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Two mechanisms for spontaneous recovery from depolarising drugs in rat muscle.
Nature. 1976 Jun 3;261(5559):416-7
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Characteristics of postjunctional carbamylcholine receptor activation and inhibition.
Am J Physiol. 1972 Mar;222(3):793-9
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The energy requirement for sodium extrusion from a frog muscle.
Proc R Soc Lond B Biol Sci. 1954 May 27;142(908):383-92
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Influence of chloride ions on changes in membrane potential during prolonged application of carbachol to frog skeletal muscle.
Br J Pharmacol. 1973 Feb;47(2):363-76
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Does curare affect transmitter release?
J Physiol. 1971 Mar;213(3):691-705
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The ultrastructure of the neuromuscular junctions of mammalian red, white, and intermediate skeletal muscle fibers.
J Cell Biol. 1970 Jul;46(1):27-41
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The distribution of acetylcholine sensitivity at the post-synaptic membrane of vertebrate skeletal twitch muscles: iontophoretic mapping in the micron range.
J Physiol. 1975 Jan;244(3):703-30
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Sodium entry in rat diaphragm induced by depolarizing drugs.
J Physiol. 1977 Nov;272(2):295-316
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Sodium fluxes in diaphragm muscle and the effects of insulin and serum proteins.
J Physiol. 1968 Jul;197(2):255-78
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Potassium induced potential changes in rat diaphragm muscle.
Pflugers Arch. 1976 Mar 11;362(1):69-79
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The M. omohyoideus of the mouse as a convenient mammalian muscle preparation. A study of junctional and extrajunctional acetylcholine receptors by noise analysis and cooperativity.
Pflugers Arch. 1976 Dec 28;367(2):115-22
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Microcalorimetric determination of energy expenditure due to active sodium-potassium transport in the soleus muscle and brown adipose tissue of the rat.
J Physiol. 1977 Feb;265(1):43-61
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A study of the desensitization produced by acetylcholine at the motor end-plate.
J Physiol. 1957 Aug 29;138(1):63-80
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The effect of voltage on the time course of end-plate currents.
J Physiol. 1972 May;223(1):151-71
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Maintenance of isolated diaphragm with normal sodium content.
J Physiol. 1961 Feb;155:343-57
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The effect of calcium on the desensitization of membrane receptors at the neuromuscular junction.
J Gen Physiol. 1966 May;49(5):963-76
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An investigation of spontaneous activity at the neuromuscular junction of the rat.
J Physiol. 1956 Jun 28;132(3):650-66
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Neuromuscular transmission in potassium-free Krebs solution.
J Physiol. 1972 Oct;226(2):95P-96P
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Mechanisms of neuromuscular blockade.
Ann N Y Acad Sci. 1971 Sep 15;183:171-82
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Voltage clamping of unparalysed cut rat diaphragm for study of transmitter release.
J Physiol. 1979 May;290(2):467-80
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Resting potentials of diaphragm muscle after prolonged anoxia.
J Physiol. 1958 Feb 17;140(2):301-17
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Location of end-plates in rat diaphragm by the use of polarizing filters [proceedings].
J Physiol. 1979 Jun;291:10P-11P
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Electrogenic sodium pump in nerve and muscle cells.
Physiol Rev. 1972 Jul;52(3):563-94
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A further analysis of the neuromuscular block caused by acetylcholine.
Acta Physiol Scand. 1956 Nov 5;37(4):330-4
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The membrane potential of rat diaphragm muscle fibres and the effect of denervation.
J Physiol. 1976 Mar;255(3):651-67
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Neuromuscular transmission in vivo and the actions of decamethonium: a micro-electrode study.
Acta Anaesthesiol Scand. 1965;9(3):165-72
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Localization of active spots within the neuromuscular junction of the frog.
J Physiol. 1956 Jun 28;132(3):630-49
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Influence of SKF-525A congeners, strophanthidin and tissue-culture media on desensitization in frog skeletal muscle.
Br J Pharmacol. 1974 Jun;51(2):259-68
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The effect of catecholamines on Na-K transport and membrane potential in rat soleus muscle.
J Physiol. 1977 Sep;270(2):383-414
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The effects of acetylcholine, decamethonium and succinylcholine on neuromuscular transmission in the rat.
Acta Physiol Scand. 1955 Oct 12;34(4):386-92
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