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. 1986;371(Suppl):149P–203P.

Proceedings of the Physiological Society, 12-14 September 1985, Cambridge Meeting: Communications

Part III

PMCID: PMC1192738

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Abercrombie R. F., Putnam R. W., Roos A. The intracellular pH of frog skeletal muscle: its regulation in isotonic solutions. J Physiol. 1983 Dec;345:175–187. doi: 10.1113/jphysiol.1983.sp014973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ashley C. C., Lea T. J. Proceedings: The influx of labelled amino acids into single muscle fibres of the barnacle Balanus nubilus. J Physiol. 1976 Jul;259(1):43P–44P. [PubMed] [Google Scholar]
  3. Bartschat D. K., Blaustein M. P. Potassium channels in isolated presynaptic nerve terminals from rat brain. J Physiol. 1985 Apr;361:419–440. doi: 10.1113/jphysiol.1985.sp015653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bean B. P. Nitrendipine block of cardiac calcium channels: high-affinity binding to the inactivated state. Proc Natl Acad Sci U S A. 1984 Oct;81(20):6388–6392. doi: 10.1073/pnas.81.20.6388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bell F. R., Drury P. L., Sly J. The effect on salt appetite and the renin-aldosterone system on replacing the depleted ions to sodium-deficient cattle. J Physiol. 1981;313:263–274. doi: 10.1113/jphysiol.1981.sp013663. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Benham C. D., Bolton T. B., Lang R. J. Acetylcholine activates an inward current in single mammalian smooth muscle cells. Nature. 1985 Jul 25;316(6026):345–347. doi: 10.1038/316345a0. [DOI] [PubMed] [Google Scholar]
  7. Berglindh T., Dibona D. R., Ito S., Sachs G. Probes of parietal cell function. Am J Physiol. 1980 Mar;238(3):G165–G176. doi: 10.1152/ajpgi.1980.238.3.G165. [DOI] [PubMed] [Google Scholar]
  8. Bers D. M. Early transient depletion of extracellular Ca during individual cardiac muscle contractions. Am J Physiol. 1983 Mar;244(3):H462–H468. doi: 10.1152/ajpheart.1983.244.3.H462. [DOI] [PubMed] [Google Scholar]
  9. Bolton T. B., Vaughan-Jones R. D. Continuous direct measurement of intracellular chloride and pH in frog skeletal muscle. J Physiol. 1977 Sep;270(3):801–833. doi: 10.1113/jphysiol.1977.sp011983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Burckhardt B. C., Sato K., Frömter E. Electrophysiological analysis of bicarbonate permeation across the peritubular cell membrane of rat kidney proximal tubule. I. Basic observations. Pflugers Arch. 1984 May;401(1):34–42. doi: 10.1007/BF00581530. [DOI] [PubMed] [Google Scholar]
  11. Butcher R. L., Collins W. E., Fugo N. W. Plasma concentration of LH, FSH, prolactin, progesterone and estradiol-17beta throughout the 4-day estrous cycle of the rat. Endocrinology. 1974 Jun;94(6):1704–1708. doi: 10.1210/endo-94-6-1704. [DOI] [PubMed] [Google Scholar]
  12. Cachelin A. B., De Peyer J. E., Kokubun S., Reuter H. Sodium channels in cultured cardiac cells. J Physiol. 1983 Jul;340:389–401. doi: 10.1113/jphysiol.1983.sp014768. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Capogrossi M. C., Lakatta E. G. Frequency modulation and synchronization of spontaneous oscillations in cardiac cells. Am J Physiol. 1985 Mar;248(3 Pt 2):H412–H418. doi: 10.1152/ajpheart.1985.248.3.H412. [DOI] [PubMed] [Google Scholar]
  14. Capogrossi M. C., Lakatta E. G. Frequency modulation and synchronization of spontaneous oscillations in cardiac cells. Am J Physiol. 1985 Mar;248(3 Pt 2):H412–H418. doi: 10.1152/ajpheart.1985.248.3.H412. [DOI] [PubMed] [Google Scholar]
  15. Chacko S., Rosenfeld A. Regulation of actin-activated ATP hydrolysis by arterial myosin. Proc Natl Acad Sci U S A. 1982 Jan;79(2):292–296. doi: 10.1073/pnas.79.2.292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Chapman R. A., Miller D. J. Structure-activity relations for caffeine: a comparative study of the inotropic effects of the methylxanthines, imidazoles and related compounds on the frog's heart. J Physiol. 1974 Nov;242(3):615–634. doi: 10.1113/jphysiol.1974.sp010726. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Cleemann L., Pizarro G., Morad M. Optical measurements of extracellular calcium depletion during a single heartbeat. Science. 1984 Oct 12;226(4671):174–177. doi: 10.1126/science.6091269. [DOI] [PubMed] [Google Scholar]
  18. Cobbold P. H., Bourne P. K. Aequorin measurements of free calcium in single heart cells. 1984 Nov 29-Dec 5Nature. 312(5993):444–446. doi: 10.1038/312444a0. [DOI] [PubMed] [Google Scholar]
  19. Crone C., Olesen S. P. Electrical resistance of brain microvascular endothelium. Brain Res. 1982 Jun 3;241(1):49–55. doi: 10.1016/0006-8993(82)91227-6. [DOI] [PubMed] [Google Scholar]
  20. Crush K. G. Carnosine and related substances in animal tissues. Comp Biochem Physiol. 1970 May 1;34(1):3–30. doi: 10.1016/0010-406x(70)90049-6. [DOI] [PubMed] [Google Scholar]
  21. Curtin N. A., Woledge R. C. A comparison of the energy balance in two successive isometric tetani of frog muscle. J Physiol. 1977 Sep;270(2):455–471. doi: 10.1113/jphysiol.1977.sp011962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Davis M. D., Hadley M. E. Pars intermedia electrical potentials: changes in spike frequency induced by regulatory factors of melanocyte stimulating hormone (MSH) secretion. Neuroendocrinology. 1978;26(5):277–282. doi: 10.1159/000122783. [DOI] [PubMed] [Google Scholar]
  23. Dawson M. J., Gadian D. G., Wilkie D. R. Mechanical relaxation rate and metabolism studied in fatiguing muscle by phosphorus nuclear magnetic resonance. J Physiol. 1980 Feb;299:465–484. doi: 10.1113/jphysiol.1980.sp013137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Dawson M. J., Gadian D. G., Wilkie D. R. Muscular fatigue investigated by phosphorus nuclear magnetic resonance. Nature. 1978 Aug 31;274(5674):861–866. doi: 10.1038/274861a0. [DOI] [PubMed] [Google Scholar]
  25. DiFrancesco D., Noble D. A model of cardiac electrical activity incorporating ionic pumps and concentration changes. Philos Trans R Soc Lond B Biol Sci. 1985 Jan 10;307(1133):353–398. doi: 10.1098/rstb.1985.0001. [DOI] [PubMed] [Google Scholar]
  26. Douglas W. W., Taraskevich P. S. Calcium component to action potentials in rat pars intermedia cells. J Physiol. 1980 Dec;309:623–630. doi: 10.1113/jphysiol.1980.sp013530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Droogmans G., Raeymaekers L., Casteels R. Electro- and pharmacomechanical coupling in the smooth muscle cells of the rabbit ear artery. J Gen Physiol. 1977 Aug;70(2):129–148. doi: 10.1085/jgp.70.2.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Dyer R. G., Mansfield S., Corbet H., Dean A. D. Fasting impairs LH secretion in female rats by activating an inhibitory opioid pathway. J Endocrinol. 1985 Apr;105(1):91–97. doi: 10.1677/joe.0.1050091. [DOI] [PubMed] [Google Scholar]
  29. Ehrenfeld J., Garcia-Romeu F., Harvey B. J. Electrogenic active proton pump in Rana esculenta skin and its role in sodium ion transport. J Physiol. 1985 Feb;359:331–355. doi: 10.1113/jphysiol.1985.sp015588. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Eisenberg R. S., McCarthy R. T., Milton R. L. Paralysis of frog skeletal muscle fibres by the calcium antagonist D-600. J Physiol. 1983 Aug;341:495–505. doi: 10.1113/jphysiol.1983.sp014819. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Eisner D. A., Lederer W. J. Na-Ca exchange: stoichiometry and electrogenicity. Am J Physiol. 1985 Mar;248(3 Pt 1):C189–C202. doi: 10.1152/ajpcell.1985.248.3.C189. [DOI] [PubMed] [Google Scholar]
  32. Elfont R. M., Epstein A. N., Fitzsimons J. T. Involvement of the renin-angiotensin system in captopril-induced sodium appetite in the rat. J Physiol. 1984 Sep;354:11–27. doi: 10.1113/jphysiol.1984.sp015359. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Ellory J. C., Jones S. E., Young J. D. Glycine transport in human erythrocytes. J Physiol. 1981 Nov;320:403–422. doi: 10.1113/jphysiol.1981.sp013958. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Elzinga G., Langewouters G. J., Westerhof N., Wiechmann A. H. Oxygen uptake of frog skeletal muscle fibres following tetanic contractions at 18 degrees C. J Physiol. 1984 Jan;346:365–377. doi: 10.1113/jphysiol.1984.sp015028. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. FALK G., FATT P. LINEAR ELECTRICAL PROPERTIES OF STRIATED MUSCLE FIBRES OBSERVED WITH INTRACELLULAR ELECTRODES. Proc R Soc Lond B Biol Sci. 1964 Apr 14;160:69–123. doi: 10.1098/rspb.1964.0030. [DOI] [PubMed] [Google Scholar]
  36. Fabiato A., Fabiato F. Contractions induced by a calcium-triggered release of calcium from the sarcoplasmic reticulum of single skinned cardiac cells. J Physiol. 1975 Aug;249(3):469–495. doi: 10.1113/jphysiol.1975.sp011026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Fabiato A., Fabiato F. Effects of pH on the myofilaments and the sarcoplasmic reticulum of skinned cells from cardiace and skeletal muscles. J Physiol. 1978 Mar;276:233–255. doi: 10.1113/jphysiol.1978.sp012231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Feltz A., Trautmann A. Desensitization at the frog neuromuscular junction: a biphasic process. J Physiol. 1982 Jan;322:257–272. doi: 10.1113/jphysiol.1982.sp014036. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Fenwick E. M., Marty A., Neher E. A patch-clamp study of bovine chromaffin cells and of their sensitivity to acetylcholine. J Physiol. 1982 Oct;331:577–597. doi: 10.1113/jphysiol.1982.sp014393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Ferreira K. T., Ferreira H. G. The regulation of volume and ion composition in frog skin. Biochim Biophys Acta. 1981 Aug 20;646(2):193–202. doi: 10.1016/0005-2736(81)90325-4. [DOI] [PubMed] [Google Scholar]
  41. Ferreira K. T. The relationship of K+ efflux at the inner surface of the isolated frog skin epithelium to the short circuit current. Biochim Biophys Acta. 1979 Jul 19;555(1):13–25. doi: 10.1016/0005-2736(79)90068-3. [DOI] [PubMed] [Google Scholar]
  42. Freund-Mercier M. J., Richard P. Electrophysiological evidence for facilitatory control of oxytocin neurones by oxytocin during suckling in the rat. J Physiol. 1984 Jul;352:447–466. doi: 10.1113/jphysiol.1984.sp015302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Gadsby D. C., Kimura J., Noma A. Voltage dependence of Na/K pump current in isolated heart cells. Nature. 1985 May 2;315(6014):63–65. doi: 10.1038/315063a0. [DOI] [PubMed] [Google Scholar]
  44. Gasko O. D., Knowles A. F., Shertzer H. G., Suolinna E. M., Racker E. The use of ion-exchange resins for studying ion transport in biological systems. Anal Biochem. 1976 May 7;72:57–65. doi: 10.1016/0003-2697(76)90506-6. [DOI] [PubMed] [Google Scholar]
  45. Grynkiewicz G., Poenie M., Tsien R. Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem. 1985 Mar 25;260(6):3440–3450. [PubMed] [Google Scholar]
  46. HODGKIN A. L., HOROWICZ P. The effect of sudden changes in ionic concentrations on the membrane potential of single muscle fibres. J Physiol. 1960 Sep;153:370–385. doi: 10.1113/jphysiol.1960.sp006540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  48. Harrison L. H., Lewis R. M. Current challenges in etiology and diagnosis of nosocomial sepsis. Urology. 1985 Jul;26(1 Suppl):8–11. [PubMed] [Google Scholar]
  49. Herzig J. W., Feile K., Rüegg J. C. Activating effects of AR-L 115 BS on the Ca2+ sensitive force, stiffness and unloaded shortening velocity (Vmax) in isolated contractile structures from mammalian heart muscle. Arzneimittelforschung. 1981;31(1A):188–191. [PubMed] [Google Scholar]
  50. Hilgemann D. W., Delay M. J., Langer G. A. Activation-dependent cumulative depletions of extracellular free calcium in guinea pig atrium measured with antipyrylazo III and tetramethylmurexide. Circ Res. 1983 Dec;53(6):779–793. doi: 10.1161/01.res.53.6.779. [DOI] [PubMed] [Google Scholar]
  51. Hodson S. Inadequacy of aldehyde fixatives in preserving the ultrastructure of corneal endothelium in rabbit and monkey. Exp Eye Res. 1968 Apr;7(2):221–224. doi: 10.1016/s0014-4835(68)80070-3. [DOI] [PubMed] [Google Scholar]
  52. Hodson S., Wigham C. The permeability of rabbit and human corneal endothelium. J Physiol. 1983 Sep;342:409–419. doi: 10.1113/jphysiol.1983.sp014859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Holzbauer M., Muscholl E., Racké K., Sharman D. F. Evidence that dopamine is a neurotransmitter in the neurointermediate lobe of the hypophysis. Prog Brain Res. 1983;60:357–364. doi: 10.1016/S0079-6123(08)64403-9. [DOI] [PubMed] [Google Scholar]
  54. Iwatsuki N., Petersen O. H. Action of tetraethylammonium on calcium-activated potassium channels in pig pancreatic acinar cells studied by patch-clamp single-channel and whole-cell current recording. J Membr Biol. 1985;86(2):139–144. doi: 10.1007/BF01870780. [DOI] [PubMed] [Google Scholar]
  55. KATZ B., THESLEFF S. A study of the desensitization produced by acetylcholine at the motor end-plate. J Physiol. 1957 Aug 29;138(1):63–80. doi: 10.1113/jphysiol.1957.sp005838. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Kammermeier H., Schmidt P., Jüngling E. Free energy change of ATP-hydrolysis: a causal factor of early hypoxic failure of the myocardium? J Mol Cell Cardiol. 1982 May;14(5):267–277. doi: 10.1016/0022-2828(82)90205-x. [DOI] [PubMed] [Google Scholar]
  57. Klyce S. D. Stromal lactate accumulation can account for corneal oedema osmotically following epithelial hypoxia in the rabbit. J Physiol. 1981 Dec;321:49–64. doi: 10.1113/jphysiol.1981.sp013971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Knight D. E., Baker P. F. Calcium-dependence of catecholamine release from bovine adrenal medullary cells after exposure to intense electric fields. J Membr Biol. 1982;68(2):107–140. doi: 10.1007/BF01872259. [DOI] [PubMed] [Google Scholar]
  59. Kraicer J., Morris A. R. In vitro release of ACTH from dispersed rat pars intermedia cells. II. Effect of neurotransmitter substances. Neuroendocrinology. 1976;21(2):175–192. doi: 10.1159/000122524. [DOI] [PubMed] [Google Scholar]
  60. Kuroda Y., Ikoma T. N-acetylhistidine isolated from frog heart. Science. 1966 May 27;152(3726):1241–1242. doi: 10.1126/science.152.3726.1241. [DOI] [PubMed] [Google Scholar]
  61. Lewis C. E., Morris J. F., Fink G. The role of microfilaments in the priming effect of LH-releasing hormone: an ultrastructural study using cytochalasin B. J Endocrinol. 1985 Aug;106(2):211–218. doi: 10.1677/joe.0.1060211. [DOI] [PubMed] [Google Scholar]
  62. Lewis S. A., Diamond J. M. Na+ transport by rabbit urinary bladder, a tight epithelium. J Membr Biol. 1976 Aug 27;28(1):1–40. doi: 10.1007/BF01869689. [DOI] [PubMed] [Google Scholar]
  63. Lim J. J., Ussing H. H. Analysis of presteady-state Na+ fluxes across the rabbit corneal endothelium. J Membr Biol. 1982;65(3):197–204. doi: 10.1007/BF01869963. [DOI] [PubMed] [Google Scholar]
  64. Lincoln D. W., Wakerley J. B. Electrophysiological evidence for the activation of supraoptic neurones during the release of oxytocin. J Physiol. 1974 Oct;242(2):533–554. doi: 10.1113/jphysiol.1974.sp010722. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Lingg G., Fischer-Colbrie R., Schmidt W., Winkler H. Exposure of an antigen of chromaffin granules on cell surface during exocytosis. Nature. 1983 Feb 17;301(5901):610–611. doi: 10.1038/301610a0. [DOI] [PubMed] [Google Scholar]
  66. Léránth C., Palkovits M., Krieger D. T. Serotonin immunoreactive nerve fibers and terminals in the rat pituitary--light- and electron-microscopic studies. Neuroscience. 1983 Jun;9(2):289–296. doi: 10.1016/0306-4522(83)90294-4. [DOI] [PubMed] [Google Scholar]
  67. MACROBBIE E. A., USSING H. H. Osmotic behaviour of the epithelial cells of frog skin. Acta Physiol Scand. 1961 Nov-Dec;53:348–365. doi: 10.1111/j.1748-1716.1961.tb02293.x. [DOI] [PubMed] [Google Scholar]
  68. Maruyama Y., Petersen O. H. Control of K+ conductance by cholecystokinin and Ca2+ in single pancreatic acinar cells studied by the patch-clamp technique. J Membr Biol. 1984;79(3):293–298. doi: 10.1007/BF01871068. [DOI] [PubMed] [Google Scholar]
  69. Maruyama Y., Petersen O. H., Flanagan P., Pearson G. T. Quantification of Ca2+-activated K+ channels under hormonal control in pig pancreas acinar cells. Nature. 1983 Sep 15;305(5931):228–232. doi: 10.1038/305228a0. [DOI] [PubMed] [Google Scholar]
  70. Mason W. T., Ho Y. W., Hatton G. I. Axon collaterals of supraoptic neurones: anatomical and electrophysiological evidence for their existence in the lateral hypothalamus. Neuroscience. 1984 Jan;11(1):169–182. doi: 10.1016/0306-4522(84)90221-5. [DOI] [PubMed] [Google Scholar]
  71. Mullins L. J. The generation of electric currents in cardiac fibers by Na/Ca exchange. Am J Physiol. 1979 Mar;236(3):C103–C110. doi: 10.1152/ajpcell.1979.236.3.C103. [DOI] [PubMed] [Google Scholar]
  72. Murphy R. A. Contractile system function in mammalian smooth muscle. Blood Vessels. 1976;13(1-2):1–23. doi: 10.1159/000158076. [DOI] [PubMed] [Google Scholar]
  73. Naik S. I., Young L. S., Charlton H. M., Clayton R. N. Pituitary gonadotropin-releasing hormone receptor regulation in mice. I: Males. Endocrinology. 1984 Jul;115(1):106–113. doi: 10.1210/endo-115-1-106. [DOI] [PubMed] [Google Scholar]
  74. Pato M. D., Adelstein R. S. Characterization of a Mg2+-dependent phosphatase from turkey gizzard smooth muscle. J Biol Chem. 1983 Jun 10;258(11):7055–7058. [PubMed] [Google Scholar]
  75. Phillips J. H., Burridge K., Wilson S. P., Kirshner N. Visualization of the exocytosis/endocytosis secretory cycle in cultured adrenal chromaffin cells. J Cell Biol. 1983 Dec;97(6):1906–1917. doi: 10.1083/jcb.97.6.1906. [DOI] [PMC free article] [PubMed] [Google Scholar]
  76. Pickering A. J., Fink G. Priming effect of luteinizing hormone releasing factor in vitro: role of protein synthesis, contractile elements, Ca2+ and cyclic AMP. J Endocrinol. 1979 Jun;81(3):223–234. doi: 10.1677/joe.0.0810223. [DOI] [PubMed] [Google Scholar]
  77. Porter D. G., Downing S. J., Bradshaw J. M. Relaxin inhibits spontaneous and prostaglandin-driven myometrial activity in anaesthetized rats. J Endocrinol. 1979 Nov;83(2):183–192. doi: 10.1677/joe.0.0830183. [DOI] [PubMed] [Google Scholar]
  78. Rand M. J., Whaler B. C. Impairment of sympathetic transmission by botulinum toxin. Nature. 1965 May 8;206(984):588–591. doi: 10.1038/206588a0. [DOI] [PubMed] [Google Scholar]
  79. Sargeant A. J., Hoinville E., Young A. Maximum leg force and power output during short-term dynamic exercise. J Appl Physiol Respir Environ Exerc Physiol. 1981 Nov;51(5):1175–1182. doi: 10.1152/jappl.1981.51.5.1175. [DOI] [PubMed] [Google Scholar]
  80. Schlue W. R., Thomas R. C. A dual mechanism for intracellular pH regulation by leech neurones. J Physiol. 1985 Jul;364:327–338. doi: 10.1113/jphysiol.1985.sp015748. [DOI] [PMC free article] [PubMed] [Google Scholar]
  81. Schultzberg M., Lundberg J. M., Hökfelt T., Terenius L., Brandt J., Elde R. P., Goldstein M. Enkephalin-like immunoreactivity in gland cells and nerve terminals of the adrenal medulla. Neuroscience. 1978;3(12):1169–1186. doi: 10.1016/0306-4522(78)90137-9. [DOI] [PubMed] [Google Scholar]
  82. Sherwood O. D., Crnekovic V. E., Gordon W. L., Rutherford J. E. Radioimmunoassay of relaxin throughout pregnancy and during parturition in the rat. Endocrinology. 1980 Sep;107(3):691–698. doi: 10.1210/endo-107-3-691. [DOI] [PubMed] [Google Scholar]
  83. Simpson L. L. The origin, structure, and pharmacological activity of botulinum toxin. Pharmacol Rev. 1981 Sep;33(3):155–188. [PubMed] [Google Scholar]
  84. Soejima M., Noma A. Mode of regulation of the ACh-sensitive K-channel by the muscarinic receptor in rabbit atrial cells. Pflugers Arch. 1984 Apr;400(4):424–431. doi: 10.1007/BF00587544. [DOI] [PubMed] [Google Scholar]
  85. Stepanova N. G., Grinio L. P. Issledovanie dipeptidov pri progressivnoi myshechnoi distrofii. Vopr Med Khim. 1968 Mar-Apr;14(2):210–214. [PubMed] [Google Scholar]
  86. Summerlee A. J., O'Byrne K. T., Paisley A. C., Breeze M. F., Porter D. G. Relaxin affects the central control of oxytocin release. Nature. 1984 May 24;309(5966):372–374. doi: 10.1038/309372a0. [DOI] [PubMed] [Google Scholar]
  87. USSING H. H. RELATIONSHIP BETWEEN OSMOTIC REACTIONS AND ACTIVE SODIUM TRANSPORT IN THE FROG SKIN EPITHELIUM. Acta Physiol Scand. 1965 Jan-Feb;63:141–155. doi: 10.1111/j.1748-1716.1965.tb04052.x. [DOI] [PubMed] [Google Scholar]
  88. Vassalle M., Musso E. On the mechanisms underlying digitalis toxicity in cardiac Purkinje fibers. Recent Adv Stud Cardiac Struct Metab. 1976;9:355–376. [PubMed] [Google Scholar]
  89. Vøllestad N. K., Vaage O., Hermansen L. Muscle glycogen depletion patterns in type I and subgroups of type II fibres during prolonged severe exercise in man. Acta Physiol Scand. 1984 Dec;122(4):433–441. doi: 10.1111/j.1748-1716.1984.tb07531.x. [DOI] [PubMed] [Google Scholar]
  90. Ward S. J., Pierson A. K., Michne W. F. Multiple opioid receptor profile in vitro and activity in vivo of the potent opioid antagonist Win 44,441-3. Life Sci. 1983;33 (Suppl 1):303–306. doi: 10.1016/0024-3205(83)90503-9. [DOI] [PubMed] [Google Scholar]
  91. Wendt I. R., Stephenson D. G. Effects of caffeine on Ca-activated force production in skinned cardiac and skeletal muscle fibres of the rat. Pflugers Arch. 1983 Aug;398(3):210–216. doi: 10.1007/BF00657153. [DOI] [PubMed] [Google Scholar]
  92. Wiggins J. R., Cranefield P. F. Effect on membrane potential and electrical activity of adding sodium to sodium-depleted cardiac purkinje fibers. J Gen Physiol. 1974 Oct;64(4):473–493. doi: 10.1085/jgp.64.4.473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  93. Williams J. T., Egan T. M., North R. A. Enkephalin opens potassium channels on mammalian central neurones. Nature. 1982 Sep 2;299(5878):74–77. doi: 10.1038/299074a0. [DOI] [PubMed] [Google Scholar]
  94. van Haeringen N. J., Glasius E. Collection method dependent concentrations of some metabolites in human tear fluid, with special reference to glucose in hyperglycaemic conditions. Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1977 Mar 29;202(1):1–7. doi: 10.1007/BF00496763. [DOI] [PubMed] [Google Scholar]

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