Main nitric oxide (NO) hallmarks to relieve arsenic stress in higher plants

Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness

Nishita, M., Park, S.-Y., Nishio, T., Kamizaki, K., Wang, Z., Tamada, K., Takumi, T., Hashimoto, R., Otani, H., Pazour, G. J., et al. (2017) · Scientific Reports · doi:10.1038/s41598-016-0028-x · Cited by 15,947

Heavy Metals in Agricultural Soils of the European Union with Implications for Food Safety

Tóth, G., Hermann, T., Da Silva, M. R., & Montanarella, L. (2016) · Environment International · doi:10.1016/j.envint.2015.12.017 · Cited by 1,654

Regulation of Ascorbate-Glutathione Pathway in Mitigating Oxidative Damage in Plants under Abiotic Stress

Hasanuzzaman, M., Bhuyan, M. H. M. B., Anee, T. I., Parvin, K., Nahar, K., Mahmud, J. A., & Fujita, M. (2019) · Antioxidants · doi:10.3390/antiox8090384 · Cited by 1,325

Arsenic uptake and metabolism in arsenic resistant and nonresistant plant species

Meharg, A. A., & Whitaker, J. (2002) · New Phytologist · doi:10.1046/j.1469-8137.2002.00363.x · Cited by 1,225

Hydrogen peroxide and nitric oxide as signalling molecules in plants

Neill, S. J., Desikan, R., Clarke, A., Hurst, R. D., & Hancock, J. T. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.372.1237 · Cited by 1,218

Arsenic uptake and metabolism in plants

Zhao, F. J., Ma, J. F., Meharg, A. A., & McGrath, S. P. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2008.02716.x · Cited by 1,185

Redox- and non-redox-metal-induced formation of free radicals and their role in human disease

Valko, M., Jomová, K., Rhodes, C. J., Kuča, K., & Musílek, K. (2015) · Archives of Toxicology · doi:10.1007/s00204-015-1579-5 · Cited by 1,062

ABA‐induced NO generation and stomatal closure in Arabidopsis are dependent on H 2 O 2 synthesis

Bright, J., Desikan, R., Hancock, J. T., Weir, I. S., & Neill, S. J. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02615.x · Cited by 1,007

Arsenic Uptake, Toxicity, Detoxification, and Speciation in Plants: Physiological, Biochemical, and Molecular Aspects

Abbas, G., Murtaza, B., Bibi, I., Shahid, M. A. R., Niazi, N. K., Khan, M. I., Amjad, M., Hussain, M., & Natasha, N. (2018) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph15010059 · Cited by 918

DNA Base Damage by Reactive Oxygen Species, Oxidizing Agents, and UV Radiation

Cadet, J., & Wagner, J. R. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a012559 · Cited by 903

Arsenic in the geosphere — a review

Matschullat, J. (2000) · Science of The Total Environment · doi:10.1016/s0048-9697(99)00524-0 · Cited by 891

Identification of a Plant Nitric Oxide Synthase Gene Involved in Hormonal Signaling

Guo, F.-Q., Okamoto, M., & Crawford, N. M. (2003) · Science · doi:10.1126/science.1086770 · Cited by 889

Nitric Oxide: The Versatility of an Extensive Signal Molecule

Lamattina, L., García‐Mata, C., Graziano, M., & Pagnussat, G. C. (2003) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.54.031902.134752 · Cited by 877

Arsenic Toxicity: The Effects on Plant Metabolism

Finnegan, P. M., & Chen, W. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00182 · Cited by 864

Protein carbonylation, cellular dysfunction, and disease progression

Dalle‐Donne, I., Aldini, G., Carini, M., Colombo, R., Rossi, R., & Milzani, A. (2006) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2006.tb00407.x · Cited by 857

Arsenic transformations in the soil–rhizosphere–plant system: fundamentals and potential application to phytoremediation

Fitz, W. J., & Wenzel, W. W. (2002) · Journal of Biotechnology · doi:10.1016/s0168-1656(02)00218-3 · Cited by 776

The light‐harvesting and protective functions of carotenoids in photosynthetic membranes

Siefermann‐Harms, D. (1987) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1987.tb09240.x · Cited by 636

EXPRESSION OF CONCERN: Modulation of drought resistance by the abscisic acid receptor PYL5 through inhibition of clade A PP2Cs

Santiago, J., Rodrigues, A., Saéz, Á., Rubio, S., Antoni, R., Dupeux, F., Park, S., Márquez, J. A., Cutler, S. R., & Rodrı́guez, P. L. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03981.x · Cited by 597

Nitric Oxide Represses the Arabidopsis Floral Transition

He, Y., Tang, R., Hao, Y., Stevens, R. D., Cook, C. W., Ahn, S. M., Jing, L., Yang, Z., Chen, L., Guo, F., et al. (2004) · Science · doi:10.1126/science.1098837 · Cited by 565

Functions and transport of silicon in plants

Ma, J. F., & Yamaji, N. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-7580-x · Cited by 563

Reduction and Coordination of Arsenic in Indian Mustard

Pickering, I. J., Prince, R. C., George, M. J., Smith, R., George, G. N., & Salt, D. E. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.122.4.1171 · Cited by 557

An Arabidopsis Glutathione Peroxidase Functions as Both a Redox Transducer and a Scavenger in Abscisic Acid and Drought Stress Responses

Miao, Y., Lv, D., Wang, P., Wang, X., Chen, J., Miao, C., & Song, C. (2006) · The Plant Cell · doi:10.1105/tpc.106.044230 · Cited by 555

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

Oracz, K., El‐Maarouf‐Bouteau, H., 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 522

Regulation of L-proline biosynthesis, signal transduction, transport, accumulation and its vital role in plants during variable environmental conditions

Meena, M., Divyanshu, K., Kumar, S., Swapnil, P., Zehra, A., Shukla, V., Yadav, M., & Upadhyay, R. S. (2019) · Heliyon · doi:10.1016/j.heliyon.2019.e02952 · Cited by 517

Nitric Reductase-Dependent Nitric Oxide Production Is Involved in Cold Acclimation and Freezing Tolerance in Arabidopsis

Zhao, M., Chen, L., Zhang, L., & Zhang, W. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.140996 · Cited by 515

ABA, hydrogen peroxide and nitric oxide signalling in stomatal guard cells

Desikan, R. (2003) · Journal of Experimental Botany · doi:10.1093/jxb/erh033 · Cited by 515

Spinal Fusion in the Next Generation: Gene and Cell Therapy Approaches

Barba, M., Cicione, C., Bernardini, C., Campana, V., Pagano, E., Michetti, F., Logroscino, G., & Lattanzi, W. (2014) · The Scientific World JOURNAL · doi:10.1155/2014/406159 · Cited by 514

Environmental Biochemistry of Arsenic

Tamaki, S., & Frankenberger, W. T. (1992) · Reviews of Environmental Contamination and Toxicology · doi:10.1007/978-1-4612-2864-6_4 · Cited by 480

Effect of arsenic on growth, oxidative stress, and antioxidant system in rice seedlings

Shri, M., Kumar, S., Chakrabarty, D., Trivedi, P. K., Mallick, S., Misra, P., Shukla, D., Mishra, S., Srivastava, S., Tripathi, R. D., et al. (2008) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2008.09.022 · Cited by 461

Proteome-Wide Characterization of Seed Aging in Arabidopsis: A Comparison between Artificial and Natural Aging Protocols

Rajjou, L., Lovigny, Y., Groot, S. P. C., Belghazi, M., Job, C., & Job, D. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.123141 · Cited by 460

Assessment of Subcellular ROS and NO Metabolism in Higher Plants: Multifunctional Signaling Molecules

Kohli, S. K., Khanna, K., Bhardwaj, R., Allah, E. F. A., Ahmad, P., & Corpas, F. J. (2019) · Antioxidants · doi:10.3390/antiox8120641 · Cited by 449

Copper‐ and arsenate‐induced oxidative stress in Holcus lanatus L. clones with differential sensitivity

Hartley‐Whitaker, J., Ainsworth, G. B., & Meharg, A. A. (2001) · Plant Cell & Environment · doi:10.1046/j.0016-8025.2001.00721.x · Cited by 421

1-Aminocyclopropane-1-Carboxylic Acid Oxidase (ACO): The Enzyme That Makes the Plant Hormone Ethylene

Houben, M., & de Poel, B. V. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00695 · Cited by 417

The Rice Aquaporin Lsi1 Mediates Uptake of Methylated Arsenic Species

Li, R.-Y., Ago, Y., Liu, W.-J., Mitani, N., Feldmann, J., McGrath, S. P., Feng, J. X., & Zhao, F. J. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.140350 · Cited by 416

A subgroup of plant aquaporins facilitate the bi-directional diffusion of As(OH)3 and Sb(OH)3across membranes

Bienert, G. P., Thorsen, M. K., Bienert, M. D., Nilsson, R. H., Wagner, A., Tamás, M. J., & Jahn, T. P. (2008) · BMC Biology · doi:10.1186/1741-7007-6-26 · Cited by 414

Nitric oxide regulates K + and Cl - channels in guard cells through a subset of abscisic acid-evoked signaling pathways

García‐Mata, C., Gay, R., Sokolovski, S. G., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1434381100 · Cited by 403

Patterns of Protein Oxidation in Arabidopsis Seeds and during Germination

Job, C., Rajjou, L., Lovigny, Y., Belghazi, M., & Job, D. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.062778 · Cited by 402

Role of Silicon in Mitigation of Heavy Metal Stresses in Crop Plants

Bhat, J. A., Shivaraj, S. M., Singh, P., Devanna, B. N., Tripathi, D. K., Dash, P. K., Solanke, A. U., Sonah, H., & Deshmukh, R. K. (2019) · Plants · doi:10.3390/plants8030071 · Cited by 399

Resistance to Sharka in Apricot: Comparison of Phase-Reconstructed Resistant and Susceptible Haplotypes of ‘Lito’ Chromosome 1 and Analysis of Candidate Genes

Mori, G. D., Falchi, R., Testolin, R., Bassi, D., Savazzini, F., Dondini, L., Tartarini, S., Palmisano, F., Minafra, A., Spadotto, A., et al. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01576 · Cited by 376

Modulation of Nitrosative Stress by S -Nitrosoglutathione Reductase Is Critical for Thermotolerance and Plant Growth in Arabidopsis

Lee, U., Wie, C., Fernandez, B. O., Feelisch, M., & Vierling, E. (2008) · The Plant Cell · doi:10.1105/tpc.107.052647 · Cited by 373

Polyamine and nitric oxide crosstalk: Antagonistic effects on cadmium toxicity in mung bean plants through upregulating the metal detoxification, antioxidant defense and methylglyoxal detoxification systems

Nahar, K., Hasanuzzaman, M., Alam, M. M., Rahman, A., Suzuki, T., & Fujita, M. (2016) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2015.12.026 · Cited by 369

Speciation and Localization of Arsenic in White and Brown Rice Grains

Meharg, A. A., Lombi, E., Williams, P. N., Scheckel, K. G., Feldmann, J., Raab, A., Zhu, Y., & Islam, M. R. (2008) · Environmental Science & Technology · doi:10.1021/es702212p · Cited by 368

Investigating the Contribution of the Phosphate Transport Pathway to Arsenic Accumulation in Rice

Wu, Z., Ren, H., McGrath, S. P., et al. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.178921 · Cited by 360

Arsenic species in an arsenic hyperaccumulating fern, Pityrogramma calomelanos: a potential phytoremediator of arsenic-contaminated soils

Francesconi, K. A., Visoottiviseth, P., Sridokchan, W., & Goessler, W. (2002) · The Science of The Total Environment · doi:10.1016/s0048-9697(01)00854-3 · Cited by 350

Dual regulation of cytosolic ascorbate peroxidase (APX) by tyrosine nitration andS-nitrosylation

Begara-Morales, J. C., Sánchez-Calvo, B., Chaki, M., Valderrama, R., Mata-Pérez, C., López-Jaramillo, J., Padilla, M. N., Carreras, A., Corpas, F. J., & Barroso, J. B. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert396 · Cited by 349

Arsenic-induced root growth inhibition in mung bean (Phaseolus aureus Roxb.) is due to oxidative stress resulting from enhanced lipid peroxidation

Singh, H. P., Batish, D. R., Kohli, R. K., & Arora, K. (2007) · Plant Growth Regulation · doi:10.1007/s10725-007-9205-z · Cited by 328

Nitric oxide and phytohormone interactions: current status and perspectives

Freschi, L. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00398 · Cited by 327

Melatonin and calcium function synergistically to promote the resilience through ROS metabolism under arsenic-induced stress

Siddiqui, M. H., Alamri, S. A., Khan, M. N., Corpas, F. J., Al-Amri, A. A., Alsubaie, Q. D., Ali, H. M., Kalaji, H. M., & Ahmad, P. (2020) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2020.122882 · Cited by 322

Antioxidant responses of hyper-accumulator and sensitive fern species to arsenic

Srivastava, M., Ma, L. Q., Singh, N., & Singh, S. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/eri134 · Cited by 317

AtNOS/AtNOA1 Is a Functional Arabidopsis thaliana cGTPase and Not a Nitric-oxide Synthase

Moreau, M., Lee, G. I., Wang, Y., Crane, B. R., & Klessig, D. F. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m804838200 · Cited by 308

Exogenous nitric oxide improves antioxidative capacity and reduces auxin degradation in roots of Medicago truncatula seedlings under cadmium stress

Xu, J., Wang, W., Yin, H., Liu, X., Sun, H., & Mi, Q. (2009) · Plant and Soil · doi:10.1007/s11104-009-0011-4 · Cited by 304

Arsenic toxicity in plants: Cellular and molecular mechanisms of its transport and metabolism

Farooq, M. A., Islam, F., Ali, B., Ullah, N., Mao, B., Gill, R. A., Yan, G., Siddique, K. H. M., & Zhou, W. (2016) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2016.08.004 · Cited by 304

Nitric oxide (NO) and phytohormones crosstalk during early plant development

Sanz, L., Albertos, P., Mateos, I., Sánchez-Vicente, I., Lechón, T., Fernández‐Marcos, M., & Lorenzo, Ó. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv213 · Cited by 300

Nitric oxide imbalance provokes a nitrosative response in plants under abiotic stress

Corpas, F. J., Leterrier, M., Valderrama, R., Airaki, M., Chaki, M., Palma, J. M., & Barroso, J. B. (2011) · Plant Science · doi:10.1016/j.plantsci.2011.04.005 · Cited by 296

Uptake, translocation and transformation of arsenate and arsenite in sunflower ( Helianthus annuus ): formation of arsenic–phytochelatin complexes during exposure to high arsenic concentrations

Raab, A., Schat, H., Meharg, A. A., & Feldmann, J. (2005) · New Phytologist · doi:10.1111/j.1469-8137.2005.01519.x · Cited by 296

Arsenate toxicity: effects on oxidative stress response molecules and enzymes in red clover plants

Mascher, R., Lippmann, B., Holzinger, S., & Bergmann, H. W. (2002) · Plant Science · doi:10.1016/s0168-9452(02)00245-5 · Cited by 290

Exogenous sodium nitroprusside alleviates arsenic-induced oxidative stress in wheat (Triticum aestivum L.) seedlings by enhancing antioxidant defense and glyoxalase system

Hasanuzzaman, M., & Fujita, M. (2013) · Ecotoxicology · doi:10.1007/s10646-013-1050-4 · Cited by 290

Contribution of glutathione to the control of cellular redox homeostasis under toxic metal and metalloid stress

Hernández, L. E., Sobrino‐Plata, J., Montero-Palmero, M. B., Carrasco-Gil, S., Flores-Cáceres, M. L., Ortega‐Villasante, C., & Escobar, C. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv063 · Cited by 284

Nitric oxide is induced by wounding and influences jasmonic acid signaling in Arabidopsis thaliana

Huang, X., Stettmaier, K., Michel, C., Hutzler, P., Mueller, M. J., & Durner, J. (2004) · Planta · doi:10.1007/s00425-003-1178-1 · Cited by 260

Phytoremediation of arsenate contaminated soil by transgenic canola and the plant growth-promoting bacterium Enterobacter cloacae CAL2

Nie, L., Shah, S., Rashid, A., et al. (2002) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(02)01375-x · Cited by 257

A review on sources, toxicity and remediation technologies for removing arsenic from drinking water

Basu, A., Saha, D., Saha, R., Ghosh, T., & Saha, B. (2013) · Research on Chemical Intermediates · doi:10.1007/s11164-012-1000-4 · Cited by 256

Nitric oxide and hydrogen sulfide in plants: which comes first?

Corpas, F. J., González‐Gordo, S., Cañas, A., & Palma, J. M. (2019) · Journal of Experimental Botany · doi:10.1093/jxb/erz031 · Cited by 253

Understanding arsenic dynamics in agronomic systems to predict and prevent uptake by crop plants

Punshon, T., Jackson, B. P., Meharg, A. A., Warczack, T., Scheckel, K. G., & Guerinot, M. L. (2016) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2016.12.111 · Cited by 252

Enhanced Abscisic Acid-Mediated Responses in nia1nia2noa1-2 Triple Mutant Impaired in NIA/NR- and AtNOA1-Dependent Nitric Oxide Biosynthesis in Arabidopsis

Lozano‐Juste, J., & León, J. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.148023 · Cited by 247

Hydrogen sulfide alleviates toxic effects of arsenate in pea seedlings through up-regulation of the ascorbate–glutathione cycle: Possible involvement of nitric oxide

Singh, V. P., Singh, S., Kumar, J., & Prasad, S. M. (2015) · Journal of Plant Physiology · doi:10.1016/j.jplph.2015.03.015 · Cited by 247

OsHAC1;1 and OsHAC1;2 Function as Arsenate Reductases and Regulate Arsenic Accumulation

Shi, S., Wang, T., Chen, Z., et al. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.01332 · Cited by 241

Omics and biotechnology of arsenic stress and detoxification in plants: Current updates and prospective

Kumar, S., Dubey, R. S., Tripathi, R. D., Chakrabarty, D., & Trivedi, P. K. (2014) · Environment International · doi:10.1016/j.envint.2014.10.019 · Cited by 240

Hydrogen sulphide may be a novel downstream signal molecule in nitric oxide‐induced heat tolerance of maize ( Z ea mays L .) seedlings

Li, Z., Yang, S., Long, W.-B., et al. (2013) · Plant Cell & Environment · doi:10.1111/pce.12092 · Cited by 238

The role of protein binding of trivalent arsenicals in arsenic carcinogenesis and toxicity

Kitchin, K. T., & Wallace, K. (2007) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2007.10.021 · Cited by 232

Proteome analysis of maize roots reveals that oxidative stress is a main contributing factor to plant arsenic toxicity

Requejo-Aguilar, R., & Tena, M. (2005) · Phytochemistry · doi:10.1016/j.phytochem.2005.05.003 · Cited by 231

Complexation of Arsenite with Phytochelatins Reduces Arsenite Efflux and Translocation from Roots to Shoots in Arabidopsis

Liu, W., Wood, B. A., Raab, A., McGrath, S. P., Zhao, F. J., & Feldmann, J. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.150862 · Cited by 230

Nitrite as the major source of nitric oxide production by Arabidopsis thaliana in response to Pseudomonas syringae

Modolo, L. V., Augusto, O., Almeida, I. M. G., Magalhaes, J. R., & Salgado, I. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.05.078 · Cited by 229

Salicylic acid-induced nitric oxide enhances arsenic toxicity tolerance in maize plants by upregulating the ascorbate-glutathione cycle and glyoxalase system

Kaya, C., Ashraf, M., Alyemeni, M. N., Corpas, F. J., & Ahmad, P. (2020) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2020.123020 · Cited by 229

Arsenic Transport in Rice and Biological Solutions to Reduce Arsenic Risk from Rice

Chen, Y., Han, Y.-H., Cao, Y., Zhu, Y., Rathinasabapathi, B., & Ma, L. Q. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00268 · Cited by 227

Effect of arsenic on some physiological parameters in bean plants

Stoeva, N., Berova, M., & Zlatev, Z. S. (2005) · Biologia Plantarum · doi:10.1007/s10535-005-3296-z · Cited by 222

Plant Haemoglobins, Nitric Oxide and Hypoxic Stress

Dordas, C. A. (2003) · Annals of Botany · doi:10.1093/aob/mcf115 · Cited by 221

An increase in the concentration of abscisic acid is critical for nitric oxide‐mediated plant adaptive responses to UV‐B irradiation

Tossi, V. E., Lamattina, L., & Cassia, R. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2008.02722.x · Cited by 219

Differential Induction of Tobacco MAP Kinases by the Defense Signals Nitric Oxide, Salicylic Acid, Ethylene, and Jasmonic Acid

Kumar, D., & Klessig, D. F. (2000) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2000.13.3.347 · Cited by 214

Transcriptomic changes and signalling pathways induced by arsenic stress in rice roots

Huang, T., Nguyen, Q. T. T., Fu, S., Lin, C.-Y., Chen, Y., & Huang, H.-J. (2012) · Plant Molecular Biology · doi:10.1007/s11103-012-9969-z · Cited by 210

Integrating nitric oxide into salicylic acid and jasmonic acid/ ethylene plant defense pathways

Mur, L. A. J., Prats, E., Pierre, S., et al. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00215 · Cited by 210

Arsenic uptake, accumulation and toxicity in rice plants: Possible remedies for its detoxification: A review

Bakhat, H. F., Zia, Z., Fahad, S., Abbas, S., Hammad, H. M., Shahzad, A. N., Abbas, F., Alharby, H. F., & Shahid, M. A. R. (2017) · Environmental Science and Pollution Research · doi:10.1007/s11356-017-8462-2 · Cited by 210

Arabidopsis NIP3;1 Plays an Important Role in Arsenic Uptake and Root-to-Shoot Translocation under Arsenite Stress Conditions

Xu, W., Dai, W., Yan, H., et al. (2015) · Molecular Plant · doi:10.1016/j.molp.2015.01.005 · Cited by 205

Nitric oxide in fruit ripening: Trends and opportunities

Manjunatha, G., Lokesh, V., & Neelwarne, B. (2010) · Biotechnology Advances · doi:10.1016/j.biotechadv.2010.03.001 · Cited by 205

The Arabidopsis thaliana aquaglyceroporin AtNIP7;1 is a pathway for arsenite uptake

Isayenkov, S. V., & Maathuis, F. J. M. (2008) · FEBS Letters · doi:10.1016/j.febslet.2008.04.022 · Cited by 205

Plant catalases as NO and H2S targets

Palma, J. M., Mateos, R. M., López-Jaramillo, J., Rodríguez-Ruiz, M., González‐Gordo, S., Lechuga-Sancho, A. M., & Corpas, F. J. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101525 · Cited by 205

The Effect of Various Nitric Oxide-Donor Agents on Hydrogen Peroxide-Mediated Toxicity: A Direct Correlation between Nitric Oxide Formation and Protection

Wink, D. A., Cook, J. A., Pacelli, R., DeGraff, W., Gamson, J., Liebmann, J., Krishna, M. C., & Mitchell, J. B. (1996) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1996.0304 · Cited by 204

S-Nitrosoglutathione Reductase Affords Protection against Pathogens in Arabidopsis, Both Locally and Systemically

Rustérucci, C., Espunya, M. C., Dı́az, M., Chabannes, M., & Martı́nez, M. C. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.091686 · Cited by 202

Current overview of S-nitrosoglutathione (GSNO) in higher plants

Corpas, F. J., Ramírez, J. D. D. A., & Barroso, J. B. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00126 · Cited by 201

Phytochelatins and Antioxidant Systems Respond Differentially during Arsenite and Arsenate Stress in Hydrilla verticillata (L.f.) Royle

Srivastava, S., Mishra, S., Tripathi, R. D., Dwivedi, S., Trivedi, P. K., & Tandon, P. K. (2007) · Environmental Science & Technology · doi:10.1021/es062167j · Cited by 197

Nitric Oxide Mediates Brassinosteroid-Induced ABA Biosynthesis Involved in Oxidative Stress Tolerance in Maize Leaves

Zhang, A., Zhang, J., Zhang, J., Ye, N., Zhang, H., Tan, M., & Jiang, M. (2010) · Plant and Cell Physiology · doi:10.1093/pcp/pcq187 · Cited by 193

Selenium and auxin mitigates arsenic stress in rice (Oryza sativa L.) by combining the role of stress indicators, modulators and genotoxicity assay

Pandey, C., & Gupta, M. (2015) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2015.01.044 · Cited by 189

Arsenic in the human food chain: the Latin American perspective

Bundschuh, J., Nath, B., Bhattacharya, P., Liu, C., Armienta, M. A., López, M. V. M., López, D. L., Jean, J., Cornejo‐Ponce, L., Macedo, L. F. L., et al. (2011) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2011.09.069 · Cited by 188

Arsenic triggers the nitric oxide (NO) and S-nitrosoglutathione (GSNO) metabolism in Arabidopsis

Leterrier, M., Airaki, M., Palma, J. M., et al. (2012) · Environmental Pollution · doi:10.1016/j.envpol.2012.03.012 · Cited by 187

Salicylic acid activates nitric oxide synthesis in Arabidopsis

Zottini, M., Costa, A., Michele, R. D., Ruzzene, M., Carimi, F., & Schiavo, F. L. (2007) · Journal of Experimental Botany · doi:10.1093/jxb/erm001 · Cited by 183

Inhibition of ribonuclease and protease activities in arsenic exposed rice seedlings: Role of proline as enzyme protectant

Mishra, S., & Dubey, R. S. (2005) · Journal of Plant Physiology · doi:10.1016/j.jplph.2005.08.003 · Cited by 181

Nitric Oxide-Releasing Polymeric Materials for Antimicrobial Applications: A Review

Rong, F., Tang, Y., Wang, T., Feng, T., Jiang, S., Li, P., & Huang, W. (2019) · Antioxidants · doi:10.3390/antiox8110556 · Cited by 178

Highly efficient xylem transport of arsenite in the arsenic hyperaccumulator Pteris vittata

Su, Y., McGrath, S. P., Zhu, Y., & Zhao, F. J. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02584.x · Cited by 177

The Predominance of Inorganic Arsenic Species in Plants from Yellowknife, Northwest Territories, Canada

Koch, I., Wang, L., Ollson, C., Cullen, W., & Reimer, K. J. (1999) · Environmental Science & Technology · doi:10.1021/es9906756 · Cited by 176

Effect of applying an arsenic-resistant and plant growth-promoting rhizobacterium to enhance soil arsenic phytoremediation by Populus deltoides LH05-17

Wang, Q., Xiong, D., Zhao, P., Yu, X., Tu, B., & Wang, G. (2011) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2011.05142.x · Cited by 173

Reduced arsenic accumulation in rice (Oryza sativa L.) shoot involves sulfur mediated improved thiol metabolism, antioxidant system and altered arsenic transporters

Awasthi, G., Singh, A. P., Kumar, A., Mishra, S., Dwivedi, S., Kumar, S., Trivedi, P. K., Pandey, V., & Tripathi, R. D. (2015) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2015.11.005 · Cited by 173

Differential molecular response of monodehydroascorbate reductase and glutathione reductase by nitration andS-nitrosylation

Begara-Morales, J. C., Sánchez-Calvo, B., Chaki, M., Mata-Pérez, C., Valderrama, R., Padilla, M. N., López-Jaramillo, J., Luque, F., Corpas, F. J., & Barroso, J. B. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv306 · Cited by 172

Fatty Acid Transduction of Nitric Oxide Signaling

Schopfer, F. J., Baker, P. R. S., Giles, G. I., Chumley, P., Batthyány, C., Crawford, J. H., Patel, R. P., Hogg, N., Branchaud, B. P., Lancaster, J. R., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m414689200 · Cited by 172

Cross Talk among Calcium, Hydrogen Peroxide, and Nitric Oxide and Activation of Gene Expression Involving Calmodulins and Calcium-Dependent Protein Kinases in Ulva compressa Exposed to Copper Excess

González, A., Cabrera, M. D. L. Á., Henríquez, M. J., Contreras, R. A., Morales, B., & Moenne, A. (2012) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.191759 · Cited by 170

Nitric oxide-mediated integrative alterations in plant metabolism to confer abiotic stress tolerance, NO crosstalk with phytohormones and NO-mediated post translational modifications in modulating diverse plant stress

Sami, F., Faizan, M., Faraz, A., et al. (2017) · Nitric Oxide · doi:10.1016/j.niox.2017.12.005 · Cited by 170

Arsenic-induced oxidative stress in the common bean legume, Phaseolus vulgaris L. seedlings and its amelioration by exogenous nitric oxide

Talukdar, D. (2012) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-012-0140-8 · Cited by 168

OXIDATIVE CHANGES AND PHOTOSYNTHESIS IN OAT PLANTS GROWN IN AS-CONTAMINATED SOIL

Stoeva, N., Bineva, T., & Pushkarov, N. (2003) · Cited by 166

Modulation of antioxidant responses by arsenic in maize

Mylona, P. V., Polidoros, A. N., & Scandalios, J. G. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00090-2 · Cited by 160

Arsenic in cooked rice: Effect of chemical, enzymatic and microbial processes on bioaccessibility and speciation in the human gastrointestinal tract

Sun, G., de Wiele, T. V., Alava, P., et al. (2011) · Environmental Pollution · doi:10.1016/j.envpol.2011.11.021 · Cited by 158

Nitric Oxide Alleviated Arsenic Toxicity by Modulation of Antioxidants and Thiol Metabolism in Rice (Oryza sativa L.)

Singh, A. P., Awasthi, G., Kumar, A., Mishra, S., Singh, P. K., Dwivedi, S., Trivedi, P. K., Chakrabarty, D., Mallick, S., Pandey, V., et al. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01272 · Cited by 158

Arsenic speciation, and arsenic and phosphate distribution in arsenic hyperaccumulator Pteris vittata L. and non-hyperaccumulator Pteris ensiformis L.

Singh, N., & Ma, L. Q. (2005) · Environmental Pollution · doi:10.1016/j.envpol.2005.08.050 · Cited by 151

A protective role for nitric oxide and salicylic acid for arsenite phytotoxicity in rice ( Oryza sativa L.)

Singh, A. P., Awasthi, G., Kumar, A., Mishra, S., Kumar, N., Dixit, S., Singh, P. K., Dwivedi, S., Trivedi, P. K., Pandey, V., et al. (2017) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2017.02.019 · Cited by 151

Arsenic Uptake and Accumulation Mechanisms in Rice Species

Abedi, T., & Mojiri, A. (2020) · Plants · doi:10.3390/plants9020129 · Cited by 145

Physical, Chemical, and Biological Methods for the Removal of Arsenic Compounds

Lim, K.-A., Shukor, M. Y., & Wasoh, H. (2014) · BioMed Research International · doi:10.1155/2014/503784 · Cited by 144

Nitric oxide alleviates arsenic-induced toxic effects in ridged Luffa seedlings

Singh, V. P., Srivastava, P. K., & Prasad, S. M. (2013) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2013.07.003 · Cited by 143

The Shoot-Specific Expression of γ-Glutamylcysteine Synthetase Directs the Long-Distance Transport of Thiol-Peptides to Roots Conferring Tolerance to Mercury and Arsenic

Li, Y., Dankher, O. P., Carreira, L. H., Smith, A. P., & Meagher, R. B. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.074815 · Cited by 139

Differential inhibition of Arabidopsis superoxide dismutases by peroxynitrite-mediated tyrosine nitration

Holzmeister, C., Gaupels, F., Geerlof, A., Sarioglu, H., Sattler, M., Durner, J., & Lindermayr, C. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru458 · Cited by 139

Irreversible Collective Migration of Cyanobacteria in Eutrophic Conditions

Dervaux, J., Méjean, A., & Brunet, P. (2015) · PLoS ONE · doi:10.1371/journal.pone.0120906 · Cited by 138

Nitric oxide mediated transcriptional modulation enhances plant adaptive responses to arsenic stress

Singh, P. K., Indoliya, Y., Chauhan, A. S., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-03923-2 · Cited by 138

Influence of the arbuscular mycorrhizal fungus Glomus mosseae on uptake of arsenate by the As hyperaccumulator fern Pteris vittata L.

Liu, Y., Zhu, Y., Chen, B., Christie, P., & Li, X. L. (2004) · Mycorrhiza · doi:10.1007/s00572-004-0320-7 · Cited by 136

Differential Transcriptomic Analysis by RNA-Seq of GSNO-Responsive Genes Between Arabidopsis Roots and Leaves

Begara-Morales, J. C., Sánchez-Calvo, B., Luque, F., Leyva‐Pérez, M. D. L. O., Leterrier, M., Corpas, F. J., & Barroso, J. B. (2014) · Plant and Cell Physiology · doi:10.1093/pcp/pcu044 · Cited by 133

Effect of nitric oxide on reactive oxygen species and antioxidant enzymes in kiwifruit during storage

Zhu, S., Sun, L., Liu, M., et al. (2008) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.3353 · Cited by 132

Physiological Response of Maize to Arsenic Contamination

Stoeva, N., Berova, M., & Zlatev, Z. S. (2003) · Biologia Plantarum · doi:10.1023/b:biop.0000023893.12939.48 · Cited by 130

Sodium Nitroprusside: Mechanism of NO Release Mediated by Sulfhydryl-Containing Molecules

Grossi, L., & D'Angelo, S. (2005) · Journal of Medicinal Chemistry · doi:10.1021/jm049857n · Cited by 129

1-Aminocyclopropane-1-carboxylic acid deaminase producing beneficial rhizobacteria ameliorate the biomass characters of Panicum maximum Jacq. by mitigating drought and salt stress

Tiwari, G., Duraivadivel, P., Sharma, S., & Hariprasad, P. (2018) · Scientific Reports · doi:10.1038/s41598-018-35565-3 · Cited by 129

Oxidative stress tolerance in plants

Krishnamurthy, A., & Rathinasabapathi, B. (2013) · Plant Signaling & Behavior · doi:10.4161/psb.25761 · Cited by 128

Arsenic accumulation in rice (Oryza sativa L.) is influenced by environment and genetic factors

Kumarathilaka, P., Seneweera, S. P., Meharg, A. A., et al. (2018) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2018.06.030 · Cited by 128

Association of inorganic arsenic exposure with liver cancer mortality: A meta-analysis

Wang, W., Cheng, S., & Zhang, D. (2014) · Environmental Research · doi:10.1016/j.envres.2014.08.034 · Cited by 127

In vitro genotoxicity of lead acetate: induction of single and double DNA strand breaks and DNA–protein cross-links

Woźniak, K., & Błasiak, J. (2003) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/s1383-5718(02)00295-4 · Cited by 125

Roles of NIA/NR/NOA1-dependent nitric oxide production and HY1 expression in the modulation of Arabidopsis salt tolerance

Xie, Y., Mao, Y., Lai, D., Zhang, W., Zheng, T., & Shen, W. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert149 · Cited by 125

Nitro-Fatty Acids in Plant Signaling: Nitro-Linolenic Acid Induces the Molecular Chaperone Network in Arabidopsis

Mata-Pérez, C., Sánchez-Calvo, B., Padilla, M. N., Begara-Morales, J. C., Luque, F., Melguizo, M., Jiménez‐Ruiz, J., Fierro-Risco, J., Peñas, A., Valderrama, R., et al. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.01671 · Cited by 125

Arsenic Hyperaccumulation Strategies: An Overview

Souri, Z., Karimi, N., & Sandalio, L. M. (2017) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2017.00067 · Cited by 125

Activity of Nitric Oxide Is Dependent On, But Is Partially Required for Function of, Salicylic Acid in the Signaling Pathway in Tobacco Systemic Acquired Resistance

Song, F., & Goodman, R. M. (2001) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2001.14.12.1458 · Cited by 124

Effect of Brassinosteroids on Germination and Seedling Growth of Radish (Raphanus sativus L.) under PEG-6000 Induced Water Stress

Mahesh, K., Balaraju, P., Ramakrishna, B., & Rao, S. S. R. (2013) · American Journal of Plant Sciences · doi:10.4236/ajps.2013.412285 · Cited by 124

Nitric Oxide Production in Plants

Planchet, É., & Kaiser, W. M. (2006) · Plant Signaling & Behavior · doi:10.4161/psb.1.2.2435 · Cited by 123

Comparative effect of calcium and EDTA on arsenic uptake and physiological attributes ofPisum sativum

Rafiq, M., Shahid, M. A. R., Abbas, G., Shamshad, S., Khalid, S., Niazi, N. K., & Dumat, C. (2017) · International Journal of Phytoremediation · doi:10.1080/15226514.2016.1278426 · Cited by 122

Inositol transporters AtINT2 and AtINT4 regulate arsenic accumulation in Arabidopsis seeds

Duan, G., Hu, Y., Schneider, S., et al. (2015) · Nature Plants · doi:10.1038/nplants.2015.202 · Cited by 119

Nitric oxide confronts arsenic stimulated oxidative stress and root architecture through distinct gene expression of auxin transporters, nutrient related genes and modulates biochemical responses in Oryza sativa L.

Praveen, A., & Gupta, M. (2018) · Environmental Pollution · doi:10.1016/j.envpol.2018.04.096 · Cited by 119

Quercetin and its metabolites improve vessel function by inducing eNOS activity via phosphorylation of AMPK

Shen, Y., Croft, K. D., Hodgson, J. M., Kyle, R. A., Lee, I.-L. E., Wang, Y., Stocker, R., & Ward, N. C. (2012) · Biochemical Pharmacology · doi:10.1016/j.bcp.2012.07.016 · Cited by 118

An aquaporin Pv TIP 4;1 from Pteris vittata may mediate arsenite uptake

He, Z., Yan, H., Chen, Y., Shen, H., Xu, W., Zhang, H., Shi, L. G., Zhu, Y., & Ma, M. (2015) · New Phytologist · doi:10.1111/nph.13637 · Cited by 116

Correction: Corrigendum: The Phosphorylation Profile of Myosin Binding Protein-C Slow is Dynamically Regulated in Slow-Twitch Muscles in Health and Disease

Ackermann, M. A., Kerr, J. P., King, B., Ward, C. W., & Kontrogianni‐Konstantopoulos, A. (2018) · Scientific Reports · doi:10.1038/srep46969 · Cited by 116

Comparative effects of various nitric oxide donors on ferritin regulation, programmed cell death, and cell redox state in plant cells

Murgia, I., de Pinto, M. C., Delledonne, M., et al. (2004) · Journal of Plant Physiology · doi:10.1016/j.jplph.2003.12.004 · Cited by 115

Sodium nitroprusside (SNP) improves tolerance to arsenic (As) toxicity in Vicia faba through the modifications of biochemical attributes, antioxidants, ascorbate-glutathione cycle and glyoxalase cycle

Ahmad, P., Alam, P., Balawi, T. H., Altalayan, F. H., Ahanger, M. A., & Ashraf, M. (2019) · Chemosphere · doi:10.1016/j.chemosphere.2019.125480 · Cited by 114

Overexpression of Rat Neurons Nitric Oxide Synthase in Rice Enhances Drought and Salt Tolerance

Cai, W., Liu, W., Wang, W., Fu, Z.-W., Han, T., & Lu, Y. (2015) · PLoS ONE · doi:10.1371/journal.pone.0131599 · Cited by 109

Accumulation and transformation of inorganic and organic arsenic in rice and role of thiol-complexation to restrict their translocation to shoot

Mishra, S., Mattusch, J., & Wennrich, R. (2017) · Scientific Reports · doi:10.1038/srep40522 · Cited by 109

Comparison of root absorption, translocation and tolerance of arsenic in the hyperaccumulator Pteris vittata and the nonhyperaccumulator Pteris tremula

Caille, N., Zhao, F. J., & McGrath, S. P. (2004) · New Phytologist · doi:10.1111/j.1469-8137.2004.01239.x · Cited by 108

Plants as Useful Vectors to Reduce Environmental Toxic Arsenic Content

Mirza, N., Mahmood, Q., Shah, M. M., Pervez, A., & Sultan, S. (2014) · The Scientific World JOURNAL · doi:10.1155/2014/921581 · Cited by 104

Arsenate disrupts ion balance, sulfur and nitric oxide metabolisms in roots and leaves of pea (Pisum sativum L.) plants

Rodríguez-Ruiz, M., Chacón, M. V. A., Palma, J. M., & Corpas, F. J. (2018) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2018.06.028 · Cited by 101

The Involvement of Nitric Oxide in Integration of Plant Physiological and Ultrastructural Adjustments in Response to Arsenic

Farnese, F. D. S., de Oliveira, J. A., Paiva, É. A. S., et al. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00516 · Cited by 99

Heterologous Expression of Pteris vittata Arsenite Antiporter PvACR3;1 Reduces Arsenic Accumulation in Plant Shoots

Chen, Y., Hua, C.-Y., Jia, M.-R., et al. (2017) · Environmental Science & Technology · doi:10.1021/acs.est.7b03369 · Cited by 98

Functional and molecular characteristics of rice and barley NIP aquaporins transporting water, hydrogen peroxide and arsenite

Katsuhara, M., Sasano, S., Horie, T., Matsumoto, T., Rhee, J., & Shibasaka, M. (2014) · Plant Biotechnology · doi:10.5511/plantbiotechnology.14.0421a · Cited by 96

Arsenic extraction and speciation in carrots using accelerated solvent extraction, liquid chromatography and plasma mass spectrometry

Vela, N. P., Heitkemper, D. T., & Stewart, K. R. (2001) · The Analyst · doi:10.1039/b102420p · Cited by 94

Induction of Class-1 Non-symbiotic Hemoglobin Genes by Nitrate, Nitrite and Nitric Oxide in Cultured Rice Cells

Ohwaki, Y., Kawagishi-Kobayashi, M., Wakasa, K., Fujihara, S., & Yoneyama, T. (2005) · Plant and Cell Physiology · doi:10.1093/pcp/pci030 · Cited by 94

Environmental exposure to arsenic and chromium in an industrial area

Vimercati, L., Gatti, M. F., Gagliardi, T., Cuccaro, F., Maria, L. D., Caputi, A., Quarato, M., & Baldassarre, A. (2017) · Environmental Science and Pollution Research · doi:10.1007/s11356-017-8827-6 · Cited by 94

Determination of arsenic species in water, soils and plants

Mattusch, J., Wennrich, R., Schmidt, A., & Reißer, W. (2000) · Fresenius Journal of Analytical Chemistry · doi:10.1007/s002160050039 · Cited by 91

Recent advances in arsenic metabolism in plants: current status, challenges and highlighted biotechnological intervention to reduce grain arsenic in rice

Shri, M., Singh, P. K., Kidwai, M., Gautam, N., Dubey, S., Verma, G., & Chakrabarty, D. (2019) · Metallomics · doi:10.1039/c8mt00320c · Cited by 90

Cadmium and arsenic-induced-stress differentially modulates Arabidopsis root architecture, peroxisome distribution, enzymatic activities and their nitric oxide content

Piacentini, D., Corpas, F. J., D’Angeli, S., Altamura, M. M., & Falasca, G. (2020) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2020.01.026 · Cited by 89

Protective role of nitric oxide against arsenic-induced damages in germinating mung bean seeds

Ismail, G. S. M. (2012) · Acta Physiologiae Plantarum · doi:10.1007/s11738-012-0927-9 · Cited by 88

Nitric oxide improves tolerance to arsenic stress in Isatis cappadocica desv. Shoots by enhancing antioxidant defenses

Souri, Z., Karimi, N., Farooq, M. A., & Sandalio, L. M. (2019) · Chemosphere · doi:10.1016/j.chemosphere.2019.124523 · Cited by 88

Insights into Nitric Oxide-Mediated Water Balance, Antioxidant Defence and Mineral Homeostasis in Rice (Oryza sativa L.) under Chilling Stress

Sohag, A. A. M., Tahjib‐Ul‐Arif, M., Afrin, S., Khan, M. K., Hannan, M. A., Skalický, M., Mortuza, M. G., Brestič, M., Hossain, M. A., & Murata, Y. (2020) · Nitric Oxide · doi:10.1016/j.niox.2020.04.001 · Cited by 86

Protective effect of nitric oxide against arsenic-induced oxidative damage in tall fescue leaves

Wei, J. J., Fei, X. Y., & Fang, H. Y. (2010) · AFRICAN JOURNAL OF BIOTECHNOLOGY · doi:10.5897/ajb10.1442 · Cited by 82

Nitric Oxide, Ethylene, and Auxin Cross Talk Mediates Greening and Plastid Development in Deetiolating Tomato Seedlings

de Melo, N. K. G., Bianchetti, R., Lira, B. S., et al. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00023 · Cited by 82

Comparative biochemical and RAPD analysis in two varieties of rice (Oryza sativa) under arsenic stress by using various biomarkers

Ahmad, M. A., Gaur, R., & Gupta, M. (2012) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2012.03.005 · Cited by 79

THB 1, a truncated hemoglobin, modulates nitric oxide levels and nitrate reductase activity

Sanz‐Luque, E., Ocaña‐Calahorro, F. J., de Montaigu, A., et al. (2014) · The Plant Journal · doi:10.1111/tpj.12744 · Cited by 78

Arsenic induced modulation of antioxidative defense system and brassinosteroids in Brassica juncea L.

Kanwar, M. K., Poonam, P., & Bhardwaj, R. (2015) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2015.02.016 · Cited by 77

Nitric Oxide Affects Rice Root Growth by Regulating Auxin Transport Under Nitrate Supply

Sun, H., Feng, F., Liu, J., & Zhao, Q. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00659 · Cited by 76

Dissecting the components controlling root‐to‐shoot arsenic translocation in Arabidopsis thaliana

Wang, C., Na, G., Bermejo, E. S., et al. (2017) · New Phytologist · doi:10.1111/nph.14761 · Cited by 75

Arsenic accumulation in lentil (Lens culinaris) genotypes and risk associated with the consumption of grains

Alam, M. Z., Hoque, M. A., Ahammed, G. J., McGee, R. J., & Carpenter‐Boggs, L. (2019) · Scientific Reports · doi:10.1038/s41598-019-45855-z · Cited by 74

Mechanisms and Role of Nitric Oxide in Phytotoxicity-Mitigation of Copper

Rather, B. A., Masood, A., Sehar, Z., Majid, A., Anjum, N. A., & Khan, N. A. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00675 · Cited by 73

Nitric oxide signaling in aluminum stress in plants

He, H., Zhan, J., He, L., & Gu, M. (2011) · PROTOPLASMA · doi:10.1007/s00709-011-0310-5 · Cited by 72

ARS5 is a component of the 26S proteasome complex, and negatively regulates thiol biosynthesis and arsenic tolerance in Arabidopsis

Sung, D., Kim, T., Komives, E. A., Mendoza‐Cózatl, D. G., & Schroeder, J. I. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03914.x · Cited by 72

Genotoxicity induced by arsenic compounds in peripheral human lymphocytes analysed by cytokinesis-block micronucleus assay

Colognato, R., Coppedè, F., Ponti, J., et al. (2007) · Mutagenesis · doi:10.1093/mutage/gem010 · Cited by 71

Inhibition of NADP‐malic enzyme activity by H2S and NO in sweet pepper (Capsicum annuum L.) fruits

Muñoz-Vargas, M. Á., González‐Gordo, S., Palma, J. M., et al. (2019) · Physiologia Plantarum · doi:10.1111/ppl.13000 · Cited by 71

Speciation by liquid chromatography-inductively coupled plasma-mass spectrometry of arsenic in mung bean seedlings used as a bio-indicator for the arsenic contamination.

den Broeck, K. V., Vandecasteele, C., & Geuns, J. M. C. (1998) · Analytica Chimica Acta · doi:10.1016/s0003-2670(97)00698-3 · Cited by 68

Nitric oxide alters nitrogen metabolism and PIN gene expressions by playing protective role in arsenic challenged Brassica juncea L.

Praveen, A., Pandey, A. K., & Gupta, M. (2019) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2019.03.054 · Cited by 68

Nitro-Fatty Acid Logistics: Formation, Biodistribution, Signaling, and Pharmacology

Schopfer, F. J., & Khoo, N. K. H. (2019) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2019.04.009 · Cited by 67

Arsenic transformation and plant growth promotion characteristics of As-resistant endophytic bacteria from As-hyperaccumulator Pteris vittata

Xu, J., Han, Y.-H., Chen, Y., et al. (2015) · Chemosphere · doi:10.1016/j.chemosphere.2015.09.102 · Cited by 66

Extraction of arsenate and arsenite species from soils and sediments

Georgiadis, M., Cai, Y. Z., & Solo‐Gabriele, H. M. (2005) · Environmental Pollution · doi:10.1016/j.envpol.2005.08.028 · Cited by 63

Effects of arsenic on nitrate metabolism in arsenic hyperaccumulating and non-hyperaccumulating ferns

Singh, N., Ma, L. Q., Vu, J. C. V., et al. (2009) · Environmental Pollution · doi:10.1016/j.envpol.2009.03.036 · Cited by 63

Arsenic-induced stress activates sulfur metabolism in different organs of garlic (Allium sativum L.) plants accompanied by a general decline of the NADPH-generating systems in roots

Ruiz, C., Feriche-Linares, R., Rodríguez-Ruiz, M., Palma, J. M., & Corpas, F. J. (2017) · Journal of Plant Physiology · doi:10.1016/j.jplph.2016.12.010 · Cited by 60

Medicago truncatula Phytoglobin 1.1 controls symbiotic nodulation and nitrogen fixation via the regulation of nitric oxide concentration

Berger, A., Guinand, S., Boscari, A., et al. (2020) · New Phytologist · doi:10.1111/nph.16462 · Cited by 60

Constitutive Expression of Mammalian Nitric Oxide Synthase in Tobacco Plants Triggers Disease Resistance to Pathogens

Chun, H. J., Park, H. C., Koo, S. C., Lee, J. H., Park, C. Y., Choi, M. S., Kang, C. H., Baek, D., Cheong, Y. H., Yun, D., et al. (2012) · Molecules and Cells · doi:10.1007/s10059-012-0213-0 · Cited by 59

Expression of the Tobacco Non-symbiotic Class 1 Hemoglobin Gene Hb1 Reduces Cadmium Levels by Modulating Cd Transporter Expression Through Decreasing Nitric Oxide and ROS Level in Arabidopsis

Bahmani, R., Kim, D.-G., Na, J., & Hwang, S. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00201 · Cited by 58

Enzymatic adaptations to arsenic-induced oxidative stress in Zea mays and genotoxic effect of arsenic in root tips of Vicia faba and Zea mays

Duquesnoy, I., Champeau, G. M., Evray, G., Ledoigt, G., & Piquet, A. (2010) · Comptes Rendus Biologies · doi:10.1016/j.crvi.2010.07.004 · Cited by 55

The application of nitric oxide delivery in nanoparticle-based tumor targeting drug delivery and treatment

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Nitro-linolenic acid is a nitric oxide donor

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Activation of NADPH-recycling systems in leaves and roots of Arabidopsis thaliana under arsenic-induced stress conditions is accelerated by knock-out of Nudix hydrolase 19 (AtNUDX19) gene

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Reactive Oxygen Species (ROS) Metabolism and Nitric Oxide (NO) Content in Roots and Shoots of Rice (Oryza sativa L.) Plants under Arsenic-Induced Stress

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Exogenous nitric oxide (as sodium nitroprusside) ameliorates arsenic-induced oxidative stress in watercress (Nasturtium officinale R. Br.) plants

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Toxicity of arsenic (As) on seed germination of sunflower (Helianthus annuus L.)

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Stably TransformedLotus japonicusPlants Overexpressing Phytoglobin LjGlb1-1 Show Decreased Nitric Oxide Levels in Roots and Nodules as Well as Delayed Nodule Senescence

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G-quadruplex structures of human telomere DNA examined by single molecule FRET and BrG-substitution

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Identification of in vivo nitrosylated phytochelatins in Arabidopsis thaliana cells by liquid chromatography-direct electrospray-linear ion trap-mass spectrometry

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ATR-FTIR Studies on the Adsorption/Desorption Kinetics of Dimethylarsinic Acid on Iron–(Oxyhydr)oxides

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Overexpression of spinach non-symbiotic hemoglobin in Arabidopsis resulted in decreased NO content and lowered nitrate and other abiotic stresses tolerance

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Effect of Phosphorus on Arsenic Accumulation and Detoxification in Arsenic Hyperaccumulator, Isatis cappadocica

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Plant Responses to Arsenic: the Role of Nitric Oxide

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Effect of Brassinosteroids on Germination and Seedling Growth of Radish ( Raphanus sativus L.) under PEG-6000 Induced Water Stress

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Nitric Oxide Attenuates Oxidative Stress Induced by Arsenic in Lettuce (Lactuca sativa) Leaves

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Nitric oxide‐fixation by non‐symbiotic haemoglobin proteins in Arabidopsis thaliana under N‐limited conditions

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Pharmacological and genetical evidence supporting nitric oxide requirement for 2,4-epibrassinolide regulation of root architecture inArabidopsis thaliana

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Adsorption of heavy metals on natural zeolites: A review

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Spatial distribution of arsenic species in soil ecosystem and their effect on plant physiology

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Application of Triple Superphosphate to Alleviate Arsenic Toxicity in Rice

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Cryptic exposure to arsenic

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METABOLIC ADAPTATIONS TO ARSENIC-INDUCED OXIDATIVE STRESS IN ISATIS CAPPADOCICA

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Co-exposure of Arsenic and Iron Causes Hepatic Injury: A Tale of Two Hits

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