Elusive roles for reactive astrocytes in neurodegenerative diseases

Calcium's Role in Mechanotransduction during Muscle Development

Damm, T. B., & Egli, M. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000356667 · Cited by 14,552

Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families

Corder, E. H., Saunders, A. M., Strittmatter, W. J., Schmechel, D. E., Gaskell, P. C., Small, G. W., Roses, A. D., Haines, J. L., & Pericak-Vance, M. A. (1993) · Science · doi:10.1126/science.8346443 · Cited by 9,429

Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity

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Mitochondrial Dysfunction and Oxidative Stress in Neurodegenerative Diseases

Lin, M. T., & Beal, M. F. (2006) · Nature · doi:10.1038/nature05292 · Cited by 6,455

Astrocytes: Biology and pathology

Sofroniew, M. V., & Vinters, H. V. (2010) · Acta Neuropathologica · doi:10.1007/s00401-009-0619-8 · Cited by 5,196

Alzheimer’s disease

Querfurth, H. W., & LaFerla, F. M. (2010) · New England Journal of Medicine · doi:10.1056/nejmra0909142 · Cited by 4,569

Glutamate uptake

Danbolt, N. C. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(00)00067-8 · Cited by 4,227

Correlative Memory Deficits, Aβ Elevation, and Amyloid Plaques in Transgenic Mice

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Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation

Gurney, M. E., Pu, H., Chiu, A. Y., Dal Canto, M. C., Polchow, C. Y., Alexander, D. D., Caliendo, J., Hentati, A., Kwon, Y. W., Deng, H.-X., et al. (1994) · Science · doi:10.1126/science.8209258 · Cited by 4,143

Triple-Transgenic Model of Alzheimer’s Disease with Plaques and Tangles

Oddo, S., Caccamo, A., Shepherd, J. D., Murphy, M. P., Golde, T. E., Kayed, R., Metherate, R., Mattson, M. P., Akbari, Y., & LaFerla, F. M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00434-3 · Cited by 4,126

Secretogranin III may be an indicator of paraquat-induced astrocyte activation and affects the recruitment of BDNF during this process

Zhan, X., Li, F., Chu, Q., & Pang, H. (2018) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2018.3909 · Cited by 8

Neuroprotective effects of selenium against lithium-induced cerebellar toxicity in rats: The role of apoptosis, gliosis, and aging markers

Helal, N. E., Ali, L. S., Elsaed, W. M., Berika, M. Y., Elhassan, Y. H., El-Bayoumi, K. S., Badawy, A. A., El-Agawy, M. S. E.-D., Dawood, A. F., & Eldesoqui, M. B. (2025) · Tissue and Cell · doi:10.1016/j.tice.2025.102779 · Cited by 7

Extracellular Vesicles Derived from Young Neural Cultures Attenuate Astrocytic Reactivity In Vitro

Almansa, D., Peinado, H., García‐Rodríguez, R., Casadomé‐Perales, Á., Dotti, C. G., & Guix, F. X. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031371 · Cited by 7

Neuroglia in neurodegeneration: Alzheimer, Parkinson, and Huntington disease

Lim, D., Matute, C., Cavaliere, F., & Verkhratsky, A. (2025) · Handbook of Clinical Neurology · doi:10.1016/b978-0-443-19102-2.00012-0 · Cited by 8

Temporal Profile of Reactive Astrocytes after Ischemic Stroke in Rats

Stadler, J., Schurr, H., Doyle, D., Garmo, L. G., Srinageshwar, B., Spencer, M. R., Petersen, R. B., Dunbar, G. L., & Rossignol, J. (2022) · Neuroglia · doi:10.3390/neuroglia3030007 · Cited by 7

The elderberry diet protection against intrahippocampal Aβ-induced memory dysfunction; the abrogated apoptosis and neuroinflammation

Jahanbakhshi, H., Moghaddam, M. H., Sani, M., Parvardeh, S., Boroujeni, M. E., Vakili, K. G., Fathi, M., Azimi, H., Mehranpour, M., Abdollahifar, M., et al. (2023) · Toxicology Research · doi:10.1093/toxres/tfad097 · Cited by 7

Examining the properties and therapeutic potential of glial restricted precursors in spinal cord injury

Fischer, I., Hayakawa, K., & Haas, C. (2016) · Neural Regeneration Research · doi:10.4103/1673-5374.180725 · Cited by 7

Intrathecal Administration of an Anti‐nociceptive Non-CpG Oligodeoxynucleotide Reduces Glial Activation and Central Sensitization

Leiguarda, C., Villarreal, A., Potilinski, M. C., Pélissier, T., Coronel, M. F., Bayo, J., Ramos, A. J., Montaner, A. D., Villar, M. J., Constandil, L., et al. (2021) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-021-09983-6 · Cited by 7

Deciphering T Cell Dynamics in Alzheimer's Disease Pathogenesis: Insights and Implications

Yang, Q., Qiu, Y., Ni, J., Li, H., & Qing, H. (2025) · Current Neuropharmacology · doi:10.2174/011570159x350611250303044527 · Cited by 7

Downregulation of STAT3 transcription factor reverses synaptotoxic phenotype of reactive astrocytes associated with prion diseases

Kushwaha, R., Molesworth, K., Makarava, N., & Baskakov, I. V. (2025) · Acta Neuropathologica Communications · doi:10.1186/s40478-025-02028-6 · Cited by 7

The Essential Role of Astrocytes in Neurodegeneration and Neuroprotection

Couselo, F. L., Saba, J., Carniglia, L., Durand, D., Lasaga, M., & Caruso, C. M. (2023) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/0118715273269881231012062255 · Cited by 6

Reactive astrocytes in prion diseases: Friend or foe?

Makarava, N., Kushwaha, R., & Baskakov, I. V. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012286 · Cited by 8

Maternal exposure to low-dose bisphenol A and its potential neurotoxic impact on male pups: A histological, immunohistochemical, and ultrastructural study

Morsy, M. M., Ahmad, M. M., & Hassan, N. H. (2024) · Tissue and Cell · doi:10.1016/j.tice.2024.102503 · Cited by 6

Rare Diseases, Spotlighting Amyotrophic Lateral Sclerosis, Huntington’s Disease, and Myasthenia Gravis: Insights from Landscape Analysis of Current Research

Iyer, K. A., Tenchov, R., Sasso, J. M., Ralhan, K., Jotshi, J., Polshakov, D. A., Maind, A., & Zhou, Q. A. (2025) · Biochemistry · doi:10.1021/acs.biochem.4c00722 · Cited by 6

Effect of prenatal exposure of green tea extract on the developing central nervous system of rat fetuses; histological, immune-histochemical and ultrastructural studies

El‐Borm, H. T., & El‐Gaber, A. S. A. (2021) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2021.04.084 · Cited by 6

Secretogranin III upregulation is involved in parkinsonian toxin-mediated astroglia activation

Zhan, X., Wen, G., Jiang, E., Li, F., Wu, X., & Pang, H. (2020) · The Journal of Toxicological Sciences · doi:10.2131/jts.45.271 · Cited by 6

Identification of highest neurotoxic amyloid-β plaque type showing reduced contact with astrocytes

Mitsubori, M., Takeda, K., Nagashima, S., Ishido, S., Matsuoka, M., Inatome, R., & Yanagi, S. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.02.081 · Cited by 6

Multimodal Benefits of Exercise in Patients With Multiple Sclerosis and COVID-19

Razi, O., Tartibian, B., Laher, I., Govindasamy, K., Zamani, N., Rocha‐Rodrigues, S., Suzuki, K., & Zouhal, H. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.783251 · Cited by 6

Glial Contributions to Lafora Disease: A Systematic Review

Vecchia, S. D., Marchese, M., & Santorelli, F. M. (2022) · Biomedicines · doi:10.3390/biomedicines10123103 · Cited by 6

Memantine suppresses the excitotoxicity but fails to rescue the ataxic phenotype in SCA1 model mice

Belozor, О. S., Vasilev, A., Mileiko, A. G., Mosina, L. D., Mikhailov, I. G., Ox, D. A., Boitsova, E. B., Shuvaev, А. N., Teschemacher, A. G., Kasparov, S., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116526 · 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

Effects on Metabolism in Astrocytes Caused by cGAMP, Which Imitates the Initial Stage of Brain Metastasis

Okawa, T., Hara, K., Goto, M., Kikuchi, M., Kogane, M., Hatakeyama, H., Tanaka, H., Shirane, D., Akita, H., Hisaka, A., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22169028 · Cited by 5

Cerebrospinal fluid glial fibrillary acidic protein, in contrast to amyloid beta protein, is associated with disease symptoms in Huntington's disease

Korpela, S., Sundblom, J., Zetterberg, H., Constantinescu, R., Svenningsson, P., Paucar, M., & Niemelä, V. (2024) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2024.122979 · Cited by 6

Effects of an Intraparenchymal Injection of Lidocaine in the Rat Cervical Spinal Cord

Sisti, M. S., Zanuzzi, C. N., Nishida, F., Cantet, R. J. C., & Portiansky, E. L. (2018) · Neurochemical Research · doi:10.1007/s11064-018-2628-2 · Cited by 5

Astrocytes as the Elements of the Regulation of Higher Brain Functions

Гомазков, О. А. (2019) · Neurochemical Journal · doi:10.1134/s1819712419030073 · Cited by 5

Ablation of Nampt in AgRP neurons leads to neurodegeneration and impairs fasting‐ and ghrelin‐mediated food intake

de Guia, R. M., Hassing, A. S., Ma, T., Plucińska, K., Holst, B., Gerhart‐Hines, Z., Emanuelli, B., & Treebak, J. T. (2021) · The FASEB Journal · doi:10.1096/fj.202002740r · Cited by 5

‘A picture is worth a thousand words’: The use of microscopy for imaging neuroinflammation

de Fraga, L. S., Tassinari, I. D., Jantsch, J., Guedes, R. P., & Bambini-Júnior, V. (2021) · Clinical & Experimental Immunology · doi:10.1111/cei.13669 · Cited by 5

Concepts toward directing human astroplasticity to promote neuroregeneration

Patel, R., Muir, M. T., Cvetkovic, C., & Krencik, R. (2018) · Developmental Dynamics · doi:10.1002/dvdy.24655 · Cited by 5

Maresin-like 1 Ameliorates Neuropathology of Alzheimer’s Disease in Brains of a Transgenic Mouse Model

Shrivastava, P., Lu, Y., Su, S., Kobayashi, Y., Zhao, Y., Lien, N., Masoud, A., Lukiw, W. J., & Hong, S. (2024) · Biomedicines · doi:10.3390/biomedicines12122865 · Cited by 5

Neurogliovascular alterations in brain pathologies across lifespan

Daigle, B., Bevilacqua, L. M., Noël, V. P., Lebel, M., Côté, D. C., Lévesque, L., & Ménard, C. (2024) · Glial health research. · doi:10.1016/j.ghres.2024.100004 · Cited by 4

Carbon ion stimulation therapy reverses iron deposits and microglia driven neuroinflammation and induces cognitive improvement in an Alzheimer’s disease mouse model

Lee, W.-S., Kokubo, T., Choi, Y., Hamano, T., Zaboronok, A., Ishikawa, T., Kwon, O. D., Kim, E., & Kim, J. (2025) · Scientific Reports · doi:10.1038/s41598-025-91689-3 · Cited by 4

Research progress on the role of exercise-regulated reactive astrocytes in the prevention and treatment of Parkinson’s disease

Yang, Q., & Zhuang, C. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1561006 · Cited by 4

Lineage specification into GABAergic, glutamatergic, dopaminergic, and astrocytic phenotypes using MUSE stem cells: a novel approach for modeling neurodegenerative and psychiatric disorders

Aprile, D., Patrone, D., Sammarraie, S. H. A. A., Alessio, N., Peluso, G., Bernardo, G. D., & Galderisi, U. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03251-2 · Cited by 4

Tau is necessary for Pseudomonas aeruginosa-induced blood-brain barrier dysfunction

Chaney, S. D., Bauman, A. J., Butlig, E.-A. R., Al-Masri, S., Sanchez, J. M., McAdams, L. H., DOAN, P., Gwin, M. S., Stevens, T., Ciernia, A. V., et al. (2026) · Communications Biology · doi:10.1038/s42003-026-09703-x · Cited by 4

DEVEA: an interactive shiny application for Differential Expression analysis, data Visualization and Enrichment Analysis of transcriptomics data

Riquelme‐Perez, M., Pérez-Sánz, F., Deleuze, J., Escartin, C., Bonnet, É., & Brohard, S. (2022) · F1000Research · doi:10.12688/f1000research.122949.1 · Cited by 4

Inflammatory Intracellular Signaling in Neurons Is Influenced by Glial Soluble Factors in iPSC-Based Cell Model of PARK2-Associated Parkinson’s Disease

Gerasimova, T., Poberezhniy, D., Nenasheva, V. V., Stepanenko, E. A., Arsenyeva, E. L., Novosadova, L. V., Grivennikov, I. A., Illarioshkin, S. N., Lagarkova, M. A., Tarantul, V. Z., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179621 · Cited by 4

Inhibition of STAT3 phosphorylation attenuates perioperative neurocognitive disorders in mice with D-galactose-induced aging by regulating pro-inflammatory reactive astrocytes

Cao, Y., Lin, X., Gao, D., Yang, J., Miao, H., & Li, T. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114095 · Cited by 4

Single cell transcriptomic profiling of neurodegeneration mediated by tau in a novel 3D neuron‐astrocyte coculture model

Rickner, H., Jiang, L., Hong, R., O’Neill, N. K., Wolozin, B. L., & Cheng, C. S. (2021) · Alzheimer s & Dementia · doi:10.1002/alz.058551 · Cited by 4

Neurodegeneration and Motor Deficits in the Absence of Astrogliosis upon Transgenic Mutant TDP-43 Expression in Mature Mice

Chan, G., van Hummel, A., van der Hoven, J., Ittner, L. M., & Ke, Y. D. (2020) · American Journal Of Pathology · doi:10.1016/j.ajpath.2020.04.009 · Cited by 4

Astrocytes réactifs et maladies cérébrales

Poulot-Becq-Giraudon, Y., Sauvage, M.-A. C.-D., & Escartin, C. (2022) · médecine/sciences · doi:10.1051/medsci/2022104 · Cited by 6

Compression injury regulates astrocyte morphology, metabolic function, and extracellular matrix modification in a 3D hydrogelPreprint

Strat, A. N., Patel, S., Thanh, M. H., Kirschner, A., Ghosh, S., Geiss, M. P., Venkatesan, A., Bernstein, A. M., Viapiano, M. S., Liu, Y., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.20.660800 · Cited by 4

Fueling Alzheimer’s Disease: Where Does Immunometabolism Stand?

Correia, S. C., Perry, G. L., & Moreira, P. I. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-240787 · Cited by 3

Moderating effects of plasma glial fibrillary acidic protein along the Alzheimer's disease continuum

Lee, S. Y., Diaz, V. E., Emanuel, O. M., Matusz, E. F., Webb, J. D., Chan, B., Lago, A. L., Wang, W., DeSimone, J. C., Rojas, J. C., et al. (2025) · Alzheimer s & Dementia · doi:10.1002/alz.70626 · Cited by 4

Plant-derived natural products modulate astrocyte function: Therapeutic strategies for Alzheimer’s disease

Wei, H., Zhang, G., Xu, Y., Zhao, A., Zheng, Y., Shao, Y. W., Yang, L., Wang, J., & Jiang, X. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.157238 · Cited by 3

Neuroprotective Effects of Strength Training on Behavioral Deficit, Oxidative Damage, Astrogliosis, and Neuronal Death in a Bipolar Disorder Model

Maidana, L. M., Guerra, J. M. D. S., Souza-Pereira, A., Dahleh, M. M. M., Godinho, D. B., Prigol, M., Royes, L. F. F., & Rambo, L. M. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70392 · Cited by 3

Space Renaissance and Neurodegeneration

Marotta, D., Stoudemire, J., Clements, T., Loring, J. F., Grisanti, P., Noggle, S., & Fossati, V. (2022) · Springer eBooks · doi:10.1007/978-3-031-18440-6_9 · Cited by 3

Mesenchymal Stem Cell Engagement Modulates Neuroma Microenviroment in Rats and Humans and Prevents Postamputation Pain

Casadei, M., Miguel, B., Rubione, J., Fiore, E. J., Mengelle, D., Guerri‐Guttenberg, R. A., Montaner, A. D., Villar, M. J., Constandil-Córdova, L., Romero-Sandoval, A. E., et al. (2024) · Journal of Pain · doi:10.1016/j.jpain.2024.03.004 · Cited by 3

A Pro-Inflammatory Stimulus versus Extensive Passaging of DITNC1 Astrocyte Cultures as Models to Study Astrogliosis

González, L. P., Palacios, E., González, M. F., Leyton-Rivera, I., Martínez-Meza, S., Pérez-Núñez, R., Jeldes, E., Avalos, A. M., Díaz, J., & Leyton, L. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179454 · Cited by 3

Modulation of SNARE-dependent exocytosis in astrocytes improves neuropathology in Huntington's disease

King, A. C., Payne, E., Stephens, E., Fowler, J. A., Wood, T. E., Rodriguez, E., & Gray, M. (2024) · Disease Models & Mechanisms · doi:10.1242/dmm.052002 · Cited by 3

Molecular interplay between oxidative and endoplasmic reticulum stress in multiple sclerosis

Kamarehei, M., & Zahednasab, H. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.148142 · Cited by 3

Tau Protein Phosphorylated at Threonine-231 is Expressed Abundantly in the Cerebellum in Prion Encephalopathies

Gómez-López, V. M., Viramontes‐Pintos, A., Ontiveros‐Torres, M. Á., Garcés‐Ramírez, L., de la Cruz, F., Villanueva‐Fierro, I., Bravo-Muñoz, M., Harrington, C. R., Martínez-Robles, S., Yescas, P., et al. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201308 · Cited by 3

Restricted Infection and Cytokine Expression in Primary Murine Astrocytes Induced by the H5N1 Influenza Virus

Pringproa, K., Srivorakul, S., Tantilertcharoen, R., & Thanawongnuwech, R. (2018) · Neurochemical Journal · doi:10.1134/s1819712418010129 · Cited by 3

Beneficial effects of atorvastatin on sex‐specific cognitive impairment induced by a cerebral microhaemorrhage in mice

Bergeron, S., Barus, R., Leboullenger, C., Auger, F., Bongiovanni, A., Tardivel, M., Jonneaux, A., Laloux, C., Potey, C., Bordet, R., et al. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15393 · Cited by 3

Capacitive Electrode-Based Electric Field Treatments on Redox-Toxic Iron Deposits in Transgenic AD Mouse Models: The Electroceutical Targeting of Alzheimer’s Disease Feasibility Study

Choi, Y., Lee, W., Lee, J., Park, S.-H., Kim, S., Kim, K. H., Park, S., Kim, E. H., & Kim, J.-K. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119552 · Cited by 3

The Role of Dopamine in Chronic Pain: Neuroinflammation and Neurogenesis

Vetlugina, А., Фокеева, Н. О., Kochneva, A., Kalueff, A. V., Евгеньевич, М. П., & Gerasimova, E. (2025) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093025020097 · Cited by 2

BDNF Mitigates Early Oxidative Stress and Promotes Release of Neuroprotective Mitochondria From Striatal Astrocytes of zQ175 Huntington's Disease Mice

Couselo, F. L., Saba, J., Frederiksen, M. F., Palmieri, M., Romero, A. C., Bigi, M. M., Carniglia, L., Durand, D., Lasaga, M., & Caruso, C. M. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70276 · Cited by 3

Astrocytes Protect Brain Metastatic Breast Cancer Cells From Chemotherapy Through CX43 Dependent STAT1 Signaling in Co‐Culture Spheroids

Yakati, V., & Rao, S. S. (2026) · Biotechnology and Bioengineering · doi:10.1002/bit.70144 · Cited by 2

Microglia-driven neuroinflammatory signaling in neurodegeneration: mechanisms and therapeutic opportunities

Saini, K., & Dhiman, P. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-12128-8 · Cited by 2

Astrocytic centrin‐2 expression in entorhinal cortex correlates with Alzheimer's disease severity

Degl’Innocenti, E., Poloni, T. E., Medici, V., Olimpico, F., Finamore, F., Profka, X., Bascarane, K., Morrone, C., Pastore, A., Escartin, C., et al. (2024) · Glia · doi:10.1002/glia.24603 · Cited by 2

In vitro biocompatibility evaluation of functional electrically stimulating microelectrodes on primary glia

Tsui, C. T., Mirkiani, S., Roszko, D. A., Churchward, M. A., Mushahwar, V. K., & Todd, K. G. (2024) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2024.1351087 · Cited by 2

Neuroglia targeting nano-therapeutic approaches to rescue aging and neurodegenerating brain

Sharma, M., Aggarwal, N., Mishra, J., & Panda, J. J. (2024) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2024.123950 · Cited by 2

Mesenchymal Stem Cells Promote an Increase in Neuronal Oscillation via Glutamate Tonic Release

Azevedo-Pereira, R. L., Aizman, I., & Nejadnik, B. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.06.015 · Cited by 2

Neuroinflammation in Huntington’s Disease

Lee, J. D., Lo, M. W., Fung, J. N., & Woodruff, T. M. (2021) · Neuromethods · doi:10.1007/978-1-0716-1712-0_9 · Cited by 2

Implementation of Neuron Astrocyte Interaction Dynamics

Kumar, S. R., & Singhal, S. (2023) · IEEE International Conference for Convergence in Technology (I2CT) · doi:10.1109/i2ct57861.2023.10126497 · Cited by 2

Proton Pump Inhibitors and Radiofrequency Ablation for Treatment of Barrett's Esophagus

Dugalić, P., Djuranovic, S. P., Pavlović-Marković, A., Dugalić, V., Tomašević, R., Gluvic, Z. M., Obradovic, M. M., Bajić, V., & Isenović, E. R. (2019) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557519666191015203636 · Cited by 2

Doxycycline, an anti-inflammatory agent, alleviates dyskinesia induced by L-DOPA in Parkinsonian ratsPreprint

Bortolanza, M., Nascimento, G. C., Raisman‐Vozari, R., & Bel, E. A. D. (2020) · doi:10.22541/au.159285563.30385356 · Cited by 2

Single-cell variations of circadian clock and immune gene expression in microglia and neurodegenerationPreprint

Ouk, K., Yalçın, M., Rigat, L., Keren‐Shaul, H., David, E., Knop, A., Böttcher, C., Kramer, A., Amit, I., Relógio, A., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.16.599193 · Cited by 2

Gene Therapy for Neurological Disorders

Malviya, R., Singh, A. K., Goyal, P., & Sundram, S. (2024) · Apple Academic Press eBooks · doi:10.1201/9781003494102 · Cited by 1

A 14‐Year Study of Serum Glial Fibrillary Acidic Protein and Total Tau in Premanifest Huntington's

Owen, N. E., Voysey, Z. J., Holbrook, J. A., Malpetti, M., Draoulec, C. L., Spindler, L. R. B., Goodman, A. O. G., Lázár, A. S., & Barker, R. A. (2025) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.70057 · Cited by 1

Tacca chantrieri André Rhizome Extract Alleviates Scopolamine‐Induced Cognitive Impairment and Neuroinflammation in Rats

Hawiset, T., Sriraksa, N., Anukanon, S., Kamsrijai, U., Praman, S., Teerapattarakan, N., & Inkaew, P. (2025) · Advances in Pharmacological and Pharmaceutical Sciences · doi:10.1155/adpp/7334303 · Cited by 1

Advances in astrocytes in aneurysmal subarachnoid haemorrhage

Liu, J., Sun, K., Chen, Q., & Ding, L. (2025) · Frontiers in Surgery · doi:10.3389/fsurg.2025.1511242 · Cited by 1

A mathematical model suggests collectivity and inconstancy enhance the efficiency of neuronal migration in the adult brain

Wakita, D., Sobu, Y., Kaneko, N., & Kano, T. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013105 · Cited by 1

Safety of 810 nm photobiomodulation in the developing brain: no evidence of glial reactivity or pro-inflammatory cytokine expression in rats

Gutiérrez‐Menéndez, A., Rodríguez‐Fernández, L., Zorzo, C., Martínez, J. A., Díez-Solinska, A., & Arias, J. L. (2025) · Lasers in Medical Science · doi:10.1007/s10103-025-04684-5 · Cited by 1

Cytoskeletal proteins regulates Tau protein in Alzheimer’s disease

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From scaffold to effector: reframing GFAP in neurodegeneration

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Evaluation of prenatal calabash chalk geophagy on the developing brain of Wistar rats

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Neuroinflammation and oxidative redox imbalance drive memory dysfunction in adolescent rats prenatally exposed to Datura Stramonium

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Mutation in Wdr45 leads to early motor dysfunction and widespread aberrant axon terminals in a beta-propeller protein associated neurodegeneration (BPAN) patient-inspired mouse model

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Behavioral and Brain Gene and Protein Changes in Female Mice Consuming Ethanol During Pregnancy and Lactation

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Molecular Network for Management of Neurodegenerative Diseases and their Translational Importance using Animal Biotechnology as a Tool in Preclinical Studies

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Neurocognitive and Neuroarchitectural Changes in the Prefrontal Cortex of Wistar Rats Treated with Highly Active Antiretroviral Therapy

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The role of astrocytes response triggered by hyperglycaemia during spinal cord injury

Sámano, C., & Mazzone, G. L. (2023) · Archives of Physiology and Biochemistry · doi:10.1080/13813455.2023.2264538 · Cited by 2

Using patient-derived cell models to investigate the role of misfolded SOD1 in ALS

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A guardian of balance: the role of BAF chromatin remodeling complex in astrogliogenesis during mouse forebrain development

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Data from STAT3-Mediated Astrocyte Reactivity Associated with Brain Metastasis Contributes to Neurovascular Dysfunction

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Reactive Astrocytes Drive Extracellular Acidification to Mediate α-Synuclein NeurodegenerationPreprint

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Sex-specific associations between astrocytic reactivity and cognitive decline in unimpaired elderlyPreprint

Plaska, C. R., Jacobs, T., Bruno, D., Lee, S. H., Imbimbo, B. P., Osorio, R., Benedet, A. L., Ashton, N. J., Zetterberg, H., Pomara, N., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.30.702902 · Cited by 1

Role of Astrocytic Serine in Learning and Memory and its Implications in Alzheimer's Disease.

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Ultrasound Induced Blood-brain Barrier Opening on Rodents : from Nanoparticles Delivery to a Therapy for Alzheimer’s Disease

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Simulating calcium signaling in fine astrocytic processes

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SETD5 dysfunction in human astrocytes drives IL-6-mediated neuronal impairments via the JAK/STAT signaling pathwayPreprint

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Ros‐Bernal, F. (2016) · Anuari de l'Agrupació Borrianenca de Cultura: revista de recerca humanística i científica · doi:10.6035/anuari.2016.27.8

Cellular Therapy for Spinal Muscular Atrophy

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Sinalização via receptor N-Metil-D-Aspartato e modulação da Na+, K+-ATPase em camundongos hipomórficos para klotho: efeitos em hipocampo e cerebelo.

Cararo-Lopes, M. M. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2017.tde-14072017-092741

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Pereira, M. D. S. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2018.tde-24042018-181827

Targeting Astrocytes With Viral Gene Therapy for Alzheimer’s Disease

Rosenthal, Z. P., Kraft, A. W., Czerniewski, L. R., & Lee, J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809813-4.00005-3

The identification of cell non-autonomous roles of astrocytes in neurodegeneration

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Reactive astrocytes in neurodegenerative diseases

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Astrocytes in Neurodegenerative Disorders

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Reactive astrocytes: The nexus of pathological and clinical hallmarks of Alzheimer’s disease

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New insights into astrocyte diversity from the lens of transcriptional regulation and their implications for neurodegenerative disease treatments

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