Temporal Processing in Cat Primary Auditory Cortex

References

• Woolsey C M., Walzl E M. Topical projection of nerve fibers from local regions of the cochlea to the cerebral cortex of the cat. Bull Johns Hopkins Hops 1942; 71: 315–44
   Google Scholar
• Merzenich M M., Knight P L., Roth G L. Representation of cochlea within primary auditory cortex in the cat. J Neurophysiol 1975; 38: 231–49
   PubMed Web of Science ®Google Scholar
• Reale R A., Imig T J. Tonotopic organization in auditory cortex of the cat. J Comp Neurol 1980; 192: 265–92
   PubMed Web of Science ®Google Scholar
• Aitkin L M., Irvine D R F, Webster W R. Central neural mechanisms of hearing. Handbook of physiology. The nervous system sensory processes. Am Physiol Soc, Washington, DC 1984; Vol. III: 675–738, Sect 1
   Google Scholar
• Schreiner C E., Mendelson J R. Functional topography of cat primary auditory cortex: distribution of integrated excitation. J Neurophysiol 1990; 64: 1442–59
   PubMedGoogle Scholar
• Heil P, Rajan R, Irvine D R F. Sensitivity of neurons in cat primary auditory cortex to tones and frequencymodulated stimuli. II: Organization of response properties along the “isofrequency” dimension. Hear Res 1992; 63: 135–56
   PubMedGoogle Scholar
• Javel E. Coding of AM tones in the chinchilla auditory nerve: implications for the pitch of complex tones. J Acoust Soc Am 1980; 68: 133–46
   PubMed Web of Science ®Google Scholar
• Creutzfeldt O, Hellweg F C., Schreiner C. Thalamocortical transformation of responses to complex auditory stimuli. Exp Brain Res 1980; 39: 87–104
   PubMed Web of Science ®Google Scholar
• Schreiner C E., Urbas J V. Representation of amplitude modulation in the auditory cortex of the cat. II. Comparison between cortical fields. Hear Res 1988; 32: 49–64
   PubMed Web of Science ®Google Scholar
• Joris P X., Yin T C. Responses to amplitude‐modulated tones in the auditory nerve of the cat. J Acoust Soc Am 1992; 91: 215–32
   PubMed Web of Science ®Google Scholar
• Eggermont J J. Rate and synchronization measures of periodicity coding in cat primary auditory cortex. Hear Res 1991; 56: 153–67
   PubMed Web of Science ®Google Scholar
• Eggermont J J. Stimulus induced and spontaneous rhythmic firing of single units in cat primary auditory cortex. Hear Res 1992; 61: 1–11
   PubMed Web of Science ®Google Scholar
• Schreiner C E., Joris P X. IUPS Satellite Symposium on Hearing. San Francisco 1988; 81
   Google Scholar
• Krueger K, Schreiner C E. Processing of tone sequences in cat primary auditory cortex. Soc Neurosci Abstr 1994; 20: 323
   Google Scholar
• Brosch M, Schreiner C E. Time course of forward masking tuning curves in cat primary auditory cortex. J Neurophysiol 1997; 77: 923–43
   PubMed Web of Science ®Google Scholar
• Calford M B., Semple M N. Monaural inhibition in cat auditory cortex. J Neurophysiol 1995; 73: 1876–91
   PubMed Web of Science ®Google Scholar
• Mendelson J R., Schreiner C E., Sutter M L. Functional topography of cat primary auditory cortex: response latencies. J Comp Physiol 1997, in press
   Google Scholar
• Phillips D P., Irvine D R. Responses of single neurons in physiologically defined primary auditory cortex (AI) of the cat: frequency tuning and responses to intensity. J Neurophysiol 1981; 45: 48–58
   PubMedGoogle Scholar
• Phillips D P., Orman S S., Musicant A D., Wilson G F. Neurons in the cat's primary auditory cortex distinguished by their responses to tones and wide‐spectrum noise. Hear Res 1985; 18: 73–86
   PubMed Web of Science ®Google Scholar
• Raggio M W., Schreiner C E. Neuronal responses in cat primary auditory cortex to electrical cochlear stimulation. I. Intensity dependence of firing rate and response latency. J Neurophysiol 1994; 72: 2334–59
   PubMedGoogle Scholar
• Reale R A., Kettner R E. Topography of binaural organization in primary auditory cortex of the cat: effects of changing interaural intensity. J Neurophysiol 1986; 56: 663–82
   PubMedGoogle Scholar
• Imig T J., Irons W A., Samson F R. Single‐unit selectivity to azimuthal direction and sound pressure level of noise bursts in cat high‐frequency primary auditory cortex. J Neurophysiol 1990; 63: 1448–66
   PubMedGoogle Scholar
• Schreiner C E., Mendelson J R. Functional topography of cat primary auditory cortex: distribution of integrated excitation. J Neurophysiol 1990; 64: 1442–59
   PubMedGoogle Scholar
• Schreiner C E., Mendelson J R., Sutter M L. Functional lopography of cal primary auditory cortex: represenla‐tion of tone inlensily. Exp Brain Res 1992; 92: 105–22
   PubMedGoogle Scholar
• Mendelson J R., Schreiner C E., Sutter M L., Grasse K L. Funclional topography of cat primary audilory cortex: responses to frequency‐modulated sweeps. Exp Brain Res 1993; 94: 65–87
   PubMedGoogle Scholar
• Schreiner C E., Sutter M L. Topography of excilalory bandwidth in cat primary auditory cortex: single‐neuron versus multiple‐neuron recordings. J Neurophysiol 1992; 68: 1487–502
   PubMedGoogle Scholar
• Sutter M L., Schreiner C E. Physiology and topography of neurons with multi‐peaked tuning curves in cat primary audilory cortex. J Neurophysiol 1995; 65: 1207–26
   Google Scholar
• Clarey J C., Barone P, Imig T J. Funclional organizalion of sound direclion and sound pressure level in primary audilory cortex of the cal. J Neurophysiol 1994; 72: 2383–405
   PubMedGoogle Scholar
• Schreiner C E. Order and disorder in audilory cortical maps. Curr Opin Neurobiol 1995; 5: 489–96
   PubMed Web of Science ®Google Scholar
• Schreiner C E., Langner G. Periodicily coding in the inferior colliculus of the cal. II. Topographical organizalion. J Neurophysiol 1988; 60: 1823–40
   PubMed Web of Science ®Google Scholar
• Schreiner C E., Raggio M W. Neuronal responses in cal primary auditory cortex lo eleclrical cochlear slimulation. II. Repelilion rale coding. J Neurophysiol 1996; 75: 1283–300
   PubMedGoogle Scholar
• Phillips D P., Hall S E., Hollett J L. Repelilion rate and signal level effecls on neuronal responses lo brief lone pulses in cat auditory cortex. J Acoust Soc Am 1989; 85: 2537–49
   PubMedGoogle Scholar
• Langner G, Schreiner C, Merzenich M M. Covarialion of latency and temporal resolulion in the inferior colliculus of the cal. Hear Res 1987; 31: 197–201
   PubMedGoogle Scholar
• Langner G, Schreiner C E. Periodicily coding in the inferior colliculus of the cat. I. Neuronal mechanisms. J Neurophysiol 1988; 60: 1799–1822
   PubMed Web of Science ®Google Scholar
• Rees A, Moller A R. Stimulus properties influencing the responses of inferior colliculus neurons to amplitudemodulated sounds. Hear Res 1987; 27: 129–143
   PubMed Web of Science ®Google Scholar
• Park T J., Pollak G D. GABA shapes a topographic organization of response latency in the mustache bat's inferior colliculus. J Neurosci 1993; 13: 5172–5187
   PubMedGoogle Scholar
• Casseday J H., Ehrlich D, Covey E. Neural tuning for sound duration: role of inhibitory mechanisms in the inferior colliculus. Science 1994; 264: 847–50
   PubMed Web of Science ®Google Scholar
• Fersler D, Lindslroem S. Synaplic excilation of neurones in area 17 of the cal by inlracorlical axon collaterals of cortico‐geniculate cells. J Physiol (London) 1985; 367: 233–52
   Google Scholar
• Welker E, Armslrong‐James M, Van der Loose H, Kraflsik R. The mode of aclivalion of a barrel column: response properties of single units in the somatosensory cortex of the mouse upon whisker deflection. Eur J Neurosci 1993; 5: 691–712
   PubMed Web of Science ®Google Scholar
• Snyder R, Leake P, Rebscher S, Beitel R. Temporal resolution of neurons in cat inferior colliculus to intracochlear electrical stimulation: effects of neonatal deafening and chronic stimulation. J Neurophysiol 1995; 73: 449–67
   PubMedGoogle Scholar