Skip to main content
NCBI home page
The Journal of Physiology logoLink to The Journal of Physiology
letter
. 1976;258(Suppl):60P–98P.

Proceedings of the Physiological Society, 19-20 March 1976, University College London Meeting: Communications

Part I

PMCID: PMC1308952  PMID: 134143

Full text

PDF
60P

Selected References

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

  1. ABBOTT B. C. The heat production associated with the maintenance of a prolonged contraction and the extra heat produced during large shortening. J Physiol. 1951 Feb;112(3-4):438–445. doi: 10.1113/jphysiol.1951.sp004541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Allen D. G., Jewell B. R., Murray J. W. The contribution of activation processes to the length-tension relation of cardiac muscle. Nature. 1974 Apr 12;248(449):606–607. doi: 10.1038/248606a0. [DOI] [PubMed] [Google Scholar]
  3. BRINDLEY G. S., MERTON P. A. The absence of position sense in the human eye. J Physiol. 1960 Aug;153:127–130. doi: 10.1113/jphysiol.1960.sp006523. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Benzonana G., Capony J. P., Pechere J. F. The binding of calcium to muscular parvalbumins. Biochim Biophys Acta. 1972 Aug 31;278(1):110–116. doi: 10.1016/0005-2795(72)90111-0. [DOI] [PubMed] [Google Scholar]
  5. Blaustein M. P., Hodgkin A. L. The effect of cyanide on the efflux of calcium from squid axons. J Physiol. 1969 Feb;200(2):497–527. doi: 10.1113/jphysiol.1969.sp008704. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Clarke P. G. The organization of visual processing in the pigeon cerebellum. J Physiol. 1974 Nov;243(1):267–285. doi: 10.1113/jphysiol.1974.sp010753. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cleland B. G., Levick W. R. Brisk and sluggish concentrically organized ganglion cells in the cat's retina. J Physiol. 1974 Jul;240(2):421–456. doi: 10.1113/jphysiol.1974.sp010617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cleworth D. R., Edman K. A. Changes in sarcomere length during isometric tension development in frog skeletal muscle. J Physiol. 1972 Dec;227(1):1–17. doi: 10.1113/jphysiol.1972.sp010016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cobb W. A., Morton H. B. Evoked potentials from the human scalp to visual half-field stimulation. J Physiol. 1970 Jun;208(2):39P–40P. [PMC free article] [PubMed] [Google Scholar]
  10. Dean P. M., Matthews E. K. Pancreatic acinar cells: measurement of membrane potential and miniature depolarization potentials. J Physiol. 1972 Aug;225(1):1–13. doi: 10.1113/jphysiol.1972.sp009926. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dicker S. E., Morris C. A. Investigation of a substance of renal origin which inhibits the growth of renal cortex explant in vitro. J Embryol Exp Morphol. 1974 Jun;31(3):655–665. [PubMed] [Google Scholar]
  12. Edman K. A. Mechanical deactivation induced by active shortening in isolated muscle fibres of the frog. J Physiol. 1975 Mar;246(1):255–275. doi: 10.1113/jphysiol.1975.sp010889. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Evans C. A., Reynolds J. M., Reynolds M. L., Saunders N. R., Segal M. B. The development of a blood-brain barrier mechanism in foetal sheep. J Physiol. 1974 Apr;238(2):371–386. doi: 10.1113/jphysiol.1974.sp010530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Fabiato A., Fabiato F. Dependence of the contractile activation of skinned cardiac cells on the sarcomere length. Nature. 1975 Jul 3;256(5512):54–56. doi: 10.1038/256054a0. [DOI] [PubMed] [Google Scholar]
  15. Fenn W. O. The relation between the work performed and the energy liberated in muscular contraction. J Physiol. 1924 May 23;58(6):373–395. doi: 10.1113/jphysiol.1924.sp002141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Glitsch H. G., Reuter H., Scholz H. The effect of the internal sodium concentration on calcium fluxes in isolated guinea-pig auricles. J Physiol. 1970 Jul;209(1):25–43. doi: 10.1113/jphysiol.1970.sp009153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Gresty M. A. Coordination of head and eye movements to fixate continuous and intermittent targets. Vision Res. 1974 Jun;14(6):395–403. doi: 10.1016/0042-6989(74)90238-7. [DOI] [PubMed] [Google Scholar]
  18. Horackova M., Vassort G. Excitation--contraction coupling in frog heart. Effect of veratrine. Pflugers Arch. 1974;352(4):291–302. doi: 10.1007/BF00585683. [DOI] [PubMed] [Google Scholar]
  19. Hoult D. I., Busby S. J., Gadian D. G., Radda G. K., Richards R. E., Seeley P. J. Observation of tissue metabolites using 31P nuclear magnetic resonance. Nature. 1974 Nov 22;252(5481):285–287. doi: 10.1038/252285a0. [DOI] [PubMed] [Google Scholar]
  20. Hyvärinen J., Poranen A. Function of the parietal associative area 7 as revealed from cellular discharges in alert monkeys. Brain. 1974 Dec;97(4):673–692. doi: 10.1093/brain/97.1.673. [DOI] [PubMed] [Google Scholar]
  21. Keatinge W. R. Ca concentration and flux in Ca-deprived arteries. J Physiol. 1972 Jul;224(1):35–59. doi: 10.1113/jphysiol.1972.sp009880. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. King-Smith P. E., More R. K., Riggs L. A. A new approach to the frequency response of human vision. J Physiol. 1976 May;257(1):36P–37P. [PubMed] [Google Scholar]
  23. Lichardus B., Nizet A. Water and sodium excretion after blood volume expansion under conditions of constant arterial, venous and plasma oncotic pressures and constant haematocrit. Clin Sci. 1972 Jun;42(6):701–709. doi: 10.1042/cs0420701. [DOI] [PubMed] [Google Scholar]
  24. Lázár G. The projection of the retinal quadrants on the optic centres in the frog. A terminal degeneration study. Acta Morphol Acad Sci Hung. 1971;19(4):325–334. [PubMed] [Google Scholar]
  25. Macknight A. D., Pilgrim J. P., Robinson B. A. The regulation of cellular volume in liver slices. J Physiol. 1974 Apr;238(2):279–294. doi: 10.1113/jphysiol.1974.sp010524. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Mancini G., Carbonara A. O., Heremans J. F. Immunochemical quantitation of antigens by single radial immunodiffusion. Immunochemistry. 1965 Sep;2(3):235–254. doi: 10.1016/0019-2791(65)90004-2. [DOI] [PubMed] [Google Scholar]
  27. Marsden C. D., Meadows J. C., Merton P. A. Isolated single motor units in human muscle and their rate of discharge during maximal voluntary effort. J Physiol. 1971;217 (Suppl):12P–13P. [PubMed] [Google Scholar]
  28. Mason R. Cell properties in the medial interlaminar nucleus of the cat's lateral geniculate complex in relation to the transient/sustained classification. Exp Brain Res. 1975 Mar 27;22(3):327–329. doi: 10.1007/BF00234773. [DOI] [PubMed] [Google Scholar]
  29. Michael W. F., Halliday A. M. Differences between the occipital distribution of upper and lower field pattern-evoked responses in man. Brain Res. 1971 Sep 24;32(2):311–324. doi: 10.1016/0006-8993(71)90327-1. [DOI] [PubMed] [Google Scholar]
  30. NAESS K., STORM-MATHISEN A. Fatique of sustained tetanic contractions. Acta Physiol Scand. 1955 Oct 12;34(4):351–366. doi: 10.1111/j.1748-1716.1955.tb01255.x. [DOI] [PubMed] [Google Scholar]
  31. Nashat F. S., Tappin J. W., Wilcox C. S. Plasma sodium concentration and sodium excretion in the anaesthetized dog. J Physiol. 1976 Jan;254(1):183–202. doi: 10.1113/jphysiol.1976.sp011228. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Nashat F. S., Tappin J. W., Wilcox C. S. The renal blood flow and the glomerular filtration rate of anaesthetized dogs during acute changes in plasma sodium concentration. J Physiol. 1976 Apr;256(3):731–745. doi: 10.1113/jphysiol.1976.sp011348. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Nyström B. Histochemistry of developing cat muscles. Acta Neurol Scand. 1968;44(4):405–439. doi: 10.1111/j.1600-0404.1968.tb05584.x. [DOI] [PubMed] [Google Scholar]
  34. Parmley W. W., Chuck L. Length-dependent changes in myocardial contractile state. Am J Physiol. 1973 May;224(5):1195–1199. doi: 10.1152/ajplegacy.1973.224.5.1195. [DOI] [PubMed] [Google Scholar]
  35. Robberecht P., Deschodt-Lanckman M., De Neef P., Borgeat P., Christophe J. In vivo effects of pancreozymin, secretin, vasoactive intestinal polypeptide and pilocarpine on the levels of cyclic AMP and cyclic GMP in the rat pancreas. FEBS Lett. 1974 Jul 15;43(2):139–143. doi: 10.1016/0014-5793(74)80986-5. [DOI] [PubMed] [Google Scholar]
  36. Rothman S. S. "Non-parallel transport" of enzyme protein by the pancreas. Nature. 1967 Feb 4;213(5075):460–462. doi: 10.1038/213460a0. [DOI] [PubMed] [Google Scholar]
  37. Rothman S. S. Protein transport by the pancreas. Science. 1975 Nov 21;190(4216):747–753. doi: 10.1126/science.1105785. [DOI] [PubMed] [Google Scholar]
  38. SIEBECK R. Wahrnehmungsstörung und Störungswahrnehmung bei Augenmuskellähmungen. Albrecht Von Graefes Arch Ophthalmol. 1954;155(1):26–34. [PubMed] [Google Scholar]
  39. Scalia F., Gregory K. Retinofugal projections in the frog: location of the postsynaptic neurons. Brain Behav Evol. 1970;3(1):16–29. doi: 10.1159/000125460. [DOI] [PubMed] [Google Scholar]
  40. Seglen P. O. Preparation of rat liver cells. 3. Enzymatic requirements for tissue dispersion. Exp Cell Res. 1973 Dec;82(2):391–398. doi: 10.1016/0014-4827(73)90357-1. [DOI] [PubMed] [Google Scholar]
  41. Silber S., Malvin R. L. Compensatory and obligatory renal growth in rats. Am J Physiol. 1974 Jan;226(1):114–117. doi: 10.1152/ajplegacy.1974.226.1.114. [DOI] [PubMed] [Google Scholar]
  42. Stein J. F., Wattam Bell J. Proceedings: The effect of cooling nucleus interpositus of the cerebellum in rhesus monkeys on the tracking of a visual target. J Physiol. 1975 Nov;252(2):47P–48P. [PubMed] [Google Scholar]
  43. Stevens J. K., Emerson R. C., Gerstein G. L., Kallos T., Neufeld G. R., Nichols C. W., Rosenquist A. C. Paralysis of the awake human: visual perceptions. Vision Res. 1976 Jan;16(1):93–98. doi: 10.1016/0042-6989(76)90082-1. [DOI] [PubMed] [Google Scholar]
  44. Tartakoff A. M., Jamieson J. D., Scheele G. A., Palade G. E. Studies on the pancreas of the guinea pig. Parallel processing and discharge of exocrine proteins. J Biol Chem. 1975 Apr 10;250(7):2671–2677. [PubMed] [Google Scholar]
  45. Taylor A., Cody F. W., Bosley M. A. Histochemical and mechanical properties of the jaw muscles of the cat. Exp Neurol. 1973 Jan;38(1):99–109. doi: 10.1016/0014-4886(73)90011-3. [DOI] [PubMed] [Google Scholar]
  46. WIESEL T. N., HUBEL D. H. EFFECTS OF VISUAL DEPRIVATION ON MORPHOLOGY AND PHYSIOLOGY OF CELLS IN THE CATS LATERAL GENICULATE BODY. J Neurophysiol. 1963 Nov;26:978–993. doi: 10.1152/jn.1963.26.6.978. [DOI] [PubMed] [Google Scholar]
  47. van Breemen C., De Weer P. Lanthanum inhibition of 45Ca efflux from the squid giant axon. Nature. 1970 May 23;226(5247):760–761. doi: 10.1038/226760a0. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES