Immune attack: the role of inflammation in Alzheimer disease

The Amyloid Hypothesis of Alzheimer’s Disease: Progress and Problems on the Road to Therapeutics

Hardy, J., & Selkoe, D. J. (2002) · Science · doi:10.1126/science.1072994 · Cited by 13,864

Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins.

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Macrophage activation and polarization: nomenclature and experimental guidelines

Murray, P. J., Allen, J. E., Biswas, S. K., Fisher, E. A., Gilroy, D. W., Goerdt, S., Gordon, S., Hamilton, J. A., Ivashkiv, L. B., Lawrence, T., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.06.008 · Cited by 6,337

Astrocytes: Biology and pathology

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

Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid β-peptide

Haass, C., & Selkoe, D. J. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2101 · Cited by 4,744

The M1 and M2 paradigm of macrophage activation: Time for reassessment

Martinez, F. O., & Gordon, S. (2014) · F1000Prime Reports · doi:10.12703/p6-13 · Cited by 4,689

Alzheimer’s disease

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

Inflammation and Alzheimer’s disease

Akiyama, H. (2000) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)00124-x · Cited by 4,514

Synaptic Pruning by Microglia Is Necessary for Normal Brain Development

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The neuroprotective role of microglial cells against amyloid beta‐mediated toxicity in organotypic hippocampal slice cultures

Richter, M., Vidovic, N., Biber, K. P. H., Dolga, A. M., Culmsee, C., & Dodel, R. C. (2019) · Brain Pathology · doi:10.1111/bpa.12807 · Cited by 31

Culprit or Bystander: Defective Mitophagy in Alzheimer’s Disease

Xie, C., Aman, Y., Adriaanse, B. A., Cader, M. Z., Plun‐Favreau, H., Xiao, J., & Fang, E. F. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00391 · Cited by 29

Transcriptome Analysis of Post-Mortem Brain Tissue Reveals Up-Regulation of the Complement Cascade in a Subgroup of Schizophrenia Patients

Carlström, E. L., Niazi, A., Etemadikhah, M., Halvardson, J., Enroth, S., Stockmeier, C. A., Rajkowska, G., Nilsson, B., & Feuk, L. (2021) · Genes · doi:10.3390/genes12081242 · Cited by 29

Deep post-GWAS analysis identifies potential risk genes and risk variants for Alzheimer’s disease, providing new insights into its disease mechanisms

Wang, Z., Zhang, Q., Lin, J.-R., Jabalameli, M. R., Mitra, J., Nguyen, N., & Zhang, Z. D. (2021) · Scientific Reports · doi:10.1038/s41598-021-99352-3 · Cited by 29

Current nano-therapeutic approaches ameliorating inflammation in cancer progression

Rehman, M. U., Khan, A., Imtiyaz, Z., Ali, S., Makeen, H. A., Rashid, S., & Arafah, A. M. (2022) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2022.02.006 · Cited by 29

Dimethyl Itaconate Reduces Cognitive Impairment and Neuroinflammation in APPswe/PS1ΔE9 Transgenic Mouse Model of Alzheimer’s Disease

Xiong, J., Lu, D., Chen, B.-Q., Liu, T., & Wang, Z. (2022) · NeuroMolecular Medicine · doi:10.1007/s12017-022-08725-y · Cited by 29

Sirtuins promote brain homeostasis, preventing Alzheimer’s disease through targeting neuroinflammation

Wątroba, M., & Szukiewicz, D. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.962769 · Cited by 29

Circulating Cell-Free Genomic DNA Is Associated with an Increased Risk of Dementia and with Change in Cognitive and Physical Function

Nidadavolu, L. S., Feger, D. M., Wu, Y., Grodstein, F., Gross, A. L., Bennett, D. A., Walston, J. D., Oh, E. S., & Abadir, P. M. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220301 · Cited by 30

Role of non‑coding RNAs as biomarkers and the application of omics technologies in Alzheimer's disease (Review)

Pierouli, K., Papakonstantinou, E., Papageorgiou, L., Diakou, I., Mitsis, Τ., Dragoumani, K., Spandidos, D. A., Bacopoulou, F., Chrousos, G. P., Goulielmos, G. N., et al. (2022) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2022.5208 · Cited by 29

Inhibition of histone methyltransferase Smyd3 rescues NMDAR and cognitive deficits in a tauopathy mouse model

Williams, J. B., Cao, Q., Wang, W., Lee, Y., Qin, L., Zhong, P., Ren, Y., Ma, K., & Yan, Z. (2023) · Nature Communications · doi:10.1038/s41467-022-35749-6 · Cited by 31

Neuroinflammation Biomarkers in the AT(N) Framework Across the Alzheimer's Disease Continuum

Bieger, A., Rocha, A., Bellaver, B., Machado, L. S., Ros, L. U. D., Borelli, W. V., Therriault, J., Macedo, A. C., Pascoal, T. A., Gauthier, S. G., et al. (2023) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2023.54 · Cited by 29

Microenvironment modulating nanogels by Shiitake-derived lentinan and a reactive oxygen species scavenging conjugated polymer for the treatment of Alzheimer’s disease

Xin, Y., Fang, F., Yue, Q., Luo, Y., Tian, S., Cheng, L., Yang, X., Yang, X., Luo, L., & Meng, F. (2024) · Nano Today · doi:10.1016/j.nantod.2024.102178 · Cited by 29

Vascular-directed responses of microglia produced by methamphetamine exposure: indirect evidence that microglia are involved in vascular repair?

Bowyer, J. F., Sarkar, S., Tranter, K. M., Hanig, J. P., Miller, D. B., & O'Callaghan, J. P. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0526-6 · Cited by 30

Impacts of Acute Hypoxia on Alzheimer's Disease-Like Pathologies in APPswe/PS1dE9 Mice and Their Wild Type Littermates

Zhang, F., Zhong, R., Qi, H., Li, S., Cheng, C., Liu, X., Liu, Y., & Le, W. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00314 · Cited by 29

Synthesis of andrographolide analogues and their neuroprotection and neurite outgrowth-promoting activities

Xu, Y., Wei, H., Wang, J., Wang, W., & Gao, J. (2019) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2019.04.025 · Cited by 29

Astrocytes regulate neuronal network activity by mediating synapse remodeling

Kim, N., & Chung, W. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.09.007 · Cited by 31

Xuefu Zhuyu decoction ameliorates obesity, hepatic steatosis, neuroinflammation, amyloid deposition and cognition impairment in metabolically stressed APPswe/PS1dE9 mice

Yeh, C.-W., Liu, H., Lin, L.-C., Liou, K.-T., Huang, Y., Lin, C., Tzeng, T.-T., Shie, F., Tsay, H.-J., & Shiao, Y. (2017) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2017.07.036 · Cited by 28

Dendritic Cells as an Alternate Approach for Treatment of Neurodegenerative Disorders

Brezováková, V., Valachova, B., Hanes, J., Novák, M., & Jadhav, S. (2018) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-018-0598-1 · Cited by 29

AVNP2 protects against cognitive impairments induced by C6 glioma by suppressing tumour associated inflammation in rats

Li, J., Liu, M., Gao, J. M., Jiang, Y., Wu, L., Cheong, Y., Ren, G., & Yang, Z. R. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.02.009 · Cited by 28

The Mechanistic Role of Bridging Integrator 1 (BIN1) in Alzheimer’s Disease

Gao, P.-R., Ye, L., Cheng, H.-R., & Li, H. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00926-y · Cited by 34

Interleukin 10 Restores Lipopolysaccharide-Induced Alterations in Synaptic Plasticity Probed by Repetitive Magnetic Stimulation

Lenz, M., Eichler, A., Kruse, P., Strehl, A., Rodriguez-Rozada, S., Goren, I., Yogev, N., Frank, S., Waisman, A., Deller, T., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.614509 · Cited by 30

Drosophila as a model to explore secondary injury cascades after traumatic brain injury

Buhlman, L. M., Krishna, G., Jones, T. B., & Thomas, T. C. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.112079 · Cited by 29

Association between Alzheimer's disease and risk of cancer: A retrospective cohort study in Shanghai, China

Ren, R., Huang, Q., Xu, G., Gu, K., Dammer, E. B., Wang, C., Xie, X., Chen, W., Shao, Z., Chen, S., et al. (2021) · Alzheimer s & Dementia · doi:10.1002/alz.12436 · Cited by 28

Odor Enrichment Attenuates the Anesthesia/Surgery-induced Cognitive Impairment

Zhang, C., Han, Y., Liu, X., Tan, H. L. E., Dong, Y., Zhang, Y., Liang, F., Zheng, H., Crosby, G. J., Culley, D. J., et al. (2022) · Annals of Surgery · doi:10.1097/sla.0000000000005599 · Cited by 28

The role of adenosine A2A receptors in Alzheimer's disease and tauopathies

Launay, A., Nebie, O., Shankara, J. V., Lebouvier, T., Buée, L., Faivre, É., & Blum, D. L. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109379 · Cited by 29

The novel function of bexarotene for neurological diseases

Liu, Y., Wang, P., Jin, G., Shi, P., Zhao, Y., Guo, J., Yin, Y., Shao, Q.-H., Li, P., & Yang, P. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102021 · Cited by 30

The mixed-lineage kinase 3 inhibitor URMC-099 facilitates microglial amyloid-β degradation

Dong, W., Embury, C. M., Lu, Y., Whitmire, S. M., Dyavarshetty, B., Gelbard, H. A., Gendelman, H. E., & Kiyota, T. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0646-z · Cited by 28

An Extract from Shrimp Processing By-Products Protects SH-SY5Y Cells from Neurotoxicity Induced by Aβ25–35

Zhang, Y., Jiao, G., Song, C., Gu, S., Brown, R. E., Zhang, J., Zhang, P., Gagnon, J., Locke, S. J., Stefanova, R., et al. (2017) · Marine Drugs · doi:10.3390/md15030083 · Cited by 28

The Microglial Response to Neurodegenerative Disease

Song, W. M., & Colonna, M. (2018) · Advances in immunology · doi:10.1016/bs.ai.2018.04.002 · Cited by 30

Short-term sleep deprivation in mice induces B cell migration to the brain compartment

Korin, B., Avraham, S., Azulay‐Debby, H., Farfara, D., Hakim, F., & Rolls, A. (2019) · SLEEP · doi:10.1093/sleep/zsz222 · Cited by 28

Cordycepin improved neuronal synaptic plasticity through CREB-induced NGF upregulation driven by MG-M2 polarization: a microglia-neuron symphony in AD

Jiao, L., Yu, Z., Zhong, X., Yao, W., Xing, L., Ma, G., Shen, J., Wu, Y., Du, K., Liu, J., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.114054 · Cited by 27

Astragaloside IV against Alzheimer's disease via microglia-mediated neuroinflammation using network pharmacology and experimental validation

Bao, M., Bade, R., Liu, H., Tsambaa, B., Shao, G., Borjigidai, A., & Cheng, Y. (2023) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2023.175992 · Cited by 27

Metal-organic frameworks derived emerging theranostic platforms

Zheng, N., Li, K., He, L., Wang, Q., Yang, B., Mao, C., Tang, W., Liu, S., & Liu, S. (2024) · Nano Today · doi:10.1016/j.nantod.2024.102404 · Cited by 27

Donanemab for Alzheimer’s disease: from preclinical research to the clinical application

Dodel, R. C., & Froelich, L. (2025) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2025.2546868 · Cited by 27

U1 snRNP Alteration and Neuronal Cell Cycle Reentry in Alzheimer Disease

Bai, B. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00075 · Cited by 28

Visceral fat-related systemic inflammation and the adolescent brain: a mediating role of circulating glycerophosphocholines

Syme, C. A., Pelletier, S., Shin, J., Abrahamowicz, M., Leonard, G. T., Perron, M., Richer, L., Veillette, S., Gaudet, D., Pike, G. B., et al. (2018) · International Journal of Obesity · doi:10.1038/s41366-018-0202-2 · Cited by 30

Anti-neuroinflammatory effects of a food-grade phenolic-enriched maple syrup extract in a mouse model of Alzheimer’s disease

Rose, K. N., Barlock, B. J., DaSilva, N. A., Johnson, S. L., Liu, C., Ma, H., Nelson, R. B., Akhlaghi, F., & Seeram, N. P. (2019) · Nutritional Neuroscience · doi:10.1080/1028415x.2019.1672009 · Cited by 28

Heart and Brain: Complex Relationships for Left Ventricular Dysfunction

Daniele, G., DiLucia, S., Masci, P. G., & del Monte, F. (2020) · Current Cardiology Reports · doi:10.1007/s11886-020-01318-w · Cited by 27

Cellular Biology of Tau Diversity and Pathogenic Conformers

Kang, S., Eskandari‐Sedighi, G., Hromádková, L., Safar, J., & Westaway, D. A. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.590199 · Cited by 29

Microglia-Derived Interleukin 23: A Crucial Cytokine in Alzheimer's Disease?

Nitsch, L., Schneider, L. H., Zimmermann, J., & Müller, M. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.639353 · Cited by 27

Better Identification of Cognitive Decline With Interleukin-2 Than With Amyloid and Tau Protein Biomarkers in Amnestic Mild Cognitive Impairment

Liang, C., Tsai, C., Lin, G., Lee, J., Lin, Y., Chu, C., Sung, Y., Tsai, C., Yeh, T., Chu, H., et al. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.670115 · Cited by 29

Cochlear Inflammaging in Relation to Ion Channels and Mitochondrial Functions

Bazard, P., Pineros, J., Frisina, R. D., Bauer, M. A., Acosta, A. A., Paganella, L. R., Borakiewicz, D., Thivierge, M., Mannering, F. L., Zhu, X., et al. (2021) · Cells · doi:10.3390/cells10102761 · Cited by 27

KYNA/Ahr Signaling Suppresses Neural Stem Cell Plasticity and Neurogenesis in Adult Zebrafish Model of Alzheimer’s Disease

Siddiqui, T., Bhattarai, P., Popova, S. D., Coşacak, M. İ., Sariya, S., Zhang, Y., Mayeux, R. P., Tosto, G., & Kızıl, Ç. (2021) · Cells · doi:10.3390/cells10102748 · Cited by 27

Landscape of immune infiltration in entorhinal cortex of patients with Alzheimerʼs disease

Zhang, H., Cao, S., Xu, Y., Sun, X., Fei, M., Jing, Q., Xu, X., Tang, J., Niu, B., & Li, C. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.941656 · Cited by 27

Ferroptosis: a potential therapeutic target for Alzheimer’s disease

Yang, L., & Nao, J. (2022) · Reviews in the Neurosciences · doi:10.1515/revneuro-2022-0121 · Cited by 28

Beyond the amyloid cascade: An update of Alzheimer's disease pathophysiology

Gouilly, D., Rafiq, M., Nogueira, L., Salabert, A., Payoux, P., Péran, P., & Pariente, J. (2023) · Revue Neurologique · doi:10.1016/j.neurol.2022.12.006 · Cited by 31

Association of PM 2.5 Exposure and Alzheimer Disease Pathology in Brain Bank Donors—Effect Modification by APOE Genotype

Christensen, G. M., Li, Z., Liang, D., Ebelt, S., Gearing, M., Levey, A. I., Lah, J. J., Wingo, A. P., Wingo, T. S., & Hüls, A. (2024) · Neurology · doi:10.1212/wnl.0000000000209162 · Cited by 27

Correlative Light and Electron Microscopy to Study Microglial Interactions with β-Amyloid Plaques

Bisht, K., Hajj, H. E., Savage, J. C., Sanchez, M. G., & Tremblay, M. (2016) · Journal of Visualized Experiments · doi:10.3791/54060 · Cited by 28

Glutaminyl cyclase activity correlates with levels of Aβ peptides and mediators of angiogenesis in cerebrospinal fluid of Alzheimer’s disease patients

Bridel, C., Hoffmann, T., Meyer, A., Durieux‐Lu, S., Simmelink, M. J. A., Orth, M., Scheltens, P., Lues, I., & Teunissen, C. E. (2017) · Alzheimer s Research & Therapy · doi:10.1186/s13195-017-0266-6 · Cited by 27

Towards a Novel Class of Multitarget-Directed Ligands: Dual P2X7–NMDA Receptor Antagonists

Karoutzou, O., Kwak, S., Lee, S., Martínez‐Falguera, D., Sureda, F. X., Vázquez, S., Kim, Y., & Barniol‐Xicota, M. (2018) · Molecules · doi:10.3390/molecules23010230 · Cited by 27

Aging exacerbates cognitive and anxiety alterations induced by an intracerebroventricular injection of amyloid-β1–42 peptide in mice

Souza, L. C., Jessé, C. R., Fabbro, L. D., de Gomes, M. G., Gomes, N. S., Filho, C. B., Goes, A. T. R., Wilhelm, E. A., Luchese, C., Roman, S. S., et al. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.01.005 · Cited by 27

Prolonged Drug-Releasing Fibers Attenuate Alzheimer’s Disease-like Pathogenesis

Salles, G. N., Calió, M. L., Afewerki, S., Soares, C. P., Porcionatto, M. A., Hölscher, C., & Lobo, A. O. (2018) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.8b12649 · Cited by 29

Integration of Machine Learning Methods to Dissect Genetically Imputed Transcriptomic Profiles in Alzheimer’s Disease

Maj, C., Azevedo, T., Giansanti, V., Borisov, O., Dimitri, G. M., Spasov, S., Initiative, A. D. N., Lió, P., & Merelli, I. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00726 · Cited by 27

Type 1 Interleukin-4 Signaling Obliterates Mouse Astroglia in vivo but Not in vitro

Mashkaryan, V., Siddiqui, T., Popova, S. D., Coşacak, M. İ., Bhattarai, P., Brandt, K., Govindarajan, N., Petzold, A., Reinhardt, S., Dahl, A., et al. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00114 · Cited by 27

Protective Activity of Aβ on Cell Cultures (PC12 and THP-1 after Differentiation) Preincubated with Lipopolysaccharide (LPS)

Wiatrak, B., & Balon, K. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-02204-w · Cited by 27

Mass spectrometry in cerebrospinal fluid uncovers association of glycolysis biomarkers with Alzheimer’s disease in a large clinical sample

de Geus, M. B., Leslie, S. N., Lam, T. T., Wang, W., Roux‐Dalvai, F., Droit, A., Kivisäkk, P., Nairn, A. C., Arnold, S. E., & Carlyle, B. C. (2023) · Scientific Reports · doi:10.1038/s41598-023-49440-3 · Cited by 28

Imeglimin Exhibits Novel Anti-Inflammatory Effects on High-Glucose-Stimulated Mouse Microglia through ULK1-Mediated Suppression of the TXNIP–NLRP3 Axis

Kato, H., Iwashita, K., Iwasa, M., Kato, S., Yamakage, H., Suganami, T., Tanaka, M., & Satoh‐Asahara, N. (2024) · Cells · doi:10.3390/cells13030284 · Cited by 26

Loss of presenilin 2 age-dependently alters susceptibility to acute seizures and kindling acquisition

Beckman, M., Knox, K. M., Koneval, Z., Smith, C., Jayadev, S., & Barker‐Haliski, M. L. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104719 · Cited by 26

The Emerging Role of COX-2, 15-LOX and PPARγ in Metabolic Diseases and Cancer: An Introduction to Novel Multi-target Directed Ligands (MTDLs)

Alaaeddine, R. A., Elzahhar, P. A., AlZaim, I., Abou-Kheir, W. G., Belal, A. S. F., & EL‐Yazbi, A. F. (2020) · Current Medicinal Chemistry · doi:10.2174/0929867327999200820173853 · Cited by 26

Modification of Glial Cell Activation through Dendritic Cell Vaccination: Promises for Treatment of Neurodegenerative Diseases

Sabahi, M., Joshaghanian, A., Dolatshahi, M., Jabbari, P., Rahmani, F., & Rezaei, N. (2021) · Journal of Molecular Neuroscience · doi:10.1007/s12031-021-01818-6 · Cited by 26

Unraveling the Speciation of β-Amyloid Peptides during the Aggregation Process by Taylor Dispersion Analysis

Deleanu, M., Hernandez, J., Cipelletti, L., Biron, J., Rossi, E., Taverna, M., Cottet, H., & Chamieh, J. (2021) · Analytical Chemistry · doi:10.1021/acs.analchem.1c00527 · Cited by 26

Design, synthesis, and in vitro evaluation of 4-aminoalkyl-1(2H)-phthalazinones as potential multifunctional anti-Alzheimer’s disease agents

Ye, C., Xu, R., Cao, Z., Song, Q., Yu, G., Shi, Y., Liu, Z., Liu, X., & Deng, Y. (2021) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2021.104895 · Cited by 26

Design and synthesis of novel diosgenin-triazole hybrids targeting inflammation as potential neuroprotective agents

Huang, Y., Huang, W., Yang, G., Wang, R., & Ma, L. (2021) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2021.128092 · Cited by 26

Neuroprotective efficacy of 4-Hydroxyisoleucine in experimentally induced intracerebral hemorrhage

Siddiqui, E. M., Mehan, S., Upadhayay, S., Khan, A., Halawi, M., Halawi, A. A., & Alsaffar, R. M. (2021) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2021.07.010 · Cited by 28

All roads lead to Rome — a review of the potential mechanisms by which exerkines exhibit neuroprotective effects in Alzheimer’s disease

So, K., Li, A., Liang, Y., Zhang, L., Luo, X., Wu, L.-L., Chen, Z.-W., Wei, G.-H., Zhang, K., Du, Z.-A., et al. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.325012 · Cited by 27

CSF-Derived CD4 + T-Cell Diversity Is Reduced in Patients With Alzheimer Clinical Syndrome

Joshi, C., Sivaprakasam, K., Christley, S., Ireland, S. J., Rivas, J. R., Zhang, W., Sader, D., Logan, R., Lambracht‐Washington, D., Rosenberg, R. N., et al. (2021) · Neurology Neuroimmunology & Neuroinflammation · doi:10.1212/nxi.0000000000001106 · Cited by 26

Roles of Fatty Acids in Microglial Polarization: Evidence from In Vitro and In Vivo Studies on Neurodegenerative Diseases

Sanjay, S., Park, M., & Lee, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137300 · Cited by 28

Mapping secretome-mediated interaction between paired neuron–macrophage single cells

Deng, J., Ji, Y., Zhu, F., Liu, L., Li, L., Bai, X., Li, H., Liu, X., Luo, Y., Lin, B., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2200944119 · Cited by 26

The pollutome-connectome axis: a putative mechanism to explain pollution effects on neurodegeneration

Pini, L., Salvalaggio, A., Wennberg, A. M. V., Dimakou, A., Matteoli, M., & Corbetta, M. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101867 · Cited by 26

Under the umbrella of depression and Alzheimer’s disease physiopathology: Can cannabinoids be a dual-pleiotropic therapy?

Fonseca, C., Ettcheto, M., Bicker, J., Fernandes, M. J., Falcão, A. C., Camins, A., & Fortuna, A. C. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101998 · Cited by 31

Reactive Oxygen Species‐Responsive Polymeric Prodrug Nanoparticles for Selective and Effective Treatment of Inflammatory Diseases

Zhang, Y., Liu, L., Wang, T., Mao, C., Shan, P., Lau, C. S., Li, Z., Guo, W., & Wang, W. (2023) · Advanced Healthcare Materials · doi:10.1002/adhm.202301394 · Cited by 26

Cis P-tau is a central circulating and placental etiologic driver and therapeutic target of preeclampsia

Jash, S., Banerjee, S., Cheng, S., Wang, B., Qiu, C., Kondo, A., Ernerudh, J., Zhou, X. Z., Lu, K. P., & Sharma, S. (2023) · Nature Communications · doi:10.1038/s41467-023-41144-6 · Cited by 26

Molecular Mechanisms Linking Osteoarthritis and Alzheimer’s Disease: Shared Pathways, Mechanisms and Breakthrough Prospects

Umoh, I. O., Reis, H. J., & de Oliveira, A. C. P. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25053044 · Cited by 28

Neuroinflammation and neurodegeneration following traumatic brain injuries

Boulton, M., & Al-Rubaie, A. (2024) · Anatomical Science International · doi:10.1007/s12565-024-00778-2 · Cited by 26

Chemical probes targeting epigenetic proteins: Applications beyond oncology

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N-Stearoylethanolamine protects the brain and improves memory of mice treated with lipopolysaccharide or immunized with the extracellular domain of α7 nicotinic acetylcholine receptor

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