Astrocyte barriers to neurotoxic inflammation

Molecular Mechanisms of Depression: Perspectives on New Treatment Strategies

Lang, U. E., & Borgwardt, S. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350094 · Cited by 8,526

Innate immune recognition

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From inflammation to sickness and depression: when the immune system subjugates the brain

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Astrocyte-endothelial interactions at the blood-brain barrier

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Astrocytes: Biology and pathology

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A Meta-Analysis of Cytokines in Major Depression

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Regeneration beyond the glial scar

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Molecular dissection of reactive astrogliosis and glial scar formation

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Genomic analysis of reactive astrogliosis

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IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel

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Generation of a perfusable three-dimensional human neurovascular chip to model brain drug delivery and immune cell extravasation

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Histological and Functional Breakdown of the Blood−Brain Barrier in Alzheimer’s Disease: A Multifactorial Intersection

Chauca, J. M. N., & Martínez, G. G. R. (2025) · Neurology International · doi:10.3390/neurolint17100166 · Cited by 14

BST2 expression at astrocyte borders promotes microglial recruitment via the C3/C3aR signaling

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Advances in electroactive bioscaffolds for repairing spinal cord injury

Liu, Z., Lai, J., Kong, D., Zhao, Y., Zhao, J., Dai, J., & Zhang, M. (2024) · Biomedical Materials · doi:10.1088/1748-605x/ad4079 · Cited by 13

Heterogeneity of brain extracellular matrix and astrocyte activation

Huber, R. E., Babbitt, C. C., & Peyton, S. R. (2024) · Journal of Neuroscience Research · doi:10.1002/jnr.25356 · Cited by 15

Navigating the nano-bio immune interface: advancements and challenges in CNS nanotherapeutics

Moulton, C., Baroni, A., Quagliarini, E., Leone, L., Digiacomo, L., Morotti, M., Caracciolo, G., Podda, M. V., & Tasciotti, E. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1447567 · Cited by 14

CAR T Cell Nanosymbionts: Revealing the Boundless Potential of a New Dyad

Baena, J. C., Pérez, L. M., Toro-Pedroza, A., Kitawaki, T., & Loukanov, A. R. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252313157 · Cited by 13

Astrocytes and Alcohol Throughout the Lifespan

Guizzetti, M., Mangieri, R. A., Ezerskiy, L. A., Hashimoto, J. G., Bajo, M., Farris, S. P., Homanics, G. E., Lasek, A. W., Mayfield, R. D., Messing, R. O., et al. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.04.013 · Cited by 13

Biomaterials in Alzheimer's Disease: An Anti‐Neuroinflammatory Perspective

Huang, N., Huang, W., Wang, M., Shi, J., Luo, Y., & Huang, J. (2025) · Advanced Healthcare Materials · doi:10.1002/adhm.202500498 · Cited by 13

Parenchymal pericytes are not the major contributor of extracellular matrix in the fibrotic scar after stroke in male mice

Roth, M., Enström, A., Aghabeick, C., Carlsson, R., Genové, G., & Paul, G. (2019) · Journal of Neuroscience Research · doi:10.1002/jnr.24557 · Cited by 14

APLN/APLNR Signaling Controls Key Pathological Parameters of Glioblastoma

Kälin, R., & Glass, R. (2021) · Cancers · doi:10.3390/cancers13153899 · Cited by 13

A Breakdown of Immune Tolerance in the Cerebellum

Hampe, C. S., & Mitoma, H. (2022) · Brain Sciences · doi:10.3390/brainsci12030328 · Cited by 15

Neuro-Immune Mechanisms of Anti-Cryptococcal Protection

Drummond, R. A. (2017) · Journal of Fungi · doi:10.3390/jof4010004 · Cited by 14

Aquaporins in neurological disorders

Hirt, L., Price, M., Benakis, C., & Badaut, J. (2018) · Clinical and Translational Neuroscience · doi:10.1177/2514183x17752902 · Cited by 13

Immune memory in the brain

Nott, A., & Glass, C. K. (2018) · Nature · doi:10.1038/d41586-018-03800-6 · Cited by 13

Retinal structure and function in monkeys with fetal alcohol exposure

Bouskila, J., Palmour, R. M., Bouchard, J., & Ptito, M. (2018) · Experimental Eye Research · doi:10.1016/j.exer.2018.07.027 · Cited by 13

Glial fibrillary acidic protein levels are associated with global histone H4 acetylation after spinal cord injury in rats

Elsner, V. R., de Menezes, M., Nicola, F., da Silva, I. V., Vizuete, A. F. K., Xavier, L., Gonçalves, C.-A. S., Netto, C. A., & Mestriner, R. G. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.239443 · Cited by 13

Spinal parenchymal occupation by neural stem cells after subpial delivery in adult immunodeficient rats

Maršala, M., Kamizato, K., Tadokoro, T., Navarro, M. R., Juhás, Š., Juhásová, J., Marsala, S., Studenovská, H., Proks, V., Hazel, T., et al. (2019) · Stem Cells Translational Medicine · doi:10.1002/sctm.19-0156 · Cited by 13

RNA interference in glial cells for nerve injury treatment

Lin, J., Jo, S. B., Kim, T.-H., Kim, H., & Chew, S. Y. (2020) · Journal of Tissue Engineering · doi:10.1177/2041731420939224 · Cited by 15

Molecular modeling on human CCR5 receptors and complex with CD4 antigens and HIV-1 envelope glycoprotein gp120.

Yang, J., & Liu, C. Q. (2000) · PubMed · Cited by 13

Specific Alterations in Astrocyte Properties via the GluA2-GAPDH Complex Associated with Multiple Sclerosis

Lee, F. H. F., Zhang, H., Jiang, A., Zai, C. C. H., & Liu, F. (2018) · Scientific Reports · doi:10.1038/s41598-018-31318-4 · Cited by 13

Nav1.5 in astrocytes plays a sex‐specific role in clinical outcomes in a mouse model of multiple sclerosis

Pappalardo, L. W., Samad, O. A., Liu, S., Zwinger, P. J., Black, J. A., & Waxman, S. G. (2018) · Glia · doi:10.1002/glia.23470 · Cited by 13

Targeting glial cells: Unveiling the neuroprotective mechanisms of Ginseng in the brain microenvironment

Wang, Y., Zhang, M., & Li, W. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.10.018 · Cited by 13

Heterogeneity of mature oligodendrocytes in the central nervous system

Weng, C., Groh, A. M. R., Yaqubi, M., Cui, Q., Stratton, J. A., Moore, G. R. W., & Antel, J. P. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00055 · Cited by 16

Endoplasmic Reticulum Stress Differently Modulates the Release of IL-6 and IL-8 Cytokines in Human Glial Cells

Sokołowska, P., Wiktorowska‐Owczarek, A., Tambor, J., Gawlak-Socka, S., Kowalczyk, E., & Jóźwiak-Bębenista, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168687 · Cited by 12

Short-chain fatty acids in Huntington's disease: Mechanisms of action and their therapeutic implications

Saadh, M. J., Ahmed, H. H., Kareem, R. A., Sanghvi, G. V., Ganesan, S., Agarwal, M., Kaur, P., Taher, W. M., Alwan, M., Jawad, M. J., et al. (2025) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2025.173972 · Cited by 12

Astrocytes, a Promising Opportunity to Control the Progress of Parkinson’s Disease

Sánchez, A., Moráles, I., Rodriguez‐Sabate, C., Solé-Sabater, M., & Rodrı́guez, M. (2021) · Biomedicines · doi:10.3390/biomedicines9101341 · Cited by 12

Exogenous polyserine and polyleucine are toxic to recipient cells

Owada, R., Mitsui, S., & Nakamura, K. (2022) · Scientific Reports · doi:10.1038/s41598-022-05720-y · Cited by 12

Astrocytic junctional adhesion molecule-A regulates T-cell entry past the glia limitans to promote central nervous system autoimmune attack

Amatruda, M., Chapouly, C., Woo, V., Safavi, F., Zhang, J., Dai, D., Therattil, A., Moon, C. Y., Villavicencio, J., Gordon, A., et al. (2022) · Brain Communications · doi:10.1093/braincomms/fcac044 · Cited by 13

Long-Term Exposure of Cultured Astrocytes to High Glucose Impact on Their LPS-Induced Activation

Abdyeva, A., Kurtova, E., Savinkova, I. G., Galkov, M., & Горбачева, Л. Р. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25021122 · Cited by 12

Proteomic and epigenomic markers of sepsis-induced delirium (SID)

Sfera, A., Price, A. I., Gradini, R., Cummings, M. A., & Osorio, C. P. (2015) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2015.00059 · Cited by 14

SUMO1 Deficiency Exacerbates Neurological and Cardiac Dysfunction after Intracerebral Hemorrhage in Aged Mice

Li, W., Chopp, M., Zacharek, A., Yang, W., Chen, Z., Landschoot‐Ward, J., Venkat, P., & Chen, J. (2020) · Translational Stroke Research · doi:10.1007/s12975-020-00837-6 · Cited by 12

Zinc finger E-Box binding homeobox 2 (ZEB2)-induced astrogliosis protected neuron from pyroptosis in cerebral ischemia and reperfusion injury

Zhao, Z., Hu, X., Wang, J., Wang, J., Hou, Y., & Chen, S. (2021) · Bioengineered · doi:10.1080/21655979.2021.2012551 · Cited by 12

Correlation Analysis of the Tinnitus Handicap Inventory and Distress Network in Chronic Tinnitus: An EEG Study

Mohsen, S. M., Mahmoudian, S., Talbian, S., & Pourbakht, A. (2018) · Basic and Clinical Neuroscience Journal · doi:10.32598/bcn.9.10.215 · Cited by 12

Monitoring maturation of neural stem cell grafts within a host microenvironment

Kopach, O. (2019) · World Journal of Stem Cells · doi:10.4252/wjsc.v11.i11.982 · Cited by 12

Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy

Bougnères, P., & Le Stunff, C. (2025) · Genes · doi:10.3390/genes16050590 · Cited by 11

Tet1 Regulates Astrocyte Development and Cognition of Mice Through Modulating GluA1

Xu, W., Zhang, X., Liang, F., Cao, Y., Li, Z., Qu, W., Zhang, J., Bi, Y., Sun, C., Zhang, J., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.644375 · Cited by 11

Probing microdomain Ca2+ activity and synaptic transmission with a node-based tripartite synapse model

Liu, L., Gao, H., Li, J., & Chen, S. (2023) · Frontiers in Network Physiology · doi:10.3389/fnetp.2023.1111306 · Cited by 11

C-X-C Motif Chemokine 3 Promotes the Inflammatory Response of Microglia after Escherichia coli-Induced Meningitis

Qu, X., Dou, B., Yang, R., Tan, C., Chen, H., & Wang, X. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310432 · Cited by 11

Augmented Mitochondrial Transfer Involved in Astrocytic PSPH Attenuates Cognitive Dysfunction in db/db Mice

Ma, H., He, S., Li, Y., Zhang, X., Chang, H., Du, M., Yan, C., Jiang, S., Gao, H., Zhao, J., et al. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04064-0 · Cited by 11

The mRNA content of plasma extracellular vesicles provides a window into molecular processes in the brain during cerebral malaria

Mwikali, K., Mwangi, S., Pance, A., Ochola‐Oyier, L. I., Kariuki, S. M., Newton, C. R. J. C., Bejon, P., Rayner, J. C., & Abdi, A. I. (2024) · Science Advances · doi:10.1126/sciadv.adl2256 · Cited by 11

Single-Cell RNA-Seq Uncovers Robust Glial Cell Transcriptional Changes in Methamphetamine-Administered Mice

Oladapo, A., Deshetty, U. M., Callen, S. E., Buch, S. J., & Periyasamy, P. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26020649 · Cited by 11

PDGFRα inhibition reduces myofibroblast expansion in the fibrotic rim and enhances recovery after ischemic stroke

Protzmann, J., Zeitelhofer, M., Stefanitsch, C., Torrente, D., Adzemovic, M. Z., Matjunins, K., Randel, S. J. I., Lewandowski, S. A., Muhl, L., Eriksson, U., et al. (2025) · Journal of Clinical Investigation · doi:10.1172/jci171077 · Cited by 11

Radiation-Induced Brain Injury with Special Reference to Astrocytes as a Therapeutic Target.

Wang, C.-P., Fan, X.-J., Shi, Y.-W., & Tang, F.-R. (2025) · Journal of Integrative Neuroscience · doi:10.31083/jin25907 · Cited by 8

Suppression of excitotoxicity and foreign body response by memantine in chronic cannula implantation into the rat brain

Hayn, L., & Koch, M. (2015) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2015.08.001 · Cited by 11

The role of regulatory T cells on the activation of astrocytes in the brain of high-fat diet mice following lead exposure

Wu, L., Li, S., Li, C., He, B., Lv, L., Wang, J., Wang, J., Wang, W., & Zhang, Y. (2021) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2021.109740 · Cited by 11

Utilization of ethanolamine phosphate phospholyase as a unique astrocytic marker

Tsujioka, H., & Yamashita, T. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1097512 · Cited by 11

In Vitro Functional Characterization of Type-I Taste Bud Cells as Monocytes/Macrophages-like Which Secrete Proinflammatory Cytokines

Hichami, A., Saidi, H., Khan, A. S., Degbeni, P., & Khan, N. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210325 · Cited by 11

Loss of maturity and homeostatic functions in Tuberous Sclerosis Complex-derived astrocytes

Luinenburg, M. J., Scheper, M., Sørensen, F. N. F., Anink, J. J., Hecke, W. V., Korshunova, I., Jansen, F. E., Riney, K., van Eijsden, P., Gosselaar, P. H., et al. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1284394 · Cited by 11

Nanomaterials for brain metastasis

Zhao, Z., Chen, Y., Sun, T., & Jiang, C. (2023) · Journal of Controlled Release · doi:10.1016/j.jconrel.2023.12.001 · Cited by 11

Optimized Model of Cerebral Ischemia In situ for the Long-Lasting Assessment of Hippocampal Cell Death

Rybachuk, O. A., Kopach, O., Krotov, V., Voitenko, N. V., & Pivneva, T. A. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00388 · Cited by 11

Report on the National Eye Institute’s Audacious Goals Initiative: Creating a Cellular Environment for Neuroregeneration

Burns, M. E., & Stevens, B. (2018) · eNeuro · doi:10.1523/eneuro.0035-18.2018 · Cited by 11

A Defined and Scalable Peptide-Based Platform for the Generation of Human Pluripotent Stem Cell-Derived Astrocytes

Raman, S., Srinivasan, G. R., Brookhouser, N., Nguyen, T., Henson, T., Morgan, D., Cutts, J., & Brafman, D. A. (2020) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.0c00067 · Cited by 11

Astrocytes-Secreted WNT5B Disrupts the Blood–Brain Barrier Via ROR1/JNK/c-JUN Cascade During Meningitic Escherichia Coli Infection

Qu, X., Yang, R., Tan, C., Chen, H., & Wang, X. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04303-4 · Cited by 10

Shh regulates M2 microglial polarization and fibrotic scar formation after ischemic stroke

Yang, Q., Jiang, P., Tang, H., Wen, J., Zhou, L., Zhao, Y., Wang, L., Wang, J., & Yang, Q. (2024) · Neurochemistry International · doi:10.1016/j.neuint.2024.105862 · Cited by 10

In vivo programming of adult pericytes aids axon regeneration by providing cellular bridges for SCI repair

Sun, W., Dion, E., Laredo, F., Okonak, A., Sepeda, J. A., Haykal, E., Zhou, M., El‐Hodiri, H. M., Fischer, A. J., Silver, J., et al. (2025) · Molecular Therapy · doi:10.1016/j.ymthe.2025.04.020 · Cited by 10

Pathological Human Astroglia in Alzheimer's Disease: Opening New Horizons with Stem Cell Technology

Mohamet, L., Jones, V. C., Dayanithi, G., & Verkhratsky, A. (2018) · Future Neurology · doi:10.2217/fnl-2017-0029 · Cited by 11

A Putative Role of Teneurin-2 and Its Related Proteins in Astrocytes

Tessarin, G. W. L., Michalec, O. M., Torres-da-Silva, K. R., da Silva, A. V., Cruz-Rizzolo, R. J., Gonçalves, A., Gasparini, D. C., Horta‐Júnior, J. D. A. C., Ervolino, E., Bittencourt, J. C., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00655 · Cited by 10

Neurotoxicities After CAR T-Cell Immunotherapy

Gust, J., Ceppi, F., & Turtle, C. J. (2019) · Elsevier eBooks · doi:10.1016/b978-0-323-66181-2.00007-x · Cited by 10

SRF Is Required for Maintenance of Astrocytes in Non-Reactive State in the Mammalian Brain

Jain, M., Das, S., Lu, P. P. Y., Virmani, G., Soman, S., Thumu, S. C. R., Gutmann, D. H., & Ramanan, N. (2021) · eNeuro · doi:10.1523/eneuro.0447-19.2020 · Cited by 10

Partial Ablation of Astrocytes Exacerbates Cerebral Infiltration of Monocytes and Neuronal Loss After Brain Stab Injury in Mice

Hu, X., Li, S., Shi, Z., Lin, W., Yang, Y., Li, Y., Li, H., Xu, Y., Zhou, M., & Tang, Y. (2022) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-022-01224-5 · Cited by 10

Therapeutic roles of plants for 15 hypothesised causal bases of Alzheimer’s disease

Tyler, S. E. B., & Tyler, L. D. K. (2022) · Natural Products and Bioprospecting · doi:10.1007/s13659-022-00354-z · Cited by 10

Novel therapeutic modulators of astrocytes for hydrocephalus

Yang, Y., Wang, C., Chen, R., Wang, Y.-C., Tan, C., Liu, J., Zhang, Q., & Xiao, G. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.932955 · Cited by 10

Targeting blood-brain barrier for sepsis-associated encephalopathy: Regulation of immune cells and ncRNAs

Tian, M., Zhan, Y., Cao, J., Gao, J., Sun, J., & Zhang, L. (2024) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2024.110922 · Cited by 11

Bumetanide Therapeutic Effect in Children and Adolescents With Autism Spectrum Disorder: A Review Study

Mollajani, R., Joghataei, M. T., & Tehrani‐Doost, M. (2019) · Basic and Clinical Neuroscience Journal · doi:10.32598/bcn.9.10.380 · Cited by 10

High Glucose Shifts the Oxylipin Profiles in the Astrocytes towards Pro-Inflammatory States

Chistyakov, D. V., Goriainov, S. V., Astakhova, A. A., & Sergeeva, M. G. (2021) · Metabolites · doi:10.3390/metabo11050311 · Cited by 10

Association between GFAP-positive astrocytes with clinically important parameters including neurological deficits and/or infarct volume in stroke-induced animals

Akhoundzadeh, K., & Shafia, S. (2021) · Brain Research · doi:10.1016/j.brainres.2021.147566 · Cited by 10

Neuroprotective effects of meloxicam on transient brain ischemia in rats: the two faces of anti-inflammatory treatments

Ugidos, I. F., González‐Rodríguez, P., Santos‐Galdiano, M., Font-Belmonte, E., Soto, B. A., Pérez‐Rodríguez, D., Gonzalo-Orden, J. M., & Fernández‐López, A. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.367846 · Cited by 10

Cerebellar Transcriptomic Analysis in a Chronic plus Binge Mouse Model of Alcohol Use Disorder Demonstrates Ethanol-Induced Neuroinflammation and Altered Glial Gene Expression

Holloway, K. N., Pinson, M. R., Douglas, J., Rafferty, T. M., Kane, C. J. M., Miranda, R. C., & Drew, P. D. (2023) · Cells · doi:10.3390/cells12050745 · Cited by 11

Fabrication and characterization of aligned fibrin nanofiber hydrogel loaded with PLGA microspheres

Yao, S., Yang, Y., Wang, X., & Wang, L. (2017) · Macromolecular Research · doi:10.1007/s13233-017-5121-x · Cited by 10

Locus Coeruleus Noradrenergic Neurons and Astroglia in Health and Disease

Zorec, R., Vardjan, N., & Verkhratsky, A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805088-0.00001-3 · Cited by 10

Human Stem Cell-derived Aggregates of Forebrain Astroglia Respond to Amyloid Beta Oligomers

Griffin, K., Bejoy, J., Song, L., Hua, T., Marzano, M., Jeske, R., Sang, Q. A., & Li, Y. (2019) · Tissue Engineering Part A · doi:10.1089/ten.tea.2019.0227 · Cited by 10

Evaluation of p21 expression and related autism‐like behavior in Bisphenol‐A exposed offspring of Wistar albino rats

Singha, S. P., Memon, S., Bano, U., Isaac, A. D., & Shahani, M. Y. (2022) · Birth Defects Research · doi:10.1002/bdr2.2022 · Cited by 9

The investigation of the molecular changes during lipopolysaccharide ‐induced systemic inflammation on rat hippocampus by using FTIR spectroscopy

Cakmak‐Arslan, G., Kaya, Y., Mamuk, S., Akarsu, E. S., & Severcan, F. (2024) · Journal of Biophotonics · doi:10.1002/jbio.202300541 · Cited by 9

Oral vancomycin treatment alters levels of indole derivatives and secondary bile acids modulating the expression of mTOR pathway genes in astrocytes during EAE

Bianchimano, P., Leone, P., Smith, E. M., Gutiérrez‐Vázquez, C., Wind-andersen, E., Bongers, G., Cristancho, S., Weiner, H. L., Clemente, J. C., & Tankou, S. K. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.01.006 · Cited by 9

The Potential Roles of Astrocytes and Microglia in the Spinal Cord and Brain After Spinal Cord Injury

Fiorin, F. D. S., & Santo, C. C. D. E. (2025) · Neuroglia · doi:10.3390/neuroglia6010012 · Cited by 9

Brosimine B and the biphasic dose-response: insights into hormesis and retinal neuroprotection

da Fonseca, S. S. S., Port’s, N. M. D. S., de Aguiar, G. P. S., Botelho, E. P., de Couto, N. M. G., Pinheiro, W. B. D. S., Khayat, A. S., Yamada, E. S., da Costa, E. T., de Sena, C. B. C., et al. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1558726 · Cited by 9

The Application of Ultrasound‐Induced Blood–Brain Barrier Opening in Neurology and Immunology

Jiang, A., Wang, Z., Song, D., Zhang, X., Guan, M., Li, X., Tan, J., He, Y., Han, W., Ding, X., et al. (2025) · Small · doi:10.1002/smll.202502699 · Cited by 9

Glial Cytokine and Metabolic Networks in Progressive Multiple Sclerosis: From Pathophysiology to Biomarkers and Therapeutic Strategies

Hohm, H. L., Schuster, R., Buciu, V. B., Serban, D.-M., Ciurescu, S., Cornea, A., Sharma, A., Nistor, D., & Kundnani, N. R. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26188817 · Cited by 9

Beyond immune privilege: the brain as a dynamic immunological interface

Kobeissy, F. H., & Salzet, M. (2026) · Cell Death and Disease · doi:10.1038/s41419-026-08561-z · Cited by 9

CD44 expression in the cuprizone model

Reinbach, C., Stadler, M.-S., Pröbstl, N., Chrzanowski, U., Schmitz, C., Kipp, M., & Hochstrasser, T. (2020) · Brain Research · doi:10.1016/j.brainres.2020.146950 · Cited by 9

Short-term systemic methotrexate administration in rats induces astrogliosis and microgliosis

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Glial Cells in Neuroinflammation in Various Disease States

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