Immune aging, dysmetabolism, and inflammation in neurological diseases

Inflammation and metabolic disorders

Hotamisligil, G. S. (2006) · Nature · doi:10.1038/nature05485 · Cited by 9,199

Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity

Polazzi, E., Mengoni, I., Caprini, M., Peña‐Altamira, E., Kurtys, E., & Monti, B. (2012) · Neurosignals · doi:10.1159/000337115 · Cited by 9,023

Molecular Mechanisms of Depression: Perspectives on New Treatment Strategies

Lang, U. E., & Borgwardt, S. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350094 · Cited by 8,526

Glutamate neurotoxicity and diseases of the nervous system

Choi, D. W. (1988) · Neuron · doi:10.1016/0896-6273(88)90162-6 · Cited by 8,188

Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo

Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827

Leptin and the regulation of body weight in mammals

Friedman, J. M., & Halaas, J. L. (1998) · Nature · doi:10.1038/27376 · Cited by 5,405

Inflamm‐aging: An Evolutionary Perspective on Immunosenescence

FRANCESCHI, C., BONAFÈ, M., VALENSIN, S., OLIVIERI, F., DE LUCA, M., OTTAVIANI, E., & DE BENEDICTIS, G. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06651.x · Cited by 5,358

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

The International Schizophrenia Consortium (2009) · Nature · doi:10.1038/nature08185 · Cited by 4,821

A Meta-Analysis of Cytokines in Major Depression

Dowlati, Y., Herrmann, N., Swardfager, W., Liu, H., Sham, L., Reim, E. K., & Lanctôt, K. L. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.09.033 · Cited by 4,729

The importance of the ratio of omega-6/omega-3 essential fatty acids

Simopoulos, A. P. (2002) · Biomedicine & Pharmacotherapy · doi:10.1016/s0753-3322(02)00253-6 · Cited by 4,286

Sicilian centenarian offspring are more resistant to immune ageing

Rubino, G., Bulati, M., Aiello, A., Aprile, S., Gambino, C. M., Gervasi, F., Caruso, C., & Accardi, G. (2018) · Aging Clinical and Experimental Research · doi:10.1007/s40520-018-0936-7 · Cited by 29

Cross‐sectional comparison of health‐span phenotypes in young versus geriatric marmosets

Ross, C. N., Adams, J., González, O., Dick, E. J., Giavedoni, L. D., Hodara, V. L., Phillips, K. A., Rigodanzo, A. D., Kasinath, B. S., & Tardif, S. D. (2019) · American Journal of Primatology · doi:10.1002/ajp.22952 · Cited by 29

Modeling tumor immunity of mouse glioblastoma by exhausted CD8+ T cells

Nakashima, H., Alayo, Q. A., Penaloza‐MacMaster, P., Freeman, G. J., Kuchroo, V. K., Reardon, D. A., Fernández, S., Caligiuri, M. A., & Chiocca, E. A. (2018) · Scientific Reports · doi:10.1038/s41598-017-18540-2 · Cited by 29

Trained Immunity Enhances Human Monocyte Function in Aging and Sepsis

Gill, P. S., Ozment, T. R., Lewis, N. H., Sherwood, E. R., & Williams, D. L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.872652 · Cited by 29

Oxidation and Inflammation in the Immune and Nervous Systems, a Link Between Aging and Anxiety

la Fuente, M. D. (2018) · Springer eBooks · doi:10.1007/978-3-319-64597-1_115-1 · Cited by 27

Immunological biomarkers of aging

Wu, F., Mu, W., Markov, N. T., Fuentealba, M., Halaweh, H., Senchyna, F., Manwaring-Mueller, M., Winer, D. A., & Furman, D. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkae036 · Cited by 28

Chronic administration of prebiotics and probiotics ameliorates pathophysiological hallmarks of Alzheimer’s disease in a APP/PS1 transgenic mouse model

Lana, D., Traini, C., Bulli, I., Sarti, G., Magni, G., Attorre, S., Giovannini, M. G., & Vannucchi, M. G. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1451114 · Cited by 27

Age-associated microglial transcriptome leads to diminished immunogenicity and dysregulation of MCT4 and P2RY12/P2RY13 related functions

Škandík, M., Frieß, L., Vázquez-Cabrera, G., Keane, L., Grabert, K., Santos, M. C. D. L., Posada-Pérez, M., Balevičiūtė, A., Cheray, M., & Joseph, B. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02295-1 · Cited by 26

Consequences of diabetes mellitus on neuronal connectivity in limbic regions

Flores‐Gómez, A. A., Gómez-Villalobos, M. D. J., & Flores, G. (2018) · Synapse · doi:10.1002/syn.22082 · Cited by 24

Old mice accumulate activated effector CD4 T cells refractory to regulatory T cell-induced immunosuppression

Harpaz, I., Bhattacharya, U., Elyahu, Y., Strominger, I., & Monsonego, A. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00283 · Cited by 22

A view of the genetic and proteomic profile of extracellular matrix molecules in aging and stroke

Chmelová, M., Androvic, P., Kirdajová, D., Turečková, J., Kriška, J., Valihrach, L., Anděrová, M., & Vargová, L. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1296455 · Cited by 24

Inflammatory and oxidative stress-related effects associated with neurotoxicity are maintained after exclusively prenatal trichloroethylene exposure

Blossom, S. J., Melnyk, S. B., Li, M., Wessinger, W. D., & Cooney, C. A. (2016) · NeuroToxicology · doi:10.1016/j.neuro.2016.01.002 · Cited by 23

A Perspective on Roles Played by Immunosenescence in the Pathobiology of Alzheimer's Disease

Zhao, Y. G., Zhan, J., & Liu, Y. (2020) · Aging and Disease · doi:10.14336/ad.2020.0205 · Cited by 23

Lactobacillus paracasei KW3110 Prevents Inflammatory-Stress-Induced Mitochondrial Dysfunction in Mouse Macrophages

Yamazaki, T., Yamada, S., Ohshio, K., Sugamata, M., & Morita, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031443 · Cited by 24

Aging Immune System in Acute Ischemic Stroke

Sykes, G. P., Tatuene, J. K., Falcione, S. R., Zehnder, S. V., Munsterman, D., Stamova, B. S., Ander, B. P., Sharp, F. R., & Jickling, G. C. (2021) · Stroke · doi:10.1161/strokeaha.120.032040 · Cited by 23

Design strategies, current applications and future perspective of aptasensors for neurological disease biomarkers

Erkmen, C., Tığ, G. A., Marrazza, G., & Uslu, B. (2022) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2022.116675 · Cited by 22

Curcuma longa L. extract improves the cortical neural connectivity during the aging process

Flores, G. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.208542 · Cited by 22

Probiotic supplementation has sex-dependent effects on immune responses in association with the gut microbiota in community-dwelling older adults: a randomized, double-blind, placebo-controlled, multicenter trial

Kim, C.-S., Jung, M. H., Choi, E. Y., & Shin, D. (2023) · Nutrition Research and Practice · doi:10.4162/nrp.2023.17.5.883 · Cited by 22

Differential Diagnosis of Suspected Multiple Sclerosis in Pediatric and Late-Onset Populations

Hua, L. H., Solomon, A. J., Tenembaum, S. N., Scalfari, A., Rovira, À., Rostasy, K. M., Newsome, S. D., Marrie, R. A., Magyari, M., Kantarci, O. H., et al. (2024) · JAMA Neurology · doi:10.1001/jamaneurol.2024.3062 · Cited by 23

Measurement of melatonin, indole‐dioxygenase, IL‐6, IL‐18, ferritin, CRP, and total homocysteine levels during herpes zoster

Khazan, M., Nasiri, S., Riahi, S., Robati, R., & Hedayati, M. (2020) · Journal of Medical Virology · doi:10.1002/jmv.25484 · Cited by 23

A comparison of hippocampal microglial responses in aged and young rodents following dependent and non-dependent binge drinking

Grifasi, I. R., Evans, W. A., Rexha, A. D., Sako, L. W., & Marshall, S. A. (2019) · International review of neurobiology · doi:10.1016/bs.irn.2019.10.018 · Cited by 21

Melatonin and Mesenchymal Stem Cells as a Key for Functional Integrity for Liver Cancer Treatment

Elmahallawy, E. K., Mohamed, Y., Abdo, W. S., & Yanai, T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124521 · Cited by 21

Genome instability: Linking ageing and brain degeneration

Barzilai, A., Schumacher, B., & Shiloh, Y. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.03.011 · Cited by 22

Does Exercise Influence Kynurenine/Tryptophan Metabolism and Psychological Outcomes in Persons With Age-Related Diseases? A Systematic Review

Lim, A., Harijanto, C., Vogrin, S., Guillemin, G. J., & Duque, G. (2021) · International Journal of Tryptophan Research · doi:10.1177/1178646921991119 · Cited by 24

Peripheral sTREM2-Related Inflammatory Activity Alterations in Early-Stage Alzheimer’s Disease

Weber, G. E., Khrestian, M., Tuason, E. D., Shao, Y. Y., Pillai, J. A., Rao, S. M., Feng, H., Zhou, Y., Cheng, F., DeSilva, T. M., et al. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100771 · Cited by 22

Partial MHC class II constructs as novel immunomodulatory therapy for stroke

Benedek, G., Vandenbark, A. A., Alkayed, N. J., & Offner, H. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.10.007 · Cited by 20

Relationship between oropharyngeal dysphagia, nutritional status, antioxidant vitamins and the inflammatory response in adults and elderly: A cross-sectional study

Homem, S. G., Moreira, E. A. M., da Silva, A. F., Barni, G. C., da Rosa, J. S., Oliveira, D. D. L., Tomio, C., de Freitas, M. B., Portari, G. V., Furkim, A. M., et al. (2020) · Clinical Nutrition ESPEN · doi:10.1016/j.clnesp.2020.04.011 · Cited by 19

Nanogels, nanodiscs, yeast cells, and metallo-complexes-based curcumin delivery for therapeutic applications

Rahmanian, M., Oroojalian, F., Pishavar, E., Kesharwani, P., & Sahebkar, A. (2023) · European Polymer Journal · doi:10.1016/j.eurpolymj.2023.112215 · Cited by 19

Sex as a Determinant of Age-Related Changes in the Brain

Burmistrov, D. E., Gudkov, S. V., Franceschi, C., & Vedunova, M. V. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25137122 · Cited by 23

Ancestral stress programs sex-specific biological aging trajectories and non-communicable disease risk

Ambeskovic, M., Ilnytskyy, Y., Kiss, D., Currie, C. L., Montina, T., Kovalchuk, I., & Metz, G. A. S. (2020) · Aging · doi:10.18632/aging.102848 · Cited by 17

A Preliminary Genetic Analysis of Complement 3 Gene and Schizophrenia

Ni, J., Hu, S., Zhang, J., Tang, W., Lu, W., & Zhang, C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136372 · Cited by 18

Lactic acid bacterium, Lactobacillus paracasei KW3110, suppresses inflammatory stress-induced caspase-1 activation by promoting interleukin-10 production in mouse and human immune cells

Yamazaki, T., Ohshio, K., Sugamata, M., & Morita, Y. (2020) · PLoS ONE · doi:10.1371/journal.pone.0237754 · Cited by 18

The growing field of immunometabolism and exercise: Key findings in the last 5 years

Padilha, C. S., Morano, A. E. V. A., Krüger, K., Neto, J. C. R., & Lira, F. S. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30866 · Cited by 23

Phenomic Microglia Diversity as a Druggable Target in the Hippocampus in Neurodegenerative Diseases

Lana, D., Magni, G., Landucci, E., Wenk, G. L., Pellegrini-Giampietro, D. E., & Giovannini, M. G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241813668 · Cited by 20

Brain Aging and Anesthesia

Pandin, P., Estruch-Pons, I., Hecke, D. V., Truong, H.-N., Marullo, L., Hublet, S., & Obbergh, L. J. V. (2019) · Journal of Cardiothoracic and Vascular Anesthesia · doi:10.1053/j.jvca.2019.03.042 · Cited by 18

Personalized Nutrition as a Key Contributor to Improving Radiation Response in Breast Cancer

Shastri, A. A., Lombardo, J. F., Okere, S. C., Higgins, S., Smith, B. C., DeAngelis, T., Palagani, A., Hines, K., Monti, D., Volpe, S. L., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010175 · Cited by 18

Longitudinal transcriptomic analysis of mouse sciatic nerve reveals pathways associated with age‐related muscle pathology

Comfort, N. T., Gade, M., Strait, M. D., Merwin, S. J., Αντωνίου, Δ., Parodi, C., Marcinczyk, L., Jean‐Francois, L., Bloomquist, T. R., Memou, A., et al. (2023) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13204 · Cited by 16

Western diet increases brain metabolism and adaptive immune responses in a mouse model of amyloidosis

Poxleitner, M., Hoffmann, S. H. L., Berezhnoy, G., Ionescu, T. M., González-Menéndez, I., Maier, F. C., Seyfried, D., Ehrlichmann, W., Quintanilla‐Martínez, L., Schmid, A. M., et al. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03080-0 · Cited by 22

Age has a role in driving host immunopathological response to alphavirus infection

Chan, Y., & Ng, L. F. P. (2017) · Immunology · doi:10.1111/imm.12799 · Cited by 17

Hypothalamic Inflammation at a Crossroad of Somatic Diseases

Mravec, B., Horváthová, Ľ., & Černáčková, A. (2018) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-018-0631-4 · Cited by 17

Aging and neuropathic pain: Mitochondria-to-glia cascade, system mechanisms, and therapeutic strategies

Majumdar, S., Samaiya, P. K., Gupta, S. K., Krishnamurthy, S., & Prajapati, S. K. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103042 · Cited by 18

Lactobacillus paracasei KW3110 Suppresses Inflammatory Stress-Induced Premature Cellular Senescence of Human Retinal Pigment Epithelium Cells and Reduces Ocular Disorders in Healthy Humans

Yamazaki, T., Suzuki, H., Yamada, S., Ohshio, K., Sugamata, M., Yamada, T., & Morita, Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21145091 · Cited by 16

CD4/CD8 ratio, comorbidities, and aging in treated HIV infected individuals on viral suppression

Passos, D. F., Bremm, J. M., da Silveira, L. L., Jantsch, M. H., da Silva, J. L. G., Disconzi, E., Rezer, J. F. P., Schwarzbold, A. V., Marques, A. C. F., Schetinger, M. R. C., et al. (2020) · Journal of Medical Virology · doi:10.1002/jmv.25911 · Cited by 20

Space-Dependent Glia–Neuron Interplay in the Hippocampus of Transgenic Models of β-Amyloid Deposition

Lana, D., Ugolini, F., & Giovannini, M. G. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249441 · Cited by 17

Lipid droplets: Emerging therapeutic targets for age-related metabolic diseases

Ma, Z., Pan, S., Yang, Y., Ren, H., Yin, S., Chen, Q., An, Z., Zhao, X., & Xu, Z. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102758 · Cited by 17

Oral curcumin supplementation improves fine motor function in the middle-aged rhesus monkey

Moore, T. L., Bowley, B. G. E., Shultz, P. L., Calderazzo, S. M., Shobin, E., Uprety, A. R., Rosene, D. L., & Moss, M. B. (2018) · Somatosensory & Motor Research · doi:10.1080/08990220.2018.1432481 · Cited by 14

Vitamin C: A Preventative, Therapeutic Agent Against Helicobacter pylori

Hussain, A., Tabrez, E. S., Peela, J. R., Honnavar, P., & Tabrez, S. S. M. (2018) · Cureus · doi:10.7759/cureus.3062 · Cited by 15

Role of Adaptive Immune and Impacts of Risk Factors on Adaptive Immune in Alzheimer’s Disease: Are Immunotherapies Effective or Off-Target?

Shi, M., Chu, F., Tian, X., Aerqin, Q., Zhu, F., & Zhu, J. (2021) · The Neuroscientist · doi:10.1177/1073858420987224 · Cited by 14

Identifying gene expression profiles associated with neurogenesis and inflammation in the human subependymal zone from development through aging

Bitar, M., Weissleder, C., North, H. F., Clearwater, M. S., Zalucki, O. H., Halliday, G. M., Webster, M. J., Piper, M., Weickert, C. S., & Barry, G. (2022) · Scientific Reports · doi:10.1038/s41598-021-03976-4 · Cited by 15

The Roles of Physical Activity and Inflammation in Mortality, Cognition, and Depressive Symptoms Among Older Mexican Americans

Shih, I., Haan, M. N., Paul, K. C., Yu, Y., Sinsheimer, J. S., & Ritz, B. R. (2019) · American Journal of Epidemiology · doi:10.1093/aje/kwz180 · Cited by 14

Immune Dysfunction Associated with Abnormal Bone Marrow-Derived Mesenchymal Stroma Cells in Senescence Accelerated Mice

Li, M., Guo, K., Adachi, Y., & Ikehara, S. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17020183 · Cited by 12

Neurochemical Aspects of Neurological Disorders

Farooqui, A. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803603-7.00016-1 · Cited by 12

Polyoxidovanadates as a pharmacological option against brain aging

Díaz, A., Vázquez‐Roque, R. A., Carreto-Meneses, K., Moroni-González, D., Moreno-Rodríguez, J. A., & Treviño, S. (2023) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2023.102256 · Cited by 11

Effects of natural source polysaccharides on neurological diseases: A review

Yang, L., Hou, H., Lu, L., Sun, Y. H., Chen, R., Deng, Q., & Chen, H. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.139697 · Cited by 11

Aging, Immunity, and Neuroinflammation: The Modulatory Potential of Nutrition

Benedetto, S. D., & Müller, L. (2019) · Springer eBooks · doi:10.1007/978-3-030-16073-9_14 · Cited by 12

Emerging Materials, Wearables, and Diagnostic Advancements in Therapeutic Treatment of Brain Diseases

Ramasubramanian, B., Reddy, V. S., Chellappan, V., & Ramakrishna, S. (2022) · Biosensors · doi:10.3390/bios12121176 · Cited by 13

Spinal cord gray matter atrophy is associated with functional decline in post‐polio syndrome

Wendebourg, M. J., Weigel, M., Richter, L., Gocheva, V., Hafner, P., Orsini, A., Crepulja, V., Schmidt, S., Huck, A., Oechtering, J., et al. (2022) · European Journal of Neurology · doi:10.1111/ene.15261 · Cited by 11

Chronic purple grape juice consumption induces age-dependent changes on cognitive function in elderly women

da Costa, P. C., Dorneles, G. P., da Silva, I. R. V., de Araújo, C. L. P., Reinaldo, G. P., Peres, A., Funchal, C., Lago, P. D., Dani, C., & Elsner, V. R. (2017) · Journal of Systems and Integrative Neuroscience · doi:10.15761/jsin.1000149 · Cited by 11

Randomized controlled trial comparing the impacts of Saccharomyces boulardii and Lactobacillus rhamnosus OF44 on intestinal flora in cerebral palsy rats: insights into inflammation biomarkers and depression-like behaviors

Chu, C., Huang, S., Wang, X., Zhao, G.-Q., Hao, W., Zhong, Y., Ma, Z., Huang, C., Peng, Y., & Wei, F. (2024) · Translational Pediatrics · doi:10.21037/tp-23-566 · Cited by 10

Chronic administration of prebiotics and probiotics prevent pathophysiological hallmarks of Alzheimer’s disease in the cortex of APP/PS1 mice

Sarti, G., Traini, C., Magni, G., Attorre, S., Tognozzi, G., Calussi, E., Giovannini, M. G., Vannucchi, M. G., & Lana, D. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1596469 · Cited by 11

Sex Differences in Hypothalamic Changes and the Metabolic Response of TgAPP Mice to a High Fat Diet

Freire‐Regatillo, A., Díaz-Pacheco, S., Frago, L. M., Arévalo, M., Argente, J., García‐Segura, L. M., CEBALLOS, M. L. D., & Chowen, J. A. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2022.910477 · Cited by 10

Relative Leukocyte Telomere Length and Genetic Variants in Telomere-Related Genes and Serum Levels Role in Age-Related Macular Degeneration

Vilkevičiūtė, A., Gedvilaitė, G., Banevičius, M., Kriaučiūnienė, L., Žaliūnienė, D., Dobilienė, O., & Liutkevičienė, R. (2022) · Cells · doi:10.3390/cells11233847 · Cited by 11

Amyloid beta-correlated plasma metabolite dysregulation in Alzheimer's disease: an untargeted metabolism exploration using high-resolution mass spectrometry toward future clinical diagnosis

Yang, J., Wu, S., Yang, J., Zhang, Q., & Dong, X. W. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1189659 · Cited by 10

Morphofunctional Investigation in a Transgenic Mouse Model of Alzheimer’s Disease: Non-Reactive Astrocytes Are Involved in Aβ Load and Reactive Astrocytes in Plaque Build-Up

Lana, D., Branca, J. J. V., Delfino, G., Giovannini, M. G., Casamenti, F., Nardiello, P., Bucciantini, M., Stefani, M., Zach, P., Zecchi‐Orlandini, S., et al. (2023) · Cells · doi:10.3390/cells12182258 · Cited by 10

Association between adherence to dietary recommendations and high-sensitivity C-reactive protein level in type 1 diabetes

Ahola, A. J., Saraheimo, M., Freese, R., Forsblom, C. M., Mäkimattila, S., & Groop, P. (2017) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2017.02.012 · Cited by 10

Microglial Inflammation and Cognitive Dysfunction in Comorbid Rat Models of Striatal Ischemic Stroke and Alzheimer’s Disease: Effects of Antioxidant Catalase-SKL on Behavioral and Cellular Pathology

MacKenzie, J. L., Ivanova, N., Nell, H. J., Giordano, C. R., Terlecky, S. R., Agca, C., Ağca, Y., Walton, P. A., Whitehead, S. N., & Cechetto, D. F. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.01.026 · Cited by 9

Deciphering the Association of Epstein–Barr Virus and Its Glycoprotein M Peptide with Neuropathologies in Mice

Rani, A., Patra, P., Verma, T., Singh, A., Jain, A. K., Jaiswal, N., Narang, S., Mittal, N., Parmar, H. S., & Jha, H. C. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00012 · Cited by 8

Morphometric analysis of the folliculostellate cells and luteinizing hormone gonadotropic cells of the anterior pituitary of the men during the aging process

Kokoris, J. Č., Jovanovic, I. D., Pantović, V., Krstić, M., Stanojkovic, M., Milošević, V., Ugrenovic, S. Z., & Stojanović, V. R. (2016) · Tissue and Cell · doi:10.1016/j.tice.2016.11.006 · Cited by 9

Altered activity of xenobiotic detoxifying enzymes at menopause – A cross-sectional study

Tsiokou, V., Kilindris, T. V., Begas, E., Kouvaras, E., Kouretas, D., & Asprodini, E. K. (2019) · Environmental Research · doi:10.1016/j.envres.2019.109074 · Cited by 9

Obesity Prevents S-Adenosylmethionine-Mediated Improvements in Age-Related Peripheral and Hippocampal Outcomes

Velden, J. W. V., & Osborne, D. M. (2021) · Nutrients · doi:10.3390/nu13041201 · Cited by 9

An evaluation of the recognised systemic inflammatory biomarkers of chronic sub-optimal inflammation provides evidence for inflammageing (IFA) during multiple sclerosis (MS)

Bolton, C. (2021) · Immunity & Ageing · doi:10.1186/s12979-021-00225-0 · Cited by 10

Intelligent Elderly People Fall Detection Based on Modified Deep Learning Deep Transfer Learning and IoT Using Thermal Imaging-Assisted Pervasive Surveillance

Rezaee, K., Khosravi, M. R., & Moghimi, M. K. (2022) · Springer eBooks · doi:10.1007/978-981-16-8150-9_6 · Cited by 9

Monocyte-Derived Macrophages Contribute to Chitinase Dysregulation in Amyotrophic Lateral Sclerosis: A Pilot Study

Gaur, N., Huß, E., Prell, T., Steinbach, R., Guerra, J., Srivastava, A., Witte, O. W., & Großkreutz, J. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.629332 · Cited by 9

Contribution of neuroinflammation to changes in [ 11 C]flumazenil binding in the rat brain: Evaluation of the inflamed pons as reference tissue

Parente, A., García, D. V., Shoji, A., Alves, I. L., Maas, B., Zijlma, R., Dierckx, R., Buchpiguel, C. A., de Vries, E. F. J., & Doorduin, J. (2017) · Nuclear Medicine and Biology · doi:10.1016/j.nucmedbio.2017.03.001 · Cited by 8

Targeting neurotransmitter-mediated inflammatory mechanisms of psychiatric drugs to mitigate the double burden of multimorbidity and polypharmacy

Matt, S. M. (2021) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2021.100353 · Cited by 8

Systematic analysis of cuproptosis-related genes in immunological characterization and predictive drugs in Alzheimer’s disease

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Neurochemical Aspects of Neurological Disorders

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Association of critically short telomeres with brain and blood markers of ageing and Alzheimer’s disease in older adults

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Wearable sensor platforms for real-time monitoring and early warning of metabolic disorders in humans

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Telomerase Depletion Accelerates Ageing of the Zebrafish Brain

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Age and sex differences in the association between Dietary Inflammatory Index and severe headache or migraine: a nationwide cross-sectional study

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Immunosenescence-related T cell phenotypes and white matter in schizophrenia patients with tardive dyskinesia

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High Body Mass Index is Associated with Elevated Blood Levels of Progerin mRNA

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The Age-Related Efficacy of Dimethyl Fumarate and Natalizumab in the Real-World Management of Multiple Sclerosis

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Differential Expression of Neurodegeneration-Related Genes in SH-SY5Y Neuroblastoma Cells Under the Influence of Cyclophilin A: Could the Enzyme be a Likely Trigger and Therapeutic Target for Alzheimer’s Disease?

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CMV Driven Immunosenescence and Alzheimer’s Disease

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