| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Julie Marie Lefort, Jean Vincent, Lucille Tallot, Frédéric Jarlier, Chris Innocentius De Zeeuw, Laure Rondi-Reig, Christelle Rochefor. Impaired cerebellar Purkinje cell potentiation generates unstable spatial map orientation and inaccurate navigation. Nature communications. vol 10. issue 1. 2019-07-01. PMID:31113954. |
these results indicate that pp2b-dependent potentiation in pcs contributes to maintain a stable hippocampal representation of a familiar environment in an allocentric reference frame as well as to support optimal trajectory toward a goal during navigation. |
2019-07-01 |
2023-08-13 |
mouse |
| William de Cothi, Hugo J Spier. Spatial Cognition: Goal-Vector Cells in the Bat Hippocampus. Current biology : CB. vol 27. issue 6. 2019-06-20. PMID:28324745. |
a new study recording from the hippocampus of flying bats has revealed populations of neurons tuned to the egocentric direction of the goal, the distance to the goal or their conjunction during spatial navigation. |
2019-06-20 |
2023-08-13 |
Not clear |
| G L West, K Konishi, M Diarra, J Benady-Chorney, B L Drisdelle, L Dahmani, D J Sodums, F Lepore, P Jolicoeur, V D Bohbo. Impact of video games on plasticity of the hippocampus. Molecular psychiatry. vol 23. issue 7. 2019-06-17. PMID:28785110. |
these results show that video games can be beneficial or detrimental to the hippocampal system depending on the navigation strategy that a person employs and the genre of the game. |
2019-06-17 |
2023-08-13 |
human |
| Mingli Liang, Michael J Starrett, Arne D Ekstro. Dissociation of frontal-midline delta-theta and posterior alpha oscillations: A mobile EEG study. Psychophysiology. vol 55. issue 9. 2019-05-28. PMID:29682758. |
numerous reports have demonstrated low-frequency oscillations during navigation using invasive recordings in the hippocampus of both rats and human patients. |
2019-05-28 |
2023-08-13 |
human |
| Ivan Soltesz, Attila Losoncz. CA1 pyramidal cell diversity enabling parallel information processing in the hippocampus. Nature neuroscience. vol 21. issue 4. 2019-05-16. PMID:29593317. |
hippocampal network operations supporting spatial navigation and declarative memory are traditionally interpreted in a framework where each hippocampal area, such as the dentate gyrus, ca3, and ca1, consists of homogeneous populations of functionally equivalent principal neurons. |
2019-05-16 |
2023-08-13 |
Not clear |
| Marcelo G Mattar, Nathaniel D Da. Prioritized memory access explains planning and hippocampal replay. Nature neuroscience. vol 21. issue 11. 2019-05-16. PMID:30349103. |
using nonlocal 'replay' of spatial locations in hippocampus as a window into memory access, we simulate a spatial navigation task in which an agent accesses memories of locations sequentially, ordered by utility: how much extra reward would be earned due to better choices. |
2019-05-16 |
2023-08-13 |
Not clear |
| John Lisman, György Buzsáki, Howard Eichenbaum, Lynn Nadel, Charan Ranganath, A David Redis. Viewpoints: how the hippocampus contributes to memory, navigation and cognition. Nature neuroscience. vol 20. issue 11. 2019-05-09. PMID:29073641. |
viewpoints: how the hippocampus contributes to memory, navigation and cognition. |
2019-05-09 |
2023-08-13 |
Not clear |
| Russell A Epstein, Eva Zita Patai, Joshua B Julian, Hugo J Spier. The cognitive map in humans: spatial navigation and beyond. Nature neuroscience. vol 20. issue 11. 2019-05-09. PMID:29073650. |
specifically, these studies indicate that (i) the human hippocampus and entorhinal cortex support map-like spatial codes, (ii) posterior brain regions such as parahippocampal and retrosplenial cortices provide critical inputs that allow cognitive maps to be anchored to fixed environmental landmarks, and (iii) hippocampal and entorhinal spatial codes are used in conjunction with frontal lobe mechanisms to plan routes during navigation. |
2019-05-09 |
2023-08-13 |
human |
| Susumu Takahash. The Hippocampal Ensemble Code for Spatial Navigation and Episodic Memory. Advances in neurobiology. vol 21. 2019-05-08. PMID:30334219. |
the hippocampal ensemble code for spatial navigation and episodic memory. |
2019-05-08 |
2023-08-13 |
mouse |
| Susumu Takahash. The Hippocampal Ensemble Code for Spatial Navigation and Episodic Memory. Advances in neurobiology. vol 21. 2019-05-08. PMID:30334219. |
in fact, loss of the hippocampus can lead to a profound disturbance to spatial navigation. |
2019-05-08 |
2023-08-13 |
mouse |
| Susumu Takahash. The Hippocampal Ensemble Code for Spatial Navigation and Episodic Memory. Advances in neurobiology. vol 21. 2019-05-08. PMID:30334219. |
and, why does the hippocampus enable flexible spatial navigation?to address these questions, in this chapter i review several compelling investigations on the firing pattern of place cells, and the temporal flow and reactivation of their ensemble activity. |
2019-05-08 |
2023-08-13 |
mouse |
| Susumu Takahash. The Hippocampal Ensemble Code for Spatial Navigation and Episodic Memory. Advances in neurobiology. vol 21. 2019-05-08. PMID:30334219. |
these pivotal reports strongly support a view that the hippocampal neuronal ensemble enables flexible spatial navigation and contributes to the capacities of episodic memory: mental time travel and foreseeing future situations. |
2019-05-08 |
2023-08-13 |
mouse |
| Caroll-Ann Blanchette, Jamila Amirova, Veronique D Bohbot, Greg L Wes. Autistic traits in neurotypical individuals are associated with increased landmark use during navigation. PsyCh journal. vol 8. issue 1. 2019-04-26. PMID:30294869. |
"spatial learners" navigate by building a cognitive map using environmental landmarks, and display more grey matter in the hippocampus. |
2019-04-26 |
2023-08-13 |
human |
| Edmund T Rolls, Sylvia Wirt. Spatial representations in the primate hippocampus, and their functions in memory and navigation. Progress in neurobiology. vol 171. 2019-04-12. PMID:30219248. |
spatial representations in the primate hippocampus, and their functions in memory and navigation. |
2019-04-12 |
2023-08-13 |
monkey |
| Edmund T Rolls, Sylvia Wirt. Spatial representations in the primate hippocampus, and their functions in memory and navigation. Progress in neurobiology. vol 171. 2019-04-12. PMID:30219248. |
these functions of the primate hippocampus in scene-related memory, provide a way for the primate hippocampus to contribute to actions in space and navigation. |
2019-04-12 |
2023-08-13 |
monkey |
| Tatsuya Haga, Tomoki Fuka. Recurrent network model for learning goal-directed sequences through reverse replay. eLife. vol 7. 2019-03-28. PMID:29969098. |
our model for the first time provides the mechanistic account for the way reverse replay contributes to hippocampal sequence learning for reward-seeking spatial navigation. |
2019-03-28 |
2023-08-13 |
Not clear |
| Katherine R Sherrill, Elizabeth R Chrastil, Irem Aselcioglu, Michael E Hasselmo, Chantal E Ster. Structural Differences in Hippocampal and Entorhinal Gray Matter Volume Support Individual Differences in First Person Navigational Ability. Neuroscience. vol 380. 2019-03-07. PMID:29673867. |
our results support the theory that hippocampus, entorhinal cortex, and thalamus are key structures for updating position and orientation during ground-level navigation. |
2019-03-07 |
2023-08-13 |
human |
| Joseph D Monaco, Rose M De Guzman, Hugh T Blair, Kechen Zhan. Spatial synchronization codes from coupled rate-phase neurons. PLoS computational biology. vol 15. issue 1. 2019-02-28. PMID:30682012. |
during spatial navigation, the frequency and timing of spikes from spatial neurons including place cells in hippocampus and grid cells in medial entorhinal cortex are temporally organized by continuous theta oscillations (6-11 hz). |
2019-02-28 |
2023-08-13 |
rat |
| Xin Hao, Xu Wang, Yiying Song, Xiangzhen Kong, Jia Li. Dual roles of the hippocampus and intraparietal sulcus in network integration and segregation support scene recognition. Brain structure & function. vol 223. issue 3. 2019-02-26. PMID:29159664. |
in short, our study demonstrated the dual roles of the hipp and ips in integration and segregation of the nn to support scene recognition, suggesting that scene recognition involves not only regions specialized in spatial navigation, but also those with general functions. |
2019-02-26 |
2023-08-13 |
Not clear |
| Hao Mei, Nikos K Logothetis, Oxana Eschenk. The activity of thalamic nucleus reuniens is critical for memory retrieval, but not essential for the early phase of "off-line" consolidation. Learning & memory (Cold Spring Harbor, N.Y.). vol 25. issue 3. 2019-02-14. PMID:29449457. |
spatial navigation depends on the hippocampal function, but also requires bidirectional interactions between the hippocampus (hpc) and the prefrontal cortex (pfc). |
2019-02-14 |
2023-08-13 |
rat |