Important Shapeshifter: Mechanisms Allowing Astrocytes to Respond to the Changing Nervous System During Development, Injury and Disease

Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo

Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827

Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue.

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The blood-brain barrier

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Molecular dissection of reactive astrogliosis and glial scar formation

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Tripartite synapses: glia, the unacknowledged partner

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Astrocyte scar formation aids central nervous system axon regeneration

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Synaptic scaling mediated by glial TNF-α

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Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis

Christopherson, K. S., Ullian, E. M., Stokes, C. C. A., Mullowney, C. E., Hell, J. W., Agah, A., Lawler, J., Mosher, D. F., Bornstein, P., & Barres, B. A. (2005) · Cell · doi:10.1016/j.cell.2004.12.020 · Cited by 1,688

Reactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury

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Protoplasmic Astrocytes in CA1 Stratum Radiatum Occupy Separate Anatomical Domains

Bushong, E. A., Martone, M. E., Jones, Y. Z., & Ellisman, M. H. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00183.2002 · Cited by 1,578

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

Current progress and challenges in the development of brain tissue models: How to grow up the changeable brain in vitro?

Salmina, A. B., Alexandrova, O. P., Сергеевич, А. А., Korsakova, S. A., Saridis, M. R., Illarioshkin, S. N., & Yurchenko, S. O. (2024) · Journal of Tissue Engineering · doi:10.1177/20417314241235527 · Cited by 17

Auditory Brainstem Deficits from Early Treatment with a CSF1R Inhibitor Largely Recover with Microglial Repopulation

Milinkeviciute, G., Chokr, S. M., & Cramer, K. S. (2021) · eNeuro · doi:10.1523/eneuro.0318-20.2021 · Cited by 12

Neuroprotective Efficacy of the Glucocorticoid Receptor Modulator PT150 in the Rotenone Mouse Model of Parkinson’s Disease

Latham, A. S., Rocha, S. M., McDermott, C. P., Reigan, P., Slayden, R. A., & Tjalkens, R. B. (2024) · NeuroToxicology · doi:10.1016/j.neuro.2024.06.017 · Cited by 12

Uncovering Astrocyte Morphological Dynamics Using Optical Diffraction Tomography and Shape‐Based Trajectory Inference

Anantha, P., Raj, P., Saracino, E., Kim, J. H., Kim, J. H., Convertino, A., Gu, L., & Barman, I. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202402960 · Cited by 9

Chronic administration of prebiotics and probiotics prevent pathophysiological hallmarks of Alzheimer’s disease in the cortex of APP/PS1 mice

Sarti, G., Traini, C., Magni, G., Attorre, S., Tognozzi, G., Calussi, E., Giovannini, M. G., Vannucchi, M. G., & Lana, D. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1596469 · Cited by 11

Traumatic brain injury in the presence of Aβ pathology affects neuronal survival, glial activation and autophagy

Streubel-Gallasch, L., Zyśk, M., Beretta, C., & Erlandsson, A. (2021) · Scientific Reports · doi:10.1038/s41598-021-02371-3 · Cited by 11

Sex-Dependent Gliovascular Interface Abnormality in the Hippocampus following Postnatal Immune Activation in Mice

Ardalan, M., Chumak, T., Quist, A., Shiadeh, S. M. J., Mallard, A.-J., Rafati, A. H., & Mallard, C. E. (2022) · Developmental Neuroscience · doi:10.1159/000525478 · Cited by 10

Circadian Control of Glial Cell Homeodynamics

Rojo, D., Badner, A., & Gibson, E. M. (2022) · Journal of Biological Rhythms · doi:10.1177/07487304221120966 · Cited by 11

Global hypo-methylation in a proportion of glioblastoma enriched for an astrocytic signature is associated with increased invasion and altered immune landscape

Boot, J. R., Rosser, G., Kancheva, D., Vinel, C., Lim, Y. M., Pomella, N., Zhang, X., Guglielmi, L., Sheer, D., Barnes, M. R., et al. (2022) · eLife · doi:10.7554/elife.77335 · Cited by 10

Neuron and astrocyte aggregation and sorting in three-dimensional neuronal constructs

Hasan, M. F., & Berdichevsky, Y. (2021) · Communications Biology · doi:10.1038/s42003-021-02104-2 · Cited by 10

Ketamine Action on Astrocytes Provides New Insights into Rapid Antidepressant Mechanisms

Stenovec, M., Li, B., Verkhratsky, A., & Zorec, R. (2021) · Advances in neurobiology · doi:10.1007/978-3-030-77375-5_14 · Cited by 10

Tuning a Bioengineered Hydrogel for Studying Astrocyte Reactivity in Glioblastoma

DePalma, T. J., Hisey, C. L., Hughes, K., Fraas, D., Tawfik, M., Scharenberg, J., Wiggins, S., Nguyen, K. T., Hansford, D. J., Reátegui, E., et al. (2024) · Acta Biomaterialia · doi:10.1016/j.actbio.2024.09.048 · Cited by 10

Induced Remodelling of Astrocytes In Vitro and In Vivo by Manipulation of Astrocytic RhoA Activity

Domingos, C., Müller, F. E., Passlick, S., Wachten, D., Ponimaskin, E. G., Schwarz, M. K., Schoch, S., Zeug, A., & Henneberger, C. (2023) · Cells · doi:10.3390/cells12020331 · Cited by 10

Friends and Foes in Alzheimer’s Disease

Pauwels, E. K. J., & Boer, G. J. (2023) · Medical Principles and Practice · doi:10.1159/000534400 · Cited by 10

Characterising murine hippocampal iron homeostasis, in relation to markers of brain inflammation and metabolism, during ageing

Ellison, G., Duong, L., Hollings, A. L., Howard, D. L., Jackaman, C., & Hackett, M. J. (2022) · Metallomics · doi:10.1093/mtomcs/mfac064 · Cited by 9

In vivo biocompatibility assessment of 3D printed bioresorbable polymers for brain tissue regeneration. A feasibility study

Clauzel, J., Colitti, N., Combeau, M., Labriji, W., Robert, L., Brilhault, A., Cirillo, C., Desmoulin, F., Raymond‐Letron, I., & Loubinoux, I. (2024) · Regenerative Therapy · doi:10.1016/j.reth.2024.10.004 · Cited by 8

The WAVE complex in developmental and adulthood brain disorders

Kim, H.-G., Berdasco, C., Nairn, A. C., & Kim, Y. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-024-01386-w · Cited by 8

L-type Voltage-Gated Calcium Channel Modulators Inhibit Glutamate-Induced Morphology Changes in U118-MG Astrocytoma Cells

Tabatabaee, M. S., & Ménard, F. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00828-z · Cited by 8

Diffusion Tensor Imaging Detects Acute Pathology-Specific Changes in the P301L Tauopathy Mouse Model Following Traumatic Brain Injury

Soni, N., Medeiros, R., Alateeq, K., To, X. V., & Nasrallah, F. A. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.611451 · Cited by 8

The cell adhesion protein dystroglycan affects the structural remodeling of dendritic spines

Figiel, I., Bączyńska, E., Wójtowicz, T., Magnowska, M., Buszka, A., Bijata, M., & Włodarczyk, J. (2022) · Scientific Reports · doi:10.1038/s41598-022-06462-7 · Cited by 9

Effects of 660-nm LED photobiomodulation on drebrin expression pattern and astrocyte migration

Yoon, S. R., Chang, S., Lee, M. Y., & Ahn, J. (2023) · Scientific Reports · doi:10.1038/s41598-023-33469-5 · Cited by 8

Multi-omic spatially resolved analysis of the neuroinflammatory response to intracortical microelectrode arrays

Druschel, L. N., Song, S. S., Kasthuri, N. M., Wang, J., Conard, J. H., Chan, E. R., Hess‐Dunning, A., & Capadona, J. R. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123477 · Cited by 7

Physical exercise influences astrocytes in the striatum of a Parkinson’s disease male mouse model

Vitorino, L. C., Oliveira, K. F., da Silva, W. A. B., Gomes, C. A. B. D. A., Romão, L. F., Allodi, S., & Corrêa, C. L. (2022) · Neuroscience Letters · doi:10.1016/j.neulet.2022.136466 · Cited by 7

IFI204 in microglia mediates traumatic brain injury-induced mitochondrial dysfunction and pyroptosis via SENP7 interaction

Guo, T., Lai, Y., Wu, S., Lin, C., Zhou, X., Lin, P., Zheng, M., Chen, J., & Lin, F. (2025) · Cell Biology and Toxicology · doi:10.1007/s10565-025-10032-8 · Cited by 6

The Potential of the Fibronectin Inhibitor Arg-Gly-Asp-Ser in the Development of Therapies for Glioblastoma

Ribeiro, M. L., Castro, V. I. B., de Castro, J. V., Pires, R. A., Reis, R. L., Costa, B. M., Ferreira, H., & Neves, N. M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094910 · Cited by 6

Understanding the Mechanobiology of Gliosis May Be the Key to Unlocking Sustained Chronic Performance of Bioelectronic Neural Interfaces

Vallejo‐Giraldo, C., Krukiewicz, K., & Biggs, M. J. P. (2021) · Advanced NanoBiomed Research · doi:10.1002/anbr.202100098 · Cited by 6

Comprehensive proteomic analysis of the differential expression of 62 proteins following intracortical microelectrode implantation

Song, S., Druschel, L. N., Kasthuri, N. M., Wang, J., Conard, J. H., Chan, E. R., Acharya, A. P., & Capadona, J. R. (2024) · Scientific Reports · doi:10.1038/s41598-024-68017-2 · Cited by 6

Platelet‐derived growth factor receptor α/glial fibrillary acidic protein expressing peritumoral astrocytes associate with shorter median overall survival in glioblastoma patients

Leiss, L. W., Mega, A., Bontell, T. O., Nistér, M., Smits, A., Corvigno, S., Rahman, M. A., Enger, P. Ø., Miletić, H., & Östman, A. (2019) · Glia · doi:10.1002/glia.23756 · Cited by 6

Glutamate Signaling and Filopodiagenesis of Astrocytoma Cells in Brain Cancers: Survey and Questions

Tabatabaee, M. S., & Ménard, F. (2022) · Cells · doi:10.3390/cells11172657 · Cited by 5

Morphological regulation of wound repair astrocytes by leucine zipper-bearing kinase-AKT signaling after spinal cord injury

Hemati-Gourabi, M., Cao, T., Mills, A. E., Rice, E. P., Baur, L., Xu, X. Q., Fenske, W. K., & Chen, M. (2025) · Experimental Neurology · doi:10.1016/j.expneurol.2025.115379 · Cited by 5

Therapeutic activities of naringenin on efavirenz-induced sleep-like disorder in the midbrain of white albino mice.

Dosumu, O. O., Edidiong, A., Faniyan, O. O., & Alani, A. (2020) · PubMed Central · doi:10.22038/ijbms.2020.47043.10852 · Cited by 5

Identification of Curcumin Targets in the Brain of Epileptic Mice Using DARTS

Zhang, N., Lin, R., Xu, H., Jing, X., Zhou, H., Wen, X., & Xie, Q. (2024) · ACS Omega · doi:10.1021/acsomega.4c00825 · Cited by 5

A macro-transection model of brain trauma for neuromaterial testing with functional electrophysiological readouts

Wiseman, J. P., Basit, R. H., Suto, A., Middya, S., Kabiri, B., Evans, M. G., George, V. T., Adams, C., Malliaras, G. G., & Chari, D. M. (2025) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00422 · Cited by 5

Isolation of ferret astrocytes reveals their morphological, transcriptional, and functional differences from mouse astrocytes

Roboon, J., Hattori, T., Nguyen, D. T., Ishii, H., Takarada‐Iemata, M., Kannon, T., Hosomichi, K., Maejima, T., Saito, K., Shinmyo, Y., et al. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.877131 · Cited by 5

The impact of wound-healing assay, phorbol myristate acetate (PMA) stimulation and siRNA-mediated FURIN gene silencing on endogenous retroviral ERVW-1 expression level in U87-MG astrocytoma cells

Machnik, G., Bułdak, Ł., Zapletal-Pudełko, K., Grabarek, B. O., Staszkiewicz, R., Sobański, D., & Okopień, B. (2024) · Advances in Medical Sciences · doi:10.1016/j.advms.2024.02.007 · Cited by 5

Astrocytes at the intersection of ageing, obesity, and neurodegeneration

Firth, W., Pye, K. R., & Potter, P. G. W. (2024) · Clinical Science · doi:10.1042/cs20230148 · Cited by 6

Quantitative analysis of astrocyte and axonal density relationships: Glia to neuron ratio in the optic nerve laminar regions

Chan, G. Z. P., Morgan, W. H., Yu, D., & Balaratnasingam, C. (2020) · Experimental Eye Research · doi:10.1016/j.exer.2020.108154 · Cited by 5

Response of astrocytes to blood exposure due to shunt insertion in vitro

Zaranek, M., Arshad, R., Zheng, K., & Harris, C. A. (2021) · AIChE Journal · doi:10.1002/aic.17485 · Cited by 5

A novel poly-ε-lysine based implant, Proliferate®, for promotion of CNS repair following spinal cord injury

Hosseinzadeh, S., Lindsay, S. L., Gallagher, A., Wellings, D. A., Riehle, M. O., Riddell, J. S., & Barnett, S. C. (2020) · Biomaterials Science · doi:10.1039/d0bm00097c · Cited by 5

The Alzheimer’s disease risk factor APOE4 drives pro-inflammation in human astrocytes via HDAC-dependent repression of TAGLN3Preprint

Arnaud, L., Benech, P. D., Greetham, L., Stephan, D., Jimenez, A., Jullien, N. D., García‐González, L., Tsvetkov, P. O., Devred, F., Sancho-Martinez, I., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.16.440108 · Cited by 5

Enteric glial cell and astrocyte melatonin regulation in Parkinson disease pathogenesis and pathophysiology

Anderson, G. (2026) · Academia Biology · doi:10.20935/acadbiol8130 · Cited by 4

Assessment and Evaluation of Contemporary Approaches for Astrocyte Differentiation from hiPSCs: A Modeling Paradigm for Alzheimer's Disease

Juráková, V., Széky, B., Zapletalová, M., Fehér, A., Zana, M., Pandey, S., Kučera, R., Šerý, O., Hudeček, J., Dinnyés, A., et al. (2024) · Biological Procedures Online · doi:10.1186/s12575-024-00257-y · Cited by 4

Drebrin Upregulation Regulates Astrocyte Polarization and Supports Tissue Recovery After Spinal Cord Injury in Mice

Šmejkalová, B., Ornaghi, M., Štěpánková, K., Schiweck, J., Urdzíková, L. M., Huelse, R., Mueller, S. G., Boehm‐Sturm, P., Kwok, J. C. F., Fawcett, J. W., et al. (2025) · Glia · doi:10.1002/glia.70048 · Cited by 4

CellRemorph: A Toolkit for Transforming, Selecting, and Slicing 3D Cell Structures on the Road to Morphologically Detailed Astrocyte Simulations

Keto, L., & Manninen, T. (2023) · Neuroinformatics · doi:10.1007/s12021-023-09627-5 · Cited by 4

Altered DTI scalars in the hippocampus are associated with morphological and structural changes after traumatic brain injury

Arora, P., Trivedi, R., Kumari, M., Singh, K., Sandhir, R., D'Souza, M. M., & Rana, P. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02758-8 · Cited by 4

The LRRK2-G2019S mutation attenuates repair of brain injury partially by reducing the release of osteopontin-containing monocytic exosome-like vesicles

An, J., Yang, H., Park, S. M., Chwae, Y., & Joe, E.-H. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106528 · Cited by 4

Clinical presentations of post ischemic and post traumatic brain injury scars associated seizures

Chavda, V. K., Patel, V. A., Parmar, H., Ramírez, M. D. J. E., Soto, G. R., Stary, C. M., & Montemurro, N. (2025) · Neurological Research · doi:10.1080/01616412.2025.2482755 · Cited by 4

Mechanical contrast between brain and leptomeninges: Insights into leptomeningeal cell and astrocyte responses to mechanical stiffness alterations

Greaney, A. J., Abubaker, M., McCarthy, C. M., Reardon, E. C., & Mulvihill, J. J. (2025) · Acta Biomaterialia · doi:10.1016/j.actbio.2025.07.019 · Cited by 4

Astrocyte reactivity in the glia limitans superficialis of the rat medial prefrontal cortex following sciatic nerve injury

Bretová, K., Svobodová, V., & Dubový, P. (2022) · Histochemistry and Cell Biology · doi:10.1007/s00418-022-02161-6 · Cited by 4

Focused ultrasound-induced blood-brain barrier opening promotes glioprotective phenotypes in ACSA-II+ murine astrocytes

Noel, R. L., Kline-Schoder, A. R., Batts, A. J., Kwon, N., Tsitsos, F., & Konofagou, E. E. (2025) · iScience · doi:10.1016/j.isci.2025.113173 · Cited by 3

Embryonic spatiotemporal expression pattern of Folded gastrulation suggests roles in multiple morphogenetic events and regulation by AbdA

Katagade, V., Kandroo, M., & Ratnaparkhi, A. (2024) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkae032 · Cited by 3

Sex differences in the single-nuclei hippocampal neurovascular unit transcriptomic response to type 2 diabetes

Nuthikattu, S., Norman, J., Milenković, D., & Villablanca, A. C. (2025) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00193.2025 · Cited by 4

Application of Light-Sheet Mesoscopy to Image Host-Pathogen Interactions in Intact Organs

Battistella, E., Quintana, J. F., & McConnell, G. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.903957 · Cited by 3

Advances in quantitative analysis of astrocytes using machine learning

Demetrio Labate, A., & Kayasandık, C. B. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.346474 · Cited by 3

DeCOOC Deconvoluted Hi‐C Map Characterizes the Chromatin Architecture of Cells in Physiologically Distinctive Tissues

Wang, J., Lu, L., Zheng, S., Wang, D., Jin, L. G., Zhang, Q., Li, M., & Zhang, Z. (2023) · Advanced Science · doi:10.1002/advs.202301058 · Cited by 3

The synergistic effects of mechanical ventilation and intrauterine inflammation on cerebral inflammation in preterm fetal sheep

Tran, N. T., Somers, A., Vidinopoulos, K., Azman, Z., Pham, Y., Zahra, V. A., Chan, K. Y. Y., Hooper, S. B., Crossley, K. J., Allison, B. J., et al. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1397658 · Cited by 3

Proteome alterations promoted by Zika virus infection

Tatara, J. M., Santi, L., & Beys‐da‐Silva, W. O. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820268-5.00028-6 · Cited by 3

Transcriptomic signatures of nine high-risk neuropsychiatric copy number variants in human brain cellsPreprint

Dugan, G., Akula, N., Marenco, S., Auluck, P. K., Raznahan, A., Liu, S., DeCasien, A. R., Xu, Q., Feng, N., Kolachana, B. S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.19.613680 · Cited by 3

Spatially patterned cytoskeletal organization shapes astrocyte branch complexityPreprint

Wynne, M. E., Barclay, W. E., Gopal, D., Jahan, N., Bergstrom, J. J. D., Ho, L. T., Nogales, E., Nogales, E., & Fu, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.10.681734 · Cited by 3

Single‐Nucleus Transcriptomics Reveals Microglial State Transitions and Astrocytic Trajectory Divergence During Glial Remodeling Induced by Intracortical Electrode Implantation

Zhao, Z., Duan, X., Huang, H., Zhang, Y., Wang, M., Qin, J., Lin, S., & Chen, H. (2026) · Glia · doi:10.1002/glia.70148 · Cited by 3

Astrocytic ankyrin-2 enables memory persistence in the mouse hippocampus

Kim, H., Lim, J., Kim, J., Özkan, E., Kim, G. H., Park, H., Park, M. G., Joo, B., Lee, S., Lee, K. J., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-75009-5 · Cited by 2

Neurogenesis and glial impairments in congenital hydrocephalus: insights from a BioGlue-induced fetal lamb model

Karakaya, D., Lampe, K., Encinas, J. L., Duru, S., Peiro, L., Oge, H., Sánchez-Margallo, F., Oria, M., & Peiro, J. L. (2025) · Fluids and Barriers of the CNS · doi:10.1186/s12987-025-00630-3 · Cited by 5

An astrocytic basis of caloric restriction action on the brain plasticityPreprint

Plata, A., Popov, A., Denisov, P., Bychkov, M. L., Brazhe, A., Lyukmanova, E. N., Lazareva, N. B., Verkhratsky, A., & Semyanov, A. V. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/625871 · Cited by 2

A Primary Neural Cell Culture Model for NeuroinflammationPreprint

Goshi, N., Morgan, R. K., Lein, P. J., & Şeker, E. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.23.914226 · Cited by 2

Forced but effective partners in crime: how astrocytes drive the progression of glioblastoma

Murk, K., & Hülse, R. (2022) · Brain · doi:10.1093/brain/awac302 · Cited by 2

“Generation of morphologically distinct astrocyte subtypes from human iPSCs reveals a link between glial shape, function and reactivity”Preprint

O’Toole, K., Guetta, L., Urbanaviciute, P., Suklai, P., Wright, C., Fisher, T., Liddelow, S. A., Luisier, R., Marzi, S. J., & Serio, A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.11.622998 · Cited by 3

mTORC1 drives cell-autonomous astrocyte reactivity in tuberous sclerosis

Li, T. L., Blair, J. D., Yoo, T., Grant, G. A., Hockemeyer, D., Porter, B. E., & Bateup, H. S. (2026) · Nature · doi:10.1038/s41586-026-11054-w · Cited by 1

Microvilli Semantic Segmentation in Microscopy Images Using a Visual Learning Pipeline

Quirós-Corella, F., Pereira, R., & Corrales-Ureña, Y. R. (2023) · International Conference on Machine Learning and Applications · doi:10.1109/icmla58977.2023.00321 · Cited by 1

Identification of glutamate-related disease-dependent alterations in subventricular NSCs of the 3xTg Alzheimer’s disease model, could they be involved in attempting damage repair?

Cerqueni, G., Terenzi, V., Preziuso, A., Serfilippi, T., Piccirillo, S., Vincenzo, M. D., Ambrogini, P., Amoroso, S., Orciani, M., Lariccia, V., et al. (2025) · Cell and Tissue Research · doi:10.1007/s00441-025-03954-6 · Cited by 2

Viability and suitability of rat pup organotypic spinal cord slice cultures in a transection injury model

Shortiss, C., Howard, L., & McMahon, S. S. (2025) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2025.110499 · Cited by 1

Improved transfection methods for observation of cytoskeletal structures in primary cultured astrocytes

Ikoma, C., Inoue, K., Kasai, K., Tsukuda, S., Tamura, A., Nakata, S., Iwata, Y., TAMAGAWA, T., Nakayama, A., Takano, K., et al. (2025) · Journal of Cell Science · doi:10.1242/jcs.264312 · Cited by 1

A Review of Nanoparticle‐Based Astrocyte Modulation in CNS Disorders: Evaluating the Underexplored Potential of Intranasal Delivery

Dlamini, S. M., Mahumane, G. D., Kumar, P., & Choonara, Y. E. (2026) · Nano Select · doi:10.1002/nano.70089 · Cited by 1

Translatome profiling of spinal cord astrocytes reveals distinct gene signatures associated with acute and chronic pain

Siliezar-Doyle, J., Perez, R. K., Stauffenberg, E., Nippert, A. R., & Tawfik, V. L. (2026) · iScience · doi:10.1016/j.isci.2026.115719 · Cited by 1

Dual CD73/A2AR blockade modulates the neurotoxic astrocyte phenotype without disrupting core inflammatory signaling

Mihajlović, K., Dragić, M., Adžić, M., Martić, T., Stevanović, I. D., Vinit, S., Bleuzé, M., Mansart, A., Adam, L., & Nedeljković, N. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1778355 · Cited by 1

Sphingosine‐1‐Phosphate Receptor 1 Regulates Competition Dependent Astrocyte Morphogenesis and Tiling in Murine Cortex

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