Neuropharmacological Effects of Quercetin: A Literature-Based Review

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 · see citing works

Mechanisms underlying inflammation in neurodegeneration

Glass, C. K., Saijo, K., Winner, B., Marchetto, M. C., & Gage, F. H. (2010) · Cell · doi:10.1016/j.cell.2010.02.016 · Cited by 3,580 · see citing works

Oxidative Stress and Neurodegenerative Diseases: A Review of Upstream and Downstream Antioxidant Therapeutic Options

Uttara, B., Singh, A., Zamboni, P., & Mahajan, R. (2009) · Current Neuropharmacology · doi:10.2174/157015909787602823 · Cited by 3,378 · see citing works

Acetylcholinesterase Inhibitors: Pharmacology and Toxicology

Colovic, M. B., Krstic, D. Z., Lazarevic-Pasti, T. D., Bondzic, A. M., & Vasic, V. M. (2013) · Current Neuropharmacology · doi:10.2174/1570159x11311030006 · Cited by 2,611 · see citing works

Excitotoxic cell death

Choi, D. W. (1992) · Journal of Neurobiology · doi:10.1002/neu.480230915 · Cited by 2,304 · see citing works

The role of autophagy in neurodegenerative disease

Nixon, R. A. (2013) · Nature Medicine · doi:10.1038/nm.3232 · Cited by 2,059 · see citing works

Lifestyle, oxidative stress, and antioxidants: Back and forth in the pathophysiology of chronic diseases

Sharifi-Rad, M., Anil Kumar, N. V., Zucca, P., Varoni, E. M., Dini, L., Panzarini, E., Rajkovic, J., Tsouh Fokou, P. V., Azzini, E., Peluso, I., et al. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00694 · Cited by 1,971 · see citing works

Aggregation of alpha-synuclein in Lewy bodies of sporadic Parkinson's disease and dementia with Lewy bodies.

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The microglial sensome revealed by direct RNA sequencing

Hickman, S. E., Kingery, N. D., Ohsumi, T. K., Borowsky, M. L., Wang, L.-C., Means, T. K., & El Khoury, J. (2013) · Nature Neuroscience · doi:10.1038/nn.3554 · Cited by 1,511 · see citing works

Molecular mechanisms of excitotoxicity and their relevance to pathogenesis of neurodegenerative diseases

Dong, X.-X., Wang, Y., & Qin, Z.-H. (2009) · Acta Pharmacologica Sinica · doi:10.1038/aps.2009.24 · Cited by 1,297 · see citing works

Role of Pro-Inflammatory Cytokines Released from Microglia in Neurodegenerative Diseases

Smith, J. A., Das, A., Ray, S. K., & Banik, N. L. (2012) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2011.10.004 · Cited by 1,165 · see citing works

Solid Lipid Nanoparticles and Nanostructured Lipid Carriers: Structure, Preparation and Application

Naseri, N., Valizadeh, H., & Zakeri‐Milani, P. (2015) · Advanced Pharmaceutical Bulletin · doi:10.15171/apb.2015.043 · Cited by 1,115 · see citing works

K -Profiles: A Nonlinear Clustering Method for Pattern Detection in High Dimensional Data

Wang, K., Zhao, Q., Lu, J., & Yu, T. (2015) · BioMed Research International · doi:10.1155/2015/918954 · Cited by 989 · see citing works

Mechanism of Oxidative Stress in Neurodegeneration

Gandhi, S., & Abramov, A. Y. (2012) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2012/428010 · Cited by 964 · see citing works

Flavonoids Protect Neuronal Cells from Oxidative Stress by Three Distinct Mechanisms

Ishige, K., Schubert, D., & Sagara, Y. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00498-6 · Cited by 841 · see citing works

Oxidative stress induced-neurodegenerative diseases: the need for antioxidants that penetrate the blood brain barrier

Gilgun‐Sherki, Y., Melamed, E., & Offen, D. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(01)00019-3 · Cited by 839 · see citing works

Dietary Quercetin and Kaempferol: Bioavailability and Potential Cardiovascular-Related Bioactivity in Humans

Dabeek, W. M., & Marra, M. V. (2019) · Nutrients · doi:10.3390/nu11102288 · Cited by 834 · see citing works

Calcium, ischemia and excitotoxicity

Szydłowska, K., & Tymianski, M. (2010) · Cell Calcium · doi:10.1016/j.ceca.2010.01.003 · Cited by 762 · see citing works

Neuroinflammation: The role and consequences

Lyman, M., Lloyd, D. G., Ji, X., Vizcaychipi, M. P., & Ma, D. (2013) · Neuroscience Research · doi:10.1016/j.neures.2013.10.004 · Cited by 740 · see citing works

A review on cholinesterase inhibitors for Alzheimer’s disease

Anand, P., & Singh, B. (2013) · Archives of Pharmacal Research · doi:10.1007/s12272-013-0036-3 · Cited by 722 · see citing works

The Pharmacological Activity, Biochemical Properties, and Pharmacokinetics of the Major Natural Polyphenolic Flavonoid: Quercetin

Batiha, G. E., Beshbishy, A. M., Ikram, M., Mulla, Z. S., El-Hack, M. E. A., Taha, A. E.-S., Algammal, A. M., & Elewa, Y. H. A. (2020) · Foods · doi:10.3390/foods9030374 · Cited by 716 · see citing works

Expression of Concern: Potent anti‐amyloidogenic and fibril‐destabilizing effects of polyphenols in vitro: implications for the prevention and therapeutics of Alzheimer's disease

Ono, K., Yoshiike, Y., Takashima, A., Hasegawa, K., Naiki, H., & Yamada, M. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01976.x · Cited by 681 · see citing works

Quercetin: Its Main Pharmacological Activity and Potential Application in Clinical Medicine

Yang, D., Wang, T., Long, M., & Li, P. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/8825387 · Cited by 647 · see citing works

Flavonoid permeability across an in situ model of the blood–brain barrier

Youdim, K. A., Qaiser, M. Z., Begley, D. J., Rice-Evans, C. A., & Abbott, N. J. (2003) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2003.11.023 · Cited by 605 · see citing works

Nanoencapsulation of Promising Bioactive Compounds to Improve Their Absorption, Stability, Functionality and the Appearance of the Final Food Products

Pateiro, M., Gómez, B., Munekata, P. E. S., Barba, F. J., Putnik, P., Kovačević, D. B., & Lorenzo, J. M. (2021) · Molecules · doi:10.3390/molecules26061547 · Cited by 603 · see citing works

Neuroprotective Effects of Quercetin in Alzheimer’s Disease

Khan, H. Z., Ullah, H., Aschner, M., Cheang, W. S., & Akkol, E. K. (2019) · Biomolecules · doi:10.3390/biom10010059 · Cited by 541 · see citing works

Alzheimer's disease results from the cerebral accumulation and cytotoxicity of amyloid ß-protein

Selkoe, D. J. (2001) · Journal of Alzheimer s Disease · doi:10.3233/jad-2001-3111 · Cited by 538 · see citing works

Application of nanotechnology in improving bioavailability and bioactivity of diet-derived phytochemicals

Wang, S. F., Su, R., Nie, S., Sun, M., Zhang, J., Wu, D., & Moustaïd‐Moussa, N. (2013) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2013.10.002 · Cited by 532 · see citing works

Mitochondrial Dysfunction and Reactive Oxygen Species in Excitotoxicity and Apoptosis: Implications for the Pathogenesis of Neurodegenerative Diseases

Rego, A. C., & Oliveira, C. R. (2003) · Neurochemical Research · doi:10.1023/a:1025682611389 · Cited by 472 · see citing works

Butyrylcholinesterase: An Important New Target in Alzheimer’s Disease Therapy

Greig, N. H., Lahiri, D. K., & Sambamurti, K. (2002) · International Psychogeriatrics · doi:10.1017/s1041610203008676 · Cited by 468 · see citing works

The Synaptic Accumulation of Hyperphosphorylated Tau Oligomers in Alzheimer Disease Is Associated With Dysfunction of the Ubiquitin-Proteasome System

Tai, H., Serrano‐Pozo, A., Hashimoto, T., Frosch, M. P., Spires‐Jones, T. L., & Hyman, B. T. (2012) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.06.033 · Cited by 456 · see citing works

The flavonoid quercetin ameliorates Alzheimer's disease pathology and protects cognitive and emotional function in aged triple transgenic Alzheimer's disease model mice

Sabogal-Guáqueta, A. M., Muñoz‐Manco, J. I., Ramírez‐Pineda, J. R., Lamprea, M. R., Osorio, E., & Cardona‐Gómez, G. P. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.01.027 · Cited by 453 · see citing works

Anti-inflammatory mechanism of intravascular neural stem cell transplantation in haemorrhagic stroke

Lee, S.-T., Chu, K., Jung, K.-H., Kim, S.-J., Kim, D.-H., Kang, K.-M., Hong, N. H., Kim, J.-H., Ban, J.-J., Park, H.-K., et al. (2008) · Brain · doi:10.1093/brain/awm306 · Cited by 424 · see citing works

Protective effect of quercetin in primary neurons against Aβ(1–42): relevance to Alzheimer's disease

Ansari, M. A., Abdul, H. M., Gururaj Joshi, A., Opii, W. O., & Butterfield, D. A. (2008) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2008.03.002 · Cited by 421 · see citing works

Microtubule-associated protein tau in development, degeneration and protection of neurons

Wang, J., & Liu, F. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.03.002 · Cited by 395 · see citing works

Molecular pharmacology of glutamate transporters, EAATs and VGLUTs

Shigeri, Y., Seal, R. P., & Shimamoto, K. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.04.004 · Cited by 391 · see citing works

Antioxidant Therapies for Alzheimer's Disease

Feng, Y., & Wang, X. (2012) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2012/472932 · Cited by 382 · see citing works

Pharmacological Properties of Chalcones: A Review of Preclinical Including Molecular Mechanisms and Clinical Evidence

Salehi, B., Quispe, C., Chamkhi, I., Omari, N. E., Balahbib, A., Sharifi‐Rad, J., Bouyahya, A., Akram, M., Iqbal, M., Docea, A. O., et al. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.592654 · Cited by 353 · see citing works

Natural AChE Inhibitors from Plants and their Contribution to Alzheimer’s Disease Therapy

Murray, A. P., Faraoni, M. B., Castro, M., Alza, N. P., & Cavallaro, V. (2013) · Current Neuropharmacology · doi:10.2174/1570159x11311040004 · Cited by 352 · see citing works

Memantine and Cholinesterase Inhibitors: Complementary Mechanisms in the Treatment of Alzheimer’s Disease

Parsons, C. G., Danysz, W., Dekundy, A., & Pulte, I. (2013) · Neurotoxicity Research · doi:10.1007/s12640-013-9398-z · Cited by 337 · see citing works

Resveratrol and quercetin, two natural polyphenols, reduce apoptotic neuronal cell death induced by neuroinflammation

Bureau, G., Longpré, F., & Martinoli, M. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21503 · Cited by 336 · see citing works

The Role of Inflammatory and Oxidative Stress Mechanisms in the Pathogenesis of Parkinson’s Disease: Focus on Astrocytes

Niranjan, R. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8483-x · Cited by 331 · see citing works

Quercetin and related polyphenols: new insights and implications for their bioactivity and bioavailability

Kawabata, K., Mukai, R., & Ishisaka, A. (2015) · Food & Function · doi:10.1039/c4fo01178c · Cited by 327 · see citing works

Neuroprotective effects of antioxidative flavonoids, quercetin, (+)-dihydroquercetin and quercetin 3-methyl ether, isolated from Opuntia ficus-indica var. saboten

Dok-Go, H., Lee, K. H., Kim, H. J., Lee, E. H., Lee, J., Song, Y. S., Lee, Y.-H., Jin, C., Lee, Y. S., & Cho, J. (2003) · Brain Research · doi:10.1016/s0006-8993(02)04150-1 · Cited by 314 · see citing works

Molecular mechanisms underlying protective role of quercetin in attenuating Alzheimer's disease

Zaplatić, E., Bule, M. H., Shah, S. Z. A., Uddin, M. S., & Niaz, K. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.03.055 · Cited by 298 · see citing works

Effects of Naturally Occurring Compounds on Fibril Formation and Oxidative Stress of β-Amyloid

Kim, H., Park, B., Lee, K., Choi, C. Y., Jang, S. S., Kim, Y., & Lee, S. (2005) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf051985c · Cited by 297 · see citing works

Diet, Lifestyle and Cardiovascular Diseases: Linking Pathophysiology to Cardioprotective Effects of Natural Bioactive Compounds

Sharifi‐Rad, J., Rodrigues, C. F., Sharopov, F. S., Docea, A. O., Karaça, A. C., Sharifi‐Rad, M., Kahveci, D., Gülseren, G., Şenol, E., Demircan, E., et al. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17072326 · Cited by 295 · see citing works

The Therapeutic Potential of Anthocyanins: Current Approaches Based on Their Molecular Mechanism of Action

Salehi, B., Sharifi-Rad, J., Cappellini, F., Reiner, Ž., Zorzan, D., Imran, M., Sener, B., Kilic, M., El-Shazly, M., Fahmy, N. M., et al. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.01300 · Cited by 293 · see citing works

Improved Oral Absorption of Quercetin from Quercetin Phytosome®, a New Delivery System Based on Food Grade Lecithin

Riva, A., Ronchi, M., Petrangolini, G., Bosisio, S., & Allegrini, P. (2018) · European Journal of Drug Metabolism and Pharmacokinetics · doi:10.1007/s13318-018-0517-3 · Cited by 291 · see citing works

Protective and Toxic Neuroinflammation in Amyotrophic Lateral Sclerosis

Hooten, K. G., Beers, D. R., Zhao, W., & Appel, S. H. (2015) · Neurotherapeutics · doi:10.1007/s13311-014-0329-3 · Cited by 287 · see citing works

Antioxidant Properties of Quercetin

Zhang, M., Swarts, S. G., Yin, L., Liu, C., Tian, Y., Cao, Y., Swarts, M., Yang, S., Zhang, S. B., Zhang, K., et al. (2011) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-7756-4_38 · Cited by 278 · see citing works

Bioavailability and metabolism of the flavonol quercetin in the pig

Ader, P. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00195-7 · Cited by 273 · see citing works

Acetylcholinesterase Inhibition by Flavonoids from Agrimonia pilosa

Jung, M., & Park, M. (2007) · Molecules · doi:10.3390/12092130 · Cited by 270 · see citing works

Inhibition of iNOS gene expression by quercetin is mediated by the inhibition of IκB kinase, nuclear factor-kappa B and STAT1, and depends on heme oxygenase-1 induction in mouse BV-2 microglia

Chen, J.-C., Ho, F., Chao, P.-D. L., Chen, C., Jeng, K.-C. G., Hsu, H.-B., Lee, S. T., Wu, W. T., & Lin, W. (2005) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2005.08.005 · Cited by 266 · see citing works

Impact of Natural Compounds on Neurodegenerative Disorders: From Preclinical to Pharmacotherapeutics

Sharifi‐Rad, M., Lankatillake, C., Dias, D. A., Docea, A. O., Mahomoodally, M. F., Lobine, D., Chazot, P. L., Kurt, B., Tumer, T. B., Moreira, A. C., et al. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9041061 · Cited by 260 · see citing works

Endogenous and exogenous mediators of quercetin bioavailability

Guo, Y., & Bruno, R. S. (2014) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2014.10.008 · Cited by 257 · see citing works

Quercetin and rutin prevent scopolamine-induced memory impairment in zebrafish

Richetti, S. K., Blank, M., Capiotti, K. M., Piato, Â., Bogo, M. R., Vianna, M. R. M. R., & Bonan, C. D. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.09.027 · Cited by 248 · see citing works

Multisite protein phosphorylation – from molecular mechanisms to kinetic models

Salazar, C., & Höfer, T. (2009) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07027.x · Cited by 247 · see citing works

Elevation of oxidative free radicals in Alzheimer's disease models can be attenuated by Ginkgo biloba extract EGb 761

Smith, J. V., & Luo, Y. (2003) · Journal of Alzheimer s Disease · doi:10.3233/jad-2003-5404 · Cited by 243 · see citing works

Quercetin and rutin exhibit antiamyloidogenic and fibril-disaggregating effects in vitro and potent antioxidant activity in APPswe cells

Jiménez‐Aliaga, K., Bermejo‐Bescós, P., Benedı́, J., & Martín‐Aragón, S. (2011) · Life Sciences · doi:10.1016/j.lfs.2011.09.023 · Cited by 239 · see citing works

Bioactive effects of quercetin in the central nervous system: Focusing on the mechanisms of actions

Suganthy, N., Devi, K. P., Nabavi, S. F., Braidy, N., & Nabavi, S. M. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.10.011 · Cited by 236 · see citing works

Flavonols and flavones as BACE-1 inhibitors: Structure–activity relationship in cell-free, cell-based and in silico studies reveal novel pharmacophore features

Shimmyo, Y., Kihara, T., Akaike, A., Niidome, T., & Sugimoto, H. (2008) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2008.01.017 · Cited by 234 · see citing works

Specificity and Regulation of Casein Kinase-Mediated Phosphorylation of ??-Synuclein

Waxman, E. A., & Giasson, B. I. (2008) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3186fc995 · Cited by 232 · see citing works

Quercetin up-regulates mitochondrial complex-I activity to protect against programmed cell death in rotenone model of Parkinson’s disease in rats

Karuppagounder, S. S., Madathil, S. K., Pandey, M., Haobam, R., Rajamma, U., & Mohanakumar, K. P. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.01.032 · Cited by 225 · see citing works

Modulation of neurotrophic signaling pathways by polyphenols

Firuzi, O., Moosavi, F., Hosseini, R., & Saso, L. (2015) · Drug Design Development and Therapy · doi:10.2147/dddt.s96936 · Cited by 224 · see citing works

Immobilized Concentration Gradients of Neurotrophic Factors Guide Neurite Outgrowth of Primary Neurons in Macroporous Scaffolds

Moore, K., Macsween, M., & Shoichet, M. S. (2006) · Tissue Engineering · doi:10.1089/ten.2006.12.267 · Cited by 221 · see citing works

Anti-ageing and rejuvenating effects of quercetin

Chondrogianni, N., Kapeta, S., Chinou, İ., Vassilatou, K., Papassideri, I. S., & Gonos, E. S. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.07.001 · Cited by 220 · see citing works

After Cellular Internalization, Quercetin Causes Nrf2 Nuclear Translocation, Increases Glutathione Levels, and Prevents Neuronal Death against an Oxidative Insult

Arredondo, F., Echeverry, C., Abin-Carriquiry, J. A., Blasina, F., Antúnez, K., Jones, D. P., Go, Y.-M., Liang, Y.-L., & Dajas, F. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.05.020 · Cited by 220 · see citing works

Inflammatory Process in Alzheimer's and Parkinson's Diseases: Central Role of Cytokines

Alam, Q., Alam, M. Z., Mushtaq, G., Damanhouri, G. A., Rasool, M., Kamal, M. A., & Haque, A. (2016) · Current Pharmaceutical Design · doi:10.2174/1381612822666151125000300 · Cited by 220 · see citing works

Hepatoprotective effect of quercetin: From chemistry to medicine

Miltonprabu, S., Tomczyk, M., Skalicka‐Woźniak, K., Rastrelli, L., Daglia, M., Nabavi, S. F., Alavian, S. M., & Nabavi, S. M. (2016) · Food and Chemical Toxicology · doi:10.1016/j.fct.2016.08.034 · Cited by 217 · see citing works

A Nondegenerate Code of Deleterious Variants in Mendelian Loci Contributes to Complex Disease Risk

Blair, D. R., Lyttle, C. S., Mortensen, J. M., Bearden, C. F., Jensen, A. B., Khiabanian, H., Melamed, R., Rabadan, R., Bernstam, E. V., Brunak, S., et al. (2013) · Cell · doi:10.1016/j.cell.2013.08.030 · Cited by 215 · see citing works

A Novel Anti-Inflammatory and Pro-Resolving Role for Resolvin D1 in Acute Cigarette Smoke-Induced Lung Inflammation

Hsiao, H.-M., Sapinoro, R., Thatcher, T. H., Croasdell, A., Levy, E. P., Fulton, R. A., Olsen, K. C., Pollock, S. J., Serhan, C. N., Phipps, R. P., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058258 · Cited by 212 · see citing works

Acute Effect of Hypervolemic Hemodilution on Retrobulbar Hemodynamics in Anterior Ischemic Optic Neuropathy

Bienert, M., Plange, N., Remky, A., Arend, O., & Kuerten, D. (2018) · BioMed Research International · doi:10.1155/2018/4756313 · Cited by 207 · see citing works

Identification of brain‐targeted bioactive dietary quercetin‐3‐ O ‐glucuronide as a novel intervention for Alzheimer's disease

Ho, L., Ferruzzi, M. G., Janle, E. M., Wang, J., Gong, B., Chen, T., Lobo, J., Cooper, B. R., Wu, Q. L., Talcott, S. T., et al. (2012) · The FASEB Journal · doi:10.1096/fj.12-212118 · Cited by 204 · see citing works

Modulation of interleukin-1β mediated inflammatory response in human astrocytes by flavonoids: Implications in neuroprotection

Sharma, V., Mishra, M., Ghosh, S., Tewari, R., Basu, A., Seth, P., & Sen, E. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2007.01.016 · Cited by 202 · see citing works

Insights into Neuroinflammation in Parkinson’s Disease: From Biomarkers to Anti-Inflammatory Based Therapies

Rocha, N. P., de Miranda, A. S., & Teixeira, A. L. (2015) · BioMed Research International · doi:10.1155/2015/628192 · Cited by 200 · see citing works

Evaluation of antioxidant and nitric oxide inhibitory activities of selected Malaysian medicinal plants

Saha, K., Lajis, N. H., Israf, D. A., Hamzah, A. S., Khozirah, S., Khamis, S., & Syahida, A. (2004) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2004.03.007 · Cited by 198 · see citing works

Amyloid β, Glutamate, Excitotoxicity in Alzheimer's Disease: Are We on the Right Track?

Esposito, Z., Belli, L., Toniolo, S., Sancesario, G., Bianconi, C., & Martorana, A. (2013) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12095 · Cited by 198 · see citing works

Curcumin’s Nanomedicine Formulations for Therapeutic Application in Neurological Diseases

Salehi, B., Călina, D. C., Docea, A. O., Koirala, N., Aryal, S., Lombardo, D., Pasqua, L., Taheri, Y., Castillo, C. M. S., Martorell, M., et al. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9020430 · Cited by 197 · see citing works

Quercetin inhibition of ROS-dependent and -independent apoptosis in rat glioma C6 cells

Chen, T.-J., Jeng, J.-Y., Lin, C., Wu, C.-Y., & Chen, Y. (2006) · Toxicology · doi:10.1016/j.tox.2006.03.007 · Cited by 192 · see citing works

Quercetin lipid nanoparticles functionalized with transferrin for Alzheimer's disease

Pinheiro, R. G. R., Granja, A., Loureiro, J. A., Pereira, M. D. C., Pinheiro, M., Neves, A. R., & Reis, S. (2020) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2020.105314 · Cited by 190 · see citing works

Quercetin reverses d-galactose induced neurotoxicity in mouse brain

Lu, J. L., Zheng, Y., Luo, L., Wu, D., Sun, D., & You-jian, F. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.03.043 · Cited by 187 · see citing works

Quercetin activates AMP‐activated protein kinase by reducing PP2C expression protecting old mouse brain against high cholesterol‐induced neurotoxicity

Lu, J. L., Wu, D., Zheng, Y., Hu, B., Zhang, Z., Shan, Q., Zheng, Z., Liu, C., & Wang, Y. (2010) · The Journal of Pathology · doi:10.1002/path.2754 · Cited by 186 · see citing works

Cholinergic Signaling Controls Conditioned Fear Behaviors and Enhances Plasticity of Cortical-Amygdala Circuits

Jiang, L., Kundu, S., Lederman, J., López‐Hernández, G. Y., Ballinger, E. C., Wang, S., Talmage, D. A., & Role, L. W. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.028 · Cited by 186 · see citing works

Cinnamomum Species: Bridging Phytochemistry Knowledge, Pharmacological Properties and Toxicological Safety for Health Benefits

Sharifi-Rad, J., Dey, A., Koirala, N., Shaheen, S., El Omari, N., Salehi, B., Goloshvili, T., Cirone Silva, N. C., Bouyahya, A., Vitalini, S., et al. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.600139 · Cited by 183 · see citing works

Current Concepts of Neurodegenerative Mechanisms in Alzheimer’s Disease

Magalingam, K. B., Radhakrishnan, A., Ping, N. S., & Haleagrahara, N. (2018) · BioMed Research International · doi:10.1155/2018/3740461 · Cited by 178 · see citing works

Quercetin Attenuates Inflammatory Responses in BV-2 Microglial Cells: Role of MAPKs on the Nrf2 Pathway and Induction of Heme Oxygenase-1

Sun, G. Y., Chen, Z., Jasmer, K. J., Chuang, D. Y., Gu, Z., Hannink, M., & Simonyi, Á. (2015) · PLoS ONE · doi:10.1371/journal.pone.0141509 · Cited by 177 · see citing works

Quercetin supplementation is effective in improving mitochondrial dysfunctions induced by 3-nitropropionic acid: Implications in Huntington's disease

Sandhir, R., & Mehrotra, A. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2012.11.018 · Cited by 171 · see citing works

SIRT1 stimulation by polyphenols is affected by their stability and metabolism

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Cognitive-Enhancing Effect of Quercetin in a Rat Model of Parkinson's Disease Induced by 6-Hydroxydopamine

Sriraksa, N., Wattanathorn, J., Muchimapura, S., Tiamkao, S., Brown, K., & Chaisiwamongkol, K. (2011) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2012/823206 · Cited by 164 · see citing works

Stimulation of Neurogenesis and Synaptogenesis by Bilobalide and Quercetin via Common Final Pathway in Hippocampal Neurons

Tchantchou, F., Lacor, P. N., Cao, Z., Lao, L., Hou, Y., Cui, C., Klein, W. L., & Luo, Y. (2009) · Journal of Alzheimer s Disease · doi:10.3233/jad-2009-1189 · Cited by 163 · see citing works

Disease‐modifying therapies in Alzheimer's disease

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Cucurbits Plants: A Key Emphasis to Its Pharmacological Potential

Salehi, B., Çapanoğlu, E., Adrar, N., Çatalkaya, G., Shaheen, S., Jaffer, M., Giri, L., Suyal, R., Jugran, A. K., Călina, D. C., et al. (2019) · Molecules · doi:10.3390/molecules24101854 · Cited by 160 · see citing works

Protective effects of Ginkgo biloba extract (EGb761) and its constituents quercetin and ginkgolide B against β-amyloid peptide-induced toxicity in SH-SY5Y cells

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Quercetin and Sesamin Protect Dopaminergic Cells from MPP+-Induced Neuroinflammation in a Microglial (N9)-Neuronal (PC12) Coculture System

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Quercetin Improves Behavioral Deficiencies, Restores Astrocytes and Microglia, and Reduces Serotonin Metabolism in 3‐Nitropropionic Acid‐Induced Rat Model of Huntington's Disease

Chakraborty, J., Singh, R. P., Dutta, D., Naskar, A., Rajamma, U., & Mohanakumar, K. P. (2013) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12189 · Cited by 145 · see citing works

Quercetin attenuates neuronal death against aluminum-induced neurodegeneration in the rat hippocampus

Sharma, D. R., Wani, W. Y., Sunkaria, A., Kandimalla, R. J., Sharma, R. K., Verma, D., Bal, A., & Gill, K. D. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.02.055 · Cited by 144 · see citing works

A Mechanistic and Pathophysiological Approach for Stroke Associated with Drugs of Abuse

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Amyloid‐beta ( A β1–42)‐induced paralysis in C aenorhabditis elegans is inhibited by the polyphenol quercetin through activation of protein degradation pathways

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Anti-depressant natural flavonols modulate BDNF and beta amyloid in neurons and hippocampus of double TgAD mice

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Ficusplants: State of the art from a phytochemical, pharmacological, and toxicological perspective

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Acetylcholine receptors in dementia and mild cognitive impairment

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Induction of Zygotic Polyembryos in Wheat: Influence of Auxin Polar Transport

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Anti‐Inflammatory Effect of Quercetin on RAW 264.7 Mouse Macrophages Induced with Polyinosinic‐Polycytidylic Acid

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A dietary regimen of caloric restriction or pharmacological activation of SIRT1 to delay the onset of neurodegeneration

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Recent Updates in the Treatment of Neurodegenerative Disorders Using Natural Compounds

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An Alzheimer's disease-specific β-amyloid fragment signature in cerebrospinal fluid

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Oxidative Stress and Inflammation Interdependence in Multiple Sclerosis

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Quercetin protects the impairment of memory and anxiogenic-like behavior in rats exposed to cadmium: Possible involvement of the acetylcholinesterase and Na+,K+-ATPase activities

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Protective effects of hyperoside (quercetin-3-o-galactoside) to PC12 cells against cytotoxicity induced by hydrogen peroxide and tert-butyl hydroperoxide

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Citrus Flavonoids Luteolin, Apigenin, and Quercetin Inhibit Glycogen Synthase Kinase-3β Enzymatic Activity by Lowering the Interaction Energy Within the Binding Cavity

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Regulation of IL‐1‐induced selective IL‐6 release from human mast cells and inhibition by quercetin

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Flavonoids inhibit myelin phagocytosis by macrophages; a structure–activity relationship study

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Oxidized quercetin inhibits α-synuclein fibrillization

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Tissue tears in the white matter after lateral fluid percussion brain injury in the rat: relevance to human brain injury

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Protective effects of quercetin against hydrogen peroxide-induced apoptosis in human neuronal SH-SY5Y cells

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Quercetin and interferon-β modulate immune response(s) in peripheral blood mononuclear cells isolated from multiple sclerosis patients

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Effect of Quercetin in the 1-Methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine-Induced Mouse Model of Parkinson's Disease

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Loading into Nanoparticles Improves Quercetin's Efficacy in Preventing Neuroinflammation Induced by Oxysterols

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Effect of Quercetin on PC12 Alzheimer’s Disease Cell Model Induced by Aβ25-35 and Its Mechanism Based on Sirtuin1/Nrf2/HO‐1 Pathway

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Quercetin Modulates NF-κ B and AP-1/JNK Pathways to Induce Cell Death in Human Hepatoma Cells

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Quercetin enhances TRAIL-induced apoptosis in prostate cancer cells via increased protein stability of death receptor 5

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Quercetin-mediated longevity in Caenorhabditis elegans: Is DAF-16 involved?

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Allium Flavonols: Health Benefits, Molecular Targets, and Bioavailability

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Avocado–Soybean Unsaponifiables: A Panoply of Potentialities to Be Exploited

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Quercetin, kaempferol and biapigenin fromhypericum perforatum are neuroprotective against excitotoxic insults

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Differential effects of quercetin on hippocampus-dependent learning and memory in mice fed with different diets related with oxidative stress

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Reversal of Aging and Chronic Ethanol-induced Cognitive Dysfunction by Quercetin a Bioflavonoid

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Synergistic neuroprotection by epicatechin and quercetin: Activation of convergent mitochondrial signaling pathways

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Antiepileptic potential of flavonoids fraction from the leaves of Anisomeles malabarica

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Antidepressant-like effect of quercetin in bulbectomized mice and involvement of the antioxidant defenses, and the glutamatergic and oxidonitrergic pathways

Holzmann, I., da Silva, L. M., da Silva, J. A. C., Steimbach, V. M. B., & de Souza, M. M. (2015) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2015.07.003 · Cited by 92 · see citing works

Paraoxonase-2 (PON2) in brain and its potential role in neuroprotection

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Epibatidine: A Promising Natural Alkaloid in Health

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Veronica Plants—Drifting from Farm to Traditional Healing, Food Application, and Phytopharmacology

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Quercetin Reverses Hypobaric Hypoxia-Induced Hippocampal Neurodegeneration and Improves Memory Function in the Rat

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Role of Quercetin Benefits in Neurodegeneration

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Quercetin Protects Against Chronic Aluminum-Induced Oxidative Stress and Ensuing Biochemical, Cholinergic, and Neurobehavioral Impairments in Rats

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Neuroprotective effects of quercetin in a mouse model of brain ischemic/reperfusion injury via anti-apoptotic mechanisms based on the Akt pathway

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Quercetin stabilizes apolipoprotein E and reduces brain Aβ levels in amyloid model mice

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The Potential Neuroprotective Role of Free and Encapsulated Quercetin Mediated by miRNA against Neurological Diseases

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Effect of quercetin and rutin in some acute seizure models in mice

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Quercetin alleviates high glucose-induced Schwann cell damage by autophagy

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Protective effect of quercetin against ICV colchicine‐induced cognitive dysfunctions and oxidative damage in rats

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The good and the bad of neuroinflammation in multiple sclerosis

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Pharmacological Activities of Psoralidin: A Comprehensive Review of the Molecular Mechanisms of Action

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In silico QSAR analysis of quercetin reveals its potential as therapeutic drug for Alzheimer's disease

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Characterization of kinases involved in the phosphorylation of aggregated α‐synuclein

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Protective effects of quercetin glycosides, rutin, and isoquercetrin against 6-hydroxydopamine (6-OHDA)-induced neurotoxicity in rat pheochromocytoma (PC-12) cells

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Enhanced neuroprotective effect of fish oil in combination with quercetin against 3‐nitropropionic acid induced oxidative stress in rat brain

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Quercetin improves cognitive deficits in rats with chronic cerebral ischemia and inhibits voltage‐dependent sodium channels in hippocampal CA1 pyramidal neurons

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Flavonoids as potential anti-platelet aggregation agents: from biochemistry to health promoting abilities

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Effects of quercetin on oxidative stress and memory retrieval in kindled rats

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Protective effects of flavonol isoquercitrin, against 6-hydroxy dopamine (6-OHDA) - induced toxicity in PC12 cells

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Acetylcholinesterase-amyloid-β-peptide interaction and Wnt signaling involvement in Aβ neurotoxicity

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Neuroprotective Effects of Quercetin: From Chemistry to Medicine

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Chronic administration of quercetin prevent spatial learning and memory deficits provoked by chronic stress in rats

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Pretreatment with Natural Flavones and Neuronal Cell Survival after Oxidative Stress: A Structure−Activity Relationship Study

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Effect of quercetin on learning and memory performance in ICR mice under neurotoxic trimethyltin exposure

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Therapeutic effects of quercetin on early inflammation in hypertriglyceridemia-related acute pancreatitis and its mechanism

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Neuroprotective effect of quercetin in ectoenzymes and acetylcholinesterase activities in cerebral cortex synaptosomes of cadmium-exposed rats

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Quercetin-3-O-β-d-glucopyranoside, a dietary flavonoid, protects PC12 cells from H2O2-induced cytotoxicity through inhibition of reactive oxygen species

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Effect of Quercetin on Paraoxonase 2 Levels in RAW264.7 Macrophages and in Human Monocytes—Role of Quercetin Metabolism

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Protective effects of onion-derived quercetin on glutamate-mediated hippocampal neuronal cell death

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Nephroprotective activities of quercetin with potential relevance to oxidative stress induced by valproic acid

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The Treatment of Cognitive, Behavioural and Motor Impairments from Brain Injury and Neurodegenerative Diseases through Cannabinoid System Modulation—Evidence from In Vivo Studies

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Quercetin attenuates spontaneous behavior and spatial memory impairment in d-galactose–treated mice by increasing brain antioxidant capacity

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Neurodegenerative diseases and neuroprotection: current views and prospects

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Molecular and cellular stratagem of brain metastases associated with melanoma (Review)

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Erratum to: Nephroprotective activities of quercetin with potential relevance to oxidative stress induced by valproic acid

Chaudhary, S., Ganjoo, P., Raisuddin, S., & Parvez, S. (2014) · PROTOPLASMA · doi:10.1007/s00709-014-0688-y · Cited by 53 · see citing works

Quercetin Stimulates NGF-induced Neurite Outgrowth in PC12 Cells via Activation of Na+/K+/2Cl- Cotransporter

Nakajima, K.-I., Niisato, N., & Marunaka, Y. (2011) · Cellular Physiology and Biochemistry · doi:10.1159/000331723 · Cited by 52 · see citing works

Quercetin reduces eIF2α phosphorylation by GADD34 induction

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Modulation of BV-2 microglia functions by novel quercetin pivaloyl ester

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Combination of lycopene, quercetin and poloxamer188 alleviates anxiety and depression in 3-nitropropionic acid-induced Huntingtons disease in rats

Jain, D. P., & Gangshettiwar, A. (2014) · Journal of Intercultural Ethnopharmacology · doi:10.5455/jice.20140903012921 · Cited by 50 · see citing works

Heterodimerization of G-protein-coupled receptors in the CNS

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Neuroprotective Properties of Standardized Extracts of Hypericum perforatum on Rotenone Model of Parkinson’s Disease

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Effect of quercetin on chronic enhancement of spatial learning and memory of mice

Liu, J., Yu, H., & Ning, X. (2006) · Science in China Series C Life Sciences · doi:10.1007/s11427-006-2037-7 · Cited by 48 · see citing works

Ameliorating effect of quercetin on acute pentylenetetrazole induced seizures in rats.

Sefil, F., Kahraman, İ., Dokuyucu, R., Gökçe, H., Öztürk, A., Tutuk, O., Aydın, M., Özkan, Ü., & Pınar, N. (2014) · PubMed Central · Cited by 47 · see citing works

Enlightening the neuroprotective effect of quercetin in epilepsy: From mechanism to therapeutic opportunities

Akyüz, E., Paudel, Y. N., Polat, A. K., Dundar, H. E., & Angelopoulou, E. (2021) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2020.107701 · Cited by 47 · see citing works

Lack of robust protective effect of quercetin in two types of 6-hydroxydopamine-induced parkinsonian models in rats and dopaminergic cell cultures

Kääriäinen, T. M., Piltonen, M., Ossola, B., Kekki, H., Lehtonen, Š., Nenonen, T., Lecklin, A., Raasmaja, A., & Männistö, P. T. (2008) · Brain Research · doi:10.1016/j.brainres.2008.01.089 · Cited by 46 · see citing works

Chemical constituents and their acetyl cholinesterase inhibitory and antioxidant activities from leaves of Acanthopanax henryi: potential complementary source against Alzheimer’s disease

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Quercetin Enhances Exercise-Mediated Neuroprotective Effects in Brain Ischemic Rats

Chang, H.-C., Yang, Y., Wang, P. S., et al. (2014) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000310 · Cited by 45 · see citing works

Neurite Outgrowth and Neuroprotective Effects of Quercetin fromCaesalpinia mimosoidesLamk. on Cultured P19-Derived Neurons

Tangsaengvit, N., Kitphati, W., Tadtong, S., Bunyapraphatsara, N., & Nukoolkarn, V. S. (2013) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2013/838051 · Cited by 44 · see citing works

Effects of Ultrahigh Temperature Pasteurization on the Liquid Components and Functional Properties of Stored Liquid Whole Eggs

Liu, T., Lv, B. S., Zhao, W., et al. (2020) · BioMed Research International · doi:10.1155/2020/3465465 · Cited by 43 · see citing works

Naringenin and quercetin reverse the effect of hypobaric hypoxia and elicit neuroprotective response in the murine model

Sarkar, A., Angeline, M. S., Anand, K., et al. (2012) · Brain Research · doi:10.1016/j.brainres.2012.08.036 · Cited by 42 · see citing works

Neuroprotective Effects of Quercetin in Pediatric Neurological Diseases

Álvarez‐Arellano, L., Salazar–García, M., & Corona, J. C. (2020) · Molecules · doi:10.3390/molecules25235597 · Cited by 42 · see citing works

Quercetin in an animal model of spinal cord compression injury: correlation of treatment duration with recovery of motor function

Schültke, E., Kamencic, H., Skihar, V., et al. (2009) · Spinal Cord · doi:10.1038/sc.2009.111 · Cited by 39 · see citing works

Comparison between the effects of quercetin on seizure threshold in acute and chronic seizure models

Nassiri‐Asl, M., Hajiali, F., Taghiloo, M., Abbasi, E., Mohseni, F., & Yousefi, F. (2014) · Toxicology and Industrial Health · doi:10.1177/0748233713518603 · Cited by 37 · see citing works

In Silico and In Vivo Studies on Quercetin as Potential Anti-Parkinson Agent

Boyina, H. K., Geethakhrishnan, S. L., Panuganti, S., et al. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-32633-3_1 · Cited by 37 · see citing works

The Flavonoid Isoquercitrin Promotes Neurite Elongation by Reducing RhoA Activity

Palazzolo, G., Horváth, P., & Zenobi‐Wong, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049979 · Cited by 36 · see citing works

A Novel Nutraceutical Formulation Can Improve Motor Activity and Decrease the Stress Level in a Murine Model of Middle-Age Animals

Tsoukalas, D., Zlatian, O. M., Mitroi, M. R., Renieri, E. A., Tsatsakis, A. M., Izotov, B. N., Burada, F., Sosoi, S. S., Burada, E., Bugă, A. M., et al. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10040624 · Cited by 36 · see citing works

Metal Binding of Flavonoids and Their Distinct Inhibition Mechanisms Toward the Oxidation Activity of Cu2+–β-Amyloid: Not Just Serving as Suicide Antioxidants!

Tay, W. M., da Silva, G. F. Z., & Ming, L. (2013) · Inorganic Chemistry · doi:10.1021/ic301832p · Cited by 34 · see citing works

The Flavonoid, Quercetin, Inhibits HIV-1 Infection in Normal Peripheral Blood Mononuclear Cells

Nair (2009) · American Journal of Infectious Diseases · doi:10.3844/ajidsp.2009.135.141 · Cited by 30 · see citing works

Thinking Outside the Ischemia Box: Advancements in the Use of Multiple Sclerosis Drugs in Ischemic Stroke

Aloizou, A., Siokas, V., Pateraki, G., Liampas, I., Bakirtzis, C., Tsouris, Z., Lazopoulos, G., Călina, D. C., Docea, A. O., Tsatsakis, A. M., et al. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10040630 · Cited by 30 · see citing works

ADORA2A rs5760423 and CYP1A2 rs762551 Polymorphisms as Risk Factors for Parkinson’s Disease

Siokas, V., Aloizou, A.-M., Tsouris, Z., Liampas, I., Liakos, P., Calina, D., Docea, A. O., Tsatsakis, A., Bogdanos, D. P., Hadjigeorgiou, G. M., et al. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10030381 · Cited by 29 · see citing works

Quercetin improved spatial memory dysfunctions in rat model of intracerebroventricular streptozotocin-induced sporadic Alzheimer's disease

Ashrafpour, M., Parsaei, S., & Sepehri, H. (2015) · National Journal of Physiology Pharmacy and Pharmacology · doi:10.5455/njppp.2015.5.2308201563 · Cited by 28 · see citing works

Erratum: microRNA Crosstalk Influences Epithelial-to-Mesenchymal, Endothelial-to-Mesenchymal, and Macrophage-to-Mesenchymal Transitions in the Kidney

Frontiers Production Office (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00011 · Cited by 27 · see citing works

Quercetin-biapigenin nanoparticles are effective to penetrate the blood–brain barrier

Oliveira, A. I., Pinho, C., Sarmento, B. F. C. C., & Dias, A. C. P. (2021) · Drug Delivery and Translational Research · doi:10.1007/s13346-021-00917-6 · Cited by 26 · see citing works

When Neuroscience Meets Pharmacology: A Neuropharmacology Literature Analysis

Yeung, A. W. K., Tzvetkov, N. T., & Atanasov, A. G. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00852 · Cited by 25 · see citing works

Effects of enzymatically modified isoquercitrin in supplementary protein powder on athlete body composition: a randomized, placebo-controlled, double-blind trial

Omi, N., Shiba, H., Nishimura, E., Tsukamoto, S., Maruki‐Uchida, H., Oda, M., & Morita, M. (2019) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-019-0303-x · Cited by 25 · see citing works

EVALUATION OF POLYPHENOLIC PROFILE AND ANTIOXIDANT ACTIVITY FOR SOME SALVIA SPECIES

Hanganu, D. (2019) · FARMACIA · doi:10.31925/farmacia.2019.5.8 · Cited by 24 · see citing works

Multi-Target Mechanisms of Phytochemicals in Alzheimer’s Disease: Effects on Oxidative Stress, Neuroinflammation and Protein Aggregation

Sharifi-Rad, J., Rapposelli, S., Sestito, S., Herrera-Bravo, J., Arancibia-Diaz, A., Salazar, L. A., Yeskaliyeva, B., Beyatli, A., Leyva-Gómez, G., González-Contreras, C., et al. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12091515 · Cited by 125 · see citing works

A Flavonoid on the Brain: Quercetin as a Potential Therapeutic Agent in Central Nervous System Disorders

Wróbel-Biedrawa, D., Grabowska, K., Galanty, A., Sobolewska, D., & Podolak, I. (2022) · Life · doi:10.3390/life12040591 · Cited by 95 · see citing works

Therapeutic Applications of Curcumin in Diabetes: A Review and Perspective

Quispe, C., Herrera-Bravo, J., Javed, Z., Khan, K., Raza, S., Gulsunoglu-Konuskan, Z., Daştan, S. D., Sytar, O., Martorell, M., Sharifi-Rad, J., et al. (2022) · BioMed Research International · doi:10.1155/2022/1375892 · Cited by 92 · see citing works

The role of Tumour Necrosis Factor in neuroinflammation associated with Parkinson’s disease and targeted therapies

Amin, R., Quispe, C., Docea, A. O., Ydyrys, A., Kulbayeva, M., Durna Daştan, S., Calina, D., & Sharifi-Rad, J. (2022) · Neurochemistry International · doi:10.1016/j.neuint.2022.105376 · Cited by 74 · see citing works

Reversal of brain aging by targeting telomerase: A nutraceutical approach

Tsoukalas, D., Buga, A., Docea, A., Sarandi, E., Mitrut, R., Renieri, E., Spandidos, D., Rogoveanu, I., Cercelaru, L., Niculescu, M., et al. (2021) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2021.5032 · Cited by 40 · see citing works

Characterization of Orange Peel Extract and Its Potential Protective Effect against Aluminum Chloride-Induced Alzheimer’s Disease

Abd El-Aziz, N. M. A., Shehata, M. G., Alsulami, T., Badr, A. N., Elbakatoshy, M. R., Ali, H. S., & El-Sohaimy, S. A. (2022) · Pharmaceuticals · doi:10.3390/ph16010012 · Cited by 31 · see citing works

Genetics of Amyotrophic Lateral Sclerosis

Gorodenker, J., & Levy, L. M. (2014) · American Journal of Neuroradiology · doi:10.3174/ajnr.a3831 · Cited by 4 · see citing works

Phosphorylated TDP-43 aggregates in peripheral motor nerves of patients with amyotrophic lateral sclerosis

Riva, N., Gentile, F., Cerri, F., Gallia, F., Podini, P., Dina, G., Falzone, Y., Fazio, R., Lunetta, C., Calvo, A., et al. (2021) · Brain · doi:10.1093/brain/awab285 · Cited by 59 · see citing works

Negative results of a phase II study of hyperbaric oxygen therapy for amyotrophic lateral sclerosis

Steele, J., Zutshi, D., & Bradley, W. G. (2007) · Amyotrophic Lateral Sclerosis · doi:10.1080/17482960701547875 · Cited by 7 · see citing works

Diagnosis and Treatment of Amyotrophic Lateral Sclerosis

Yang, F. (2011) · Zhongguo quanke yixue

Amyotrophic Lateral Sclerosis Sera Applied to Cultured Motor Neurons

Horwich, M., Engel, W. K., & Chauvin, P. B. (1974) · Archives of Neurology · doi:10.1001/archneur.1974.00490340060015 · Cited by 39 · see citing works