The Many Faces of Astrocytes in Alzheimer's Disease

Neurotoxic reactive astrocytes are induced by activated microglia

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Neuroinflammation in Alzheimer's disease

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2016 Alzheimer's disease facts and figures

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Glutamate uptake

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Neuropathological alterations in Alzheimer disease

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Single-cell transcriptomic analysis of Alzheimer’s disease

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Reactive astrocyte nomenclature, definitions, and future directions

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2020 Alzheimer's disease facts and figures

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The glymphatic system: a beginner's guide

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Amyloid Precursor Protein Processing and Alzheimer's Disease

O'Brien, R. J., & Wong, P. C. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113613 · Cited by 2,061 · see citing works

RAGE and amyloid-β peptide neurotoxicity in Alzheimer's disease

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Alzheimer Mechanisms and Therapeutic Strategies

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The glymphatic pathway in neurological disorders.

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Reactive Gliosis and the Multicellular Response to CNS Damage and Disease

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Understanding RAGE, the receptor for advanced glycation end products

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Human and mouse single-nucleus transcriptomics reveal TREM2-dependent and TREM2-independent cellular responses in Alzheimer’s disease

Zhou, Y., Song, W. M., Andhey, P. S., Swain, A., Levy, T., Miller, K. R., Poliani, P. L., Cominelli, M., Grover, S., Gilfillan, S., et al. (2020) · Nature Medicine · doi:10.1038/s41591-019-0695-9 · Cited by 1,150 · see citing works

Disease-associated astrocytes in Alzheimer’s disease and aging

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A single-cell atlas of entorhinal cortex from individuals with Alzheimer’s disease reveals cell-type-specific gene expression regulation

Grubman, A., Chew, G., Ouyang, J. F., Sun, G., Choo, X. Y., McLean, C., Simmons, R. K., Buckberry, S., Vargas-Landin, D. B., Poppe, D., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0539-4 · Cited by 956 · see citing works

Spatial Transcriptomics and In Situ Sequencing to Study Alzheimer’s Disease

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Astrocytes and Brain Injury

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The genetic landscape of Alzheimer disease: clinical implications and perspectives

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GABA from reactive astrocytes impairs memory in mouse models of Alzheimer's disease

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Neural Circuit-Specialized Astrocytes: Transcriptomic, Proteomic, Morphological, and Functional Evidence

Chai, H., Diaz-Castro, B., Shigetomi, E., Monte, E., Octeau, J. C., Yu, X., Cohn, W., Rajendran, P. S., Vondriska, T. M., Whitelegge, J. P., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.029 · Cited by 769 · see citing works

Astrocytes: a central element in neurological diseases

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Astrocyte Reactivity: Subtypes, States, and Functions in CNS Innate Immunity

Sofroniew, M. V. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.07.004 · Cited by 721 · see citing works

Hyperphosphorylation of Microtubule-Associated Protein Tau: A Promising Therapeutic Target for Alzheimer Disease

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Transcription factor NF-κB is activated in primary neurons by amyloid β peptides and in neurons surrounding early plaques from patients with Alzheimer disease

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Amyloid cascade hypothesis: Pathogenesis and therapeutic strategies in Alzheimer's disease

Barage, S. H., & Sonawane, K. D. (2015) · Neuropeptides · doi:10.1016/j.npep.2015.06.008 · Cited by 579 · see citing works

Involvement of Astrocytes in Alzheimer’s Disease from a Neuroinflammatory and Oxidative Stress Perspective

González-Reyes, R. E., Nava-Mesa, M. O., Vargas-Sánchez, K., Ariza-Salamanca, D. F., & Mora-Muñoz, L. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00427 · Cited by 525 · see citing works

Identification of diverse astrocyte populations and their malignant analogs

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Astrocytic neuroligins control astrocyte morphogenesis and synaptogenesis

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YKL-40: A Novel Prognostic Fluid Biomarker for Preclinical Alzheimer's Disease

Craig-Schapiro, R., Perrin, R. J., Roe, C. M., Xiong, C., Carter, D., Cairns, N. J., Mintun, M. A., Peskind, E. R., Li, G., Galasko, D. R., et al. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.08.025 · Cited by 504 · see citing works

Astrocyte layers in the mammalian cerebral cortex revealed by a single-cell in situ transcriptomic map

Bayraktar, O. A., Bartels, T., Holmqvist, S., Kleshchevnikov, V., Martirosyan, A., Polioudakis, D., Ben Haim, L., Young, A. M. H., Batiuk, M. Y., Prakash, K., et al. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0602-1 · Cited by 489 · see citing works

The Emerging Nature of Astrocyte Diversity

Khakh, B. S., & Deneen, B. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050443 · Cited by 485 · see citing works

Single-nucleus transcriptome analysis reveals dysregulation of angiogenic endothelial cells and neuroprotective glia in Alzheimer’s disease

Lau, S.-F., Cao, H., Fu, A. K. Y., & Ip, N. Y. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2008762117 · Cited by 476 · see citing works

Complement C3 Is Activated in Human AD Brain and Is Required for Neurodegeneration in Mouse Models of Amyloidosis and Tauopathy

Wu, T., Dejanovic, B., Gandham, V. D., Gogineni, A., Edmonds, R., Schauer, S., Srinivasan, K., Huntley, M. A., Wang, Y., Wang, T.-M., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.07.060 · Cited by 466 · see citing works

Astrocytes in Alzheimer's Disease

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Evidence for Astrocytosis in Prodromal Alzheimer Disease Provided by ¹¹ C-Deuterium-L-Deprenyl: A Multitracer PET Paradigm Combining ¹¹ C-Pittsburgh Compound B and ¹⁸ F-FDG

Carter, S. F., Schöll, M., Almkvist, O., Wall, A., Engler, H., Långström, B., & Nordberg, A. (2012) · Journal of Nuclear Medicine · doi:10.2967/jnumed.110.087031 · Cited by 442 · see citing works

Environmental risk factors for dementia: a systematic review

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The role of astrocytes in amyloid production and Alzheimer's disease

Frost, G. R., & Li, Y. (2017) · Open Biology · doi:10.1098/rsob.170228 · Cited by 435 · see citing works

Neuron loss in the 5XFAD mouse model of Alzheimer’s disease correlates with intraneuronal Aβ42 accumulation and Caspase-3 activation

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Altered Insulin Signaling in Alzheimer’s Disease Brain – Special Emphasis on PI3K-Akt Pathway

Gabbouj, S., Ryhänen, S., Marttinen, M., Wittrahm, R., Takalo, M., Kemppainen, S., Martiskainen, H., Tanila, H., Haapasalo, A., Hiltunen, M., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00629 · Cited by 401 · see citing works

Reactive astrocytes in neurodegenerative diseases

Li, K., Li, J., Zheng, J., & Qin, S. (2019) · Aging and disease · doi:10.14336/ad.2018.0720 · Cited by 398 · see citing works

Fibrous and protoplasmic astrocytes are biochemically and developmentally distinct

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Astrocytes, neurons, synapses: a tripartite view on cortical circuit development

Farhy-Tselnicker, I., & Allen, N. J. (2018) · Neural Development · doi:10.1186/s13064-018-0104-y · Cited by 396 · see citing works

Isolation of glia from Alzheimer’s mice reveals inflammation and dysfunction

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Tumor Necrosis Factor-α, Interleukin-1β, and Interferon-γ Stimulate γ-Secretase-mediated Cleavage of Amyloid Precursor Protein through a JNK-dependent MAPK Pathway

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The contribution of activated astrocytes to Aβ production: Implications for Alzheimer's disease pathogenesis

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Receptor for AGEs (RAGE) as Mediator of NF-kB Pathway Activation in Neuroinflammation and Oxidative Stress

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Astrocyte Biomarkers in Alzheimer’s Disease

Carter, S. F., Herholz, K., Rosa-Neto, P., Pellerin, L., Nordberg, A., & Zimmer, E. R. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2018.11.006 · Cited by 355 · see citing works

Inhibition of Stat3‐mediated astrogliosis ameliorates pathology in an Alzheimer's disease model

Reichenbach, N., Delekate, A., Plescher, M., Schmitt, F., Krauss, S., Blank, N., Halle, A., & Petzold, G. C. (2019) · EMBO Molecular Medicine · doi:10.15252/emmm.201809665 · Cited by 343 · see citing works

Untangling the brain’s neuroinflammatory and neurodegenerative transcriptional responses

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The JAK/STAT3 pathway is a common inducer of astrocyte reactivity in Alzheimer’s and Huntington’s diseases

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Metabotropic P2Y1 receptor signalling mediates astrocytic hyperactivity in vivo in an Alzheimer’s disease mouse model

Delekate, A., Füchtemeier, M., Schumacher, T., Ulbrich, C., Foddis, M., & Petzold, G. C. (2014) · Nature Communications · doi:10.1038/ncomms6422 · Cited by 332 · see citing works

Connexin 30 sets synaptic strength by controlling astroglial synapse invasion

Pannasch, U., Freche, D., Dallérac, G. M., Ghézali, G., Escartin, C., Ezan, P., Cohen‐Salmon, M., Benchenane, K., Abudara, V., Dufour, A., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3662 · Cited by 329 · see citing works

Cognitive Decline in Alzheimer's Disease Is Associated with Selective Changes in Calcineurin/NFAT Signaling

Abdul, H. M., Sama, M. A., Furman, J. L., Mathis, D. M., Beckett, T. L., Weidner, A. M., Patel, E., Baig, I., Murphy, M. P., LeVine, H., et al. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1064-09.2009 · Cited by 319 · see citing works

Alterations in Expression of Glutamatergic Transporters and Receptors in Sporadic Alzheimer's Disease

Jacob, C. P., Koutsilieri, E., Bartl, J., Neuen-Jacob, E., Arzberger, T., Zander, N., Ravid, R., Roggendorf, W., Riederer, P., & Grünblatt, E. (2007) · Journal of Alzheimer's Disease · doi:10.3233/jad-2007-11113 · Cited by 317 · see citing works

Astrogliosis: An integral player in the pathogenesis of Alzheimer's disease

Osborn, L. M., Kamphuis, W., Wadman, W. J., & Hol, E. M. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.01.001 · Cited by 312 · see citing works

Protein phosphatase 2A dysfunction in Alzheimer’s disease

Sontag, J.-M., & Sontag, E. (2014) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00016 · Cited by 304 · see citing works

The Transforming Growth Factor‐βs

Bottner, M. B., KRIEGLSTEIN, K. G., & Unsicker, K. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0752227.x · Cited by 302 · see citing works

Role of RAGE in Alzheimer’s Disease

Cai, Z., Liu, N., Wang, C., Qin, B., Zhou, Y., Xiao, M., Chang, L., Yan, L., & Zhao, B. (2015) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-015-0233-3 · Cited by 286 · see citing works

Deciphering the astrocyte reaction in Alzheimer's disease

Perez-Nievas, B. G., & Serrano-Pozo, A. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00114 · Cited by 282 · see citing works

Modulation of astrocyte reactivity improves functional deficits in mouse models of Alzheimer’s disease

Ceyzériat, K., Ben Haim, L., Denizot, A., Pommier, D., Matos, M., Guillemaud, O., Palomares, M.-A., Abjean, L., Petit, F., Gipchtein, P., et al. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0606-1 · Cited by 256 · see citing works

Epidemiological and Economic Burden of Alzheimer's Disease: A Systematic Literature Review of Data across Europe and the United States of America

Takizawa, C., Thompson, P. L., van Walsem, A., Faure, C., & Maier, W. C. (2014) · Journal of Alzheimer s Disease · doi:10.3233/jad-141134 · Cited by 253 · see citing works

Immunohistochemical distribution of the receptor for advanced glycation end products in neurons and astrocytes in Alzheimer’s disease

Sasaki, N., Toki, S., Chowei, H., Saito, T., Nakano, N., Hayashi, Y., Takeuchi, M., & Makita, Z. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03075-4 · Cited by 253 · see citing works

Vascular amyloid alters astrocytic water and potassium channels in mouse models and humans with Alzheimer's disease

Wilcock, D. M., Vitek, M. P., & Colton, C. A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.01.023 · Cited by 249 · see citing works

Tau Proteins and Tauopathies in Alzheimer’s Disease

Chong, F. P., Ng, K. Y., Koh, R. Y., & Chye, S. M. (2018) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-017-0574-1 · Cited by 248 · see citing works

Cellular Functions of the Amyloid Precursor Protein from Development to Dementia

van der Kant, R., & Goldstein, L. S. B. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.01.022 · Cited by 246 · see citing works

Alterations in cholesterol metabolism as a risk factor for developing Alzheimer’s disease: Potential novel targets for treatment

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Microglia and Astrocytes in Disease: Dynamic Duo or Partners in Crime?

Liddelow, S. A., Marsh, S. E., & Stevens, B. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.07.006 · Cited by 226 · see citing works

Astroglial Glutamate Signaling and Uptake in the Hippocampus

Rose, C. R., Felix, L., Zeug, A., Dietrich, D., Reiner, A., & Henneberger, C. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00451 · Cited by 224 · see citing works

Amyloid-beta peptide decreases glutamate uptake in cultured astrocytes: Involvement of oxidative stress and mitogen-activated protein kinase cascades

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Structural Remodeling of Astrocytes in the Injured CNS

Sun, D., & Jakobs, T. (2011) · The Neuroscientist · doi:10.1177/1073858411423441 · Cited by 219 · see citing works

Regulation of neural process growth, elaboration and structural plasticity by NF-κB

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Towards a Better Understanding of GABAergic Remodeling in Alzheimer’s Disease

Govindpani, K., Calvo-Flores Guzmán, B., Vinnakota, C., Waldvogel, H., Faull, R., & Kwakowsky, A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081813 · Cited by 208 · see citing works

Overexpression of human S100B exacerbates cerebral amyloidosis and gliosis in the Tg2576 mouse model of Alzheimer's disease

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Astrocyte-Derived TGF-β1 Accelerates Disease Progression in ALS Mice by Interfering with the Neuroprotective Functions of Microglia and T Cells

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Activated MAO-B in the brain of Alzheimer patients, demonstrated by [11C]-l-deprenyl using whole hemisphere autoradiography

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TGF‐β1 is an organizer of responses to neurodgeneration

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Diverse subtypes of astrocytes and their development during corticogenesis

Tabata, H. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00114 · Cited by 192 · see citing works

Transcriptomic profiling of microglia and astrocytes throughout aging

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Astrocyte Senescence and Alzheimer’s Disease: A Review

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TGF-β1 mRNA Increases in Macrophage/Microglial Cells of the Hippocampus in Response to Deafferentation and Kainic Acid-Induced Neurodegeneration

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Early-onset Alzheimer's Disease: Nonamnestic Subtypes and Type 2 AD

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GLT-1 Loss Accelerates Cognitive Deficit Onset in an Alzheimer's Disease Animal Model

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Alzheimer's disease β‐secretase BACE1 is not a neuron‐specific enzyme

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Modifiable Risk Factors for Prevention of Dementia in Midlife, Late Life and the Oldest-Old: Validation of the LIBRA Index

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Photocleavable Mass-Tagged Oligonucleotide Probes for Multiplexed and Multiomic Tissue Imaging of Targeted Transcripts

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Role of astrocytes in Alzheimer's disease pathogenesis and the impact of exercise-induced remodeling

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The GPCR Connection: Linking Alzheimer's Disease and Glioblastoma

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Generating PET scan patterns in Alzheimer’s by a mathematical model

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Transactivation Response DNA-Binding Protein of 43 (TDP-43) and Glial Cell Roles in Neurological Disorders

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SOX9 Expression Is Increased in Alzheimer’s Disease (AD) and Is Associated With Disease Progression and APOE4 Genotype: A Computational Approach

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Human brain single nucleus cell type enrichments in neurodegenerative diseasesPreprint

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Characterization of Isolated Human Astrocytes from Aging Brain

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Senescence as a Central Node in Alzheimer’s Disease: Molecular Triggers, Cellular Effectors, and RNA-Based Interventions

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AstroGreen transgenic mouse illuminates the trafficking of astrocyte-derived extracellular vesicles

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Therapeutic Potential of HAEEPGP Peptide Against β-Amyloid Induced Neuropathology

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Material considerations for delivering therapeutics across the blood–brain barrier

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Glial cells are involved in day–night protein dysregulation in the hippocampus of a mouse model of Alzheimer’s disease

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Altered metabolic function induced by amyloid-beta oligomers and PSEN1-mutations in iPSC-derived astrocytesPreprint

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Dexmedetomidine Exerts Multi-level Effects to Ameliorate Alzheimer’s Disease Pathology in the Adult Zebrafish Brain

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Ancestry-related differences in chromatin accessibility and gene expression of APOE4 are associated with Alzheimer disease riskPreprint

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Cellular underpinnings of the selective vulnerability to tauopathic insults in Alzheimer’s diseasePreprint

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β-asarone inhibits autophagic neuron death by downregulating reactive astrocytes-derived SPARC expression in LPS-induced SH-SY5Y cellsPreprint

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Cognitive Function Involving Glial Cells

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Formaldehyde, Neuroinflammation, and Cognitive Impairment

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Divergent CNS –Peripheral Signaling Reflects Astrocyte Dysfunction and Contributes to Insulin Resistance in Early Aβ Pathology

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Progressive changes in synapses and glial cells in AppNL-G-F mice, a model of Alzheimer’s disease

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Additional file 7 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700856

Additional file 19 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700892

Additional file 9 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700862

Additional file 26 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700913

Additional file 3 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700844

Additional file 20 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700895

Additional file 12 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700871

Additional file 25 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700910

Additional file 2 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.25530408

Additional file 8 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700859

Additional file 5 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700850

Additional file 17 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700886

Additional file 6 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700853

Additional file 21 of Insights for disease modeling from single-cell transcriptomics of iPSC-derived Ngn2-induced neurons and astrocytes across differentiation time and co-culture

Das, D., Sonthalia, S., Stein-O.’Brien, G., Wahbeh, M., Feuer, K., Goff, L. A., Colantuoni, C., Mahairaki, V., & Avramopoulos, D. (2024) · Figshare · doi:10.6084/m9.figshare.26700898

Role of Reactive Astrocytes in Alzheimer’s Disease

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