Erratum: Dynamics of spatial resolution of single units in the lateral geniculate nucleus of cat during brief visual stimulation (Journal of Neurophysiology (2007) 97, (1445-1456) DOI: 10.1152/jn.01338.2005);Dynamics of spatial resolution of single units in the lateral geniculate nucleus of cat during brief visual stimulation

Journal of Neurophysiology

Volumn 97, Issue 2, 2007, Pages 1445-1456

  Ruksenas, O ^a,b   Bulatov, A ^a,c   Heggelund, P ^a  

^a UNIVERSITY OF OSLO   (Norway)

^b VILNIUS UNIVERSITY   (Lithuania)

^c KAUNAS UNIVERSITY OF MEDICINE   (Lithuania)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ARTICLE; BRAIN NERVE CELL; CAT; DYNAMICS; LATERAL GENICULATE NUCLEUS; NEUROTRANSMISSION; NONHUMAN; PRIORITY JOURNAL; SPATIAL SUMMATION; STIMULUS RESPONSE; VISUAL STIMULATION;

EID: 33846917135     PISSN: 00223077     EISSN: 15221598     Source Type: Journal    
DOI: 10.1152/jn.z9k-8581-corr.2007     Document Type: Erratum

References (57)

1. Albrecht DG, Geisler WS, Crane AM. Visual cortex nonlinearities. In: The Visual Neurosciences, edited by Chalupa LM, Werner JS. Cambridge, MA: MIT Press, 2003, p. 747-764.
2. Bishop PO, Burke W, Davis R. Synapse discharge by single fibre in mam-malian visual system. Nature 182: 728-730, 1958.
3. Bredfeldt CE, Ringach DL. Dynamics of spatial frequency tuning in macaque V1. J Neurosci 22: 1976-1984, 2002.
4. Bullier J, Norton TT. X and Y relay cells in cat lateral geniculate nucleus: quantitative analysis of receptive field properties and classification. J Neurophysiol 42: 244-273, 1979.
5. Cai D, DeAngelis GC, Freeman RD. Spatiotemporal receptive field organization in the lateral geniculate nucleus of cats and kittens. J Neurophysiol 78: 1045-1061, 1997.
6. Cleland BG, Dubin MW, Levick WR. Sustained and transient neurones in the cat's retina and lateral geniculate nucleus. J Physiol 217: 473-496, 1971.
7. Cleland BG, Lee BB. A comparison of visual responses of cat lateral genic-ulate nucleus neurones with those of ganglion cells afferent to them. J Physiol 369: 249-268, 1985.
8. DeAngelis GC, Ohzawa I, Freeman RD. Spatiotemporal organization of simple-cell receptive fields in the cat striate cortex. 1. General characteristics of postnatal development. J Neurophysiol 69: 1091-1117, 1993.
9. DeBoer E, Kuyper P. Triggered correlation. Trans IEEE Biomed Eng 15: 169-179, 1968.
10. Demb JB, Zaghloul K, Haarsma L, Sterling P. Bipolar cells contribute to nonlinear spatial summation in the brisk-transient (Y) ganglion cell in mammalian retina. J Neurosci 21: 7447-7454, 2001.
11. Derrington AM, Lennie P. The influence of temporal frequency and adaptation level on receptive field organization of retinal ganglion cells in cat. J Physiol 333: 343-366, 1982.
12. Dubin MW, Cleland BG. Organization of visual inputs to interneurones of lateral geniculate nucleus of the cat. J Neurophysiol 40: 410-427, 1977.
13. Eckhorn R, Krause F, Nelson JJ. The RF-cinematogram - a cross-correlation technique for mapping several visual receptive fields at once. Biol Cybern 69: 37-55, 1993.
14. Enroth-Cugell C, Robson JG, Schweizer-Tong DE, Watson AB. Spatio-temporal interaction in cat retinal ganglion cells showing linear spatial summation. J Physiol 341: 279-307, 1983.
15. Evinger C, Fuchs AF. Saccadic, smooth pursuit, and optokinetic eye movements of the trained cat. J Physiol 285: 209-229, 1978.
16. Fjeld IT, Ruksenas O, Heggelund P. Brainstem modulation of visual response properties of single cells in the dorsal lateral geniculate nucleus of cat. J Physiol 543: 541-554, 2002.
17. Flores-Herr N, Protti DA, Wässle H. Synaptic currents generating the inhibitory surround of ganglion cells in the mammalian retina. J Neurosci 21: 4852-4863, 2001.
18. Frazor RA, Albrecht DG, Geisler WS, Crane AM. Temporal dynamics of the spatial frequency response function. J Neurophysiol 91: 2607-2627, 2004.
19. Frishman LJ, Freeman AM, Troy JB, Schwitzer-Tong DE, Enroth-Cugell C. Spatiotemporal frequency responses of cat retinal ganglion cells. J Gen Physiol 89: 599-628, 1987.
20. Golomb D, Kleinfeldt D, Reid RC, Shapley RM, Shraiman BI. On temporal codes and the spatiotemporal response of neurons in the lateral geniculate nucleus. J Neurophysiol 72: 2990-3003, 1994.
21. Hamos JE, Van Horn SC, Raczkowski D, Sherman SM. Synaptic circuits involving an individual retinogeniculate axon in the cat. J Comp Neurol 259: 165-192, 1987.
22. Hartveit E, Heggelund P. The effect of contrast on the visual response of lagged and nonlagged cells in the cat lateral geniculate nucleus. Vis Neurosci 9: 515-525, 1992.
23. Hartveit E, Heggelund P. Brain-stem influence on visual response of lagged and nonlagged cells in the cat lateral geniculate nucleus. Vis Neurosci 10: 325-339, 1993.
24. Hartveit E, Ramberg SI, Heggelund P. Brainstem modulation of spatial receptive field properties in the dorsal lateral geniculate nucleus of cat. J Neurophysiol 70: 1644-1655, 1993.
25. Hegdé J, Van Essen DC. Temporal dynamics of shape analysis in macaque visual area V2. J Neurophysiol 92: 3030-3042, 2004.
26. Heggelund P, Hartveit E. Neurotransmitter receptors mediating excitatory input to cells in the cat lateral geniculate nucleus. I. Lagged cells. J Neurophysiol 63: 1347-1360, 1990.
27. Hubel DH, Wiesel TN. Integrative action in the cat's lateral geniculate body. J Physiol 155: 385-398, 1961.
28. Kamermans M, Spekreijse H. The feedback pathway from horizontal cells to cones. Vision Res 39: 2449-2468, 1999.
29. Kaplan E, Shapley RM. The origin of the S (slow) potential in the mammalian lateral geniculate nucleus. Exp Brain Res 55: 111-116, 1984.
30. Knierim JJ, Van Essen DC. Neuronal responses to static texture patterns in area V1 of the alert macaque monkey. J Neurophysiol 67: 961-980, 1992.
31. Lee D, Malpeli JG. Effects of saccades on the activity of neurons in the cat lateral geniculate nucleus. J Neurophysiol 79: 922-936, 1998.
32. Levick WR. Another tungsten microelectrode. Med Biol Eng 10: 510-515, 1972.
33. Livingstone MS, Hubel DH. Effects of sleep and arousal on the processing of visual information in the cat. Nature 291: 554-561, 1981.
34. Mastronarde DN. Two classes of single-input X-cells in cat lateral geniculate nucleus. I. Receptive field properties and classification of cells. J Neurophysiol 57: 357-380, 1987a.
35. Mastronarde DN. Two classes of single-input X-cells in cat lateral geniculate nucleus. II. Retinal inputs and generation of receptive-field properties. J Neurophysiol 57: 381-413, 1987b.
36. Mastronarde DN. Nonlagged relay cells and interneurons in the cat lateral geniculate nucleus: receptive field properties and retinal inputs. Vis Neurosci 8: 407-441, 1992.
37. McMahon MJ, Packer OS, Dacey DM. The classical receptive field surround of primate parasol ganglion cells is mediated primarily by a non-GABAergic pathway. J Neurosci 24: 3736-3745, 2004.
38. Menz MD, Freeman RD. Stereoscopic depth processing in the visual cortex: a coarse-to-fine mechanism. Nat Neurosci 6: 59-65, 2003.
39. Menz MD, Freeman RD. Temporal dynamics of binocular disparity processing in the central visual pathway. J Neurophysiol 91: 1782-1793, 2004.
40. Müller JR, Metha AB, Krauskopf J, Lennie P. Information conveyed by onset transients in responses of striate cortical neurons. J Neurosci 21: 6978-6990, 2001.
41. Reid RC, Victor JD, Shapley RM. The use of m-series in the analysis of visual neurons: linear receptive field properties. Vis Neurosci 14: 1015-1027, 1997.
42. Reppas RC, Usrey WM, Reid RC. Saccadic eye movements modulate visual responses in the lateral geniculate nucleus. Neuron 35: 961-974, 2002.
43. Ringach DL, Hawken MJ, Shapley R. Dynamics of orientation tuning in macaque primary visual cortex. Nature 387: 281-284, 1997.
44. Robson JA. Qualitative and quantitative analyses of the patterns of retinal input to neurons in the dorsal lateral geniculate nucleus of the cat. J Comp Neurol 334: 324-336, 1993.
45. Rodieck RW. Quantitative analysis of cat retinal ganglion cell response to visual stimuli. Vision Res 5: 583-601, 1965.
46. Rodieck RW, Pettigrew JD, Bishop PO, Nikara T. Residual eye movements in receptive field studies of paralysed cats. Vision Res 7: 107-110, 1967.
47. Ruksenas O, Fjeld IT, Heggelund P. Spatial summation and center-surround antagonism in the receptive field of single units in the dorsal lateral geniculate nucleus of cat: comparison with retinal input. Vis Neurosci 17: 855-870, 2000.
48. Shapley RM, Lennie P. Spatial frequency analysis in the visual system. Annu Rev Neurosci 8: 547-583, 1985.
49. Stevens JK, Gerstein GL. Spatiotemporal organization of cat lateral geniculate receptive fields. J Neurophysiol 39: 213-238, 1976.
50. Stryker M, Blakemore C. Saccadic and disjunctive eye movements in cats. Vision Res 12: 2005-2013, 1972.
51. Suder K, Funke K, Zhao Y, Kerscher N, Wennekers T, Wörgötter F. Spatial dynamics of receptive fields in cat primary visual cortex related to the temporal structure of thalamocortical feedforward activity. Experiments and models. Exp Brain Res 144: 430-444, 2002.
52. Wolfe J, Palmer LA. Temporal diversity in the lateral geniculate nucleus of cat. Vis Neurosci 15: 653-675, 1998.
53. Wörgötter F, Suder K, Zhao Y, Kerscher N, Eysel U, Funke K. State-dependent receptive field restructuring in the visual cortex. Nature 396: 165-168, 1998.
54. Xing D, Shapley RM, Haeken MJ, Ringach DL. Effect of stimulus size on the dynamics of orientation selectivity in macaque V1. J Neurophysiol 94: 799-812, 2005.
55. Yarbus AL. Eye Movements and Vision. New York: Plenum Press, 1967.
56. Zisper K, Lamme VA, Schiller PH. Contextual modulation in primary visual cortex. J Neurosci 16: 7376-7389, 1996.
57. Zohary E, Hillman P, Hochstein S. Time course of perceptual discrimination and single neuron reliability. Biol Cybern 62: 475-486, 1990.