Innate Immunity and Neurodegeneration

Neuroinflammation in Alzheimer's disease

Heneka, M. T., Carson, M. J., Khoury, J. E., Landreth, G. E., Brosseron, F., Feinstein, D. L., Jacobs, A. H., Wyss-Coray, T., Vitorica, J., Ransohoff, R. M., et al. (2015) · The Lancet Neurology · doi:10.1016/s1474-4422(15)70016-5 · Cited by 6,226

Parkinson's disease

Kalia, L. V., & Lang, A. E. (2015) · The Lancet · doi:10.1016/s0140-6736(14)61393-3 · Cited by 6,184

The amyloid hypothesis of Alzheimer's disease at 25 years

Selkoe, D. J., & Hardy, J. (2016) · EMBO Molecular Medicine · doi:10.15252/emmm.201606210 · Cited by 6,164

Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages

Ginhoux, F., Greter, M., Leboeuf, M., Nandi, S., See, P., Gokhan, S., Mehler, M. F., Conway, S. J., Ng, L. G., Stanley, E. R., et al. (2010) · Science · doi:10.1126/science.1194637 · Cited by 5,175

Synaptic Pruning by Microglia Is Necessary for Normal Brain Development

Paolicelli, R. C., Bolasco, G., Pagani, F., Maggi, L., Scianni, M., Panzanelli, P., Giustetto, M., Ferreira, T. A., Guiducci, E., Dumas, L., et al. (2011) · Science · doi:10.1126/science.1202529 · Cited by 4,244

Microglia-mediated neurotoxicity: uncovering the molecular mechanisms

Block, M. L., Zecca, L., & Hong, J.-S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2038 · Cited by 4,110

ATP mediates rapid microglial response to local brain injury in vivo

Davalos, D., Grutzendler, J., Yang, G., Kim, J. V., Zuo, Y., Jung, S., Littman, D. R., Dustin, M. L., & Gan, W.-B. (2005) · Nature Neuroscience · doi:10.1038/nn1472 · Cited by 3,913

Host microbiota constantly control maturation and function of microglia in the CNS

Erny, D., Hrabě de Angelis, A. L., Jaitin, D., Wieghofer, P., Staszewski, O., David, E., Keren-Shaul, H., Mahlakoiv, T., Jakobshagen, K., Buch, T., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4030 · Cited by 3,569

Complement and microglia mediate early synapse loss in Alzheimer mouse models

Hong, S., Beja-Glasser, V. F., Nfonoyim, B. M., Frouin, A., Li, S., Ramakrishnan, S., Merry, K. M., Shi, Q., Rosenthal, A., Barres, B. A., et al. (2016) · Science · doi:10.1126/science.aad8373 · Cited by 3,343

The Classical Complement Cascade Mediates CNS Synapse Elimination

Stevens, B., Allen, N. J., Vazquez, L. E., Howell, G. R., Christopherson, K. S., Nouri, N., Micheva, K. D., Mehalow, A. K., Huberman, A. D., Stafford, B., et al. (2007) · Cell · doi:10.1016/j.cell.2007.10.036 · Cited by 3,313

Adamantoyl chloride inhibited replication of the largemouth bass virus via enhanced immunity and inhibition of apoptosis

Wang, M., Yang, B., Liu, T., Li, P., Bai, S., Zhou, Z., Liu, X., He, M., Ling, F., & Wang, G. (2023) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2023.109167 · Cited by 11

When nature’s robots go rogue: exploring protein homeostasis dysfunction and the implications for understanding human aging disease pathologies

Reisz, J. A., Barrett, A. S., Nemkov, T. G., Hansen, K. C., & D’Alessandro, A. (2018) · Expert Review of Proteomics · doi:10.1080/14789450.2018.1453362 · Cited by 11

Suppressing immunotherapy by organ-specific tumor microenvironments: what is in the brain?

Zhang, C., & Yu, D. (2019) · Cell & Bioscience · doi:10.1186/s13578-019-0349-0 · Cited by 11

Lysophosphatidic Acid Receptor 5 (LPA5) Knockout Ameliorates the Neuroinflammatory Response In Vivo and Modifies the Inflammatory and Metabolic Landscape of Primary Microglia In Vitro

Joshi, L., Plastira, I., Bernhart, E. M., Reicher, H., Koshenov, Z., Graier, W. F., Vujić, N., Kratky, D., Rivera, R. R., Chun, J. J. M., et al. (2022) · Cells · doi:10.3390/cells11071071 · Cited by 11

Modeling neurodegenerative diseases using non-human primates: advances and challenges

Li, B., He, D., Li, X., & Guo, X. (2022) · Ageing and Neurodegenerative Diseases · doi:10.20517/and.2022.14 · Cited by 11

Polymicrobial Infections and Neurodegenerative Diseases

Carrasco, L., Pisa, D., & Alonso, R. (2020) · Current Clinical Microbiology Reports · doi:10.1007/s40588-020-00139-3 · Cited by 11

Three rare anti-inflammatory sesquiterpene lactones from Magnolia grandiflora

Xu, S.-Y., ZHANG, F., Tao, L., JIANG, Y., HUANG, T., Li, Y., Hu, Z., Yang, J., Hao, X., & Yuan, C. (2024) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(24)60601-1 · Cited by 10

Low-intensity exercise combined with sodium valproate attenuates kainic acid-induced seizures and associated co-morbidities by inhibiting NF-κB signaling in mice

Jia, Y., Tang, L., Yao, Y., Zhuo, L., Qu, D., Chen, X., Ji, Y., Tao, J., & Zhu, Y. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.993405 · Cited by 10

Defective phagocytosis leads to neurodegeneration through systemic increased innate immune signaling

Elguero, J., Liu, G., Tiemeyer, K. H., Bandyadka, S., Gandevia, H., Duro, L., Yan, Z., & McCall, K. (2023) · iScience · doi:10.1016/j.isci.2023.108052 · Cited by 10

Fibrinogen drives neuroinflammation and neuropathology in perioperative neurocognitive disorders

Wang, X., Jiang, S., Di, L., Li, S., Chen, H., Huang, P., Cao, T., Jin, W., & Huang, L. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115906 · Cited by 9

Heterochromatic silencing of immune‐related genes in glia is required for BBB integrity and normal lifespan in drosophila

Shu, S., Jiang, M., Deng, X., Yue, W., Cao, X., Zhang, K., Wang, Z., He, H., Cui, J., Wang, Q., et al. (2023) · Aging Cell · doi:10.1111/acel.13947 · Cited by 9

Parkinson's Disease and Mitotherapy-Based Approaches towards α-Synucleinopathies

Bhatt, V., Shukla, H., & Tiwari, A. K. (2024) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2306109 · Cited by 9

Revisiting Inbred Mouse Models to Study the Developing Brain: The Potential Role of Intestinal Microbiota

Oriá, R. B., Malva, J. O., Foley, P. L., Freitas, R. S., Bolick, D. T., & Guerrant, R. L. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00358 · Cited by 9

Neurodegenerative disease-associated microRNAs acting as signaling molecules modulate CNS neuron structure and viability

Kumbol, V., Ivanov, A., McGurran, H., Schüler, J., Zhai, Y., Ludwik, K., Hinkelmann, L., Brehm, M., Krüger, C., Küchler, J., et al. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02199-8 · Cited by 8

Novel insights into sevoflurane-induced developmental neurotoxicity mechanisms

Gao, T., & Huang, Z. (2024) · Epigenomics · doi:10.1080/17501911.2024.2395250 · Cited by 8

The enigma of mitochondrial epigenetic alterations in air pollution-induced neurodegenerative diseases

Acharyya, S., Kumar, S. H., Chouksey, A., Soni, N., Nazeer, N., & Mishra, P. K. (2024) · NeuroToxicology · doi:10.1016/j.neuro.2024.10.002 · Cited by 8

Insights into the mechanisms of non-coding RNAs’ implication in the pathogenesis of Alzheimer’s disease

Khodayi-Shahrak, M., Khalaj‐Kondori, M., Feizi, M. A. H., & Talebi, M. (2022) · EXCLI journal · doi:10.17179/excli2022-5006 · Cited by 8

Disease mechanisms as subtypes: Microbiome

Bonvegna, S., & Cilia, R. (2023) · Handbook of clinical neurology · doi:10.1016/b978-0-323-85555-6.00006-0 · Cited by 8

Immunotherapy with an antibody against CD1d modulates neuroinflammation in an α-synuclein transgenic model of Lewy body like disease

Iba, M., Kwon, S., Kim, C., Szabo, M. P., Horan-Portelance, L., Lopez-Ocasio, M. D., Dagur, P. K., Overk, C., Rissman, R. A., & Masliah, E. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03087-7 · Cited by 7

Nicotinamide N-oxide Inhibits Microglial Pyroptosis by Upregulating Mitophagy and Alleviates Neural Damage in Rats after TBI

Li, X., Luo, L., Duan, P., Bi, Y., Meng, Y., Zhang, X., Feng, W., Jin, Z., Zuo, K., Zhao, X., et al. (2024) · Inflammation · doi:10.1007/s10753-024-02171-7 · Cited by 7

Cellular inhibitor of apoptosis 2 (cIAP2) restricts neuroinflammation during experimental autoimmune encephalomyelitis

Biswas, D. D., Martin, R., Brown, L. N., Mockenhaupt, K., Gupta, A. S., Surace, M. J., Tharakan, A., Yester, J., Bhardwaj, R., Conrad, D. H., et al. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02527-6 · Cited by 7

SDS3 regulates microglial inflammation by modulating the expression of the upstream kinase ASK1 in the p38 MAPK signaling pathway

Shen, J., Lai, W., Li, Z., Zhu, W., Bai, X., Yang, Z., Wang, Q., & Ji, J. (2024) · Inflammation Research · doi:10.1007/s00011-024-01913-5 · Cited by 7

PGC-1α-siRNA suppresses inflammation in substantia nigra of PD mice by inhibiting microglia

Guan, X., Wu, P., Cao, B., Liu, X., Chen, X., Zhang, W., Zhang, Y., Guan, Z., & Wang, Y. (2021) · International Journal of Neuroscience · doi:10.1080/00207454.2021.1910257 · Cited by 7

Metabolomic Investigation of Synergistic Mechanism for Fangfeng Extract Preventing LPS Induced Neuroinflammation in BV-2 Microglia Cells

Zhu, X., Wang, X., Zhang, S., Li, X., Li, Z., Chen, X., Liu, X., Li, H., & Zhang, J. (2021) · Applied Sciences · doi:10.3390/app11178155 · Cited by 7

Loss of the NF-κB negative regulator Pirk in Drosophila links brain and gut immunity to neurodegeneration

Arora, S., Critchley, G., Dekmak, A. S., Miesenböck, G., Kempf, A., & Ligoxygakis, P. (2025) · Brain Communications · doi:10.1093/braincomms/fcaf144 · Cited by 6

Disruption of lysosomal nutrient sensing scaffold contributes to pathogenesis of a fatal neurodegenerative lysosomal storage disease

Bagh, M. B., Appu, A. P., Sadhukhan, T., Mondal, A., Plavelil, N., Raghavankutty, M., Supran, A. M., Sadhukhan, S., Liu, A., & Mukherjee, A. B. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.105641 · Cited by 7

An Alzheimer’s disease-associated common regulatory variant in a PTK2B intron alters microglial function

Bello, E., Long, K. R., Iwama, S., Steer, J., Cooper, S., Alasoo, K., Kumasaka, N., Schwartzentruber, J., Panousis, N. I., & Bassett, A. R. (2026) · iScience · doi:10.1016/j.isci.2026.115688 · Cited by 7

Lutein and zeaxanthin: The possible contribution, mechanisms of action and implications of modern dietary intake for cognitive development in children.

Loskutova, E., Shah, K., Flitcroft, I., Setti, A., Butler, J. S., Nolan, Y. M., Paudel, N., & Loughman, J. (2019) · HRB Open Research · doi:10.12688/hrbopenres.12903.1 · Cited by 6

The role of Aβ in Alzheimer's Disease as an Evolutionary Outcome of Optimized Innate Immune Defense

Tatar, M. (2022) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2022.68 · Cited by 6

Toll-like receptors in Immunity and inflammation

Kumar, V., & Stewart, J. H. (2024) · IntechOpen eBooks · doi:10.5772/intechopen.1003992 · Cited by 6

Tabersonine ameliorates depressive-like behavior by inhibiting NLRP3 inflammasome activation in a mouse model

Shi, Y., Hu, Y., Gan, Y., Mi, Z., Luo, S., Lei, J., Fang, Q., & Li, H. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110432 · Cited by 6

Advances in the Study of APOE and Innate Immunity in Alzheimer’s Disease

Li, Y., Chang, J., Chen, X., Liu, J., & Zhao, L. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230179 · Cited by 6

Arsenic Exposure Induces Neuro-immune Toxicity in the Cerebral Cortex and the Hippocampus via Neuroglia and NLRP3 Inflammasome Activation in C57BL/6 Mice

Yan, N., Wang, Z., Li, Z., Zheng, Y., Chang, N., Xu, K., Wang, Q., & Duan, X. (2023) · Biological Trace Element Research · doi:10.1007/s12011-023-04012-4 · Cited by 6

Epigenetic memory astrocytes are likely an artifact of immune cell contaminationPreprint

O’Dea, M. R., & Liddelow, S. A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.04.647246 · Cited by 6

Innate Immune Tolerance Regulates Microglia Response to Aβ Oligomers

Valerio, R. R., Santos, Á. R., Nóbrega, A. H. L., Martins, R., Felice, F. G. D., Ferreira, S. T., Savino, W., Bonomo, A. C., Bernardi, A., & Frozza, R. L. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70341 · Cited by 5

Renal IL-23–Dependent Type 3 Innate Lymphoid Cells Link Crystal-induced Intrarenal Inflammasome Activation with Kidney Fibrosis

Frasconi, T. M., Kurts, C., Dhana, E., Kaiser, R., Reichelt, M., Lukacs‐Kornek, V., Boor, P., Hauser, A. E., Reguant, A. P., Bedoui, S., et al. (2024) · The Journal of Immunology · doi:10.4049/jimmunol.2400041 · Cited by 5

Involvement of Microglia in Retinal Ganglion Cell Injury Induced by IOP Elevation in a Rat Ex Vivo Acute Glaucoma Model

Sato, T., Ishikawa, M., Izumi, Y., Shibata, N., Sato, K., Ohno‐Oishi, M., Tawarayama, H., Kunikata, H., Zorumski, C. F., & Nakazawa, T. (2025) · Biomedicines · doi:10.3390/biomedicines13071670 · Cited by 5

Intrinsic antiviral immunity drives neurodegeneration in Alzheimer disease

Pluchino, S., & Willis, C. M. (2020) · Journal of Clinical Investigation · doi:10.1172/jci135906 · Cited by 5

Defective Astrocyte Maturation Drives Cerebellar Neuroinflammation and Degeneration

Mockenhaupt, K., Zarei‐Kheirabadi, M., Gonsiewski, A. K., Hariprashad, A., Dain, L., Verheijen, J., Singh, S. K., & Kordula, T. (2025) · The FASEB Journal · doi:10.1096/fj.202501225rr · Cited by 4

Brain Functional and Structural Changes of Breast Cancer After Chemotherapy: A Systematic Review and Meta-analysis

Chen, Y., Wang, B., Wang, X., Wu, M., Yan, Z., Xu, X., & Yan, S. (2025) · Neuropsychology Review · doi:10.1007/s11065-025-09681-7 · Cited by 4

Role of the NLRP3-Q705K polymorphism in the pathogenesis of inflammatory-mediated diseases: A brief look at impacts of the Q705 polymorphism and NLRP3 activation on cancer immunotherapy

Asgharifar, S. F., & Heris, M. J. (2022) · Human Gene · doi:10.1016/j.humgen.2022.201057 · Cited by 4

Ras, RhoA, and vascular pharmacology in neurodevelopment and aging

Nussinov, R., Jang, H., & Cheng, F. (2024) · Neurochemistry International · doi:10.1016/j.neuint.2024.105883 · Cited by 4

Aggregatin is a mitochondrial regulator of MAVS activation to drive innate immunity

Gao, J., Ding, M., Xiyang, Y., Qin, S., Shukla, D., Xu, J., Miyagi, M., Fujioka, H., Liang, J., & Wang, X. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkae019 · Cited by 4

Exploring the Correlation between the Cognitive Benefits of Drug Combinations in a Clinical Database and the Efficacies of the Same Drug Combinations Predicted from a Computational Model

Anastasio, T. J. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-190144 · Cited by 4

Molecular and genetic landscapes of retina and brain microglia in neurodegenerative diseasesPreprint

Ma, K., & Ratnapriya, R. (2025) · Genome Research · doi:10.1101/gr.280554.125 · Cited by 4

Proteomics: Unraveling the Cross Talk Between Innate Immunity and Disease Pathophysiology, Diagnostics, and Treatment Options

Luz, I. S., Takaya, R., Ribeiro, D. G., Castro, M. S., & Fontes, W. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-50624-6_12 · Cited by 3

Decoding spontaneous intracerebral hemorrhage: mechanistic breakthroughs and disruptive revolution in pharmacological treatment

Chen, Y., Wu, G., Zhang, W., Zou, Z., Huang, L., Shi, H., Wang, Q. J., Chen, W., Luo, Z., Zhao, Z., et al. (2026) · Experimental & Molecular Medicine · doi:10.1038/s12276-026-01733-z · Cited by 3

Unlocking the aging brain: mTORC1 as a convergent integrator for neurodegeneration and therapeutic intervention

Rejili, M., Al‐kuraishy, H. M., Shokr, M. M., & Batiha, G. E. (2026) · Biogerontology · doi:10.1007/s10522-026-10457-6 · Cited by 3

Regulation of NLRP3 inflammasome signaling in Alzheimer’s disease: emerging neuroprotective role of phytochemicals

Gupta, A. K., Singh, S., & Singh, T. D. (2026) · Inflammopharmacology · doi:10.1007/s10787-026-02324-0 · Cited by 3

The systemic costs of hematopoietic stem cell aging

Puri, G., & Blanc, R. S. (2025) · Development · doi:10.1242/dev.205103 · Cited by 3

Epstein–Barr virus and multiple sclerosis

Skliar, A. I., Torianyk, I., Осолодченко, Т. П., & Ponomarenko, S. V. (2020) · Pathologia · doi:10.14739/2310-1237.2020.3.221870 · Cited by 3

Intestinal microbiota and neuroinflammation in Parkinson's disease: At the helm of the gut-brain axis

Manfready, R. A., Goetz, C. G., & Keshavarzian, A. (2022) · International review of neurobiology · doi:10.1016/bs.irn.2022.07.008 · Cited by 2

Selective Destabilization of Transcripts by mRNA Decapping Regulates Oocyte Maturation and Innate Immunity Gene Expression during Ageing in C. elegans

Borbolis, F., Ranti, D., Papadopoulou, M.-D., Dimopoulou, S., Malatras, A., Michalopoulos, I., & Syntichaki, P. (2023) · Biology · doi:10.3390/biology12020171 · Cited by 3

Advanced Chemometric Modeling Approaches for the Design of Multitarget Drugs Against Neurodegenerative Diseases

Halder, A. K., Moura, A. S., & Cordeiro, M. N. D. S. (2018) · Methods in pharmacology and toxicology · doi:10.1007/7653_2018_14 · Cited by 3

Etiology of Neuroinflammatory Pathologies in Neurodegenerative Diseases: A Treatise

Downs, B. W., Kushner, S. W., Bagchi, M., Blum, K., Badgaiyan, R. D., Chakraborty, S., & Bagchi, D. (2021) · Current Psychopharmacologye · doi:10.2174/2211556010666210122145526 · Cited by 3

Innate Immunity and Parkinson's DiseasePreprint

Oludipe, D. B., Du, X., Akter, S., Zhang, C., Mosley, R. L., Gendelman, H. E., & Sil, S. (2025) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a041640 · Cited by 3

The multifaceted role of antimicrobial peptides in neurodegeneration: Insights from Drosophila and beyond

Behera, P., Rangappa, N., Chandrashekar, M., Mishra, A., Chinnathambi, S., & Mishra, M. (2025) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2025.08.003 · Cited by 2

Calsyntenin-3 suppresses inflammation via inhibition of TLR N-glycosylation and membrane localization

Duan, J., Zhang, S., Wang, B., Liu, Y., Liu, L., Liu, Y., Wu, J., & Cao, X. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2528269123 · Cited by 2

Dementias Caused by Persistent Pathogens and the Protective Role of HLA Against them

James, L. M., & Georgopoulos, A. P. (2020) · Journal of Neurology and Neuromedicine · doi:10.29245/2572.942x/2019/1.1260 · Cited by 2

Immunity as key factors that influence cognitive development on children

Oktarina, M. D., Sekartini, R., Wasito, E., & Kartjito, M. S. (2023) · World Nutrition Journal · doi:10.25220/wnj.v06.s2.0003 · Cited by 2

Inflammation as the Common Pathophysiology Linking Stress, Mental Illness, Autoimmunity and Chronic Disease: Implications for Public Health Policy

Kinderlehrer, D. A. (2024) · Journal of Biomedical Research & Environmental Sciences · doi:10.37871/jbres1889 · Cited by 2

Neuroprotective Immunity for Neurodegenerative and Neuroinfectious Diseases

Olson, K. E., Mosley, R. L., & Gendelman, H. E. (2020) · Springer eBooks · doi:10.1007/978-3-030-33946-3_8 · Cited by 2

Innate Immune Status of Glia Modulates Prion Propagation in Early Stage of Infection

Kang, S., Kim, C., Aiken, J. M., & McKenzie, D. I. (2023) · Cells · doi:10.3390/cells12141878 · Cited by 2

Prominent role of PM10 but not of circulating inflammation in the link between air pollution and the risk of neurodegenerative disordersPreprint

Gialluisi, A., Costanzo, S., Veronesi, G., Cembalo, A., Tirozzi, A., Falciglia, S., Ricci, M., Martone, F., Zazzaro, G., Ferrario, M., et al. (2023) · medRxiv · doi:10.1101/2023.05.17.23289154 · Cited by 2

Ayurvedic formulations Guduchi and Madhuyashti triggers JNK signaling mediated immune response and adversely affects Huntington phenotype

Singh, S., & Tapadia, M. G. (2022) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-022-03724-9 · Cited by 1

Neurotoxicity induced by the microbial metabolite β-methylamino-L-alanine: pathways and mechanisms

Candeias, E., Nunes‐Costa, D., Pereira-Santos, A. R., Magalhães, J. D., Melo-Marques, I., Guedes, B., Esteves, A. R., Empadinhas, N., & Cardoso, S. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-23763-8.00068-3 · Cited by 1

Integrative omics in Parkinson’s disease: An introduction

Laß, J., & Trinh, J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13550-7.00003-3 · Cited by 1

Cross-disease transcriptomic analysis reveals DOK3 and PAPOLA as therapeutic targets for neuroinflammatory and tumorigenic processes

Wang, X., Bian, Y., & Chen, W.-G. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1504629 · Cited by 1

Nanotherapeutic formulations of enzyme inhibitors targeting cancer and neuroinflammation: An updated review

Liu, Y., Thiruvengadam, M., Arcot, R., Shariati, M. A., Edis, Z., Chung, I.-M., Liu, S., & Xi, Q. (2025) · Industrial Crops and Products · doi:10.1016/j.indcrop.2025.121803 · Cited by 1

Endothelial miR-7052 Safeguards Blood–Brain Barrier Integrity During Endotoxemia by Co-repressing ANGPT2 and PDE5A

Yang, W., & Wu, H. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-05716-z · Cited by 1

Cellular and Molecular Mechanisms Contributing to Parkinson’s Disease

Madhuranthagan, M., Benito Johnson., D., Essly Selva Jasmine., P., Suresh., R., & Senthil Kumar., C. (2026) · Research Journal of Pharmacology and Pharmacodynamics · doi:10.52711/2321-5836.2026.00005 · Cited by 1

Caspase-1 variant influencing CSF tau and FDG PET levels in non-demented elders from the ADNI cohort

Liu, Y., Tan, M., Wang, Z.-T., Xu, W., & Tan, L. (2022) · BMC Neurology · doi:10.1186/s12883-022-02582-9 · Cited by 1

The Significance of Lysosome in the Diagnosis and Subclassification of Alzheimer’s Disease

Li, C., Zheng, Z., & Jin, M. (2023) · Science of Advanced Materials · doi:10.1166/sam.2023.4441 · Cited by 1

Expression of Toll-like receptors in the cerebellum during pathogenesis of prion disease

Liao, X., Zhu, W., Liao, X., Liu, W., Hou, Y., & Wan, J. (2024) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2024.1341901 · Cited by 1

MET receptor tyrosine kinase promotes the generation of functional synapses in adult cortical circuits

Cui, Y., Ma, X., Wei, J., Chen, C., Shakir, N., Guirram, H., Dai, Z., Anderson, T. R., Ferguson, D., & Qiu, S. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01471 · Cited by 2

Steroids and terpenoids from Aglaia edulis and their anti-inflammatory activities

Chen, X., Li, Z., Yang, X., Li, Y., Jin, J. H., Liu, J., Hao, X., Yuan, C., & Yi, P. (2024) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2024.141195 · Cited by 1

Neurodegeneration meets immunology – A chemical biology perspective

Araman, C., & Hart, B. A. ‘. (2019) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2019.03.038

Arf1-Ablation-Induced Neuronal Damage Promotes Neurodegeneration Through an NLRP3 Inflammasome–Meningeal γδ T cell–IFNγ-Reactive Astrocyte PathwayPreprint

Wang, G., Yin, W., Shin, H., & Hou, X. S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.27.012526

Searching for Possible Links between Alzheimer’s Disease and Systemic Sclerosis

Dardiotis, E., & Bogdanos, D. P. (2020) · Mediterranean Journal of Rheumatology · doi:10.31138/mjr.31.4.378

Letter from the Editor: 2021

Adler, A. J. (2021) · Immunological Investigations · doi:10.1080/08820139.2021.1956723

Faculty Opinions recommendation of Fragmented mitochondria released from microglia trigger A1 astrocytic response and propagate inflammatory neurodegeneration.

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Wang, J., Li, J., Wang, J., Sun, W., Fang, Q., Meng, M., Zhang, X., Jia, R., Li, X., Meng, X., et al. (2020) · Research Square · doi:10.21203/rs.3.rs-90903/v1

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KUŞAT, T., & Emrah, S. U. R. (2023) · doi:10.59287/sbyc.582

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Borst, K., & Prinz, M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-823848-6.00006-3

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Sharma, S. K. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-21752-4.00041-9

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Badesso, S. (2024) · Deposito Adademico Digital Universidad De Navarra (University of Navarra) · doi:10.15581/10171/70194

Early-Life Systemic Inflammation Modulate Microglia Phenotype to Slow Down Aβ Pathology in the 5xFAD Mouse Model of Alzheimer’s DiseasePreprint

Yang, Y., García-Cruzado, M., Zeng, H., Wang, X., Bachiller, S., Camprubí-Ferrer, L., Bahatyrevich-Kharitonik, B., Fernández‐Calle, R., & Deierborg, T. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.19.624204

TGF-β3-mediated phagocytosis protects mammary epithelial cells of ketotic dairy cows against metabolic stress–induced inflammatory damage

Chang, R., Jia, H., Chen, Y., Loor, J. J., Xu, Q., Ma, L., Li, M., Shen, T., Li, X., Xu, C., et al. (2025) · Journal of Dairy Science · doi:10.3168/jds.2025-26828

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Additional file 7 of MicroRNA-100-5p and microRNA-298-5p released from apoptotic cortical neurons are endogenous Toll-like receptor 7/8 ligands that contribute to neurodegeneration

Wallach, T., Mossmann, Z. J., Szczepek, M., Wetzel, M., Machado, R. S. R., Raden, M., Miladi, M., Kleinau, G., Krüger, C., Dembny, P., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17088344

Additional file 5 of MicroRNA-100-5p and microRNA-298-5p released from apoptotic cortical neurons are endogenous Toll-like receptor 7/8 ligands that contribute to neurodegeneration

Wallach, T., Mossmann, Z. J., Szczepek, M., Wetzel, M., Machado, R. S. R., Raden, M., Miladi, M., Kleinau, G., Krüger, C., Dembny, P., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17088338

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Additional file 2 of MicroRNA-100-5p and microRNA-298-5p released from apoptotic cortical neurons are endogenous Toll-like receptor 7/8 ligands that contribute to neurodegeneration

Wallach, T., Mossmann, Z. J., Szczepek, M., Wetzel, M., Machado, R. S. R., Raden, M., Miladi, M., Kleinau, G., Krüger, C., Dembny, P., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17088329

Additional file 3 of MicroRNA-100-5p and microRNA-298-5p released from apoptotic cortical neurons are endogenous Toll-like receptor 7/8 ligands that contribute to neurodegeneration

Wallach, T., Mossmann, Z. J., Szczepek, M., Wetzel, M., Machado, R. S. R., Raden, M., Miladi, M., Kleinau, G., Krüger, C., Dembny, P., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17088332

Additional file 4 of MicroRNA-100-5p and microRNA-298-5p released from apoptotic cortical neurons are endogenous Toll-like receptor 7/8 ligands that contribute to neurodegeneration

Wallach, T., Mossmann, Z. J., Szczepek, M., Wetzel, M., Machado, R. S. R., Raden, M., Miladi, M., Kleinau, G., Krüger, C., Dembny, P., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17088335

Additional file 8 of MicroRNA-100-5p and microRNA-298-5p released from apoptotic cortical neurons are endogenous Toll-like receptor 7/8 ligands that contribute to neurodegeneration

Wallach, T., Mossmann, Z. J., Szczepek, M., Wetzel, M., Machado, R. S. R., Raden, M., Miladi, M., Kleinau, G., Krüger, C., Dembny, P., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17088347

Additional file 1 of Immunotherapy with an antibody against CD1d modulates neuroinflammation in an α-synuclein transgenic model of Lewy body like disease

Iba, M., Kwon, S., Kim, C., Szabo, M. P., Horan-Portelance, L., Lopez-Ocasio, M. D., Dagur, P. K., Overk, C., Rissman, R. A., & Masliah, E. (2024) · Figshare · doi:10.6084/m9.figshare.25608801

Additional file 1 of Intestinal microbiome-mediated resistance against vibriosis for Cynoglossus semilaevis

Zhou, Q., Zhu, X., Li, Y., Yang, P., Wang, S., Ning, K., & Chen, S. (2022) · Figshare · doi:10.6084/m9.figshare.21192147

Additional file 11 of MicroRNA-100-5p and microRNA-298-5p released from apoptotic cortical neurons are endogenous Toll-like receptor 7/8 ligands that contribute to neurodegeneration

Wallach, T., Mossmann, Z. J., Szczepek, M., Wetzel, M., Machado, R. S. R., Raden, M., Miladi, M., Kleinau, G., Krüger, C., Dembny, P., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17088317

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