Inflammation, the complement system and the diseases of aging

Inflammation, Atherosclerosis, and Coronary Artery Disease

Hansson, G. K. (2005) · New England Journal of Medicine · doi:10.1056/nejmra043430 · Cited by 8,773

Complement factor H polymorphism in age-related macular degeneration

Klein, R. J., Zeiss, C., Chew, E. Y., Tsai, J.-Y., Sackler, R. S., Haynes, C., Henning, A. K., SanGiovanni, J. P., Mane, S. M., Mayne, S. T., et al. (2005) · Science · doi:10.1126/science.1109557 · Cited by 4,492

Reactive microglia are positive for HLA‐DR in the substantia nigra of Parkinson's and Alzheimer's disease brains

McGeer, P. L., Itagaki, S., Boyes, B. E., & McGeer, E. G. (1988) · Neurology · doi:10.1212/wnl.38.8.1285 · Cited by 2,990

Complement factor H polymorphism and age-related macular degeneration

Edwards, A. O., Ritter, R., Abel, K. J., Manning, A., Panhuysen, C., & Farrer, L. A. (2005) · Science · doi:10.1126/science.1110189 · Cited by 2,449

Complement factor H variant increases the risk of age-related macular degeneration

Haines, J. L., Hauser, M. A., Schmidt, S., Scott, W. K., Olson, L. M., Gallins, P., Spencer, K. L., Kwan, S. Y., Noureddine, M., Gilbert, J. R., et al. (2005) · Science · doi:10.1126/science.1110359 · Cited by 2,424

A common haplotype in the complement regulatory gene factor H ( HF1/CFH ) predisposes individuals to age-related macular degeneration

Hageman, G. S., Anderson, D. H., Johnson, L. V., Hancox, L. S., Taiber, A. J., Hardisty, L. I., Hageman, J. L., Stockman, H. A., Borchardt, J. D., Gehrs, K. M., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501536102 · Cited by 1,961

The many faces of macrophage activation

Mosser, D. M. (2003) · Journal of Leukocyte Biology · doi:10.1189/jlb.0602325 · Cited by 1,902

A role for local inflammation in the formation of drusen in the aging eye

Anderson, D. H., Mullins, R. F., Hageman, G. S., & Johnson, L. V. (2002) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(02)01624-0 · Cited by 1,087

Complement activation by beta-amyloid in Alzheimer disease.

Rogers, J., Cooper, N. R., Webster, S., Schultz, J., McGeer, P. L., Styren, S. D., Civin, W. H., Brachova, L., Bradt, B., & Ward, P. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.21.10016 · Cited by 817

Nonsteroidal Anti-inflammatory Drugs and the Risk of Parkinson Disease

Chen, H., Zhang, S. M., Hernán, M. Á., Schwarzschild, M. A., Willett, W. C., Colditz, G. A., Speizer, F. E., & Ascherio, A. (2003) · Archives of Neurology · doi:10.1001/archneur.60.8.1059 · Cited by 641

Pulmonary toxicity and global gene expression changes in response to sub-chronic inhalation exposure to crystalline silica in rats

Umbright, C., Sellamuthu, R., Roberts, J. R., Young, S., Richardson, D. L., Schwegler‐Berry, D., McKinney, W., Chen, B. T., Gu, J. K., Kashon, M. L., et al. (2017) · Journal of Toxicology and Environmental Health · doi:10.1080/15287394.2017.1384773 · Cited by 27

Saponins isolated from Radix polygalae extent lifespan by modulating complement C3 and gut microbiota

Wu, J., Wu, A., Zhou, X., Khan, I., Zhang, R. L., Lo, H. H., Li, Q., Song, L., Yun, X. Y., Wang, H. M., et al. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105697 · Cited by 27

Brain expression of the calcineurin inhibitor RCAN1 (Adapt78)

Mitchell, A. N., Jayakumar, L., Koleilat, I., Qian, J., Sheehan, C., Bhoiwala, D. L., Hushmendy, S. F., Heuring, J. M., & Crawford, D. R. (2007) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2007.08.030 · Cited by 27

Auraptene consolidates memory, reverses scopolamine-disrupted memory in passive avoidance task, and ameliorates retention deficits in mice.

Tabrizian, K., Yaghoobi, N. S., Iranshahi, M., Shahraki, J., Rezaee, R., & Hashemzaei, M. (2015) · PubMed · Cited by 26

Effect of CR1 Genetic Variants on Cerebrospinal Fluid and Neuroimaging Biomarkers in Healthy, Mild Cognitive Impairment and Alzheimer's Disease Cohorts

Initiative, A. D. N., Zhu, X., Wang, H.-F., Jiang, T., Lu, H., Tan, M., Tan, C., Tan, L., Tan, L., & Yu, J. (2016) · Molecular Neurobiology · doi:10.1007/s12035-015-9638-8 · Cited by 26

CD4+ T-Cell Senescence in Neurodegenerative Disease: Pathogenesis and Potential Therapeutic Targets

Gao, Y., Lu, Y., Liang, X., Zhao, M., Yu, X., Fu, H., & Yang, W. (2024) · Cells · doi:10.3390/cells13090749 · Cited by 27

Auraptene and Its Role in Chronic Diseases

Derosa, G., Maffioli, P., & Sahebkar, A. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-41342-6_19 · Cited by 24

Effects of Age on Thermal Sensitivity in the Rat

Yezierski, R. P., King, C. D., Morgan, D., Carter, C. S., & Vierck, C. J. (2010) · The Journals of Gerontology Series A · doi:10.1093/gerona/glq024 · Cited by 24

Parkin negatively regulates the antiviral signaling pathway by targeting TRAF3 for degradation

Xin, D., Gu, H., Liu, E., & Sun, Q. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra117.001201 · Cited by 23

Age-Associated Glia Remodeling and Mitochondrial Dysfunction in Neurodegeneration: Antioxidant Supplementation as a Possible Intervention

Picca, A., Ferri, E., Calvani, R., Coelho‐Júnior, H. J., Marzetti, E., & Arosio, B. (2022) · Nutrients · doi:10.3390/nu14122406 · Cited by 24

Complement 3 and metabolic syndrome induced by clozapine: a cross-sectional study and retrospective cohort analysis

Zhang, C., Zhang, Y., Cai, J., Chen, M., & Song, L. (2015) · The Pharmacogenomics Journal · doi:10.1038/tpj.2015.68 · Cited by 22

Complement Factor H Y402H Polymorphism is not Associated with Late-onset Alzheimer’s Disease

Hamilton, G., Proitsi, P., Williams, J. H., O’Donovan, M. C., Owen, M. J., Powell, J. F., & Lovestone, S. (2007) · NeuroMolecular Medicine · doi:10.1007/s12017-007-8013-y · Cited by 21

Normal Aging Involves Modulation of Specific Inflammatory Markers in the Rat Retina and Choroid

Steinle, J. J., Sharma, S., Smith, C. P., & McFayden-Ketchum, L. S. (2009) · The Journals of Gerontology Series A · doi:10.1093/gerona/gln052 · Cited by 21

Neuroinflammation-Induced Upregulation of Glial Cathepsin X Expression and Activity in vivo

Pišlar, A. H., Tratnjek, L., Glavan, G., Zidar, N., Živin, M., & Kos, J. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.575453 · Cited by 21

Inflammation — a lifelong companion

Ferencĭk, M., Štvrtinová, V., Hulín, I., & Novák, M. (2007) · Folia Microbiologica · doi:10.1007/bf02932155 · Cited by 20

The peel of Citrus kawachiensis (kawachi bankan) ameliorates microglial activation, tau hyper-phosphorylation, and suppression of neurogenesis in the hippocampus of senescence-accelerated mice

Okuyama, S., Kotani, Y., Yamamoto, K., Sawamoto, A., Sugawara, K., Sudo, M., Ohkubo, Y., Tamanaha, A., Nakajima, M., & Furukawa, Y. (2018) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2018.1433993 · Cited by 20

Neuronal RING finger protein 11 (RNF11) regulates canonical NF-κB signaling

Pranski, E. L., Dalal, N. V., Herskowitz, J. H., Orr, A. L., Roesch, L. A., Fritz, J. J., Heilman, C. J., Lah, J. J., Levey, A. I., & Betarbet, R. S. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-67 · Cited by 19

Degeneration of dopaminergic neurons induced by thrombin injection in the substantia nigra of the rat is enhanced by dexamethasone: Role of monoamine oxidase enzyme

Argüelles, S., Herrera, A. J., Carreño‐Müller, E., de Pablos, R. M., Villarán, R. F., Espinosa‐Oliva, A. M., Machado, A., & Cano, J. (2009) · NeuroToxicology · doi:10.1016/j.neuro.2009.12.001 · Cited by 19

Chemiexcitation: Mammalian Photochemistry in the Dark†

Brash, D. E., & Goncalves, L. C. P. (2023) · Photochemistry and Photobiology · doi:10.1111/php.13781 · Cited by 16

Anti-Inflammatory Properties of Acetylcholinesterase Inhibitors Administred in Alzheimers Disease

Kamal, M. A., Greig, N. H., & Reale, M. (2009) · Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry · doi:10.2174/187152309787580810 · Cited by 14

Inhibition of Proteasome Activity Upregulates IL-6 Expression in RPE Cells through the Activation of P38 MAPKs

Qin, T., & Gao, S. (2018) · Journal of Ophthalmology · doi:10.1155/2018/5392432 · Cited by 13

A static magnetic field attenuates lipopolysaccharide-induced neuro-inflammatory response via IL-6-mediated pathway

Shen, L.-K., Huang, H., Yang, P.-C., Huang, Y.-K., Wang, P. D.-Y., Leung, T., Chen, C., & Chang, W. (2013) · Electromagnetic Biology and Medicine · doi:10.3109/15368378.2013.794734 · Cited by 14

Type 2 Diabetes: Local Inflammation and Direct Effect of Bacterial Toxic Components

Judith Miklossy, A., Martins, R. N., Darbinian, N., Khalili, K., & McGeer, P. L. (2008) · The Open Pathology Journal · doi:10.2174/1874375700802010086 · Cited by 13

Opposite Modulation of Peripheral Inflammation and Neuroinflammation by Adenosine A2A Receptors

Cunha, R. A., Chen, J., & Sitkovsky, M. V. (2007) · Springer eBooks · doi:10.1007/978-0-387-70830-0_3 · Cited by 12

Gazing into the future: Parkinson's disease gene therapeutics to modify natural history

Maguire‐Zeiss, K. A., Mhyre, T. R., & Federoff, H. J. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2007.09.030 · Cited by 11

Regional Gene Expression of Inflammation and Oxidative Stress Responses Does Not Predict Neurodegeneration in Aging

López‐González, I., Cordomí, C. T., & Ferrer, I. (2017) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlw117 · Cited by 10

Inflammation and the Aging Process: Devil or Angel

Gauldie, J. (2008) · Nutrition Reviews · doi:10.1111/j.1753-4887.2007.tb00356.x · Cited by 10

Targeting shared pathways in tauopathies and age-related macular degeneration: implications for novel therapies

Rinaldi, M., Pezone, A., Quadrini, G. I., Abbadessa, G., Laezza, M. P., Passaro, M. L., Porcellini, A., & Costagliola, C. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1371745 · Cited by 9

Antibodies against small heat-shock proteins in Alzheimer’s disease as a part of natural human immune repertoire or activation of humoral response?

Papuć, E., Krupski, W., Kurys-Denis, E., & Rejdak, K. (2015) · Journal of Neural Transmission · doi:10.1007/s00702-015-1477-2 · Cited by 9

Spontaneous complement activation on human B cells results in localized membrane depolarization and the clustering of complement receptor type 2 and C3 fragments

Løbner, M., Leslie, R. G. Q., Prodinger, W. M., & Nielsen, C. H. (2009) · Immunology · doi:10.1111/j.1365-2567.2009.03056.x · Cited by 9

Association Between Serum Complement C3 Levels and Age-Related Cataract

Shao, M., Li, D., Teng, J., Zhang, Y., Li, S., & Cao, W. (2017) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.17-22522 · Cited by 8

Die Bedeutung der posttraumatischen Entzündungsreaktion im verletzten Gehirn

Schmidt, O. I., Leinhase, I., Hasenboehler, E. A., Morgan, S. J., & Stahel, P. F. (2007) · Der Orthopäde · doi:10.1007/s00132-007-1061-z · Cited by 7

A journey with Tony Hugli up the inflammatory cascade towards the auto-digestion hypothesis

Schmid‐Schönbein, G. W. (2007) · International Immunopharmacology · doi:10.1016/j.intimp.2007.07.015 · Cited by 7

Role of inflammation in the pathogenesis of age-related macular degeneration

Scholl, S., Kirchhof, J., & Augustin, A. J. (2009) · Expert Review of Ophthalmology · doi:10.1586/eop.09.51 · Cited by 7

Immune Responses in Neurodegenerative Diseases

Shrestha, R., Shrestha, S., Millington, O. R., Brewer, J. M., & Bushell, T. J. (2015) · Kathmandu University Medical Journal · doi:10.3126/kumj.v12i1.13646 · Cited by 7

Long-term intake of α-glycerophosphocholine (GPC) suppresses microglial inflammation and blood-brain barrier (BBB) disruption and promotes neurogenesis in senescence-accelerated mice prone 8 (SAMP8)

Umino, M., Okuda, M., Ohkubo, T., Fujii, T., & Matsubara, K. (2023) · Bioscience Biotechnology and Biochemistry · doi:10.1093/bbb/zbad135 · Cited by 7

Designing of multi-target-directed ligands against the enzymes associated with neuroinflammation: anin silicoapproach

Dileep, K. V., Remya, C., Tintu, I., & Sadasivan, C. (2013) · Frontiers in Life Science · doi:10.1080/21553769.2014.901924 · Cited by 7

Effectiveness and Safety of Oral Azvudine for Elderly Hospitalized Patients With COVID‐19: A Multicenter, Retrospective, Real‐World Study

Sun, R., Wang, H., Sun, J., Yang, M., Zhang, S., Hu, X., Yu, B., Song, Z., Han, N., Luo, H., et al. (2025) · Advanced Science · doi:10.1002/advs.202404450 · Cited by 5

Neuroinflammation as a Potential Mechanism Underlying Parkinsons Disease

Cebrián, C., & Sulzer, D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803783-6.00008-0 · Cited by 7

Amyloid and Neurodegeneration: Alzheimer's Disease and Retinal Degeneration

Prakasam, A., Venugopal, C., Suram, A., Pacheco‐Quinto, J., Zhou, Y., Pappolla, M. A., Sharpe, K. A., Lahiri, D. K., Greig, N. H., Rohrer, B. ̈., et al. (2008) · Springer eBooks · doi:10.1007/978-0-387-30375-8_7 · Cited by 4

Terminal complement complex deposition on chondrocytes promotes premature senescence in age- and trauma-related osteoarthritis

Ruths, L., Hengge, J., Teixeira, G. Q., Haffner‐Luntzer, M., Ignatius, A. A., & Riegger, J. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1470907 · Cited by 3

Microglial Response to Inflammatory Stimuli-Impact of Protein Acetylation and Phosphorylation

Huuskonen, J. (2007) · Cited by 3

The inner fire: the shifting paradigm of complement system in aging

Triggianese, P., & Della-Morte, D. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1795833 · Cited by 3

Protective effect of Auraptene, a novel acetylcholinesterase inhibitor, on hydrogen peroxide-induced cell toxicity in PC12 cells

Hadipour, E., Khodadadi, M., Emami, S. A., Rahamouz-Haghighi, S., Ramazani, E., & Tayarani‐Najaran, Z. (2024) · Toxicology Research · doi:10.1093/toxres/tfae217 · Cited by 2

Central Nervous System Distribution of the Poxviral Proteins After Intranasal Administration of Proteins and Titering of Vaccinia Virus in the Brain After Intracranial Administration

Kulkarni, A. P., Govender, D., Kellaway, L. A., & Kotwal, G. J. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-876-4_18 · Cited by 2

Younger Siblings, C-Reactive Protein, and Risk of Age-Related Macular Degeneration

Cohn, A., Busija, L., Robman, L. D., Dimitrov, P. N., Varsamidis, M., Lim, L. L., Baird, P. N., & Guymer, R. H. (2013) · American Journal of Epidemiology · doi:10.1093/aje/kws332 · Cited by 2

Kognitive Defizite nach Strahlentherapie von Hirntumoren

Buthut, M., Haußmann, R., Seidlitz, A., Krause, M., & Donix, M. (2017) · Der Nervenarzt · doi:10.1007/s00115-017-0423-y · Cited by 2

Search for Neuroprotective Compounds ―From 4-Methycatechol to Citrus Compounds―

Furukawa, Y. (2020) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.20-00164 · Cited by 2

Macrophages, Microglia, and Dendritic C

Ghorpade, A., Gendelman, H. E., & Kipnis, J. (2008) · Springer eBooks · doi:10.1007/978-0-387-72573-4_9 · Cited by 2

Evolving Pharmacotherapies Involving Neuroimmune Crosstalk

Maurya, R., Ali, K., Soni, H., Mhatre, A., & Naqvi, S. (2026) · Springer eBooks · doi:10.1007/978-981-95-5088-3_12 · Cited by 1

Animal Models of Parkinson’s Disease Induced by Toxins and Genetic Manipulation

Hisahara, S., & Shimoham, S. (2012) · InTech eBooks · doi:10.5772/19860 · Cited by 1

KAJIAN EFEK ALFA-PINEN TERHADAP i-NOS (INDUCIBLE NITRIC OXIDE SYNTHASE) PADA KULTUR SEL NEURON-GLIA YANG DIPAPAR LIPOPOLISAKARIDA

Murtyastami, S. W. K. (2010) · Farmasains Jurnal Farmasi dan Ilmu Kesehatan · doi:10.22219/far.v1i1.421 · Cited by 1

Vascular Cognitive Impairment

Windon, C., & Elahi, F. M. (2024) · Springer eBooks · doi:10.1007/978-3-031-49963-0_30 · Cited by 1

Genetic Basis of Age-related Macular Degeneration

Othman, M., Branham, K. E. H., & Heckenlively, J. R. (2011) · touchREVIEWS in Ophthalmology · doi:10.17925/usor.2011.04.02.119 · Cited by 1

Identifying Key Networks Linked to Light-Independent Photoreceptor Degeneration in Visual Arrestin 1 Knockout Mice

Kim, H. S., Huang, S., Lee, E.-J., & Craft, C. M. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-75402-4_34 · Cited by 1

Bcl-2 Upregulation is Significantly Enhanced in the Hippocampus of Normal Aging Mice After an Acute Challenge Elicited by Pro-inflammatory Cytokines Circulating in the Cerebrospinal Fluid

Xu, Y., Bentivoglio, M., & Deng, X. (2007) · Neurochemical Research · doi:10.1007/s11064-007-9531-6

C-reactive protein (CRP) and anti-CRP autoantibodies in systemic lupus erythematosus - a study on the occurrence and clinical implications of anti- CRP antibodies and CRP-mediated complement activation

Sjöwall, C. (2006) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

The influence of common infections on clinical course and neurodegeneration in an animal model of multiple sclerosis

Kumar, P. (2015) · doi:10.53846/goediss-4967

Estudo das alterações motoras e comportamentais induzidas por rotenona em ratos machos e fêmeas

Ferreira, F. F. (2015) · UFPR Digital Collection (Federal University of Paraná)

The Impact of Stress and Inflammatory Processes on Cognitive Change in Late Adulthood

Balasubramanian, A. B. (2010) · eScholarship (California Digital Library)

Therapeutic potential of inhibition of the neuroinflammation induced cathepsin X: in vivo evidencePreprint

Pišlar, A. H., Tratnjek, L., Glavan, G., Zidar, N., Živin, M., & Kos, J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/513671

Masitinib mediates TGF-Beta1 and Nitric Oxide Secretion and Ameliorates MPTP/Microglia-Induced Degeneration of Differentiated SH-SY5Y CellsPreprint

Erol, A. Y. G., Akıncı, E., Koçancı, F. G., Kaba, F. A., Dora, D. D., & Uysal, H. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.16.206094

Neuroinflammatory mechanisms of Parkinson's Disease

Mangano, E. N. (2011) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2011-09648

Tailoring Vaccines for Older Individuals: Aging of the Immune System and the Impact on Vaccine Efficacy

Bashir, S., Wilson, M., Ashiru-Oredope, D. A. I., & Murdan, S. (2023) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-3-031-35811-1_9

Bradykinin in ocular health and diseases

Bhat, M., Couture, R., & Vaucher, E. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-28907-1.00007-4

Evaluation of Immune Risk Factors for Developing Complications After Bacterial Meningitis in Children

Kadziszewska, A., & Gowin, E. (2025) · Journal of Child Neurology · doi:10.1177/08830738251374541

Die Rolle des Toll-like Rezeptors 4 bei der Entstehung von Bluthochdruck und der Kontraktilität von Widerstandsgefäßen

Eißler, R. (2011) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.14426

Association of nonfribrillar amyloid oligomers with drusen of aging and age-related macular degeneration

Luibl, V. (2006) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.5701

Lipopolysaccharide-mediated macrophage polarization, conserved pathogenesis, and implications for peripheral neuropathy: a systematic review

Elson, L., Eijkelkamp, N., & Coert, J. H. (2026) · Inflammation Research · doi:10.1007/s00011-026-02317-3

BindingDB Entry 50007267: Synthesis and evaluation of isoprenylation-resveratrol dimer derivatives against Alzheimer's disease.

BindingDB (2021) · UC San Diego · doi:10.7270/q2mc939p

BindingDB Entry 50012637: Design, synthesis, in-vitro, in-vivo and in-silico studies of pyrrolidine-2,5-dione derivatives as multitarget anti-inflammatory agents.

BindingDB (2022) · UC San Diego · doi:10.7270/q27s7sfq

Neurochemical Aspects of Traumatic Brain Injury

Farooqui, A. A. (2010) · Springer eBooks · doi:10.1007/978-1-4419-6652-0_6

Complement, neuroinflammation and neuronal degeneration in Alzheimer disease

McGeer, P. L., McGeer, E. G., & Yasojima, K. (2001) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-8225-5_2 · Cited by 1

Inflammation and the Degenerative Diseases of Aging

McGeer, P. L., & McGeer, E. G. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1332.007 · Cited by 530

Role of complement in neurodegeneration and neuroinflammation

Bonifati, D. M., & Kishore, U. (2006) · Molecular Immunology · doi:10.1016/j.molimm.2006.03.007 · Cited by 314

Microglial Cell Dysregulation in the Aged Brain and Neurodegeneration

Triolo-Mieses, M., Fadić, R., & Rommy von Bernhardi, M. (2022) · Springer eBooks · doi:10.1007/978-3-031-15080-7_180 · Cited by 1

Innate Immunity, Local Inflammation, and Degenerative Disease

McGeer, P. L., & McGeer, E. G. (2002) · Science of Aging Knowledge Environment · doi:10.1126/sageke.2002.29.re3 · Cited by 75