All Relations between navigation and hippocampal formation
| Publication | Sentence | Publish Date | Extraction Date | Species |
|---|---|---|---|---|
| Manu S Madhav, Ravikrishnan P Jayakumar, Shahin G Lashkari, Francesco Savelli, Hugh T Blair, James J Knierim, Noah J Cowa. The Dome: A virtual reality apparatus for freely locomoting rodents. Journal of neuroscience methods. 2021-09-26. PMID:34453979. | the cognitive map in the hippocampal formation of rodents and other mammals integrates multiple classes of sensory and motor information into a coherent representation of space. | 2021-09-26 | 2023-08-13 | rat |
| Christina N Rogers Flattery, Rebecca F Rosen, Aaron S Farberg, Jeromy M Dooyema, Patrick R Hof, Chet C Sherwood, Lary C Walker, Todd M Preus. Quantification of neurons in the hippocampal formation of chimpanzees: comparison to rhesus monkeys and humans. Brain structure & function. vol 225. issue 8. 2021-08-11. PMID:32909100. | the hippocampal formation is important for higher brain functions such as spatial navigation and the consolidation of memory, and it contributes to abilities thought to be uniquely human, yet little is known about how the human hippocampal formation compares to that of our closest living relatives, the chimpanzees. | 2021-08-11 | 2023-08-13 | human |
| Zoltán Kraboth, Bernadette Kálmá. Neuroscience highlights: Main cell types underlying memory and spatial navigation. Ideggyogyaszati szemle. vol 73. issue 9-10. 2020-10-28. PMID:33035420. | interest in the hippocampal formation and its role in navigation and memory arose in the second part of the 20th century, at least in part due to the curious case of henry g. molaison, who underwent brain surgery for intractable epilepsy. | 2020-10-28 | 2023-08-13 | Not clear |
| Zoltán Kraboth, Bernadette Kálmá. Neuroscience highlights: Main cell types underlying memory and spatial navigation. Ideggyogyaszati szemle. vol 73. issue 9-10. 2020-10-28. PMID:33035420. | by this brief survey, we highlight main cell types in the hippocampal formation, and describe their roles in spatial navigation and memory processes. | 2020-10-28 | 2023-08-13 | Not clear |
| Paulo E Jorge, Belmiro V Pinto, Verner P Bingman, John B Phillip. Involvement of the Avian Dorsal Thalamic Nuclei in Homing Pigeon Navigation. Frontiers in behavioral neuroscience. vol 11. 2020-09-29. PMID:29163085. | in the brain, regions like the piriform cortex, olfactory bulbs, hippocampal formation, vestibular nuclei, and the wulst, are among the brain regions often discussed as involved in avian navigation. | 2020-09-29 | 2023-08-13 | pigeon |
| Deepa Jain, Indraja R Jakhalekar, Sachin S Deshmuk. Navigational Strategies and Their Neural Correlates. Journal of the Indian Institute of Science. vol 97. issue 4. 2020-09-29. PMID:29657367. | then we move on to outline what we know about the brain area most associated with spatial navigation, namely the hippocampal formation. | 2020-09-29 | 2023-08-13 | Not clear |
| Jean Simonnet, Michael Brech. Burst Firing and Spatial Coding in Subicular Principal Cells. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 39. issue 19. 2020-06-11. PMID:30819796. | the subiculum is the major output structure of the hippocampal formation and is involved in learning and memory as well as in spatial navigation. | 2020-06-11 | 2023-08-13 | Not clear |
| Larry W Swanson, Joel D Hah. A qualitative solution with quantitative potential for the mouse hippocampal cortex flatmap problem. Proceedings of the National Academy of Sciences of the United States of America. vol 117. issue 6. 2020-05-11. PMID:31988117. | the hippocampal formation (hpf) is a focus of intense experimental investigation, particularly because of its roles in conscious memory consolidation, spatial navigation, emotion, and motivated behaviors. | 2020-05-11 | 2023-08-13 | mouse |
| G Torromino, L Autore, V Khalil, V Mastrorilli, M Griguoli, A Pignataro, E Centofante, G M Biasini, V De Turris, M Ammassari-Teule, A Rinaldi, A Mel. Offline ventral subiculum-ventral striatum serial communication is required for spatial memory consolidation. Nature communications. vol 10. issue 1. 2020-04-02. PMID:31844154. | the hippocampal formation is considered essential for spatial navigation. | 2020-04-02 | 2023-08-13 | Not clear |
| Marian Tsano. Differential and complementary roles of medial and lateral septum in the orchestration of limbic oscillations and signal integration. The European journal of neuroscience. vol 48. issue 8. 2019-11-14. PMID:29044802. | we discuss the heterogeneous anatomy of the lateral septum, which is composed of diverse subregions with distinct ascending and descending projections, and we relate the physiological characteristics of septal nuclei to their functional relationships with the hippocampal formation, the hypothalamus and the brainstem reticular formation during motivated spatial navigation. | 2019-11-14 | 2023-08-13 | Not clear |
| A Yin, P H Tseng, S Rajangam, M A Lebedev, M A L Nicoleli. Place Cell-Like Activity in the Primary Sensorimotor and Premotor Cortex During Monkey Whole-Body Navigation. Scientific reports. vol 8. issue 1. 2019-10-11. PMID:29907789. | these observations suggest that primary sensorimotor and premotor cortical areas in primates are likely involved in allocentrically representing body position in space during whole-body navigation, which is an unexpected finding given the classical hierarchical model of cortical processing that attributes functional specialization for spatial processing to the hippocampal formation. | 2019-10-11 | 2023-08-13 | monkey |
| Sang Ah Lee, Jonathan F Miller, Andrew J Watrous, Michael R Sperling, Ashwini Sharan, Gregory A Worrell, Brent M Berry, Joshua P Aronson, Kathryn A Davis, Robert E Gross, Bradley Lega, Sameer Sheth, Sandhitsu R Das, Joel M Stein, Richard Gorniak, Daniel S Rizzuto, Joshua Jacob. Electrophysiological Signatures of Spatial Boundaries in the Human Subiculum. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 38. issue 13. 2019-10-08. PMID:29467145. | to address this gap in the literature, we analyzed intracranial recordings from the hippocampal formation of surgical epilepsy patients (of both sexes) while they performed a virtual spatial navigation task and compared the power in three frequency bands (1-4, 4-10, and 30-90 hz) for target locations near and far from the environmental boundaries. | 2019-10-08 | 2023-08-13 | human |
| Nobuyoshi Matsumoto, Takuma Kitanishi, Kenji Mizusek. The subiculum: Unique hippocampal hub and more. Neuroscience research. vol 143. 2019-07-23. PMID:30121285. | the hippocampal formation, which comprises the hippocampus proper, dentate gyrus, and subiculum, is crucial for learning, memory, and spatial navigation. | 2019-07-23 | 2023-08-13 | Not clear |
| James R Hinman, G William Chapman, Michael E Hasselm. Neuronal representation of environmental boundaries in egocentric coordinates. Nature communications. vol 10. issue 1. 2019-07-05. PMID:31235693. | cognitive maps of environments are encoded in the hippocampal formation in an allocentric reference frame, but motor movements that comprise physical navigation are represented within an egocentric reference frame. | 2019-07-05 | 2023-08-13 | Not clear |
| Joshua P Bassett, Thomas J Wills, Francesca Cacucc. Self-Organized Attractor Dynamics in the Developing Head Direction Circuit. Current biology : CB. vol 28. issue 4. 2019-07-03. PMID:29398220. | they are a fundamental component of the wider circuit of spatially responsive hippocampal formation neurons that make up the neural cognitive map of space [4]. | 2019-07-03 | 2023-08-13 | rat |
| Matthias Nau, Joshua B Julian, Christian F Doelle. How the Brain's Navigation System Shapes Our Visual Experience. Trends in cognitive sciences. vol 22. issue 9. 2019-06-06. PMID:30031670. | here we review growing evidence that the mammalian hippocampal formation, extensively studied in the context of navigation and memory, mediates a representation of visual space that is stably anchored to the external world. | 2019-06-06 | 2023-08-13 | Not clear |
| Jacob L S Bellmund, Peter Gärdenfors, Edvard I Moser, Christian F Doelle. Navigating cognition: Spatial codes for human thinking. Science (New York, N.Y.). vol 362. issue 6415. 2019-05-08. PMID:30409861. | the hippocampal formation has long been suggested to underlie both memory formation and spatial navigation. | 2019-05-08 | 2023-08-13 | human |
| Bryan C Souza, Rodrigo Pavão, Hindiael Belchior, Adriano B L Tor. On Information Metrics for Spatial Coding. Neuroscience. vol 375. 2019-02-21. PMID:29432886. | the hippocampal formation is involved in navigation, and its neuronal activity exhibits a variety of spatial correlates (e.g., place cells, grid cells). | 2019-02-21 | 2023-08-13 | Not clear |
| Derrek P Hibar, Hieab H H Adams, Neda Jahanshad, Ganesh Chauhan, Jason L Stein, Edith Hofer, Miguel E Renteria, Joshua C Bis, Alejandro Arias-Vasquez, M Kamran Ikram, Sylvane Desrivières, Meike W Vernooij, Lucija Abramovic, Saud Alhusaini, Najaf Amin, Micael Andersson, Konstantinos Arfanakis, Benjamin S Aribisala, Nicola J Armstrong, Lavinia Athanasiu, Tomas Axelsson, Ashley H Beecham, Alexa Beiser, Manon Bernard, Susan H Blanton, Marc M Bohlken, Marco P Boks, Janita Bralten, Adam M Brickman, Owen Carmichael, M Mallar Chakravarty, Qiang Chen, Christopher R K Ching, Vincent Chouraki, Gabriel Cuellar-Partida, Fabrice Crivello, Anouk Den Braber, Nhat Trung Doan, Stefan Ehrlich, Sudheer Giddaluru, Aaron L Goldman, Rebecca F Gottesman, Oliver Grimm, Michael E Griswold, Tulio Guadalupe, Boris A Gutman, Johanna Hass, Unn K Haukvik, David Hoehn, Avram J Holmes, Martine Hoogman, Deborah Janowitz, Tianye Jia, Kjetil N Jørgensen, Nazanin Karbalai, Dalia Kasperaviciute, Sungeun Kim, Marieke Klein, Bernd Kraemer, Phil H Lee, David C M Liewald, Lorna M Lopez, Michelle Luciano, Christine Macare, Andre F Marquand, Mar Matarin, Karen A Mather, Manuel Mattheisen, David R McKay, Yuri Milaneschi, Susana Muñoz Maniega, Kwangsik Nho, Allison C Nugent, Paul Nyquist, Loes M Olde Loohuis, Jaap Oosterlaan, Martina Papmeyer, Lukas Pirpamer, Benno Pütz, Adaikalavan Ramasamy, Jennifer S Richards, Shannon L Risacher, Roberto Roiz-Santiañez, Nanda Rommelse, Stefan Ropele, Emma J Rose, Natalie A Royle, Tatjana Rundek, Philipp G Sämann, Arvin Saremi, Claudia L Satizabal, Lianne Schmaal, Andrew J Schork, Li Shen, Jean Shin, Elena Shumskaya, Albert V Smith, Emma Sprooten, Lachlan T Strike, Alexander Teumer, Diana Tordesillas-Gutierrez, Roberto Toro, Daniah Trabzuni, Stella Trompet, Dhananjay Vaidya, Jeroen Van der Grond, Sven J Van der Lee, Dennis Van der Meer, Marjolein M J Van Donkelaar, Kristel R Van Eijk, Theo G M Van Erp, Daan Van Rooij, Esther Walton, Lars T Westlye, Christopher D Whelan, Beverly G Windham, Anderson M Winkler, Katharina Wittfeld, Girma Woldehawariat, Christiane Wolf, Thomas Wolfers, Lisa R Yanek, Jingyun Yang, Alex Zijdenbos, Marcel P Zwiers, Ingrid Agartz, Laura Almasy, David Ames, Philippe Amouyel, Ole A Andreassen, Sampath Arepalli, Amelia A Assareh, Sandra Barral, Mark E Bastin, Diane M Becker, James T Becker, David A Bennett, John Blangero, Hans van Bokhoven, Dorret I Boomsma, Henry Brodaty, Rachel M Brouwer, Han G Brunner, Randy L Buckner, Jan K Buitelaar, Kazima B Bulayeva, Wiepke Cahn, Vince D Calhoun, Dara M Cannon, Gianpiero L Cavalleri, Ching-Yu Cheng, Sven Cichon, Mark R Cookson, Aiden Corvin, Benedicto Crespo-Facorro, Joanne E Curran, Michael Czisch, Anders M Dale, Gareth E Davies, Anton J M De Craen, Eco J C De Geus, Philip L De Jager, Greig I De Zubicaray, Ian J Deary, Stéphanie Debette, Charles DeCarli, Norman Delanty, Chantal Depondt, Anita DeStefano, Allissa Dillman, Srdjan Djurovic, Gary Donohoe, Wayne C Drevets, Ravi Duggirala, Thomas D Dyer, Christian Enzinger, Susanne Erk, Thomas Espeseth, Iryna O Fedko, Guillén Fernández, Luigi Ferrucci, Simon E Fisher, Debra A Fleischman, Ian Ford, Myriam Fornage, Tatiana M Foroud, Peter T Fox, Clyde Francks, Masaki Fukunaga, J Raphael Gibbs, David C Glahn, Randy L Gollub, Harald H H Göring, Robert C Green, Oliver Gruber, Vilmundur Gudnason, Sebastian Guelfi, Asta K Håberg, Narelle K Hansell, John Hardy, Catharina A Hartman, Ryota Hashimoto, Katrin Hegenscheid, Andreas Heinz, Stephanie Le Hellard, Dena G Hernandez, Dirk J Heslenfeld, Beng-Choon Ho, Pieter J Hoekstra, Wolfgang Hoffmann, Albert Hofman, Florian Holsboer, Georg Homuth, Norbert Hosten, Jouke-Jan Hottenga, Matthew Huentelman, Hilleke E Hulshoff Pol, Masashi Ikeda, Clifford R Jack, Mark Jenkinson, Robert Johnson, Erik G Jönsson, J Wouter Jukema, René S Kahn, Ryota Kanai, Iwona Kloszewska, David S Knopman, Peter Kochunov, John B Kwok, Stephen M Lawrie, Hervé Lemaître, Xinmin Liu, Dan L Longo, Oscar L Lopez, Simon Lovestone, Oliver Martinez, Jean-Luc Martinot, Venkata S Mattay, Colm McDonald, Andrew M McIntosh, Francis J McMahon, Katie L McMahon, Patrizia Mecocci, Ingrid Melle, Andreas Meyer-Lindenberg, Sebastian Mohnke, Grant W Montgomery, Derek W Morris, Thomas H Mosley, Thomas W Mühleisen, Bertram Müller-Myhsok, Michael A Nalls, Matthias Nauck, Thomas E Nichols, Wiro J Niessen, Markus M Nöthen, Lars Nyberg, Kazutaka Ohi, Rene L Olvera, Roel A Ophoff, Massimo Pandolfo, Tomas Paus, Zdenka Pausova, Brenda W J H Penninx, G Bruce Pike, Steven G Potkin, Bruce M Psaty, Simone Reppermund, Marcella Rietschel, Joshua L Roffman, Nina Romanczuk-Seiferth, Jerome I Rotter, Mina Ryten, Ralph L Sacco, Perminder S Sachdev, Andrew J Saykin, Reinhold Schmidt, Helena Schmidt, Peter R Schofield, Sigurdur Sigursson, Andrew Simmons, Andrew Singleton, Sanjay M Sisodiya, Colin Smith, Jordan W Smoller, Hilkka Soininen, Vidar M Steen, David J Stott, Jessika E Sussmann, Anbupalam Thalamuthu, Arthur W Toga, Bryan J Traynor, Juan Troncoso, Magda Tsolaki, Christophe Tzourio, Andre G Uitterlinden, Maria C Valdés Hernández, Marcel Van der Brug, Aad van der Lugt, Nic J A van der Wee, Neeltje E M Van Haren, Dennis van 't Ent, Marie-Jose Van Tol, Badri N Vardarajan, Bruno Vellas, Dick J Veltman, Henry Völzke, Henrik Walter, Joanna M Wardlaw, Thomas H Wassink, Michael E Weale, Daniel R Weinberger, Michael W Weiner, Wei Wen, Eric Westman, Tonya White, Tien Y Wong, Clinton B Wright, Ronald H Zielke, Alan B Zonderman, Nicholas G Martin, Cornelia M Van Duijn, Margaret J Wright, W T Longstreth, Gunter Schumann, Hans J Grabe, Barbara Franke, Lenore J Launer, Sarah E Medland, Sudha Seshadri, Paul M Thompson, M Arfan Ikra. Novel genetic loci associated with hippocampal volume. Nature communications. vol 8. 2018-11-19. PMID:28098162. | the hippocampal formation is a brain structure integrally involved in episodic memory, spatial navigation, cognition and stress responsiveness. | 2018-11-19 | 2023-08-13 | Not clear |
| Ann B Butle. Of Horse-Caterpillars and Homologies: Evolution of the Hippocampus and Its Name. Brain, behavior and evolution. vol 90. issue 1. 2018-04-27. PMID:28866677. | the hippocampal formation of amniotes participates in allocentric (external landmark) spatial navigation, memory, and attention to novel stimuli, and these functions generally are shared across amniotes despite variation in its morphological features. | 2018-04-27 | 2023-08-13 | Not clear |