Immune attack: the role of inflammation in Alzheimer disease

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

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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

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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

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

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Alzheimer’s disease

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Inflammation and Alzheimer’s disease

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Synaptic Pruning by Microglia Is Necessary for Normal Brain Development

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Prevention and Treatment of Alzheimer’s Disease: Biological Mechanisms of Exercise

McGurran, H., Glenn, J. M., Madero, E. N., & Bott, N. T. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-180958 · Cited by 63

Quantification of white matter cellularity and damage in preclinical and early symptomatic Alzheimer's disease

Wang, Q., Wang, Y., Liu, J., Sutphen, C. L., Cruchaga, C., Blazey, T., Gordon, B. A., Su, Y., Chen, C., Shimony, J. S., et al. (2019) · NeuroImage: Clinical · doi:10.1016/j.nicl.2019.101767 · Cited by 63

HMGB1 gene silencing inhibits neuroinflammation via down-regulation of NF-κB signaling in primary hippocampal neurons induced by Aβ25–35

Nan, K., Han, Y., Fang, Q., Huang, C., Yu, L., Ge, W., Xiang, F., Tao, Y.-X., Cao, H., & Li, J. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2018.12.027 · Cited by 62

Targeting Microglia-Synapse Interactions in Alzheimer’s Disease

Piccioni, G., Mango, D., Saidi, A., Corbo, M., & Nisticò, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052342 · Cited by 64

Is cyclooxygenase‐1 involved in neuroinflammation?

Ghazanfari, N., van Waarde, A., Dierckx, R., Doorduin, J., & de Vries, E. F. J. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24934 · Cited by 65

Curcumin improves memory deficits by inhibiting HMGB1‐RAGE/TLR4‐NF‐κB signalling pathway in APPswe/PS1dE9 transgenic mice hippocampus

Han, Y., Chen, R., Lin, Q., Liu, Y., Ge, W., Cao, H., & Li, J. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16855 · Cited by 64

Epigenetic mechanisms of particulate matter exposure: air pollution and hazards on human health

Covarrubias, D. G., Ramírez‐Díaz, I., Guzmán-Linares, J., Limón, I. D., Manuel-Sánchez, D. M., Molina-Herrera, A., Coral-García, M. Á., Anastasio, E., Anaya‐Hernández, A., López‐Salazar, P., et al. (2024) · Frontiers in Genetics · doi:10.3389/fgene.2023.1306600 · Cited by 65

Diet Supplementation with Hydroxytyrosol Ameliorates Brain Pathology and Restores Cognitive Functions in a Mouse Model of Amyloid-β Deposition

Nardiello, P., Pantano, D., Lapucci, A., Stefani, M., & Casamenti, F. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-171124 · Cited by 62

Multi-cohort cerebrospinal fluid proteomics identifies robust molecular signatures across the Alzheimer disease continuum

Ali, M., Timsina, J., Western, D., Liu, M., Beric, A., Budde, J., Do, A., Heo, G., Wang, L., Gentsch, J., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.02.014 · Cited by 61

Peptidylarginine Deiminases—Roles in Cancer and Neurodegeneration and Possible Avenues for Therapeutic Intervention via Modulation of Exosome and Microvesicle (EMV) Release?

Lange, S., Gallagher, M., Kholia, S., Kosgodage, U. S., Hristova, M., Hardy, J., & Inal, J. M. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18061196 · Cited by 62

Multimodal, label-free fluorescence and Raman imaging of amyloid deposits in snap-frozen Alzheimer’s disease human brain tissue

Lochocki, B., Boon, B. D. C., Verheul, S. R., Zada, L., Hoozemans, J. J. M., Ariese, F., & de Boer, J. F. (2021) · Communications Biology · doi:10.1038/s42003-021-01981-x · Cited by 61

Profiling the oral microbiomes in patients with Alzheimer's disease

Guo, H., Li, B., Yao, H., Liu, D., Chen, R., Zhou, S., Ji, Y., Zeng, L., & Du, M. (2021) · Oral Diseases · doi:10.1111/odi.14110 · Cited by 62

N-Benzyl Benzamide Derivatives as Selective Sub-Nanomolar Butyrylcholinesterase Inhibitors for Possible Treatment in Advanced Alzheimer’s Disease

Du, C., Wang, L., Guan, Q., Yang, H., Chen, T., Liu, Y., Li, Q., Lyu, W., Lü, X., Chen, Y., et al. (2022) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c00944 · Cited by 61

Berberine alleviates Alzheimer's disease by regulating the gut microenvironment, restoring the gut barrier and brain-gut axis balance

Sun, C., Dong, S., Chen, W., Li, S., Luo, E., & Ji, J. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155624 · Cited by 64

Melatonin protects against A β ‐induced neurotoxicity in primary neurons via miR‐132/PTEN/AKT/FOXO3a pathway

Zhao, Y., Zhao, R., Wu, J., Wang, Q., Pang, K., Shi, Q., Gao, Q., Hu, Y., Dong, X., Zhang, J., et al. (2018) · BioFactors · doi:10.1002/biof.1411 · Cited by 55

Novel targets in Alzheimer’s disease: A special focus on microglia

Balducci, C., & Forloni, G. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.01.017 · Cited by 62

Innate Immunity Cells and the Neurovascular Unit

Presta, I., Vismara, M. F. M., Novellino, F., Donato, A., Zaffino, P., Scali, E., Pirrone, K. C., Spadea, M. F., Malara, N., & Donato, G. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19123856 · Cited by 61

Alterations of Transcription of Genes Coding Anti-oxidative and Mitochondria-Related Proteins in Amyloid β Toxicity: Relevance to Alzheimer’s Disease

Cieślik, M., Czapski, G. A., Wójtowicz, S., Wieczorek, I., Wencel, P. L., Strosznajder, R. P., Jaber, V. R., Lukiw, W. J., & Strosznajder, J. B. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-01819-y · Cited by 61

The Neuroimmune Axis in the Tumor Microenvironment

Shurin, M. R., Shurin, G. V., Zlotnikov, S. B., & Bunimovich, Y. L. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1900828 · Cited by 61

Proteomic Profiling of Plasma and Brain Tissue from Alzheimer’s Disease Patients Reveals Candidate Network of Plasma Biomarkers

Chen, M., & Xia, W. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-200110 · Cited by 63

Investigation of the peripheral inflammation (neutrophil–lymphocyte ratio) in two neurodegenerative diseases of the central nervous system

Kara, S. P., Altunan, B., & Ünal, A. (2021) · Neurological Sciences · doi:10.1007/s10072-021-05507-5 · Cited by 61

Genetic Deletion of Tumor Necrosis Factor-α Attenuates Amyloid-β Production and Decreases Amyloid Plaque Formation and Glial Response in the 5XFAD Model of Alzheimer’s Disease

Paouri, E., Tzara, O., Zenelak, S., & Georgopoulos, S. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-170065 · Cited by 61

Structural Modification, In Vitro, In Vivo, Ex Vivo, and In Silico Exploration of Pyrimidine and Pyrrolidine Cores for Targeting Enzymes Associated with Neuroinflammation and Cholinergic Deficit in Alzheimer’s Disease

Javed, M. A., Ashraf, N., Jan, M. S., Mahnashi, M. H., Alqahtani, Y. S., Alyami, B. A., Alqarni, A. O., Asiri, Y. I., Ikram, M., Sadiq, A., et al. (2021) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.1c00507 · Cited by 60

Inflammation, tau pathology, and synaptic integrity associated with sleep spindles and memory prior to β-amyloid positivity

Mander, B. A., Dave, A., Lui, K. K., Sprecher, K. E., Berisha, D. E., Chappel-Farley, M. G., Chen, I. Y., Riedner, B. A., Heston, M. B., Suridjan, I., et al. (2022) · SLEEP · doi:10.1093/sleep/zsac135 · Cited by 62

Exosomes Derived from M2 Microglial Cells Modulated by 1070‐nm Light Improve Cognition in an Alzheimer's Disease Mouse Model

Chen, C., Bao, Y., Lü, X., Jiang, C., Guo, Y., Tong, S., Zhang, J., Chen, L., & Mao, Y. Q. (2023) · Advanced Science · doi:10.1002/advs.202304025 · Cited by 60

Alzheimer’s disease and cytokine IL-10 gene polymorphisms: is there an association?

Magalhaes, C. A., Ferriani, M. D. G. C., Sousa, L. P., Caramelli, P., & Gomes, K. B. (2017) · Arquivos de Neuro-Psiquiatria · doi:10.1590/0004-282x20170110 · Cited by 60

Theaflavins Improve Memory Impairment and Depression-Like Behavior by Regulating Microglial Activation

Ano, Y., Ohya, R., Kita, M., Taniguchi, Y., & Kondô, K. (2019) · Molecules · doi:10.3390/molecules24030467 · Cited by 61

Scavenger Receptor-A deficiency impairs immune response of microglia and astrocytes potentiating Alzheimer’s disease pathophysiology

Cornejo, F., Vruwink, M., Metz, C., Muñoz, P., Salgado, N., Poblete, J., Andrés, M. E., Eugenín, J., & von Bernhardi, R. (2018) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2017.12.007 · Cited by 59

Effects and mechanisms of natural products on Alzheimer’s disease

Yang, Z., Zhou, D.-D., Huang, S., Fang, A., Li, H., & Zhu, H. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1985428 · Cited by 59

Anti-herpetic tau preserves neurons via the cGAS-STING-TBK1 pathway in Alzheimer’s disease

Hyde, V. R., Zhou, C., y Fernández, J. R. M., Chatterjee, K., Ramakrishna, P., Lin, A., Fisher, G. W., Celiker, O. T., Caldwell, J., Bender, O., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2024.115109 · Cited by 61

Mesenchymal stem cell-mediated immunomodulation in cell therapy of neurodegenerative diseases

Chen, X., Wang, S., & Cao, W. (2017) · Cellular Immunology · doi:10.1016/j.cellimm.2017.06.006 · Cited by 61

Targeting NLRP3 Inflammasome in Translational Treatment of Nervous System Diseases: An Update

Yu, Q., Zhao, T., Liu, M., Cao, D., Li, J., Li, Y., Xia, M., Wang, X., Zheng, T., Liu, C., et al. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.707696 · Cited by 61

The Role of Microglia in the Homeostasis of the Central Nervous System and Neuroinflammation

Gogoleva, V. S., Drutskaya, M. S., & Атретханы, К.-С. Н. (2019) · Molecular Biology · doi:10.1134/s0026893319050054 · Cited by 61

Substance P and Antagonists of the Neurokinin-1 Receptor in Neuroinflammation Associated with Infectious and Neurodegenerative Diseases of the Central Nervous System

Philipp, M. (2016) · Journal of Neurology and Neuromedicine · doi:10.29245/2572.942x/2016/2.1020 · Cited by 58

The Immune System's Role in the Consequences of Mild Traumatic Brain Injury (Concussion)

Verboon, L. N., Patel, H. C., & Greenhalgh, A. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.620698 · Cited by 63

Caffeic Acid Phenethyl Ester (CAPE): Biosynthesis, Derivatives and Formulations with Neuroprotective Activities

Pérez, R., Burgos, V., Marín, V., Camins, A., Olloquequi, J., González‐Chavarría, I., Ulrich, H., Wyneken, Ú., Luarte, A., Ortíz, L., et al. (2023) · Antioxidants · doi:10.3390/antiox12081500 · Cited by 58

Neuroimmune mechanisms in K rabbe's disease

Potter, G. B., & Petryniak, M. A. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23804 · Cited by 58

Potassium channel expression and function in microglia: Plasticity and possible species variations

Nguyen, H. M., Blomster, L. V., Christophersen, P., & Wulff, H. (2017) · Channels · doi:10.1080/19336950.2017.1300738 · Cited by 58

Search for Alzheimer's Disease Biomarkers in Blood Cells: Hypotheses-Driven Approach

Wojsiat, J., Laskowska-Kaszub, K., Mietelska‐Porowska, A., & Wojda, U. (2017) · Biomarkers in Medicine · doi:10.2217/bmm-2017-0041 · Cited by 61

Methotrexate causes persistent deficits in memory and executive function in a juvenile animal model

Wen, J., Maxwell, R. R., Wolf, A. J., Spira, M., Gulinello, M. E., & Cole, P. D. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.07.007 · Cited by 58

Neuroinflammation

Mukhara, D., Oh, U., & Neigh, G. N. (2020) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64123-6.00017-5 · Cited by 60

Neuroinflammatory processes in cognitive disorders: Is there a role for flavonoids and n-3 polyunsaturated fatty acids in counteracting their detrimental effects?

Vauzour, D., Martinsen, A., & Layé, S. (2015) · Neurochemistry International · doi:10.1016/j.neuint.2015.08.004 · Cited by 60

Transcriptome sequencing study implicates immune-related genes differentially expressed in schizophrenia: new data and a meta-analysis

Sanders, A. R., Drigalenko, E. I., Duan, J., Moy, W., Freda, J., Göring, H. H. H., Gejman, P. V., & on behalf of, M. G. S. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.47 · Cited by 58

Imperatorin ameliorates lipopolysaccharide induced memory deficit by mitigating proinflammatory cytokines, oxidative stress and modulating brain-derived neurotropic factor

Chowdhury, A. A., Gawali, N. B., Shinde, P., Munshi, R., & Juvekar, A. R. (2018) · Cytokine · doi:10.1016/j.cyto.2018.04.018 · Cited by 57

modCHIMERA: a novel murine closed-head model of moderate traumatic brain injury

Sauerbeck, A. D., Fanizzi, C., Kim, J. H., Gangolli, M., Bayly, P. V., Wellington, C. L., Brody, D. L., & Kummer, T. T. (2018) · Scientific Reports · doi:10.1038/s41598-018-25737-6 · Cited by 57

Rubus chingii Hu: an overview of botany, traditional uses, phytochemistry, and pharmacology

SHENG, J.-Y., Wang, S., Liu, K., Zhu, B., Zhang, Q., Qin, L., & Jian-Jun, W. U. (2020) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(20)30048-0 · Cited by 57

Sirtuins as Potential Therapeutic Targets for Mitigating Neuroinflammation Associated With Alzheimer’s Disease

Fernando, K., & Wijayasinghe, Y. S. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.746631 · Cited by 57

Inhibition of Inflammation Mediated Through the Tumor Necrosis Factor α Biochemical Pathway Can Lead to Favorable Outcomes in Alzheimer Disease

Shamim, D., & Laskowski, M. C. (2017) · Journal of Central Nervous System Disease · doi:10.1177/1179573517722512 · Cited by 56

Serum Hepcidin Levels, Iron Dyshomeostasis and Cognitive Loss in Alzheimer’s Disease

Sternberg, Z., Hu, Z., Sternberg, D. S., Waseh, S., Quinn, J. F., Wild, K., Kaye, J. A., Zhao, L., & Garrick, M. D. (2017) · Aging and Disease · doi:10.14336/ad.2016.0811 · Cited by 57

Visible-light-mediated direct synthesis of phosphorotrithioates as potent anti-inflammatory agents from white phosphorus

Lu, G., Chen, J., Huangfu, X., Li, X., Fang, M., Tang, G., & Zhao, Y. (2018) · Organic Chemistry Frontiers · doi:10.1039/c8qo01087k · Cited by 56

Importance of extracellular vesicle secretion at the blood–cerebrospinal fluid interface in the pathogenesis of Alzheimer’s disease

Vandendriessche, C., Balusu, S., Cauwenberghe, C. V., Brkić, M., Pauwels, M. J., Plehiers, N., Bruggeman, A., Dujardin, P., Imschoot, G. V., Wonterghem, E. V., et al. (2021) · Acta Neuropathologica Communications · doi:10.1186/s40478-021-01245-z · Cited by 58

Peripheral inflammatory biomarkers are associated with cognitive function and dementia: Framingham Heart Study Offspring cohort

Chen, J., Doyle, M. F., Fang, Y., Mez, J., Crane, P. K., Scollard, P., ADSP Data Harmonization Consortium Cognitive Harmonization Core, Satizabal, C. L., Alosco, M. L., Qiu, W. Q., et al. (2023) · Aging Cell · doi:10.1111/acel.13955 · Cited by 56

Iridoids and other monoterpenes in the Alzheimer’s brain: Recent development and future prospects

Habtemariam, S. (2018) · Molecules · doi:10.3390/molecules23010117 · Cited by 55

Exercise-Induced Modulation of Neuroinflammation in Models of Alzheimer’s Disease

Kelly, Á. M. (2018) · Brain Plasticity · doi:10.3233/bpl-180074 · Cited by 55

Targeting Insulin Resistance to Treat Cognitive Dysfunction

Tyagi, A., & Pugazhenthi, S. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02283-3 · Cited by 59

Microglial TLR4/NLRP3 Inflammasome Signaling in Alzheimer’s Disease

Li, Y., Chen, X., Zhou, M., Feng, S., Peng, X., & Wang, Y. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230273 · Cited by 58

Targeting CCR3 to Reduce Amyloid-β Production, Tau Hyperphosphorylation, and Synaptic Loss in a Mouse Model of Alzheimer’s Disease

Zhu, C., Xu, B., Sun, X., Zhu, Q., & Sui, Y. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0269-5 · Cited by 59

CD44 Splice Variants as Potential Players in Alzheimer’s Disease Pathology

Pinner, E., Gruper, Y., Zimra, M. B., Kristt, D., Laudon, M., Naor, D., & Zisapel, N. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-161245 · Cited by 55

Shedding of membrane-associated LDL receptor-related protein-1 from microglia amplifies and sustains neuroinflammation

Brifault, C., Gilder, A. S., Laudati, E., Banki, M. A., & Gonias, S. L. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.798413 · Cited by 58

Cerebrospinal fluid phosphorylated tau, visinin-like protein-1, and chitinase-3-like protein 1 in mild cognitive impairment and Alzheimer’s disease

Initiative, T. A. D. N., Zhang, H., Ng, K. P., Therriault, J., Kang, M. S., Pascoal, T. A., Rosa‐Neto, P., & Gauthier, S. G. (2018) · Translational Neurodegeneration · doi:10.1186/s40035-018-0127-7 · Cited by 57

Synaptic Loss, ER Stress and Neuro-Inflammation Emerge Late in the Lateral Temporal Cortex and Associate with Progressive Tau Pathology in Alzheimer’s Disease

Buchanan, H. M., Mackay, M., PALMER, K., Tothová, K., Katsur, M., Platt, B., & Koss, D. J. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-01950-1 · Cited by 58

The acute phase protein lactoferrin is a key feature of Alzheimer’s disease and predictor of Aβ burden through induction of APP amyloidogenic processing

Tsatsanis, A., McCorkindale, A. N., Wong, B. X. W., Patrick, E., Ryan, T. M., Evans, R. W., Bush, A. I., Sutherland, G. T., Sivaprasadarao, A., Guennewig, B., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01248-1 · Cited by 57

Intranasal delivery of pro-resolving lipid mediators rescues memory and gamma oscillation impairment in AppNL-G-F/NL-G-F mice

Emre, C., Arroyo-García, L. E., Do, K. V., Jun, B., Ohshima, M., Alcalde, S. G., Cothern, M. L., Maioli, S., Nilsson, P., Hjorth, E., et al. (2022) · Communications Biology · doi:10.1038/s42003-022-03169-3 · Cited by 55

Microglial innate memory and epigenetic reprogramming in neurological disorders

Martins-Ferreira, R., Leal, B., Costa, P., & Ballestar, E. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101971 · Cited by 55

Precise gene delivery systems with detachable albumin shell remodeling dysfunctional microglia by TREM2 for treatment of Alzheimer's disease

Wang, P., Yang, P., Qian, K., Li, Y., Xu, S., Meng, R., Guo, Q., Cheng, Y., Cao, J., Xu, M., et al. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121360 · Cited by 56

An integrated cytokine and kynurenine network as the basis of neuroimmune communication

Stone, T. W., Clanchy, F. I. L., Huang, Y., Chiang, N., Darlington, L. G., & Williams, R. O. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1002004 · Cited by 57

Trace elements and Alzheimer dementia in population-based studies: A bibliometric and meta-analysis

Li, K., Li, A., Mei, Y., Zhao, J., Zhou, Q., Li, Y., Yang, M., & Xu, Q. (2022) · Environmental Pollution · doi:10.1016/j.envpol.2022.120782 · Cited by 55

Neural stem/progenitor cells in Alzheimer's disease.

Tincer, G., Mashkaryan, V., Bhattarai, P., & Kızıl, Ç. (2016) · Europe PMC (PubMed Central) · Cited by 56

A multiomic approach to characterize the temporal sequence in Alzheimer's disease-related pathology

Marttinen, M., Paananen, J., Neme, A., Mitra, V., Takalo, M., Natunen, T., Paldanius, K. M. A., Mäkinen, P. M., Bremang, M., Kurki, M., et al. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.12.009 · Cited by 55

N , N ′-Diacetyl- p -phenylenediamine restores microglial phagocytosis and improves cognitive defects in Alzheimer’s disease transgenic mice

Park, M. H., Lee, M., Nam, G., Kim, M., Kang, J., Choi, B. J., Jeong, M. S., Park, K. H., Han, W. H., Tak, E., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1916318116 · Cited by 54

Recent advances in understanding the mechanisms of PM2.5-mediated neurodegenerative diseases

Zhu, X., Ji, X., Shou, Y., Huang, Y., Hu, Y., & Wang, H. (2020) · Toxicology Letters · doi:10.1016/j.toxlet.2020.04.017 · Cited by 55

Retinal Pigment Epithelium Remodeling in Mouse Models of Retinitis Pigmentosa

Napoli, D., Biagioni, M., Billeri, F., Marco, B. D., Orsini, N., Novelli, E., & Strettoi, E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105381 · Cited by 54

Two‐level diagnostic classification using cerebrospinal fluid YKL‐40 in Alzheimer's disease

Baldacci, F., Toschi, N., Lista, S., Zetterberg, H., Blennow, K., Kilimann, I., Teipel, S., Cavedo, E., dos Santos, A. M., Epelbaum, S., et al. (2017) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2017.01.021 · Cited by 53

Inflammation: major denominator of obesity, Type 2 diabetes and Alzheimer’s disease-like pathology?

Kacířová, M., Zmeškalová, A., Kořínková, L., Železná, B., Kuneš, J., & Maletı́nská, L. (2020) · Clinical Science · doi:10.1042/cs20191313 · Cited by 56

Benzo(a)pyrene exposure induced neuronal loss, plaque deposition, and cognitive decline in APP/PS1 mice

Liu, D., Zhao, Y., Qi, Y., Gao, Y., Tu, D., Wang, Y., Gao, H., & Zhou, H. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01925-y · Cited by 54

Cognitive Dysfunction after Heart Disease: A Manifestation of the Heart‐Brain Axis

Xu, C., Tao, X., Ma, X., Zhao, R., & Cao, Z. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/4899688 · Cited by 53

Targeting cytokine networks in neuroinflammatory diseases

Becher, B., Derfuss, T. J., & Liblau, R. (2024) · Nature Reviews Drug Discovery · doi:10.1038/s41573-024-01026-y · Cited by 56

Roles of the Receptor for Advanced Glycation End Products and Its Ligands in the Pathogenesis of Alzheimer’s Disease

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Modeling neurodegenerative diseases with patient-derived induced pluripotent cells: Possibilities and challenges

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