Astrocyte glypicans 4 and 6 promote formation of excitatory synapses via GluA1 AMPA receptors

Glutamate Receptor Ion Channels: Structure, Regulation, and Function

Traynelis, S. F., Wollmuth, L. P., McBain, C. J., Menniti, F. S., Vance, K. M., Ogden, K. K., Hansen, K. B., Yuan, H., Myers, S. J., & Dingledine, R. (2010) · Pharmacological Reviews · doi:10.1124/pr.109.002451 · Cited by 3,568

A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function

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AMPA Receptor Trafficking and Synaptic Plasticity

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Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis

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Control of Synapse Number by Glia

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Control of Synaptic Strength by Glial TNFα

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A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

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Gabapentin Receptor α2δ-1 Is a Neuronal Thrombospondin Receptor Responsible for Excitatory CNS Synaptogenesis

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Neuroligins Determine Synapse Maturation and Function

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Array tomography: a new tool for imaging the molecular architecture and ultrastructure of neural circuits

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The Effects of Immune System Modulation on Prion Disease Susceptibility and Pathogenesis

Mabbott, N. A., Bradford, B. M., Pal, R., Young, R. A., & Donaldson, D. S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197299 · Cited by 22

Modulation of network activity and induction of homeostatic synaptic plasticity by enzymatic removal of heparan sulfates

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Puzzling out presynaptic differentiation

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The Role of Astrocytes in the Molecular Pathophysiology of Schizophrenia: Between Neurodevelopment and Neurodegeneration

Vellucci, L., Mazza, B., Barone, A., Nasti, A., Simone, G. D., Iasevoli, F., & de Bartolomeis, A. (2025) · Biomolecules · doi:10.3390/biom15050615 · Cited by 23

The HSPG Glypican Regulates Experience-Dependent Synaptic and Behavioral Plasticity by Modulating the Non-Canonical BMP Pathway

Kamimura, K., Odajima, A., Ikegawa, Y., Chikako, M., & Maeda, N. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.08.032 · Cited by 19

Running Promotes Transformation of Brain Astrocytes Into Neuroprotective Reactive Astrocytes and Synaptic Formation by Targeting Gpc6 Through the STAT3 Pathway

Chen, Z., Gao, M. Q., Su, Y., Liu, P., & Sun, B. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.633618 · Cited by 20

Astrocytic NMDA Receptors in the Basolateral Amygdala Contribute to Facilitation of Fear Extinction

Shelkar, G. P., Liu, J., & Dravid, S. M. (2021) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyab055 · Cited by 20

Electrophysiological Properties of Human Cortical Organoids: Current State of the Art and Future Directions

Zourray, C., Kurian, M. A., Barral, S., & Lignani, G. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.839366 · Cited by 20

Novel model of cortical–meningeal organoid co-culture system improves human cortical brain organoid cytoarchitecture

Jalilian, E., & Shin, S. (2023) · Scientific Reports · doi:10.1038/s41598-023-35077-9 · Cited by 19

Talking to the Synapse: How Antidepressants Can Target Glial Cells to Reshape Brain Circuits

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Loss of Local Astrocyte Support Disrupts Action Potential Propagation and Glutamate Release Synchrony from Unmyelinated Hippocampal Axon Terminals In Vitro

Sobieski, C. A., Jiang, X., Crawford, D. C., & Mennerick, S. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1289-15.2015 · Cited by 21

Intracellular protein complexes involved in synapse assembly in presynaptic neurons

Han, K. A., Um, J. W., & Ko, J. (2018) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2018.11.008 · Cited by 19

HSPGs glypican‐1 and glypican‐4 are human neuronal proteins characteristic of different neural phenotypes

Oikari, L. E., Yu, C., Okolicsanyi, R. K., Avgan, N., Peall, I. W., Griffiths, L. R., & Haupt, L. M. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24666 · Cited by 20

Star power: the emerging role of astrocytes as neuronal partners during cortical plasticity

Wahis, J., Hennes, M., Arckens, L., & Holt, M. G. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.12.001 · Cited by 21

Stem and Progenitor Cell-Derived Astroglia Therapies for Neurological Diseases

Chen, C., Chan, A., Han, W., Chung, S., Deng, W., & Jiang, P. (2015) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2015.09.003 · Cited by 20

Nasal Delivery of Engineered Exosomes via a Thermo‐Sensitive Hydrogel Depot Reprograms Glial Cells for Spinal Cord Repair

Wang, Y., Liu, J., Li, P., Peng, Z., Zhang, Y., Liu, Y., Li, M., Gong, X., Liu, D., Xu, E., et al. (2025) · Advanced Science · doi:10.1002/advs.202504486 · Cited by 20

Circadian Regulation of the Neuroimmune Environment Across the Lifespan: From Brain Development to Aging

Chen, R., Routh, B. N., Gaudet, A. D., & Fonken, L. K. (2023) · Journal of Biological Rhythms · doi:10.1177/07487304231178950 · Cited by 21

Glial modulation of synapse development and plasticity: oligodendrocyte precursor cells as a new player in the synaptic quintet

Akinlaja, Y. O., & Nishiyama, A. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1418100 · Cited by 23

Role of astrocyte in neuroinflammation‐induced loss in neuroplasticity and subsequent onset of depression: A systematic review

Singhal, G., Singhal, S., & Baune, B. T. (2025) · Neuroprotection/Neuroprotection (Chichester, England. Print) · doi:10.1002/nep3.70009 · Cited by 22

The past, present, and future of research on neuroinflammation-induced mild cognitive impairment: A bibliometric analysis

Cai, M., Zhang, Y., Chen, S. X., Wu, Z., & Zhu, L. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.968444 · Cited by 20

Astrocytes-Derived Small Extracellular Vesicles Hinder Glioma Growth

Serpe, C., Michelucci, A., Monaco, L., Rinaldi, A., Luca, M. D., Familiari, P., Relucenti, M., Pietro, E. D., Castro, M. A. D., D’Agnano, I., et al. (2022) · Biomedicines · doi:10.3390/biomedicines10112952 · Cited by 17

A three‐dimensional spheroid co‐culture system of neurons and astrocytes derived from Alzheimer's disease patients for drug efficacy testing

Park, H. J., Kim, J., & Ryou, C. (2023) · Cell Proliferation · doi:10.1111/cpr.13399 · Cited by 18

Intracellular accumulation of tau oligomers in astrocytes and their synaptotoxic action rely on Amyloid Precursor Protein Intracellular Domain-dependent expression of Glypican-4

Puliatti, G., Puma, D. D. L., Aceto, G., Lazzarino, G., Acquarone, E., Mangione, R., D'adamio, L., Ripoli, C., Arancio, O., Piacentini, R., et al. (2023) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2023.102482 · Cited by 19

Astrocytes in the adult dentate gyrus—balance between adult and developmental tasks

Chalmers, N., Masouti, E., & Beckervordersandforth, R. (2024) · Molecular Psychiatry · doi:10.1038/s41380-023-02386-4 · Cited by 19

A Novel In Vitro Live-imaging Assay of Astrocyte-mediated Phagocytosis Using pH Indicator-conjugated Synaptosomes

Byun, Y. G., & Chung, W. (2018) · Journal of Visualized Experiments · doi:10.3791/56647 · Cited by 18

3-O-sulfated heparan sulfate interactors target synaptic adhesion molecules from neonatal mouse brain and inhibit neural activity and synaptogenesis in vitro

Maïza, A., Sidahmed‐Adrar, N., Michel, P. P., Carpentier, G., Habert, D., Dalle, C., Redouane, W., Hamza, M. M., van Kuppevelt, T., Ouidja, M. O., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-76030-4 · Cited by 21

Type IIa RPTPs and Glycans: Roles in Axon Regeneration and Synaptogenesis

Sakamoto, K., Ozaki, T., Suzuki, Y., & Kadomatsu, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115524 · Cited by 18

Transcriptome profiling of the Olig2-expressing astrocyte subtype reveals their unique molecular signature

Ohayon, D., Aguirrebengoa, M., Escalas, N., Jungas, T., & Soula, C. (2021) · iScience · doi:10.1016/j.isci.2021.102806 · Cited by 20

Response of Astrocyte Subpopulations Following Spinal Cord Injury

Allahyari, R. V., Heinsinger, N. M., Hwang, D. H., Jaffe, D. A., Rasouli, J., Shiers, S. I., Thomas, S. J., Price, T. J., Rostami, A. M., & Lepore, A. C. (2022) · Cells · doi:10.3390/cells11040721 · Cited by 18

CRISPRi screens in human astrocytes elucidate regulators of distinct inflammatory reactive statesPreprint

Leng, K., Rose, I. V. L., Kim, H., Xia, W., Romero‐Fernandez, W., Rooney, B., Koontz, M., Li, E., Ao, Y., Wang, S., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.23.457400 · Cited by 18

Characterization of Glycosaminoglycan Disaccharide Composition in Astrocyte Primary Cultures and the Cortex of Neonatal Rats

Zhang, X., Hashimoto, J. G., Han, X., Zhang, F., Linhardt, R. J., & Guizzetti, M. (2021) · Neurochemical Research · doi:10.1007/s11064-020-03195-9 · Cited by 17

Case Report: A Novel De Novo Missense Mutation of the GRIA2 Gene in a Chinese Case of Neurodevelopmental Disorder With Language Impairment

Zhou, B., Zhang, C., Zheng, L., Wang, Z., Chen, X., Feng, X., Zhang, Q., Hao, S., Wei, L., Gu, W., et al. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.794766 · Cited by 17

Cocaine preference and neuroadaptations are maintained by astrocytic NMDA receptors in the nucleus accumbens

Shelkar, G. P., Gandhi, P. J., Liu, J., & Dravid, S. M. (2022) · Science Advances · doi:10.1126/sciadv.abo6574 · Cited by 18

Beyond NMDA Receptors: Homeostasis at the Glutamate Tripartite Synapse and Its Contributions to Cognitive Dysfunction in Schizophrenia

Bauminger, H., & Gaisler‐Salomon, I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158617 · Cited by 16

Novel Antidepressant Mechanism of Ginsenoside Rg1 in Regulating the Dysfunction of the Glutamatergic System in Astrocytes

Zhang, N., Jiang, H., Wang, H., Wang, Y., Peng, Y., Liu, Y., Xia, C., Xu, Y., Chu, S., Zhang, Y., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010575 · Cited by 17

Astrocytes Excessively Engulf Synapses in a Mouse Model of Alzheimer’s Disease

Li, L., Lü, S., Zhu, J., Yu, X., Hou, S., Huang, Y., Niu, X., Du, X., & Liu, R. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25021160 · Cited by 17

Gliomas: a reflection of temporal gliogenic principles

Sojka, C., & Sloan, S. A. (2024) · Communications Biology · doi:10.1038/s42003-024-05833-2 · Cited by 18

Astrocytes as a target for Nogo‐A and implications for synapse formation in vitro and in a model of acute demyelination

Espírito‐Santo, S., Coutinho, V. G., Dezonne, R. S., Stipursky, J., dos Santos‐Rodrigues, A., Batista, C., Paes‐de‐Carvalho, R., Fuss, B., & Gomes, F. C. A. (2021) · Glia · doi:10.1002/glia.23971 · Cited by 19

Astrocytes increase the activity of synaptic GluN2B NMDA receptors

Hahn, J., Wang, X., & Margeta, M. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00117 · Cited by 18

Synapse-specific roles for microglia in development: New horizons in the prefrontal cortex

Blagburn-Blanco, S. V., Chappell, M. S., Biase, L. M. D., & DeNardo, L. A. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.965756 · Cited by 16

β-Adrenergic Signaling Promotes Morphological Maturation of Astrocytes in Female Mice

Rosenberg, M. F., Godoy, M. I., Wade, S. D., Paredes, M. F., Zhang, Y., & Molofsky, A. V. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0357-23.2023 · Cited by 18

Circadian Biology and the Neurovascular Unit

Li, W., Tiedt, S., Lawrence, J. H., Harrington, M. E., Musiek, E. S., & Lo, E. H. (2024) · Circulation Research · doi:10.1161/circresaha.124.323514 · Cited by 17

Acute and Chronic Mu Opioids Differentially Regulate Thrombospondins 1 and 2 Isoforms in Astrocytes

Phamduong, E., Rathore, M. K., Crews, N. R., D’Angelo, A. S., Leinweber, A. L., Kappera, P., Krenning, T. M., Rendell, V. R., Belcheva, M. M., & Coscia, C. J. (2013) · ACS Chemical Neuroscience · doi:10.1021/cn400172n · Cited by 18

GPR30 disrupts the balance of GABAergic and glutamatergic transmission in the spinal cord driving to the development of bone cancer pain

Luo, J. D., Huang, X., Li, Y., Yang, L., Xu, X., Gao, Y., Shi, R., Yao, W., Liu, J., & Ke, C. (2016) · Oncotarget · doi:10.18632/oncotarget.11867 · Cited by 16

Microglia and Astrocytes in Postnatal Neural Circuit Formation

Duffy, A., & Eyo, U. B. (2024) · Glia · doi:10.1002/glia.24650 · Cited by 15

The role of reactive astrocytes in neurotoxicity induced by ultrafine particulate matter

Li, B., Chang, X., Liang, X., Liu, T., Shen, Y., Zhang, Q., Yang, X., Lyu, Y., Liu, L., Guo, J., et al. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.161416 · Cited by 17

Cytosolic DNA sensors and glial responses to endogenous DNA

Suptela, A. J., & Marriott, I. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1130172 · Cited by 15

Dysregulation of astrocyte-secreted pleiotrophin contributes to neuronal structural and functional deficits in Down syndrome

Brandebura, A. N., Paumier, A., Asbell, Q. N., Tao, T., Micael, M. K. B., Sanchez, S., & Allen, N. J. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116300 · Cited by 17

High-Resolution Microfluidic Single-Cell Transcriptional Profiling Reveals Clinically Relevant Subtypes among Human Stem Cell Populations Commonly Utilized in Cell-Based Therapies

Rennert, R. C., Schäfer, R., Bliss, T. M., Januszyk, M., Sorkin, M., Achrol, A. S., Rodrigues, M., Maan, Z. N., Kluba, T., Steinberg, G. K., et al. (2016) · Frontiers in Neurology · doi:10.3389/fneur.2016.00041 · Cited by 15

Astrocytic‐neuronal crosstalk gets jammed: Alternative perspectives on the onset of neuropsychiatric disorders

Román, C., Egert, L., & Benedetto, B. D. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14900 · Cited by 16

Limb-clasping, cognitive deficit and increased vulnerability to kainic acid-induced seizures in neuronal glycosylphosphatidylinositol deficiency mouse models

Kandasamy, L. C., Tsukamoto, M., Banov, V., Sambuu, T., Nagasawa, Y., Kato, M., Matsumoto, N., Takeda, J., Itohara, S., Ogawa, S., et al. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddab052 · Cited by 15

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

Acupuncture Treatment of Epilepsy

Chao, D., & Xia, Y. (2012) · Springer eBooks · doi:10.1007/978-1-4614-3357-6_6 · Cited by 14

The Effect of Dexmedetomidine Post-treatment on the Inflammatory Response of Astrocyte Induced by Lipopolysaccharide

Xie, C., Wang, Z., Tang, J., Shi, Z., & He, Z. (2014) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-014-0213-0 · Cited by 15

Gestational Hypothyroxinemia Affects Glutamatergic Synaptic Protein Distribution and Neuronal Plasticity Through Neuron-Astrocyte Interplay

Cisternas, P., Louveau, A., Bueno, S. M., Kalergis, A. M., Boudin, H., & Riedel, C. A. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9609-0 · Cited by 15

Antiepileptogenic repair of excitatory and inhibitory synaptic connectivity after neocortical trauma

Prince, D. A., Gu, F., & Parada, I. (2016) · Progress in brain research · doi:10.1016/bs.pbr.2016.03.013 · Cited by 15

Neutrophils-astrocyte interactions in central nervous system inflammation

Yuan, B., Zhang, X., Liu, L., Chai, Y., Zhang, J., & Chen, X. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-07945-x · Cited by 15

Necl2/3-mediated mechanism for tripartite synapse formation

Nozawa, O., Miyata, M., Shiotani, H., Kameyama, T., Komaki, R., Shimizu, T., Kuriu, T., Kashiwagi, Y., Sato, Y., Koebis, M., et al. (2022) · Development · doi:10.1242/dev.200931 · Cited by 13

How Are Synapses Born? A Functional and Molecular View of the Role of the Wnt Signaling Pathway

Bonansco, C., Cerpa, W. F., & Inestrosa, N. C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010708 · Cited by 13

Abnormal Morphology and Synaptogenic Signaling in Astrocytes Following Prenatal Opioid Exposure

Niebergall, E. B., Weekley, D., Mazur, A., Olszewski, N. A., DeSchepper, K. M., Radant, N. P., Vijay, A., & Risher, W. C. (2024) · Cells · doi:10.3390/cells13100837 · Cited by 14

CNS / PNS proteoglycans functionalize neuronal and astrocyte niche microenvironments optimizing cellular activity by preserving membrane polarization dynamics, ionic microenvironments, ion fluxes, neuronal activation, and network neurotransductive capacity

Melrose, J. (2024) · Journal of Neuroscience Research · doi:10.1002/jnr.25361 · Cited by 15

A smarter mouse with human astrocytes

Zhang, Y., & Barres, B. A. (2013) · BioEssays · doi:10.1002/bies.201300070 · Cited by 14

Heparan sulfate proteoglycans in Drosophila neuromuscular development

Kamimura, K., & Maeda, N. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.06.015 · Cited by 14

Friends Turn Foe—Astrocytes Contribute to Neuronal Damage in NeuroAIDS

Pandey, H. S., & Seth, P. (2019) · Journal of Molecular Neuroscience · doi:10.1007/s12031-019-01357-1 · Cited by 13

Trans-synaptic interactions of ionotropic glutamate receptors

Fossati, M., & Charrier, C. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.09.001 · Cited by 19

VER/VEGF receptors regulate AMPA receptor surface levels and glutamatergic behavior

Luth, E. S., Hodul, M., Rennich, B. J., Riccio, C., Hofer, J., Markoja, K., & Juo, P. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009375 · Cited by 16

The Astrogenic Balance in the Aging Brain

Andromidas, F., Atashpanjeh, S., Myers, A. J., MacKinnon, B., Shaffer, M. M., & Koob, A. O. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210420095118 · Cited by 13

Reconstitution of Giant Mammalian Synapses in Culture for Molecular Functional and Imaging Studies

Dimitrov, D., Takagi, H., Guillaud, L., Saitoh, N., Eguchi, K., & Takahashi, T. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3869-15.2016 · Cited by 14

Glia Development and Function in the NematodeCaenorhabditis elegansPreprint

Singhvi, A., Shaham, S., & Rapti, G. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041346 · Cited by 15

Senescent Astrocytes: A New Player in Brain Aging and Cognitive Decline

Pessoa, B., Hayashide, L. D. S., Dias, G. R., Pontes, B., Pinto, R. S., & Diniz, L. P. (2026) · Brain Sciences · doi:10.3390/brainsci16010076 · Cited by 13

Crosstalk between Blood Vessels and Glia during the Central Nervous System Development

Tabata, H. (2022) · Life · doi:10.3390/life12111761 · Cited by 14

Impact of Aβ40 and Aβ42 Fibrils on the Transcriptome of Primary Astrocytes and Microglia

Zhu, X. A., Schrader, J. M., Irizarry, B. A., Smith, S. O., & Nostrand, W. E. V. (2022) · Biomedicines · doi:10.3390/biomedicines10112982 · Cited by 14

Erythropoietin alleviates astrocyte pyroptosis by targeting the miR-325-3p/Gsdmd axis in rat spinal cord injury

Shan, W., Wang, J., Cheng, R., Xuan, Y., & Yin, Z. (2023) · Inflammopharmacology · doi:10.1007/s10787-023-01311-z · Cited by 13

Astrocyte coverage of excitatory synapses correlates to measures of synapse structure and function in ferret primary visual cortex

Thomas, C. I., Ryan, M. A., McNabb, M. C., Kamasawa, N., & Scholl, B. (2024) · Glia · doi:10.1002/glia.24582 · Cited by 19

Glial Control of Cortical Neuronal Circuit Maturation and Plasticity

Faust, T. E., Devlin, B. A., Farhy-Tselnicker, I., Ferro, A., Postolache, M., & Xin, W. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1208-24.2024 · Cited by 13

Physiology of Astroglia: Channels, Receptors, Transporters, Ion Signaling and Gliotransmission

Verkhratsky, A., & Parpura, V. (2015) · Colloquium Series on Neuroglia in Biology and Medicine From Physiology to Disease · doi:10.4199/c00123ed1v01y201501ngl004 · Cited by 12

Astrocytes, Makers of New Neurons

Kempermann, G. (2015) · Neuron · doi:10.1016/j.neuron.2015.11.017 · Cited by 13

Glypican 6 Enhances N-Methyl-D-Aspartate Receptor Function in Human-Induced Pluripotent Stem Cell-Derived Neurons

Sato, K., Takahashi, K., Shigemoto‐Mogami, Y., Chujo, K., & Sekino, Y. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00259 · Cited by 13

Histone Deacetylases in Neurodegenerative Diseases and Their Potential Role as Therapeutic Targets: Shedding Light on Astrocytes

Pinheiro, P. D. S. M., Diniz, L. P., Franco, L. S., Siqueira, M., & Gomes, F. C. A. (2025) · Pharmaceuticals · doi:10.3390/ph18101471 · Cited by 13

Translational modulator ISRIB alleviates synaptic and behavioral phenotypes in Fragile X syndrome

Coulson, R. L., Frattini, V., Moyer, C. E., Hodges, J., Walter, P., Mourrain, P., Zuo, Y., & Wang, G. X. (2024) · iScience · doi:10.1016/j.isci.2024.109259 · Cited by 12

Running exercise improves astrocyte loss, morphological complexity and astrocyte-contacted synapses in the hippocampus of CUS-induced depression model mice

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