| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Ellen K W Brennan, Shyam Kumar Sudhakar, Izabela Jedrasiak-Cape, Tibin T John, Omar J Ahme. Hyperexcitable Neurons Enable Precise and Persistent Information Encoding in the Superficial Retrosplenial Cortex. Cell reports. vol 30. issue 5. 2021-03-16. PMID:32023472. |
the retrosplenial cortex (rsc) is essential for memory and navigation, but the neural codes underlying these functions remain largely unknown. |
2021-03-16 |
2023-08-13 |
mouse |
| Neal W Morton, Alison R Presto. Concept formation as a computational cognitive process. Current opinion in behavioral sciences. vol 38. 2021-02-27. PMID:33628870. |
navigation within hippocampal cognitive maps, which is guided by grid coding in entorhinal cortex, may contribute to imagination through recombination of event elements or concept features. |
2021-02-27 |
2023-08-13 |
Not clear |
| Caitlin S Mallory, Kiah Hardcastle, Malcolm G Campbell, Alexander Attinger, Isabel I C Low, Jennifer L Raymond, Lisa M Giocom. Mouse entorhinal cortex encodes a diverse repertoire of self-motion signals. Nature communications. vol 12. issue 1. 2021-02-22. PMID:33510164. |
here, we identify multiple self-motion signals, related to the position and velocity of the head and eyes, encoded by neurons in a key node of the navigation circuitry of mice, the medial entorhinal cortex (mec). |
2021-02-22 |
2023-08-13 |
mouse |
| Robert Gk Munn, Lisa M Giocom. Multiple head direction signals within entorhinal cortex: origin and function. Current opinion in neurobiology. vol 64. 2021-01-27. PMID:32088661. |
here, we discuss recent evidence illustrating that the signaling of direction within the mammalian brain is likewise transformed and multiplexed as it progresses from subcortical regions that contain tightly direction-coupled neurons through thalamus to regions that support navigation, such as the subiculum, entorhinal cortex and hippocampus. |
2021-01-27 |
2023-08-13 |
Not clear |
| Arianna Rinaldi, Elvira De Leonibus, Alessandra Cifra, Giulia Torromino, Elisa Minicocci, Elisa De Sanctis, Rosa María López-Pedrajas, Alberto Oliverio, Andrea Mel. Flexible use of allocentric and egocentric spatial memories activates differential neural networks in mice. Scientific reports. vol 10. issue 1. 2020-12-31. PMID:32647258. |
successful navigation was correlated with the activation of ca1, posterior-dorsomedial striatum, nucleus accumbens core and infralimbic cortex when allocentric-trained mice needed to use a novel route. |
2020-12-31 |
2023-08-13 |
mouse |
| Arianna Rinaldi, Elvira De Leonibus, Alessandra Cifra, Giulia Torromino, Elisa Minicocci, Elisa De Sanctis, Rosa María López-Pedrajas, Alberto Oliverio, Andrea Mel. Flexible use of allocentric and egocentric spatial memories activates differential neural networks in mice. Scientific reports. vol 10. issue 1. 2020-12-31. PMID:32647258. |
allocentric navigation from a familiar route activated dorsomedial striatum, nucleus accumbens, prelimbic and infralimbic cortex. |
2020-12-31 |
2023-08-13 |
mouse |
| Ana Belén de Landeta, Magdalena Pereyra, Jorge H Medina, Cynthia Katch. Anterior retrosplenial cortex is required for long-term object recognition memory. Scientific reports. vol 10. issue 1. 2020-11-23. PMID:32152383. |
the retrosplenial cortex (rsc) is implicated on navigation and contextual memory. |
2020-11-23 |
2023-08-13 |
Not clear |
| Seongmin A Park, Douglas S Miller, Hamed Nili, Charan Ranganath, Erie D Boorma. Map Making: Constructing, Combining, and Inferring on Abstract Cognitive Maps. Neuron. vol 107. issue 6. 2020-11-20. PMID:32702288. |
we tested whether the hippocampus (hc), entorhinal cortex (ec), and ventromedial prefrontal cortex (vmpfc)/medial orbitofrontal cortex (mofc) organize abstract and discrete relational information into a cognitive map to guide novel inferences. |
2020-11-20 |
2023-08-13 |
human |
| Gillian Coughlan, Peter Zhukovsky, Vaisakh Puthusseryppady, Rachel Gillings, Anne-Marie Minihane, Donnie Cameron, Michael Hornberge. Functional connectivity between the entorhinal and posterior cingulate cortices underpins navigation discrepancies in at-risk Alzheimer's disease. Neurobiology of aging. vol 90. 2020-10-29. PMID:32171591. |
navigation processes that are selectively mediated by functional activity in the entorhinal cortex may be a marker of preclinical alzheimer's disease (ad). |
2020-10-29 |
2023-08-13 |
Not clear |
| Ford Burles, Alberto Umiltá, Liam H McFarlane, Kendra Potocki, Giuseppe Iari. Ventral-Dorsal Functional Contribution of the Posterior Cingulate Cortex in Human Spatial Orientation: A Meta-Analysis. Frontiers in human neuroscience. vol 12. 2020-10-01. PMID:29867414. |
the retrosplenial cortex has long been implicated in human spatial orientation and navigation. |
2020-10-01 |
2023-08-13 |
human |
| Timo Oess, Jeffrey L Krichmar, Florian Röhrbei. A Computational Model for Spatial Navigation Based on Reference Frames in the Hippocampus, Retrosplenial Cortex, and Posterior Parietal Cortex. Frontiers in neurorobotics. vol 11. 2020-09-30. PMID:28223931. |
a computational model for spatial navigation based on reference frames in the hippocampus, retrosplenial cortex, and posterior parietal cortex. |
2020-09-30 |
2023-08-13 |
rat |
| Timo Oess, Jeffrey L Krichmar, Florian Röhrbei. A Computational Model for Spatial Navigation Based on Reference Frames in the Hippocampus, Retrosplenial Cortex, and Posterior Parietal Cortex. Frontiers in neurorobotics. vol 11. 2020-09-30. PMID:28223931. |
in this paper, we construct a computational model of the posterior parietal cortex and the retrosplenial cortex for spatial navigation. |
2020-09-30 |
2023-08-13 |
rat |
| Xin Hao, Yi Huang, Yiying Song, Xiangzhen Kong, Jia Li. Experience with the Cardinal Coordinate System Contributes to the Precision of Cognitive Maps. Frontiers in psychology. vol 8. 2020-09-30. PMID:28744248. |
neurally, the extent to which individuals relied on the cardinal coordinate system was positively correlated with the gray matter volume of the entorhinal cortex, suggesting that the entorhinal cortex may serve as the neuroanatomical basis of coordinate-based navigation (the entorhinal coordinate area, eca). |
2020-09-30 |
2023-08-13 |
Not clear |
| Anna L Powell, Emma Hindley, Andrew Jd Nelson, Moira Davies, Eman Amin, John P Aggleton, Seralynne D Van. Lesions of retrosplenial cortex spare immediate-early gene activity in related limbic regions in the rat. Brain and neuroscience advances. vol 2. 2020-09-28. PMID:32166157. |
the retrosplenial cortex forms part of a network of cortical and subcortical structures that have particular importance for spatial learning and navigation in rodents. |
2020-09-28 |
2023-08-13 |
rat |
| Xiaoli Chen, Paula Vieweg, Thomas Wolber. Computing distance information from landmarks and self-motion cues - Differential contributions of anterior-lateral vs. posterior-medial entorhinal cortex in humans. NeuroImage. vol 202. 2020-09-11. PMID:31386919. |
in humans, however, if and how the entorhinal cortex supports landmark-based navigation and path integration is poorly understood. |
2020-09-11 |
2023-08-13 |
human |
| Xiaoli Chen, Paula Vieweg, Thomas Wolber. Computing distance information from landmarks and self-motion cues - Differential contributions of anterior-lateral vs. posterior-medial entorhinal cortex in humans. NeuroImage. vol 202. 2020-09-11. PMID:31386919. |
together, these findings suggest that subdivisions of entorhinal cortex encode fine-grained spatial information for different spatial cues, which provides important insights into how the entorhinal cortex supports different modes of spatial navigation. |
2020-09-11 |
2023-08-13 |
human |
| Simone Viganò, Manuela Piazz. Distance and Direction Codes Underlie Navigation of a Novel Semantic Space in the Human Brain. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 40. issue 13. 2020-09-01. PMID:32060171. |
using whole-brain fmri adaptation and searchlight model-based representational similarity analysis, we found evidence of both distance-based and direction-based responses in brain regions typically involved in spatial navigation: the medial prefrontal cortex and the right entorhinal cortex (ehc). |
2020-09-01 |
2023-08-13 |
human |
| Matthias Nau, Tobias Navarro Schröder, Markus Frey, Christian F Doelle. Behavior-dependent directional tuning in the human visual-navigation network. Nature communications. vol 11. issue 1. 2020-08-31. PMID:32591544. |
to examine these processes, we combined 7t-fmri with a kernel-based encoding model of virtual navigation to map world-centered directional tuning across the human cortex. |
2020-08-31 |
2023-08-13 |
human |
| Qiliang He, Thackery I Brow. Environmental Barriers Disrupt Grid-like Representations in Humans during Navigation. Current biology : CB. vol 29. issue 16. 2020-08-03. PMID:31378608. |
collectively, these results provide mechanistic insight into why barriers compartmentalize our cognitive map, indicating that boundaries exert a powerful influence on the way environments are represented in human entorhinal cortex. |
2020-08-03 |
2023-08-13 |
human |
| Travis P Todd, Danielle I Fournier, David J Bucc. Retrosplenial cortex and its role in cue-specific learning and memory. Neuroscience and biobehavioral reviews. vol 107. 2020-07-28. PMID:31055014. |
the retrosplenial cortex (rsc) contributes to spatial navigation, as well as contextual learning and memory. |
2020-07-28 |
2023-08-13 |
Not clear |