Commentary on the Pinotsis and Friston Neural Fields DCM and the Cadonic and Albensi Oscillations and NMDA Receptors Articles

2014, Volume 1, Issue 2: 158-162. doi: 10.3934/Neuroscience.2014.2.158

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Commentary Special Issues

Received: 03 July 2014 Accepted: 17 August 2014 Published: 16 September 2014

Citation: Robert A. Moss, Jarrod Moss. Commentary on the Pinotsis and Friston Neural Fields DCM and the Cadonic and Albensi Oscillations and NMDA Receptors Articles[J]. AIMS Neuroscience, 2014, 1(2): 158-162. doi: 10.3934/Neuroscience.2014.2.158

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[1]	Pinotsis D, Friston K. (2014) Gamma Oscillations and Neural Field DCMs can reveal cortical excitability and microstructure. AIMS Neurosci 1: 18-38.
[2]	Moss RA, Moss J. (2014) The role of dynamic columns in explaining Gamma-band synchronization and NMDA receptors in cognitive functions. AIMS Neurosci 1: 65-88.
[3]	Edelman GM. (1993) Neural Darwinism: selection and reentrant signaling in higher brain function. Neuron 10: 115-125. doi: 10.1016/0896-6273(93)90304-A
[4]	Edelman GM, Gally JA. (2013) Reentry: a key mechanism for integration of brain function. Front Integr Neurosci 7: 63.
[5]	Henson RNA, Rugg MD. (2003) Neural response suppression, haemodynamic repetition effects, and behavioural priming. Neuropsychologia 41: 263-270. doi: 10.1016/S0028-3932(02)00159-8
[6]	McClelland JL, Rumelhart DE. (1981) An interactive activation model of context effects in letter perception: I. An account of basic findings. Psychol Rev 88: 375-407.
[7]	Cadonic C, Albensi BC. (2014) The role of dynamic columns in explaining gamma-band synchronization and NMDA receptors in cognitive functions. AIMS Neurosci 1: 52-64.
[8]	Hennequin G, Vogels TP, Gerstner W. (2014) Optimal control of transient dynamics in balanced networks supports generation of complex movements. Neuron 82: 1394-1406. doi: 10.1016/j.neuron.2014.04.045

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