. |
| Q28085320 | Genetic evidence in the mouse solidifies the calcium hypothesis of myofiber death in muscular dystrophy |
| Q36757538 | Heterokaryon myotubes with normal mouse and Duchenne nuclei exhibit sarcolemmal dystrophin staining and efficient intracellular free calcium control. |
| Q34204770 | How calcium influx through calcium leak channels is responsible for the elevated levels of calcium-dependent proteolysis in dystrophic myotubes |
| Q24308714 | Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle |
| Q77959497 | Hypotonic medium increases calcium permeant channels activity in human normal and dystrophic myotubes |
| 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 |
| Q44826878 | Increased sarcolipin expression and decreased sarco(endo)plasmic reticulum Ca2+ uptake in skeletal muscles of mouse models of Duchenne muscular dystrophy |
| Q27438151 | Inhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expression |
| Q37056368 | Insights into bone health in Duchenne muscular dystrophy |
| Q72111438 | Intracellular Ca2+ concentrations are not elevated in resting cultured muscle from Duchenne (DMD) patients and in MDX mouse muscle fibres |
| Q73087615 | Intracellular calcium signals measured with indo-1 in isolated skeletal muscle fibres from control and mdx mice |
| Q44006756 | Intracellular pH regulation in isolated fast-twitch skeletal muscle from dystrophin-deficient mouse |
| Q33339391 | L-type Ca2+ channel function is linked to dystrophin expression in mammalian muscle |
| Q70671305 | Lack of dystrophin but normal calcium homeostasis in smooth muscle from dystrophic mdx mice |
| 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 |
| Q74558580 | Long-term study of Ca(2+) homeostasis and of survival in collagenase-isolated muscle fibres from normal and mdx mice |
| Q41432538 | Loss, restoration, and maintenance of plasma membrane integrity |
| Q74529467 | Mdx myotubes have normal excitability but show reduced contraction-relaxation dynamics |
| Q36235185 | Mechanical function of dystrophin in muscle cells |
| Q33950716 | Mechanisms of muscle weakness in muscular dystrophy |
| Q36185924 | Mechanisms of stretch-induced muscle damage in normal and dystrophic muscle: role of ionic changes. |
| Q72681998 | Membrane potential, resting calcium and calcium transients in isolated muscle fibres from normal and dystrophic mice |
| Q26772002 | Metabogenic and Nutriceutical Approaches to Address Energy Dysregulation and Skeletal Muscle Wasting in Duchenne Muscular Dystrophy |
| Q44640506 | Mini-dystrophin restores L-type calcium currents in skeletal muscle of transgenic mdx mice. |
| Q34627089 | Mitigation of muscular dystrophy in mice by SERCA overexpression in skeletal muscle |
| Q37428682 | Mitochondrial alterations and oxidative stress in an acute transient mouse model of muscle degeneration: implications for muscular dystrophy and related muscle pathologies. |
| Q35873186 | Modulation by prednisolone of calcium handling in skeletal muscle cells. |
| Q70680908 | Monoclonal antibodies targeted against the C-terminal domain of dystrophin or utrophin |
| Q74702690 | Multivariate evaluation of the functional recovery obtained by the overexpression of utrophin in skeletal muscles of the mdx mouse |
| Q74495850 | Muscle cells from mdx mice have an increased susceptibility to oxidative stress |
| Q35630800 | Muscle degeneration without mechanical injury in sarcoglycan deficiency |
| Q38329774 | Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of Ca(V)1.1 calcium channel |
| Q35928235 | Mutation of delta-sarcoglycan is associated with Ca(2+) -dependent vascular remodeling in the Syrian hamster |
| Q37368276 | Myonuclear apoptosis in dystrophic mdx muscle occurs by perforin-mediated cytotoxicity |
| Q34445717 | Myotubes from transgenic mdx mice expressing full-length dystrophin show normal calcium regulation |
| Q72798826 | N-terminal domain of dystrophin |
| Q51781252 | NO may prompt calcium leakage in dystrophic muscle. |
| Q44122960 | Na(+)/Ca(2+) exchange in human myotubes: intracellular calcium rises in response to external sodium depletion are enhanced in DMD. |
| Q39546119 | Na+ dysregulation coupled with Ca2+ entry through NCX1 promotes muscular dystrophy in mice |
| 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 |
| Q34807192 | Pharmacological control of cellular calcium handling in dystrophic skeletal muscle |
| Q71857802 | Phenotype of dystrophinopathy in old MDX mice |
| Q89723303 | Pigs with δ-sarcoglycan deficiency exhibit traits of genetic cardiomyopathy |
| Q34271469 | Plasma Membrane Disruption: Repair, Prevention, Adaptation |
| Q28296676 | Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix |
| Q46669833 | Propagation in the transverse tubular system and voltage dependence of calcium release in normal and mdx mouse muscle fibres |
| Q45982332 | Proteolysis results in altered leak channel kinetics and elevated free calcium in mdx muscle. |
| Q42035368 | Re-evaluation of the distributions of dystrophin and utrophin in sciatic nerve |
| Q35873884 | Regulation of cytosolic calcium in skeletal muscle cells of the mdx mouse under conditions of stress |
| Q47665947 | Ryanodine channel complex stabilizer compound S48168/ARM210 as a disease modifier in dystrophin-deficient mdx mice: proof-of-concept study and independent validation of efficacy |
| Q33840940 | Sarcoglycans in muscular dystrophy |
| Q79733822 | Sarcoplasmic reticulum Ca2+ release and depletion fail to affect sarcolemmal ion channel activity in mouse skeletal muscle |
| Q52277880 | Similarity of ATP-dependent K+ channels in skeletal muscle fibres from normal and mutant mdx mice. |
| Q39905014 | Specific knockdown of delta-sarcoglycan gene in C2C12 in vitro causes post-translational loss of other sarcoglycans without mechanical stress |
| Q35903669 | The Effects of Experimental Sleep Apnea on Cardiac and Respiratory Functions in 6 and 18 Month Old Dystrophic (mdx) Mice |
| Q36031274 | The absence of dysferlin induces the expression of functional connexin-based hemichannels in human myotubes |
| Q44788698 | The action potential-evoked sarcoplasmic reticulum calcium release is impaired in mdx mouse muscle fibres |
| Q40500531 | The dystrophin superfamily: variability and complexity |
| Q41738877 | The molecular basis of activity-induced muscle injury in Duchenne muscular dystrophy |
| Q41701568 | The oculomotor periphery: the clinician's focus is no longer a basic science stepchild |
| Q38654037 | The role of mechanobiology in progression of rotator cuff muscle atrophy and degeneration |
| Q34800803 | The role of proteases in excitation-contraction coupling failure in muscular dystrophy |
| Q77587714 | The therapeutic potential of oral creatine supplementation in muscle disease |
| Q53946062 | The tubular vacuolation process in amphibian skeletal muscle. |
| Q48309004 | Touch channels sense blood pressure. |
| Q33836366 | Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse |
| Q50657212 | [Current care strategies for Duchenne muscular dystrophy]. |
| Q73080448 | [Molecular pathogenesis of muscular diseases] |
| Q52581401 | rAAV6-microdystrophin rescues aberrant Golgi complex organization in mdx skeletal muscles. |
Search more.