The DOI matches its Crossref record; 80 of the 82 references it cites were found in a registry or an index.
The role of reactive oxygen species in homeostasis and degradation of cartilage
Open accessAbstract
Objectives The metabolism of cells in articular joint tissues in normal and pathological conditions is subject to a complex environmental control. In addition to soluble mediators such as cytokines and growth factors, as well as mechanical stimuli, reactive oxygen species (ROS) emerge as major factors in this regulation. ROS production has been found to increase in joint diseases, such as osteoarthritis and rheumatoid arthritis, but their role in joint diseases initiation and progression remains questionable.Method This review is focused on the role of ROS, mainly nitric oxide, peroxynitrite and superoxide anion radicals, in the signaling mechanisms implied in the main cellular functions, including synthesis and degradation of matrix components. The direct effects of ROS on cartilage matrix components as well as their inflammatory and immunomodulatory effects are also considered.Results Some intracellular signaling pathways are redox sensitive and ROS are involved in the regulation of the production of some biochemical factors involved in cartilage degradation and joint inflammation. Further, ROS may cause damage to all matrix components, either by a direct attack or indirectly by reducing matrix components synthesis, by inducing apoptosis or by activating latent metalloproteinases. Finally, we have highlighted the uncoupling effect of ROS on tissue remodeling and synovium inflammation, suggesting that antioxidant therapy could be helpful to treat structural changes but not to relieve symptoms.Conclusions This review of the literature supports the concept that ROS are not only deleterious agents involved in cartilage degradation, but that they also act as integral factors of intracellular signaling mechanisms. Further investigation is required to support the concept of antioxidant therapy in the management of joint diseases.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“One disease whose aetiology is well known to be bound up with ROSs is rheumatoid arthritis (RA) [36,1241-1246].”
From Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases (2009) · cites this paper as [1245]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Redox Regulation of Fos and Jun DNA-Binding Activity in Vitro
Abate, C., Patel, L., Rauscher, F. J., & Curran, T. (1990) · Science · doi:10.1126/science.2118682 · Cited by 1,573
Reactive Oxygen Species as Intracellular Messengers During Cell Growth and Differentiation
Sauer, H., Wartenberg, M., & Hescheler, J. (2001) · Cellular Physiology and Biochemistry · doi:10.1159/000047804 · Cited by 1,118
Xanthoudakis, S., & Curran, T. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05097.x · Cited by 708
Clancy, R. M., Leszczynska-Piziak, J., & Abramson, S. B. (1992) · Journal of Clinical Investigation · doi:10.1172/jci115929 · Cited by 686
Siwik, D. A., Pagano, P. J., & Colucci, W. S. (2001) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2001.280.1.c53 · Cited by 674
Chondrocyte apoptosis induced by nitric oxide.
Blanco, F. J., Ochs, R., Schwarz, H., & Lotz, M. (1995) · PubMed Central · Cited by 623
Lo, Y. Y. C., & Cruz, T. F. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.20.11727 · Cited by 530
Articular chondrocytes synthesize nitric oxide in response to cytokines and lipopolysaccharide
Stadler, J., Stefanović-Račić, M., Billiar, T. R., CURRAN, R. D., McIntyre, L. A., Georgescu, H. I., Simmons, R. L., & Evans, C. H. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.147.11.3915 · Cited by 438
Landino, L. M., Crews, B. C., Timmons, M. D., Morrow, J. D., & Marnett, L. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.26.15069 · Cited by 423
Nitric Oxide Activates Metalloprotease Enzymes in Articular Cartilage
Murrell, G. A. C., Jang, D., & Williams, R. J. (1995) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1995.1003 · Cited by 407
Research works printed but not linked: 1
- Henrotin, 2002, Type II collagen derived fragment (Coll2-1) is a new marker predictive of osteoarthritic progression, Osteoporos Int, 13, S17
Cited by
Sorted by citations
Items 601–700 of 740
Herrero‐Beaumont, G., Marco-Bonilla, M., Migliore, A., López-Reyes, A. G., Irigaray-Moreno, A., Mediero, A., & Largo, R. (2025) · BMC Musculoskeletal Disorders · doi:10.1186/s12891-025-09061-5 · Cited by 3
Luo, T. D., Marquez-Lara, A. J., Stone, A. V., Mannava, S., Howse, E. A., Rosas, S., Schallmo, M. S., Atilla, H. A., & Stubbs, A. J. (2018) · Hip International · doi:10.1177/1120700018813829 · Cited by 3
Drug Delivery Approaches for Rheumatoid Arthritis: Recent Advances and Clinical Translation Aspects
Thangadurai, M., Sethuraman, S., & Subramanian, A. (2025) · Critical Reviews in Therapeutic Drug Carrier Systems · doi:10.1615/critrevtherdrugcarriersyst.v42.i3.10 · Cited by 3
Dawn, I. (2013) · IOSR Journal of Dental and Medical Sciences · doi:10.9790/0853-0366063 · Cited by 3
Palma, H. E., Gallio, M., Silva, G. B., Cantarelli, C., Wolkmer, P., Salazar, R. F. D. S., Wergutz, J., Krause, L. M. F., Krause, A., Brass, K. E., et al. (2019) · Ciência Rural · doi:10.1590/0103-8478cr20180263 · Cited by 3
Abdel‐Rahman, A. A. ‐., Hamouda, H. E., Zeid, I. F., El‐Barbary, A. M., & Al-Ashwah, A. A. (2020) · Indian Journal of Rheumatology · doi:10.4103/injr.injr_71_19 · Cited by 3
Cellular signaling pathways with reactive oxygen species (ROS)
Madkour, L. H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-822481-6.00003-7 · Cited by 3
Effect of prophylactic administration of vitamin C in chickens with staphylococcal septic arthritis
Nematollahi, F., Shomali, T., Abdi‐Hachesoo, B., Derakhshandeh, A., Khodakaram‐Tafti, A., & Moezzi, M. S. (2021) · Veterinary Medicine and Science · doi:10.1002/vms3.649 · Cited by 3
RetractedVasconcellos, R. S., Volpato, J. A., Komarcheuski, A. S., & Costa, J. L. G. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99196-4.00025-5 · Cited by 4
Effects of radical oxygen species and antioxidants on macrophage polarization
Lurier, E. B., Levy, R. J., Barbee, K., Golomb, G., & Spiller, K. L. (2015) · Annual Northeast Biomedical Engineering Conference · doi:10.1109/nebec.2015.7117113 · Cited by 3
Milner, P., Smith, H. C., Robinson, R., Wilkins, R. J., & Gibson, J. S. (2012) · Journal of Orthopaedic Research® · doi:10.1002/jor.22221 · Cited by 3
Exogenous luteinizing hormone for assisted reproduction techniques in poor response patients
Spremović-Radjenović, S., Gudović, A., & Lazovic, G. (2010) · Vojnosanitetski pregled · doi:10.2298/vsp1007569s · Cited by 3
Crystal structures and in vitro biological effects of two protocatechuic acid complexes
Wei, J., Nong, W., He, C., Zhou, Y. G., Lu, D., & Lin, C. (2016) · Molecular Crystals and Liquid Crystals · doi:10.1080/15421406.2016.1222049 · Cited by 3
Value of Biomarkers in Osteoarthritis
Dinçel, Y. M. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.79946 · Cited by 3
Primary Glenohumeral Osteoarthritis
Altieri, B. A. B., & Ricchetti, E. T. (2024) · Springer eBooks · doi:10.1007/978-3-031-30518-4_92 · Cited by 3
El-Gamal, Y., Elmaksoud, S. S. A., Saad, M., & Lateef, H. M. A. E. (2022) · The Egyptian Journal of Pediatric Allergy and Immunology · doi:10.21608/ejpa.2022.126121.1038 · Cited by 2
Çıçek, H., Tuhanıoğlu, Ü., & Çiçek, F. A. (2024) · Acta Orthopaedica et Traumatologica Turcica · doi:10.5152/j.aott.2024.22172 · Cited by 2
Konar, M., Kaur, B., Saini, U. C., Bhadada, S. K., & Sharma, S. (2025) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2025.141067 · Cited by 2
Molybdenum nanoclusters as potent antioxidants for the treatment of osteoarthritis
Yang, H., Liu, W., Wang, R., Zhang, B., Wang, W., Wu, J., Jiang, P., Zhao, Y., Liang, X., Feng, X., et al. (2026) · Journal of Materials Chemistry B · doi:10.1039/d5tb02482j · Cited by 2
Theranostic MnO2 nanoparticles alleviate oxidative stress and visualize cartilage in osteoarthritis
Chen, T., Mei, Y., Xu, J., Gu, Y., Zhang, X., Jiang, S., Chen, Z., & Zhu, J. (2026) · Journal of Materials Science · doi:10.1007/s10853-026-12670-7 · Cited by 2
there any association of metabolic disturbances with joint destruction and pain?
Chetina, E. V., Markova, G. A., & Sharapova, E. P. (2019) · Biomeditsinskaya Khimiya · doi:10.18097/pbmc20196506441 · Cited by 2
Active Constituents Isolated from Zingiber zerumbet with Anti-Arthritis Activity
Wu, M., Cheng, M., Chen, M., & Yech, Y. (2022) · Chemistry of Natural Compounds · doi:10.1007/s10600-022-03828-1 · Cited by 2
Tumor Microenvironment-Responsive Nanoplatforms for Triggering Drug Delivery
Melia, F., Udomjarumanee, P., Rogoyski, R., & Pranjol, M. Z. I. (2023) · Springer eBooks · doi:10.1007/978-3-030-80962-1_412-1 · Cited by 2
Signaling of Nociceptors and Pain Perception: Impact of Age
Vinayak, M., & Singh, A. K. (2019) · Springer eBooks · doi:10.1007/978-981-13-3585-3_5 · Cited by 2
Rose, S., & Bennuri, S. C. (2018) · Springer eBooks · doi:10.1007/978-981-10-5311-5_5 · Cited by 2
Biochemical Mediators Involved in Cartilage Degradation and the Induction of Pain in Osteoarthritis
Michael, B., Yan, D., Chen, D., & Im, H. (2012) · InTech eBooks · doi:10.5772/26805 · Cited by 2
Physiopathologie de l'arthrose
Chevalier, X. (2008) · EMC - Appareil locomoteur · doi:10.1016/s0246-0521(08)45638-3 · Cited by 2
Chevalier, X. (2009) · EMC - Aparato Locomotor · doi:10.1016/s1286-935x(09)70905-0 · Cited by 2
Thioredoxin Gene Expression in Rat Knee Articular Cartilage After Full-Thickness Injury
Kakimaru, H., Kataoka, H. C., Enomoto, K., Kumahashi, N., Ohira, A., Yodoi, J., Uchio, Y., & Ochi, M. (2005) · Connective Tissue Research · doi:10.1080/03008200590935529 · Cited by 2
Viscosupplementation for the treatment of osteoarthritis of the knee
Ostałowska, A., Skowron, M., Birkner, E., Kasperczyk, S., Święchowicz, S., Koczy, B., & Nowak, D. (2017) · Annales Academiae Medicae Silesiensis · doi:10.18794/aams/62723 · Cited by 2
Millican, A. A., Leatherwood, J. L., Coverdale, J. A., Arnold, C. E., Bradbery, A. N., Larson, C. K., Lamprecht, E. D., White-Springer, S. H., Paulk, C. B., Welsh, T. H., et al. (2020) · Translational Animal Science · doi:10.1093/tas/txaa006 · Cited by 2
Can hydrogen retard the progression of osteoarthritis?
Li, D. (2012) · African Journal of Pharmacy and Pharmacology · doi:10.5897/ajpp11.515 · Cited by 2
Nutrigenomics, Inflammaging, and Osteoarthritis
Mobasheri, A., Barrett‐Jolley, R., Staunton, C. A., Ford, C., & Henrotin, Y. E. (2015) · Wiley eBooks · doi:10.1002/9781118930458.ch7 · Cited by 2
Self-citationCharakterisierung der radikalfangenden Eigenschaften pflanzlicher Entzündungshemmer
Germann, I. (2005) · Cited by 2
Megawati, S., Rahmadi, M., Susilo, I., & Khotib, J. (2017) · Folia Medica Indonesiana · doi:10.20473/fmi.v52i2.5219 · Cited by 1
Deng, C., Presle, N., Pizard, A., Guillaume, C., Bianchi, A., & Kempf, H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031810 · Cited by 1
Lohberger, B., Grote, V., Kaltenegger, H., Glänzer, D., Sadoghi, P., Kraus, T., & Steinecker-Frohnwieser, B. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262210934 · Cited by 1
Efficacy of Some Antibiotics in Curing Resistant Escherichia coli Infection
El-Banna, T., El-Aziz, A. A., El‐Mahdy, N. A., & Samy, Y. (2015) · Journal of Biosciences and Medicines · doi:10.4236/jbm.2015.37005 · Cited by 1
M2 Macrophages in the Integument and in the Musculoskeletal System
Rőszer, T. (2020) · Progress in inflammation research · doi:10.1007/978-3-030-50480-9_7 · Cited by 1
El-Sayed, J. M., Khadrawy, S. M., Mohamed, A. E., Mohamed, H. M., Mohamed, T. A., & Aly, M. S. (2025) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2025.113150 · Cited by 1
Estrogen-Dependent Transcriptional Activity: A Protection Against ROS in Osteoarthritis
Lugo, L., & Herrero‐Beaumont, G. (2012) · Springer eBooks · doi:10.1007/978-1-4614-6166-1_20 · Cited by 1
Post-Traumatic Osteoarthritis: Biologic Approaches to Treatment
Lidder, S., & Chubinskay, S. (2012) · InTech eBooks · doi:10.5772/26454 · Cited by 1
Knee osteoarthritis a pathological basis for use of newer drug therapies
Keny, M., Bhounsule, S. A., & Rataboli, P. V. (2014) · International Journal of Basic & Clinical Pharmacology · doi:10.5455/2319-2003.ijbcp20140602 · Cited by 1
Mandal, A., Das, R. S., Singh, B., Banerjee, R., & Mukhopadhyay, S. (2017) · Journal of Coordination Chemistry · doi:10.1080/00958972.2017.1303488 · Cited by 1
Biological Markers Associated Osteoarthritis
Mahakkanukrauh, P. (2017) · Medicine & health · doi:10.17576/mh.2017.1201.03 · Cited by 1
Ferrara, V., Toti, A., Lucarini, E., Parisio, C., Micheli, L., Ciampi, C., Margiotta, F., Crocetti, L., Vergelli, C., Giovannoni, M. P., et al. (2023) · Antioxidants · doi:10.3390/antiox12061207 · Cited by 1
Regulation of Cartilage and Bone Metabolism by Oxidative Stress
Niehoff, A., & Ziskoven, C. (2012) · Springer eBooks · doi:10.1007/978-1-4614-6166-1_5 · Cited by 1
Oxidative Stress in Human Autoimmune Joint Diseases
kurlov, M. (2012) · InTech eBooks · doi:10.5772/33460 · Cited by 1
Dillemans, M., Appelboom, T., & Nedervelde, L. V. (2008) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2008.06.032 · Cited by 1
Cantagrel, A. G., & Degboé, Y. (2015) · Revue du Rhumatisme · doi:10.1016/j.rhum.2015.10.002 · Cited by 1
Yoshimura, K. (2016) · Journal of Oral Biosciences · doi:10.1016/j.job.2016.02.002 · Cited by 1
Pathophysiology, Epidemiology, and Prognosis of Aortic Aneurysms
Pande, R. L., & Beckman, J. A. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-2930-6.00037-9 · Cited by 1
Yoshioka, H., Yui, N., Yatabe, K., Fujiya, H., Musha, H., Niki, H., Karasawa, R., & Yudoh, K. (2016) · International Journal of Clinical Rheumatology · Cited by 1
Nitric Oxide Signaling and Nitrosative Stress in the Musculoskeletal System 128
szer, T. R. ̋. (2014) · Cited by 1
Wade-Vallance, A. K., Ng, M., Kuo, K., Luo, C., Adams, S., Dhaliwal, G. K., & Yu, C. W. (2017) · Cited by 1
Wilson, A. M. M., & Balandrán‐Quintana, R. R. (2018) · Current Organic Chemistry · doi:10.2174/1385272822666180828114021 · Cited by 1
Green Tea Polyphenols in the Amelioration of Osteoarthritis: Memoir on the Preclinical Observations
Mathai, N. J., Murali, S. D., Adnan, M. M., Naik, T. S., George, T., Abraham, S., & Baliga, M. S. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813006-3.00028-3 · Cited by 1
Shivnath, N., Rawat, V., Sahabjada, S., Jafri, A., Rais, J., Khan, H., & Arshad, M. (2018) · Journal of Ecophysiology and Occupational Health · doi:10.18311/jeoh/2018/21062 · Cited by 1
Lee, J., & Woo, C. (2019) · Journal of Korean Medicine Rehabilitation · doi:10.18325/jkmr.2019.29.2.115 · Cited by 1
Consequences of Oxidative Stress and ROS-Mediated Pathways Cellular Signaling Stress Response
Madkour, L. H. (2020) · Nanomedicine and nanotoxicology · doi:10.1007/978-3-030-37297-2_5 · Cited by 1
Faculty Opinions recommendation of Rotenone prevents impact-induced chondrocyte death.
Ratcliffe, A. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.5012956.4945054 · Cited by 1
Ojha, A., Chatterjee, P., Kippner, L. E., Stevens, H. Y., Boden, S. D., Drissi, H., Mautner, K., Yeago, C., Roy, K., & Sinha, S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.26.678886 · Cited by 1
Bezine, M. (2017) · theses.fr (ABES) · doi:10.70675/a634c389z7b07z4830zb56dzbf7b53a56944 · Cited by 1
Palma, L., & José, M. (2010) · Universidad de Chile
The Non-operative Management of Hip Disease in Young Adults
Pollock, N., & Hulse, D. (2013) · Springer eBooks · doi:10.1007/978-1-4471-5412-9_12
New Drugs and Nutraceuticals in the Treatment of Osteoarthritis
Henrotin, Y. E., & Reginster, J. (2011) · Pharmaceutical Sciences Encyclopedia · doi:10.1002/9780470571224.pse454
Self-citationOxidative stress and XIAP signalling in neuronal cells
Kairisalo, M. (2010) · Työväentutkimus Vuosikirja
The role of transcription factor Nrf2 in osteoarthritis
Abusarah, J. (2014) · doi:10.71781/31868
Role of myeloperoxidase in lung inflammation'
Haegens, A. (2008) · doi:10.26481/dis.20080606ah
Brossi, P. M. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.10.2014.tde-17092014-111507
Defining the Role of GGTase-I in the Development of Rheumatoid Arthritis and Atherosclerosis
Khan, O. M. (2012) · Gothenburg University Publications Electronic Archive (Gothenburg University)
Mnaimneh, S., Damaj, M. B., Barhoumi, R., Mouneimne, Y., Geffard, M., Veyret, B., & Vincendeau, P. (2004) · The Pain Clinic · doi:10.1163/1568569041798407
Guo, D., Tan, W., Wang, F., Lv, Z., Hu, J., Lv, T., Chen, Q., Gu, X., Wan, B., & Zhang, Z. (2008) · Revue du Rhumatisme · doi:10.1016/j.rhum.2007.12.009
Nitric oxide production in association with osteoarthritis
Kalpakcioglu, B. B., & Şenel, K. (2007) · The Pain Clinic · doi:10.1179/016911107x268648
Oxidant and Antioxidant Status in Children with Juvenile Idiopathic Arthritis
Poyrazoğlu, H., Yazıcı, C., Gökçek, İ., Gündüz, Z., Dursun, İ., & Düşünsel, R. (2012) · Annals of Paediatric Rheumatology · doi:10.5455/apr.092020120807
MikroRNA’lar ve OSTEOARTRİT / MicroRNAs and OSTEOARTHRITIS
Soyocak, A., Özgen, M., Kurt, H., Değirmenci, İ., & Güneş, H. V. (2016) · OSMANGAZİ JOURNAL OF MEDICINE · doi:10.20515/otd.04339
Downey, C. M., & Jirik, F. R. (2011) · Springer eBooks · doi:10.1007/978-1-4614-1025-6_45
Evaluation of potential therapeutic agents for antiinflammatory activity
Sahu, D. (2012) · INFLIBNET
Sepúlveda, M., & Julieta, A. (2008) · Universidad de Chile
Rothenberg, A. R., & Elisseeff, J. H. (2010) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789814313568_0012
A proteomics survey of human articular chondrocytes in osteoarthritis
Lambrecht, S. (2007) · Ghent University Academic Bibliography (Ghent University)
Role of endothelial progenitor cells and redox potential in synovium neovascularisation
Rzodkiewicz, P., Gajewski, M., Maśliński, S., & Wojtecka-Lukasik, E. (2012) · Reumatologia/Rheumatology · doi:10.5114/reum.2012.31406
Potential Mechanisms of PTA: Cell Death
Grogan, S. P., Lotz, M., & DʼLima, D. D. (2015) · Springer eBooks · doi:10.1007/978-1-4899-7606-2_15
Aging and Post-Traumatic Arthritis
Loeser, R. F., Ferguson, C. M., & Lotz, M. (2015) · Springer eBooks · doi:10.1007/978-1-4899-7606-2_14
Oxidative stress in osteoarticular diseases
Alcaraz, M. J., Portal‐Núñez, S., Ardura, J. A., & Esbrit, P. (2016) · Wiley eBooks · doi:10.1002/9781118832431.ch12
Vos, L. M. (2014) · University of Groningen research database (University of Groningen / Centre for Information Technology)
Rastmanesh, R., & Weber, C. E. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-397156-2.00127-7
Autophagy Regulates Osteoarthritis-Like Gene Expression Changes
Takayama, K., & Matsushita, T. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405529-2.00021-4
Ye, W., Zhong, Z., Zhu, S., Zheng, S., Xiao, J., Song, S., Yu, H., Wu, Q., Lin, Z., & Chen, J.-T. (2017) · APOPTOSIS · doi:10.1007/s10495-017-1373-3
RetractedTikhova, Y., Дворщенко, К. О., Korotkyi, O., & Valentyno, V. V. (2017) · ScienceRise Biological Science · doi:10.15587/2519-8025.2017.109318
Szíjgyártó, Z. (2007) · University of Debrecen Electronic Archive (University of Debrecen)
Optimization of Vitrification for Human Articular Cartilage
Hahn, J. N. (2015) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3901zq1h
Arthia, R., Kuppusamy, M., Vijayakumar, V., Mangairkarasi, N., Manikannan, M., & Poonguzhali, S. (2019) · PharmaNutrition · doi:10.1016/j.phanu.2019.100170
Mora, R., Pedrotti, L., Bertani, B., Tuvo, G., & Nicoletta, M. (2020)
Metadata
- Authors
- Henrotin, Y. E., Bruckner, P., & Pujol, J.-P. L.
- Affiliations
- University of Liège (BE)
- Université de Caen Normandie (FR)
- Corresponding author
- Henrotin, Y.E
- ORCID
- Henrotin, Y.E
- Venue
- Osteoarthritis and Cartilage
- Publisher
- Elsevier BV
- Published
- 2003-10
- Volume
- 11
- Issue
- 10
- Pages
- 747-755
- ISSN
- 1063-4584 (ISSN-L)
- OpenAlex
- W2044924856
- Cited by
- 740
- References
- 82
- Citations by year
- 2026: 15 · 2025: 29 · 2024: 30 · 2023: 35 · 2022: 34 · 2021: 37 · 2020: 39 · 2019: 35 · 2018: 45 · 2017: 36 · 2016: 32 · 2015: 33 · 2014: 35 · 2013: 34 · 2012: 45
- FWCI
- 3.61
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Osteoarthritis and Cartilage (publishedVersion)
- PubMed (publishedVersion)
- ORBi (University of Liège) (submittedVersion)
- Funders
- UCB Pharma
- Topics
- Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Keywords
- reactive oxygen species, cartilage degeneration, cartilage homeostasis, nitric oxide, peroxynitrite, superoxide, redox signaling, joint inflammation, synovium, matrix metalloproteinases, apoptosis, antioxidant therapy, osteoarthritis, rheumatoid arthritis
- MeSH terms
- Cartilage, Articular, Extracellular Matrix, Homeostasis, Humans, Osteoarthritis, Oxidation-Reduction, Synovial Membrane, Signal Transduction, Cytokines, Apoptosis, Reactive Oxygen Species, Chondrocytes, Metalloproteases
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review