The thalamic matrix and thalamocortical synchrony.

By Edward G. Jones. Trends in Neurosciences, 2001

634 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Cognitive Neuroscience

View Paper: https://www.semanticscholar.org/paper/31df2d277a69ce0f95433f11f0b81298b169e82c

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In Cellular and Molecular Neuroscience

In Cognitive Neuroscience

Citations in the corpus

Sound-Induced Enhancement of Low-Intensity Vision: Multisensory Influences on Human Sensory-Specific Cortices and Thalamic Bodies Relate to Perceptual Enhancement of Visual Detection Sensitivity (2010, background): “At a very different level to human fMRI data, one possible mechanism for audiovisual interplay between thalamic and cortical structures might involve calbindinpositive neurons within the thalamus, which could directly link thalamic with cortical structures (Jones, 2001; Lakatos et al., 2007).”
The functional logic of cortico-pulvinar connections. (2003, background): “1997); these are envisaged to condition the temporal patterning of activity (Engel et al. 2001; Jones 2001) for example, acting to synchronize V1 cortico-cortical and cortico-thalamic neurons, ultimately recruiting elements of V1 to the coherently oscillating neural assembly.”
Separating semantic conflict and response conflict in the Stroop task: A functional MRI study (2005, background): “This area of the thalamus projects to the motor cortices (Jones, 2001; Rausell et al., 1992), consistent with the interpretation of increased response activation in this contrast but not in the semantic contrast.”
Neuronal oscillations and multisensory interaction in primary auditory cortex. (2007, background): “The possibility that nonspecific thalamic projections may mediate somatosensory modulation of A1 activity through phase resetting fits with the proposition that this system may be uniquely important in promoting cortical synchrony (Jones, 2001).”
Exploring the Thalamus and its Role in Cortical Function, S.M. Sherman, R.W. Guillery (Eds.). The MIT Press (2006), ISBN: 0-262-19532-1 (2007, result): “The recent claim (Jones, 2001) that corticothalamic axons arising in layer 5 of cortex, that is, the driving corticothalamic axons (see below), form diffuse and widespread terminals in the thalamus is contrary to the many observations cited above showing welllocalized terminal arbors comparable to…”
Persistent EEG overactivation in the cortical pain matrix of neurogenic pain patients (2006, background): “As a part of the medial thalamus, the nucleus CL is diffusely connected to wide cortical areas (Steriade et al., 1997; Jones, 2001) and is thought to serve as a nonspecific amplifier of thalamocortical activity (Llinas et al.”
Breakdown of within- and between-network Resting State Functional Magnetic Resonance Imaging Connectivity during Propofol-induced Loss of Consciousness (2010, background): “In this context, it could be suggested that the pattern of reduced cerebral connectivity observed in our study matches the cortical projections of thalamic matrix cells (as previously observed in monkey), which were suggested to be involved in cortico-thalamocortical connectivity.(74) In the hypothe”
Is perception discrete or continuous? (2003, background): “The non-specific network or ‘matrix’ [ 46 ] is a distributed neuronal network occupying the entire thalamus, and connected with virtually all sensory and motor cortices.”
Synaptic Mechanisms of Memory Consolidation during Sleep Slow Oscillations (2016, methodology): “The thalamus model consisted of core and matrix systems (Jones, 2001).”
Towards a Mathematical Theory of Cortical Micro-circuits (2009, background): “It is assumed that the belief-timing neurons project to non-specific thalamic regions (the thalamic matrix) [54] which implement a variable delay mechanism that projects back to layer 1 to complete a timing loop, as shown in Figure 7.”
The Human Thalamus Is an Integrative Hub for Functional Brain Networks (2016, background): “Every cortical region receives projections from the thalamus and in turn sends outputs to one or multiple thalamic nuclei (Jones, 2001).”
Low-frequency neuronal oscillations as instruments of sensory selection (2008, positive): “Although it is beyond the scope of this paper to cover this topic in detail, it is noteworthy that so-called ‘non-specific’ thalamic afferents are widespread and project both within [23] (Figure 2d) and across modalities [24].”