Forward and reverse hippocampal place-cell sequences during ripples
By Kamran Diba, György Buzsáki. 2007
1,136 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Cognitive Neuroscience
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cellular and Molecular Neuroscience
- David J. Foster
- György Buzsáki
- Loren M. Frank
- Brad E. Pfeiffer
- Y. Dudai
- Jan Born
- Giulio Tononi
- James J. Knierim
In Cognitive Neuroscience
- György Buzsáki
- David J. Foster
- Loren M. Frank
- Brad E. Pfeiffer
- Jan Born
- Y. Dudai
- Giulio Tononi
- Chiara Cirelli
Citations in the corpus
- Hippocampal replay in the awake state: a potential physiological substrate of memory consolidation and retrieval (2011, background): “Further examination of SWR activity revealed that awake replay can occur in either the same (forward) or the opposite (reverse) direction as that observed during behavio”
- Hippocampal Replay is Not a Simple Function of Experience (2010, background): “…1989; Sutherland and McNaughton, 2000), incorporation or consolidation of information into cognitive schemas or cognitive maps (O’Keefe and Nadel, 1978; Tse et al., 2007), and learning and planning future experiences (Foster and Wilson, 2006; Diba and Buzsáki, 2007; Karlsson and Frank, 2009).”
- Hippocampal place cells construct reward related sequences through unexplored space (2015, methodology): “The extent to which templates were represented in the spiking events was assessed using templatematching (Lee and Wilson, 2002; Foster and Wilson, 2006; Diba and Buzsaki, 2007).”
- Hippocampal replay of extended experience (2009, neutral): “There are significantly more remote replay events than the number of false positives expected to be generated by our replay detection procedure (52 of 1656 events; p < 10 11 under a binomial distribution, using false-positive rate of 1%).”
- About sleep's role in memory. (2013, background): “In a task requiring the rat to run back and forth on the same elevated linear track, replay in the reverse order occurred mainly at the end of a run, whereas replay in a forward direction transpired in the anticipatory period before a new run (288, 492).”
- Distinct hippocampal-cortical memory representations for experiences associated with movement versus immobility (2017, positive): “These reinstated activity patterns correspond to representations of trajectories through space (Csicsvari et al., 2007; Davidson et al., 2009; Diba and Buzsáki, 2007; Foster and Wilson, 2006; Gupta et al., 2010; Jackson et al., 2006; Karlsson and Frank, 2009; Pfeiffer and Foster, 2013; Wu and Foster”
- Sequence Learning and the Role of the Hippocampus in Rodent Navigation (2012, positive): “Consistent with a role in learning, reverse replay appears to be more prevalent on a novel track than a familiar one [52], whereas forward ordered sequences display the opposite pattern [54].”
- Hippocampus Leads Ventral Striatum in Replay of Place-Reward Information (2009, background): “Reactivation of neuronal sequences In addition to cross-correlograms, a ranked-order sequence analysis of multi-neuron spike trains has been applied to hippocampal and neocortical datasets to demonstrate temporally structured replay [1-3].”