Oxidative Stress, Synaptic Dysfunction, and Alzheimer’s Disease

Free Radicals in the Physiological Control of Cell Function

Dröge, W. (2002) · Physiological Reviews · doi:10.1152/physrev.00018.2001 · Cited by 9,855

Oxyl radicals, redox-sensitive signalling cascades and antioxidants

Genestra, M. (2007) · Cellular Signalling · doi:10.1016/j.cellsig.2007.04.009 · Cited by 4,930

Hypothetical model of dynamic biomarkers of the Alzheimer's pathological cascade

Jack, C. R., Knopman, D. S., Jagust, W. J., Shaw, L. M., Aisen, P. S., Weiner, M. W., Petersen, R. C., & Trojanowski, J. Q. (2010) · The Lancet Neurology · doi:10.1016/s1474-4422(09)70299-6 · Cited by 4,806

Physical basis of cognitive alterations in alzheimer's disease: Synapse loss is the major correlate of cognitive impairment

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Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling

Ray, P. D., Huang, B.-W., & Tsuji, Y. (2012) · Cellular Signalling · doi:10.1016/j.cellsig.2012.01.008 · Cited by 4,373

Oxidative mechanisms in the toxicity of metal ions

Stohs, S. J., & Bagchi, D. (1995) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(94)00159-h · Cited by 4,219

Triple-Transgenic Model of Alzheimer’s Disease with Plaques and Tangles

Oddo, S., Caccamo, A., Shepherd, J. D., Murphy, M. P., Golde, T. E., Kayed, R., Metherate, R., Mattson, M. P., Akbari, Y., & LaFerla, F. M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00434-3 · Cited by 4,126

LTP and LTD

Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968

Clinical and biomarker changes in dominantly inherited Alzheimer's disease

Bateman, R. J., Xiong, C., Benzinger, T. L. S., Fagan, A. M., Goate, A., Fox, N. C., Marcus, D. S., Cairns, N. J., Xie, X., Blazey, T. M., et al. (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1202753 · Cited by 3,814

Cell Survival Responses to Environmental Stresses Via the Keap1-Nrf2-ARE Pathway

Kensler, T. W., Wakabayashi, N., & Biswal, S. (2007) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.46.120604.141046 · Cited by 3,630

Inhibiting amyloid beta (1–42) peptide-induced mitochondrial dysfunction prevents the degradation of synaptic proteins in the entorhinal cortex

Olajide, O. J., Rue, C. L., Bergdahl, A., & Chapman, C. A. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.960314 · Cited by 24

Ginsenoside Rg1 alleviates learning and memory impairments and Aβ disposition through inhibiting NLRP1 inflammasome and autophagy dysfunction in APP/PS1 mice

Li, X., Huang, L., Kong, L., Su, Y., Zhou, H., Ji, P., Sun, R., Wang, C., Li, W., & Li, W. (2022) · Molecular Medicine Reports · doi:10.3892/mmr.2022.12893 · Cited by 25

The shift in the fatty acid composition of the circulating lipidome in Alzheimer's disease

Dakterzada, F., Jové, M., Cantero, J. L., Mota‐Martorell, N., Pamplona, R., & Piñoll‐Ripoll, G. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.13792 · Cited by 23

Post-translational Modifications of the Peptidyl-Prolyl Isomerase Pin1

Chen, D., Wang, L., & Lee, T. H. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00129 · Cited by 23

Conservation and divergence of vulnerability and responses to stressors between human and mouse astrocytesPreprint

Li, J., Pan, L., Godoy, M. I., Pembroke, W. G., Rexach, J. E., Condro, M. C., Alvarado, A. G., Harteni, M., Chen, Y.-W., Stiles, L., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.17.044222 · Cited by 23

Arachidonic Acid Mobilization and Peroxidation Promote Microglial Dysfunction in Aβ Pathology

Lin, D., Gold, A., Kaye, S., Atkinson, J., Tol, M. J., Sas, A., Segal, B. M., Tontonoz, P., Zhu, J., & Gao, J. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0202-24.2024 · Cited by 23

Interplay Between Aging and Tau Pathology in Alzheimer’s Disease: Mechanisms and Translational Perspectives

Alrouji, M., Alshammari, M. S., Syed, T., & Shamsi, A. (2025) · Antioxidants · doi:10.3390/antiox14070774 · Cited by 21

Mitochondrial complex I deficiency induces Alzheimer's disease–like signatures that are reversible by targeted therapy

Gao, H., Jensen, K. N., Nesbitt, J. J., Ostroot, M., Cary, G. A., Wiley, J. C., Trushin, S., Watzlawik, J. O., Springer, W., Galkin, A. S., et al. (2025) · Alzheimer s & Dementia · doi:10.1002/alz.70519 · Cited by 22

Novel multi target-directed ligands targeting 5-HT4 receptors with in cellulo antioxidant properties as promising leads in Alzheimer's disease

Lanthier, C., Payan, H., Liparulo, I., Hatat, B., Lecoutey, C., Since, M., Davis, A., Bergamini, C., Claeysen, S., Dallemagne, P., et al. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.111596 · Cited by 24

Natural Food Supplements Reduce Oxidative Stress in Primary Neurons and in the Mouse Brain, Suggesting Applications in the Prevention of Neurodegenerative Diseases

Bobadilla, M., Garcı́a-Sanmartı́n, J., & Martı́nez, A. (2021) · Antioxidants · doi:10.3390/antiox10010046 · Cited by 22

Synergistic Neuroprotective Effects of a Natural Product Mixture against AD Hallmarks and Cognitive Decline in Caenorhabditis elegans and an SAMP8 Mice Model

Griñán‐Ferré, C., Bellver‐Sanchís, A., Olivares-Martín, M., Bañuelos, Ó., & Pallàs, M. (2021) · Nutrients · doi:10.3390/nu13072411 · Cited by 22

Modified Low-Temperature Extraction Method for Isolation of Bletilla striata Polysaccharide as Antioxidant for the Prevention of Alzheimer’s Disease

Lin, Y.-W., Fang, C.-H., Liang, Y., Liao, H.-H., & Lin, F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222312760 · Cited by 23

Saffron reduces some inflammation and oxidative stress markers in donepezil-treated mild-to-moderate Alzheimer's Disease patients: A randomized double-blind placebo-control trial

Marzabadi, L. R., Fazljou, S. M. B., Araj‐Khodaei, M., Sadigh‐Eteghad, S., Naseri, A., & Talebi, M. (2022) · Journal of Herbal Medicine · doi:10.1016/j.hermed.2022.100574 · Cited by 22

Sweroside Ameliorated Memory Deficits in Scopolamine-Induced Zebrafish (Danio rerio) Model: Involvement of Cholinergic System and Brain Oxidative Stress

Brinza, I., Raey, M. A. E., El‐Kashak, W. A., Eldahshan, O. A., & Hriţcu, L. (2022) · Molecules · doi:10.3390/molecules27185901 · Cited by 22

Clinical relevance of biomarkers, new therapeutic approaches, and role of post-translational modifications in the pathogenesis of Alzheimer’s disease

Mumtaz, I., Ayaz, M. O., Khan, M. S., Manzoor, U., Ganayee, M. A., Bhat, A. Q., Dar, G. H., Alghamdi, B. S. A., Hashem, A. M., Dar, M. J., et al. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.977411 · Cited by 23

Risk of neurodegenerative diseases in patients with sleep disorders: A nationwide population-based case-control study

Lin, W., Lin, Y., Yang, F., Chung, C., Hu, J., Tsao, C., Weng, Z., Ko, C.-A., & Chien, W. (2023) · Sleep Medicine · doi:10.1016/j.sleep.2023.05.014 · Cited by 24

Pathological Impact of Tau Proteolytical Process on Neuronal and Mitochondrial Function: a Crucial Role in Alzheimer’s Disease

Olesen, M. A., & Quintanilla, R. A. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03434-4 · Cited by 23

Integrated transcriptomics reveals the brain and blood biomarkers in Alzheimer's disease

Yu, H., Wang, F., Wu, J., Gong, J., Bi, S., Mao, Y., Jia, D., & Chai, G. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14316 · Cited by 21

Polysaccharides: potential bioactive macromolecules for Alzheimer’s disease

Peng, G., Li, M., & Meng, Z. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1249018 · Cited by 23

P2X7 Receptor: an Emerging Target in Alzheimer’s Disease

Huang, Q., Ying, J., Yu, W., Dong, Y., Xiong, H., Zhang, Y., Liu, J., Wang, X., & Hua, F. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03699-9 · Cited by 26

Discovery of novel deoxyvasicinone derivatives with benzenesulfonamide substituents as multifunctional agents against Alzheimer's disease

Dong, S., Xia, J., Wang, F., Yang, L., Xing, S., Du, J., Zhang, T., & Li, Z. (2023) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2023.116013 · Cited by 23

Exploring the complexities of 1C metabolism: implications in aging and neurodegenerative diseases

Ghanem, A. B., Hussayni, Y., Kadbey, R., Ratel, Y., Yehya, S., Khouzami, L., Ghadieh, H. E., Kanaan, A., Azar, S. T., & Harb, F. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1322419 · Cited by 24

Functional interplay between plasma membrane Ca2+-ATPase, amyloid β-peptide and tau

Mata, A. M. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.08.004 · Cited by 22

An Insight in Pathophysiological Mechanism of Alzheimer's Disease and its Management Using Plant Natural Products

Firdaus, Z., & Singh, T. D. (2020) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557520666200730155928 · Cited by 23

FoxO3 transcription factor promotes autophagy after oxidative stress injury in HT22 cells

Deng, A., Ma, L., Zhou, X., Wang, X., Wang, S., & Chen, X. (2020) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2020-0448 · Cited by 22

Exploring the multifaceted role of ginkgolides and bilobalide from Ginkgo biloba in mitigating metabolic disorders

Kim, H., Kang, S., & Go, G. (2024) · Food Science and Biotechnology · doi:10.1007/s10068-024-01656-3 · Cited by 22

Impaired peroxisomal beta-oxidation in microglia triggers oxidative stress and impacts neurons and oligodendrocytes

Tawbeh, A., Gondcaille, C., Saih, F.-E., Raas, Q., Loichot, D., Hamon, Y., Keime, C., Benani, A., Di Cara, F., Cherkaoui-Malki, M., et al. (2025) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2025.1542938 · Cited by 21

Impact of diet and exercise on mitochondrial quality and mitophagy in Alzheimer's disease

Pradeepkiran, J. A., Islam, M. A., Sehar, U., Reddy, A. P., Vijayan, M., & Reddy, P. H. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102734 · Cited by 25

Alzheimer's Disease and Frontotemporal Dementia: A Review of Pathophysiology and Therapeutic Approaches

Kelliny, S., Zhou, X., & Bobrovskaya, L. (2025) · Journal of Neuroscience Research · doi:10.1002/jnr.70046 · Cited by 27

Association of aerobic glycolysis with the structural connectome reveals a benefit–risk balancing mechanism in the human brain

Chen, Y., Lin, Q., Liao, X., Zhou, C., & Yong He, A. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2013232118 · Cited by 22

Involvement of Hepcidin in Cognitive Damage Induced by Chronic Intermittent Hypoxia in Mice

Zhao, Y., Tan, M., Song, J., An, J., Yang, X., Li, W., Guo, Y., & Ji, E. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/8520967 · Cited by 21

Long-Term Treatment of Cuban Policosanol Attenuates Abnormal Oxidative Stress and Inflammatory Response via Amyloid Plaques Reduction in 5xFAD Mice

Kim, J., Lim, D.-K., Suh, Y., & Chang, K. (2021) · Antioxidants · doi:10.3390/antiox10081321 · Cited by 20

NXP032 Ameliorates Aging-Induced Oxidative Stress and Cognitive Impairment in Mice through Activation of Nrf2 Signaling

Lee, J. M., Lee, J. H., Song, M. K., & Kim, Y. (2022) · Antioxidants · doi:10.3390/antiox11010130 · Cited by 21

Maternal High Fat Diet Anticipates the AD-like Phenotype in 3xTg-AD Mice by Epigenetic Dysregulation of Aβ Metabolism

Natale, F., Spinelli, M., Rinaudo, M., Cocco, S., Sarrapochiello, I. N., Fusco, S., & Grassi, C. (2023) · Cells · doi:10.3390/cells12020220 · Cited by 21

Hydroxytyrosol–Donepezil Hybrids Play a Protective Role in an In Vitro Induced Alzheimer’s Disease Model and in Neuronal Differentiated Human SH-SY5Y Neuroblastoma Cells

Maiuolo, J., Costanzo, P., Masullo, M., D'Errico, A. A., Nasso, R., Bonacci, S., Mollace, V., Oliverio, M., & Arcone, R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713461 · Cited by 23

Metabolomics profiling reveals distinct, sex‐specific signatures in serum and brain metabolomes in mouse models of Alzheimer's disease

Pandey, R. S., Arnold, M., Batra, R., Krumsiek, J., Kotredes, K. P., Garceau, D. T., Williams, H. M., Sasner, M., Howell, G. R., Kaddurah‐Daouk, R., et al. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.13851 · Cited by 22

Ameliorative effect of vanillic acid against scopolamine-induced learning and memory impairment in rat via attenuation of oxidative stress and dysfunctional synaptic plasticity

Choi, G.-Y., Lee, I.-S., Moon, E., Choi, H., Je, A. R., Park, J.-H., & Kweon, H. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117000 · Cited by 23

S-Adenosylmethionine and Superoxide Dismutase 1 Synergistically Counteract Alzheimer’s Disease Features Progression in TgCRND8 Mice

Cavallaro, R. A., Nicolia, V., Fiorenza, M. T., Scarpa, S., & Fuso, A. (2017) · Antioxidants · doi:10.3390/antiox6040076 · Cited by 21

GAPT regulates cholinergic dysfunction and oxidative stress in the brains of learning and memory impairment mice induced by scopolamine

Liu, Z., Qin, G., Mana, L., Dong, Y., Huang, S., Wang, Y., Wu, Y., Shi, J., Tian, J., & Wang, P. (2020) · Brain and Behavior · doi:10.1002/brb3.1602 · Cited by 21

Real-time evolution of Aβ40 metal-catalyzed oxidation reveals Asp1 as the main target and a dependence on metal binding site

Cheignon, C., Hureau, C., & Collin, F. (2017) · Inorganica Chimica Acta · doi:10.1016/j.ica.2017.07.031 · Cited by 21

Analysis of shared underlying mechanism in neurodegenerative disease

Butler, R., Bradford, D. R., & Rodgers, K. E. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1006089 · Cited by 24

Embryonic Zebrafish as a Model for Investigating the Interaction between Environmental Pollutants and Neurodegenerative Disorders

Yin, J., & Horzmann, K. A. (2024) · Biomedicines · doi:10.3390/biomedicines12071559 · Cited by 20

The molecular mechanism of nitric oxide in memory consolidation and its role in the pathogenesis of memory-related disorders

Bahdar, Z. I., Abu‐El‐Rub, E., Almazari, R., Alzu’bi, A., & Al‐Zoubi, R. M. (2025) · Neurogenetics · doi:10.1007/s10048-025-00803-0 · Cited by 20

Serotonergic Regulation in Alzheimer’s Disease

Долгачева, Л. П., Зинченко, В. П., Nadeev, A. D., & Goncharov, N. V. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26115218 · Cited by 21

The Therapeutic Potential of Butyrate and Lauric Acid in Modulating Glial and Neuronal Activity in Alzheimer’s Disease

Wtpsk, S., Oikari, L. E., Bharadwaj, P., Jayasena, V., Martins, R. N., & Fernando, W. M. A. D. B. (2025) · Nutrients · doi:10.3390/nu17142286 · Cited by 23

Human Induced Pluripotent Stem Cell-Derived Neural Cells from Alzheimer's Disease Patients Exhibited Different Susceptibility to Oxidative Stress

Zhang, L., Xu, M., Ren, Q., Liu, G., Meng, S., Xiahou, K., Zhang, Y., Jiang, N., & Zhou, W. (2020) · Stem Cells and Development · doi:10.1089/scd.2020.0103 · Cited by 20

The Dose and Duration-dependent Association between Melatonin Treatment and Overall Cognition in Alzheimer’s Dementia: A Network Meta- Analysis of Randomized Placebo-Controlled Trials

Shiue, Y., Tseng, P., Zeng, B., Chen, Y., Yang, C., Su, K., Chen, T., Wu, Y., Tu, Y., Lin, P., et al. (2022) · Current Neuropharmacology · doi:10.2174/1570159x20666220420122322 · Cited by 21

Effect of Mediterranean diet and Mediterranean diet plus calorie restriction on cognition, lifestyle, and cardiometabolic health: A randomized clinical trial

Tussing-Humphreys, L. M., Lamar, M., McLeod, A., Schiffer, L. A., Blumstein, L. B., Dakers, R., Karstens, A. J., Hemphill, N. O., Strahan, D. C., Siegel, L., et al. (2022) · Preventive Medicine Reports · doi:10.1016/j.pmedr.2022.101955 · Cited by 25

The effect of ghrelin on antioxidant status in the rat’s model of Alzheimer's disease induced by amyloid-beta

Sarlaki, F., Shahsavari, Z., Goshadrou, F., Naseri, F., Keimasi, M., & Sirati‐Sabet, M. (2022) · Biomedicine · doi:10.37796/2211-8039.1341 · Cited by 20

Practical Three-Component Regioselective Synthesis of Drug-Like 3-Aryl(or heteroaryl)-5,6-dihydrobenzo[h]cinnolines as Potential Non-Covalent Multi-Targeting Inhibitors To Combat Neurodegenerative Diseases

Mousavi, H., Rimaz, M., & Zeynizadeh, B. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00055 · Cited by 21

Gingko biloba Extract (EGb) Inhibits Oxidative Stress in Neuro 2A Cells Overexpressing APPsw

Chen, L., Zhang, C., Han, Y., Meng, X., Zhang, Y., Chu, H., & Ma, H. (2019) · BioMed Research International · doi:10.1155/2019/7034983 · Cited by 20

Multiple target-based combination therapy of galantamine, memantine and lycopene for the possible treatment of Alzheimer’s disease

Vishwas, S., Awasthi, A., Corrie, L., Singh, S. K., & Gulati, M. (2020) · Medical Hypotheses · doi:10.1016/j.mehy.2020.109879 · Cited by 20

MERCs. The Novel Assistant to Neurotransmission?

Shirokova, O. M., Pchelin, P. V., & Mukhina, I. V. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.589319 · Cited by 20

Synergistic enhancing-memory effect of D-serine and RU360, a mitochondrial calcium uniporter blocker in rat model of Alzheimer's disease

Nikseresht, Z., Ahangar, N., Badrikoohi, M., & Babaei, P. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113307 · Cited by 20

Age-Dependent Decrease of Mitochondrial Complex II Activity in a Familial Mouse Model for Alzheimer’s Disease

Emmerzaal, T. L., Rodenburg, R. J., Tanila, H., Verweij, V., Kiliaan, A. J., & Kozicz, T. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-180337 · Cited by 21

Mitochondrial vulnerability to oxidation in human brain organoids modelling Alzheimer's disease

Holubiec, M. I., Alloatti, M., Bianchelli, J., Greloni, F., Arnaiz, C., Gonzalez Prinz, M., Fernandez Bessone, I., Pozo Devoto, V., & Falzone, T. L. (2023) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2023.08.028 · Cited by 20

Pathogenesis, Animal Models, and Drug Discovery of Alzheimer’s Disease

Xia, Z.-D., Ma, R.-X., Wen, J.-F., Zhai, Y.-F., Wang, Y.-Q., Wang, F.-Y., Liu, D., Zhao, X.-L., Sun, B., Jia, P., et al. (2023) · Journal of Alzheimer's Disease · doi:10.3233/jad-230326 · Cited by 19

The new perspective of Alzheimer's Disease Research: Mechanism and therapeutic strategy of neuronal senescence

Niu, Q., Li, D., Zhang, J., Piao, Z., Xi, Y., Xi, Y., Kamal, N. N. S. N. M., Li, P., Li, P., & Yin, Y. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102593 · Cited by 19

Unraveling the cGAS-STING pathway in Alzheimer’s disease: A new Frontier in neuroinflammation and therapeutic strategies

Kaur, A., & Aran, K. R. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.04.001 · Cited by 23

Miro, a Rho GTPase genetically interacts with Alzheimer's disease-associated genes (Tau, Aβ42andAppl) inDrosophila melanogaster

Panchal, K., & Tiwari, A. K. (2020) · Biology Open · doi:10.1242/bio.049569 · Cited by 21

Methionine-Mediated Protein Phosphatase 2A Catalytic Subunit (PP2Ac) Methylation Ameliorates the Tauopathy Induced by Manganese in Cell and Animal Models

Wu, B., Cai, H., Tang, S., Xu, Y., Shi, Q., Wei, L., Meng, L., Zhang, N., Wang, X., Xiao, D., et al. (2020) · Neurotherapeutics · doi:10.1007/s13311-020-00930-6 · Cited by 19

Association between Acrylamide Hemoglobin Adduct Levels and Depressive Symptoms in US Adults: NHANES 2013–2016

Li, Z., Sun, J., & Zhang, D. (2021) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c04647 · Cited by 20

Ginsenoside Rf inhibits human tau proteotoxicity and causes specific LncRNA, miRNA and mRNA expression changes in Caenorhabditis elegans model of tauopathy

Zhang, S., Wang, H., Wang, J., Jin, W., Yan, X., Chen, X., Wang, D., Zhao, D., Wang, Y., Cong, D., et al. (2022) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2022.174887 · Cited by 19

Late-onset epilepsy and the risk of dementia: a systematic review and meta-analysis

Huang, L., Fu, C., Li, J., & Peng, S. (2022) · Aging Clinical and Experimental Research · doi:10.1007/s40520-022-02118-8 · Cited by 19

Cerebral Oxidative Stress in Early Alzheimer’s Disease Evaluated by 64Cu-ATSM PET/MRI: A Preliminary Study

Okazawa, H., Ikawa, M., Tsujikawa, T., Mori, T., Makino, A., Kiyono, Y., Nakamoto, Y., Kosaka, H., & Yoneda, M. (2022) · Antioxidants · doi:10.3390/antiox11051022 · Cited by 21

5-Methyltetrahydrofolate Alleviates Memory Impairment in a Rat Model of Alzheimer’s Disease Induced by D-Galactose and Aluminum Chloride

Zhang, Z., Wu, H., Qi, S., Tang, Y., Qin, C., Liu, R., Zhang, J., Cao, Y., & Gao, X. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph192416426 · Cited by 19

Discovery of Multitarget-Directed Ligands from Piperidine Alkaloid Piperine as a Cap Group for the Management of Alzheimer’s Disease

Bhanukiran, K., Singh, S. K., Singh, R., Kumar, A., & Hemalatha, S. (2023) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.3c00269 · Cited by 19

Monitoring Alzheimer’s disease via ultraweak photon emission

Sefati, N., Esmaeilpour, T., Salari, V., Zarifkar, A., Dehghani, F., Ghaffari, M. K., Zadeh‐Haghighi, H., Császár, N., Bókkon, I., Rodrigues, S., et al. (2023) · iScience · doi:10.1016/j.isci.2023.108744 · Cited by 20

TNF-α Levels Are Increased in Patients with Subjective Cognitive Impairment and Are Negatively Correlated with β Amyloid-42

Serafini, S., Ferretti, G., Monterosso, P., Angiolillo, A., Costanzo, A. D., & Matrone, C. (2024) · Antioxidants · doi:10.3390/antiox13020216 · Cited by 19

Effects of Supplementation with a Microalgae Extract from Phaeodactylum tricornutum Containing Fucoxanthin on Cognition and Markers of Health in Older Individuals with Perceptions of Cognitive Decline

Yoo, C., Maury, J., Gonzalez, D. E., Ko, J., Xing, D., Jenkins, V. M., Dickerson, B. L., Leonard, M., Estes, L., Johnson, S., et al. (2024) · Nutrients · doi:10.3390/nu16172999 · Cited by 21

p62/sequestosome-1 knockout delays neurodegeneration induced by Drp1 loss

Yamada, T., Adachi, Y., Yanagawa, T., Iijima, M., & Sesaki, H. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.05.012 · Cited by 18

Galantamine-memantine combination superior to donepezil-memantine combination in Alzheimer's disease: critical dissection with an emphasis on kynurenic acid and mismatch negativity.

Koola, M. M., Nikiforuk, A., Pillai, A., & Parsaik, A. K. (2018) · PubMed · Cited by 19

Synaptic Activity and (Neuro)Inflammation in Alzheimer’s Disease: Could Exosomes be an Additional Link?

Counil, H., & Krantic, S. M. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-191237 · Cited by 20

Application of Nanomaterials in Neurodegenerative Diseases

Cui, W., Fu, W., Lin, Y., & Zhang, T. (2020) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x15666200326093410 · Cited by 20

Deciphering Alzheimer’s disease: predicting new therapeutic strategies via improved understanding of biology and pathogenesis

Khoury, R., & Grossberg, G. T. (2020) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2020.1790530 · Cited by 19

Novel Acetylcholinesterase Inhibitors Based on Uracil Moiety for Possible Treatment of Alzheimer Disease

Semenov, V. E., Zueva, I. V., Mukhamedyarov, M. A., Lushchekina, S. V., Petukhova, E. O., Gubaidullina, L. M., Krylova, E. S., Saifina, L. F., Lenina, O. A., & Petrov, K. A. (2020) · Molecules · doi:10.3390/molecules25184191 · Cited by 19

An Analysis of the Neurological and Molecular Alterations Underlying the Pathogenesis of Alzheimer’s Disease

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