Reactive oxygen species, antioxidants and signaling in plants

Reactive oxygen species: Metabolism, oxidative stress, and signal transduction

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Oxidative stress, antioxidants and stress tolerance

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Quantitative Monitoring of Gene Expression Patterns with a Complementary DNA Microarray

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Oxidants, oxidative stress and the biology of ageing

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ASCORBATE AND GLUTATHIONE: Keeping Active Oxygen Under Control

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Reactive oxygen gene network of plants

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Genomic Expression Programs in the Response of Yeast Cells to Environmental Changes

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Biochemistry and molecular biology of plants

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Redox Homeostasis and Antioxidant Signaling: A Metabolic Interface between Stress Perception and Physiological Responses

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The role of active oxygen in the response of plants to water deficit and desiccation

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Oxygen Stress and Superoxide Dismutases

Scandalios, J. G. (1993) · Plant Physiology · doi:10.1104/pp.101.1.7 · Cited by 1,690

P LANT M ITOCHONDRIA AND O XIDATIVE S TRESS: Electron Transport, NADPH Turnover, and Metabolism of Reactive Oxygen Species

Møller, I. M. (2001) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.52.1.561 · Cited by 1,664

Functional analysis of oxidative stress-activated mitogen-activated protein kinase cascade in plants

Kovtun, Y., Chiu, W.-L., Tena, G., & Sheen, J. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.6.2940 · Cited by 1,530

The evolution of free radicals and oxidative stress

McCord, J. M. (2000) · The American Journal of Medicine · doi:10.1016/s0002-9343(00)00412-5 · Cited by 1,407

Remodeling of Yeast Genome Expression in Response to Environmental Changes

Causton, H. C., Ren, B., Koh, S. S., Harbison, C. T., Kanin, E., Jennings, E. G., Lee, T. I., True, H. L., Lander, E. S., & Young, R. A. (2001) · Molecular Biology of the Cell · doi:10.1091/mbc.12.2.323 · Cited by 1,370

Reactive oxygen species and temperature stresses: A delicate balance between signaling and destruction

Suzuki, N., & Mittler, R. (2006) · Physiologia Plantarum · doi:10.1111/j.0031-9317.2005.00582.x · Cited by 1,117

Positive control of a regulon for defenses against oxidative stress and some heat-shock proteins in Salmonella typhimurium

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Flavonoid oxidation in plants: from biochemical properties to physiological functions

POURCEL, L., ROUTABOUL, J., CHEYNIER, V, LEPINIEC, L., & DEBEAUJON, I. (2007) · Trends in Plant Science · doi:10.1016/j.tplants.2006.11.006 · Cited by 966

Regulation of the Arabidopsis Transcriptome by Oxidative Stress

Desikan, R., A.-H.-Mackerness, S., Hancock, J. T., & Neill, S. J. (2001) · Plant Physiology · doi:10.1104/pp.127.1.159 · Cited by 922

Systemic Signaling and Acclimation in Response to Excess Excitation Energy in Arabidopsis

Karpinski, S., Reynolds, H., Karpinska, B., Wingsle, G., Creissen, G., & Mullineaux, P. (1999) · Science · doi:10.1126/science.284.5414.654 · Cited by 875

DNA Microarray-Mediated Transcriptional Profiling of the Escherichia coli Response to Hydrogen Peroxide

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Global transcriptional responses of fission yeast to environmental stress

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Responses to Abiotic Stresses

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Complexity, Cross Talk and Integration of Plant MAP Kinase Signalling

Jonak, C. (2002) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(02)00285-6 · Cited by 706

The role of active oxygen species in plant signal transduction

Van Breusegem, F., Vranová, E., Dat, J. F., & Inzé, D. (2001) · Plant Science · doi:10.1016/s0168-9452(01)00452-6 · Cited by 603

Photorespiration protects C3 plants from photooxidation

Kozaki, A., & Takeba, G. (1996) · Nature · doi:10.1038/384557a0 · Cited by 593

Changes in the antioxidant enzyme efficacy in two high yielding genotypes of mulberry (Morus alba L.) under NaCl salinity

Sudhakar, C., Lakshmi, A., & Giridarakumar, S. (2001) · Plant Science · doi:10.1016/s0168-9452(01)00450-2 · Cited by 583

Oxidative Stress and Autophagy

Kiffin, R., Bandyopadhyay, U., & Cuervo, A. M. (2006) · Antioxidants & Redox Signaling · doi:10.1089/ars.2006.8.152 · Cited by 525

Control of Plant Development by Reactive Oxygen Species

Gapper, C., & Dolan, L. (2006) · Plant Physiology · doi:10.1104/pp.106.079079 · Cited by 519

The role of active oxygen species in plant signal transduction

Vranová, E., Breusegem, F. V., Dat, J. F., Belles‐Boix, E., & Inzé, D. (2002) · Ghent University Academic Bibliography (Ghent University) · Cited by 508

Chilling stress-induced changes of antioxidant enzymes in the leaves of cucumber: in gel enzyme activity assays

Lee, D. H., & Lee, C. B. (2000) · Plant Science · doi:10.1016/s0168-9452(00)00326-5 · Cited by 480

Response of the cultivated tomato and its wild salt‐tolerant relative Lycopersiconpennellii to salt‐dependent oxidative stress: The root antioxidative system

Shalata, A., Mittova, V., Volokita, M., Guy, M., & Tal, M. (2001) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2001.1120405.x · Cited by 448

NDP kinase 2 interacts with two oxidative stress-activated MAPKs to regulate cellular redox state and enhances multiple stress tolerance in transgenic plants

Moon, H., Lee, B., Choi, G., Shin, D., Prasad, D. T., Lee, O., Kwak, S.-S., Kim, D. H., Nam, J., Bahk, J., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.252641899 · Cited by 441

Dissecting the Superoxide Dismutase-Ascorbate-Glutathione-Pathway in Chloroplasts by Metabolic Modeling. Computer Simulations as a Step towards Flux Analysis

Polle, A. (2001) · Plant Physiology · doi:10.1104/pp.126.1.445 · Cited by 420

Effects of silicon on enzyme activity and sodium, potassium and calcium concentration in barley under salt stress

Liang, Y. (1999) · Plant and Soil · doi:10.1023/a:1004526604913 · Cited by 406

Elevated Glutathione Biosynthetic Capacity in the Chloroplasts of Transgenic Tobacco Plants Paradoxically Causes Increased Oxidative Stress

Creissen, G., Firmin, J., Fryer, M., Kular, B., Leyland, N., Reynolds, H., Pastori, G., Wellburn, F., Baker, N., Wellburn, A., et al. (1999) · The Plant Cell · doi:10.1105/tpc.11.7.1277 · Cited by 356

Harpin and hydrogen peroxide both initiate programmed cell death but have differential effects on defence gene expression in Arabidopsis suspension cultures

DESIKAN, R., REYNOLDS, A., HANCOCK, T. J., & NEILL, J. S. (1998) · Biochemical Journal · doi:10.1042/bj3300115 · Cited by 354

Double antisense plants lacking ascorbate peroxidase and catalase are less sensitive to oxidative stress than single antisense plants lacking ascorbate peroxidase or catalase

Rizhsky, L., Hallak‐Herr, E., Van Breusegem, F., Rachmilevitch, S., Barr, J. E., Rodermel, S., Inzé, D., & Mittler, R. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01427.x · Cited by 346

Signaling through MAP kinase networks in plants

Mishra, N. S., Tuteja, R., & Tuteja, N. (2006) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2006.05.001 · Cited by 345

The Roles of Reactive Oxygen Species in Plant Cells

Bailey-Serres, J. N., & Mittler, R. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.900191 · Cited by 337

Formation and possible roles of nitric oxide in plant roots

Stöhr, C., & Stremlau, S. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/erj058 · Cited by 242

Enhanced tolerance to oxidative stress in transgenic tobacco plants expressing three antioxidant enzymes in chloroplasts

Lee, Y.-P., Kim, S.-H., Bang, J.-W., Lee, H.-S., Kwak, S.-S., & Kwon, S.-Y. (2007) · Plant Cell Reports · doi:10.1007/s00299-006-0253-z · Cited by 239

Response of antioxidative defence system to temperature and water stress combinations in wheat seedlings

Keleş, Y., & Öncel, İ. (2002) · Plant Science · doi:10.1016/s0168-9452(02)00213-3 · Cited by 215

Superoxide Dismutase, Catalase, and α-Tocopherol Content of Stored Potato Tubers

Spychalla, J. P., & Desborough, S. L. (1990) · PLANT PHYSIOLOGY · doi:10.1104/pp.94.3.1214 · Cited by 200

Spatial Dependence for Hydrogen Peroxide-Directed Signaling in Light-Stressed Plants

Mullineaux, P. M., Karpinski, S., & Baker, N. R. (2006) · Plant Physiology · doi:10.1104/pp.106.078162 · Cited by 198

Comprehensive analysis of gene expression in Nicotiana tabacum leaves acclimated to oxidative stress

Vranová, E., Atichartpongkul, S., Villarroel, R., Van Montagu, M., Inzé, D., & Van Camp, W. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152337999 · Cited by 172

Characterization of membrane polypeptides from pea leaf peroxisomes involved in superoxide radical generation

López‐Huertas, E., Corpas, F. J., Sandalio, L. M., & del Río, L. A. (1999) · Biochemical Journal · doi:10.1042/0264-6021:3370531 · Cited by 150

Changes of some anti-oxidative physiological indices under soil water deficits among 10 wheat (Triticum aestivum L.) genotypes at tillering stage

Shao, H., Chu, L.-Y., Wu, G., Zhang, J., Lu, Z., & Hu, Y.-C. (2006) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2006.09.004 · Cited by 138

Hydrogen peroxide–induced gene expression in Arabidopsis thaliana

Desikan, R., Neill, S. J., & Hancock, J. T. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00157-x · Cited by 134

Transcription Profiling of the Early Gravitropic Response in Arabidopsis Using High-Density Oligonucleotide Probe Microarrays,

Moseyko, N., Zhu, T., Chang, H., Wang, X., & Feldman, L. J. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.009688 · Cited by 112

Apoplastic peroxidases and ascorbate are involved in manganese toxicity and tolerance of Vigna unguiculata

Fecht‐Christoffers, M. M., Maier, P., & Horst, W. J. (2003) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2003.00022.x · Cited by 109

The mutual responses of higher plants to environment: Physiological and microbiological aspects

Wu, G., Zhen-Kuan, W., Wang, Y., Chu, L.-Y., & Shao, H. (2007) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2007.05.003 · Cited by 70

The Mechanism of Superoxide Scavenging byArchaeoglobus fulgidus Neelaredoxin

Abreu, I. A., Saraiva, L. M., Soares, C. M., Teixeira, M. S., & Cabelli, D. E. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m103232200 · Cited by 41

Stress hormones mediated lipid accumulation and modulation of specific fatty acids in Nannochloropsis oceanica CASA CC201

Udayan, A., Sabapathy, H., & Arumugam, M. (2020) · Bioresource Technology · doi:10.1016/j.biortech.2020.123437 · Cited by 51

Ecotoxicological effects of ibuprofen on plant growth of Vigna unguiculata L

Wijaya, L., Alyemeni, M., Ahmad, P., Alfarhan, A., Barcelo, D., El-Sheikh, M. A., & Pico, Y. (2020) · Plants · doi:10.3390/plants9111473 · Cited by 51