Reactieve zuurstofcomponent (Dutch Wikipedia)

Analysis of information sources in references of the Wikipedia article "Reactieve zuurstofcomponent" in Dutch language version.

refsWebsite

Global rank Dutch rank

17doi.org

2^nd place

8^th place

15nih.gov

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12^th place

1springer.com

274^th place

340^th place

1biomedcentral.com

2,747^th place

785^th place

biomedcentral.com

jbiomedsci.biomedcentral.com

Aleksey V. Belikov, Burkhart Schraven, Luca Simeoni. (2015). T cells and reactive oxygen species Journal of Biomedical Science. 22 pag.: 85 DOI:10.1186/s12929-015-0194-3 Internetpagina: T cells and reactive oxygen species (alleen samenvatting, voor volledig artikel is betaald abonnement nodig) PubMed: 26471060

doi.org

dx.doi.org

E. Novo, M. Parola. (2008). Redox mechanisms in hepatic chronic wound healing and fibrogenesis Fibrogenesis Tissue Repair. 1 (1): pag.: 5 DOI:10.1186/1755-1536-1-5 PubMed Central: 2584013 PubMed: 19014652
M.Hayyan, M.A. Hashim, I.M. AlNashef. (2016). Superoxide Ion: Generation and Chemical Implications Chem.Rev.. 116 (5): pag.: 3029–3085 DOI:10.1021/acs.chemrev.5b00407
Martha E. Sosa Torres, Juan P. Saucedo-Vázquez, Peter M.H. Kroneck. (2015). Sustaining Life on Planet Earth: Metalloenzymes Mastering Dioxygen and Other Chewy Gases, Chapter 1, Section 3 The dark side of dioxygen' Ed.: Peter M.H. Kroneck, Martha E. Sosa Torres Metal Ions in Life Sciences. 15 pag.: 1–12 Springer DOI:10.1007/978-3-319-12415-5_1
J.F. Turrens. (2003). Mitochondrial formation of reactive oxygen species J.Physiol.. 552 (Pt 2): pag.: 335–344 DOI:10.1113/jphysiol.2003.049478 PubMed Central: 2343396 PubMed: 14561818
F. Muller. (2000). The nature and mechanism of superoxide production by the electron transport chain: Its relevance to aging J.Amer.Aging Assoc.. 23 (4): pag.: 227–253 DOI:10.1007/s11357-000-0022-9 PubMed Central: 3455268 PubMed: 23604868
D. Han, E. Williams, E. Cadenas. (2001). Mitochondrial respiratory chain-dependent generation of superoxide anion and its release into the intermembrane space The Biochemical Journal. 353 (2): pag.: 411–416 DOI:10.1042/0264-6021:3530411 PubMed Central: 1221585 PubMed: 11139407
X. Li, P. Fang, J. Mai, E.T. Choi, H. Wang, X.F. Yang. (2013). Targeting mitochondrial reactive oxygen species as novel therapy for inflammatory diseases and cancers J.Hematology & Oncology. 6 (19): pag.: 19 DOI:10.1186/1756-8722-6-19 PubMed Central: 3599349 PubMed: 23442817
C. Laloi, M. Havaux. (2015). Key players of singlet oxygen-induced cell death in plants Front Plant Sci. 6 pag.: 39 DOI:10.3389/fpls.2015.00039 PubMed Central: 4316694 PubMed: 25699067
B. Rada, T.L.Leto. (2008). Oxidative innate immune defenses by Nox/Duox family NADPH oxidases Contributions to Microbiology Contributions to Microbiology. 15 pag.: 164–187 – ISBN 978-3-8055-8548-4 DOI:10.1159/000136357 PubMed Central: 2776633 PubMed: 18511861
G.E. Conner, M. Salathe, R. Forteza. (2002). Lactoperoxidase and hydrogen peroxide metabolism in the airway American Journal of Respiratory and Critical Care Medicine. 166 (12 pt2): pag.: S57-61 DOI:10.1164/rccm.2206018 PubMed: 12471090
H.J. Kim, C.H. Kim, J.H. Ryu, M.J. Kim, C.Y. Park, J.M. Lee, M.J. Holtzman, J.H. Yoon. (2013). Reactive oxygen species induce antiviral innate immune response through IFN-λ regulation in human nasal epithelial cells American Journal of Respiratory Cell and Molecular Biology. 49 (5): pag.: 855–865 DOI:10.1165/rcmb.2013-0003OC PubMed: 23786562
C. Deffert, J. Cachat, K.H. Krause. (2014). Phagocyte NADPH oxidase, chronic granulomatous disease and mycobacterial infections Cellular Microbiology. 16 (8): pag.: 1168–1178 DOI:10.1111/cmi.12322 PubMed: 24916152
Aleksey V. Belikov, Burkhart Schraven, Luca Simeoni. (2015). T cells and reactive oxygen species Journal of Biomedical Science. 22 pag.: 85 DOI:10.1186/s12929-015-0194-3 Internetpagina: T cells and reactive oxygen species (alleen samenvatting, voor volledig artikel is betaald abonnement nodig) PubMed: 26471060
J. Liu, E. Head, A.M. Gharib, W. Yuan, R.T. Ingersoll, T.M. Hagen, C.W. Cotman, B.N. Ames. (2002). Memory loss in old rats is associated with brain mitochondrial decay and RNA/DNA oxidation: partial reversal by feeding acetyl-L-carnitine and/or R-alpha -lipoic acid Proceedings of the National Academy of Sciences of the United States of America. 99 (4): pag.: 2356–2361 DOI:10.1073/pnas.261709299 PubMed Central: 122369 PubMed: 11854529
E.R. Stadtman. (1992). Protein oxidation and aging Science. 257 (5074): pag.: 1220–1224 DOI:10.1126/science.1355616 PubMed: 1355616
J.M. Carney, P.E. Starke-Reed, C.N. Oliver, R.W. Landum, M.S. Cheng, J.F. Wu, R.A. Floyd. (1991). Reversal of age-related increase in brain protein oxidation, decrease in enzyme activity, and loss in temporal and spatial memory by chronic administration of the spin-trapping compound N-tert-butyl-alpha-phenylnitrone Proceedings of the National Academy of Sciences of the United States of America. 88 (9): pag.: 3633–3636 DOI:10.1073/pnas.88.9.3633 PubMed Central: 51506 PubMed: 1673789
Zie voor de verscjillende soorten beschadigingen bijvoorbeeld:
- G. Waris, H. Ahsan. (2006). Reactive oxygen species: role in the development of cancer and various chronic conditions J.Carcinogenesis. 5 pag.: 14 DOI:10.1186/1477-3163-5-14 PubMed Central: 1479806 PubMed: 16689993

nih.gov

ncbi.nlm.nih.gov

E. Novo, M. Parola. (2008). Redox mechanisms in hepatic chronic wound healing and fibrogenesis Fibrogenesis Tissue Repair. 1 (1): pag.: 5 DOI:10.1186/1755-1536-1-5 PubMed Central: 2584013 PubMed: 19014652
J.F. Turrens. (2003). Mitochondrial formation of reactive oxygen species J.Physiol.. 552 (Pt 2): pag.: 335–344 DOI:10.1113/jphysiol.2003.049478 PubMed Central: 2343396 PubMed: 14561818
F. Muller. (2000). The nature and mechanism of superoxide production by the electron transport chain: Its relevance to aging J.Amer.Aging Assoc.. 23 (4): pag.: 227–253 DOI:10.1007/s11357-000-0022-9 PubMed Central: 3455268 PubMed: 23604868
D. Han, E. Williams, E. Cadenas. (2001). Mitochondrial respiratory chain-dependent generation of superoxide anion and its release into the intermembrane space The Biochemical Journal. 353 (2): pag.: 411–416 DOI:10.1042/0264-6021:3530411 PubMed Central: 1221585 PubMed: 11139407
X. Li, P. Fang, J. Mai, E.T. Choi, H. Wang, X.F. Yang. (2013). Targeting mitochondrial reactive oxygen species as novel therapy for inflammatory diseases and cancers J.Hematology & Oncology. 6 (19): pag.: 19 DOI:10.1186/1756-8722-6-19 PubMed Central: 3599349 PubMed: 23442817
C. Laloi, M. Havaux. (2015). Key players of singlet oxygen-induced cell death in plants Front Plant Sci. 6 pag.: 39 DOI:10.3389/fpls.2015.00039 PubMed Central: 4316694 PubMed: 25699067
B. Rada, T.L.Leto. (2008). Oxidative innate immune defenses by Nox/Duox family NADPH oxidases Contributions to Microbiology Contributions to Microbiology. 15 pag.: 164–187 – ISBN 978-3-8055-8548-4 DOI:10.1159/000136357 PubMed Central: 2776633 PubMed: 18511861
G.E. Conner, M. Salathe, R. Forteza. (2002). Lactoperoxidase and hydrogen peroxide metabolism in the airway American Journal of Respiratory and Critical Care Medicine. 166 (12 pt2): pag.: S57-61 DOI:10.1164/rccm.2206018 PubMed: 12471090
H.J. Kim, C.H. Kim, J.H. Ryu, M.J. Kim, C.Y. Park, J.M. Lee, M.J. Holtzman, J.H. Yoon. (2013). Reactive oxygen species induce antiviral innate immune response through IFN-λ regulation in human nasal epithelial cells American Journal of Respiratory Cell and Molecular Biology. 49 (5): pag.: 855–865 DOI:10.1165/rcmb.2013-0003OC PubMed: 23786562
C. Deffert, J. Cachat, K.H. Krause. (2014). Phagocyte NADPH oxidase, chronic granulomatous disease and mycobacterial infections Cellular Microbiology. 16 (8): pag.: 1168–1178 DOI:10.1111/cmi.12322 PubMed: 24916152
Aleksey V. Belikov, Burkhart Schraven, Luca Simeoni. (2015). T cells and reactive oxygen species Journal of Biomedical Science. 22 pag.: 85 DOI:10.1186/s12929-015-0194-3 Internetpagina: T cells and reactive oxygen species (alleen samenvatting, voor volledig artikel is betaald abonnement nodig) PubMed: 26471060
J. Liu, E. Head, A.M. Gharib, W. Yuan, R.T. Ingersoll, T.M. Hagen, C.W. Cotman, B.N. Ames. (2002). Memory loss in old rats is associated with brain mitochondrial decay and RNA/DNA oxidation: partial reversal by feeding acetyl-L-carnitine and/or R-alpha -lipoic acid Proceedings of the National Academy of Sciences of the United States of America. 99 (4): pag.: 2356–2361 DOI:10.1073/pnas.261709299 PubMed Central: 122369 PubMed: 11854529
E.R. Stadtman. (1992). Protein oxidation and aging Science. 257 (5074): pag.: 1220–1224 DOI:10.1126/science.1355616 PubMed: 1355616
J.M. Carney, P.E. Starke-Reed, C.N. Oliver, R.W. Landum, M.S. Cheng, J.F. Wu, R.A. Floyd. (1991). Reversal of age-related increase in brain protein oxidation, decrease in enzyme activity, and loss in temporal and spatial memory by chronic administration of the spin-trapping compound N-tert-butyl-alpha-phenylnitrone Proceedings of the National Academy of Sciences of the United States of America. 88 (9): pag.: 3633–3636 DOI:10.1073/pnas.88.9.3633 PubMed Central: 51506 PubMed: 1673789
Zie voor de verscjillende soorten beschadigingen bijvoorbeeld:
- G. Waris, H. Ahsan. (2006). Reactive oxygen species: role in the development of cancer and various chronic conditions J.Carcinogenesis. 5 pag.: 14 DOI:10.1186/1477-3163-5-14 PubMed Central: 1479806 PubMed: 16689993

springer.com

link.springer.com

Yun Jeong Kim, Yong Kyoo Shin, Dong Suep Sohn, Chung Soo Lee. (2014). Menadione induces the formation of reactive oxygen species and depletion of GSH-mediated apoptosis and inhibits the FAK-mediated cell invasion Naunyn-Schmiedeberg's Archives of Pharmacology. 387 (9): pag.: 799–809 springer.com: Menadione induces the formation of reactive oxygen species geraadpleegd op 8 mei 2018 (alleen samenvatting, voor volledig artikel is betaald abonnement nodig)