Brassinosteroids regulate growth in plants under stressful environments and crosstalk with other potential phytohormones

Mechanisms of Salinity Tolerance

Munns, R., & Tester, M. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092911 · Cited by 13,792 · see citing works

Temperature extremes: Effect on plant growth and development

Hatfield, J. L., & Prueger, J. H. (2015) · Weather and Climate Extremes · doi:10.1016/j.wace.2015.08.001 · Cited by 2,691 · see citing works

Soil Salinity: Effect on Vegetable Crop Growth. Management Practices to Prevent and Mitigate Soil Salinization

Machado, R., & Serralheiro, R. P. (2017) · Horticulturae · doi:10.3390/horticulturae3020030 · Cited by 1,436 · see citing works

Roles of enzymatic and nonenzymatic antioxidants in plants during abiotic stress

Ahmad, P., Jaleel, C. A., Salem, M. A., Nabi, G., & Sharma, S. (2010) · Critical Reviews in Biotechnology · doi:10.3109/07388550903524243 · Cited by 1,213 · see citing works

Effects of brassinosteroids on the plant responses to environmental stresses

Bajguz, A., & Hayat, S. (2008) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2008.10.002 · Cited by 929 · see citing works

Reactive Oxygen Species Are Involved in Brassinosteroid-Induced Stress Tolerance in Cucumber

Xia, X., Wang, Y., Zhou, Y., Tao, Y., Mao, W., Shi, K., Asami, T., Chen, Z., & Yu, J. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.138230 · Cited by 713 · see citing works

Nitric Oxide Mitigates Salt Stress by Regulating Levels of Osmolytes and Antioxidant Enzymes in Chickpea

Ahmad, P., Latef, A. A. H. A., Hashem, A., Allah, E. F. A., Gücel, S., & Tran, L. P. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00347 · Cited by 587 · see citing works

Recent developments in understanding salinity tolerance

Türkan, İ., & Demiral, T. (2009) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2009.05.008 · Cited by 571 · see citing works

Brassinosteroid confers tolerance in Arabidopsis thaliana and Brassica napus to a range of abiotic stresses

Kagale, S., Divi, U. K., Krochko, J. E., Keller, W. A., & Krishna, P. (2006) · Planta · doi:10.1007/s00425-006-0361-6 · Cited by 552 · see citing works

Brassinosteroid regulates stomatal development by GSK3-mediated inhibition of a MAPK pathway

Kim, T., Michniewicz, M., Bergmann, D. C., & Wang, Z. (2012) · Nature · doi:10.1038/nature10794 · Cited by 530 · see citing works

An Essential Role for 14-3-3 Proteins in Brassinosteroid Signal Transduction in Arabidopsis

Gampala, S. S. L., Kim, T., He, J., Tang, W., Deng, Z., Bai, M.-Y., Guan, S., Lalonde, S., Sun, Y., Gendron, J. M., et al. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.06.009 · Cited by 524 · see citing works

Selenium and sulfur influence ethylene formation and alleviate cadmium-induced oxidative stress by improving proline and glutathione production in wheat

Khan, M. I. R., Nazir, F., Asgher, M., Per, T. S., & Khan, N. A. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.09.011 · Cited by 490 · see citing works

Brassinolide Application Improves the Drought Tolerance in Maize Through Modulation of Enzymatic Antioxidants and Leaf Gas Exchange

Anjum, S. A., Wang, L., Farooq, M., Hussain, M. B., Xue, L. L., & Zou, C. (2011) · Journal of Agronomy and Crop Science · doi:10.1111/j.1439-037x.2010.00459.x · Cited by 488 · see citing works

Plant growth under water/salt stress: ROS production; antioxidants and significance of added potassium under such conditions

Ahanger, M. A., Tomar, N. S., Tittal, M., Argal, S., & Agarwal, R. M. (2017) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-017-0462-7 · Cited by 486 · see citing works

Brassinosteroid Regulates Cell Elongation by Modulating Gibberellin Metabolism in Rice

Tong, H., Xiao, Y., Liu, D., Gao, S., Liu, L., Yin, Y., Jin, Y. H., Qian, Q., & Chu, C. (2014) · The Plant Cell · doi:10.1105/tpc.114.132092 · Cited by 461 · see citing works

Brassinosteroid-mediated stress tolerance in Arabidopsis shows interactions with abscisic acid, ethylene and salicylic acid pathways

Divi, U. K., Rahman, T., & Krishna, P. (2010) · BMC Plant Biology · doi:10.1186/1471-2229-10-151 · Cited by 457 · see citing works

Auxin and ethylene: collaborators or competitors?

Muday, G. K., Rahman, A., & Binder, B. M. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2012.02.001 · Cited by 442 · see citing works

Cytokinin‐mediated source/sink modifications improve drought tolerance and increase grain yield in rice under water‐stress

Peleg, Z., Reguera, M., Tumimbang-Raiz, E., Walia, H., & Blumwald, E. (2011) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2010.00584.x · Cited by 439 · see citing works

Brassinosteroid enhanced the level of antioxidants under cadmium stress in Brassica juncea

Hayat, S., Ali, B., Hasan, S. A., & Ahmad, A. (2006) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2006.06.002 · Cited by 390 · see citing works

Brassinosteroids Interact with Auxin to Promote Lateral Root Development in Arabidopsis

Bao, F., Shen, J., Brady, S. R., Muday, G. K., Asami, T., & Yang, Z. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.036897 · Cited by 382 · see citing works

Arabidopsis WRKY46, WRKY54 and WRKY70 Transcription Factors Are Involved in Brassinosteroid-Regulated Plant Growth and Drought Response

Chen, J., Nolan, T. M., Ye, H., Zhang, M., Tong, H., Xin, P., Chu, J., Chu, C., Li, Z., & Yin, Y. (2017) · The Plant Cell · doi:10.1105/tpc.17.00364 · Cited by 380 · see citing works

Effect of 24-epibrassinolide on growth, yield, antioxidant system and cadmium content of bean (Phaseolus vulgaris L.) plants under salinity and cadmium stress

Rady, M. M. (2011) · Scientia Horticulturae · doi:10.1016/j.scienta.2011.03.035 · Cited by 378 · see citing works

Salinity stress induced alterations in antioxidant metabolism and nitrogen assimilation in wheat ( Triticum aestivum L) as influenced by potassium supplementation

Ahanger, M. A., & Agarwal, R. M. (2017) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2017.04.017 · Cited by 372 · see citing works

Jasmonates act with salicylic acid to confer basal thermotolerance in Arabidopsis thaliana

Clarke, S., Cristescu, S. M., Miersch, O., Harren, F. J. M., Wasternack, C. H., & Mur, L. A. J. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2008.02735.x · Cited by 368 · see citing works

Auxin: a master regulator in plant root development

Saini, S., Sharma, I., Kaur, N., & Pati, P. K. (2013) · Plant Cell Reports · doi:10.1007/s00299-013-1430-5 · Cited by 357 · see citing works

Alleviation of Cadmium Toxicity in Brassica juncea L. (Czern. & Coss.) by Calcium Application Involves Various Physiological and Biochemical Strategies

Ahmad, P., Sarwat, M., Bhat, N. A., Wani, M. R., Kazi, A. G., & Tran, L. P. (2015) · PLoS ONE · doi:10.1371/journal.pone.0114571 · Cited by 338 · see citing works

Nitrogen availability regulates proline and ethylene production and alleviates salinity stress in mustard (Brassica juncea)

Iqbal, N., Umar, S., & Khan, N. A. (2015) · Journal of Plant Physiology · doi:10.1016/j.jplph.2015.02.006 · Cited by 320 · see citing works

BRASSINOSTEROID INSENSITIVE2 Interacts with ABSCISIC ACID INSENSITIVE5 to Mediate the Antagonism of Brassinosteroids to Abscisic Acid during Seed Germination inArabidopsis

Hu, Y., & Yu, D. (2014) · The Plant Cell · doi:10.1105/tpc.114.130849 · Cited by 312 · see citing works

The Mechanisms of Brassinosteroids' Action: From Signal Transduction to Plant Development

Yang, C.-J., Zhang, C., Lu, Y., Jin, J., & Wang, X. (2011) · Molecular Plant · doi:10.1093/mp/ssr020 · Cited by 311 · see citing works

Cadmium-induced oxidative damage in mustard [Brassica juncea (L.) Czern. & Coss.] plants can be alleviated by salicylic acid

Ahmad, P., Nabi, G., & Ashraf, M. (2010) · South African Journal of Botany · doi:10.1016/j.sajb.2010.05.003 · Cited by 310 · see citing works

H2O2 mediates the crosstalk of brassinosteroid and abscisic acid in tomato responses to heat and oxidative stresses

Zhou, J., Wang, J., Li, X., Xia, X., Zhou, Y., Shi, K., Chen, Z., & Yu, J. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru217 · Cited by 306 · see citing works

A role for brassinosteroids in the amelioration of aluminium stress through antioxidant system in mung bean (Vigna radiata L. Wilczek)

Ali, B., Hasan, S. A., Hayat, S., Hayat, Q., Yadav, S., Fariduddin, Q., & Ahmad, A. (2007) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2007.07.014 · Cited by 303 · see citing works

Brassinosteroids Alleviate Heat-Induced Inhibition of Photosynthesis by Increasing Carboxylation Efficiency and Enhancing Antioxidant Systems in Lycopersicon esculentum

Ogweno, J. O., Song, X., Shi, K., Hu, W. H., Mao, W. H., Zhou, Y. H., Yu, J. Q., & Nogués, S. (2007) · Journal of Plant Growth Regulation · doi:10.1007/s00344-007-9030-7 · Cited by 300 · see citing works

An Interaction Between BZR1 and DELLAs Mediates Direct Signaling Crosstalk Between Brassinosteroids and Gibberellins in Arabidopsis

Li, Q., Wang, C., Jiang, L., Li, S., Sun, S. S. M., & He, J. (2012) · Science Signaling · doi:10.1126/scisignal.2002908 · Cited by 300 · see citing works

BRX mediates feedback between brassinosteroid levels and auxin signalling in root growth

Mouchel, C. F., Sanguinet, K. A., & Hardtke, C. S. (2006) · Nature · doi:10.1038/nature05130 · Cited by 296 · see citing works

Spatiotemporal Brassinosteroid Signaling and Antagonism with Auxin Pattern Stem Cell Dynamics in Arabidopsis Roots

Chaiwanon, J., & Wang, Z. (2015) · Current Biology · doi:10.1016/j.cub.2015.02.046 · Cited by 294 · see citing works

The primary signaling outputs of brassinosteroids are regulated by abscisic acid signaling

Zhang, S., Cai, Z., & Wang, X. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900349106 · Cited by 284 · see citing works

RD26 mediates crosstalk between drought and brassinosteroid signalling pathways

Ye, H., Liu, S., Tang, B., Chen, J., Xie, Z., Nolan, T. M., Jiang, H., Guo, H., Lin, H.-Y., Li, L., et al. (2017) · Nature Communications · doi:10.1038/ncomms14573 · Cited by 272 · see citing works

Silicon (Si) Supplementation Alleviates NaCl Toxicity in Mung Bean [Vigna radiata (L.) Wilczek] Through the Modifications of Physio-biochemical Attributes and Key Antioxidant Enzymes

Ahmad, P., Ahanger, M. A., Alam, P., Alyemeni, M. N., Wijaya, L., Ali, S., & Ashraf, M. (2018) · Journal of Plant Growth Regulation · doi:10.1007/s00344-018-9810-2 · Cited by 269 · see citing works

Brassinosteroids Antagonize Gibberellin- and Salicylate-Mediated Root Immunity in Rice

Vleesschauwer, D. D., Buyten, E. V., Satoh, K., Balidion, J., Mauleon, R., Choi, I., VeraCruz, C. M., Kikuchi, S., & Höfte, M. (2012) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.193672 · Cited by 257 · see citing works

Calcium and Potassium Supplementation Enhanced Growth, Osmolyte Secondary Metabolite Production, and Enzymatic Antioxidant Machinery in Cadmium-Exposed Chickpea (Cicer arietinum L.)

Ahmad, P., Latef, A. A. H. A., Allah, E. F. A., Hashem, A., Sarwat, M., Anjum, N. A., & Gücel, S. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00513 · Cited by 252 · see citing works

Brassinosteroid Homeostasis in Arabidopsis Is Ensured by Feedback Expressions of Multiple Genes Involved in Its Metabolism

Tanaka, K., Asami, T., Yoshida, S., Nakamura, Y. K., Matsuo, T., & Okamoto, S. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.058040 · Cited by 247 · see citing works

Overexpression of the brassinosteroid biosynthetic gene DWF4 in Brassica napus simultaneously increases seed yield and stress tolerance

Sahni, S., Prasad, B. D., Liu, Q., Grbić, V., Sharpe, A. G., Singh, S. P., & Krishna, P. (2016) · Scientific Reports · doi:10.1038/srep28298 · Cited by 244 · see citing works

Treatment with 24-epibrassinolide, a brassinosteroid, increases the basic thermotolerance of Brassica napus and tomato seedlings

Dhaubhadel, S., Chaudhary, S., Dobinson, K. F., & Krishna, P. (1999) · Plant Molecular Biology · doi:10.1023/a:1006283015582 · Cited by 239 · see citing works

Brassinosteroids Are Master Regulators of Gibberellin Biosynthesis in Arabidopsis

Unterholzner, S. J., Rozhon, W., Papacek, M., Ciomas, J., Lange, T., Kugler, K., Mayer, K., Sieberer, T., & Poppenberger, B. (2015) · The Plant Cell · doi:10.1105/tpc.15.00433 · Cited by 239 · see citing works

The auxin response factor, OsARF 19, controls rice leaf angles through positively regulating OsGH 3‐5 and OsBRI 1

Zhang, S., Wang, S., Xu, Y., Yu, C., Shen, C., Qian, Q., Geisler, M. M., Jiang, D. A., & Qi, Y. (2014) · Plant Cell & Environment · doi:10.1111/pce.12397 · Cited by 238 · see citing works

Brassinosteroid functions to protect the translational machinery and heat‐shock protein synthesis following thermal stress

Dhaubhadel, S., Browning, K. S., Gallie, D., & Krishna, P. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01257.x · Cited by 233 · see citing works

Potassium up-regulates antioxidant metabolism and alleviates growth inhibition under water and osmotic stress in wheat (Triticum aestivum L)

Ahanger, M. A., & Agarwal, R. M. (2016) · PROTOPLASMA · doi:10.1007/s00709-016-1037-0 · Cited by 232 · see citing works

Exogenous application of brassinosteroid offers tolerance to salinity by altering stress responses in rice variety Pusa Basmati-1

Sharma, I., Ching, E., Saini, S., Bhardwaj, R., & Pati, P. K. (2013) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2013.04.013 · Cited by 230 · see citing works

28-Homobrassinolide protects chickpea (Cicer arietinum) from cadmium toxicity by stimulating antioxidants

Hasan, S. A., Hayat, S., Ali, B., & Ahmad, A. (2007) · Environmental Pollution · doi:10.1016/j.envpol.2007.03.006 · Cited by 227 · see citing works

Effect of 24-epibrassinolide on ROS content, antioxidant system, lipid peroxidation and Ni uptake in Solanum nigrum L. under Ni stress

Soares, C., de Sousa, A., Pinto, A., Azenha, M., Teixeira, J., Azevedo, R. A., & Fidalgo, F. (2015) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2015.09.010 · Cited by 225 · see citing works

Effect of 28-homobrassinolide on photosynthesis, fluorescence and antioxidant system in the presence or absence of salinity and temperature in Vigna radiata

Hayat, S., Hasan, S. A., Yusuf, M., Hayat, Q., & Ahmad, A. (2010) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2010.03.004 · Cited by 225 · see citing works

Plant steroidal hormone epibrassinolide regulate – Heavy metal stress tolerance in Oryza sativa L. by modulating antioxidant defense expression

Sharma, P., Kumar, A., & Bhardwaj, R. (2015) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2015.08.005 · Cited by 221 · see citing works

Salicylic acid and methyl jasmonate improve chilling tolerance in cold-stored lemon fruit (Citrus limon)

Siboza, X. I., Bertling, I., & Odindo, A. O. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.05.012 · Cited by 212 · see citing works

Brassinosteroids protect photosynthetic machinery against the cadmium induced oxidative stress in two tomato cultivars

Hasan, S. A., Hayat, S., & Ahmad, A. (2011) · Chemosphere · doi:10.1016/j.chemosphere.2011.04.047 · Cited by 209 · see citing works

Ethylene Modulates Flavonoid Accumulation and Gravitropic Responses in Roots of Arabidopsis

Buer, C. S., Sukumar, P., & Muday, G. K. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.075671 · Cited by 208 · see citing works

Involvement of Auxin and Brassinosteroid in the Regulation of Petiole Elongation under the Shade

Kozuka, T., Kobayashi, J., Horiguchi, G., Demura, T., Sakakibara, H., Tsukaya, H., & Nagatani, A. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.156802 · Cited by 202 · see citing works

Versatile roles of brassinosteroid in plants in the context of its homoeostasis, signaling and crosstalks

Saini, S., Sharma, I., & Pati, P. K. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00950 · Cited by 193 · see citing works

Plant responses to environmental stresses—from gene to biotechnology

Ahanger, M. A., Akram, N. A., Ashraf, M., Alyemeni, M. N., Wijaya, L., & Ahmad, P. (2017) · AoB Plants · doi:10.1093/aobpla/plx025 · Cited by 192 · see citing works

28-Homobrassinolide ameliorates the saline stress in chickpea (Cicer arietinum L.)

Ali, B., Hayat, S., & Ahmad, A. (2006) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2005.12.002 · Cited by 191 · see citing works

Seed priming with brassinolide improves lucerne (Medicago sativa L.) seed germination and seedling growth in relation to physiological changes under salinity stress

Zhang, S., Hu, J., Zhang, Y., Xie, X., & Knapp, A. D. (2007) · Australian Journal of Agricultural Research · doi:10.1071/ar06253 · Cited by 191 · see citing works

Drought Tolerance: Role of Organic Osmolytes, Growth Regulators, and Mineral Nutrients

Ahanger, M. A., Tyagi, S. R., Wani, M. R., & Ahmad, P. (2013) · Springer eBooks · doi:10.1007/978-1-4614-8591-9_2 · Cited by 180 · see citing works

Brassinosteroid-regulated GSK3/Shaggy-like Kinases Phosphorylate Mitogen-activated Protein (MAP) Kinase Kinases, Which Control Stomata Development in Arabidopsis thaliana

Khan, M., Rozhon, W., Bigeard, J., Pflieger, D., Husar, S., Andrea Pitzschke, A., Teige, M., Jonak, C., Heribert Hirt, A., & Poppenberger, B. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.384453 · Cited by 176 · see citing works

24-Epibrassinolide protects against the stress generated by salinity and nickel in Brassica juncea

Ali, B., Hayat, S., Fariduddin, Q., & Ahmad, A. (2008) · Chemosphere · doi:10.1016/j.chemosphere.2008.04.012 · Cited by 176 · see citing works

Plant growth under drought stress

Ahanger, M. A., Moradtalab, N., Allah, E. F. A., Ahmad, P., & Hajiboland, R. (2016) · doi:10.1002/9781119054450.ch37 · Cited by 174 · see citing works

Zygotic Genome Activation Occurs Shortly after Fertilization in Maize

Chen, J., Strieder, N., Krohn, N. G., Cyprys, P., Sprunck, S., Engelmann, J. C., & Dresselhaus, T. (2017) · The Plant Cell · doi:10.1105/tpc.17.00099 · Cited by 174 · see citing works

28-homobrassinolide regulates antioxidant enzyme activities and gene expression in response to salt- and temperature-induced oxidative stress in Brassica juncea

Kaur, H., Sirhindi, G., Bhardwaj, R., Alyemeni, M. N., Siddique, K. H. M., & Ahmad, P. (2018) · Scientific Reports · doi:10.1038/s41598-018-27032-w · Cited by 168 · see citing works

BAK1 is required for the attenuation of ethylene-inducing xylanase (Eix)-induced defense responses by the decoy receptor LeEix1

Bar, M., Sharfman, M., Ron, M., & Avni, A. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04282.x · Cited by 167 · see citing works

Auxin stimulates DWARF4 expression and brassinosteroid biosynthesis in Arabidopsis

Chung, Y., Maharjan, P. M., Lee, O., Fujioka, S., Jang, S., Kim, B., Takatsuto, S., Tsujimoto, M., Kim, H., Cho, S., et al. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04513.x · Cited by 166 · see citing works

Ethylene production is associated with alleviation of cadmium-induced oxidative stress by sulfur in mustard types differing in ethylene sensitivity

Asgher, M., Khan, N. A., Khan, M. I. R., Fatma, M., & Masood, A. (2014) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2014.04.017 · Cited by 164 · see citing works

Brassinosteroids interact negatively with jasmonates in the formation of anti-herbivory traits in tomato

Campos, M. L., de Almeida, M., Rossi, M. L., Martinelli, A. P., Litholdo, C. G., Figueira, A., Rampelotti-Ferreira, F. T., Vendramim, J. D., Benedito, V. A., & Peres, L. E. P. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp270 · Cited by 157 · see citing works

Brassinosteroid Ameliorates Zinc Oxide Nanoparticles-Induced Oxidative Stress by Improving Antioxidant Potential and Redox Homeostasis in Tomato Seedling

Li, M., Ahammed, G. J., Li, C., Bao, X. Q., Yu, J., Huang, C., Yin, H., & Zhou, J. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00615 · Cited by 155 · see citing works

The F-box Protein KIB1 Mediates Brassinosteroid-Induced Inactivation and Degradation of GSK3-like Kinases in Arabidopsis

Zhu, J.-Y., Li, Y., Cao, D.-M., Yang, H., Oh, E., Bi, Y., Zhu, S., & Wang, Z. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.05.012 · Cited by 152 · see citing works

Application of brassinosteroids to rice seeds (Oryza sativa L.) reduced the impact of salt stress on growth, prevented photosynthetic pigment loss and increased nitrate reductase activity

Anuradha, S. M. J., & Rao, S. S. R. (2003) · Plant Growth Regulation · doi:10.1023/a:1023080720374 · Cited by 150 · see citing works

Brassinosteroid effects on some physical and biochemical properties and secondary metabolite accumulation in peppermint (Mentha piperita L.) under salt stress

Çoban, Ö., & Baydar, N. G. (2016) · Industrial Crops and Products · doi:10.1016/j.indcrop.2016.03.049 · Cited by 149 · see citing works

Physiological and Molecular Effects of 24-Epibrassinolide, a Brassinosteroid on Thermotolerance of Tomato

Singh, I., & Shono, M. (2005) · Plant Growth Regulation · doi:10.1007/s10725-005-3252-0 · Cited by 148 · see citing works

Ethylene and hydrogen peroxide are involved in brassinosteroid-induced salt tolerance in tomato

Zhu, T., Deng, X., Zhou, X., Zhu, L., Zou, L., Li, P., Zhang, D., & Lin, H. (2016) · Scientific Reports · doi:10.1038/srep35392 · Cited by 148 · see citing works

24-Epibrassinolide regulates photosynthesis, antioxidant enzyme activities and proline content of Cucumis sativus under salt and/or copper stress

Fariduddin, Q., Khalil, R., Mir, B. A., Yusuf, M., & Ahmad, A. (2013) · Environmental Monitoring and Assessment · doi:10.1007/s10661-013-3139-x · Cited by 147 · see citing works

BRL1, a leucine‐rich repeat receptor‐like protein kinase, is functionally redundant with BRI1 in regulating Arabidopsis brassinosteroid signaling

Zhou, A., Wang, H., Walker, J. C., & Li, J. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02214.x · Cited by 145 · see citing works

Brassinolide alleviates salt stress and increases antioxidant activity of cowpea plants (Vigna sinensis)

El-Mashad, A. A. A., & Mohamed, H. I. (2011) · PROTOPLASMA · doi:10.1007/s00709-011-0300-7 · Cited by 142 · see citing works

Foliar spray of brassinosteroid enhances yield and quality of Solanum lycopersicum under cadmium stress

Hayat, S., Alyemeni, M. N., & Hasan, S. A. (2012) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2012.03.005 · Cited by 142 · see citing works

Alleviation of drought-induced oxidative stress in maize (Zea mays L.) plants by dual application of 24-epibrassinolide and spermine

Talaat, N. B., Shawky, B. T., & Ibrahim, A. S. (2015) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2015.01.006 · Cited by 134 · see citing works

Brassinosteroids accelerate recovery of photosynthetic apparatus from cold stress by balancing the electron partitioning, carboxylation and redox homeostasis in cucumber

Jiang, Y., Huang, L., Cheng, F., Zhou, Y., Xia, X., Mao, W., Shi, K., & Yu, J. (2012) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2012.01696.x · Cited by 132 · see citing works

Potassium induces positive changes in nitrogen metabolism and antioxidant system of oat (Avena sativaL cultivar Kent)

Ahanger, M. A., Agarwal, R. M., Tomar, N. S., & Shrivastava, M. (2015) · Journal of Plant Interactions · doi:10.1080/17429145.2015.1056260 · Cited by 131 · see citing works

Effect of 28-homobrassinolide on the drought stress-induced changes in photosynthesis and antioxidant system of Brassica juncea L.

Fariduddin, Q., Khanam, S., Hasan, S. A., Ali, B., Hayat, S., & Ahmad, A. (2009) · Acta Physiologiae Plantarum · doi:10.1007/s11738-009-0302-7 · Cited by 128 · see citing works

Brassinosteroid Enhances Jasmonate‐Induced Anthocyanin Accumulation in Arabidopsis Seedlings

Peng, Z., Han, C., Yuan, L., Zhang, K., Huang, H., & Ren, C. (2011) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2011.01042.x · Cited by 126 · see citing works

Modification of Osmolytes and Antioxidant Enzymes by 24-Epibrassinolide in Chickpea Seedlings Under Mercury (Hg) Toxicity

Ahmad, P., Ahanger, M. A., Egamberdieva, D., Alam, P., Alyemeni, M. N., & Ashraf, M. (2017) · Journal of Plant Growth Regulation · doi:10.1007/s00344-017-9730-6 · Cited by 125 · see citing works

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 · see citing works

Brassinosteroids alleviate chilling-induced oxidative damage by enhancing antioxidant defense system in suspension cultured cells of Chorispora bungeana

Liu, Y., Zhao, Z., Si, J., Di, C., Han, J., & An, L. (2009) · Plant Growth Regulation · doi:10.1007/s10725-009-9405-9 · Cited by 123 · see citing works

Involvement of Auxin and Brassinosteroid in Dwarfism of Autotetraploid Apple (Malus × domestica)

Ma, Y., Xue, H., Zhang, L., Zhang, F., Ou, C., Wang, F., & Zhang, Z. (2016) · Scientific Reports · doi:10.1038/srep26719 · Cited by 123 · see citing works

The effect of brassinosteroids on radish (Raphanus sativus L.) seedlings growing under cadmium stress

Anuradha, S. M. J., & Rao, S. (2007) · Plant Soil and Environment · doi:10.17221/2307-pse · Cited by 123 · see citing works

Interactive effect of brassinosteroids and cytokinins on growth, chlorophyll, monosaccharide and protein content in the green alga Chlorella vulgaris (Trebouxiophyceae)

Bajguz, A., & Piotrowska‐Niczyporuk, A. (2014) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2014.04.009 · Cited by 119 · see citing works

NONEXPRESSOR OF PATHOGENESIS‐RELATED PROTEINS1 (NPR1) and some NPR1‐related proteins are sensitive to salicylic acid

Maier, F., ZWICKER, S., Hückelhoven, A. G., MEISSNER, M., FUNK, J., Pfitzner, A. J. P., & Pfitzner, U. M. (2010) · Molecular Plant Pathology · doi:10.1111/j.1364-3703.2010.00653.x · Cited by 116 · see citing works

28-homobrassinolide improves growth and photosynthesis in Cucumis sativus L. through an enhanced antioxidant system in the presence of chilling stress

Fariduddin, Q., Yusuf, M., Chalkoo, S., Hayat, S., & Ahmad, A. (2011) · Photosynthetica · doi:10.1007/s11099-011-0022-2 · Cited by 115 · see citing works

Synergistic effect of auxins and brassinosteroids on the growth and regulation of metabolite content in the green alga Chlorella vulgaris (Trebouxiophyceae)

Bajguz, A., & Piotrowska‐Niczyporuk, A. (2013) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2013.08.003 · Cited by 115 · see citing works

A Leaky Mutation in DWARF4 Reveals an Antagonistic Role of Brassinosteroid in the Inhibition of Root Growth by Jasmonate in Arabidopsis

Ren, C., Han, C., Peng, W., Huang, Y., Peng, Z., Xiong, X., Zhu, Q., Gao, B., & Xie, D. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.140202 · Cited by 115 · see citing works

Impact of postharvest brassinosteroids treatment on PAL activity in tomato fruit in response to chilling stress

Aghdam, M. S., Asghari, M., Farmani, B., Mohayeji, M., & Moradbeygi, H. (2012) · Scientia Horticulturae · doi:10.1016/j.scienta.2012.07.008 · Cited by 114 · see citing works

Effect of brassinolide on chilling injury of green bell pepper in storage

Wang, Q., Ding, T., Gao, L., Pang, J., & Yang, N. (2012) · Scientia Horticulturae · doi:10.1016/j.scienta.2012.07.018 · Cited by 112 · see citing works

24-Epibrassinolide modulates growth, nodulation, antioxidant system, and osmolyte in tolerant and sensitive varieties of Vigna radiata under different levels of nickel: A shotgun approach

Yusuf, M., Fariduddin, Q., & Ahmad, A. (2012) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2012.05.004 · Cited by 112 · see citing works

Gene expression and functional analyses in brassinosteroid‐mediated stress tolerance

Divi, U. K., Rahman, T., & Krishna, P. (2015) · Plant Biotechnology Journal · doi:10.1111/pbi.12396 · Cited by 111 · see citing works

Effects of 24-epibrassinolide on antioxidation defense and osmoregulation systems of young grapevines (V. vinifera L.) under chilling stress

Xi, Z., Wang, Z., Fang, Y., Hu, Z., Hu, Y., Deng, M., & Zhang, Z. (2013) · Plant Growth Regulation · doi:10.1007/s10725-013-9809-4 · Cited by 108 · see citing works

Effect of 24-epibrassinolide on drought stress-induced changes in Chorispora bungeana

Li, Y. H., Liu, Y. J., Xu, X., Jin, M., An, L., & Zhang, H. (2012) · Biologia Plantarum · doi:10.1007/s10535-012-0041-2 · Cited by 108 · see citing works

The antagonistic regulation of abscisic acid‐inhibited root growth by brassinosteroids is partially mediated via direct suppression of ABSCISIC ACID INSENSITIVE 5 expression by BRASSINAZOLE RESISTANT 1

Yang, X., Bai, Y., Shang, J., Xin, R., & Tang, W. (2016) · Plant Cell & Environment · doi:10.1111/pce.12763 · Cited by 108 · see citing works

Receptor-like kinase complexes in plant innate immunity

Greeff, C., Roux, M. E., Mundy, J., & Petersen, M. (2012) · Frontiers in Plant Science · doi:10.3389/fpls.2012.00209 · Cited by 107 · see citing works

Foliar application of brassinosteroids alleviates adverse effects of zinc toxicity in radish (Raphanus sativus L.) plants

Ramakrishna, B., & Rao, S. S. R. (2014) · PROTOPLASMA · doi:10.1007/s00709-014-0714-0 · Cited by 105 · see citing works

Brassinosteroids regulate pectin methylesterase activity and AtPME41 expression in Arabidopsis under chilling stress

Qu, T., Liu, R., Wang, W., An, L., Chen, T., Liu, G., & Zhao, Z. (2011) · Cryobiology · doi:10.1016/j.cryobiol.2011.07.003 · Cited by 105 · see citing works

24-Epibrassinosteroid alleviate drought-induced inhibition of photosynthesis in Capsicum annuum

Hu, W., Yan, X., Xiao, Y.-A., Zeng, J., Qi, H.-J., & Ogweno, J. O. (2012) · Scientia Horticulturae · doi:10.1016/j.scienta.2012.11.012 · Cited by 105 · see citing works

14-3-3 Proteins fine-tune plant nutrient metabolism

Shin, R., Jez, J. M., Basra, A. S., Zhang, B., & Schachtman, D. P. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.11.025 · Cited by 102 · see citing works

Effects of Brassmosteroids on Growth, Nodulation, Phytohormone Content and Nitrogenase Activity in French Bean Under Water Stress

Upreti, K. K., & Murti, G. S. R. (2004) · Biologia Plantarum · doi:10.1023/b:biop.0000041094.13342.1b · Cited by 99 · see citing works

Epibrassinolide ameliorates Cr (VI) stress via influencing the levels of indole-3-acetic acid, abscisic acid, polyamines and antioxidant system of radish seedlings

Pal, S., Kanwar, M. K., Bhardwaj, R., Gupta, B. D., & Gupta, R. K. (2011) · Chemosphere · doi:10.1016/j.chemosphere.2011.03.056 · Cited by 96 · see citing works

Role of brassinosteroid signaling in modulating Tobacco mosaic virus resistance in Nicotiana benthamiana

Deng, X., Zhu, T., Peng, X., Xi, D., Guo, H., Yin, Y., Zhang, D., & Lin, H. (2016) · Scientific Reports · doi:10.1038/srep20579 · Cited by 95 · see citing works

Enhancement of Chilling Stress Tolerance of Tomato Fruit by Postharvest Brassinolide Treatment

Aghdam, M. S., & Mohammadkhani, N. (2013) · Food and Bioprocess Technology · doi:10.1007/s11947-013-1165-x · Cited by 93 · see citing works

Effects of brassinosteroid and brassinosteroid mimic on photosynthetic efficiency and rice yield under heat stress

Thussagunpanit, J., Jutamanee, K., Sonjaroon, W., Kaveeta, L., Chai-arree, W., Pankean, P., & Suksamrarn, A. (2015) · Photosynthetica · doi:10.1007/s11099-015-0106-5 · Cited by 91 · see citing works

Kinetics of nitrate uptake by Citrus seedlings and inhibitory effects of salinity

Cerezo, M., García‐Agustín, P., Serna, M. D., & Primo‐Millo, E. (1997) · Plant Science · doi:10.1016/s0168-9452(97)00095-2 · Cited by 86 · see citing works

Role of 24‐Epibrassinolide in Wheat Production: Physiological Effects and Uptake

Janeczko, A., Biesaga‐Kościelniak, J., Oklešťková, J., Filek, M., Dziurka, M., Szarek‐Łukaszewska, G., & Kościelniak, J. (2010) · Journal of Agronomy and Crop Science · doi:10.1111/j.1439-037x.2009.00413.x · Cited by 84 · see citing works

Barley Brassinosteroid Mutants Provide an Insight into Phytohormonal Homeostasis in Plant Reaction to Drought Stress

Gruszka, D., Janeczko, A., Dziurka, M., Pociecha, E., Oklešťková, J., & Szarejko, I. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01824 · Cited by 82 · see citing works

Zinc application mitigates the adverse effects of NaCl stress on mustard [Brassica juncea(L.) Czern & Coss] through modulating compatible organic solutes, antioxidant enzymes, and flavonoid content

Ahmad, P., Ahanger, M. A., Alyemeni, M. N., Wijaya, L., Egamberdieva, D., Bhardwaj, R., & Ashraf, M. (2017) · Journal of Plant Interactions · doi:10.1080/17429145.2017.1385867 · Cited by 82 · see citing works

Brassinosteroids and lead as stimulators of phytochelatins synthesis in Chlorella vulgaris

Bajguz, A. (2002) · Journal of Plant Physiology · doi:10.1078/0176-1617-00654 · Cited by 81 · see citing works

Brassinosteroids alleviate high-temperature injury in Ficus concinna seedlings via maintaining higher antioxidant defence and glyoxalase systems

Jin, S. H., Li, X. Q., Wang, G. G., & Zhu, X. T. (2015) · AoB Plants · doi:10.1093/aobpla/plv009 · Cited by 81 · see citing works

Dual Application of 24-Epibrassinolide and Spermine Confers Drought Stress Tolerance in Maize (Zea mays L.) by Modulating Polyamine and Protein Metabolism

Talaat, N. B., & Shawky, B. T. (2016) · Journal of Plant Growth Regulation · doi:10.1007/s00344-015-9557-y · Cited by 81 · see citing works

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 · see citing works

Chill-induced inhibition of photosynthesis was alleviated by 24-epibrassinolide pretreatment in cucumber during chilling and subsequent recovery

Hu, W., Wu, Y., Zeng, J. Z., He, L., & Zeng, Q. M. (2010) · Photosynthetica · doi:10.1007/s11099-010-0071-y · Cited by 75 · see citing works

Combining Enhanced Root and Shoot Growth Reveals Cross Talk between Pathways That Control Plant Organ Size in Arabidopsis

Vercruyssen, L., González, N., Werner, T., Schmülling, T., & Inzé, D. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.167049 · Cited by 74 · see citing works

Transcriptome Response Mediated by Cold Stress in Lotus japonicus

Calzadilla, P. I., Maiale, S. J., RUIZ, O. A., & Escaray, F. J. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00374 · Cited by 73 · see citing works

A History of Brassinosteroid Research from 1970 through 2005: Thirty-Five Years of Phytochemistry, Physiology, Genes, and Mutants

Clouse, S. D. (2015) · Journal of Plant Growth Regulation · doi:10.1007/s00344-015-9540-7 · Cited by 72 · see citing works

Overexpression of WsSGTL1 Gene of Withania somnifera Enhances Salt Tolerance, Heat Tolerance and Cold Acclimation Ability in Transgenic Arabidopsis Plants

Mishra, M. K., Chaturvedi, P., Singh, R., Singh, G., Sharma, L. K., Pandey, V., Kumari, N., & Misra, P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063064 · Cited by 72 · see citing works

Effect of short-term cold stress on oxidative damage and transcript accumulation of defense-related genes in chickpea seedlings

Kazemi-Shahandashti, S.-S., Maali-Amiri, R., Zeinali, H., Khazaei, M., Talei, A., & Ramezanpour, S. S. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.03.020 · Cited by 71 · see citing works

Physiological and biochemical effect of 24-epibrassinoslide on cold tolerance in maize seedlings

Singh, I., Kumar, U., Singh, S. K., Gupta, C., Singh, M., & Kushwaha, S. R. (2012) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-012-0122-x · Cited by 70 · see citing works

Hormonal crosstalk for root development: a combined experimental and modeling perspective

Liu, J., Rowe, J. H., & Lindsey, K. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00116 · Cited by 69 · see citing works

Effects of brassinosteroid infiltration prior to cold treatment on ion leakage and pigment contents in rape leaves

Janeczko, A., Gullner, G., Skoczowski, A., Dubert, F., & Barna, B. (2007) · Biologia Plantarum · doi:10.1007/s10535-007-0072-2 · Cited by 67 · see citing works

24-epibrassinolide and/or putrescine trigger physiological and biochemical responses for the salt stress mitigation in Cucumis sativus L.

Fariduddin, Q., Mir, B. A., Yusuf, M., & Ahmad, A. (2014) · Photosynthetica · doi:10.1007/s11099-014-0052-7 · Cited by 67 · see citing works

INFLUENCE OF EXOGENOUS APPLICATION OF BRASSINOSTEROID ON GROWTH AND MINERAL NUTRIENTS OF WHEAT (TRITICUM AESTIVUM L.) UNDER SALINE CONDITIONS

Shahbaz, M., & Ashraf, M. (2007) · Cited by 66 · see citing works

Mechanisms of signaling crosstalk between brassinosteroids and gibberellins

Li, Q., & He, J. (2013) · Plant Signaling & Behavior · doi:10.4161/psb.24686 · Cited by 65 · see citing works

Microarray analysis of brassinosteroids- and gibberellin-regulated gene expression in rice seedlings

Yang, G., Jan, A., Shen, S., Yazaki, J., Ishikawa, M., Shimatani, Z., Kishimoto, N., Kikuchi, S., Matsumoto, H., & Komatsu, S. (2004) · Molecular Genetics and Genomics · doi:10.1007/s00438-004-0998-4 · Cited by 64 · see citing works

Structure-activity relationship of brassinosteroids and their agricultural practical usages

Liu, J., Zhang, D., Sun, X., Ding, T., Lei, B., & Zhang, C. (2017) · Steroids · doi:10.1016/j.steroids.2017.05.005 · Cited by 64 · see citing works

Heat shock response in tomato brassinosteroid mutants indicates that thermotolerance is independent of brassinosteroid homeostasis

Mazorra, L. M., Holton, N. J., Bishop, G. J., & Núñez, M. (2011) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2011.09.005 · Cited by 63 · see citing works

Brassinosteroid enhances cytokinin-induced anthocyanin biosynthesis in Arabidopsis seedlings

Yuan, L., Peng, Z., Zhi, T., Zho, Z., Liu, Y., Zhu, Q., Xiong, X., & Ren, C. (2014) · Biologia Plantarum · doi:10.1007/s10535-014-0472-z · Cited by 59 · see citing works

Brassinosteroid control of shoot gravitropism interacts with ethylene and depends on auxin signaling components

Vandenbussche, F., Callebert, P., Žádníková, P., Benková, E., & Straeten, D. V. D. (2012) · American Journal of Botany · doi:10.3732/ajb.1200264 · Cited by 54 · see citing works

Biochemical aspects of cadmium in plants.

Ernst, W. H. O. (1980) · Cited by 53 · see citing works

Role of foliar application of 24-epibrassinolide in response of peanut seedlings to iron deficiency

Song, Y. L., Dong, Y., Tian, X., Kong, J., Bai, X., Xu, L., & He, Z. L. (2016) · Biologia Plantarum · doi:10.1007/s10535-016-0596-4 · Cited by 49 · see citing works

24-epibrassinolide induced antioxidative defense system of Brassica juncea L. under Zn metal stress

Arora, P., Bhardwaj, R., & Kanwar, M. K. (2010) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-010-0031-9 · Cited by 48 · see citing works

Brassinosteroid signaling: from receptor kinases to transcription factors

Li, J. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.07.009 · Cited by 46 · see citing works

Cytokinin oxidase is involved in the regulation of cytokinin content by 24-epibrassinolide in wheat seedlings

Адикович, Ю. Р., Мэлсович, А. А., Безрукова, М. В., Vysotskaya, L. B., Khripach, V. A., & Шакирова, Ф. М. (2012) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2012.03.004 · Cited by 46 · see citing works

Brassinosteroid-mediated evaluation of antioxidant system and nitrogen metabolism in two contrasting cultivars of Vigna radiata under different levels of nickel

Yusuf, M., Fariduddin, Q., Ahmad, I., & Ahmad, A. (2014) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-014-0259-x · Cited by 45 · see citing works

Transcriptome analysis reveals the regulation of brassinosteroids on petal growth in Gerbera hybrida

Huang, G., Han, M., Yao, W., & Wang, Y. (2017) · PeerJ · doi:10.7717/peerj.3382 · Cited by 45 · see citing works

Homeostasis of Brassinosteroids Regulated by DRL1, a Putative Acyltransferase in Arabidopsis

Zhu, W., Wang, H., Fujioka, S., Zhou, T., Tian, H., Tian, W., & Wang, X. (2012) · Molecular Plant · doi:10.1093/mp/sss144 · Cited by 43 · see citing works

Protective Roles of Brassinolide on Rice Seedlings under High Temperature Stress

Yun-ying, C. A. O., & Hua, Z. H. A. O. (2008) · Rice Science · doi:10.1016/s1672-6308(08)60021-9 · Cited by 41 · see citing works

Photoinhibition-induced reduction in photosynthesis is alleviated by abscisic acid, cytokinin and brassinosteroid in detached tomato leaves

Ogweno, J. O., Hu, W. H., Song, X., Shi, K., Mao, W. H., Zhou, Y. H., & Yu, J. Q. (2010) · Plant Growth Regulation · doi:10.1007/s10725-009-9439-z · Cited by 41 · see citing works

Effect of 28-homobrassinolide on growth, zinc metal uptake and antioxidative enzyme activities in Brassica juncea L. seedlings

Sharma, P., Bhardwaj, R., Arora, N., & Arora, H. K. (2007) · Brazilian Journal of Plant Physiology · doi:10.1590/s1677-04202007000300004 · Cited by 41 · see citing works

Brassinosteroids signal through two receptor-like kinases

Li, J. (2003) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(03)00088-8 · Cited by 40 · see citing works

BIN2/DWF12 Antagonistically Transduces Brassinosteroid and Auxin Signals in the Roots of Arabidopsis

Maharjan, P. M., Schulz, B., & Choe, S. (2011) · Journal of Plant Biology · doi:10.1007/s12374-010-9138-3 · Cited by 40 · see citing works

Regulation of growth and antioxidant enzyme activities by 28-homobrassinolide in seedlings of Raphanus sativus L. under cadmium stress.

Sharma, I., Pati, P. K., & Bhardwaj, R. (2010) · PubMed · Cited by 40 · see citing works

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

Kommavarapu, Mahesh, M., Parshavaneni, Balaraju, Bellamkonda, Ramakrishna, Sadhu, Seeta, Ram, R., & Rao (2013) · Acta Scientiarum Naturalium Universitatis Sunyatseni · Cited by 40 · see citing works

A molecular mechanism realizing sequence-specific recognition of nucleic acids by TDP-43

Furukawa, Y., Suzuki, Y., Fukuoka, M., Nagasawa, K., Nakagome, K., Shimizu, H., Mukaiyama, A., & Akiyama, S. (2016) · Scientific Reports · doi:10.1038/srep20576 · Cited by 39 · see citing works

High Temperature Stimulates DWARF4 (DWF4) Expression to Increase Hypocotyl Elongation in Arabidopsis

Maharjan, P. M., & Choe, S. (2011) · Journal of Plant Biology · doi:10.1007/s12374-011-9183-6 · Cited by 35 · see citing works

Brassinosteroids regulate the thylakoid membrane architecture and the photosystem II function

Krumova, S., Zhiponova, M., Dankov, K. G., Velikova, V., Balashev, K., Andreeva, T. D., Russinova, E., & Taneva, S. G. (2013) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2013.07.008 · Cited by 35 · see citing works

Regulation of 2,4-epibrassinolide on mineral nutrient uptake and ion distribution in Ca(NO3)2 stressed cucumber plants

Yuan, L., Zhu, S., Shu, S., Sun, J., & Guo, S. (2015) · Journal of Plant Physiology · doi:10.1016/j.jplph.2015.06.010 · Cited by 34 · see citing works

Sequential Regulation of Gibberellin, Brassinosteroid, and Jasmonic Acid Biosynthesis Occurs in Rice Coleoptiles to Control the Transcript Levels of Anti-MicrobialThioninGenes

Kitanaga, Y., Cui, J., Hasegawa, M., Yazaki, J., Kishimoto, N., Kikuchi, S., Nakamura, H., Ichikawa, H., Asami, T., Yoshida, S., et al. (2006) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.60145 · Cited by 33 · see citing works

24-Epibrassinolide Mediated Changes in Photosynthetic pigments and Antioxidative Defence System of Radish Seedlings under Cadmium and Mercury Stress

Kapoor, D., Rattan, A., Gautam, V., Kapoor, N., & Bhardwaj, R. (2014) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 28 · see citing works

Effect of brassinosteroids on ammonium uptake via regulation of ammonium transporter and N-metabolism genes in Arabidopsis

Zhao, B., Zhu, X. F., Jung, J. H., & Xuan, Y. (2016) · Biologia Plantarum · doi:10.1007/s10535-016-0627-1 · Cited by 28 · see citing works

24-epibrassinolide regulated diminution of Cr metal toxicity in Brassica juncea L. plants

Arora, P., Bhardwaj, R., & Kanwar, M. K. (2010) · Brazilian Journal of Plant Physiology · doi:10.1590/s1677-04202010000300002 · Cited by 26 · see citing works

The effects of brassinosteroids on photosynthetic parameters in leaves of two field-grown maize inbred lines and their F1 hybrid

Kočová, M., Rothová, O., Hola, D., Kvasnica, M., & Kohout, L. (2010) · Biologia Plantarum · doi:10.1007/s10535-010-0143-7 · Cited by 25 · see citing works

Physiological and Biochemical Effects of 24-Epibrassinolide on Heat-Stress Adaptation in Maize (Zea mays L.)

Yadava, P., Kaushal, J., Gautam, A., Parmar, H., & Singh, I. (2016) · Natural Science · doi:10.4236/ns.2016.84020 · Cited by 24 · see citing works

Protective Roles of Brassinolide on Tomato Seedlings under Drought Stress

behnamnia, M. (2015) · International Journal of Agriculture and Crop Sciences (IJACS) · Cited by 22 · see citing works

Stimulation of Wheat Germ Agglutinin Gene Expression in Root Seedlings by 24-Epibrassinolide

Шакирова, Ф. М., Безрукова, М. В., Мэлсович, А. А., & Гималов, Ф. Р. (2002) · Russian Journal of Plant Physiology · doi:10.1023/a:1014805724231 · Cited by 19 · see citing works

[Salt resistance and its mechanism of cucumber under effects of exogenous chemical activators].

Song, S., Liu, W., Guo, S., Shang, Q., & Zhang, Z. (2006) · PubMed · Cited by 15 · see citing works

Brassinosteroid-independent functions of the BRI1-associated kinase BAK1/SERK3

Kemmerling, B., & Nürnberger, T. (2008) · Plant Signaling & Behavior · doi:10.4161/psb.3.2.4981 · Cited by 14 · see citing works

Mitigation of Drought Stress by 24-Epibarassinolide and 28-Homobrassinolide in Pigeon Pea Seedlings

Shahana, T., Rao, P. A., Ram, S., & Sujatha, E. (2015) · International Journal of Multidisciplinary and Current Research · Cited by 14 · see citing works

[Alleviation effects of brassinolide on cucumber seedlings under NaCl stress].

Lu, X.-M., & Yang, W. (2013) · PubMed · Cited by 12 · see citing works

Protective Roles of Brassinolide in Rice Seedlings under Heat Stress

Hua, Z. (2007) · Zhongguo shuidao kexue · Cited by 11 · see citing works

Potassium in plants: Growth regulation, signaling, and environmental stress tolerance

Johnson, R., Vishwakarma, K., Hossen, M. S., Kumar, V., Shackira, A. M., Puthur, J. T., Abdi, G., Sarraf, M., & Hasanuzzaman, M. (2022) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2022.01.001 · Cited by 550 · see citing works

Plant salt response: Perception, signaling, and tolerance

Xiao, F., & Zhou, H. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1053699 · Cited by 286 · see citing works

Crosstalk of nanoparticles and phytohormones regulate plant growth and metabolism under abiotic and biotic stress

Tripathi, D., Singh, M., & Rai, S. P. (2022) · Plant Stress · doi:10.1016/j.stress.2022.100107 · Cited by 266 · see citing works

Lead Toxicity in Cereals: Mechanistic Insight Into Toxicity, Mode of Action, and Management

Aslam, M., Aslam, A., Sheraz, M., Ali, B., Ulhassan, Z., Ullah, N., Zhou, W., & Gill, R. A. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2020.587785 · Cited by 215 · see citing works

Combined effects of brassinosteroid and kinetin mitigates salinity stress in tomato through the modulation of antioxidant and osmolyte metabolism

Ahanger, M. A., Mir, R. A., Alyemeni, M. N., & Ahmad, P. (2019) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2019.12.007 · Cited by 189 · see citing works

24-Epibrassinolide (EBR) Confers Tolerance against NaCl Stress in Soybean Plants by Up-Regulating Antioxidant System, Ascorbate-Glutathione Cycle, and Glyoxalase System

Alam, P., Albalawi, T., Altalayan, F. H., Bakht, M. A., Ahanger, M. A., Raja, V., Ashraf, M., & Ahmad, P. (2019) · Biomolecules · doi:10.3390/biom9110640 · Cited by 168 · see citing works

Comprehensive Overview of the Brassinosteroid Biosynthesis Pathways: Substrates, Products, Inhibitors, and Connections

Bajguz, A., Chmur, M., & Gruszka, D. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.01034 · Cited by 165 · see citing works

Protective mechanisms of melatonin against selenium toxicity in Brassica napus: insights into physiological traits, thiol biosynthesis and antioxidant machinery

Ulhassan, Z., Huang, Q., Gill, R. A., Ali, S., Mwamba, T. M., Ali, B., Hina, F., & Zhou, W. (2019) · BMC Plant Biology · doi:10.1186/s12870-019-2110-6 · Cited by 131 · see citing works

Combined Kinetin and Spermidine Treatments Ameliorate Growth and Photosynthetic Inhibition in Vigna angularis by Up-Regulating Antioxidant and Nitrogen Metabolism under Cadmium Stress

Ahanger, M. A., Aziz, U., Alsahli, A. A., Alyemeni, M. N., & Ahmad, P. (2020) · Biomolecules · doi:10.3390/biom10010147 · Cited by 120 · see citing works

Zinc oxide nanoparticles and 24-epibrassinolide alleviates Cu toxicity in tomato by regulating ROS scavenging, stomatal movement and photosynthesis

Faizan, M., Bhat, J. A., Noureldeen, A., Ahmad, P., & Yu, F. (2021) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2021.112293 · Cited by 119 · see citing works

Biosynthetic Pathways of Hormones in Plants

Bajguz, A., & Piotrowska‐Niczyporuk, A. (2023) · Metabolites · doi:10.3390/metabo13080884 · Cited by 119 · see citing works

Improving Performance of Salt-Grown Crops by Exogenous Application of Plant Growth Regulators

Quamruzzaman, M., Manik, S. M. N., Shabala, S. N., & Zhou, M. (2021) · Biomolecules · doi:10.3390/biom11060788 · Cited by 109 · see citing works

Plant Hormones in Phytoplasma Infected Plants

Dermastia, M. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00477 · Cited by 90 · see citing works

Distinct Morphological, Physiological, and Biochemical Responses to Light Quality in Barley Leaves and Roots

Klem, K., Gargallo‐Garriga, A., Rattanapichai, W., Oravec, M., Holub, P., Veselá, B., Sardans, J., Peñuelas, J., & Urban, O. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01026 · Cited by 86 · see citing works

Pre-sowing seed treatment with kinetin and calcium mitigates salt induced inhibition of seed germination and seedling growth of choysum (Brassica rapa var. parachinensis)

Kamran, M., Wang, D., Xie, K., Lu, Y., Shi, C., Sabagh, A. E., Gu, W., & Xu, P. (2021) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2021.112921 · Cited by 86 · see citing works

Aluminum Toxicity in Plants: Present and Future

Hajiboland, R., Panda, C., Lastochkina, O. V., Gavassi, M. A., Habermann, G., & Pereira, J. F. (2022) · Journal of Plant Growth Regulation · doi:10.1007/s00344-022-10866-0 · Cited by 83 · see citing works

Integrative mechanisms of plant salt tolerance: Biological pathways, phytohormonal regulation, and technological innovations

Waheed, A., Zhuo, L., Wang, M., Hailiang, X., Tong, Z., Wang, C., & Aili, A. (2024) · Plant Stress · doi:10.1016/j.stress.2024.100652 · Cited by 80 · see citing works

Brassinosteroids Regulate Functional Components of Antioxidative Defense System in Salt Stressed Maize Seedlings

Rattan, A., Kapoor, D., Kapoor, N., Bhardwaj, R., & Sharma, A. (2020) · Journal of Plant Growth Regulation · doi:10.1007/s00344-020-10097-1 · Cited by 72 · see citing works

Role of Phytohormones in Regulating Heat Stress Acclimation in Agricultural Crops

Jha, U. C., Nayyar, H., & Siddique, K. H. M. (2021) · Journal of Plant Growth Regulation · doi:10.1007/s00344-021-10362-x · Cited by 69 · see citing works

Exogenous application of β-sitosterol mediated growth and yield improvement in water-stressed wheat (Triticum aestivum) involves up-regulated antioxidant system

Elkelish, A., Awad, Y. M., Soliman, M. H., Abu-Elsaoud, A. M., Abdelhamid, M. T., & El–Metwally, I. M. (2019) · Journal of Plant Research · doi:10.1007/s10265-019-01143-5 · Cited by 66 · see citing works

Saponin biopriming positively stimulates antioxidants defense, osmolytes metabolism and ionic status to confer salt stress tolerance in soybean

Soliman, M. H., Abdulmajeed, A. M., Alhaithloul, H. A. S., Alharbi, B. M., El-Esawi, M. A., Hasanuzzaman, M., & Elkelish, A. (2020) · Acta Physiologiae Plantarum · doi:10.1007/s11738-020-03098-w · Cited by 66 · see citing works

Triacontanol as a dynamic growth regulator for plants under diverse environmental conditions

Islam, S., & Mohammad, F. (2020) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-020-00815-0 · Cited by 64 · see citing works

Arbuscular Mycorrhizal Fungi and Compost-Based Biostimulants Enhance Fitness, Physiological Responses, Yield, and Quality Traits of Drought-Stressed Tomato Plants

Soussani, F.-E., Boutasknit, A., Ben-Laouane, R., Benkirane, R., Baslam, M., & Meddich, A. (2023) · Plants · doi:10.3390/plants12091856 · Cited by 69 · see citing works

The Jasmonic Acid Pathway Positively Regulates the Polyphenol Oxidase-Based Defense against Tea Geometrid Caterpillars in the Tea Plant (Camellia sinensis)

Zhang, J., Zhang, X., Ye, M., Li, X.-W., Lin, S., & Sun, X. (2020) · Journal of Chemical Ecology · doi:10.1007/s10886-020-01158-6 · Cited by 59 · see citing works

Exogenous EBR Ameliorates Endogenous Hormone Contents in Tomato Species under Low-Temperature Stress

Heidari, P., Entazari, M., Ebrahimi, A., Ahmadizadeh, M., Vannozzi, A., Palumbo, F., & Barcaccia, G. (2021) · Horticulturae · doi:10.3390/horticulturae7040084 · Cited by 57 · see citing works

PGPR-Enabled bioremediation of pesticide and heavy metal-contaminated soil: A review of recent advances and emerging challenges

Sharma, I., Sharma, S., Sharma, V., Singh, A. K., Sharma, A., Kumar, A., Singh, J., & Sharma, A. (2024) · Chemosphere · doi:10.1016/j.chemosphere.2024.142678 · Cited by 59 · see citing works

Foliar Spray of Stigmasterol Regulates Physiological Processes and Antioxidant Mechanisms to Improve Yield and Quality of Sunflower Under Drought Stress

Hanafy, R. S., & Sadak, M. S. (2023) · Journal of soil science and plant nutrition · doi:10.1007/s42729-023-01197-4 · Cited by 54 · see citing works

Nanoparticles and their crosstalk with stress mitigators: A novel approach towards abiotic stress tolerance in agricultural systems

Khan, A. R., Salam, A., Li, G., Iqbal, B., Ulhassan, Z., Liu, Q., Azhar, W., Liaquat, F., Shah, I. H., Hassan, S. S. U., et al. (2024) · The Crop Journal · doi:10.1016/j.cj.2024.09.010 · Cited by 53 · see citing works

Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones

Arif, Y., Singh, P., Bajguz, A., & Hayat, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158664 · Cited by 50 · see citing works

The reliance of phytohormone biosynthesis on primary metabolite precursors

Fàbregas, N., & Fernie, A. R. (2021) · Journal of Plant Physiology · doi:10.1016/j.jplph.2021.153589 · Cited by 47 · see citing works

Plant development and heat stress: role of exogenous nutrients and phytohormones in thermotolerance

Angon, P. B., Das, A., Roy, A. R., Khan, J. J., Ahmad, I., Biswas, A., Pallob, A. T., Mondol, M., & Yeasmin, S. T. (2024) · Discover Plants. · doi:10.1007/s44372-024-00020-3 · Cited by 45 · see citing works

24-Epibrassinolide promotes arsenic tolerance in Arabidopsis thaliana L. by altering stress responses at biochemical and molecular level

Surgun-Acar, Y., & Zemheri‐Navruz, F. (2019) · Journal of Plant Physiology · doi:10.1016/j.jplph.2019.05.002 · Cited by 44 · see citing works

24-epibrassinolide induces protection against waterlogging and alleviates impacts on the root structures, photosynthetic machinery and biomass in soybean

Pereira, Y. C., da Silva, F. R., da Silva, B. R. S., Cruz, F. J. R., Marques, D. J., & Lobato, A. K. D. S. (2020) · Plant Signaling & Behavior · doi:10.1080/15592324.2020.1805885 · Cited by 44 · see citing works

Co-Application of 24-Epibrassinolide and Titanium Oxide Nanoparticles Promotes Pleioblastus pygmaeus Plant Tolerance to Cu and Cd Toxicity by Increasing Antioxidant Activity and Photosynthetic Capacity and Reducing Heavy Metal Accumulation and Translocation

Emamverdian, A., Ding, Y., Barker, J., Liu, G., Hasanuzzaman, M., Li, Y., Ramakrishnan, M., & Mokhberdoran, F. (2022) · Antioxidants · doi:10.3390/antiox11030451 · Cited by 42 · see citing works

Brassinosteroids-Mediated Amelioration of Iron Deficiency in Soybean Plants: Beneficial Effects on the Nutritional Status, Photosynthetic Pigments and Chlorophyll Fluorescence

dos Santos, L. R., Paula, L. D. S., Pereira, Y. C., da Silva, B. R. S., Batista, B. L., Alsahli, A. A., & Lobato, A. K. D. S. (2020) · Journal of Plant Growth Regulation · doi:10.1007/s00344-020-10232-y · Cited by 36 · see citing works

Foliar brassinosteroid analogue (DI-31) sprays increase drought tolerance by improving plant growth and photosynthetic efficiency in lulo plants

Castañeda-Murillo, C. C., Rojas-Ortiz, J. G., Sánchez-Reinoso, A. D., Chávez-Arias, C. C., & Restrepo-Díaz, H. (2022) · Heliyon · doi:10.1016/j.heliyon.2022.e08977 · Cited by 36 · see citing works

Allelopathy of uncomposted and composted invasive aster (Ageratina adenophora) on ryegrass

Jiao, Y., Yong, L., Yuan, L., & Huang, J. (2020) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2020.123727 · Cited by 35 · see citing works

Plant Growth Regulators and Salt Stress: Mechanism of Tolerance Trade-Off

Fariduddin, Q., Zaid, A., & Mohammad, F. (2019) · Springer eBooks · doi:10.1007/978-981-13-8801-9_4 · Cited by 32 · see citing works

Adapting Crops to Rising Temperatures: Understanding Heat Stress and Plant Resilience Mechanisms

Kumar, A., Muthuramalingam, P., Kumar, R., Tiwari, S., Verma, L., Park, S., & Shin, H. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262110426 · Cited by 31 · see citing works

24-Epibrassinolide Positively Modulate Leaf Structures, Antioxidant System and Photosynthetic Machinery in Rice Under Simulated Acid Rain

da Fonseca, S. S., da Silva, B. R. S., & Lobato, A. K. D. S. (2020) · Journal of Plant Growth Regulation · doi:10.1007/s00344-020-10167-4 · Cited by 29 · see citing works

In situ aerobic composting eliminates the toxicity of Ageratina adenophora to maize and converts it into a plant- and soil-friendly organic fertilizer

Jiao, Y., Ruilian, J., Sun, Y., Yang, G., Li, Y., Huang, J., & Yuan, L. (2020) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2020.124554 · Cited by 30 · see citing works

Potassium enhances cadmium resistance ability of Panax notoginseng by brassinolide signaling pathway-regulated cell wall pectin metabolism

Liu, P., Jin, Z., Dai, C., Guo, L., Cui, X., & Yang, Y. J. (2021) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2021.112906 · Cited by 29 · see citing works

Brassinolide Soaking Reduced Nitrite Content and Extended Color Change and Storage Time of Toona sinensis Bud during Low Temperature and Near Freezing-Point Temperature Storage

Xu, X., Guo, C., Ma, C., Li, M., Chen, Y., Liu, C., Chu, J., & Yao, X. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113110 · Cited by 29 · see citing works

Role of Brassinosteroids (BRs) in Modulating Antioxidative Defense Mechanism in Plants Growing Under Abiotic and Biotic Stress Conditions

Sharma, N., Kour, S., Kumar, D., Kaur, R., Khajuria, A., & Ohri, P. (2022) · Springer eBooks · doi:10.1007/978-981-16-7981-0_15 · Cited by 28 · see citing works

24-epibrassinolide promotes selenium uptake in grapevine under selenium stress

Lin, L., Li, Z., Wang, J., Liang, D., Xia, H., Lv, X., Tang, Y., Wang, X., Deng, Q., & Liao, M. (2022) · Scientia Horticulturae · doi:10.1016/j.scienta.2022.111564 · Cited by 28 · see citing works

Triacontanol: a Multifunctional Growth Regulator for Enhancing Stress Tolerance

EL-BELTAGI, H. S., Gad, M., Abdel‐Haleem, M., Shalaby, T., Adel Abdel-Sabour, R. E. Z. K., & Khedr, E. H. (2025) · Journal of Plant Diseases and Protection · doi:10.1007/s10343-025-01144-6 · Cited by 27 · see citing works

Hydrogen sulfide induced by hydrogen peroxide mediates brassinosteroid-induced stomatal closure of Arabidopsis thaliana

Ma, Y., Shao, L., Zhang, W., & Zheng, F. (2020) · Functional Plant Biology · doi:10.1071/fp20205 · Cited by 26 · see citing works

Brassinolide Enhances the Level of Brassinosteroids, Protein, Pigments, and Monosaccharides in Wolffia arrhiza Treated with Brassinazole

Chmur, M., & Bajguz, A. (2021) · Plants · doi:10.3390/plants10071311 · Cited by 26 · see citing works

Comprehensive Insights into Flavonoids: Biosynthesis, Stress Modulation, and Plant Growth Regulation

Parveen, Z., Zaidi, S., Bajguz, A., Arif, Y., & Hayat, S. (2025) · Journal of Plant Growth Regulation · doi:10.1007/s00344-025-11841-1 · Cited by 23 · see citing works

Rice seedlings showed a higher heat tolerance through the foliar application of biostimulants

QUINTERO-CALDERÓN, E. H., Sánchez-Reinoso, A. D., Chávez-Arias, C. C., Garcés-Varón, G., & Restrepo-Díaz, H. (2021) · Notulae Botanicae Horti Agrobotanici Cluj-Napoca · doi:10.15835/nbha49112120 · Cited by 24 · see citing works

MAPK Pathway under Chronic Copper Excess in Green Macroalgae (Chlorophyta): Involvement in the Regulation of Detoxification Mechanisms

Rodríguez-Rojas, F., Celis‐Plá, P. S. M., Méndez, L., Moenne, F., Muñoz, P. T., Lobos, M. G., Díaz, P., Sánchez‐Lizaso, J. L., Brown, M. T., Moenne, A., et al. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20184546 · Cited by 23 · see citing works

Alleviation of Oxidative Stress Induced by 24-Epibrassinolide in Soybean Plants Exposed to Different Manganese Supplies: UpRegulation of Antioxidant Enzymes and Maintenance of Photosynthetic Pigments

Rodrigues, W. D. S., Pereira, Y. C., de Souza, A. L. M., Batista, B. L., & Lobato, A. K. D. S. (2020) · Journal of Plant Growth Regulation · doi:10.1007/s00344-020-10091-7 · Cited by 24 · see citing works

Mitigation of arsenic stress in Brassica juncea L. using zinc oxide-nanoparticles produced by novel hydrothermal synthesis

Bhat, J. A., Faizan, M., Bhat, M. A., Sharma, G., Rinklebe, J., Alyemeni, M. N., Bajguz, A., & Ahmad, P. (2023) · South African Journal of Botany · doi:10.1016/j.sajb.2023.10.059 · Cited by 21 · see citing works

Abiotic Stress Tolerance in Crop Plants: Role of Phytohormones

Alhaithloul, H. A. S., Abu-Elsaoud, A. M., & Soliman, M. H. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.93710 · Cited by 21 · see citing works

Hormonal response of Acutodesmus obliquus exposed to combined treatment with 24-epibrassinolide and lead

Talarek-Karwel, M., Bajguz, A., & Piotrowska‐Niczyporuk, A. (2020) · Journal of Applied Phycology · doi:10.1007/s10811-020-02191-4 · Cited by 20 · see citing works

Drought Stress Responses in Arabica Coffee Genotypes: Physiological and Metabolic Insights

Chekol, H., Warkineh, B., Shimber, T., Mierek‐Adamska, A., Dąbrowska, G. B., & Degu, A. (2024) · Plants · doi:10.3390/plants13060828 · Cited by 19 · see citing works

The Impact of Nanoparticles on Plant Growth, Development, and Stress Tolerance Through Regulating Phytohormones

Karabulut, F. (2024) · Springer eBooks · doi:10.1007/978-981-97-0851-2_4 · Cited by 19 · see citing works

Leaf application of 24‐epibrassinolide mitigates cadmium toxicity in young Eucalyptus urophylla plants by modulating leaf anatomy and gas exchange

Cunha, L. F. S., de Oliveira, V. P., Nascimento, A. W. S., da Silva, B. R. S., Batista, B. L., Alsahli, A. A., & Lobato, A. K. D. S. (2020) · Physiologia Plantarum · doi:10.1111/ppl.13182 · Cited by 19 · see citing works

24-Epibrasinolide Delays Chlorophyll Degradation and Stimulates the Photosynthetic Machinery in Magnesium-Stressed Soybean Plants

dos Santos, L. A., Batista, B. L., & Lobato, A. K. D. S. (2021) · Journal of Plant Growth Regulation · doi:10.1007/s00344-021-10539-4 · Cited by 18 · see citing works

A brassinosteroid functional analogue increases soybean drought resilience

Perez-Borroto, L. S., Guzzo, M. C., Posada, G. A., Malavera, A. N. P., Castagnaro, A. P., González-Olmedo, J. L., Coll-García, Y., & Pardo, E. M. (2022) · Scientific Reports · doi:10.1038/s41598-022-15284-6 · Cited by 16 · see citing works

Integrated transcriptomics and metabolomics revealed the mechanism of catechin biosynthesis in response to lead stress in tung tree (Vernicia fordii)

Dong, X. B., Li, W., Li, C., Akan, O. D., Liao, C., Cao, J., & Zhang, L. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.172796 · Cited by 16 · see citing works

Principal Component Analysis to Assess the Changes of Yield and Quality of Two Pinellia ternata Cultivars After Brassinolide Treatments

Guo, C., Shen, Y., Li, M., Ying, C., Xu, X., Chu, J., & Yao, X. (2021) · Journal of Plant Growth Regulation · doi:10.1007/s00344-021-10434-y · Cited by 16 · see citing works

Medicinal and Aromatic Plants Under Abiotic Stress: A Crosstalk on Phytohormones’ Perspective

Zaid, A., Ahmad, B., & Wani, S. H. (2021) · Springer eBooks · doi:10.1007/978-3-030-61153-8_5 · Cited by 16 · see citing works

The role of phytohormones in reducing the arsenic-induced stress in plants

Garg, T., Kumar, A., Joshi, A., Awasthi, A., Rana, A., Kumar, V., & Kaur, S. (2024) · South African Journal of Botany · doi:10.1016/j.sajb.2024.03.020 · Cited by 15 · see citing works

Mitigating Effect of Trans-Zeatin on Cadmium Toxicity in Desmodesmus armatus

Piotrowska‐Niczyporuk, A., Bonda-Ostaszewska, E., & Bajguz, A. (2024) · Cells · doi:10.3390/cells13080686 · Cited by 14 · see citing works

Overdominance at the Gene Expression Level Plays a Critical Role in the Hybrid Root Growth of Brassica napus

Shalby, N., Mohamed, I. A. A., Xiong, J., Hu, K., Yang, Y., Nishawy, E., Yi, B., Wen, J., Ma, C., Shen, J., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179246 · Cited by 15 · see citing works

Ascorbate–Glutathione Cycle

Chauhan, P., Mir, R. A., & Khah, M. A. (2022) · Wiley eBooks · doi:10.1002/9781119800156.ch8 · Cited by 16 · see citing works

Phytohormonal modulation alleviates arsenic toxicity in rice by enhancing antioxidant defenses, proline metabolism, and arsenic detoxification mechanisms

Shaghaleh, H., Hamoud, Y. A., Saleem, M. H., Elansary, H. O., Mahmoud, E. A., & Sheteiwy, M. S. A. (2025) · Scientific Reports · doi:10.1038/s41598-025-11629-z · Cited by 14 · see citing works

Transcriptional and metabolic responses of apple to different potassium environments

Sun, T., Zhang, J., Zhang, Q., Li, X., Li, M., Yang, Y., Zhou, J., Wei, Q., & Zhou, B. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1131708 · Cited by 14 · see citing works

Occurrence of plant hormones in composts made from organic fraction of agri-food industry waste

Sienkiewicz, A., Krasowska, M., Kowczyk-Sadowy, M., Obidziński, S., Piotrowska‐Niczyporuk, A., & Bajguz, A. (2024) · Scientific Reports · doi:10.1038/s41598-024-57524-x · Cited by 14 · see citing works

Exogenously applied spermidine confers protection against cinnamic acid-mediated oxidative stress in Pisum sativum

Kapoor, R. T., Alyemeni, M. N., & Ahmad, P. (2021) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2021.02.052 · Cited by 14 · see citing works

Exogenous Application of 24-Epibrassinolide Improves Manganese Tolerance in Arabidopsis thaliana L. via the Modulation of Antioxidant System

Surgun-Acar, Y., & Zemheri‐Navruz, F. (2021) · Journal of Plant Growth Regulation · doi:10.1007/s00344-021-10320-7 · Cited by 14 · see citing works

Brassinosteroids: A Multifunctional Phytohormone of Plant Development and Stress Responses

Praveena, J., Dash, S., Behera, L., & Rout, G. R. (2020) · Current Journal of Applied Science and Technology · doi:10.9734/cjast/2020/v39i2530896 · Cited by 12 · see citing works

Deciphering the mechanism of action and crosstalk of brassinosteroids with other plant growth regulators in orchestrating physio-biochemical responses in plants under salt stress

Shah, S. H., Parrey, Z. A., Barwal, S. K., Mohammad, F., & Siddiqui, M. H. (2024) · Plant Growth Regulation · doi:10.1007/s10725-024-01226-x · Cited by 12 · see citing works

24-Epibrassinolide induces protection against nickel excess in soybean plants: anatomical evidences

Saraiva, M. P., Maia, C. F., da Silva, B. R. S., Batista, B. L., & Lobato, A. K. D. S. (2021) · Revista Brasileira de Botânica · doi:10.1007/s40415-021-00701-3 · Cited by 12 · see citing works

Nitrogen-Driven Orchestration of Lateral Root Development: Molecular Mechanisms and Systemic Integration

Sun, X., Gu, Y., Liu, Y., Liu, Z., & Wang, P. (2025) · Biology · doi:10.3390/biology14081099 · Cited by 11 · see citing works

Multiple Pathways Revealing the CeO2 Nanoparticle-Biostimulant-Based “Stress Training” Strategy for Enhanced Medicago sativa L. Antiviral Capability

Guo, Z., Zhang, T., Chen, Z., Niu, J., Rasel, M., Luo, E., Li, Y., Xu, N., Hassan, M. U., Kareem, H. A., et al. (2025) · ACS Nano · doi:10.1021/acsnano.4c10637 · Cited by 11 · see citing works

Unravelling the metabolic signatures and associated pathways underlying saline‐alkali stress resilience in the halophyte Salvadora persica

Kumari, A., Fatnani, D., Seth, C. S., & Parida, A. K. (2025) · Physiologia Plantarum · doi:10.1111/ppl.70114 · Cited by 10 · see citing works

Brassinosteroid-Mediated Resistance to Cobalt-Induced Toxicity by Regulating Hormonal Balance, Cellular Metabolism, and Antioxidant Defense in Maize

Salam, A., Chang, J., Yang, L., Zeeshan, M., Iqbal, A., Khan, A. R., Afridi, M. S., Ulhassan, Z., Azhar, W., Zhang, Z., et al. (2025) · Plants · doi:10.3390/plants14132076 · Cited by 10 · see citing works

Effect of Foliar Application of 24-Epibrassinolide on Water Use Efficiency and Morpho-Physiological Characteristics of Lilium LA Hybrid under Deficit Irrigation

Omidian, M., Roein, Z., & Shiri, M. A. (2021) · Journal of Plant Growth Regulation · doi:10.1007/s00344-021-10400-8 · Cited by 10 · see citing works

Comparative Physiological and Transcriptomic Analysis Provide New Insights of Crucial Pathways and Genes Regulating Kenaf Salt Tolerance

Hu, Y., Li, Z., Tang, M., Luo, D., Kashif, M. H., Cao, S., Wang, C., Yue, J., Huang, Z., Pan, J., et al. (2022) · Journal of Plant Growth Regulation · doi:10.1007/s00344-022-10822-y · Cited by 9 · see citing works

Exogenous brassinosteroid alleviates calcium deficiency induced tip-burn by regulating calcium transport in Brassica rapa L. ssp. pekinensis

Li, Y., Wu, Y., Tang, Z., Xiao, X., Gao, X., Qiao, Y., Ma, J., Hu, L., & Yu, J. (2023) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2023.114534 · Cited by 9 · see citing works

Comparative Efficacy of Melatonin and Brassinolide in Mitigating the Adverse Effects of Cadmium on Wolffia arrhiza

Chmur, M., & Bajguz, A. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26020692 · Cited by 8 · see citing works

Use of chemical labeling-assisted liquid chromatography-mass spectrometry for discovering derivatives of brassinosteroids

Xiong, C.-F., Bai, Y., Yin, X.-M., Ye, T.-T., & Feng, Y. (2022) · Journal of Chromatography A · doi:10.1016/j.chroma.2022.463639 · Cited by 8 · see citing works

Methyl esters of 23,24-Dinor-5α-cholan-22-oic acids as brassinosteroid Analogues. Synthesis, evaluation of plant growth promoting activity and Molecular docking

Cimino, P. F., Núñez, G. M., Rosado‐Abón, A., Amesty, Á., Estévez‐Braun, A., Díaz, K., Espinoza, C. L., & Iglesias‐Arteaga, M. A. (2023) · Steroids · doi:10.1016/j.steroids.2023.109248 · Cited by 8 · see citing works

Bark tissue transcriptome analyses of inverted Populus yunnanensis cuttings reveal the crucial role of plant hormones in response to inversion

Zhou, A., Gan, P., Zong, D., Fei, X., Zhong, Y.-Y., Li, S., Yu, J., & He, C. (2019) · PeerJ · doi:10.7717/peerj.7740 · Cited by 8 · see citing works

Involvement of brassinosteroids in plant response to salt stress

Rattan, A., Kapoor, D., Ashish, Kapoor, N., Bhardwaj, R., & Sharma, A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-813227-2.00003-5 · Cited by 7 · see citing works

Appropriate mowing can promote the growth of Anabasis aphylla through the auxin metabolism pathway

Jiang, P., Han, P., He, M., Shui, G., Guo, C., Shah, S. E., Wang, Z., Wu, H., Li, J., & Pan, Z. (2024) · BMC Plant Biology · doi:10.1186/s12870-024-05204-3 · Cited by 7 · see citing works

Implications of Phytohormones as Agrochemicals in Dynamic Environmental Conditions

Madaan, I., Dogra, N., Kaushik, S., Kaur, G., Sidhu, A., Bhardwaj, R., & Sirhindi, G. (2022) · Springer eBooks · doi:10.1007/978-981-16-9310-6_23 · Cited by 7 · see citing works

Lights Out. The Chloroplast Under Attack During Phytoplasma Infection?

Janik, K., Mittelberger, C., & Moser, M. (2020) · Annual Plant Reviews online · doi:10.1002/9781119312994.apr0747 · Cited by 7 · see citing works

Ecophysiological characterisation of a Klebsormidium strain isolated from a cave environment

Futó, P., Lengyel, E., Futó, M., Németh, Z., Pirger, Z., Komáromy, A., Padisák, J., Felföldi, T., Kutasi, J., & Bernát, G. (2023) · Journal of Applied Phycology · doi:10.1007/s10811-023-03161-2 · Cited by 7 · see citing works

Soil Management and Crop Adaptation in Saline Areas

Mannan, M. A., Karim, M. A., Higichi, H., Akter, M., & Akter, M. T. (2024) · Springer eBooks · doi:10.1007/978-981-97-6635-2_13 · Cited by 6 · see citing works

Role of phytohormones in biotic vs abiotic stresses with respect to PGPR and autophagy

Gul, A., Huda, N.-U., & Nawaz, S. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-91883-1.00016-4 · Cited by 6 · see citing works

Role of brassinosteroids in regulating physiological and molecular aspects of plants under abiotic stress

Ghorbel, M., & Brini, F. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-98332-7.00019-6 · Cited by 6 · see citing works

Influence of 24-Epibrassinolide on Water Exchange of Wheat Varieties Various in Dry Resistance under Osmotic Stress

Безрукова, М. В., Kudoyarova, G. R., Lubyanova, A. R., Maslennikova, D., & Шакирова, Ф. М. (2021) · Russian Journal of Plant Physiology · doi:10.1134/s1021443721010040 · Cited by 6 · see citing works

Methyl Jasmonate and Brassinosteroids: Emerging Plant Growth Regulators in Plant Abiotic Stress Tolerance and Environmental Changes

Alhaithloul, H. A. S., & Soliman, M. H. (2021) · Springer eBooks · doi:10.1007/978-3-030-61153-8_8 · Cited by 6 · see citing works

Brassinosteroids and Salicylic Acid as Chemical Agents to Ameliorate Diverse Environmental Stresses in Plants

Vardhini, B. V. (2020) · doi:10.1002/9781119552154.ch19 · Cited by 6 · see citing works

Nitrogen application enhances thermotolerance in Pinellia ternata via modulation of antioxidant capacity

Chen, Y., Zhou, Y., Chao, Q., RongZhi, Y., Duan, Y., Xue, J., Wang, R., & Xue, T. (2025) · Scientia Horticulturae · doi:10.1016/j.scienta.2025.114343 · Cited by 5 · see citing works

Comparative Response of Red and Green Algae to the Quality of Coastal Water of Red Sea, Haql, Saudi Arabia

AlSolami, M. A. (2020) · Journal of Environmental Protection · doi:10.4236/jep.2020.1110049 · Cited by 5 · see citing works

The Beneficial Effect of 24-Epibrassinolide Against High-Temperature Stress in Gracilariopsis lemaneiformis Revealed by Physiological Response and Transcriptomic Profiling

Chu, L., Luo, S., Chen, Q., Chen, X., Xu, N., & Sun, X. K. (2024) · Journal of Plant Growth Regulation · doi:10.1007/s00344-024-11454-0 · Cited by 5 · see citing works

Understanding brassinosteroid-regulated mechanisms to improve stress tolerance in plants: a critical review

Nawaz, F., Naeem, M. S., Zulfiqar, B., Akram, A., Ashraf, M. Y., Raheel, M., Shabbir, R. N., Hussain, R. A., Anwar, I., & Aurangzaib, M. (2017) · Environmental Science and Pollution Research · doi:10.1007/s11356-017-9163-6 · Cited by 113 · see citing works

The physiological and molecular mechanism of brassinosteroid in response to stress: a review

Anwar, A., Liu, Y., Dong, R., Bai, L., Yu, X., & Li, Y. (2018) · Biological Research · doi:10.1186/s40659-018-0195-2 · Cited by 275 · see citing works

Brassinosteroids as a multidimensional regulator of plant physiological and molecular responses under various environmental stresses

Basit, F., Liu, J., An, J., Chen, M., He, C., Zhu, X., Li, Z., Hu, J., & Guan, Y. (2021) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-15087-8 · Cited by 59 · see citing works

Brassinosteroid receptors as multidimensional regulators in brassinosteroid perception, plant growth, and stress adaptation

Ali, M. S., Kumar, D., Parkirti, P., Sharma, A. E., Sharma, R., Singh, A., Sharma, M., Mir, N. R., Singh, A. D., Ibrahim, M. F. M., et al. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-30244-2.00013-0 · Cited by 1 · see citing works

The molecular mechanism of brassinosteroids in mediating the abiotic stress responses of plants

Liaqat, S., Saffeullah, P., Umar, S., & Siddiqi, T. O. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-90943-3.00003-1 · Cited by 1 · see citing works