Neuroprotective and Neurorescue Effects of a Novel Polymeric Nanoparticle Formulation of Curcumin (NanoCurc™) in the Neuronal Cell Culture and Animal Model: Implications for Alzheimer's disease

GLUTATHIONE

Meister, A., & Anderson, M. E. (1983) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.52.070183.003431 · Cited by 5,694 · see citing works

Bioavailability of curcumin: Problems and promises

Anand, P., Kunnumakkara, A. B., Newman, R. A., & Aggarwal, B. B. (2007) · Molecular Pharmaceutics · doi:10.1021/mp700113r · Cited by 5,543 · see citing works

Cellular response to oxidative stress: Signaling for suicide and survival *

Martindale, J., & Holbrook, N. (2002) · Journal of Cellular Physiology · doi:10.1002/jcp.10119 · Cited by 2,392 · see citing works

Curcumin as “Curecumin”: From kitchen to clinic

Goel, A., Kunnumakkara, A. B., & Aggarwal, B. B. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.08.016 · Cited by 2,220 · see citing works

Glutathione and its role in cellular functions

Sies, H. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00177-x · Cited by 1,735 · see citing works

Curcumin: The story so far

Sharma, R. A., Gescher, A. J., & Steward, W. P. (2005) · European Journal of Cancer · doi:10.1016/j.ejca.2005.05.009 · Cited by 1,701 · see citing works

The Curry Spice Curcumin Reduces Oxidative Damage and Amyloid Pathology in an Alzheimer Transgenic Mouse

Lim, G. P., Chu, T., Yang, F., Beech, W., Frautschy, S. A., & Cole, G. M. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-21-08370.2001 · Cited by 1,530 · see citing works

Dose escalation of a curcuminoid formulation

Lao, C. D., Ruffin, M. T., Normolle, D. P., Heath, D. D., Murray, S. I., Bailey, J. M., Boggs, M. E., Crowell, J. A., Rock, C. L., & Brenner, D. E. (2006) · BMC Complementary and Alternative Medicine · doi:10.1186/1472-6882-6-10 · Cited by 1,400 · see citing works

A Stable Nonfluorescent Derivative of Resorufin for the Fluorometric Determination of Trace Hydrogen Peroxide: Applications in Detecting the Activity of Phagocyte NADPH Oxidase and Other Oxidases

Zhou, M., Diwu, Z. J., Panchuk-Voloshina, N., & Haugland, R. P. (1997) · Analytical Biochemistry · doi:10.1006/abio.1997.2391 · Cited by 1,400 · see citing works

Polymeric nanoparticle-encapsulated curcumin ("nanocurcumin"): a novel strategy for human cancer therapy

Bisht, S., Feldmann, G., Soni, S., Ravi, R. K., Karikar, C., Maitra, A., & Maitra, A. (2007) · Journal of Nanobiotechnology · doi:10.1186/1477-3155-5-3 · Cited by 1,091 · see citing works

Biotransformation of Curcumin Through Reduction and Glucuronidation in Mice

Pan, M., Huang, T., & Lin, J. (1999) · Drug Metabolism and Disposition · doi:10.1016/s0090-9556(24)15211-7 · Cited by 950 · see citing works

Oxidative damage in Alzheimer's

Smith, M. A., Perry, G. L., Richey, P. L., Sayrec, L. M., Anderson, V. E., Beal, M. F., & Kowall, N. W. (1996) · Nature · doi:10.1038/382120b0 · Cited by 897 · see citing works

Studies of curcumin and curcuminoids. XXVII. Cyclodextrin complexation: solubility, chemical and photochemical stability

Tønnesen, H. H., Másson, M., & Loftsson, Þ. (2002) · International Journal of Pharmaceutics · doi:10.1016/s0378-5173(02)00323-x · Cited by 768 · see citing works

Curcumin Structure-Function, Bioavailability, and Efficacy in Models of Neuroinflammation and Alzheimer’s Disease

Begum, A. N., Jones, M. R., Lim, G. P., Morihara, T., Kim, P., Heath, D. D., Rock, C. L., Pruitt, M. A., Yang, F., Hudspeth, B., et al. (2008) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.108.137455 · Cited by 604 · see citing works

ΔΨ _m ‐Dependent and ‐independent production of reactive oxygen species by rat brain mitochondria

Votyakova, T. V., & Reynolds, I. J. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00548.x · Cited by 601 · see citing works

Six-Month Randomized, Placebo-Controlled, Double-Blind, Pilot Clinical Trial of Curcumin in Patients With Alzheimer Disease

Baum, L., Lam, C. W. K., Cheung, S. K. K., Kwok, T. C. Y., Lui, V. W.-C., Tsoh, J., LAM, L. C. W., Leung, V., Hui, E., Ng, C., et al. (2008) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0b013e318160862c · Cited by 594 · see citing works

Metabolism of the cancer chemopreventive agent curcumin in human and rat intestine.

Ireson, C. R., Jones, D. J. L., Orr, S., Coughtrie, M. W. H., Boocock, D. J., Williams, M. L., Farmer, P. B., Steward, W. P., & Gescher, A. J. (2002) · PubMed · Cited by 561 · see citing works

CD36, a Class B Scavenger Receptor, Is Expressed on Microglia in Alzheimer's Disease Brains and Can Mediate Production of Reactive Oxygen Species in Response to β-Amyloid Fibrils

Coraci, I. S., Husemann, J., Berman, J. W., Hulette, C., Dufour, J. H., Campanella, G. K., Luster, A. D., Silverstein, S. C., & El Khoury, J. B. (2002) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)64354-4 · Cited by 398 · see citing works

Are reactive oxygen species involved in Alzheimer's disease?

Benzi, G. (1995) · Neurobiology of Aging · doi:10.1016/0197-4580(95)00066-n · Cited by 365 · see citing works

Curcumin Stimulates Proliferation of Embryonic Neural Progenitor Cells and Neurogenesis in the Adult Hippocampus

Kim, S. J., Son, T. G., Park, H. R., Park, M.-K., Kim, M., Kim, H. S., Chung, H. Y., Mattson, M. P., & Lee, J. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m708373200 · Cited by 357 · see citing works

Compartmentation of Glutathione: Implications for the Study of Toxicity and Disease

Smith, C. V., Jones, D. P., Guenthner, T. M., Lash, L. H., & Lauterburg, B. H. (1996) · Toxicology and Applied Pharmacology · doi:10.1006/taap.1996.0191 · Cited by 331 · see citing works

Structure–activity Relationships of Amyloid Beta‐aggregation Inhibitors Based on Curcumin: Influence of Linker Length and Flexibility

Reinke, A. A., & Gestwicki, J. E. (2007) · Chemical Biology & Drug Design · doi:10.1111/j.1747-0285.2007.00557.x · Cited by 330 · see citing works

Evidence suggesting a role for hydroxyl radical in gentamicin-induced acute renal failure in rats.

Walker, P. D., & Shah, S. V. (1988) · Journal of Clinical Investigation · doi:10.1172/jci113325 · Cited by 298 · see citing works

Tissue distribution & elimination of capsaicin, piperine & curcumin following oral intake in rats.

Suresh, D., & Srinivasan, K. (2010) · PubMed · Cited by 268 · see citing works

Reactive oxygen and DNA damage in mitochondria

Richter, C. (1992) · Mutation Research/DNAging · doi:10.1016/0921-8734(92)90029-o · Cited by 240 · see citing works

Neuroprotective mechanisms of curcumin against cerebral ischemia-induced neuronal apoptosis and behavioral deficits

Wang, Q., Sun, A. Y., Simonyi, Á., Jensen, M. D., Shelat, P. B., Rottinghaus, G. E., MacDonald, R. S., Miller, D. K., Lubahn, D. E., Weisman, G. A., et al. (2005) · Journal of Neuroscience Research · doi:10.1002/jnr.20610 · Cited by 233 · see citing works

Apoptosis and autophagy: Regulation of caspase‐9 by phosphorylation

Allan, L. A., & Clarke, P. R. (2009) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07330.x · Cited by 226 · see citing works

Curcumin induces chemo/radio-sensitization in ovarian cancer cells and curcumin nanoparticles inhibit ovarian cancer cell growth

Yallapu, M. M., Maher, D. M., Sundram, V., Bell, M. C., Jaggi, M., & Chauhan, S. C. (2010) · Journal of Ovarian Research · doi:10.1186/1757-2215-3-11 · Cited by 221 · see citing works

Systemic Administration of Polymeric Nanoparticle-Encapsulated Curcumin (NanoCurc) Blocks Tumor Growth and Metastases in Preclinical Models of Pancreatic Cancer

Bisht, S., Mizuma, M., Feldmann, G., Ottenhof, N. A., Hong, S., Pramanik, D., Chenna, V., Karikari, C. A., Sharma, R. B., Goggins, M., et al. (2010) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-10-0172 · Cited by 216 · see citing works

Curcumin Protected PC12 Cells against Beta-Amyloid-Induced Toxicity through the Inhibition of Oxidative Damage and Tau Hyperphosphorylation

Park, S.-Y., Kim, H.-S., Cho, E.-K., Kwon, B.-Y., Phark, S., Hwang, K.-W., & Sul, D. (2008) · Food and Chemical Toxicology · doi:10.1016/j.fct.2008.05.030 · Cited by 209 · see citing works

High‐performance liquid chromatography analysis of curcumin in rat plasma: application to pharmacokinetics of polymeric micellar formulation of curcumin

Ma, Z., Shayeganpour, A., Brocks, D. R., Lavasanifar, A., & Samuel, J. (2007) · Biomedical Chromatography · doi:10.1002/bmc.795 · Cited by 203 · see citing works

A Critical Analysis of New Molecular Targets and Strategies for Drug Developments in Alzheimers Disease

Lahiri, D. K., Farlow, M. R., Sambamurti, K., Greig, N. H., Giacobini, E., & Schneider, L. S. S. (2003) · Current Drug Targets · doi:10.2174/1389450033346957 · Cited by 185 · see citing works

Stability-indicating HPTLC determination of curcumin in bulk drug and pharmaceutical formulations

Ansari, M. J., Ahmad, S., Kohli, K., et al. (2005) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2005.03.021 · Cited by 172 · see citing works

Mitochondrial function, GSH and iron in neurodegeneration and Lewy body diseases

Gu, M., Owen, A., Toffa, S., Cooper, J. A. D., Dexter, D. T., Jenner, P. G., MARSDEN, C. D., & Schapira, A. H. V. (1998) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(98)00095-1 · Cited by 164 · see citing works

Alterations in brain antioxidant enzymes and redox proteomic identification of oxidized brain proteins induced by the anti-cancer drug adriamycin: implications for oxidative stress-mediated chemobrain

Gururaj Joshi, A., Aluise, C. D., Cole, M. P., Rukhsana Sultana, A., Pierce, W. M. J., Vore, M. E., Clair, D. K. S., & Butterfield, D. A. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.01.021 · Cited by 156 · see citing works

Curcumin attenuates gentamicin-induced renal oxidative damage in rats

Farombi, E. O., & Ekor, M. (2006) · Food and Chemical Toxicology · doi:10.1016/j.fct.2006.05.005 · Cited by 155 · see citing works

Neuroinflammation in Alzheimer's disease: different molecular targets and potential therapeutic agents including curcumin

Ray, B., & Lahiri, D. K. (2009) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2009.06.012 · Cited by 152 · see citing works

Salvianolic acid B inhibits Aβ fibril formation and disaggregates preformed fibrils and protects against Aβ-induced cytotoxicty

Durairajan, S. S. K., Yuan, Q., Xie, L., Chan, W. S., Kum, W.-F., Koo, I., Liu, C., Song, Y., Huang, J., Klein, W. L., et al. (2007) · Neurochemistry International · doi:10.1016/j.neuint.2007.09.006 · Cited by 149 · see citing works

Effect of Turmeric, Turmerin and Curcumin on H2O2-Induced Renal Epithelial (LLC-PK1) Cell Injury

Cohly, H., Taylor, A., Angel, M. F., et al. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00140-8 · Cited by 140 · see citing works

Amyloid β Peptide–Induced Cerebral Endothelial Cell Death Involves Mitochondrial Dysfunction and Caspase Activation

Xu, J., Chen, S., Ku, G., Ahmed, S. H., Xu, J., Chen, H., & Hsu, C. Y. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200106000-00008 · Cited by 127 · see citing works

Fibrillar beta-amyloid peptide Aβ1–40 activates microglial proliferation via stimulating TNF-α release and H2O2 derived from NADPH oxidase: a cell culture study

Jekabsone, A., Mander, P. K., Tickler, A. K., Sharpe, M. A., & Brown, G. C. (2006) · Journal of Neuroinflammation · doi:10.1186/1742-2094-3-24 · Cited by 127 · see citing works

Memantine lowers amyloid‐β peptide levels in neuronal cultures and in APP/PS1 transgenic mice

Alley, G. M., Bailey, J. A., Chen, D., Ray, B., Puli, L., Tanila, H., Banerjee, P., & Lahiri, D. K. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22172 · Cited by 124 · see citing works

Systemic Delivery of Curcumin: 21st Century Solutions for an Ancient Conundrum

Bisht, S., & Maitra, A. (2009) · Current Drug Discovery Technologies · doi:10.2174/157016309789054933 · Cited by 124 · see citing works

A Role for NOX NADPH Oxidases in Alzheimer's Disease and Other Types of Dementia?

Zekry, D., Epperson, T. K., & Krause, K. (2003) · IUBMB Life · doi:10.1080/1521654031000153049 · Cited by 112 · see citing works

Role of the APP Non-Amyloidogenic Signaling Pathway and Targeting α-Secretase as an Alternative Drug Target for Treatment of Alzheimers Disease

Bandyopadhyay, S., Goldstein, L. E., Lahiri, D. K., & Rogers, J. T. (2007) · Current Medicinal Chemistry · doi:10.2174/092986707782360060 · Cited by 95 · see citing works

Gender differences in glutathione metabolism in Alzheimer's disease

Liu, H., Harrell, L. E., Shenvi, S. V., Hagen, T. M., & Liu, R.-M. (2005) · Journal of Neuroscience Research · doi:10.1002/jnr.20424 · Cited by 83 · see citing works

In vivocharacterization of a polymeric nanoparticle platform with potential oral drug delivery capabilities

Bisht, S., Feldmann, G., Koorstra, J.-B. M., Mullendore, M. E., Alvarez, H., Karikari, C. A., Rudek, M. A., Lee, C. K., Maitra, A., & Maitra, A. (2008) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-08-0476 · Cited by 68 · see citing works

An immediate endothelial cell signaling response to lung ischemia

Song, C. H., Al‐Mehdi, A. B., & Fisher, A. B. (2001) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.2001.281.4.l993 · Cited by 66 · see citing works

Ethane production as a measure of lipid peroxidation after renal ischemia

Paller, M. S., & Hebbel, R. P. (1986) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.1986.251.5.f839 · Cited by 49 · see citing works

Striatal Damage and Oxidative Stress Induced by the Mitochondrial Toxin Malonate Are Reduced in Clorgyline-Treated Rats and MAO-A Deficient Mice

Maragos, W. F., Young, K. L., Altman, C. S., et al. (2004) · Neurochemical Research · doi:10.1023/b:nere.0000018845.82808.45 · Cited by 47 · see citing works

Effects of amyloid-beta peptides on hydrogen peroxide-metabolizing enzymes in rat brainin vivo

Kaminsky, Y. G., & Kosenko, E. A. (2008) · Free Radical Research · doi:10.1080/10715760802159057 · Cited by 47 · see citing works

The oxidase systems of Ascaris-muscle mitochondria

Cheah, K. S., & Chance, B. (1970) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(70)90131-3 · Cited by 45 · see citing works

Memantine treatment decreases levels of secreted Alzheimer's amyloid precursor protein (APP) and amyloid beta (Aβ) peptide in the human neuroblastoma cells

Ray, B., Banerjee, P., Greig, N. H., & Lahiri, D. K. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.11.016 · Cited by 45 · see citing works

Role of oxygen free radical species in in vitro models of proximal tubular ischemia

Borkan, S. C., & Schwartz, J. H. (1989) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.1989.257.1.f114 · Cited by 43 · see citing works

Potential protection of curcumin against amyloid β-induced toxicity on cultured rat prefrontal cortical neurons

Qin, X., Cheng, Y., Cui, J., Zhang, Y., & Yu, L. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.07.047 · Cited by 38 · see citing works

Molecular and immunocytochemical characterization of primary neuronal cultures from adult rat brain: Differential expression of neuronal and glial protein markers

Ray, B., Bailey, J. A., Sarkar, S., & Lahiri, D. K. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.08.018 · Cited by 32 · see citing works

Expression of the apoptosis-related proteins caspase-3 and NF-κB in the hippocampus of Tg2576 mice

Niu, Y., Zhang, W., Wu, P., Liu, B., Sun, G.-T., Yu, D., & Deng, J. (2010) · Neuroscience Bulletin · doi:10.1007/s12264-010-6122-3 · Cited by 28 · see citing works

Determination of high-affinity choline uptake (HACU) and choline acetyltransferase (ChAT) activity in the same population of cultured cells

Ray, B., Simon, J. R., & Lahiri, D. K. (2009) · Brain Research · doi:10.1016/j.brainres.2009.07.096 · Cited by 18 · see citing works

[Epidemiology of Alzheimer's disease].

Dufouil, C., & Alpérovitch, A. (2005) · PubMed · Cited by 8 · see citing works

Nanotechnology: A Promising Approach for Delivery of Neuroprotective Drugs

Naqvi, S., Panghal, A., & Flora, S. J. S. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00494 · Cited by 305 · see citing works

Curcumin loaded solid lipid nanoparticles: an efficient formulation approach for cerebral ischemic reperfusion injury in rats.

Kakkar, V., Muppu, S. K., Chopra, K., & Kaur, I. P. (2013) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2013.02.005 · Cited by 222 · see citing works

Curcumin nanoparticles attenuate neurochemical and neurobehavioral deficits in experimental model of huntington’s disease.

Sandhir, R., Yadav, A., Mehrotra, A., Sunkaria, A., Singh, A., & Sharma, S. (2014) · NeuroMolecular Medicine · doi:10.1007/s12017-013-8261-y · Cited by 204 · see citing works

Effect of Curcumin-Associated and Lipid Ligand-Functionalized Nanoliposomes on Aggregation of the Alzheimer's Aβ Peptide

Taylor, M., Moore, S., Mourtas, S., Niarakis, A., Re, F., Zona, C., Ferla, B. L., Nicotra, F., Masserini, M., Antimisiaris, S. G., et al. (2011) · Nanomedicine Nanotechnology Biology and Medicine · doi:10.1016/j.nano.2011.06.015 · Cited by 149 · see citing works

Novel upregulation of amyloid-β precursor protein (APP) by microRNA-346 via targeting of APP mRNA 5′-untranslated region: Implications in Alzheimer’s disease

Long, J. M., Maloney, B., Rogers, J. T., & Lahiri, D. K. (2019) · Molecular Psychiatry · doi:10.1038/s41380-018-0266-3 · Cited by 141 · see citing works

Oxidant/antioxidant imbalance and the risk of Alzheimer's disease

Moneim, A. (2015) · Current Alzheimer Research · doi:10.2174/1567205012666150325182702 · Cited by 136 · see citing works

Neurotheranostics as Personalized Medicines

Kevadiya, B. D., Ottemann, B. M., Thomas, M. B., Mukadam, I., Nigam, S., McMillan, J., Gorantla, S., Bronich, T. K., Edagwa, B., & Gendelman, H. E. (2019) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2018.10.011 · Cited by 124 · see citing works

Ergothioneine protects against neuronal injury induced by β-amyloid in mice

Yang, N.-C., Lin, H.-C., Wu, J.-H., Ou, H.-C., Chai, Y.-C., Tseng, C.-Y., Liao, J.-W., & Song, T.-Y. (2012) · Food and Chemical Toxicology · doi:10.1016/j.fct.2012.08.021 · Cited by 123 · see citing works

Translation of Pre-Clinical Studies into Successful Clinical Trials for Alzheimer’s Disease: What are the Roadblocks and How Can They Be Overcome?

Banik, A., Brown, R. E., Bamburg, J., Lahiri, D. K., Khurana, D., Friedland, R. P., Chen, W., Ding, Y., Mudher, A., Padjen, A. L., et al. (2015) · Journal of Alzheimer’s Disease · doi:10.3233/jad-150136 · Cited by 102 · see citing works

The “Aged Garlic Extract” (AGE) and One of its Active Ingredients S-Allyl-LCysteine (SAC) as Potential Preventive and Therapeutic Agents for Alzheimer's Disease (AD)

Ray, B., B. Chauhan, N., & K. Lahiri, D. (2011) · Current Medicinal Chemistry · doi:10.2174/092986711796504664 · Cited by 100 · see citing works

Dendrimer Architectonics to Treat Cancer and Neurodegenerative Diseases with Implications in Theranostics and Personalized Medicine

Moorthy, H., & Govindaraju, T. (2021) · ACS Applied Bio Materials · doi:10.1021/acsabm.0c01319 · Cited by 64 · see citing works

Rescuing apoptotic neurons in Alzheimer’s disease using wheat germ agglutinin-conjugated and cardiolipin-conjugated liposomes with encapsulated nerve growth factor and curcumin

Kuo, Y.-C., & Lin, C.-C. (2015) · International Journal of Nanomedicine · doi:10.2147/ijn.s79528 · Cited by 56 · see citing works

Nanotechnology in the diagnostic and therapy for Alzheimer's disease

Panghal, A., & Flora, S. J. S. (2024) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2024.130559 · Cited by 31 · see citing works

Investigation of therapeutic effect of curcumin α and β glucoside anomers against Alzheimer’s disease by the nose to brain drug delivery

Ahmadi, N., Hosseini, M.-J., Rostamizadeh, K., & Anoush, M. (2021) · Brain Research · doi:10.1016/j.brainres.2021.147517 · Cited by 28 · see citing works

Metabolic Fate of Curcumin in the Gastrointestinal Tract in Mice

Li, Z., Sun, Y., Song, M., et al. (2016) · The FASEB Journal · doi:10.1096/fasebj.30.1_supplement.690.9 · Cited by 1 · see citing works

Anti Oxidant Potential of “Cureit”- A Novel BioAvailable Curcumin Formulation

Gopia, S., Georgea, R., & .Sriraamb, V. T. (2014) · Asian Journal of Pharmaceutical Technology and Innovation · Cited by 5 · see citing works

Evaluation of Curcumin Nanoparticles against Rabbit Skin Infection

Fatthi, D. A. (2023) · E3S Web of Conferences · doi:10.1051/e3sconf/202339101119

Analysis of the anticancer activity of curcuminoids, thiotryptophan and 4-phenoxyphenol derivatives

Parsai, S., Keck, R. W., Skrzypczak‐Jankun, E., & Jankun, J. (2013) · Oncology Letters · doi:10.3892/ol.2013.1679 · Cited by 24 · see citing works

Curcumin and Curcumin-like Molecules: From Spice to Drugs

Marchiani, A., Rozzo, C., Fadda, A., Delogu, G., & Ruzza, P. (2013) · Current Medicinal Chemistry · doi:10.2174/092986732102131206115810 · Cited by 194 · see citing works