Reactive oxygen species in plant development

Glutathione S-Transferases

Habig, W. H., Pabst, M. J., & Jakoby, W. B. (1974) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)42083-8 · Cited by 18,221

ROS Are Good

Mittler, R. (2017) · Trends in Plant Science · doi:10.1016/j.tplants.2016.08.002 · Cited by 3,499

ROS signaling: the new wave?

Mittler, R., Vanderauwera, S., Suzuki, N., Miller, G., Tognetti, V. B., Vandepoele, K., Gollery, M., Shulaev, V., & Van Breusegem, F. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2011.03.007 · Cited by 2,305

Reactive oxygen species produced by NADPH oxidase regulate plant cell growth

Foreman, J., Demidchik, V., Bothwell, J. H. F., Mylona, P., Miedema, H., Torres, M. A., Linstead, P., Costa, S., Brownlee, C., Jones, J. D. G., et al. (2003) · Nature · doi:10.1038/nature01485 · Cited by 2,239

Leaf Senescence

Lim, P. O., Kim, H. J., & Gil Nam, H. (2007) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105316 · Cited by 1,978

Glutathione in plants: an integrated overview

NOCTOR, G., MHAMDI, A., CHAOUCH, S., HAN, Y., NEUKERMANS, J., MARQUEZ‐GARCIA, B., QUEVAL, G., & FOYER, C. H. (2012) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2011.02400.x · Cited by 1,589

Reactive Oxygen Species in Plant Signaling

Waszczak, C., Carmody, M., & Kangasjärvi, J. (2018) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042817-040322 · Cited by 1,563

Redox Regulation in Photosynthetic Organisms: Signaling, Acclimation, and Practical Implications

Foyer, C. H., & Noctor, G. (2009) · Antioxidants & Redox Signaling · doi:10.1089/ars.2008.2177 · Cited by 1,431

Superoxide Anion Radical (O·̄2), Superoxide Dismutases, and Related Matters

Fridovich, I. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.30.18515 · Cited by 1,337

Seed Germination and Vigor

Rajjou, L., Duval, M., Gallardo, K., Catusse, J., Bally, J., Job, C., & Job, D. (2012) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042811-105550 · Cited by 1,237

Transcriptional Regulation of ROS Controls Transition from Proliferation to Differentiation in the Root

Tsukagoshi, H., Busch, W., & Benfey, P. N. (2010) · Cell · doi:10.1016/j.cell.2010.10.020 · Cited by 1,081

Reactive Oxygen Species in Plant Cell Death

Van Breusegem, F., & Dat, J. F. (2006) · Plant Physiology · doi:10.1104/pp.106.078295 · Cited by 1,000

Catalase function in plants: a focus on Arabidopsis mutants as stress-mimic models

Mhamdi, A., Queval, G., Chaouch, S., Vanderauwera, S., Van Breusegem, F., & Noctor, G. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq282 · Cited by 989

Performing the paradoxical: how plant peroxidases modify the cell wall

PASSARDI, F., PENEL, C., & DUNAND, C. (2004) · Trends in Plant Science · doi:10.1016/j.tplants.2004.09.002 · Cited by 932

ROS-related redox regulation and signaling in plants

Noctor, G., Reichheld, J.-P., & Foyer, C. H. (2018) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2017.07.013 · Cited by 903

High-Resolution Temporal Profiling of Transcripts during Arabidopsis Leaf Senescence Reveals a Distinct Chronology of Processes and Regulation

Breeze, E., Harrison, E., McHattie, S., Hughes, L., Hickman, R., Hill, C., Kiddle, S., Kim, Y.-S., Penfold, C. A., Jenkins, D., et al. (2011) · The Plant Cell · doi:10.1105/tpc.111.083345 · Cited by 868

From intracellular signaling networks to cell death: the dual role of reactive oxygen species in seed physiology

Bailly, C., El-Maarouf-Bouteau, H., & Corbineau, F. (2008) · Comptes Rendus. Biologies · doi:10.1016/j.crvi.2008.07.022 · Cited by 861

Singlet oxygen in plants: production, detoxification and signaling

Triantaphylidès, C., & Havaux, M. (2009) · Trends in Plant Science · doi:10.1016/j.tplants.2009.01.008 · Cited by 713

JUNGBRUNNEN1 , a Reactive Oxygen Species–Responsive NAC Transcription Factor, Regulates Longevity in Arabidopsis

Wu, A., Allu, A. D., Garapati, P., Siddiqui, H., Dortay, H., Zanor, M.-I., Asensi-Fabado, M. A., Munné-Bosch, S., Antonio, C., Tohge, T., et al. (2012) · The Plant Cell · doi:10.1105/tpc.111.090894 · Cited by 601

Genetic and molecular identification of genes required for female gametophyte development and function in Arabidopsis

Pagnussat, G. C., Yu, H.-J., Ngo, Q. A., Rajani, S., Mayalagu, S., Johnson, C. S., Capron, A., Xie, L.-F., Ye, D., & Sundaresan, V. (2005) · Development · doi:10.1242/dev.01595 · Cited by 591

The ROOT MERISTEMLESS1/CADMIUM SENSITIVE2 Gene Defines a Glutathione-Dependent Pathway Involved in Initiation and Maintenance of Cell Division during Postembryonic Root Development

Vernoux, T., Wilson, R. C., Seeley, K. A., Reichheld, J.-P., Muroy, S., Brown, S., Maughan, S. C., Cobbett, C. S., Van Montagu, M., Inzé, D., et al. (2000) · The Plant Cell · doi:10.1105/tpc.12.1.97 · Cited by 576

Oxidative scission of plant cell wall polysaccharides by ascorbate-induced hydroxyl radicals

FRY, S. C. (1998) · Biochemical Journal · doi:10.1042/bj3320507 · Cited by 558

Distribution of superoxide and hydrogen peroxide in Arabidopsis root and their influence on root development: possible interaction with peroxidases

Dunand, C., Crèvecoeur, M., & Penel, C. (2007) · New Phytologist · doi:10.1111/j.1469-8137.2007.01995.x · Cited by 554

Leaf Vitamin C Contents Modulate Plant Defense Transcripts and Regulate Genes That Control Development through Hormone Signaling[W]

Pastori, G. M., Kiddle, G., Antoniw, J., Bernard, S., Veljovic-Jovanovic, S., Verrier, P. J., Noctor, G., & Foyer, C. H. (2003) · The Plant Cell · doi:10.1105/tpc.010538 · Cited by 537

Identification of Genes Required for Embryo Development in Arabidopsis

Tzafrir, I., Pena-Muralla, R., Dickerman, A., Berg, M., Rogers, R., Hutchens, S., Sweeney, T. C., McElver, J., Aux, G., Patton, D., et al. (2004) · Plant Physiology · doi:10.1104/pp.104.045179 · Cited by 535

Local Positive Feedback Regulation Determines Cell Shape in Root Hair Cells

Takeda, S., Gapper, C., Kaya, H., Bell, E., Kuchitsu, K., & Dolan, L. (2008) · Science · doi:10.1126/science.1152505 · Cited by 518

ROS production and protein oxidation as a novel mechanism for seed dormancy alleviation

Oracz, K., Bouteau, H. E., Farrant, J. M., Cooper, K., Belghazi, M., Job, C., Job, D., Corbineau, F., & Bailly, C. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03063.x · Cited by 518

The Role and Regulation of ABI5 (ABA-Insensitive 5) in Plant Development, Abiotic Stress Responses and Phytohormone Crosstalk

Skubacz, A., Daszkowska-Golec, A., & Szarejko, I. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01884 · Cited by 499

A gene regulatory network controlled by the NAC transcription factor ANAC092/AtNAC2/ORE1 during salt-promoted senescence: ANAC092 gene regulatory network

Balazadeh, S., Siddiqui, H., Allu, A. D., Matallana-Ramirez, L. P., Caldana, C., Mehrnia, M., Zanor, M.-I., Köhler, B., & Mueller-Roeber, B. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04151.x · Cited by 480

Perturbation of Indole-3-Butyric Acid Homeostasis by the UDP-Glucosyltransferase UGT74E2 Modulates Arabidopsis Architecture and Water Stress Tolerance

Tognetti, V. B., Van Aken, O., Morreel, K., Vandenbroucke, K., van de Cotte, B., De Clercq, I., Chiwocha, S., Fenske, R., Prinsen, E., Boerjan, W., et al. (2010) · The Plant Cell · doi:10.1105/tpc.109.071316 · Cited by 473

Molecular Definition of the Ascorbate-Glutathione Cycle in Arabidopsis Mitochondria Reveals Dual Targeting of Antioxidant Defenses in Plants

Chew, O., Whelan, J., & Millar, A. H. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m307525200 · Cited by 471

A plate reader method for the measurement of NAD, NADP, glutathione, and ascorbate in tissue extracts: Application to redox profiling during Arabidopsis rosette development

Queval, G., & Noctor, G. (2007) · Analytical Biochemistry · doi:10.1016/j.ab.2007.01.005 · Cited by 468

Two genes in Arabidopsis thaliana encoding GDP‐l‐galactose phosphorylase are required for ascorbate biosynthesis and seedling viability

Dowdle, J., Ishikawa, T., Gatzek, S., Rolinski, S., & Smirnoff, N. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03266.x · Cited by 459

Spreading the news: subcellular and organellar reactive oxygen species production and signalling

Mignolet-Spruyt, L., Xu, E., Idänheimo, N., Hoeberichts, F. A., Mühlenbock, P., Brosché, M., Van Breusegem, F., & Kangasjärvi, J. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw080 · Cited by 459

Conditional oxidative stress responses in the Arabidopsis photorespiratory mutant cat2 demonstrate that redox state is a key modulator of daylength‐dependent gene expression, and define photoperiod as a crucial factor in the regulation of H 2 O 2 ‐induced cell death

Queval, G., Issakidis‐Bourguet, E., Hoeberichts, F. A., Vandorpe, M., Gakière, B., Vanacker, H., Miginiac‐Maslow, M., Van Breusegem, F., & Noctor, G. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03263.x · Cited by 446

Peroxiredoxins in Plants and Cyanobacteria

Dietz, K.-J. (2011) · Antioxidants & Redox Signaling · doi:10.1089/ars.2010.3657 · Cited by 407

Oxidative stress and antioxidative systems: recipes for successful data collection and interpretation

Noctor, G., Mhamdi, A., & Foyer, C. H. (2016) · Plant, Cell & Environment · doi:10.1111/pce.12726 · Cited by 406

Plant glutathione peroxidases: Emerging role of the antioxidant enzymes in plant development and stress responses

Bela, K., Horváth, E., Gallé, Á., Szabados, L., Tari, I., & Csiszár, J. (2015) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.12.014 · Cited by 404

Intracellular Redox Compartmentation and ROS-Related Communication in Regulation and Signaling

Noctor, G., & Foyer, C. H. (2016) · Plant Physiology · doi:10.1104/pp.16.00346 · Cited by 403

Different Modes of Hydrogen Peroxide Action During Seed Germination

Wojtyla, Ł., Lechowska, K., Kubala, S., & Garnczarska, M. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00066 · Cited by 400

In Vivo Cell Wall Loosening by Hydroxyl Radicals during Cress Seed Germination and Elongation Growth

Müller, K., Linkies, A., Vreeburg, R. A. M., Fry, S. C., Krieger-Liszkay, A., & Leubner-Metzger, G. (2009) · Plant Physiology · doi:10.1104/pp.109.139204 · Cited by 399

Glutathione – linking cell proliferation to oxidative stress

Diaz-Vivancos, P., de Simone, A., Kiddle, G., & Foyer, C. H. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.09.023 · Cited by 391

Ascorbate Biosynthesis in Mitochondria Is Linked to the Electron Transport Chain between Complexes III and IV

Bartoli, C. G., Pastori, G. M., & Foyer, C. H. (2000) · Plant Physiology · doi:10.1104/pp.123.1.335 · Cited by 387

Lateral root formation and the multiple roles of auxin

Du, Y., & Scheres, B. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/erx223 · Cited by 383

A Tripartite Amplification Loop Involving the Transcription Factor WRKY75, Salicylic Acid, and Reactive Oxygen Species Accelerates Leaf Senescence

Guo, P., Li, Z., Huang, P., Li, B., Fang, S., Chu, J., & Guo, H. (2017) · The Plant Cell · doi:10.1105/tpc.17.00438 · Cited by 376

Arabidopsis GLUTATHIONE REDUCTASE1 Plays a Crucial Role in Leaf Responses to Intracellular Hydrogen Peroxide and in Ensuring Appropriate Gene Expression through Both Salicylic Acid and Jasmonic Acid Signaling Pathways

Mhamdi, A., Hager, J., Chaouch, S., Queval, G., Han, Y., Taconnat, L., Saindrenan, P., Gouia, H., Issakidis-Bourguet, E., Renou, J.-P., et al. (2010) · Plant Physiology · doi:10.1104/pp.110.153767 · Cited by 371

Reactive Oxygen Species (ROS): Beneficial Companions of Plants’ Developmental Processes

Singh, R., Singh, S., Parihar, P., Mishra, R. K., Tripathi, D. K., Singh, V. P., Chauhan, D. K., & Prasad, S. M. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01299 · Cited by 363

Reactive oxygen species mediate pollen tube rupture to release sperm for fertilization in Arabidopsis

Duan, Q., Kita, D., Johnson, E. A., Aggarwal, M., Gates, L., Wu, H.-M., & Cheung, A. Y. (2014) · Nature Communications · doi:10.1038/ncomms4129 · Cited by 343

ORS1, an H2O2-Responsive NAC Transcription Factor, Controls Senescence in Arabidopsis thaliana

Balazadeh, S., Kwasniewski, M., Caldana, C., Mehrnia, M., Zanor, M. I., Xue, G.-P., & Mueller-Roeber, B. (2011) · Molecular Plant · doi:10.1093/mp/ssq080 · Cited by 327

Spatiotemporal Production of Reactive Oxygen Species by NADPH Oxidase Is Critical for Tapetal Programmed Cell Death and Pollen Development in Arabidopsis

Xie, H.-T., Wan, Z.-Y., Li, S., & Zhang, Y. (2014) · The Plant Cell · doi:10.1105/tpc.114.125427 · Cited by 323

Interplay between the NADP-Linked Thioredoxin and Glutathione Systems in Arabidopsis Auxin Signaling

Bashandy, T., Guilleminot, J., Vernoux, T., Caparros-Ruiz, D., Ljung, K., Meyer, Y., & Reichheld, J.-P. (2010) · The Plant Cell · doi:10.1105/tpc.109.071225 · Cited by 319

The NADPH-dependent thioredoxin system constitutes a functional backup for cytosolic glutathione reductase in Arabidopsis

Marty, L., Siala, W., Schwarzländer, M., Fricker, M. D., Wirtz, M., Sweetlove, L. J., Meyer, Y., Meyer, A. J., Reichheld, J.-P., & Hell, R. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900206106 · Cited by 314

Plastidial Thioredoxin z Interacts with Two Fructokinase-Like Proteins in a Thiol-Dependent Manner: Evidence for an Essential Role in Chloroplast Development in Arabidopsis and Nicotiana benthamiana

Arsova, B., Hoja, U., Wimmelbacher, M., Greiner, E., Üstün, Ş., Melzer, M., Petersen, K., Lein, W., & Börnke, F. (2010) · The Plant Cell · doi:10.1105/tpc.109.071001 · Cited by 314

Ca2+-Activated Reactive Oxygen Species Production by Arabidopsis RbohH and RbohJ Is Essential for Proper Pollen Tube Tip Growth

Kaya, H., Nakajima, R., Iwano, M., Kanaoka, M. M., Kimura, S., Takeda, S., Kawarazaki, T., Senzaki, E., Hamamura, Y., Higashiyama, T., et al. (2014) · The Plant Cell · doi:10.1105/tpc.113.120642 · Cited by 312

The Impact of Global Change Factors on Redox Signaling Underpinning Stress Tolerance

Munné-Bosch, S., Queval, G., & Foyer, C. H. (2012) · Plant Physiology · doi:10.1104/pp.112.205690 · Cited by 309

Redox Regulation of Plant Development

Considine, M. J., & Foyer, C. H. (2014) · Antioxidants & Redox Signaling · doi:10.1089/ars.2013.5665 · Cited by 295

A redox cycle within the cell cycle: ring in the old with the new

Menon, S. G., & Goswami, P. C. (2007) · Oncogene · doi:10.1038/sj.onc.1209895 · Cited by 294

Senescence‐specific regulation of catalases in Arabidopsis thaliana (L.) Heynh

ZIMMERMANN, P., HEINLEIN, C., ORENDI, G., & ZENTGRAF, U. (2006) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2005.01459.x · Cited by 294

The Timing of Senescence and Response to Pathogens Is Altered in the Ascorbate-Deficient Arabidopsis Mutant vitamin c-1

Barth, C., Moeder, W., Klessig, D. F., & Conklin, P. L. (2004) · Plant Physiology · doi:10.1104/pp.103.032185 · Cited by 288

A nuclear glutathione cycle within the cell cycle

Diaz Vivancos, P., Wolff, T., Markovic, J., Pallardó, F. V., & Foyer, C. H. (2010) · Biochemical Journal · doi:10.1042/bj20100409 · Cited by 277

Role of Reactive Oxygen Species in the Regulation of Arabidopsis Seed Dormancy

Leymarie, J., Vitkauskaité, G., Hoang, H. H., Gendreau, E., Chazoule, V., Meimoun, P., Corbineau, F., El-Maarouf-Bouteau, H., & Bailly, C. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcr129 · Cited by 276

Redox regulation of plant stem cell fate

Zeng, J., Dong, Z., Wu, H., Tian, Z., & Zhao, Z. (2017) · The EMBO Journal · doi:10.15252/embj.201695955 · Cited by 273

Inactivation of Thioredoxin Reductases Reveals a Complex Interplay between Thioredoxin and Glutathione Pathways in Arabidopsis Development

Reichheld, J.-P., Khafif, M., Riondet, C., Droux, M., Bonnard, G., & Meyer, Y. (2007) · The Plant Cell · doi:10.1105/tpc.107.050849 · Cited by 270

Molecular link between auxin and ROS-mediated polar growth

Mangano, S., Denita-Juarez, S. P., Choi, H.-S., Marzol, E., Hwang, Y., Ranocha, P., Velasquez, S. M., Borassi, C., Barberini, M. L., Aptekmann, A. A., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1701536114 · Cited by 268

Functional Analysis of Arabidopsis Mutants Points to Novel Roles for Glutathione in Coupling H 2 O 2 to Activation of Salicylic Acid Accumulation and Signaling

Han, Y., Chaouch, S., Mhamdi, A., Queval, G., Zechmann, B., & Noctor, G. (2013) · Antioxidants & Redox Signaling · doi:10.1089/ars.2012.5052 · Cited by 262

Convergence and divergence in gene expression profiles induced by leaf senescence and 27 senescence‐promoting hormonal, pathological and environmental stress treatments

GUO, Y., & GAN, S. (2012) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2011.02442.x · Cited by 258

The metabolomics of oxidative stress

Noctor, G., Lelarge-Trouverie, C., & Mhamdi, A. (2015) · Phytochemistry · doi:10.1016/j.phytochem.2014.09.002 · Cited by 252

Arabidopsis Basic Leucine-Zipper Transcription Factors TGA9 and TGA10 Interact with Floral Glutaredoxins ROXY1 and ROXY2 and Are Redundantly Required for Anther Development

Murmu, J., Bush, M. J., DeLong, C., Li, S., Xu, M., Khan, M., Malcolmson, C., Fobert, P. R., Zachgo, S., & Hepworth, S. R. (2010) · Plant Physiology · doi:10.1104/pp.110.159111 · Cited by 252

Control of Arabidopsis meristem development by thioredoxin-dependent regulation of intercellular transport

Benitez-Alfonso, Y., Cilia, M., Roman, A. S., Thomas, C., Maule, A., Hearn, S., & Jackson, D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808717106 · Cited by 251

Control of root growth and development by reactive oxygen species

Tsukagoshi, H. (2016) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2015.10.012 · Cited by 245

Specific checkpoints regulate plant cell cycle progression in response to oxidative stress

Reichheld, J., Vernoux, T., Lardon, F., Van Montagu, M., & Inzé, D. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00413.x · Cited by 243

Functions and Regulation of Programmed Cell Death in Plant Development

Daneva, A., Gao, Z., Van Durme, M., & Nowack, M. K. (2016) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-111315-124915 · Cited by 243

Peroxisomal Hydrogen Peroxide Is Coupled to Biotic Defense Responses by ISOCHORISMATE SYNTHASE1 in a Daylength-Related Manner

Chaouch, S., Queval, G., Vanderauwera, S., Mhamdi, A., Vandorpe, M., Langlois-Meurinne, M., Van Breusegem, F., Saindrenan, P., & Noctor, G. (2010) · Plant Physiology · doi:10.1104/pp.110.153957 · Cited by 236

Interaction between hydrogen peroxide and plant hormones during germination and the early growth of pea seedlings

BARBA‐ESPIN, G., DIAZ‐VIVANCOS, P., CLEMENTE‐MORENO, M. J., ALBACETE, A., FAIZE, L., FAIZE, M., PÉREZ‐ALFOCEA, F., & HERNÁNDEZ, J. A. (2010) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2010.02120.x · Cited by 232

Extranuclear protection of chromosomal DNA from oxidative stress

Vanderauwera, S., Suzuki, N., Miller, G., van de Cotte, B., Morsa, S., Ravanat, J.-L., Hegie, A., Triantaphylidès, C., Shulaev, V., Van Montagu, M. C. E., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018359108 · Cited by 229

Hypoxia Triggers Meiotic Fate Acquisition in Maize

Kelliher, T., & Walbot, V. (2012) · Science · doi:10.1126/science.1220080 · Cited by 228

ROXY1 and ROXY2, two Arabidopsis glutaredoxin genes, are required for anther development

Xing, S., & Zachgo, S. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03375.x · Cited by 215

Targeted mRNA Oxidation Regulates Sunflower Seed Dormancy Alleviation during Dry After-Ripening

Bazin, J., Langlade, N., Vincourt, P., Arribat, S., Balzergue, S., El-Maarouf-Bouteau, H., & Bailly, C. (2011) · The Plant Cell · doi:10.1105/tpc.111.086694 · Cited by 212

A membrane-associated thioredoxin required for plant growth moves from cell to cell, suggestive of a role in intercellular communication

Meng, L., Wong, J. H., Feldman, L. J., Lemaux, P. G., & Buchanan, B. B. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913759107 · Cited by 211

Crosstalk between reactive oxygen species and hormonal signalling pathways regulates grain dormancy in barley

BAHIN, E., BAILLY, C., SOTTA, B., KRANNER, I., CORBINEAU, F., & LEYMARIE, J. (2011) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2011.02298.x · Cited by 209

Quiescent center formation in maize roots is associated with an auxin-regulated oxidizing environment

Jiang, K., Meng, Y. L., & Feldman, L. J. (2003) · Development · doi:10.1242/dev.00359 · Cited by 207

Restricting glutathione biosynthesis to the cytosol is sufficient for normal plant development

Pasternak, M., Lim, B., Wirtz, M., Hell, R., Cobbett, C. S., & Meyer, A. J. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03389.x · Cited by 202

Licensed to Kill: Mitochondria, Chloroplasts, and Cell Death

Van Aken, O., & Van Breusegem, F. (2015) · Trends in Plant Science · doi:10.1016/j.tplants.2015.08.002 · Cited by 202

ABNORMAL INFLORESCENCE MERISTEM1 Functions in Salicylic Acid Biosynthesis to Maintain Proper Reactive Oxygen Species Levels for Root Meristem Activity in Rice

Xu, L., Zhao, H., Ruan, W., Deng, M., Wang, F., Peng, J., Luo, J., Chen, Z., & Yi, K. (2017) · The Plant Cell · doi:10.1105/tpc.16.00665 · Cited by 200

Nuclear Activity of ROXY1, a Glutaredoxin Interacting with TGA Factors, Is Required for Petal Development in Arabidopsis thaliana

Li, S., Lauri, A., Ziemann, M., Busch, A., Bhave, M., & Zachgo, S. (2009) · The Plant Cell · doi:10.1105/tpc.108.064477 · Cited by 194

ROXY1 , a member of the plant glutaredoxin family, is required for petal development in Arabidopsis thaliana

Xing, S., Rosso, M. G., & Zachgo, S. (2005) · Development · doi:10.1242/dev.01725 · Cited by 193

ORS1, an H2O2-Responsive NAC Transcription Factor, Controls Senescence in Arabidopsis thaliana

Salma, Balazadeh, Miroslaw, KWASNIEWSKI, V., Camila, C., Caldana, Mohammad, Mehrnia, María, Inês, et al. (2011) · 分子植物：英文版 · Cited by 189

The hydroxyl radical in plants: from seed to seed

Richards, S. L., Wilkins, K. A., Swarbreck, S. M., Anderson, A. A., Habib, N., Smith, A. G., McAinsh, M., & Davies, J. M. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/eru398 · Cited by 187

Transcriptional control of ROS homeostasis by KUODA1 regulates cell expansion during leaf development

Lu, D., Wang, T., Persson, S., Mueller‐Roeber, B., & Schippers, J. H. M. (2014) · Nature Communications · doi:10.1038/ncomms4767 · Cited by 186

The MAP Kinase MPK4 Is Required for Cytokinesis in Arabidopsis thaliana

Kosetsu, K., Matsunaga, S., Nakagami, H., Colcombet, J., Sasabe, M., Soyano, T., Takahashi, Y., Hirt, H., & Machida, Y. (2010) · The Plant Cell · doi:10.1105/tpc.110.077164 · Cited by 182

Pollen tube NAD(P)H oxidases act as a speed control to dampen growth rate oscillations during polarized cell growth

Lassig, R., Gutermuth, T., Bey, T. D., Konrad, K. R., & Romeis, T. (2014) · The Plant Journal · doi:10.1111/tpj.12452 · Cited by 180

Reactive oxygen species, abscisic acid and ethylene interact to regulate sunflower seed germination

EL‐MAAROUF‐BOUTEAU, H., SAJJAD, Y., BAZIN, J., LANGLADE, N., CRISTESCU, S. M., BALZERGUE, S., BAUDOUIN, E., & BAILLY, C. (2015) · Plant, Cell & Environment · doi:10.1111/pce.12371 · Cited by 175

Defective Tapetum Cell Death 1 (DTC1) Regulates ROS Levels by Binding to Metallothionein during Tapetum Degeneration

Yi, J., Moon, S., Lee, Y.-S., Zhu, L., Liang, W., Zhang, D., Jung, K.-H., & An, G. (2016) · Plant Physiology · doi:10.1104/pp.15.01561 · Cited by 165

Production and Scavenging of Reactive Oxygen Species and Redox Signaling during Leaf and Flower Senescence: Similar But Different

Rogers, H., & Munné-Bosch, S. (2016) · Plant Physiology · doi:10.1104/pp.16.00163 · Cited by 164

Cross-species approaches to seed dormancy and germination: conservation and biodiversity of ABA-regulated mechanisms and the Brassicaceae DOG1 genes

Graeber, K., Linkies, A., Müller, K., Wunchova, A., Rott, A., & Leubner-Metzger, G. (2010) · Plant Molecular Biology · doi:10.1007/s11103-009-9583-x · Cited by 159

The Emerging Role of Reactive Oxygen Species Signaling during Lateral Root Development

Manzano, C., Pallero-Baena, M., Casimiro, I., De Rybel, B., Orman-Ligeza, B., Van Isterdael, G., Beeckman, T., Draye, X., Casero, P., & del Pozo, J. C. (2014) · Plant Physiology · doi:10.1104/pp.114.238873 · Cited by 158

Redox regulation at the site of primary growth: auxin, cytokinin and ROS crosstalk

Tognetti, V. B., Bielach, A., & Hrtyan, M. (2017) · Plant Cell & Environment · doi:10.1111/pce.13021 · Cited by 152

Salt stress and senescence: identification of cross-talk regulatory components

Allu, A. D., Soja, A. M., Wu, A., Szymański, J., & Balazadeh, S. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru173 · Cited by 148

Redox regulation in shoot growth, SAM maintenance and flowering

Schippers, J. H. M., Foyer, C. H., & van Dongen, J. T. (2016) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2015.11.009 · Cited by 148

Hydroperoxide reduction by thioredoxin‐specific glutathione peroxidase isoenzymes of Arabidopsis thaliana

Iqbal, A., Yabuta, Y., Takeda, T., Nakano, Y., & Shigeoka, S. (2006) · FEBS Journal · doi:10.1111/j.1742-4658.2006.05548.x · Cited by 145

Alterations in the Endogenous Ascorbic Acid Content Affect Flowering Time in Arabidopsis

Kotchoni, S. O., Larrimore, K. E., Mukherjee, M., Kempinski, C. F., & Barth, C. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.132324 · Cited by 145

Arabidopsis root growth dependence on glutathione is linked to auxin transport

Kopřivová, A., Mugford, S. T., & Kopřiva, S. (2010) · Plant Cell Reports · doi:10.1007/s00299-010-0902-0 · Cited by 144

Plant primary meristems: shared functions and regulatory mechanisms

Stahl, Y., & Simon, R. G. (2009) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.09.008 · Cited by 142

Arabidopsis Monothiol Glutaredoxin, AtGRXS17, Is Critical for Temperature-dependent Postembryonic Growth and Development via Modulating Auxin Response

Cheng, N.-H., Liu, J., Liu, X., Wu, Q., Thompson, S. M., Lin, J., Chang, J., Whitham, S. A., Park, S., Cohen, J. D., et al. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.201707 · Cited by 141

FASCIATED EAR4 Encodes a bZIP Transcription Factor That Regulates Shoot Meristem Size in Maize

Pautler, M., Eveland, A. L., LaRue, T., Yang, F., Weeks, R., Lunde, C. F., Je, B. I., Meeley, R. B., Komatsu, M., Vollbrecht, E., et al. (2015) · The Plant Cell · doi:10.1105/tpc.114.132506 · Cited by 141

ASCORBATE PEROXIDASE6 Protects Arabidopsis Desiccating and Germinating Seeds from Stress and Mediates Cross Talk between Reactive Oxygen Species, Abscisic Acid, and Auxin

Chen, C., Letnik, I., Hacham, Y., Dobrev, P. I., Ben-Daniel, B.-H., Vaňková, R., Amir, R., & Miller, G. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.245324 · Cited by 138

Role of Reactive Oxygen Species during Cell Expansion in Leaves

Schmidt, R., Kunkowska, A. B., & Schippers, J. H. M. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00426 · Cited by 136

Low glutathione regulates gene expression and the redox potentials of the nucleus and cytosol in A rabidopsis thaliana

Schnaubelt, D., Queval, G., Dong, Y., et al. (2013) · Plant Cell & Environment · doi:10.1111/pce.12252 · Cited by 130

The Interrelationship between Abscisic Acid and Reactive Oxygen Species Plays a Key Role in Barley Seed Dormancy and Germination

Ishibashi, Y., Aoki, N., Kasa, S., Sakamoto, M., Kai, K., Tomokiyo, R., Watabe, G., Yuasa, T., & Iwaya‐Inoue, M. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00275 · Cited by 129

Lack of GLYCOLATE OXIDASE1, but Not GLYCOLATE OXIDASE2, Attenuates the Photorespiratory Phenotype of CATALASE2-Deficient Arabidopsis

Kerchev, P., Waszczak, C., Lewandowska, A., Willems, P., Shapiguzov, A., Li, Z., Alseekh, S., Mühlenbock, P., Hoeberichts, F. A., Huang, J., et al. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00359 · Cited by 128

The effects of redox controls mediated by glutathione peroxidases on root architecture in Arabidopsis thaliana

Passaia, G., Queval, G., Bai, J., Margis-Pinheiro, M. M. A. N., & Foyer, C. H. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/ert486 · Cited by 123

Plastid-Localized Glutathione Reductase2-Regulated Glutathione Redox Status Is Essential for Arabidopsis Root Apical Meristem Maintenance

Yu, X., Pasternak, T. P., Eiblmeier, M., Ditengou, F. A., Kochersperger, P., Sun, J., Wang, H., Rennenberg, H., Teale, W., Paponov, I. A., et al. (2013) · The Plant Cell · doi:10.1105/tpc.113.117028 · Cited by 123

Nuclear glutathione

García‐Giménez, J. L., Marković, J., Dasí, F., Queval, G., Schnaubelt, D., Foyer, C. H., & Pallardó, F. V. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.10.005 · Cited by 123

A mutation in GDP-mannose pyrophosphorylase causes conditional hypersensitivity to ammonium, resulting in Arabidopsis root growth inhibition, altered ammonium metabolism, and hormone homeostasis

Barth, C., Gouzd, Z. A., Steele, H. P., & Imperio, R. M. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp310 · Cited by 120

Cytosolic and Chloroplastic DHARs Cooperate in Oxidative Stress-Driven Activation of the Salicylic Acid Pathway

Rahantaniaina, M.-S., Li, S., Innocenti, G., Tuzet, A., Issakidis‐Bourguet, E., Mhamdi, A., & Noctor, G. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.00317 · Cited by 114

Glutathione peroxidase‐like enzymes cover five distinct cell compartments and membrane surfaces in Arabidopsis thaliana

Attacha, S., Solbach, D., Bela, K., Moseler, A., Wagner, S., Schwarzländer, M., Aller, I., Müller, S. J., & Meyer, A. J. (2017) · Plant Cell & Environment · doi:10.1111/pce.12919 · Cited by 112

oiwa, a Female Gametophytic Mutant Impaired in a Mitochondrial Manganese-Superoxide Dismutase, Reveals Crucial Roles for Reactive Oxygen Species during Embryo Sac Development and Fertilization in Arabidopsis

Martin, M. V., Fiol, D. F., Sundaresan, V., Zabaleta, E. J., & Pagnussat, G. C. (2013) · The Plant Cell · doi:10.1105/tpc.113.109306 · Cited by 111

Auxin controls petal initiation in Arabidopsis

Lampugnani, E. R., Kilinc, A., & Smyth, D. R. (2012) · Development · doi:10.1242/dev.084582 · Cited by 109

NADPH oxidase activity in pollen tubes is affected by calcium ions, signaling phospholipids and Rac/Rop GTPases

Potocký, M., Pejchar, P., Gutkowska, M., Jimenez-Quesada, M. J., Potocká, A., Ramírez, J. D. D. A., Kost, B., & Žárský, V. (2012) · Journal of Plant Physiology · doi:10.1016/j.jplph.2012.05.014 · Cited by 106

Global Identification of DELLA Target Genes during Arabidopsis Flower Development

Hou, X., Hu, W., Shen, L., Lee, L. Y. C., Tao, Z., Han, J.-H., & Yu, H. Q. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.121301 · Cited by 106

Germination induction of dormant Avena fatua caryopses by KAR1 and GA3 involving the control of reactive oxygen species (H2O2 and O2−) and enzymatic antioxidants (superoxide dismutase and catalase) both in the embryo and the aleurone layers

Cembrowska-Lech, D., Koprowski, M., & Kępczyński, J. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.11.010 · Cited by 104

Redox Changes During the Cell Cycle in the Embryonic Root Meristem of Arabidopsis thaliana

Simone, A. D., Hubbard, R., de la Torre, N. V., et al. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6959 · Cited by 104

Expression analyses of Arabidopsis oligopeptide transporters during seed germination, vegetative growth and reproduction

Stacey, M. G., Osawa, H., Patel, A., Gassmann, W., & Stacey, G. S. (2005) · Planta · doi:10.1007/s00425-005-0087-x · Cited by 103

Organelles Contribute Differentially to Reactive Oxygen Species-Related Events during Extended Darkness

Rosenwasser, S., Rot, I., Sollner, E., Meyer, A. J., Smith, Y., Leviatan, N., Fluhr, R., & Friedman, H. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.169797 · Cited by 102

Arabidopsis ABI5 plays a role in regulating ROS homeostasis by activating CATALASE 1 transcription in seed germination

Bi, C., Yu, M., Wu, Z., Yu, Y., Liang, S., Lü, K., & Wang, X. (2017) · Plant Molecular Biology · doi:10.1007/s11103-017-0603-y · Cited by 100

PFT 1, a transcriptional M ediator complex subunit, controls root hair differentiation through reactive oxygen species ( ROS ) distribution in A rabidopsis

Kalaipandian, S., Chandrika, N. N. P., & Schmidt, W. (2012) · New Phytologist · doi:10.1111/nph.12000 · Cited by 97

Disturbance of reactive oxygen species homeostasis induces atypical tubulin polymer formation and affects mitosis in root‐tip cells of Triticum turgidum and Arabidopsis thaliana

Livanos, P., Galatis, B., Quader, H., & Apostolakos, P. (2011) · Cytoskeleton · doi:10.1002/cm.20538 · Cited by 92

Plant-specific CC-type glutaredoxins: functions in developmental processes and stress responses

Gutsche, N., Thurow, C., Zachgo, S., & Gatz, C. (2015) · Biological Chemistry · doi:10.1515/hsz-2014-0300 · Cited by 89

Pyridine Nucleotide Cycling and Control of Intracellular Redox State in Relation to Poly (ADP-Ribose) Polymerase Activity and Nuclear Localization of Glutathione during Exponential Growth of Arabidopsis Cells in Culture

Pellny, T. K., Locato, V., Díaz‐Vivancos, P., Marković, J., Gara, L. D., Pallardó, F. V., & Foyer, C. H. (2009) · Molecular Plant · doi:10.1093/mp/ssp008 · Cited by 89

Redox Modulation of Plant Developmental Regulators from the Class I TCP Transcription Factor Family

Viola, I. L., Güttlein, L. N., & González, D. H. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.216416 · Cited by 89

Arabidopsis Glutaredoxin S17 and Its Partner, the Nuclear Factor Y Subunit C11/Negative Cofactor 2α, Contribute to Maintenance of the Shoot Apical Meristem under Long-Day Photoperiod

Knuesting, J., Riondet, C., María, C., Kruse, I., Bécuwe, N., König, N., Berndt, C., Tourrette, S., Guilleminot, J., Herrero, E., et al. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.00049 · Cited by 88

NTR/NRX Define a New Thioredoxin System in the Nucleus of Arabidopsis thaliana Cells

Marchal, C., Delorme‐Hinoux, V., Bariat, L., Siala, W., Belin, C., Sáez‐Vasquez, J., Riondet, C., & Reichheld, J. (2013) · Molecular Plant · doi:10.1093/mp/sst162 · Cited by 87

A Maize Glutaredoxin Gene, Abphyl2, Regulates Shoot Meristem Size and Phyllotaxy

Yang, F., Bui, H., Pautler, M., Llaca, V., Johnston, R., Lee, B., Kolbe, A. R., Sakai, H., & Jackson, D. P. (2015) · The Plant Cell · doi:10.1105/tpc.114.130393 · Cited by 86

Redox regulation of cell proliferation: Bioinformatics and redox proteomics approaches to identify redox-sensitive cell cycle regulators

Foyer, C. H., Wilson, M. H., & Wright, M. H. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.03.047 · Cited by 86

Peroxisomal ATP-Binding Cassette Transporter COMATOSE and the Multifunctional Protein ABNORMAL INFLORESCENCE MERISTEM Are Required for the Production of Benzoylated Metabolites in Arabidopsis Seeds

Bussell, J. D., Reichelt, M., Wiszniewski, A. A. G., Gershenzon, J., & Smith, S. M. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.229807 · Cited by 84

The Arabidopsis thaliana Class III Peroxidase AtPRX71 Negatively Regulates Growth under Physiological Conditions and in Response to Cell Wall Damage.

Raggi, S., Ferrarini, A., Delledonne, M., Dunand, C., Ranocha, P., Lorenzo, G. D., Cervone, F., & Ferrari, S. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.01464 · Cited by 82

NADPH Oxidase-Dependent Superoxide Production in Plant Reproductive Tissues

Jimenez-Quesada, M. J., Traverso, J. A., & Ramírez, J. D. D. A. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00359 · Cited by 75

A new role for glutathione in the regulation of root architecture linked to strigolactones

Márquez‐García, B., Njo, M. F., Beeckman, T., Goormachtig, S., & Foyer, C. H. (2013) · Plant Cell & Environment · doi:10.1111/pce.12172 · Cited by 71

Auxin and Its Role in Plant Senescence

Mueller‐Roeber, B., & Balazadeh, S. (2013) · Journal of Plant Growth Regulation · doi:10.1007/s00344-013-9398-5 · Cited by 71

Fluorescent in vivo imaging of reactive oxygen species and redox potential in plants

Ortega‐Villasante, C., Burén, S., Blázquez‐Castro, A., Barón‐Sola, Á., & Hernández, L. E. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.04.005 · Cited by 71

Plant cell division

Livanos, P., Apostolakos, P., & Galatis, B. (2012) · Plant Signaling & Behavior · doi:10.4161/psb.20530 · Cited by 69

Activation of auxin signalling counteracts photorespiratory H2O2 ‐dependent cell death

Kerchev, P., Mühlenbock, P., Denecker, J., Morreel, K., Hoeberichts, F. A., Kelen, K. V. D., Vandorpe, M., Nguyen, L., Audenaert, D., & Breusegem, F. V. (2013) · Plant Cell & Environment · doi:10.1111/pce.12250 · Cited by 67

Reactive oxygen species are involved in regulation of pollen wall cytomechanics

Smirnova, A. V., Matveyeva, N. P., & Yermakov, I. P. (2013) · Plant Biology · doi:10.1111/plb.12004 · Cited by 60

5′ to 3′ mRNA Decay Contributes to the Regulation of Arabidopsis Seed Germination by Dormancy

Basbouss-Serhal, I., Pateyron, S., Cochet, F., Leymarie, J., & Bailly, C. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.01933 · Cited by 57

SHORT-ROOT Deficiency Alleviates the Cell Death Phenotype of the Arabidopsis catalase2 Mutant under Photorespiration-Promoting Conditions

Waszczak, C., Kerchev, P., Mühlenbock, P., Hoeberichts, F. A., Kelen, K. V. D., Mhamdi, A., Willems, P., Denecker, J., Kumpf, R. P., Noctor, G., et al. (2016) · The Plant Cell · doi:10.1105/tpc.16.00038 · Cited by 53

Decreased glutathione reductase2 leads to early leaf senescence in Arabidopsis

Ding, S., Wang, L., Yang, Z., Lu, Q., Wen, X., & Lu, C. (2015) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12371 · Cited by 50

Mitochondrial AtTrxo1 is transcriptionally regulated by AtbZIP9 and AtAZF2 and affects seed germination under saline conditions

Ortiz‐Espín, A., Iglesias‐Fernández, R., Pérez, A. C., Carbonero, P., Sevilla, F., & Jiménez, A. (2017) · Journal of Experimental Botany · doi:10.1093/jxb/erx012 · Cited by 47

Cell-cycle-dependent regulation of oxidative stress responses and Ca2+ permeable channels NtTPC1A/B in tobacco BY-2 cells

Kadota, Y., Furuichi, T., Sano, T., Kaya, H., Gunji, W., Murakami, Y., Muto, S., Hasezawa, S., & Kuchitsu, K. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.09.004 · Cited by 42

DNA double‐strand breaks induce the expression of flavin‐containing monooxygenase and reduce root meristem size in A rabidopsis thaliana

Chen, P., & Umeda, M. (2015) · Genes to Cells · doi:10.1111/gtc.12255 · Cited by 29

PETAL LOSS and ROXY1 Interact to Limit Growth Within and between Sepals But to Promote Petal Initiation in Arabidopsis thaliana

Quon, T., Lampugnani, E. R., & Smyth, D. R. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00152 · Cited by 29

Mechanisms of ROS Regulation of Plant Development and Stress Responses

Huang, H., Ullah, F., Zhou, D.-X., Yi, M., & Zhao, Y. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00800 · Cited by 1,468

The Role of the Plant Antioxidant System in Drought Tolerance

Laxa, M., Liebthal, M., Telman, W., Chibani, K., & Dietz, K.-J. (2019) · Antioxidants · doi:10.3390/antiox8040094 · Cited by 855

Developing climate‐resilient crops: improving plant tolerance to stress combination

Rivero, R. M., Mittler, R., Blumwald, E., & Zandalinas, S. I. (2022) · The Plant Journal · doi:10.1111/tpj.15483 · Cited by 622

ROS production and signalling in chloroplasts: cornerstones and evolving concepts

Foyer, C. H., & Hanke, G. (2022) · The Plant Journal · doi:10.1111/tpj.15856 · Cited by 357

Nanobiotechnology-based strategies for enhanced crop stress resilience

Zhao, L., Bai, T., Wei, H., Gardea-Torresdey, J. L., Keller, A., & White, J. C. (2022) · Nature Food · doi:10.1038/s43016-022-00596-7 · Cited by 270