The DOI matches its Crossref record; 120 of the 120 references it cites were found in a registry or an index.
Do stars govern our actions? Astrocyte involvement in rodent behavior
Open accessAbstract
Astrocytes have emerged as important partners of neurons in information processing. Important progress has been made in the past two decades in understanding the role of astrocytes in the generation of neuron-astrocyte network outputs resulting in behavior. We review evidence for astrocyte involvement across four different behavioral domains: cognition, emotion, motor, and sensory processing. Accumulating evidence from animal models has provided a wealth of data that largely supports a direct involvement of astrocytes on diverse aspects of behavior. The development of tools for selectively controlling the temporal and spatial properties of astrocyte activity will help to consolidate our knowledge of the mechanisms underlying this involvement.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“recent evidence for glial (Han et al., 2012) and mitochondrial CB1R (Hebert-Chatelain et al., 2016) in eCB-mediated mnemonic processes, together with a known role for astrocytes (Oliveira et al., 2015) and mitochondria (Manji et al., 2012) in stress- and anxiety-related processes.”
From The endocannabinoid system as a target for novel anxiolytic drugs (2017) · cites this paper as Oliveira et al., 2015
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
CRISPR-Cas systems for editing, regulating and targeting genomes
Sander, J. D., & Joung, J. K. (2014) · Nature Biotechnology · doi:10.1038/nbt.2842 · Cited by 3,153
Cahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129
Tripartite synapses: glia, the unacknowledged partner
Araque, A., Parpura, V., Sanzgiri, R. P., & Haydon, P. G. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01349-6 · Cited by 2,529
Self-citationGlutamate Induces Calcium Waves in Cultured Astrocytes: Long-Range Glial Signaling
Cornell-Bell, A. H., Finkbeiner, S. M., Cooper, M. S., & Smith, S. J. (1990) · Science · doi:10.1126/science.1967852 · Cited by 1,846
Tripartite synapses: astrocytes process and control synaptic information
Perea, G., Navarrete, M., & Araque, A. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.05.001 · Cited by 1,820
Self-citationGlutamate-mediated astrocyte–neuron signalling
Parpura, V., Basarsky, T. A., Liu, F., Jeftinija, K., Jeftinija, S., & Haydon, P. G. (1994) · Nature · doi:10.1038/369744a0 · Cited by 1,768
Astrocyte-Neuron Lactate Transport Is Required for Long-Term Memory Formation
Suzuki, A., Stern, S. A., Bozdagi, O., Huntley, G. W., Walker, R. H., Magistretti, P. J., & Alberini, C. M. (2011) · Cell · doi:10.1016/j.cell.2011.02.018 · Cited by 1,711
Long-term potentiation depends on release of d-serine from astrocytes
Henneberger, C., Papouin, T., Oliet, S. H. R., & Rusakov, D. A. (2010) · Nature · doi:10.1038/nature08673 · Cited by 1,389
Gliotransmitters Travel in Time and Space
Araque, A., Carmignoto, G., Haydon, P. G., Oliet, S. H. R., Robitaille, R., & Volterra, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.007 · Cited by 1,308
Self-citationAstrocytic Purinergic Signaling Coordinates Synaptic Networks
Pascual, O., Casper, K. B., Kubera, C., Zhang, J., Revilla-Sanchez, R., Sul, J.-Y., Takano, H., Moss, S. J., McCarthy, K., & Haydon, P. G. (2005) · Science · doi:10.1126/science.1116916 · Cited by 1,280
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–188 of 188
Ma, Z., Du, X., Wang, F., Ding, R., Li, Y., Liu, A., Wei, L., Hou, S., Chen, F., Hu, Q., et al. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00400 · Cited by 22
Kaczmarczyk, L., Reichenbach, N., Blank-Stein, N., Jonson, M., Dittrich, L., Petzold, G. C., & Jackson, W. S. (2021) · Scientific Reports · doi:10.1038/s41598-021-84887-2 · Cited by 18
Intra-generational protein malnutrition impairs temporal astrogenesis in rat brain
Naik, A. A., Patro, N., Seth, P., & Patro, I. K. (2017) · Biology Open · doi:10.1242/bio.023432 · Cited by 21
Liu, L., Kelly, M. G., Yang, X. R., Fernandez, T. G., Wierzbicki, E. L., Skrobach, A., & Doré, S. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00807-4 · Cited by 20
IP 3 R2 null mice display a normal acquisition of somatic and neurological development milestones
Guerra‐Gomes, S., Cunha‐Garcia, D., Nascimento, D. S. M., Duarte‐Silva, S., Loureiro‐Campos, E., Sardinha, V. M., Viana, J. F., Sousa, N., Maciel, P., Pinto, L., et al. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14724 · Cited by 20
Self-citationSpatial and Temporal Diversity of Astrocyte Phenotypes in Spinocerebellar Ataxia Type 1 Mice
Rosa, J. S., Hamel, K. A., Sheeler, C. A., Borgenheimer, E., Gilliat, S., Soles, A., Ghannoum, F. J., Sbrocco, K., Handler, H. P., Rainwater, O., et al. (2022) · Cells · doi:10.3390/cells11203323 · Cited by 19
The Duality of Astrocyte Neuromodulation: Astrocytes Sense Neuromodulators and Are Neuromodulators
Lines, J., Corkrum, M., Aguilar, J., & Araque, A. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70054 · Cited by 19
Self-citationCalcium‐Dependent Signaling in Astrocytes: Downstream Mechanisms and Implications for Cognition
Veiga, A., Abreu, D. S., Dias, J. D., Azenha, P., Barsanti, S., & Oliveira, J. F. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70019 · Cited by 21
Self-citationZhang, Y., Wu, S., Xie, L., Yu, S., Zhang, L., Liu, C., Zhou, W., & Yu, T. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00240 · Cited by 18
Modelling the modulation of cortical Up-Down state switching by astrocytes
Moyse, L. B., & Berry, H. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010296 · Cited by 16
Gliotransmission and adenosinergic modulation: insights from mammalian spinal motor networks
Acton, D. G., & Miles, G. B. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00230.2017 · Cited by 17
Impact of Coffee Intake on Measures of Wellbeing in Mice
Machado, N. J., Ardais, A. P., Nunes, A., Szabó, E. C., Silveirinha, V., Silva, H. B. L., Kaster, M. P., & Cunha, R. A. (2024) · Nutrients · doi:10.3390/nu16172920 · Cited by 16
Sensory response in host and engrafted astrocytes of adult brain in Vivo
Zhang, K., & Chen, X. (2017) · Glia · doi:10.1002/glia.23181 · Cited by 14
Lin, Z., You, F., Li, T., Feng, Y., Zhao, X., Yang, J., Yao, Z., Gao, Y., & Chen, J. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00782-w · Cited by 16
The role of astrocytes in behaviors related to emotion and motivation
Shigetomi, E., & Koizumi, S. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.09.015 · Cited by 16
Astroglial cannabinoid signaling and behavior
Ramon‐Duaso, C., Conde-Moro, A. R., & Busquets-García, A. (2022) · Glia · doi:10.1002/glia.24171 · Cited by 13
A Neuron–Glial Perspective for Computational Neuroscience
Pittà, M. D., & Berry, H. (2019) · Springer series in computational neuroscience · doi:10.1007/978-3-030-00817-8_1 · Cited by 13
Central amygdala astrocyte plasticity underlies GABAergic dysregulation in ethanol dependence
Nentwig, T. B., Obray, J. D., Kruyer, A., Wilkes, E. T., Vaughan, D. T., Scofield, M. D., & Chandler, L. J. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03337-z · Cited by 14
From Pathology to Physiology of Calcineurin Signalling in Astrocytes
Lim, D., Rocchio, F., Mapelli, L., & Moccia, F. D. (2016) · Russian Agency for Digital Standardization · doi:10.20388/omp2016.002.0029 · Cited by 12
Antonelli, F., Casciati, A., Bellés, M., Serra, N., Linares, V., Marino, C., Mancuso, M., & Pazzaglia, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222212605 · Cited by 12
Melzer, L., Freiman, T. M., & Derouiche, A. (2021) · Cells · doi:10.3390/cells10010072 · Cited by 14
Tackling Dysfunction of Mitochondrial Bioenergetics in the Brain
Zanfardino, P., Doccini, S., Santorelli, F. M., & Petruzzella, V. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158325 · Cited by 13
Astroengrams: rethinking the cellular substrate for memory
Romero, J. S., & Navarrete, M. (2026) · Nature reviews. Neuroscience · doi:10.1038/s41583-025-01012-2 · Cited by 13
Martins‐Macedo, J., Salgado, A. J., Gomes, E. D., & Pinto, L. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.09.030 · Cited by 11
Gao, Z., Wu, L., Zhao, X., Wei, Z., Lu, L., & Yi, M. (2023) · Cognitive Neurodynamics · doi:10.1007/s11571-023-10002-y · Cited by 10
Shining the Light on Astrocytic Ensembles
Delgado, L., & Navarrete, M. (2023) · Cells · doi:10.3390/cells12091253 · Cited by 12
Angeles-López, Q. D., García‐Lara, L., Aguirre-Pineda, N., Castañeda‐Arellano, R., Elizondo, G., Pérez‐Severiano, F., & Segovia, J. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113230 · Cited by 9
Nuriya, M., Takeuchi, M., & Yasui, M. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.12.073 · Cited by 9
Genetics and Traumatic Brain Injury: Findings from an Exome-Based Study of a 50-Patient Case Series
Gracheva, A. S., Kashatnikova, D. A., Redkin, I. V., Zakharchenko, V. E., Kuzovlev, A. N., & Salnikova, L. E. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46090616 · Cited by 7
Campos, J., Guerra‐Gomes, S., Serra, S. C., Baltazar, G., Oliveira, J. F., Teixeira, F. G., & Salgado, A. J. (2020) · Brain Research · doi:10.1016/j.brainres.2020.146700 · Cited by 8
Self-citationde Suduiraut, I. G., Grosse, J., Ramos‐Fernández, E., Sandi, C., & Hollis, F. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14892 · Cited by 8
Ontogeny of the circadian system: a multiscale process throughout development
Comas, M., Tonelli, D. D. P., Berdondini, L., & Astiz, M. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2023.11.004 · Cited by 7
Control of Dopamine Signal in High-Order Receptor Complex on Striatal Astrocytes
Amato, S., Averna, M., Farsetti, E., Guidolin, D., Pedrazzi, M., Gatta, E., Candiani, S., Maura, G., Agnati, L. F., Cervetto, C., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168610 · Cited by 9
AstroWars: the return of the astrocytic metabotropic glutamate receptor 5
Dias, J. D., Viana, J. F., Alves, L. S., Veiga, A., Matos, B. G. D. O., Machado, J. L., & Oliveira, J. F. (2025) · The Journal of Physiology · doi:10.1113/jp288403 · Cited by 7
Self-citationTurk, A. Z., & SheikhBahaei, S. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25230 · Cited by 7
Astrocytic GABA controls fidelity of temporal cortical processing in Fragile X Syndrome
Wagner, V. A., Thapa, R., Norman, A. O., Varallo, A., Wimberly, J., Rais, M., Gerasymchuk, D., Piepponen, P. T., Razak, K. A., Castrén, M. L., et al. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107233 · Cited by 8
Sex-specific astrocyte regulation of spinal motor circuits by Nkx6.1
Huerta, N. A. B., Lee, Z.-F., Song, E. C., Woo, J., Cheng, Y.-T., Sardar, D., Sert, O., Maleki, E., Yu, K., Akdemir, E. S., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.115121 · Cited by 5
Astrocytes phenomics as new druggable targets in healthy aging and Alzheimer’s disease progression
Lana, D., Ugolini, F., Iovino, L., Attorre, S., & Giovannini, M. G. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1512985 · Cited by 6
Barsanti, S., Viana, J. F., Veiga, A., Machado, J. L., Abreu, D. S., Dias, J. D., Monteiro, S., Silva, N. A., Pinto, L., & Oliveira, J. F. (2024) · Cells · doi:10.3390/cells13110969 · Cited by 5
Self-citationNuriya, M., Yasui, D., Yamada, T., Aoki, T., & Yasui, M. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.02.142 · Cited by 5
Brain-wide circuit-specific targeting of astrocytes
Thompson, A., Arano, R., Saleem, U., Preciado, R., Munoz, L., Nelson, I., Ramos, K., Kim, Y., Li, Y., & Xu, W. (2023) · Cell Reports Methods · doi:10.1016/j.crmeth.2023.100653 · Cited by 4
Dual Oxytocin Signals in Striatal Astrocytes
Farsetti, E., Amato, S., Averna, M., Guidolin, D., Pedrazzi, M., Maura, G., Agnati, L. F., Cervetto, C., & Marcoli, M. (2025) · Biomolecules · doi:10.3390/biom15081122 · Cited by 4
Signal encoding performance of astrocyte-dressed Morris Lecar neurons
Erkan, E. (2023) · Chaos Solitons & Fractals · doi:10.1016/j.chaos.2023.114223 · Cited by 4
Astroglial CB1 Reveal Sex‐Specific Synaptic Effects of Amphetamine
Mariani, Y., Tor, T. D., Garavaldi, T., Julio‐Kalajzić, F., Gisquet, D., Gómez-Sotres, P., Cannich, A., Gambino, G., Drago, F., Serrat, R., et al. (2025) · Glia · doi:10.1002/glia.70026 · Cited by 4
Insights on nervous system biology and anatomy
Esteves, M., Almeida, A., & Leite‐Almeida, H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818084-6.00001-5 · Cited by 5
Mitterauer, B. (2019) · Open Journal of Medical Psychology · doi:10.4236/ojmp.2019.82002 · Cited by 4
Allometry unleashed: an adaptationist approach of brain scaling in mammalian evolutionPreprint
Willemet, R. (2019) · doi:10.7287/peerj.preprints.27872v1 · Cited by 4
A spatial threshold for astrocyte calcium surgePreprint
Lines, J., Baraibar, A. M., Nanclares, C., Martín, E. D., Aguilar, J., Kofuji, P., Navarrete, M., & Araque, A. (2024) · eLife · doi:10.7554/elife.90046.2 · Cited by 4
Self-citationHomeostasis to Allostasis: Prefrontal Astrocyte Roles in Cognitive Flexibility and Stress Biology
Wulaer, B., Holtz, M., & Nagai, J. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-64839-7_6 · Cited by 4
Astrocytic α7-nicotinic acetylcholine receptors mediate pain information processing and perception
Teng, T., Yang, S., Li, J., Wang, H., Wu, F., He, Y., Fan, J., Shi, H., Huang, M., Zhou, X. R., et al. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107245 · Cited by 3
The multiple scales of astrocytic functional units
Oliveira, J. F., Agarwal, A., Beckervordersandforth, R., Curreli, S., Denizot, A., Dulla, C. G., Enger, R., Goda, Y., Goshen, I., Holt, M. G., et al. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02308-x · Cited by 4
Self-citationDeciphering the role of siRNA in anxiety and depression
Bale, R., & Doshi, G. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176868 · Cited by 3
A spatial threshold for astrocyte calcium surge
Lines, J., Baraibar, A. M., Nanclares, C., Martín, E. D., Aguilar, J., Kofuji, P., Navarrete, M., & Araque, A. (2024) · eLife · doi:10.1101/2023.07.18.549563 · Cited by 5
Self-citationKosuge, A., Kunisawa, K., Iida, T., Wulaer, B., Kawai, T., Tanabe, M., Saito, K., Nabeshima, T., & Mouri, A. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16100 · Cited by 3
Melanopsin for Time-Controlling Activation of Astrocyte–Neuron Networks
Mederos, S., González-Arias, C., & Perea, G. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0755-8_3 · Cited by 3
Astrocyte subdomains respond independently in vivoPreprint
López-Hidalgo, M. A., Kellner, V., & Schummers, J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/675769 · Cited by 3
Rais (2022) · doi:10.1101/2022.02.08.479618 · Cited by 2
Non-neuronal brain biology and its relevance to animal welfare
Lawrence, A. B., Brown, S. M., Bradford, B. M., Mabbott, N. A., Bombail, V., & Rutherford, K. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106136 · Cited by 3
Computational Role of Astrocytes in Bayesian Inference and Probability Distribution Encoding
Dimkovski, M., & An, A. (2016) · Lecture notes in computer science · doi:10.1007/978-3-319-47103-7_3 · Cited by 2
Inferences of glia‐mediated control in Caenorhabditis elegans
Bowles, S. N., & Johnson, C. M. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24803 · Cited by 2
Gau, Y. A., Hsu, E. T., Cha, J., Pak, R. W., Looger, L. L., Kang, J. U., & Bergles, D. E. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.18.541390 · Cited by 2
Reversal of Postnatal Brain Astrocytes and Ependymal Cells towards a Progenitor Phenotype in Culture
Kakogiannis, D., Kourla, M., Dimitrakopoulos, D., & Kazanis, I. (2024) · Cells · doi:10.3390/cells13080668 · Cited by 1
Ferreira, G. A. M., & Pinto, L. (2025) · Glia · doi:10.1002/glia.70031 · Cited by 2
Mancini, A., Bellingacci, L., Canonichesi, J., & Filippo, M. D. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-85841-0.00017-1 · Cited by 1
Sardar, D., Cheng, Y.-T., Woo, J., Choi, D., Lee, Z.-F., Kwon, W., Chen, H., Lozzi, B., Cervantes, A., Rajendran, K., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.24.529904 · Cited by 1
Astrocytic Foxo1 regulates hippocampal spinogenesis and synaptic plasticity to enhance fear memoryPreprint
Viana, J. F., Guerra‐Gomes, S., Abreu, D. S., Machado, J. L., Barsanti, S., Gonçalves, M., Martín, C., Sardinha, V. M., Nascimento, D. S. M., Tavares, G., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.01.538923 · Cited by 1
Self-citationA spatial threshold for astrocyte calcium surgePreprint
Lines, J., Baraibar, A. M., Nanclares, C., Martín, E. D., Aguilar, J., Kofuji, P., Navarrete, M., & Araque, A. (2023) · eLife · doi:10.7554/elife.90046.1 · Cited by 1
Self-citationSimulating calcium signaling in fine astrocytic processes
Denizot, A. (2019) · theses.fr (ABES) · doi:10.70675/970a38b3z8898z4ac0z896ez5ae9336af7f7 · Cited by 1
Kaczmarczyk, L., Reichenbach, N., Blank-Stein, N., Jonson, M., Dittrich, L., Petzold, G. C., & Jackson, W. S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.06.027714
Astrocytes mediate analogous memory in a multi-layer neuron-astrocytic networkPreprint
Tsybina, Y., Kastalskiy, I. A., Krivonosov, M., Zaikin, A. A., Kazantsev, V., Gorban, A. N., & Gordleeva, S. (2021) · arXiv (Cornell University) · doi:10.48550/arxiv.2108.13414
Delepine, C., Li, K., Shih, J., Gaudeaux, P., & Sur, M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.20.477039
Kyriacou, C. P. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734831688.793555633
Friedman, W. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.738597157.793578735
Neudecker, V., Perez‐Zoghbi, J. F., & Brambrink, A. M. (2024) · Journal of Immunological Sciences · doi:10.29245/2578-3009/2024/2.1255
Astrocytic mGluR5 signaling tunes emotional and cognitive processing in the adult brainPreprint
Viana, J. F., Dias, J. D., González-Arias, C., Alves, L. S., Veiga, A., Abreu, D. S., Machado, J. L., Barsanti, S., Nobre, R. J., de Almeida, L. P., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.07.663457
Self-citationGenetic-Designed Tools to Unveil the Role of Astrocytes in Neuronal Circuits and Animal Behavior
Ashouri, F., Sánchez-Ruiz, A., Alberquilla, S., & Perea, G. (2025) · Springer eBooks · doi:10.1007/978-3-031-94215-0_5
Ventral striatal astrocytes contribute to reinforcement learningPreprint
Pai, J., Sogukpinar, F., Ogasawara, K., Smith, G. J., Fiocchi, F. R., Dai, Y., Wu, Y., Frank, M. J., Ching, S., Lucantonio, F., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.20.683205 · Cited by 1
Lituma, P. J., Deveci, A., Barrio-Alonso, E., Tan, K., Wilkinson, M., Castillo, P. E., & Çolak, D. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.18.689044
Pellegrino, G. (2017) · theses.fr (ABES) · doi:10.70675/49c584f3z87f6z4320z924bz64015ded1e39
Circuits neuronaux sous-tendant la régulation émotionnelle par le système ocytocinergique
Goyon, S. (2018) · theses.fr (ABES) · doi:10.70675/c8c9bec0z7b79z4826z862az93b128e1ada6
Visser, J. (2022) · theses.fr (ABES) · doi:10.70675/bd2669fdzfb7az41aezb634z91c7e005996c
Cannabinoid modulation of behavioral processes : from adolescence to adulthood
Ioannidou, C. (2021) · theses.fr (ABES) · doi:10.70675/85fe2023za70dz4d65z83c9z9828ec89522f
New regulators in oxytocin and vasopressin release : role of the endolysosomal two-pore channels
Martucci, L. L. (2021) · theses.fr (ABES) · doi:10.70675/027d1ae2zd2ebz4677za019ze6ccd94cafe9
The role of astrocytes in the social transmission of stress
Gómez-Sotres, P. (2024) · theses.fr (ABES) · doi:10.70675/1d3b266aze7c4z4968z98c6za5ffe9fe383a
Preface to the Special Issue “Astrocytes in Cognition and Behavior”
Oliveira, J. F., & Araque, A. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70501
Self-citationLituma, P. J., Deveci, A., Barrio-Alonso, E., Tan, K., Wilkinson, M., Castillo, P. E., & Colak, D. (2026) · eLife · doi:10.7554/elife.111940
Lituma, P. J., Deveci, A., Barrio-Alonso, E., Tan, K., Wilkinson, M., Castillo, P. E., & Colak, D. (2026) · eLife · doi:10.7554/elife.111940.1
Metadata
- Authors
- Oliveira, J. F., Sardinha, V. M., Guerra-Gomes, S., Araque, A., & Sousa, N.
- Affiliations
- University of Minho (PT)
- University of Minnesota (US)
- Corresponding author
- Oliveira, João Filipe
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 2015-09
- Volume
- 38
- Issue
- 9
- Pages
- 535-549
- ISSN
- 0166-2236 (ISSN-L)
- OpenAlex
- W1646393677
- Cited by
- 189
- References
- 120
- Citations by year
- 2026: 5 · 2025: 17 · 2024: 15 · 2023: 22 · 2022: 15 · 2021: 24 · 2020: 21 · 2019: 23 · 2018: 15 · 2017: 17 · 2016: 14 · 2015: 1
- FWCI
- 1.86
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Trends in Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- RepositóriUM (Universidade do Minho) (submittedVersion, other-oa)
- Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (submittedVersion, cc-by-nc-nd)
- Funders
- European Commission (273936)
- National Science Council
- Fundação Bial
- Fundação para a Ciência e a Tecnologia (SFRH/BD/101298/2014, COMPETE, PTDC/SAU-NSC/118194/2010, SFRH/BPD/97281/2013)
- FP7 People: Marie-Curie Actions
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- astrocytes, astrocyte-neuron interaction, behavior, cognition, emotions, motor behavior, sensory processing, rodent models
- MeSH terms
- Animals, Astrocytes, Behavior, Animal, Mental Processes, Neurons, Rodentia
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
