| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Yinghan Zhuang, Chuhan Li, Fang Zhao, Yan Yan, Hongjie Pan, Jianmin Zhan, Thomas Behnisc. E3 Ubiquitin Ligase International journal of molecular sciences. vol 25. issue 3. 2024-02-10. PMID:38338822. |
e3 ubiquitin ligase the hippocampal formation, particularly the ca2 subregion, is critical for social memory formation and memory processing, relying on synaptic plasticity-a fundamental mechanism by which synapses strengthen. |
2024-02-10 |
2024-02-12 |
mouse |
| Samuel Brandon Lassers, Yash S Vakilna, William C Tang, Gregory J Brewe. The flow of axonal information among hippocampal sub-regions 2: patterned stimulation sharpens routing of information transmission. Frontiers in neural circuits. vol 17. 2023-12-25. PMID:38144878. |
the sub-regions of the hippocampal formation are essential for episodic learning and memory formation, yet the spike dynamics of each region contributing to this function are poorly understood, in part because of a lack of access to the inter-regional communicating axons. |
2023-12-25 |
2023-12-27 |
Not clear |
| Olayemi Joseph Olajide, Marcus E Suvanto, Clifton Andrew Chapma. Molecular mechanisms of neurodegeneration in the entorhinal cortex that underlie its selective vulnerability during the pathogenesis of Alzheimer's disease. Biology open. vol 10. issue 1. 2021-07-15. PMID:33495355. |
the entorhinal cortex (ec) is a vital component of the medial temporal lobe, and its contributions to cognitive processes and memory formation are supported through its extensive interconnections with the hippocampal formation. |
2021-07-15 |
2023-08-13 |
Not clear |
| Ziyang Liu, Cheng Peng, Yinghan Zhuang, Ying Chen, Thomas Behnisc. Direct Medial Entorhinal Cortex Input to Hippocampal CA3 Is Crucial for eEF2K Inhibitor-Induced Neuronal Oscillations in the Mouse Hippocampus. Frontiers in cellular neuroscience. vol 14. 2020-09-28. PMID:32210764. |
the hippocampal formation plays a vital role in memory formation and takes part in the control of the default neuronal network activity of the brain. |
2020-09-28 |
2023-08-13 |
mouse |
| 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 |
| Loreta Medina, Antonio Abellán, Ester Desfili. Contribution of Genoarchitecture to Understanding Hippocampal Evolution and Development. Brain, behavior and evolution. vol 90. issue 1. 2018-04-27. PMID:28866679. |
the hippocampal formation is a highly conserved structure of the medial pallium that works in association with the entorhinal cortex, playing a key role in memory formation and spatial navigation. |
2018-04-27 |
2023-08-13 |
mouse |
| Shweta Hegde, Will R Capell, Baher A Ibrahim, Jennifer Klett, Neema S Patel, Alexander T Sougiannis, Michy P Kell. Phosphodiesterase 11A (PDE11A), Enriched in Ventral Hippocampus Neurons, is Required for Consolidation of Social but not Nonsocial Memories in Mice. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. vol 41. issue 12. 2017-09-11. PMID:27339393. |
camp signaling in the ventral hippocampal formation (vhipp) appears to be required for social memory formation, but the phosphodiesterase (pde) involved remains unknown. |
2017-09-11 |
2023-08-13 |
mouse |
| He Tang, Gui-Sheng Wu, Jing Xie, Xiaobin He, Ke Deng, Huadong Wang, Fuqiang Xu, Huai-Rong Lu. Brain-wide map of projections from mice ventral subiculum. Neuroscience letters. vol 629. 2017-07-26. PMID:27422730. |
the hippocampal formation plays a critical role in episodic memory formation and spatial navigation. |
2017-07-26 |
2023-08-13 |
mouse |
| Hitoshi Nagura, Tomoko Doi, Yoshinori Fujiyosh. Characterization of physiological phenotypes of dentate gyrus synapses of PDZ1/2 domain-deficient PSD-95-knockin mice. The European journal of neuroscience. vol 43. issue 5. 2016-12-13. PMID:26684546. |
the hippocampal formation is involved in several important brain functions of animals, such as memory formation and pattern separation, and the synapses in the dentate gyrus (dg) play critical roles as the first step in the hippocampal circuit. |
2016-12-13 |
2023-08-13 |
mouse |
| Christopher D Whelan, Derrek P Hibar, Laura S van Velzen, Anthony S Zannas, Tania Carrillo-Roa, Katie McMahon, Gautam Prasad, Sinéad Kelly, Joshua Faskowitz, Greig deZubiracay, Juan E Iglesias, Theo G M van Erp, Thomas Frodl, Nicholas G Martin, Margaret J Wright, Neda Jahanshad, Lianne Schmaal, Philipp G Sämann, Paul M Thompso. Heritability and reliability of automatically segmented human hippocampal formation subregions. NeuroImage. vol 128. 2016-12-13. PMID:26747746. |
the human hippocampal formation can be divided into a set of cytoarchitecturally and functionally distinct subregions, involved in different aspects of memory formation. |
2016-12-13 |
2023-08-13 |
human |
| Marian Tsanov, Shane M O'Mar. Decoding signal processing in thalamo-hippocampal circuitry: implications for theories of memory and spatial processing. Brain research. vol 1621. 2016-05-23. PMID:25498107. |
one of the main information streams to the hippocampal formation, vital for episodic memory formation, arises from thalamo-hippocampal projections, as there is extensive connectivity between these structures. |
2016-05-23 |
2023-08-13 |
Not clear |
| Jacob Raber, Emil Rudobeck, Mary Campbell-Beachler, Antiño R Allen, Barrett Allen, Susanna Rosi, Gregory A Nelson, Shaila Ramachandran, Jennifer Turner, John R Fike, Roman Vlkolinsk. (28)Silicon radiation-induced enhancement of synaptic plasticity in the hippocampus of naïve and cognitively tested mice. Radiation research. vol 181. issue 4. 2014-06-23. PMID:24673255. |
while low doses of (56)fe radiation do not induce cell death of mature neurons, they affect synaptic plasticity in the ca1 region, the principal neuronal output of the hippocampal formation involved in memory formation. |
2014-06-23 |
2023-08-12 |
mouse |
| Yoshifumi Abe, Masaki Sekino, Yasushi Terazono, Hiroyuki Ohsaki, Yugo Fukazawa, Seiichiro Sakai, Hiromu Yawo, Tatsuhiro Hisatsun. Opto-fMRI analysis for exploring the neuronal connectivity of the hippocampal formation in rats. Neuroscience research. vol 74. issue 3-4. 2013-07-22. PMID:22982343. |
our study suggests that opto-fmri could be a tool for exploring the neuronal connectivity of the hippocampal formation, to understand the neural basis of memory formation and retrieval. |
2013-07-22 |
2023-08-12 |
rat |
| Yoshifumi Abe, Masaki Sekino, Yasushi Terazono, Hiroyuki Ohsaki, Yugo Fukazawa, Seiichiro Sakai, Hiromu Yawo, Tatsuhiro Hisatsun. Opto-fMRI analysis for exploring the neuronal connectivity of the hippocampal formation in rats. Neuroscience research. vol 74. issue 3-4. 2013-07-22. PMID:22982343. |
although the hippocampal formation is very important for memory formation and retrieval, there is little information on its neuronal connectivity, especially on its longitudinal axis of connection. |
2013-07-22 |
2023-08-12 |
rat |
| Nathaniel J Killian, Michael J Jutras, Elizabeth A Buffal. A map of visual space in the primate entorhinal cortex. Nature. vol 491. issue 7426. 2013-01-16. PMID:23103863. |
place-modulated activity among neurons in the hippocampal formation presents a means to organize contextual information in the service of memory formation and recall. |
2013-01-16 |
2023-08-12 |
rat |
| Tracey J Shor. Opposite effects of stressful experience on memory formation in males versus females. Dialogues in clinical neuroscience. vol 4. issue 2. 2012-09-10. PMID:22033590. |
these opposite effects of stress on memory formation are accompanied by similarly opposite effects on neuroanatomical measures, such as dendritic spines in the hippocampal formation. |
2012-09-10 |
2023-08-12 |
rat |
| Marian Joëls, Henk Kars. Corticosteroid effects on calcium signaling in limbic neurons. Cell calcium. vol 51. issue 3-4. 2012-08-03. PMID:22153720. |
these receptors are highly expressed in neurons of the hippocampal formation and the amygdala, areas that play a role in (emotional) memory formation. |
2012-08-03 |
2023-08-12 |
rat |
| Jean-Marie C Bouteiller, Michel Baudry, Sushmita L Allam, Renaud J Greget, Serge Bischoff, Theodore W Berge. Modeling glutamatergic synapses: insights into mechanisms regulating synaptic efficacy. Journal of integrative neuroscience. vol 7. issue 2. 2008-12-12. PMID:18763719. |
the hippocampal formation is critically involved for the long-term storage of various forms of information, and it is widely believed that the phenomenon of long-term potentiation (ltp) of synaptic transmission is a molecular/cellular mechanism participating in memory formation. |
2008-12-12 |
2023-08-12 |
Not clear |
| A Mohedano-Moriano, A Martinez-Marcos, P Pro-Sistiaga, X Blaizot, M M Arroyo-Jimenez, P Marcos, E Artacho-Pérula, R Insaust. Convergence of unimodal and polymodal sensory input to the entorhinal cortex in the fascicularis monkey. Neuroscience. vol 151. issue 1. 2008-04-22. PMID:18065153. |
the hippocampal formation is a key structure in memory formation and consolidation. |
2008-04-22 |
2023-08-12 |
monkey |
| Li Zhang, Wei Yu, Tai-Zhen Han, Wen Xie, Yu Lu. [Changes of NMDA receptor expression in rat hippocampal formation after establishment of spatial memory by different training modes]. Sheng li xue bao : [Acta physiologica Sinica]. vol 58. issue 5. 2008-01-03. PMID:17041728. |
these results suggest that the short reinforcing training mode can establish long-term spatial memory, which is almost the same as that established by the long-term training mode, and that the increase of nmda/nr1 expression in ca1 area and dentate gyrus of the hippocampal formation may be one of the mechanisms of spatial long-term memory formation. |
2008-01-03 |
2023-08-12 |
rat |