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. 1968 Aug;60(4):1069–1080. doi: 10.1073/pnas.60.4.1069

The neuronal membrane.

A L Lehninger
PMCID: PMC224883  PMID: 4299940

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Selected References

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

  1. Barondes S. H. Incorporation of radioactive glucosamine into macromolecules at nerve endings. J Neurochem. 1968 Jul;15(7):699–706. doi: 10.1111/j.1471-4159.1968.tb08970.x. [DOI] [PubMed] [Google Scholar]
  2. Benson A. A. On the orientation of lipids in chloroplast and cell membranes. J Am Oil Chem Soc. 1966 May;43(5):265–270. doi: 10.1007/BF02609671. [DOI] [PubMed] [Google Scholar]
  3. Changeux J. P., Podleski T. R. On the excitability and cooperativity of the electroplax membrane. Proc Natl Acad Sci U S A. 1968 Mar;59(3):944–950. doi: 10.1073/pnas.59.3.944. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Changeux J. P. Responses of acetylcholinesterase from Torpedo marmorata to salts and curarizing drugs. Mol Pharmacol. 1966 Sep;2(5):369–392. [PubMed] [Google Scholar]
  5. Changeux J. P., Thiéry J., Tung Y., Kittel C. On the cooperativity of biological membranes. Proc Natl Acad Sci U S A. 1967 Feb;57(2):335–341. doi: 10.1073/pnas.57.2.335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chapman D., Penkett S. A. Nuclear magnetic resonance spectroscopic studies of the interaction of phospholipids with cholesterol. Nature. 1966 Sep 17;211(5055):1304–1305. doi: 10.1038/2111304a0. [DOI] [PubMed] [Google Scholar]
  7. Cohen L. B., Keynes R. D., Hille B. Light scattering and birefringence changes during nerve activity. Nature. 1968 May 4;218(5140):438–441. doi: 10.1038/218438a0. [DOI] [PubMed] [Google Scholar]
  8. Derry D. M., Wolfe L. S. Gangliosides in isolated neurons and glial cells. Science. 1967 Dec 15;158(3807):1450–1452. doi: 10.1126/science.158.3807.1450. [DOI] [PubMed] [Google Scholar]
  9. Finean J. B. The molecular organization of cell membranes. Prog Biophys Mol Biol. 1966;16:143–170. doi: 10.1016/0079-6107(66)90005-8. [DOI] [PubMed] [Google Scholar]
  10. Hopfer U., Lehninger A. L., Thompson T. E. Protonic conductance across phospholipid bilayer membranes induced by uncoupling agents for oxidative phosphorylation. Proc Natl Acad Sci U S A. 1968 Feb;59(2):484–490. doi: 10.1073/pnas.59.2.484. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kilbourn B. T., Dunitz J. D., Pioda L. A., Simon W. Structure of the K+ complex with nonactin, a macrotetrolide antibiotic possessing highly specific K+ transport properties. J Mol Biol. 1967 Dec 28;30(3):559–563. doi: 10.1016/0022-2836(67)90370-1. [DOI] [PubMed] [Google Scholar]
  12. Korn E. D. Structure of biological membranes. Science. 1966 Sep 23;153(3743):1491–1498. doi: 10.1126/science.153.3743.1491. [DOI] [PubMed] [Google Scholar]
  13. LOWDEN J. A., WOLFE L. S. STUDIES ON BRAIN GANGLIOSIDES. IV. THE EFFECT OF HYPERCAPNIA ON GANGLIOSIDES IN VIVO. Can J Biochem. 1964 Dec;42:1703–1710. doi: 10.1139/o64-181. [DOI] [PubMed] [Google Scholar]
  14. Lardy H. A., Graven S. N., Estrada S. Specific induction and inhibition of cation and anion transport in mitochondria. Fed Proc. 1967 Sep;26(5):1355–1360. [PubMed] [Google Scholar]
  15. Laurent T. C. In vitro studies on the transport of macromolecules through the connective tissue. Fed Proc. 1966 May-Jun;25(3):1128–1134. [PubMed] [Google Scholar]
  16. Lehninger A. L., Carafoli E., Rossi C. S. Energy-linked ion movements in mitochondrial systems. Adv Enzymol Relat Areas Mol Biol. 1967;29:259–320. doi: 10.1002/9780470122747.ch6. [DOI] [PubMed] [Google Scholar]
  17. Lenard J., Singer S. J. Alteration of the conformation of proteins in red blood cell membranes and in solution by fixatives used in electron microscopy. J Cell Biol. 1968 Apr;37(1):117–121. doi: 10.1083/jcb.37.1.117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. MONOD J., CHANGEUX J. P., JACOB F. Allosteric proteins and cellular control systems. J Mol Biol. 1963 Apr;6:306–329. doi: 10.1016/s0022-2836(63)80091-1. [DOI] [PubMed] [Google Scholar]
  19. Maddy A. H., Huang C., Thompson T. E. Studies on lipid bilayer membranes: a model for the plasma membrane. Fed Proc. 1966 May-Jun;25(3):933–936. [PubMed] [Google Scholar]
  20. Moore J. W., Narahashi T., Shaw T. I. An upper limit to the number of sodium channels in nerve membrane? J Physiol. 1967 Jan;188(1):99–105. doi: 10.1113/jphysiol.1967.sp008126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Moore J. W., Narahashi T. Tetrodotoxin's highly selective blockage of an ionic channel. Fed Proc. 1967 Nov-Dec;26(6):1655–1663. [PubMed] [Google Scholar]
  22. Mueller P., Rudin D. O. Action potentials induced in biomolecular lipid membranes. Nature. 1968 Feb 24;217(5130):713–719. doi: 10.1038/217713a0. [DOI] [PubMed] [Google Scholar]
  23. Nachmansohn D. Chemical control of the permeability cycle in excitable membranes during electrical activity. Ann N Y Acad Sci. 1966 Jul 14;137(2):877–900. doi: 10.1111/j.1749-6632.1966.tb50207.x. [DOI] [PubMed] [Google Scholar]
  24. Pressman B. C. Induced active transport of ions in mitochondria. Proc Natl Acad Sci U S A. 1965 May;53(5):1076–1083. doi: 10.1073/pnas.53.5.1076. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Prezbindowski K. S., Ruzicka F. J., Sun F. F., Crane F. L. A double layer of protein in mitochondrial cristae. Biochem Biophys Res Commun. 1968 Apr 19;31(2):164–169. doi: 10.1016/0006-291x(68)90724-9. [DOI] [PubMed] [Google Scholar]
  26. RICHARDSON S. H., HULTIN H. O., FLEISCHER S. INTERACTIONS OF MITOCHONDRIAL STRUCTURAL PROTEIN WITH PHOSPHOLIPIDS. Arch Biochem Biophys. 1964 May;105:254–260. doi: 10.1016/0003-9861(64)90006-2. [DOI] [PubMed] [Google Scholar]
  27. Rand R. P., Luzzati V. X-ray diffraction study in water of lipids extracted from human erythrocytes: the position of cholesterol in the lipid lamellae. Biophys J. 1968 Jan;8(1):125–137. doi: 10.1016/S0006-3495(68)86479-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Robertson J. D. Granulo-fibrillar and globular substructure in unit membranes. Ann N Y Acad Sci. 1966 Jul 14;137(2):421–440. doi: 10.1111/j.1749-6632.1966.tb50174.x. [DOI] [PubMed] [Google Scholar]
  29. SVENNERHOLM L. CHROMATOGRAPHIC SEPARATION OF HUMAN BRAIN GANGLIOSIDES. J Neurochem. 1963 Sep;10:613–623. doi: 10.1111/j.1471-4159.1963.tb08933.x. [DOI] [PubMed] [Google Scholar]
  30. SVENNERHOLM L. THE DISTRIBUTION OF LIPIDS IN THE HUMAN NERVOUS SYSTEM. I. ANALYTICAL PROCEDURE. LIPIDS OF FOETAL AND NEWBORN BRAIN. J Neurochem. 1964 Dec;11:839–853. doi: 10.1111/j.1471-4159.1964.tb06735.x. [DOI] [PubMed] [Google Scholar]
  31. Wallach D. F., Kamat V. B. The contribution of sialic acid to the surface change of fragments of plasma membrane and endoplasmic reticulum. J Cell Biol. 1966 Sep;30(3):660–663. doi: 10.1083/jcb.30.3.660. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Watanabe A., Tasaki I., Lerman L. Bi-ionic action potentials in squid giant axons internally perfused with sodium saltssalts. Proc Natl Acad Sci U S A. 1967 Dec;58(6):2246–2252. doi: 10.1073/pnas.58.6.2246. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Watanabe A., Tasaki I., Singer I., Lerman L. Effects of tetrodotoxin on excitability of squid giant axons in sodium-free media. Science. 1967 Jan 6;155(3758):95–97. doi: 10.1126/science.155.3758.95. [DOI] [PubMed] [Google Scholar]

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