All Relations between navigation and hippocampus

Publication Sentence Publish Date Extraction Date Species
Michiel H G Claessen, Martine J E van Zandvoort, Frans S S Leijten, Ineke J M van der Ha. Memory for novel and familiar environments relies on the hippocampus: A case study on a patient with a right anteromesial temporal lobectomy. Hippocampus. vol 29. issue 9. 2020-05-26. PMID:30847996. while the hippocampus has been ascribed a prominent role in navigation ability, it is still a subject of debate whether it contributes to learning novel environments only or to remembering familiar environments as well. 2020-05-26 2023-08-13 human
Michiel H G Claessen, Martine J E van Zandvoort, Frans S S Leijten, Ineke J M van der Ha. Memory for novel and familiar environments relies on the hippocampus: A case study on a patient with a right anteromesial temporal lobectomy. Hippocampus. vol 29. issue 9. 2020-05-26. PMID:30847996. this pattern of findings suggests that the hippocampus is not only important for navigation in novel environments, but also for familiar environments learned long ago. 2020-05-26 2023-08-13 human
Iva K Brunec, Jessica Robin, Eva Zita Patai, Jason D Ozubko, Amir-Homayoun Javadi, Morgan D Barense, Hugo J Spiers, Morris Moscovitc. Cognitive mapping style relates to posterior-anterior hippocampal volume ratio. Hippocampus. vol 29. issue 8. 2020-05-25. PMID:30714271. we find that greater reported cognitive map use was related to significantly greater posterior, relative to anterior, hippocampal volume in two separate samples of young adults. 2020-05-25 2023-08-13 human
Stephen Ramanoël, Elizabeth York, Marine Le Petit, Karine Lagrené, Christophe Habas, Angelo Arle. Age-Related Differences in Functional and Structural Connectivity in the Spatial Navigation Brain Network. Frontiers in neural circuits. vol 13. 2020-05-25. PMID:31736716. within these networks, areas such as the hippocampus (hc) are known to be affected by aging and to be associated with cognitive decline and navigation impairments. 2020-05-25 2023-08-13 human
Stephen Ramanoël, Elizabeth York, Marine Le Petit, Karine Lagrené, Christophe Habas, Angelo Arle. Age-Related Differences in Functional and Structural Connectivity in the Spatial Navigation Brain Network. Frontiers in neural circuits. vol 13. 2020-05-25. PMID:31736716. the opa is known to be involved in egocentric navigation, as opposed to allocentric strategies which are more related to the hippocampal region. 2020-05-25 2023-08-13 human
Ian A Clark, Misun Kim, Eleanor A Maguir. Verbal Paired Associates and the Hippocampus: The Role of Scenes. Journal of cognitive neuroscience. vol 30. issue 12. 2020-05-19. PMID:30063178. this vpa deficit is not well understood and is particularly difficult for hippocampal theories with a visuospatial bias to explain (e.g., cognitive map and scene construction theories). 2020-05-19 2023-08-13 human
Roddy M Grieves, Selim Jedidi-Ayoub, Karyna Mishchanchuk, Anyi Liu, Sophie Renaudineau, Kate J Jeffer. The place-cell representation of volumetric space in rats. Nature communications. vol 11. issue 1. 2020-05-18. PMID:32034157. place cells are spatially modulated neurons found in the hippocampus that underlie spatial memory and navigation: how these neurons represent 3d space is crucial for a full understanding of spatial cognition. 2020-05-18 2023-08-13 rat
Lukas Kunz, Liang Wang, Daniel Lachner-Piza, Hui Zhang, Armin Brandt, Matthias Dümpelmann, Peter C Reinacher, Volker A Coenen, Dong Chen, Wen-Xu Wang, Wenjing Zhou, Shuli Liang, Philip Grewe, Christian G Bien, Anne Bierbrauer, Tobias Navarro Schröder, Andreas Schulze-Bonhage, Nikolai Axmache. Hippocampal theta phases organize the reactivation of large-scale electrophysiological representations during goal-directed navigation. Science advances. vol 5. issue 7. 2020-05-13. PMID:31281882. hippocampal theta phases organize the reactivation of large-scale electrophysiological representations during goal-directed navigation. 2020-05-13 2023-08-13 Not clear
Lukas Kunz, Liang Wang, Daniel Lachner-Piza, Hui Zhang, Armin Brandt, Matthias Dümpelmann, Peter C Reinacher, Volker A Coenen, Dong Chen, Wen-Xu Wang, Wenjing Zhou, Shuli Liang, Philip Grewe, Christian G Bien, Anne Bierbrauer, Tobias Navarro Schröder, Andreas Schulze-Bonhage, Nikolai Axmache. Hippocampal theta phases organize the reactivation of large-scale electrophysiological representations during goal-directed navigation. Science advances. vol 5. issue 7. 2020-05-13. PMID:31281882. our findings suggest shared neural mechanisms between working memory and goal-directed navigation and provide new insights into the functions of the hippocampal theta rhythm. 2020-05-13 2023-08-13 Not clear
Mojtaba Bandarabadi, Richard Boyce, Carolina Gutierrez Herrera, Claudio L Bassetti, Sylvain Williams, Kaspar Schindler, Antoine Adamantidi. Dynamic modulation of theta-gamma coupling during rapid eye movement sleep. Sleep. vol 42. issue 12. 2020-05-11. PMID:31410477. theta phase modulates gamma amplitude in hippocampal networks during spatial navigation and rapid eye movement (rem) sleep. 2020-05-11 2023-08-13 mouse
Suijuan Zhong, Wenyu Ding, Le Sun, Yufeng Lu, Hao Dong, Xiaoying Fan, Zeyuan Liu, Ruiguo Chen, Shu Zhang, Qiang Ma, Fuchou Tang, Qian Wu, Xiaoqun Wan. Decoding the development of the human hippocampus. Nature. vol 577. issue 7791. 2020-05-07. PMID:31942070. the hippocampus is an important part of the limbic system in the human brain that has essential roles in spatial navigation and the consolidation of information from short-term memory to long-term memory 2020-05-07 2023-08-13 human
Baburam Bhattarai, Jong Won Lee, Min Whan Jun. Distinct effects of reward and navigation history on hippocampal forward and reverse replays. Proceedings of the National Academy of Sciences of the United States of America. vol 117. issue 1. 2020-05-05. PMID:31871185. distinct effects of reward and navigation history on hippocampal forward and reverse replays. 2020-05-05 2023-08-13 rat
Baburam Bhattarai, Jong Won Lee, Min Whan Jun. Distinct effects of reward and navigation history on hippocampal forward and reverse replays. Proceedings of the National Academy of Sciences of the United States of America. vol 117. issue 1. 2020-05-05. PMID:31871185. to better understand the functional roles of hippocampal forward and reverse replays, we trained rats in a spatial sequence memory task and examined how these replays are modulated by reward and navigation history. 2020-05-05 2023-08-13 rat
Baburam Bhattarai, Jong Won Lee, Min Whan Jun. Distinct effects of reward and navigation history on hippocampal forward and reverse replays. Proceedings of the National Academy of Sciences of the United States of America. vol 117. issue 1. 2020-05-05. PMID:31871185. we propose that hippocampal forward and reverse replays might contribute to constructing a map of potential navigation trajectories and their associated values (a "value map") via distinct mechanisms. 2020-05-05 2023-08-13 rat
Ethan A Solomon, Bradley C Lega, Michael R Sperling, Michael J Kahan. Hippocampal theta codes for distances in semantic and temporal spaces. Proceedings of the National Academy of Sciences of the United States of America. vol 116. issue 48. 2020-04-27. PMID:31723043. studies in humans and animals support the idea that the hippocampal theta rhythm (4 to 8 hz) is key to this mapping function, as it has been repeatedly observed during spatial navigation tasks. 2020-04-27 2023-08-13 human
Maria Kovalska, Petra Hnilicova, Dagmar Kalenska, Barbara Tothova, Marian Adamkov, Jan Lehotsk. Effect of Methionine Diet on Metabolic and Histopathological Changes of Rat Hippocampus. International journal of molecular sciences. vol 20. issue 24. 2020-04-27. PMID:31835644. the hippocampus has a crucial role in spatial navigation and memory processes and is being constantly studied for neurodegenerative disorders. 2020-04-27 2023-08-13 rat
Lihui Lu, Yuqi Ren, Tao Yu, Zhixiang Liu, Sice Wang, Lubin Tan, Jiawei Zeng, Qiru Feng, Rui Lin, Yang Liu, Qingchun Guo, Minmin Lu. Control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus. Nature communications. vol 11. issue 1. 2020-04-23. PMID:31937768. navigation requires not only the execution of locomotor programs but also high arousal and real-time retrieval of spatial memory that is often associated with hippocampal theta oscillations. 2020-04-23 2023-08-13 mouse
Roberto A Gulli, Lyndon R Duong, Benjamin W Corrigan, Guillaume Doucet, Sylvain Williams, Stefano Fusi, Julio C Martinez-Trujill. Context-dependent representations of objects and space in the primate hippocampus during virtual navigation. Nature neuroscience. vol 23. issue 1. 2020-04-13. PMID:31873285. context-dependent representations of objects and space in the primate hippocampus during virtual navigation. 2020-04-13 2023-08-13 monkey
Roberto A Gulli, Lyndon R Duong, Benjamin W Corrigan, Guillaume Doucet, Sylvain Williams, Stefano Fusi, Julio C Martinez-Trujill. Context-dependent representations of objects and space in the primate hippocampus during virtual navigation. Nature neuroscience. vol 23. issue 1. 2020-04-13. PMID:31873285. the hippocampus is implicated in associative memory and spatial navigation. 2020-04-13 2023-08-13 monkey
Yanpei Wang, Lei Hao, Yuning Zhang, Chenyi Zuo, Daoyang Wan. Entorhinal cortex volume, thickness, surface area and curvature trajectories over the adult lifespan. Psychiatry research. Neuroimaging. vol 292. 2020-04-07. PMID:31521943. the entorhinal cortex (erc) acts as a connection between the hippocampus and temporal cortex and plays a key role in memory retrieval and navigation. 2020-04-07 2023-08-13 human