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. 1962 Aug;162(3):432–450. doi: 10.1113/jphysiol.1962.sp006943

Single-unit recording from antidromically activated optic radiation neurones

P O Bishop, W Burke, R Davis
PMCID: PMC1359668  PMID: 13869505

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Selected References

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

  1. ARAKI T., OTANI T., FURUKAWA T. The electrical activities of single motoneurones in toad's spinal cord, recorded with intracellular electrodes. Jpn J Physiol. 1953 Dec 15;3(4):254–267. doi: 10.2170/jjphysiol.3.254. [DOI] [PubMed] [Google Scholar]
  2. ARAKI T., OTANI T. Response of single motoneurons to direct stimulation in toad's spinal cord. J Neurophysiol. 1955 Sep;18(5):472–485. doi: 10.1152/jn.1955.18.5.472. [DOI] [PubMed] [Google Scholar]
  3. BENNETT M. V., CRAIN S. M., GRUNDFEST H. Electrophysiology of supramedullary neurons in Spheroides maculatus. I. Orthodromic and antidromic responses. J Gen Physiol. 1959 Sep;43:159–188. doi: 10.1085/jgp.43.1.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BISHOP P. O., BURKE W., DAVIS R. The identification of single units in central visual pathways. J Physiol. 1962 Aug;162:409–431. doi: 10.1113/jphysiol.1962.sp006942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. BISHOP P. O., BURKE W., DAVIS R. The interpretation of the extracellular response of single lateral geniculate cells. J Physiol. 1962 Aug;162:451–472. doi: 10.1113/jphysiol.1962.sp006944. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. BISHOP P. O., EVANS W. A. The refractory period of the sensory synapses of the lateral geniculate nucleus. J Physiol. 1956 Dec 28;134(3):538–557. doi: 10.1113/jphysiol.1956.sp005664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. BROCK L. G., COOMBS J. S., ECCLES J. C. Intracellular recording from antidromically activated motoneurones. J Physiol. 1953 Dec 29;122(3):429–461. doi: 10.1113/jphysiol.1953.sp005013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. COOMBS J. S., CURTIS D. R., ECCLES J. C. The generation of impulses in motoneurones. J Physiol. 1957 Dec 3;139(2):232–249. doi: 10.1113/jphysiol.1957.sp005888. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. COOMBS J. S., CURTIS D. R., ECCLES J. C. The interpretation of spike potentials of motoneurones. J Physiol. 1957 Dec 3;139(2):198–231. doi: 10.1113/jphysiol.1957.sp005887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. DOTY R. W. Potentials evoked in cat cerebral cortex by diffuse and by punctiform photic stimuli. J Neurophysiol. 1958 Sep;21(5):437–464. doi: 10.1152/jn.1958.21.5.437. [DOI] [PubMed] [Google Scholar]
  11. ECCLES J. C., ECCLES R. M., IGGO A., LUNDBERG A. Electrophysiological studies on gamma motoneurones. Acta Physiol Scand. 1960 Sep 30;50:32–40. doi: 10.1111/j.1748-1716.1960.tb02070.x. [DOI] [PubMed] [Google Scholar]
  12. ECCLES J. C., FATT P., KOKETSU K. Cholinergic and inhibitory synapses in a pathway from motor-axon collaterals to motoneurones. J Physiol. 1954 Dec 10;126(3):524–562. doi: 10.1113/jphysiol.1954.sp005226. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. EDWARDS C., OTTOSON D. The site of impulse initiation in a nerve cell of a crustacean stretch receptor. J Physiol. 1958 Aug 29;143(1):138–148. doi: 10.1113/jphysiol.1958.sp006049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. FATT P. Electric potentials occurring around a neurone during its antidromic activation. J Neurophysiol. 1957 Jan;20(1):27–60. doi: 10.1152/jn.1957.20.1.27. [DOI] [PubMed] [Google Scholar]
  15. FRANK K., FUORTES M. G. Potentials recorded from the spinal cord with microelectrodes. J Physiol. 1955 Dec 29;130(3):625–654. doi: 10.1113/jphysiol.1955.sp005432. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. FREYGANG W. H., Jr, FRANK K. Extracellular potentials from single spinal motoneurons. J Gen Physiol. 1959 Mar 20;42(4):749–760. doi: 10.1085/jgp.42.4.749. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. FUORTES M. G., FRANK K., BECKER M. C. Steps in the production of motoneuron spikes. J Gen Physiol. 1957 May 20;40(5):735–752. doi: 10.1085/jgp.40.5.735. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. GRANIT R., PHILLIPS C. G. Excitatory and inhibitory processes acting upon individual Purkinje cells of the cerebellum in cats. J Physiol. 1956 Sep 27;133(3):520–547. doi: 10.1113/jphysiol.1956.sp005606. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. KANDEL E. R., SPENCER W. A., BRINLEY F. J., Jr Electrophysiology of hippocampal neurons. I. Sequential invasion and synaptic organization. J Neurophysiol. 1961 May;24:225–242. doi: 10.1152/jn.1961.24.3.225. [DOI] [PubMed] [Google Scholar]
  20. LI C. L., ORTIZ-GALVIN A., CHOU S. N., HOWARD S. Y. Cortical intracellular potentials in response to stimulation to lateral geniculate body. J Neurophysiol. 1960 Nov;23:592–601. doi: 10.1152/jn.1960.23.6.592. [DOI] [PubMed] [Google Scholar]
  21. MACHNE X., FADIGA E., BROOKHART J. M. Antidromic and synaptic activation of frog motor neurons. J Neurophysiol. 1959 Sep;22:483–503. doi: 10.1152/jn.1959.22.5.483. [DOI] [PubMed] [Google Scholar]
  22. MARTIN A. R., BRANCH C. L. Spontaneous activity of Betz cells in cats with midbrain lesions. J Neurophysiol. 1958 Jul;21(4):368–370. doi: 10.1152/jn.1958.21.4.368. [DOI] [PubMed] [Google Scholar]
  23. NISHI S., KOKETSU K. Electrical properties and activities of single sympathetic neurons in frogs. J Cell Comp Physiol. 1960 Feb;55:15–30. doi: 10.1002/jcp.1030550104. [DOI] [PubMed] [Google Scholar]
  24. TASAKI I. Properties of myelinated fibers in frog sciatic nerve and in spinal cord as examined with micro-electrodes. Jpn J Physiol. 1952 Nov;3(1):73–94. doi: 10.2170/jjphysiol.3.73. [DOI] [PubMed] [Google Scholar]
  25. VASTOLA E. F. Antidromic action potentials in lateral geniculate body. J Neurophysiol. 1957 Mar;20(2):167–185. doi: 10.1152/jn.1957.20.2.167. [DOI] [PubMed] [Google Scholar]
  26. WIDEN L., AJMONE MARSAN C. Effects of corticipetal and corticifugal impulses upon single elements of the dorsolateral geniculate nucleus. Exp Neurol. 1960 Oct;2:468–502. doi: 10.1016/0014-4886(60)90028-5. [DOI] [PubMed] [Google Scholar]

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