| scholarly article | Q13442814 |
| P356 | DOI | 10.1152/AJPCELL.1996.271.4.C1325 |
| P698 | PubMed publication ID | 8897840 |
| P2093 | author name string | P Reddy | |
| R A Steinhardt | |||
| W F Denetclaw | |||
| P R Turner | |||
| F W Hopf | |||
| P2860 | cites work | Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity | Q45874117 |
| Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice | Q46266620 | ||
| Functional expression of a rapidly inactivating neuronal calcium channel | Q46427777 | ||
| Calcium entry through stretch-inactivated ion channels in mdx myotubes | Q46603395 | ||
| Functional diversity of L-type calcium channels in rat cerebellar neurons | Q48326006 | ||
| Developmental regulation of mechanosensitive calcium channels in skeletal muscle from normal and mdx mice. | Q52235615 | ||
| Barium- and calcium-permeable channels open at negative membrane potentials in rat ventricular myocytes. | Q54105106 | ||
| Dystrophin expression in myotubes formed by the fusion of normal and dystrophic myoblasts | Q33517754 | ||
| Myotubes from transgenic mdx mice expressing full-length dystrophin show normal calcium regulation | Q34445717 | ||
| Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse | Q35009267 | ||
| Dystrophin protects the sarcolemma from stresses developed during muscle contraction | Q36259954 | ||
| Fura-2 measurement of cytosolic free Ca2+ in monolayers and suspensions of various types of animal cells | Q36473522 | ||
| Changes in cytosolic resting ionized calcium level and in calcium transients during in vitro development of normal and Duchenne muscular dystrophy cultured skeletal muscle measured by laser cytofluorimetry using indo-1. | Q36773101 | ||
| New fluorescent calcium indicators designed for cytosolic retention or measuring calcium near membranes | Q36793083 | ||
| Mechanisms of Exercise-Induced Muscle Fibre Injury | Q36937768 | ||
| Calcium channels, stores, and oscillations | Q37902933 | ||
| Assessment of Fura-2 for measurements of cytosolic free calcium | Q37932223 | ||
| Fluorescent probes of cell signaling | Q38613270 | ||
| Muscular dystrophy and activation of proteinases | Q39249665 | ||
| Expression of the putative Duchenne muscular dystrophy gene in differentiated myogenic cell cultures and in the brain | Q39707657 | ||
| The structural and functional diversity of dystrophin | Q40644356 | ||
| Accumulation of calcium by normal and dystrophin-deficient mouse muscle during contractile activity in vitro | Q41083740 | ||
| Regulation of cytosolic Ca2+ in clonal human muscle cell cultures | Q42492425 | ||
| Calcium rises abruptly and briefly throughout the cell at the onset of anaphase | Q42525633 | ||
| Methods for calibration of fluorescent calcium indicators in skeletal muscle fibers | Q42630798 | ||
| Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin | Q44177784 | ||
| Alteration of intracellular Fura-2 fluorescence by viscosity: a simple correction | Q44434955 | ||
| P433 | issue | 4 Pt 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | C1325-39 | |
| P577 | publication date | 1996-10-01 | |
| P1433 | published in | American Journal of Physiology | Q2160146 |
| P1476 | title | A critical evaluation of resting intracellular free calcium regulation in dystrophic mdx muscle | |
| P478 | volume | 271 |
| Q36422465 | Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy. |
| Q34178063 | Ca(2+) influx and opening of Ca(2+)-activated K(+) channels in muscle fibers from control and mdx mice |
| Q73070067 | Calcium homeostasis in dystrophic muscle |
| Q54519217 | Cellular mechanism underlying the facilitation of contractile response of vas deferens smooth muscle by sodium orthovanadate. |
| Q33644573 | Characteristics of skeletal muscle in mdx mutant mice |
| Q46388856 | Comparison of the myoplasmic calcium transient elicited by an action potential in intact fibres of mdx and normal mice |
| Q36855555 | Congenital muscular dystrophies involving the O-mannose pathway |
| Q44473148 | Consequence of parvalbumin deficiency in the mdx mouse: histological, biochemical and mechanical phenotype of a new double mutant. |
| Q44424989 | Depolarization-induced contraction and SR function in mechanically skinned muscle fibers from dystrophic mdx mice |
| Q47704855 | Duchenne and Becker Muscular Dystrophies: A Review of Animal Models, Clinical End Points, and Biomarker Quantification. |
| Q52566595 | Dystrophin and the cardiomyocyte membrane cytoskeleton in the healthy and failing heart. |
| Q37263246 | Electrically silent divalent cation entries in resting and active voltage-controlled muscle fibers |
| Q35700706 | Elevated subsarcolemmal Ca2+ in mdx mouse skeletal muscle fibers detected with Ca2+-activated K+ channels. |
| Q35903075 | Evidence of a Role for Fibroblast Transient Receptor Potential Canonical 3 Ca2+ Channel in Renal Fibrosis |
| Q36293416 | Extensive but coordinated reorganization of the membrane skeleton in myofibers of dystrophic (mdx) mice |
| Q59489917 | Extrajunctional resting Ca2+ influx is not increased in a severely dystrophic expiratory muscle (triangularis sterni) of the mdx mouse |
| Q34204770 | How calcium influx through calcium leak channels is responsible for the elevated levels of calcium-dependent proteolysis in dystrophic myotubes |
| Q33581470 | Hyperactive intracellular calcium signaling associated with localized mitochondrial defects in skeletal muscle of an animal model of amyotrophic lateral sclerosis |
| Q33950422 | Identification of a neuronal nitric oxide synthase in isolated cardiac mitochondria using electrochemical detection |
| Q40542404 | Improvement of calcium handling and changes in calcium-release properties after mini- or full-length dystrophin forced expression in cultured skeletal myotubes |
| Q40682466 | Increase in cytosolic Ca2+ induced by elevation of extracellular Ca2+ in skeletal myogenic cells. |
| Q37011991 | Interactions between sarco-endoplasmic reticulum and mitochondria in cardiac and skeletal muscle - pivotal roles in Ca²⁺ and reactive oxygen species signaling |
| Q73087615 | Intracellular calcium signals measured with indo-1 in isolated skeletal muscle fibres from control and mdx mice |
| Q41882302 | Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers |
| Q30813768 | Large-scale analysis of differential gene expression in the hindlimb muscles and diaphragm of mdx mouse |
| 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 |
| Q33950716 | Mechanisms of muscle weakness in muscular dystrophy |
| Q28593398 | Mice lacking Homer 1 exhibit a skeletal myopathy characterized by abnormal transient receptor potential channel activity |
| Q38901391 | Mitochondrial Ca(2+) uptake in skeletal muscle health and disease. |
| Q57286631 | Muscle membrane integrity in Duchenne muscular dystrophy: recent advances in copolymer-based muscle membrane stabilizers |
| Q77129602 | Muscular degeneration in the absence of dystrophin is a calcium-dependent process |
| Q39546119 | Na+ dysregulation coupled with Ca2+ entry through NCX1 promotes muscular dystrophy in mice |
| Q43565183 | Nifedipine-activated Ca(2+) permeability in newborn rat cortical collecting duct cells in primary culture |
| Q73778888 | Oxidative stress as a potential pathogenic mechanism in an animal model of Duchenne muscular dystrophy |
| Q82037630 | Posttetanic potentiation in mdx muscle |
| Q35048538 | Role of basal extracellular Ca2+ entry during 5-HT-induced vasoconstriction of canine pulmonary arteries |
| Q36549710 | RyR isoforms and fibre type-specific expression of proteins controlling intracellular calcium concentration in skeletal muscles |
| Q36549694 | Sarcolemmal ion channels in dystrophin-deficient skeletal muscle fibres |
| Q44400229 | Store operated Ca2+ influx by selective depletion of ryanodine sensitive Ca2+ pools in primary human skeletal muscle cells |
| Q42934651 | Synthesis and properties of Asante Calcium Red--a novel family of long excitation wavelength calcium indicators |
| Q33828179 | Systems analysis of biological networks in skeletal muscle function. |
| Q39529041 | The heart in Duchenne muscular dystrophy: early detection of contractile performance alteration |
| Q41701568 | The oculomotor periphery: the clinician's focus is no longer a basic science stepchild |
| Q34800803 | The role of proteases in excitation-contraction coupling failure in muscular dystrophy |
| 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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