Dual Roles of Astrocyte-Derived Factors in Regulation of Blood-Brain Barrier Function after Brain Damage

Apolipoprotein E and Alzheimer disease: risk, mechanisms and therapy

Liu, C.-C., Kanekiyo, T., Xu, H., & Bu, G. (2013) · Nature Reviews Neurology · doi:10.1038/nrneurol.2012.263 · Cited by 3,459

Matrix metalloproteinase-mediated disruption of tight junction proteins in cerebral vessels is reversed by synthetic matrix metalloproteinase inhibitor in focal ischemia in rat

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Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia

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The Hedgehog Pathway Promotes Blood-Brain Barrier Integrity and CNS Immune Quiescence

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Astrocyte roles in traumatic brain injury

Burda, J. E., Bernstein, A. M., & Sofroniew, M. V. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.03.020 · Cited by 791

Crosstalk of tight junction components with signaling pathways

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Astrocyte-derived VEGF-A drives blood-brain barrier disruption in CNS inflammatory disease

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VEGF-mediated disruption of endothelial CLN-5 promotes blood-brain barrier breakdown

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Tight junctions at the blood brain barrier: physiological architecture and disease-associated dysregulation

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Pericyte, but not astrocyte, hypoxia inducible factor-1 (HIF-1) drives hypoxia-induced vascular permeability in vivo

Baumann, J., Tsao, C.-C., Patkar, S., Huang, S., Francia, S., Magnussen, S. N., Gassmann, M., Vogel, J., Köster-Hegmann, C., & Ogunshola, O. O. (2022) · Fluids and Barriers of the CNS · doi:10.1186/s12987-021-00302-y · Cited by 28

Effect of retinoic acid on the neurovascular unit: A review

Pouso, M. R., & Cairrão, E. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.03.011 · Cited by 27

The Neuroprotection Effects of Exosome in Central Nervous System Injuries: a New Target for Therapeutic Intervention

Zhang, L., Mao, L., & Wang, H. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-03028-6 · Cited by 27

Developing a transwell millifluidic device for studying blood–brain barrier endothelium

Harding, I. C., O’Hare, N. R., Vigliotti, M., Caraballo, A., Lee, C. I., Millican, K., Herman, I. M., & Ebong, E. E. (2022) · Lab on a Chip · doi:10.1039/d2lc00657j · Cited by 28

Astrocytes in Post-Stroke Depression: Roles in Inflammation, Neurotransmission, and Neurotrophin Signaling

Jing, D., Hou, X., Guo, X., Zhao, X., Zhang, K., Zhang, J., Kan, C., Han, F., Liu, J., & Sun, X. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01386-w · Cited by 27

Exosomes; multifaceted nanoplatform for targeting brain cancers

Mardi, N., Salahpour‐Anarjan, F., Nemati, M., Baher, N. S., Rahbarghazi‬, R., & Zarebkohan, A. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216077 · Cited by 25

Blood–Brain Barrier: Structure, Function, Diseases, and Drug Delivery Systems

He, Y., Qu, M., Yu, L., He, L., Lu, Y., Hong, J., Sun, M., Yang, H., Mi, W., Guo, H., et al. (2026) · MedComm · doi:10.1002/mco2.70712 · Cited by 24

Modeling the blood-brain barrier for treatment of central nervous system (CNS) diseases

Rice, O., Surian, A., & Chen, Y. (2022) · Journal of Tissue Engineering · doi:10.1177/20417314221095997 · Cited by 25

Endothelial deletion of EPH receptor A4 alters single-cell profile and Tie2/Akap12 signaling to preserve blood–brain barrier integrity

Cash, A., de Jager, C., Brickler, T., Soliman, E., Ladner, L. R., Kaloss, A. M., Zhu, Y., Pridham, K. J., Mills, J., Ju, J., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2204700120 · Cited by 24

Astroglial cells as neuroendocrine targets in forebrain development: Implications for sex differences in psychiatric disease

Rurak, G. M., Woodside, B. C., Aguilar‐Valles, A., & Salmaso, N. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100897 · Cited by 24

Inactivation of Hedgehog signal transduction in adult astrocytes results in region-specific blood–brain barrier defects

Wang, H., Xu, Z., Xia, Z., Rallo, M. S., Duffy, A., & Matise, M. P. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2017779118 · Cited by 23

Food Reward Alterations during Obesity Are Associated with Inflammation in the Striatum in Mice: Beneficial Effects of Akkermansia muciniphila

Huwart, S. J. P., d’Oplinter, A. D. W., Rastelli, M., Hul, M. V., de Vos, W. M., Luquet, S. H., Cani, P. D., & Everard, A. (2022) · Cells · doi:10.3390/cells11162534 · Cited by 24

Blood-brain barrier biomarkers

Zapata-Acevedo, J. F., Mantilla-Galindo, A., Vargas-Sánchez, K., & González-Reyes, R. E. (2024) · Advances in clinical chemistry · doi:10.1016/bs.acc.2024.04.004 · Cited by 23

Down-regulation of astrocytic sonic hedgehog by activation of endothelin ETB receptors: Involvement in traumatic brain injury-induced disruption of blood brain barrier in a mouse model

Michinaga, S., Inoue, A., Sonoda, K., Mizuguchi, H., & Kōyama, Y. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105042 · Cited by 23

Resveratrol Attenuates Meningitic Escherichia coli-Mediated Blood–Brain Barrier Disruption

Yang, R., Lv, Y., Miao, L., Zhang, H., Qu, X., Chen, J., Xu, B., Yang, B., Fu, J., Tan, C., et al. (2021) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.0c00564 · Cited by 22

Synergistic Impairment of the Neurovascular Unit by HIV-1 Infection and Methamphetamine Use: Implications for HIV-1-Associated Neurocognitive Disorders

Fattakhov, N. S., Torices, S., Stangis, M., Park, M., & Toborek, M. J. (2021) · Viruses · doi:10.3390/v13091883 · Cited by 22

Optogenetic Activation of Astrocytes Reduces Blood-Brain Barrier Disruption via IL-10 In Stroke

Suo, Q., Deng, L., Chen, T., Wu, S., Qi, L., Liu, Z., He, T., Tian, H.-L., Li, W., Tang, Y., et al. (2023) · Aging and Disease · doi:10.14336/ad.2023.0226 · Cited by 23

Post-Ischemic Permeability of the Blood–Brain Barrier to Amyloid and Platelets as a Factor in the Maturation of Alzheimer’s Disease-Type Brain Neurodegeneration

Pluta, R. M., Miziak, B., & Czuczwar, S. J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310739 · Cited by 22

Astroglial Cells: Emerging Therapeutic Targets in the Management of Traumatic Brain Injury

Czyżewski, W., Mazurek, M., Sakwa, L., Szymoniuk, M., Pham, J., Pasierb, B., Litak, J., Czyżewska, E., Turek, M., Piotrowski, B., et al. (2024) · Cells · doi:10.3390/cells13020148 · Cited by 22

Bridging metabolic syndrome and cognitive dysfunction: role of astrocytes

Li, Z., Jiang, Y., Long, C., Peng, X., Tao, J., Pu, Y., & Yue, R. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1393253 · Cited by 22

Retinoic acid in Parkinson's disease: Molecular insights, therapeutic advances, and future prospects

Pareek, A., Singhal, R., Pareek, A., Ghazi, T., Kapoor, D. U., Ratan, Y., Singh, A. K., Jain, V., & Chuturgoon, A. A. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.123010 · Cited by 21

Astrocyte phenotypes: Emphasis on potential markers in neuroinflammation.

Bozic, I. D., Savić, D. Z., & Lavrnja, I. C. (2021) · PubMed · doi:10.14670/hh-18-284 · Cited by 22

Protective Effects of Complement Component 8 Gamma Against Blood-Brain Barrier Breakdown

Kim, J., Han, J., & Suk, K. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.671250 · Cited by 21

Cooperation between neurovascular dysfunction and Aβ in Alzheimer’s disease

Wang, N., Yang, X., Zhao, Z., Liu, D., Wang, X., Tang, H., Zhong, C., Chen, X., Chen, W. K., & Meng, Q. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1227493 · Cited by 22

MiRNA-125a-5p attenuates blood–spinal cord barrier permeability under hypoxia in vitro

Wang, J., Zhikui, N., Zhao, H., Gao, K., & Cao, Y. (2019) · Biotechnology Letters · doi:10.1007/s10529-019-02753-8 · Cited by 20

Estradiol Inhibits Human Brain Vascular Pericyte Migration Activity: A Functional and Transcriptomic Analysis

Kurmann, L., Okoniewski, M. J., & Dubey, R. K. (2021) · Cells · doi:10.3390/cells10092314 · Cited by 20

Molecular and biophysical remodeling of the blood–brain barrier in glioblastoma: mechanistic drivers of tumor–neurovascular crosstalk

Abikenari, M. A., Sjöholm, M., Liu, J., Nageeb, G., Ha, J. H., Wu, J. Y., Ren, A. L., Sayadi, J. J., Lim, J., Cho, K. B., et al. (2025) · Frontiers in Physics · doi:10.3389/fphy.2025.1723329 · Cited by 20

Astrocyte responses to nanomaterials: Functional changes, pathological changes and potential applications

Dai, D., He, L., Chen, Y., & Zhang, C. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.12.013 · Cited by 20

Regulatory T Cell Therapeutics for Neuroinflammatory Disorders

Harkins, A. L., Kopec, A. L., & Keeler, A. M. (2022) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.2022045080 · Cited by 19

Tong-Qiao-Huo-Xue decoction activates PI3K/Akt/mTOR pathway to reduce BMECs autophagy after cerebral ischemia/reperfusion injury

Hua, Y., Zhai, Y. W., Wang, G., Wang, N., Wu, Q., Huang, Q., Seto, S. W., & Wang, Y. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.115585 · Cited by 18

The Need for New Biomarkers to Assist with Stroke Prevention and Prediction of Post-Stroke Therapy Based on Plasma-Derived Extracellular Vesicles

Popescu-Drigă, M. V., Cătălin, B., Olaru, D. G., Słowik, A., Plesnila, N., Hermann, D. M., & Popa‐Wagner, A. (2021) · Biomedicines · doi:10.3390/biomedicines9091226 · Cited by 19

Repetitive head trauma and apoE4 induce chronic cerebrovascular alterations that impair tau elimination from the brain

Eisenbaum, M., Pearson, A., Ortiz, C., Koprivica, M., Cembran, A., MULLAN, M. J., Crawford, F., Ojo, J. O., & Bachmeier, C. J. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.114702 · Cited by 18

The Role of Neuroglia in the Development and Progression of Schizophrenia

Rawani, N. S., Chan, A. W., Todd, K. G., Baker, G. B., & Dursun, S. M. (2024) · Biomolecules · doi:10.3390/biom15010010 · Cited by 19

Activated microglia promote invasion and barrier dysfunction of brain endothelial cells via regulating the CXCL13/CXCR5 axis

Zhang, Q., Jiang, J., Liu, Y., Ma, G., Wang, X., & Fang, B. (2022) · Cell Biology International · doi:10.1002/cbin.11832 · Cited by 17

Neural and Glial Regulation of Angiogenesis in CNS in Ischemic Stroke

Grinchevskaya, L. R., Salikhova, D. I., Silachev, D. N., & Goldshtein, D. V. (2024) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-024-06219-4 · Cited by 16

Expression of IL-20 Receptor Subunit β Is Linked to EAE Neuropathology and CNS Neuroinflammation

Dayton, J. R., Yuan, Y., Pacumio, L. P., Dorflinger, B. G., Yoo, S. C., Olson, M. J., Hernández-Suárez, S. I., McMahon, M. M., & Cruz-Orengo, L. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.683687 · Cited by 16

Key brain cell interactions and contributions to the pathogenesis of Alzheimer’s disease

Saavedra, J., Nascimento, M., Liz, M. A., & Cardoso, I. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1036123 · Cited by 16

FUS aggregation following ischemic stroke favors brain astrocyte activation through inducing excessive autophagy

Wu, S., Yin, Y., & Du, L. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114144 · Cited by 15

Emerging Roles of Microglia in Blood-Brain Barrier Integrity in Aging and Neurodegeneration

Zhang, S., Meng, R., Jiang, M., Qing, H., & Ni, J. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230203103910 · Cited by 16

Secretomics reveals gelatinase substrates at the blood-brain barrier that are implicated in astroglial barrier function

Burmeister, M., Frauenstein, A., Kahms, M., Arends, L., Gerwien, H., Deshpande, T., Kuhlmann, T., Groß, C. C., Naik, V. N., Wiendl, H., et al. (2023) · Science Advances · doi:10.1126/sciadv.adg0686 · Cited by 16

The battle of lipid-based nanocarriers against blood-brain barrier: a critical review

Abla, K. K., & Mehanna, M. M. (2023) · Journal of drug targeting · doi:10.1080/1061186x.2023.2247583 · Cited by 15

Nanotechnology-Based Diagnostics and Therapy for Pathogen-Related Infections in the CNS

Selvan, S. T., Padmanabhan, P., & Gulyás, B. Z. (2019) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.9b00470 · Cited by 15

Lab-On-A-Chip for the Development of Pro-/Anti-Angiogenic Nanomedicines to Treat Brain Diseases

Parimalam, S. S., Bǎdilescu, S., Sonenberg, N., Bhat, R., & Packirisamy, M. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20246126 · Cited by 15

Beta-Secretase 1 Underlies Reactive Astrocytes and Endothelial Disruption in Neurodegeneration

Chacón-Quintero, M. V., Pineda-López, L. G., Villegas‐Lanau, C. A., Posada‐Duque, R., & Cardona‐Gómez, G. P. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.656832 · Cited by 15

Glial cell activity in cardiovascular diseases and risk of acute myocardial infarction

Truter, N., Malan, L., & Essop, M. F. (2023) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00332.2022 · Cited by 14

Cerebral malaria – modelling interactions at the blood–brain barrier in vitro

Adams, Y., & Jensen, A. T. R. (2022) · Disease Models & Mechanisms · doi:10.1242/dmm.049410 · Cited by 15

Roles of astrocytic sonic hedgehog production and its signal for regulation of the blood-brain barrier permeability

(2024) · Vitamins and Hormones · doi:10.1016/bs.vh.2024.04.006 · Cited by 13

Modeling the Blood–Brain Barrier to Understand Drug Delivery in Alzheimer’s Disease

Wasielewska, J. M., Chaves, J., White, A. R., & Oikari, L. E. (2020) · Exon Publications eBooks · doi:10.36255/exonpublications.alzheimersdisease.2020.ch7 · Cited by 13

Glial Cell-Based Vascular Mechanisms and Transplantation Therapies in Brain Vessel and Neurodegenerative Diseases

Zhao, Y., Wang, S., Song, X., Yuan, J., Qi, D., Gu, X., Yin, M. Y., Han, Z., Zhu, Y., Liu, Z., et al. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.627682 · Cited by 13

Neuroinflammation in Bilirubin Neurotoxicity

Zhang, F., Chen, L., & Jiang, K. (2023) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2201009 · Cited by 13

Roles of Extracellular Vesicles in Multiple Sclerosis: From Pathogenesis to Potential Tools as Biomarkers and Therapeutics

Pistono, C., Osera, C., Cuccia, M., & Bergamaschi, R. (2023) · Sclerosis · doi:10.3390/sclerosis1020011 · Cited by 13

Apolipoprotein E-Containing Lipoproteins and LRP1 Protect From NMDA-Induced Excitotoxicity Associated With Reducing α2-Macroglobulin in Müller Glia

Hayashi, H., Mori, M., Harashima, M., Hashizume, T., Furiya, M., Mukaigaito, C., Takemura, E., Yamada, M., Mise, K., Yuan, B., et al. (2021) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.62.13.23 · Cited by 13

Neurosurgery at the crossroads of immunology and nanotechnology. New reality in the COVID-19 pandemic

Ljubimov, V. A., Ramesh, A., Davani, S., Danielpour, M., Breunig, J. J., & Black, K. L. (2021) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2021.114033 · Cited by 13

PRMT7 can prevent neurovascular uncoupling, blood-brain barrier permeability, and mitochondrial dysfunction in repetitive and mild traumatic brain injury

Acosta, C. H., Clemons, G. A., Citadin, C. T., Carr, W. C., Udo, M. S. B., Tešić, V., Sanicola, H. W., Freelin, A. H., Toms, J., Jordan, J. D., et al. (2023) · Experimental Neurology · doi:10.1016/j.expneurol.2023.114445 · Cited by 12

Exploring lipophilic compounds that induce BDNF secretion in astrocytes beyond the BBB using a new multi-cultured human in vitro BBB model

Fujisawa, M., Takeshita, Y., Fujikawa, S., Matsuo, K., Okamoto, M., Tamada, M., Shimizu, F., Sano, Y., Koga, M., & Kanda, T. (2021) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2021.577783 · Cited by 12

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

Mechanisms of Astrocyte Action in the Blood Brain Barrier: From Structural Support to Dynamic Regulation

Feng, D. N., Wang, L. N., Hu, A. N., & Zhang, S. (2025) · Journal of Integrative Neuroscience · doi:10.31083/jin45223 · Cited by 11

Culturing astrocytes on substrates that mimic brain tumors promotes enhanced mechanical forces

Bizanti, A., Chandrashekar, P., & Steward, R. L. (2021) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.112751 · Cited by 11

Beta-caryophyllene inhibits the permeability of the blood–brain barrier in MPTP-induced parkinsonism

Ramos-Molina, A. R., Tejeda-Martínez, A. R., Paredes, J. M. V., Chaparro-Huerta, V., Urmeneta-Ortíz, M. F., Ramírez-Jirano, L. J., & Flores-Soto, M. E. (2023) · Neurología · doi:10.1016/j.nrl.2022.11.004 · Cited by 11

Microfluidics for brain endothelial cell-astrocyte interactions

Sanapathi, J., Vipparthi, P., Mishra, S., Sosnik, A., & Kumarasamy, M. (2023) · Organs-on-a-Chip · doi:10.1016/j.ooc.2023.100033 · Cited by 11

Neurological Infection, Kynurenine Pathway, and Parasitic Infection by Neospora caninum

Del’Arco, A. E., Argolo, D. S., Guillemin, G. J., Costa, M. D. F. D., Costa, S. L., & Pinheiro, A. M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.714248 · Cited by 11

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

YES-10, A Combination of Extracts from Clematis mandshurica RUPR. and Erigeron annuus (L.) PERS., Prevents Ischemic Brain Injury in A Gerbil Model of Transient Forebrain Ischemia

Lee, T.-K., Park, J. H., Kim, B., Park, Y. E., Lee, J., Ahn, J. H., Park, C. W., Noh, Y., Lee, J.-W., Kim, S.-S., et al. (2020) · Plants · doi:10.3390/plants9020154 · Cited by 10

Development of Brain Permeable Drugs and Novel Strategies to Overcome the Brain Barriers for Treatment Purposes

Chauhan, A., & Jain, S. (2025) · Current Pharmaceutical Design · doi:10.2174/0113816128386983250410092649 · Cited by 10

Evolution of glial cells: a non-bilaterian perspective

Sheloukhova, L., & Watanabe, H. (2024) · Neural Development · doi:10.1186/s13064-024-00184-4 · Cited by 9

New perspectives on the role of biological factors in anorexia nervosa: Brain volume reduction or oxidative stress, which came first?

Gaiaschi, L., Priori, E. C., Mensi, M. M., Verri, M., Buonocore, D., Parisi, S., Hernandez, L. N. Q., Brambilla, I., Ferrari, B., Luca, F. D., et al. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106580 · Cited by 9

17β-Estradiol Abrogates TNF-α-Induced Human Brain Vascular Pericyte Migration by Downregulating miR-638 via ER-β

Kurmann, L., Azzarito, G., Leeners, B., Rosselli, M., & Dubey, R. K. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252111416 · Cited by 9

Neurovascular dysfunction in the development and progression of neuroinflammatory diseases

Gowdy, J., Ahn, J. J., Miller, R. H., & Islam, Y. (2026) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2026.1741928 · Cited by 7

Do astrocytes act as immune cells after pediatric TBI?

Panchenko, P. E., Hippauf, L., Konsman, J. P., & Badaut, J. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106231 · Cited by 9

Astrocytic S100B, Blood-Brain Barrier and Neurodegenerative Diseases

Krishnan, A., Wu, H., & Venkataraman, V. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.92146 · Cited by 8

The adhesion GPCR ADGRV1 controls glutamate homeostasis in hippocampal astrocytes supporting neurons

Güler, B. E., Zorin, M., Linnert, J., Nagel‐Wolfrum, K., & Wolfrum, U. (2026) · Acta Neuropathologica Communications · doi:10.1186/s40478-026-02282-2 · Cited by 8

Solute transport in the brain tissue: what are the key biophysical parameters tying in vivo and in vitro studies together?

Alcaide, D., Cacheux, J., Bancaud, A., Muramatsu, R., & Matsunaga, Y. T. (2023) · Biomaterials Science · doi:10.1039/d3bm00027c · Cited by 7

Neurotrophic extracellular matrix proteins promote neuronal and iPSC astrocyte progenitor cell‐ and nano‐scale process extension for neural repair applications

O’Connor, C., Mullally, R. E., McComish, S. F., O'Sullivan, J., Woods, I., Schoen, I., Garrè, M., Caldwell, M. A., Dervan, A. G., & O’Brien, F. J. (2024) · Journal of Anatomy · doi:10.1111/joa.14163 · Cited by 8

The Potential Role of Exosomes in Communication Between Astrocytes and Endothelial Cells

Czpakowska, J., Glabinski, A. R., & Szpakowski, P. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104676 · Cited by 7

Glial cells in the center of future ischemic stroke treatments

Pérez-Álvarez, M. J., & Hernández, I. H. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.339480 · Cited by 7

The chronic stress risk phenotype mirrored in the human retina as a neurodegenerative condition

Malan, L., van Wyk, R., von Känel, R., Ziemssen, T., Vilser, W., Nilsson, P. M., Magnusson, M., Jujić, A., Mak, D. W., Steyn, F., et al. (2023) · Stress · doi:10.1080/10253890.2023.2210687 · Cited by 7

Populus tomentiglandulosa Extract Is Rich in Polyphenols and Protects Neurons, Astrocytes, and the Blood-Brain Barrier in Gerbil Striatum Following Ischemia-Reperfusion Injury

Lee, T.-K., Lee, J., Kim, J.-D., Kim, D. W., Ahn, J., Park, J.-H., Kim, H. I., Cho, J.-H., Choi, S., Won, M., et al. (2021) · Molecules · doi:10.3390/molecules26185430 · Cited by 7

A New Insight in Cellular and Molecular Signaling Regulation for Neural Differentiation Program

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