Cultured muscle from myotonic muscular dystrophy patients: altered membrane electrical properties

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Cultured muscle from myotonic muscular dystrophy patients: altered membrane electrical properties is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode1981PNAS...78..648M
P356DOI10.1073/PNAS.78.1.648
P932PMC publication ID319112
P698PubMed publication ID6941262
P5875ResearchGate publication ID16258296

P2093author name stringGray R
Appel S
Chauvin P
Merickel M
P2860cites workDestruction of sodium conductance inactivation in squid axons perfused with pronaseQ24655917
Sodium, Potassium, and Chloride Fluxes in Intercostal Muscle from Normal Goats and Goats with Hereditary MyotoniaQ24656067
Cable parameters, sodium, potassium, chloride, and water content, and potassium efflux in isolated external intercostal muscle of normal volunteers and patients with myotonia congenitaQ34064967
EFFECTS OF VARIOUS POTASSIUM SALTS AND PROTEASES UPON EXCITABILITY OF INTRACELLULARLY PERFUSED SQUID GIANT AXONSQ34413169
Scanning Electron Microscopy Studies in Muscular DystrophyQ39080078
The electrical properties of muscle fiber membranes in dystrophia myotonica and myotonia congenitaQ39443849
Effects of motor nerve anesthesia and tenotomy on muscle membrane propertiesQ43461216
Electrophysiologic properties of intercostal muscle fibers in human neuromuscular diseasesQ43869949
A quantitative technique for growing human adult skeletal muscle in culture starting from mononucleated cellsQ43878653
Growth of human muscle in tissue culture. An improved techniqueQ45106394
Electrophysiology of hippocampal neurons. II. After-potentials and repetitive firing.Q51302393
Electrical properties of chick skeletal muscle fibers developing in cell cultureQ52997888
Myotonic Muscular Dystrophy: Altered Calcium Transport in ErythrocytesQ67312904
A study of individual neuro-muscular junctions in myotoniaQ70068945
Design of a single electrode voltage clampQ71069670
Application of the freeze fracture technique to the study of human neuromuscular diseaseQ71193417
Delayed depolarization in cat spinal motoneuronsQ72206892
Pattern of regeneration of muscle from progressive muscular dystrophy patients cultivated in vitro as compared to normal human skeletal muscleQ74659739
Multiple-spike discharge evoking after-depolarizations in the slowly adapting stretch receptor neuron of the lobster. II. The slow after-depolarizationQ95800672
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectmuscular dystrophyQ1137767
electrical propertiesQ110583288
P1104number of pages5
P304page(s)648-652
P577publication date1981-01-01
P1433published inProceedings of the National Academy of Sciences of the United States of AmericaQ1146531
P1476titleCultured muscle from myotonic muscular dystrophy patients: altered membrane electrical properties
P478volume78

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cites work (P2860)
Q36022588A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ Release
Q67912803Abnormal M-wave responses during exercise in myotonic muscular dystrophy: A Na+-K+ pump defect?
Q45553677Alglucosidase alfa enzyme replacement therapy as a therapeutic approach for glycogen storage disease type III.
Q67699845Altered Na+ channel activity and reduced Cl? conductance cause hyperexcitability in recessive generalized myotonia (becker)
Q54095533Characteristics of Na+ channels and Cl- conductance in resealed muscle fibre segments from patients with myotonic dystrophy
Q69242857Cultivation, morphology, and electrophysiology of contractile rat myoballs
Q42181355Deficiency of Na+/K(+)-ATPase and sarcoplasmic reticulum Ca(2+)-ATPase in skeletal muscle and cultured muscle cells of myotonic dystrophy patients
Q47950306Expression of apamin receptor in muscles of patients with myotonic muscular dystrophy
Q41878069In vivo assessment of muscle membrane properties in myotonic dystrophy
Q36715356Ionic transporting systems of skeletal muscle in relation with innervation and their involvement in myotonic diseases
Q28588083Myotonic dystrophy protein kinase is involved in the modulation of the Ca2+ homeostasis in skeletal muscle cells
Q34071934Physiologic basis of potentials recorded in electromyography
Q37007575Sodium Channel and Sodium Pump in Normal and Pathological Muscles from Patients with Myotonic Muscular Dystrophy and Lower Motor Neuron Impairment
Q37683689The all-or-none role of innervation in expression of apamin receptor and of apamin-sensitive Ca2+-activated K+ channel in mammalian skeletal muscle

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