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1 s to act as excitatory pacemakers for the V1 gamma rhythm.
2 zures) and with the power change of the high-gamma rhythm.
3 excitatory/inhibitory equilibrium and on the gamma rhythm.
4 e associated with brain rhythms, notably the gamma rhythm.
5 on the functional significance of the visual gamma rhythm.
6 ronounced for the beta and strongest for the gamma rhythm.
7 f generating delta/theta (ie, 2 to 6 Hz) and gamma rhythms.
8 emporal-parietal structures and expressed in gamma rhythms.
9 tial inhibitory neuron subtype necessary for gamma rhythms.
10 ty characteristic of assembly formation with gamma rhythms.
11  high frequency oscillations associated with gamma rhythms.
12  interneurons that contribute to hippocampal gamma rhythms.
13 rain) that apparently cannot be tolerated by gamma rhythms.
14 gic stimulation can generate theta-modulated gamma rhythms.
15 lity (GC) in the theta, beta, high-beta, and gamma rhythms.
16 auditory scene and in the associated induced gamma rhythms.
17 a) and PING (pyramidal-interneuronal network gamma) rhythms.
18                                              Gamma rhythm (30-70 Hz), thought to represent the intera
19 te a prokinetic state by inducing narrowband gamma rhythms (65-90 Hz).
20 rated by as little as 400 microm, making the gamma rhythm a poor candidate for binding or communicati
21 of the PIC prevents the normalization of the gamma rhythm, a waveband of neural oscillations thought
22 theories of schizophrenia and that theta and gamma rhythm abnormalities are evident in schizophrenic
23 g-predicted inputs by inhibiting feedforward gamma rhythms and associated spiking.
24 cal field potential, observable as theta and gamma rhythms and coupling between these rhythms, is pre
25 Consistent with this prediction, hippocampal gamma rhythms and pyramidal cell coupling to theta phase
26  in PV interneurons for expression of normal gamma rhythms and specific cognitive behaviors.
27                                    Theta and gamma rhythms and their cross-frequency coupling play cr
28 aspartate (NMDA) receptor antagonists alters gamma rhythms, and can induce cognitive as well as psych
29 tabilize cortical network activity, generate gamma rhythms, and regulate experience-dependent plastic
30  are thought to be organized by co-occurring gamma rhythms ( approximately 25-100 Hz).
31                                     Although gamma rhythms are abnormal in schizophrenia, it remains
32                                              Gamma rhythms are commonly observed in many brain region
33                                              Gamma rhythms are known to contribute to the process of
34 memory retrieval, depending on which type of gamma rhythms are recruited.
35 ies are consistent with data suggesting that gamma rhythms are used for relatively local computations
36        Instead, our results suggest that the gamma rhythm arises from local interactions between exci
37 ematical analysis, we study the breakdown of gamma rhythms as the driven ensembles become too small,
38  whose contrast varies across space generate gamma rhythms at significantly different frequencies in
39 est that robust nesting of hippocampal theta-gamma rhythms at the time of retrieval is a specific rec
40 t in a network with realistic heterogeneity, gamma rhythms based on the interaction of excitatory and
41  Primary visual cortex exhibits two types of gamma rhythm: broadband activity in the 30-90 Hz range a
42               Surprisingly, stimulus-induced gamma rhythms, but not alpha or steady-state visually ev
43 s of several parts of the brain suggest that gamma rhythms can be generated by pools of excitatory ne
44            Large gratings, however, induce a gamma rhythm characterized by a distinctive spectral "bu
45 mple of a place in which slow theta and fast gamma rhythms coexist.
46 ndependently predicts that context-dependent gamma rhythms depend critically on SOM interneurons.
47 tially impact local and global properties of gamma rhythms depending on visual stimulus statistics.
48 pocampal subfield CA1 and that slow and fast gamma rhythms differentially coordinate place cells duri
49  potentials increases with attention, the V1 gamma rhythm does not engage V4 excitatory-neurons, but
50                      We discuss that a given gamma rhythm does not per se implement any specific cogn
51  the emergence of the AS-related hippocampal gamma rhythm during the first postnatal week, as well as
52 d the mPFC's involvement in modulating theta-gamma rhythms during reward-related decision-making.
53 und" gamma rhythm (resembling the persistent gamma rhythms evoked in vitro by cholinergic agonists) i
54 ations may expand the computational power of gamma rhythms for optimizing the synthesis and storage o
55                     For these functions, the gamma rhythm frequency must be consistent across neural
56 The results suggest the presence of a single gamma rhythm generator with a frequency range of 65-75 H
57 a phase-locking and show that the endogenous gamma rhythm has cell-type- and layer-specific effects o
58              The synaptic bases of theta and gamma rhythms have been extensively studied but the cell
59                                        While gamma rhythms have been extensively studied in the adult
60 tional role in vision.SIGNIFICANCE STATEMENT Gamma rhythms have been proposed to be a robust encoding
61 tant mice exhibit enhanced baseline cortical gamma rhythms, impaired gamma rhythm induction after opt
62 n: (i) spike times are entrained to a global Gamma rhythm (implying a consistent representation of th
63                                       As the gamma rhythm in area 21a did not spread backward to area
64 arp stimulus-onset transient and a sustained gamma rhythm in local field potential recorded from the
65 e coincident expression of multiple types of gamma rhythm in sensory cortex suggests a mechanistic su
66 al for a visually induced, context-dependent gamma rhythm in visual cortex.
67                       Models of the 30-80 Hz gamma rhythm in which network oscillations arise through
68 ggested diagnostic and therapeutic value for gamma rhythms in brain, the same has not been rigorously
69 this interaction contributes to nested theta/gamma rhythms in hippocampus.
70 onse to smell: Odor induces theta, beta, and gamma rhythms in human piriform cortex.
71 cover a previously unappreciated function of gamma rhythms in recruiting both neuronal and glial resp
72   The parameter range chosen is motivated by gamma rhythms, in which the gamma-aminobutyric acid type
73 ed baseline cortical gamma rhythms, impaired gamma rhythm induction after optogenetic drive of PV int
74                The preference of this global gamma rhythm is sensitive to adaptation, in a manner con
75 icularly strongly linked to cognition is the gamma rhythm: it is involved in attention, short- and lo
76 cordings in slice preparations we found that gamma rhythms lead to activity-dependent modification of
77 oral theta oscillations and occipitoparietal gamma rhythms leads to significant dose-dependent improv
78                                          The gamma rhythm manifests as a broad resonance peak in the
79                                              Gamma rhythms may be generated locally by interactions w
80 y glutamatergic drive, we show that top-down gamma rhythms may block sensory signals.
81                In this paper, we discuss how gamma rhythm, one of the main components of the extracel
82 nsory-motor cortex and a significant rise of gamma rhythm over right somatosensory-motor cortex.
83                                 The model of gamma rhythm predicts an average zero phase lag between
84 ed scopolamine on movement-induced theta and gamma rhythms recorded in the superficial layers of the
85 onous spontaneous activity to a "background" gamma rhythm (resembling the persistent gamma rhythms ev
86 ast) cells, that may contribute to theta and gamma rhythms, respectively.
87 isual stimuli that induce a strong, coherent gamma rhythm result in enhanced pairwise and higher-orde
88 ikely reflect the hypothesis that the mu and gamma rhythms specifically index the downstream modulati
89 ch the MCs fire at rates lower than the fast gamma rhythm they create.
90                 Entraining M1 neurons at the gamma rhythm through tACS may be an effective method to
91  gamma regimes can interact with a bottom-up gamma rhythm to provide regulation of signals between th
92 olved in the projection of locally generated gamma rhythms to distal sites.
93 The model makes novel use of on-going faster gamma rhythms to form a set of discrete clocks that prov
94  requires coupling of approximately 30-100Hz gamma rhythms to particular phases of the theta cycle.
95 sic relationship of both CA1 place cells and gamma rhythms to theta rhythm in the hippocampus is prof
96 , covering a broad range of timescales, from gamma rhythms to ultra-slow rhythms lasting up to hundre
97            The significance of this induced "gamma rhythm" to brain function remains unclear.
98                                       Third, gamma rhythm typically concurs with irregular firing of
99  of excitatory and inhibitory neurons in the gamma rhythm varies across local circuits and conditions
100                             As in neocortex, gamma rhythms were dependent on GABA(A) receptor-mediate
101        (5) Cholinergically elicited beta and gamma rhythms were eliminated by antagonists of either A
102                          Additionally, these gamma rhythms were linked back to mismatched expectation
103                             Hippocampal slow gamma rhythms were strongly associated to neocortical tr
104                  The model also reproduces a gamma rhythm whose frequency changes with time, at theta
105 hanges in the association of place cells and gamma rhythms with theta rhythm, suggesting that the ove

 
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