Drought response in wheat: key genes and regulatory mechanisms controlling root system architecture and transpiration efficiency

The role of stomata in sensing and driving environmental change

Hetherington, A. M., & Woodward, F. I. (2003) · Nature · doi:10.1038/nature01843 · Cited by 2,413 · see citing works

Crops that feed the world 6. Past successes and future challenges to the role played by maize in global food security

Shiferaw, B. A., Prasanna, B. M., Hellin, J., & Bänziger, M. (2011) · Food Security · doi:10.1007/s12571-011-0140-5 · Cited by 1,676 · see citing works

Control of root system architecture by DEEPER ROOTING 1 increases rice yield under drought conditions

Uga, Y., Sugimoto, K., Ogawa, S., Rane, J., Ishitani, M., Hara, N., Kitomi, Y., Inukai, Y., Ono, K., Kanno, N., et al. (2013) · Nature Genetics · doi:10.1038/ng.2725 · Cited by 1,618 · see citing works

A chromosome-based draft sequence of the hexaploid bread wheat ( <i>Triticum aestivum</i> ) genome

The International Wheat Genome Sequencing Consortium (IWGSC), Mayer, K. F. X., Rogers, J., Doležel, J., Pozniak, C., Eversole, K., Feuillet, C., Gill, B., Friebe, B., Lukaszewski, A. J., et al. (2014) · Science · doi:10.1126/science.1251788 · Cited by 1,583 · see citing works

Crops that feed the world 10. Past successes and future challenges to the role played by wheat in global food security

Shiferaw, B. A., Smale, M., Braun, H., Duveiller, E., Reynolds, M. P., & Muricho, G. (2013) · Food Security · doi:10.1007/s12571-013-0263-y · Cited by 1,467 · see citing works

A Critical Evaluation of Traits for Improving Crop Yields in Water-Limited Environments

Ludlow, M. M., & Muchow, R. C. (1990) · Advances in agronomy · doi:10.1016/s0065-2113(08)60477-0 · Cited by 1,318 · see citing works

Breeding for high water-use efficiency

Condon, A. G. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh277 · Cited by 1,218 · see citing works

Tuning gene expression to changing environments: from rapid responses to evolutionary adaptation

López-Maury, L., Marguerat, S., & Bähler, J. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2398 · Cited by 1,061 · see citing works

APETALA 2/Ethylene Responsive Factor ( AP 2/ ERF ) transcription factors: mediators of stress responses and developmental programs

Licausi, F., Ohme‐Takagi, M., & Pierdomenico Perata, A. (2013) · New Phytologist · doi:10.1111/nph.12291 · Cited by 1,022 · see citing works

NINJA connects the co-repressor TOPLESS to jasmonate signalling

Pauwels, L., Barbero, G. F., Geerinck, J., Tilleman, S., Grunewald, W., Pérez, A. C., Chico, J. M., Bossche, R. V., Sewell, J. A., Gil, E., et al. (2010) · Nature · doi:10.1038/nature08854 · Cited by 1,022 · see citing works

The Influence of Climate Change on Global Crop Productivity1

Lobell, D., & Gourdji, S. (2012) · Plant Physiology · doi:10.1104/pp.112.208298 · Cited by 919 · see citing works

Repression Domains of Class II ERF Transcriptional Repressors Share an Essential Motif for Active Repression

Ohta, M., Matsui, K., Hiratsu, K., Shinshi, H., & Ohme‐Takagi, M. (2001) · The Plant Cell · doi:10.1105/tpc.010127 · Cited by 865 · see citing works

Transcription Factors and Plants Response to Drought Stress: Current Understanding and Future Directions

Joshi, R., Wani, S. H., Singh, B., Bohra, A., Dar, Z. A., Lone, A. A., Pareek, A., & Singla-Pareek, S. L. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01029 · Cited by 857 · see citing works

Dominant repression of target genes by chimeric repressors that include the EAR motif, a repression domain, in Arabidopsis

Hiratsu, K., Matsui, K., Koyama, T., & Ohme‐Takagi, M. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01759.x · Cited by 816 · see citing works

TOPLESS Mediates Auxin-Dependent Transcriptional Repression During Arabidopsis Embryogenesis

Szemenyei, H. J., Hannon, M., & Long, J. A. (2008) · Science · doi:10.1126/science.1151461 · Cited by 807 · see citing works

WRKY Transcription Factors: Molecular Regulation and Stress Responses in Plants

Phukan, U. J., Jeena, G. S., & Shukla, R. K. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00760 · Cited by 751 · see citing works

Wheat yield loss attributable to heat waves, drought and water excess at the global, national and subnational scales

Zampieri, M., Ceglar, A., Dentener, F. J., & Toreti, A. (2017) · Environmental Research Letters · doi:10.1088/1748-9326/aa723b · Cited by 713 · see citing works

Raising yield potential in wheat

Reynolds, M. P., Foulkes, J. M., Slafer, G. A., Berry, P., Parry, M. A. J., Snape, J. W., & Angus, W. J. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp016 · Cited by 697 · see citing works

Root growth maintenance during water deficits: physiology to functional genomics

Sharp, R. E. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh276 · Cited by 676 · see citing works

The ERECTA gene regulates plant transpiration efficiency in Arabidopsis

Masle, J., Gilmore, S. R., & Farquhar, G. D. (2005) · Nature · doi:10.1038/nature03835 · Cited by 579 · see citing works

AtMYBL2, a protein with a single MYB domain, acts as a negative regulator of anthocyanin biosynthesis in Arabidopsis

Matsui, K., Umemura, Y., & Ohme‐Takagi, M. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03565.x · Cited by 574 · see citing works

Increasing crop productivity when water is scarce—from breeding to field management

Passioura, J. B. (2005) · Agricultural Water Management · doi:10.1016/j.agwat.2005.07.012 · Cited by 557 · see citing works

Is photosynthesis limited by decreased Rubisco activity and RuBP content under progressive water stress?

Bota, J., Medrano, H., & Flexas, J. (2004) · New Phytologist · doi:10.1111/j.1469-8137.2004.01056.x · Cited by 546 · see citing works

Role of an Arabidopsis AP2/EREBP-Type Transcriptional Repressor in Abscisic Acid and Drought Stress Responses

Song, C., Agarwal, M., Ohta, M., Guo, Y., Halfter, U., Wang, P., & Zhu, J. (2005) · The Plant Cell · doi:10.1105/tpc.105.033043 · Cited by 525 · see citing works

Gain‐ and loss‐of‐function mutations in Zat10 enhance the tolerance of plants to abiotic stress

Mittler, R., Kim, Y., Song, L., Coutu, J., Coutu, A., Ciftci-Yilmaz, S., Lee, H., Stevenson, B., & Zhu, J. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.11.002 · Cited by 504 · see citing works

EAR motif-mediated transcriptional repression in plants

Kagale, S., & Rozwadowski, K. L. (2011) · Epigenetics · doi:10.4161/epi.6.2.13627 · Cited by 491 · see citing works

Physiological traits used in the breeding of new cultivars for water-scarce environments.

Richards, R. (2006) · Agricultural Water Management · doi:10.1016/j.agwat.2005.07.013 · Cited by 429 · see citing works

Stress-induced expression in wheat of the Arabidopsis thaliana DREB1A gene delays water stress symptoms under greenhouse conditions

Pellegrineschi, A., Reynolds, M. P., Pacheco, M., Brito, R. M., Almeraya, R., Yamaguchi‐Shinozaki, K., & Hoisington, D. A. (2004) · Genome · doi:10.1139/g03-140 · Cited by 426 · see citing works

Drought-responsive WRKY transcription factor genes TaWRKY1 and TaWRKY33 from wheat confer drought and/or heat resistance in Arabidopsis

He, G., Xu, J.-Y., Wang, Y., Liu, J.-M., Li, P.-S., Chen, M., Ma, Y., & Xu, Z. (2016) · BMC Plant Biology · doi:10.1186/s12870-016-0806-4 · Cited by 409 · see citing works

Mechanisms of Stomatal Development

Pillitteri, L. J., & Torii, K. U. (2012) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042811-105451 · Cited by 393 · see citing works

Isolation and molecular characterization of the Triticum aestivum L. ethylene-responsive factor 1 (TaERF1) that increases multiple stress tolerance

Xu, Z., Xia, L., Chen, M., Cheng, X., Zhang, R.-Y., Li, L., Zhao, Y., Lu, Y., Ni, Z., Liu, L., et al. (2007) · Plant Molecular Biology · doi:10.1007/s11103-007-9237-9 · Cited by 368 · see citing works

Dro1, a major QTL involved in deep rooting of rice under upland field conditions

Uga, Y., Okuno, K., & Yano, M. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/erq429 · Cited by 364 · see citing works

The ERF transcription factor Ta ERF 3 promotes tolerance to salt and drought stresses in wheat

Rong, W., Qi, L., Wang, A., Ye, X., Du, L., Liang, H.-X., Zhiyong, X., & Zhang, Z. (2014) · Plant Biotechnology Journal · doi:10.1111/pbi.12153 · Cited by 350 · see citing works

The Arabidopsis GTL1 Transcription Factor Regulates Water Use Efficiency and Drought Tolerance by Modulating Stomatal Density via Transrepression of SDD1

Yoo, C. Y., Pence, H. E., Jin, J. B., Miura, K., Gosney, M. J., Hasegawa, P. M., & Mickelbart, M. V. (2010) · The Plant Cell · doi:10.1105/tpc.110.078691 · Cited by 350 · see citing works

The EAR-motif of the Cys2/His2-type Zinc Finger Protein Zat7 Plays a Key Role in the Defense Response of Arabidopsis to Salinity Stress

Ciftci-Yilmaz, S., Morsy, M. R., Song, L., Coutu, A., Krizek, B. A., Lewis, M. W., Warren, D., Cushman, J. C., Connolly, E. L., & Mittler, R. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611093200 · Cited by 323 · see citing works

Abscisic acid accumulation modulates auxin transport in the root tip to enhance proton secretion for maintaining root growth under moderate water stress

Xu, W., Jia, L., Shi, W., Liang, J., Zhou, F., Li, Q., & Zhang, J. (2012) · New Phytologist · doi:10.1111/nph.12004 · Cited by 312 · see citing works

Genome-Wide Analysis of Ethylene-Responsive Element Binding Factor-Associated Amphiphilic Repression Motif-Containing Transcriptional Regulators in Arabidopsis

Kagale, S., Links, M. G., & Rozwadowski, K. L. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.151704 · Cited by 304 · see citing works

Repression Domains of Class II ERF Transcriptional Repressors Share an Essential Motif for Active Repression

Ohta, M. (2001) · The Plant Cell · doi:10.1105/tpc.13.8.1959 · Cited by 296 · see citing works

A Novel Group of Transcriptional Repressors in Arabidopsis

Ikeda, M., & Ohme‐Takagi, M. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp048 · Cited by 263 · see citing works

A novel rice C2H2-type zinc finger protein, ZFP36, is a key player involved in abscisic acid-induced antioxidant defence and oxidative stress tolerance in rice

Zhang, H., Liu, Y., Wen, F., Yao, D., Wang, L., Guo, J., Ni, L., Zhang, A., Tan, M., & Jiang, M. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru313 · Cited by 262 · see citing works

A Wheat WRKY Transcription Factor TaWRKY10 Confers Tolerance to Multiple Abiotic Stresses in Transgenic Tobacco

Wang, C., Deng, P., Chen, L., Wang, X., Ma, H., Hu, W., Yao, N., Feng, Y., Chai, R., Yang, G., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065120 · Cited by 255 · see citing works

Negative regulation of defence and stress genes by EAR-motif-containing repressors

Kazan, K. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2006.01.004 · Cited by 250 · see citing works

Silicon Application Alleviates Drought Stress in Wheat Through Transcriptional Regulation of Multiple Antioxidant Defense Pathways

Ma, D., Sun, D., Wang, C., Qin, H., Ding, H., Li, Y., & Guo, T. (2015) · Journal of Plant Growth Regulation · doi:10.1007/s00344-015-9500-2 · Cited by 242 · see citing works

A systems biology perspective on the role of WRKY transcription factors in drought responses in plants

Tripathi, P., Rabara, R., & Rushton, P. J. (2013) · Planta · doi:10.1007/s00425-013-1985-y · Cited by 235 · see citing works

Arabidopsis Cys2/His2 Zinc-Finger Proteins AZF1 and AZF2 Negatively Regulate Abscisic Acid-Repressive and Auxin-Inducible Genes under Abiotic Stress Conditions

Kodaira, K., Qin, F., Tran, L. P., Maruyama, K., Kidokoro, S., Fujita, Y., Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.182683 · Cited by 231 · see citing works

Ectopic expression of a wheat MYB transcription factor gene, TaMYB73, improves salinity stress tolerance in Arabidopsis thaliana

He, Y., Li, W., Lv, J. C., Jia, Y., Wang, M., & Xia, G. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err389 · Cited by 231 · see citing works

Gm WRKY 27 interacts with Gm MYB 174 to reduce expression of Gm NAC 29 for stress tolerance in soybean plants

Wang, F., Chen, H., Li, Q., Wei, W., Li, W., Zhang, W., Ma, B., Bi, Y., Lai, Y., Liu, X., et al. (2015) · The Plant Journal · doi:10.1111/tpj.12879 · Cited by 222 · see citing works

Breeding wheat for drought tolerance: Progress and technologies

Mwadzingeni, L., Shimelis, H., Dube, E., Laing, M., & Tsilo, T. (2016) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(15)61102-9 · Cited by 205 · see citing works

Global profiling of alternative splicing landscape responsive to drought, heat and their combination in wheat ( Triticum aestivum L.)

Liu, Z., Qin, J., Tian, X., Xu, S., Wang, Y., Li, H., Wang, X., Peng, H., Yao, Y., Hu, Z., et al. (2017) · Plant Biotechnology Journal · doi:10.1111/pbi.12822 · Cited by 203 · see citing works

Changes in the water status and osmotic solute contents in response to drought and salicylic acid treatments in four different cultivars of wheat (Triticum aestivum)

Loutfy, N., El‐Tayeb, M. A., Hassanen, A. M., Moustafa, M., Sakuma, Y., & Inouhe, M. (2011) · Journal of Plant Research · doi:10.1007/s10265-011-0419-9 · Cited by 201 · see citing works

Genome-wide association analysis of agronomic traits in wheat under drought-stressed and non-stressed conditions

Mwadzingeni, L., Shimelis, H., Rees, D. J. G., & Tsilo, T. J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171692 · Cited by 191 · see citing works

Transcription factors involved in drought tolerance and their possible role in developing drought tolerant cultivars with emphasis on wheat (Triticum aestivum L.)

Gahlaut, V., Jaiswal, V., Kumar, A., & Gupta, P. K. (2016) · Theoretical and Applied Genetics · doi:10.1007/s00122-016-2794-z · Cited by 185 · see citing works

Transcriptome-wide identification of bread wheat WRKY transcription factors in response to drought stress

Okay, S., Derelli, E., & Ünver, T. (2014) · Molecular Genetics and Genomics · doi:10.1007/s00438-014-0849-x · Cited by 183 · see citing works

QTL Analysis for Drought Tolerance in Wheat: Present Status and Future Possibilities

Gupta, P. K., Balyan, H. S., & Gahlaut, V. (2017) · Agronomy · doi:10.3390/agronomy7010005 · Cited by 183 · see citing works

Deep rooting conferred by DEEPER ROOTING 1 enhances rice yield in paddy fields

Arai‐Sanoh, Y., Takai, T., Yoshinaga, S., Nakano, H., Kojima, M., Sakakibara, H., Kondo, M., & Uga, Y. (2014) · Scientific Reports · doi:10.1038/srep05563 · Cited by 181 · see citing works

Citrulline and DRIP-1 Protein (ArgE Homologue) in Drought Tolerance of Wild Watermelon

Yokota, A. (2002) · Annals of Botany · doi:10.1093/aob/mcf074 · Cited by 181 · see citing works

Complexity and coordination of root growth at low water potentials: recent advances from transcriptomic and proteomic analyses

YAMAGUCHI, M., & Sharp, R. E. (2009) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2009.02064.x · Cited by 180 · see citing works

The Arabidopsis EAR-motif-containing protein RAP2.1 functions as an active transcriptional repressor to keep stress responses under tight control

Dong, C., & Liu, J. (2010) · BMC Plant Biology · doi:10.1186/1471-2229-10-47 · Cited by 177 · see citing works

Benefits of increased soil exploration by wheat roots

Lilley, J. M., & Kirkegaard, J. A. (2011) · Field Crops Research · doi:10.1016/j.fcr.2011.03.010 · Cited by 171 · see citing works

Overexpression of GmERF5, a new member of the soybean EAR motif-containing ERF transcription factor, enhances resistance to Phytophthora sojae in soybean

Dong, L., Cheng, Y., Wu, J., Cheng, Q., Li, W., Fan, S., Jiang, L., Xu, Z., Kong, F., Zhang, D., et al. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv078 · Cited by 170 · see citing works

Expression of TaWRKY44, a wheat WRKY gene, in transgenic tobacco confers multiple abiotic stress tolerances

Wang, X., Zeng, J., Li, Y., Rong, X., Sun, J., Sun, T., Li, M., Wang, L., Feng, Y., Chai, R., et al. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00615 · Cited by 169 · see citing works

DRO 1 influences root system architecture in Arabidopsis and Prunus species

Guseman, J. M., Webb, K., Srinivasan, C., & Dardick, C. D. (2016) · The Plant Journal · doi:10.1111/tpj.13470 · Cited by 168 · see citing works

Performance of wheat genotypes under osmotic stress at germination and early seedling growth stage

Rauf, M., Munir, M., Hassan, M., Ahmad, M. I., & Afzal, M. (2007) · AFRICAN JOURNAL OF BIOTECHNOLOGY · doi:10.5897/ajb2007.000-2119 · Cited by 165 · see citing works

TOPLESS mediates brassinosteroid-induced transcriptional repression through interaction with BZR1

Oh, E., Zhu, J.-Y., Ryu, H., Hwang, I., & Wang, Z. (2014) · Nature Communications · doi:10.1038/ncomms5140 · Cited by 162 · see citing works

A wheat salinity-induced WRKY transcription factor TaWRKY93 confers multiple abiotic stress tolerance in Arabidopsis thaliana

Qin, Y., Tian, Y., & Liu, X. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.06.128 · Cited by 161 · see citing works

A TFIIIA-type zinc finger protein confers multiple abiotic stress tolerances in transgenic rice (Oryza sativa L.)

Huang, J., Sun, S., Xu, D., Lan, H., Sun, H., Wang, Z., Bao, Y., Wang, J., Tang, H., & Zhang, H. (2012) · Plant Molecular Biology · doi:10.1007/s11103-012-9955-5 · Cited by 152 · see citing works

Transcriptomics Analyses Reveal Wheat Responses to Drought Stress during Reproductive Stages under Field Conditions

Ma, J., Li, R., Wang, H., Li, D., Wang, X., Zhang, Y., Zhen, W., Duan, H., Yan, G., & Li, Y. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00592 · Cited by 149 · see citing works

Relationships between ash content, carbon isotope discrimination and yield in durum wheat

Araus, J. L., Amaro, T., Casadesús, J., Asbati, A., & Nachit, M. M. (1998) · Australian Journal of Plant Physiology · doi:10.1071/pp98071 · Cited by 148 · see citing works

Transcriptome pathways unique to dehydration tolerant relatives of modern wheat

Ergen, N. Z., Thimmapuram, J., Bohnert, H. J., & Budak, H. (2009) · Functional & Integrative Genomics · doi:10.1007/s10142-009-0123-1 · Cited by 146 · see citing works

Discovery and expression profile analysis of AP2/ERF family genes from Triticum aestivum

Zhuang, J., Chen, J.-M., Yao, Q., Xiong, F., ChaoCai, S., Zhou, X., Zhang, J., & Xiong, A. (2010) · Molecular Biology Reports · doi:10.1007/s11033-010-0162-7 · Cited by 141 · see citing works

Photosynthetic characteristics and enzymatic antioxidant capacity of leaves from wheat cultivars exposed to drought

Huseynova, I. M. (2012) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2012.02.037 · Cited by 136 · see citing works

The evolution of nuclear auxin signalling

Paponov, I. A., Teale, W., Lang, D., Paponov, M., Ralf Reski, A., Rensing, S. A., & Palme, K. J. (2009) · BMC Evolutionary Biology · doi:10.1186/1471-2148-9-126 · Cited by 131 · see citing works

GsZFP1, a new Cys2/His2-type zinc-finger protein, is a positive regulator of plant tolerance to cold and drought stress

Luo, X., Bai, X., Zhu, D., Li, Y., Ji, W., Cai, H., Wu, J., Liu, B., & Zhu, Y. (2011) · Planta · doi:10.1007/s00425-011-1563-0 · Cited by 119 · see citing works

Genetic association of stomatal traits and yield in wheat grown in low rainfall environments

Shahinnia, F., Roy, J. L., Laborde, B., Sznajder, B., Kalambettu, P., Mahjourimajd, S., Tilbrook, J., & Fleury, D. (2016) · BMC Plant Biology · doi:10.1186/s12870-016-0838-9 · Cited by 114 · see citing works

Dominant Repression by Arabidopsis Transcription Factor MYB44 Causes Oxidative Damage and Hypersensitivity to Abiotic Stress

Persak, H., & Pitzschke, A. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15022517 · Cited by 113 · see citing works

Overexpression of the Wheat Expansin Gene TaEXPA2 Improved Seed Production and Drought Tolerance in Transgenic Tobacco Plants

Chen, Y., Han, Y., Zhang, M., Zhou, S., Kong, X., & Wang, W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0153494 · Cited by 105 · see citing works

EAR motif mutation of rice OsERF3 alters the regulation of ethylene biosynthesis and drought tolerance

Zhang, H., Zhang, J., Quan, R., Pan, X., Wan, L., & Huang, R. (2013) · Planta · doi:10.1007/s00425-013-1852-x · Cited by 104 · see citing works

A novel ERF transcription activator in wheat and its induction kinetics after pathogen and hormone treatments

Zhang, Z., Yao, W., Dong, N., Liang, H., Liu, H., & Huang, R. (2007) · Journal of Experimental Botany · doi:10.1093/jxb/erm151 · Cited by 101 · see citing works

A D53 repression motif induces oligomerization of TOPLESS corepressors and promotes assembly of a corepressor-nucleosome complex

Ma, H., Duan, J., Ke, J., He, Y., Gu, X., Xu, T.-H., Yu, H. J., Wang, Y., Brunzelle, J. S., Jiang, Y., et al. (2017) · Science Advances · doi:10.1126/sciadv.1601217 · Cited by 100 · see citing works

Genetic Yield Gains of the CIMMYT International Semi‐Arid Wheat Yield Trials from 1994 to 2010

Manès, Y., Gomez, H. F., Puhl, L. E., Reynolds, M. P., Braun, H., & Trethowan, R. M. (2012) · Crop Science · doi:10.2135/cropsci2011.10.0574 · Cited by 98 · see citing works

QTL mapping for nine drought-responsive agronomic traits in bread wheat under irrigated and rain-fed environments

Gahlaut, V., Jaiswal, V., Tyagi, B. S., Singh, G. P., Sareen, S., Balyan, H. S., & Gupta, P. K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182857 · Cited by 96 · see citing works

Genome-Wide Investigation of WRKY Transcription Factors Involved in Terminal Drought Stress Response in Common Bean

Wu, J., Chen, J., Wang, L., & Wang, S. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00380 · Cited by 95 · see citing works

Comparative proteomics illustrates the complexity of drought resistance mechanisms in two wheat (Triticum aestivum L.) cultivars under dehydration and rehydration

Cheng, L., Wang, Y., He, Q., Li, H., Zhang, X., & Zhang, F. (2016) · BMC Plant Biology · doi:10.1186/s12870-016-0871-8 · Cited by 94 · see citing works

Genome-Wide Identification and Expression Analysis of WRKY Transcription Factors under Multiple Stresses in Brassica napus

He, Y., Mao, S., Gao, Y., Zhu, L., Wu, D., Cui, Y., Li, J., & Qian, W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0157558 · Cited by 90 · see citing works

Transcriptome analysis of drought-responsive genes regulated by hydrogen sulfide in wheat (Triticum aestivum L.) leaves

Li, H., Li, M., Wei, X., Zhang, X., Xue, R., Zhao, Y., & Zhao, H. (2017) · Molecular Genetics and Genomics · doi:10.1007/s00438-017-1330-4 · Cited by 90 · see citing works

Conservative water use under high evaporative demand associated with smaller root metaxylem and limited trans-membrane water transport in wheat

Schoppach, R., Wauthelet, D., Jeanguenin, L., & Sadok, W. (2013) · Functional Plant Biology · doi:10.1071/fp13211 · Cited by 87 · see citing works

Variation for stomatal characteristics and water use efficiency among diploid, tetraploid and hexaploid Iranian wheat landraces

Khazaeı, H., Monneveux, P., Hongbo, S., & Mohammady-D, S. (2009) · Genetic Resources and Crop Evolution · doi:10.1007/s10722-009-9471-x · Cited by 87 · see citing works

Dissecting the old Mediterranean durum wheat genetic architecture for phenology, biomass and yield formation by association mapping and QTL meta-analysis

Soriano, J. M., Malosetti, M., Roselló, M., Sorrells, M. E., & Royo, C. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178290 · Cited by 86 · see citing works

QTL mapping for yield and photosynthetic related traits under different water regimes in wheat

Xu, Y.-F., Li, S.-S., Li, L.-H., Ma, F., Fu, X.-Y., Shi, Z.-L., Xu, H., Ma, P., & An, D.-G. (2017) · Molecular breeding · doi:10.1007/s11032-016-0583-7 · Cited by 81 · see citing works

Transcriptional Repression: Conserved and Evolved Features

Payankaulam, S., Li, L. M., & Arnosti, D. N. (2010) · Current Biology · doi:10.1016/j.cub.2010.06.037 · Cited by 79 · see citing works

Physiology in the production and improvement of cereals.

Sylvester-Bradley, R., Scott, R. K., & Wright, C. E. (1990) · OpenGrey (Institut de l'Information Scientifique et Technique) · Cited by 77 · see citing works

Overexpression ofAtERF019delays plant growth and senescence and improves drought tolerance in Arabidopsis

Scarpeci, T. E., Frea, V. S., Zanor, M. I., & Valle, E. M. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw429 · Cited by 72 · see citing works

Mapping QTL for Root and Shoot Morphological Traits in a Durum Wheat × T. dicoccumSegregating Population at Seedling Stage

Iannucci, A., Marone, D., Russo, M. A., Vita, P. D., Miullo, V., Ferragonio, P., Blanco, A., Gadaleta, Á., & Mastrangelo, A. M. (2017) · International Journal of Genomics · doi:10.1155/2017/6876393 · Cited by 69 · see citing works

Ectopic expression of an EAR motif deletion mutant of SlERF3 enhances tolerance to salt stress and Ralstonia solanacearum in tomato

Pan, I.-C., Li, C.-W., Su, R., Cheng, C., Lin, C., & Chan, M. (2010) · Planta · doi:10.1007/s00425-010-1235-5 · Cited by 66 · see citing works

Overexpression of wheat geneTaMORimproves root system architecture and grain yield inOryza sativa

Li, B., Liu, D., Li, Q., Mao, X., Li, A., Wang, J., Chang, X., & Jing, R. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw193 · Cited by 63 · see citing works

Ancestral QTL Alleles from Wild Emmer Wheat Enhance Root Development under Drought in Modern Wheat

Merchuk-Ovnat, L., Fahima, T., Ephrath, J. E., Krugman, T., & Saranga, Y. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00703 · Cited by 63 · see citing works

SlERF36, an EAR-motif-containing ERF gene from tomato, alters stomatal density and modulates photosynthesis and growth

Upadhyay, R. K., Soni, D. K., Singh, R., Dwivedi, U. N., Pathre, U. V., Nath, P., & Sane, A. P. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert162 · Cited by 61 · see citing works

Breeding for Yield Potential has Increased Deep Soil Water Extraction Capacity in Irrigated Wheat

Pask, A., & Reynolds, M. (2013) · Crop Science · doi:10.2135/cropsci2013.01.0011 · Cited by 60 · see citing works

The Solanum lycopersicum Zinc Finger2 Cysteine-2/Histidine-2 Repressor-Like Transcription Factor Regulates Development and Tolerance to Salinity in Tomato and Arabidopsis

Hichri, I., Muhovski, Y., Žižková, E., Dobrev, P. I., Franco‐Zorrilla, J. M., Solano, R., López‐Vidriero, I., Motyka, V., & Lutts, S. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.225920 · Cited by 60 · see citing works

A transcriptional repressor of the ERF family confers drought tolerance to rice and regulates genes preferentially located on chromosome 11

Joo, J., Choi, H. J., Lee, Y. H., Kim, Y.-K., & Song, S. I. (2013) · Planta · doi:10.1007/s00425-013-1880-6 · Cited by 57 · see citing works

Physiological and transcriptome analysis of He-Ne laser pretreated wheat seedlings in response to drought stress

Qiu, Z., Yuan, M., He, Y., Li, Y.-F., & Zhang, L. (2017) · Scientific Reports · doi:10.1038/s41598-017-06518-z · Cited by 57 · see citing works

Comprehensive Functional Analyses of Expressed Sequence Tags in Common Wheat (Triticum aestivum)

Manickavelu, A., Kawaura, K., Oishi, K., Shin‐I, T., Kohara, Y., Yahiaoui, N., Keller, B., Abe, R., Suzuki, A., Nagayama, T., et al. (2012) · DNA Research · doi:10.1093/dnares/dss001 · Cited by 55 · see citing works

Wheat WRKY Type Transcription Factor Gene TaWRKY1 is Essential in Mediating Drought Tolerance Associated with an ABA-Dependent Pathway

Ding, W., Fang, W., Shi, S., Zhao, Y., Li, X., & Xiao, K. (2016) · Plant Molecular Biology Reporter · doi:10.1007/s11105-016-0991-1 · Cited by 52 · see citing works

Change of function of the wheat stress‐responsive transcriptional repressor Ta RAP 2.1L by repressor motif modification

Amalraj, A., Luang, S., Yadav, M. K., Sornaraj, P., Eini, O., Kovalchuk, N., Bazanova, N., Li, Y., Yang, N., Eliby, S., et al. (2015) · Plant Biotechnology Journal · doi:10.1111/pbi.12432 · Cited by 50 · see citing works

Abiotic stress upregulated TaZFP34 represses the expression of type-B response regulator and SHY2 genes and enhances root to shoot ratio in wheat

Chang, H., Chen, D., Kam, J., Richardson, T. M., Drenth, J., Guo, X., McIntyre, C. L., Chai, S., Rae, A. L., & Xue, G. (2016) · Plant Science · doi:10.1016/j.plantsci.2016.07.011 · Cited by 50 · see citing works

Genome wide identification of C1-2i zinc finger proteins and their response to abiotic stress in hexaploid wheat

Cheuk, A., & Houde, M. (2015) · Molecular Genetics and Genomics · doi:10.1007/s00438-015-1152-1 · Cited by 47 · see citing works

Identification and validation of root length QTLs for water stress resistance in hexaploid wheat (Titicum aestivum L.)

Ayalew, H., Liu, H., & Yan, G. (2017) · Euphytica · doi:10.1007/s10681-017-1914-4 · Cited by 47 · see citing works

Transcriptomic and proteomic analyses of a pale-green durum wheat mutant shows variations in photosystem components and metabolic deficiencies under drought stress

Peremartí, A., Marè, C., Aprile, A., Roncaglia, E., Cattivelli, L., Villegas, D., & Royo, C. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-125 · Cited by 43 · see citing works

Water-deficit stress-responsive microRNAs and their targets in four durum wheat genotypes

Liu, H., Able, A. J., & Able, J. A. (2016) · Functional & Integrative Genomics · doi:10.1007/s10142-016-0515-y · Cited by 42 · see citing works

High-throughput SNP genotyping of modern and wild emmer wheat for yield and root morphology using a combined association and linkage analysis

Lucas, S. J., Salantur, A., Yazar, S., & Budak, H. (2017) · Functional & Integrative Genomics · doi:10.1007/s10142-017-0563-y · Cited by 34 · see citing works

Small yet effective

Kagale, S., & Rozwadowski, K. L. (2010) · Plant Signaling & Behavior · doi:10.4161/psb.5.6.11576 · Cited by 33 · see citing works

Genome-Wide Associations for Water-Soluble Carbohydrate Concentration and Relative Maturity in Wheat Using SNP and DArT Marker Arrays

Ovenden, B. W., Milgate, A., Wade, L. J., Rebetzke, G. J., & Holland, J. B. (2017) · G3 Genes Genomes Genetics · doi:10.1534/g3.117.039842 · Cited by 32 · see citing works

QTLs for cell wall-bound phenolics in relation to the photosynthetic apparatus activity and leaf water status under drought stress at different growth stages of triticale

Hura, T., Tyrka, M., Hura, K., Ostrowska, A., & Dziurka, K. (2016) · Molecular Genetics and Genomics · doi:10.1007/s00438-016-1276-y · Cited by 30 · see citing works

The EAR Motif Controls the Early Flowering and Senescence Phenotype Mediated by Over-Expression of SlERF36 and Is Partly Responsible for Changes in Stomatal Density and Photosynthesis

Upadhyay, R. K., Gupta, A., Ranjan, S., Singh, R., Pathre, U. V., Nath, P., & Sane, A. P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101995 · Cited by 28 · see citing works

TaER Expression Is Associated with Transpiration Efficiency Traits and Yield in Bread Wheat

Zheng, J., Yang, Z., Madgwick, P. J., Carmo‐Silva, E., Parry, M. A. J., & Hu, Y.-G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0128415 · Cited by 27 · see citing works

Altered gene expression by sedaxane increases PSII efficiency, photosynthesis and growth and improves tolerance to drought in wheat seedlings

Ajigboye, O. O., Lu, C., Murchie, E. H., Schlatter, C., Swart, G., & Ray, R. V. (2016) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2016.09.008 · Cited by 27 · see citing works

Quantitative Trait Loci Associated with Drought Tolerance in Brachypodium distachyon

Jiang, Y., Wang, X., Yu, X., Zhao, X., Luo, N., Pei, Z., Liu, H., & Garvin, D. F. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00811 · Cited by 27 · see citing works

Identification of quantitative trait loci for seedling root traits from Tibetan semi-wild wheat (Triticum aestivum subsp. tibetanum)

Ma, J., Luo, W., Zhang, H., Zhou, X.-H., Qin, N., Wei, Y., Liu, Y., Jiang, Q., Chen, G., Zheng, Y., et al. (2017) · Genome · doi:10.1139/gen-2017-0097 · Cited by 27 · see citing works

Engineering drought and salt tolerance in plants using SodERF3, a novel sugarcane ethylene responsive factor

Trujillo, L. E., Menéndez, C., Ochagavia, M. E., Hernández, I. M., Borrás, O., Rodríguez, R., Coll, Y., Arrieta, J. G., Banguela‐Castillo, A., Ramírez, R., et al. (2009) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 26 · see citing works

Identification of drought stress related proteins from 1Sl(1B) chromosome substitution line of wheat variety Chinese Spring

Zhou, J., Ma, C., Zhen, S., Cao, M., Zeller, F. J., Hsam, S. L. K., & Yan, Y. (2016) · Botanical studies · doi:10.1186/s40529-016-0134-x · Cited by 26 · see citing works

Isolation and characterization of a novel transcriptional repressor GmERF6 from soybean

Zhai, Y., Li, J. W., Li, X. W., Lei, T., Yan, F., Zhao, Y., Li, Y., Su, L., Wang, Y., & Wang, Q. Y. (2012) · Biologia Plantarum · doi:10.1007/s10535-012-0146-7 · Cited by 22 · see citing works

Selection For Flag Leaf Stomatal Frequency In Bread Wheat

Bkagwat, S. G., & Bhatia, C. R. (1993) · Plant Breeding · doi:10.1111/j.1439-0523.1993.tb01224.x · Cited by 18 · see citing works

Morpho-physiological characterization of spring wheat genotypes under drought stress

Baloch, M. J., Dunwell, J. M., Khan, N. U., Jatoi, W. A., Khakhwani, A. A., Veesar, N. F., & Gul, S. (2013) · CentAUR (University of Reading) · Cited by 15 · see citing works

PpERF3b, a transcriptional repressor from peach, contributes to disease susceptibility and side branching in EAR-dependent and -independent fashions

Sherif, S. M., El‐Sharkawy, I., Paliyath, G., & Jayasankar, S. (2013) · Plant Cell Reports · doi:10.1007/s00299-013-1405-6 · Cited by 15 · see citing works

Response to water deficit in glume of wheat: expression profiling by microarray analysis

Liu, C., Mi, H., Liu, H., Xie, S., Wu, Y., Ning, P., Liang, T., & Lv, J. (2016) · Euphytica · doi:10.1007/s10681-016-1827-7 · Cited by 14 · see citing works

Association mapping for photosynthesis and yield traits under two moisture conditions and their drought indices in winter bread wheat (Triticum aestivum L.) using SSR markers

Iqbal, S., NIFA, P. B. 4., Chen, X., Daoura, B. G., Chen, L., & Hu, Y. (2017) · Australian Journal of Crop Science · doi:10.21475/ajcs.17.11.03.pne252 · Cited by 13 · see citing works

Association Mapping of Root Traits for Drought Tolerance in Bread Wheat

Ahmad, I., Ali, N., Ahmad, H., & Inamullah (2017) · InTech eBooks · doi:10.5772/67242 · Cited by 11 · see citing works

Physiological Responses of Two Wheat Cultivars to Soil Drought

Chipilski, R. R., Kocheva, K. V., Nenova, V. R., & Georgiev, G. (2012) · Zeitschrift für Naturforschung C · doi:10.1515/znc-2012-3-410 · Cited by 10 · see citing works

QTL Mapping for Early Ground Cover in Wheat (Triticum aestivum L.) under Drought Stress

Mondal, B., Singh, A., Yadav, A., Tomar, R. S. S., Vinod, V., Singh, G. P., & Prabhu, K. V. (2017) · Current Science · doi:10.18520/cs/v112/i06/1266-1271 · Cited by 10 · see citing works

Isolation and characterization of ERECTA genes and their expression patterns in common wheat (Triticum aestivum L.)

Huang, L., Yasir, T. A., Phillips, A. L., & Hu, Y. (2013) · Rothamsted Repository (Rothamsted Repository) · Cited by 9 · see citing works

Physiological Responses of Two Wheat Cultivars to Soil Drought

Chipilski, R. R., Kochev, K. V., Nenova, V. R., & Georgiev, G. (2012) · Zeitschrift für Naturforschung C · doi:10.5560/znc.2012.67c0181 · Cited by 9 · see citing works

Genetic Dissection of Stem Water-Soluble Carbohydrates and Agronomic Traits in Wheat under Different Water Regimes

Khan, N. I., Chang, X., & Jing, R. (2017) · Journal of Agricultural Science · doi:10.5539/jas.v9n3p42 · Cited by 7 · see citing works

AP2/ERF Transcription Factor Regulatory Networks in Hormone and Abiotic Stress Responses in Arabidopsis

Xie, Z., Nolan, T. M., Jiang, H., & Yin, Y. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00228 · Cited by 763 · see citing works

Heat and Drought Stresses in Crops and Approaches for Their Mitigation

Lamaoui, M., Jemo, M., Datla, R. S. S., & Bekkaoui, F. (2018) · Frontiers in Chemistry · doi:10.3389/fchem.2018.00026 · Cited by 752 · see citing works

Plant Transcription Factors Involved in Drought and Associated Stresses

Hrmová, M., & Hussain, S. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115662 · Cited by 238 · see citing works

Responses of root system architecture to water stress at multiple levels: A meta-analysis of trials under controlled conditions

Kou, X., Han, W., & Kang, J. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1085409 · Cited by 223 · see citing works

MdMYB88 and MdMYB124 Enhance Drought Tolerance by Modulating Root Vessels and Cell Walls in Apple

Geng, D., Chen, P., Shen, X., Zhang, Y., Li, X., Jiang, L., Xie, Y., Niu, C., Zhang, J., Huang, X., et al. (2018) · PLANT PHYSIOLOGY · doi:10.1104/pp.18.00502 · Cited by 208 · see citing works

Root system architecture in cereals: progress, challenges and perspective

Maqbool, S., Hassan, M. A., Xia, X., York, L. M., Rasheed, A., & He, Z. (2022) · The Plant Journal · doi:10.1111/tpj.15669 · Cited by 210 · see citing works

Is Silicon a Panacea for Alleviating Drought and Salt Stress in Crops?

Thorne, S. J., Hartley, S. E., & Maathuis, F. J. M. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.01221 · Cited by 198 · see citing works

Shaping the root system architecture in plants for adaptation to drought stress

Ranjan, A., Sinha, R., Singla-Pareek, S. L., Pareek, A., & Singh, A. K. (2022) · Physiologia Plantarum · doi:10.1111/ppl.13651 · Cited by 181 · see citing works

Genetic Improvement of Wheat for Drought Tolerance: Progress, Challenges and Opportunities

Bapela, T., Shimelis, H., Tsilo, T. J., & Mathew, I. (2022) · Plants · doi:10.3390/plants11101331 · Cited by 199 · see citing works

Genetic dissection of drought and heat‐responsive agronomic traits in wheat

Li, L., Mao, X., Wang, J., Chang, X., Reynolds, M. P., & Jing, R. (2019) · Plant Cell & Environment · doi:10.1111/pce.13577 · Cited by 170 · see citing works

Addressing Research Bottlenecks to Crop Productivity

Reynolds, M. P., Atkin, O. K., Bennett, M. J., Cooper, M., Dodd, I. C., Foulkes, J. M., Frohberg, C., Hammer, G., Henderson, I. R., Huang, B., et al. (2021) · Trends in Plant Science · doi:10.1016/j.tplants.2021.03.011 · Cited by 177 · see citing works

Understanding role of roots in plant response to drought: Way forward to climate‐resilient crops

Kalra, A., Goel, S., & Elias, A. A. (2023) · The Plant Genome · doi:10.1002/tpg2.20395 · Cited by 149 · see citing works

Advances in Wheat Physiology in Response to Drought and the Role of Plant Growth Promoting Rhizobacteria to Trigger Drought Tolerance

Camaille, M., Fabre, N., Clément, C., & Barka, E. A. (2021) · Microorganisms · doi:10.3390/microorganisms9040687 · Cited by 149 · see citing works

Alleviation of drought and salt stress in vegetables: crop responses and mitigation strategies

Khalid, M. F., Huda, S., Yong, M., Li, L., Li, L., Chen, Z., & Ahmed, T. A.-F. (2022) · Plant Growth Regulation · doi:10.1007/s10725-022-00905-x · Cited by 125 · see citing works

Stress responsive gene regulation in relation to hydrogen sulfide in plants under abiotic stress

Pandey, A. K., & Gautam, A. (2020) · Physiologia Plantarum · doi:10.1111/ppl.13064 · Cited by 118 · see citing works

Recognizing the hidden half in wheat: root system attributes associated with drought tolerance

Li, C., Li, L., Reynolds, M. P., Wang, J., Chang, X., Mao, X., & Jing, R. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab124 · Cited by 114 · see citing works

Root system architecture, physiological and transcriptional traits of soybean ( Glycine max L.) in response to water deficit: A review

Xiong, R., Liu, S., Considine, M. J., Siddique, K. H. M., Lam, H., & Chen, Y. (2020) · Physiologia Plantarum · doi:10.1111/ppl.13201 · Cited by 111 · see citing works

Phenotypic variability in bread wheat root systems at the early vegetative stage

Chen, Y., Palta, J. A., Prasad, P. V. V., & Siddique, K. H. M. (2020) · BMC Plant Biology · doi:10.1186/s12870-020-02390-8 · Cited by 101 · see citing works

Profiling, isolation and characterisation of beneficial microbes from the seed microbiomes of drought tolerant wheat

Hone, H., Mann, R. C., Yang, G., Kaur, J. P., Tannenbaum, I., Li, T., SPANGENBERG, G. C., & Sawbridge, T. (2021) · Scientific Reports · doi:10.1038/s41598-021-91351-8 · Cited by 97 · see citing works

Barley with improved drought tolerance: Challenges and perspectives

Elakhdar, A., Solanki, S., Kubo, T., Abed, A., El-Akhdar, I., Khedr, R., Hamwieh, A., Capo-chichi, L. J. A., Abdelsattar, M., Franckowiak, J. D., et al. (2022) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2022.104965 · Cited by 127 · see citing works

Engineering drought tolerance in plants through CRISPR/Cas genome editing

Joshi, R. K., Bharat, S. S., & Mishra, R. (2020) · 3 Biotech · doi:10.1007/s13205-020-02390-3 · Cited by 96 · see citing works

Photosynthetic and ascorbate-glutathione metabolism in the flag leaves as compared to spikes under drought stress of winter wheat (Triticum aestivum L.)

Lou, L., Li, X., Chen, J., Li, Y., Tang, Y., & Lv, J. (2018) · PLoS ONE · doi:10.1371/journal.pone.0194625 · Cited by 92 · see citing works

Genome-Wide Identification and Analysis of the AP2 Transcription Factor Gene Family in Wheat (Triticum aestivum L.)

Zhao, Y., Ma, R., Xu, D., Bi, H., Xia, Z., & Peng, H. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01286 · Cited by 73 · see citing works

High-Temperature and Drought Stress Effects on Growth, Yield and Nutritional Quality with Transpiration Response to Vapor Pressure Deficit in Lentil

Haddad, N. E., Choukri, H., Ghanem, M. E., Smouni, A., Mentag, R., Rajendran, K., Hejjaoui, K., Maalouf, F., & Kumar, S. (2021) · Plants · doi:10.3390/plants11010095 · Cited by 73 · see citing works

Effective Use of Water in Crop Plants in Dryland Agriculture: Implications of Reactive Oxygen Species and Antioxidative System

Rane, J., Singh, A. K., Tiwari, M., Prasad, P. V. V., & Jagadish, S. V. K. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2021.778270 · Cited by 72 · see citing works

Variation Among Spring Wheat (Triticum aestivum L.) Genotypes in Response to the Drought Stress. II—Root System Structure

Grzesiak, M. T., Hordyńska, N., Maksymowicz, A., Grzesiak, S., & Szechyńska‐Hebda, M. (2019) · Plants · doi:10.3390/plants8120584 · Cited by 69 · see citing works

Major genomic regions responsible for wheat yield and its components as revealed by meta-QTL and genotype–phenotype association analyses

Liu, H., Mullan, D. J., Zhang, C., Zhao, S., Li, X., Zhang, A., Lu, Z., Wang, Y., & Yan, G. (2020) · Planta · doi:10.1007/s00425-020-03466-3 · Cited by 68 · see citing works

Physiological, Biochemical and Molecular Response of Different Winter Wheat Varieties under Drought Stress at Germination and Seedling Growth Stage

Vuković, R., Čamagajevac, I. Š., Vuković, A., Šunić, K., Begović, L., Mlinarić, S., Sekulić, R., Sabo, N., & Španić, V. (2022) · Antioxidants · doi:10.3390/antiox11040693 · Cited by 73 · see citing works

Genome-Wide Association Studies Reveal Genomic Regions Associated With the Response of Wheat (Triticum aestivum L.) to Mycorrhizae Under Drought Stress Conditions

Lehnert, H., Serfling, A., Friedt, W., & Ordon, F. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.01728 · Cited by 66 · see citing works

Ameliorating Drought Effects in Wheat Using an Exclusive or Co-Applied Rhizobacteria and ZnO Nanoparticles

Muhammad, F., Raza, M. A. S., Iqbal, R., Zulfiqar, F., Aslam, M. U., Yong, J. W. H., Altaf, M. A., Zulfiqar, B., Amin, J., & Ibrahim, M. A. (2022) · Biology · doi:10.3390/biology11111564 · Cited by 65 · see citing works

Comparative RNA-seq analysis of the drought-sensitive lentil (Lens culinaris) root and leaf under short- and long-term water deficits

Morgil, H., Tardu, M., Cevahir, G., & Kavaklı, İ. H. (2019) · Functional & Integrative Genomics · doi:10.1007/s10142-019-00675-2 · Cited by 64 · see citing works

Bottom-up perspective – The role of roots and rhizosphere in climate change adaptation and mitigation in agroecosystems

George, T., Bulgarelli, D., Carminati, A., Chen, Y., Jones, D. L., Kuzyakov, Y. V., Schnepf, A., Wissuwa, M., & Roose, T. (2024) · Plant and Soil · doi:10.1007/s11104-024-06626-6 · Cited by 61 · see citing works

Rice SnRK protein kinase OsSAPK8 acts as a positive regulator in abiotic stress responses

Zhong, R., Wang, Y., Gai, R., Xi, D., Mao, C., & Ming, F. (2019) · Plant Science · doi:10.1016/j.plantsci.2019.110373 · Cited by 58 · see citing works

Response of potato (Solanum tuberosum L.) cultivars to drought stress under in vitro and field conditions

Zaki, H. E. M., & Radwan, K. S. A. (2022) · Chemical and Biological Technologies in Agriculture · doi:10.1186/s40538-021-00266-z · Cited by 58 · see citing works

Genetic components of root architecture and anatomy adjustments to water‐deficit stress in spring barley

Oyiga, B. C., Palczak, J., Wojciechowski, T., Lynch, J. P., Naz, A. A., Léon, J., & Ballvora, A. (2019) · Plant Cell & Environment · doi:10.1111/pce.13683 · Cited by 58 · see citing works

Why Is the Correct Selection of Trichoderma Strains Important? The Case of Wheat Endophytic Strains of T. harzianum and T. simmonsii

Pedrero-Méndez, A., Insuasti, H. C., Neagu, T., Illescas, M., Rubio, M. B., Monte, E., & Hermosa, R. (2021) · Journal of Fungi · doi:10.3390/jof7121087 · Cited by 57 · see citing works

Functional phenomics and genetics of the root economics space in winter wheat using high‐throughput phenotyping of respiration and architecture

Guo, H., Ayalew, H., Seethepalli, A., Dhakal, K., Griffiths, M., Ma, X., & York, L. M. (2021) · New Phytologist · doi:10.1111/nph.17329 · Cited by 53 · see citing works

The MYB33 , MYB65 , and MYB101 transcription factors affect Arabidopsis and potato responses to drought by regulating the ABA signaling pathway

Wyrzykowska, A., Bielewicz, D., Plewka, P., Sołtys‐Kalina, D., Wasilewicz‐Flis, I., Marczewski, W., Jarmołowski, A., & Szweykowska-Kulińska, Z. (2022) · Physiologia Plantarum · doi:10.1111/ppl.13775 · Cited by 51 · see citing works

RNA-seq analysis reveals different drought tolerance mechanisms in two broadly adapted wheat cultivars ‘TAM 111’ and ‘TAM 112’

Chu, C., Wang, S., Paetzold, L., Wang, Z., Hui, K., Rudd, J. C., Xue, Q., Ibrahim, A. M. H., Metz, R. P., Johnson, C. D., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-83372-0 · Cited by 48 · see citing works

Effect of Trichoderma asperellum on Wheat Plants’ Biochemical and Molecular Responses, and Yield under Different Water Stress Conditions

Illescas, M., Morán-Diez, M. E., de Alba, Á. E. M., Hermosa, R., & Monte, E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126782 · Cited by 48 · see citing works

Transgenic solutions to increase yield and stability in wheat: shining hope or flash in the pan?

Araus, J. L., Serret, M. D., & Lopes, M. S. (2019) · Journal of Experimental Botany · doi:10.1093/jxb/erz077 · Cited by 46 · see citing works

Emerging applications of gene editing technologies for the development of climate-resilient crops

Chavhan, R. L., Jaybhaye, S. G., Hinge, V. R., Deshmukh, A. S., Shaikh, U. S., Jadhav, P. K., Kadam, U. S., & Hong, J. C. (2025) · Frontiers in Genome Editing · doi:10.3389/fgeed.2025.1524767 · Cited by 43 · see citing works

Transcription factors – Insights into abiotic and biotic stress resilience and crop improvement

Bhoite, R. N., Onyemaobi, O., Halder, T., Shankar, M., & Sharma, D. L. (2025) · Current Plant Biology · doi:10.1016/j.cpb.2025.100434 · Cited by 43 · see citing works

Bioprospecting the roles of Trichoderma in alleviating plants’ drought tolerance: Principles, mechanisms of action, and prospects

Akbari, S. I., Prismantoro, D., Permadi, N., Rossiana, N., Miranti, M., Mispan, M. S., Mohamed, Z., & Doni, F. (2024) · Microbiological Research · doi:10.1016/j.micres.2024.127665 · Cited by 42 · see citing works

Elucidating the Drought Responsiveness in Wheat Genotypes

Pandey, A., Khobra, R., Mamrutha, H. M., Wadhwa, Z., Krishnappa, G., Singh, G. P., & Singh, G. P. (2022) · Sustainability · doi:10.3390/su14073957 · Cited by 41 · see citing works

Transcriptomic analysis of drought stress responses of sea buckthorn (Hippophae rhamnoidessubsp. sinensis) by RNA-Seq

Ye, G., Ma, Y., Feng, Z., & Zhang, X. (2018) · PLoS ONE · doi:10.1371/journal.pone.0202213 · Cited by 41 · see citing works

Differentiate responses of tetraploid and hexaploid wheat (Triticum aestivum L.) to moderate and severe drought stress: a cue of wheat domestication

Gui, Y.-W., Sheteiwy, M. S. A., Zhu, S., Zhu, L., Batool, A., Jia, T., & Xiong, Y. (2020) · Plant Signaling & Behavior · doi:10.1080/15592324.2020.1839710 · Cited by 40 · see citing works

Exploring the Genetic Architecture of Root-Related Traits in Mediterranean Bread Wheat Landraces by Genome-Wide Association Analysis

Rufo, R., Salvi, S., Royo, C., & Soriano, J. M. (2020) · Agronomy · doi:10.3390/agronomy10050613 · Cited by 40 · see citing works

Genetic analyses of root traits: Implications for environmental adaptation and new variety development: A review

Mathew, I., & Shimelis, H. (2022) · Plant Breeding · doi:10.1111/pbr.13049 · Cited by 40 · see citing works

A systematic review on the role of miRNAs in plant response to stresses under the changing climatic conditions

Li, Z., Yang, J., Cai, X., Zeng, X., Zou, J., & Xing, W. (2024) · Plant Stress · doi:10.1016/j.stress.2024.100674 · Cited by 39 · see citing works

Integrated transcriptome and metabolome analysis revealed differential drought stress response mechanisms of wheat seedlings with varying drought tolerance

Guo, X., Lv, L., Zhao, A., Zhao, W., Liu, Y., Li, Z., Li, H., & Chen, X. (2025) · BMC Plant Biology · doi:10.1186/s12870-025-06603-w · Cited by 39 · see citing works

Plant Tolerance to Drought Stress with Emphasis on Wheat

Adel, S., & Carels, N. (2023) · Plants · doi:10.3390/plants12112170 · Cited by 37 · see citing works

Shaping Durum Wheat for the Future: Gene Expression Analyses and Metabolites Profiling Support the Contribution of BCAT Genes to Drought Stress Response

Buffagni, V., Vurro, F., Janni, M., Gullì, M., Keller, A. A., & Marmiroli, N. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00891 · Cited by 37 · see citing works

Assessment of the Biochemical Responses of Wheat Seedlings to Soil Drought after Application of Selective Herbicide

Todorova, D., Sergiev, I., Katerova, Z., Shopova, E., Dimitrova, L., & Brankova, L. (2021) · Plants · doi:10.3390/plants10040733 · Cited by 36 · see citing works

The potassium transporter TaNHX2 interacts with TaGAD1 to promote drought tolerance via modulating stomatal aperture in wheat

Li, J., Liu, X., Chang, S., Chu, W., Lin, J., Zhou, H., Hu, Z., Zhang, M., Xin, M., Yao, Y., et al. (2024) · Science Advances · doi:10.1126/sciadv.adk4027 · Cited by 35 · see citing works

Approaches and determinants to sustainably improve crop production

Gojon, A., Nussaume, L., Luu, D., Murchie, E. H., Baekelandt, A., Saltenis, V. L. R., Cohan, J., Desnos, T., Inzé, D., Ferguson, J. N., et al. (2022) · Food and Energy Security · doi:10.1002/fes3.369 · Cited by 35 · see citing works

Transcriptome unveiled the gene expression patterns of root architecture in drought-tolerant and sensitive wheat genotypes

Rasool, F., Khan, M. R., Schneider, M. C., Uzair, M., Aqeel, M., Ajmal, W., Léon, J., & Naz, A. A. (2022) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2022.02.025 · Cited by 34 · see citing works

Genetic approaches to exploit landraces for improvement of Triticum turgidum ssp. durum in the age of climate change

Broccanello, C., Bellin, D., DalCorso, G., Furini, A., & Taranto, F. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1101271 · Cited by 37 · see citing works

Comprehensive genomic survey, structural classification and expression analysis of C2H2-type zinc finger factor in wheat (Triticum aestivum L.)

Li, Y., Sun, A., Wu, Q. J., Zou, X., Chen, F., Cai, R., Xie, H., Zhang, M., & Guo, X. (2021) · BMC Plant Biology · doi:10.1186/s12870-021-03016-3 · Cited by 34 · see citing works

Analysis of transcriptional responses in root tissue of bread wheat landrace (Triticum aestivum L.) reveals drought avoidance mechanisms under water scarcity

Chaichi, M., Sanjarian, F., Razavi, K., & González-Hernández, J. L. (2019) · PLoS ONE · doi:10.1371/journal.pone.0212671 · Cited by 34 · see citing works

Silicon improves root system and canopy physiology in wheat under drought stress

Ashfaq, W., Brodie, G. I., Fuentes, S., Pang, A., & Gupta, S. (2023) · Plant and Soil · doi:10.1007/s11104-023-06202-4 · Cited by 32 · see citing works

Genome-wide association mapping of genomic regions associated with drought stress tolerance at seedling and reproductive stages in bread wheat

Reddy, S. S., Saini, D. K., Singh, G., Sharma, S., Mishra, V. K., & Joshi, A. K. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1166439 · Cited by 29 · see citing works

OsSCL30 overexpression reduces the tolerance of rice seedlings to low temperature, drought and salt

Zhang, J., Sun, Y., Zhou, Z., Zhang, Y., Yang, Y., Zan, X., Li, X., Wan, J., Gao, X., Chen, R., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-12438-4 · Cited by 28 · see citing works

Physiological, biochemical and molecular responses of finger millet (Eleusine coracana) genotypes exposed to short-term drought stress induced by PEG-6000

Rakkammal, K., Maharajan, T., Shriram, R. N., Ram, P. S. J., Ceasar, S. A., & Ramesh, M. (2023) · South African Journal of Botany · doi:10.1016/j.sajb.2023.01.053 · Cited by 27 · see citing works

Association mapping unravels the genetics controlling seedling drought stress tolerance in winter wheat

Schierenbeck, M., Alqudah, A. M., Thabet, S. G., Lohwasser, U., Simón, M. R., & Börner, A. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1061845 · Cited by 27 · see citing works

Comparative Analysis of the Transcriptional Response of Tolerant and Sensitive Wheat Genotypes to Drought Stress in Field Conditions

Lv, S., Feng, K., Peng, S., Wang, J., Zhang, Y., Bian, J., & Nie, X. (2018) · Agronomy · doi:10.3390/agronomy8110247 · Cited by 26 · see citing works

Root transcriptome profiling of contrasting wheat genotypes provides an insight to their adaptive strategies to water deficit

Mia, M. S., Liu, H., Wang, X., Zhang, C., & Yan, G. (2020) · Scientific Reports · doi:10.1038/s41598-020-61680-1 · Cited by 26 · see citing works

Insight of transcriptional regulators reveals the tolerance mechanism of carpet-grass (Axonopus compressus) against drought

Nawaz, M., Liao, L., Azeem, F., Shabbir, S., Zohaib, A., Ashraf, U., Yang, H., & Wang, Z. (2021) · BMC Plant Biology · doi:10.1186/s12870-021-02844-7 · Cited by 26 · see citing works

Morpho-Physiological and Hormonal Response of Winter Wheat Varieties to Drought Stress at Stem Elongation and Anthesis Stages

Duvnjak, J., Lončarić, A., Brkljačić, L., Šamec, D., Šarčević, H., Salopek‐Sondi, B., & Španić, V. (2023) · Plants · doi:10.3390/plants12030418 · Cited by 29 · see citing works

Drought in acid soil increases aluminum toxicity especially of the Al-sensitive wheat

Siecińska, J., Wiącek, D., Przysucha, B., & Nosalewicz, A. (2019) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2019.06.007 · Cited by 25 · see citing works

Drought stress tolerance mechanisms and their potential common indicators to salinity, insights from the wild watermelon (Citrullus lanatus): A review

Malambane, G., Madumane, K., Sewelo, L. T., & Batlang, U. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1074395 · Cited by 25 · see citing works

Enhancing crop resilience: Understanding the role of drought priming in wheat stress response

Wang, X., Ge, J., He, M., Li, Q., Cai, J., Zhou, Q., Zhong, Y., Wollenweber, B., & Jiang, D. (2023) · Field Crops Research · doi:10.1016/j.fcr.2023.109083 · Cited by 25 · see citing works

Enhancing Wheat Growth, Physiology, Yield, and Water Use Efficiency under Deficit Irrigation by Integrating Foliar Application of Salicylic Acid and Nutrients at Critical Growth Stages

El-Hendawy, S., Mohammed, N. A., & Al-Suhaibani, N. (2024) · Plants · doi:10.3390/plants13111490 · Cited by 24 · see citing works

A review on applications of plant network biology to understand the drought stress response in economically important cereal crops

Thanmalagan, R. R., Jayaprakash, A., Roy, A. D., Annamalai, A., & Lakshmi, P. T. V. (2021) · Plant Gene · doi:10.1016/j.plgene.2021.100345 · Cited by 24 · see citing works

UAV‐based RGB imagery and ground measurements for high‐throughput phenotyping of senescence and QTL mapping in bread wheat

Li, L., Hassan, M. A., Song, J., Xie, Y., Rasheed, A., Yang, S., Li, H., Liu, P., Xia, X., He, Z., et al. (2023) · Crop Science · doi:10.1002/csc2.21086 · Cited by 24 · see citing works

Exploring the Genotype-Dependent Toolbox of Wheat under Drought Stress

Vassileva, V., Georgieva, M. S., Zehirov, G., & Dimitrova, A. (2023) · Agriculture · doi:10.3390/agriculture13091823 · Cited by 23 · see citing works

Comparing transcriptional responses to Fusarium crown rot in wheat and barley identified an important relationship between disease resistance and drought tolerance

Su, Z., Powell, J. J., Gao, S., Zhou, M., & Liu, C. (2021) · BMC Plant Biology · doi:10.1186/s12870-020-02818-1 · Cited by 22 · see citing works

Transcriptome Analyses of Near Isogenic Lines Reveal Putative Drought Tolerance Controlling Genes in Wheat

Nouraei, S., Mia, M. S., Liu, H., Turner, N. C., & Yan, G. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.857829 · Cited by 22 · see citing works

Cellular mechanisms of drought tolerance in wheat

Ali, M., Gul, A., Hasan, H., Gul, S., Fareed, A., Nadeem, M., Siddique, R., Jan, S. U., & Jamil, M. A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819527-7.00009-1 · Cited by 22 · see citing works

Identification and characterization of multiple abiotic stress tolerance genes in wheat

Kumar, R., Mamrutha, H. M., Kaur, A., Bhusal, N., Pandey, A., Kumar, S., V, Mishra, C. N., Singh, G. P., & Singh, G. P. (2020) · Molecular Biology Reports · doi:10.1007/s11033-020-05906-5 · Cited by 22 · see citing works

Genome-Wide Approach to Identify Quantitative Trait Loci for Drought Tolerance in Tetraploid Potato (Solanum tuberosum L.)

Schumacher, C., Thümecke, S., Schilling, F., Köhl, K. I., Kopka, J., Sprenger, H., Hincha, D. K., Walther, D., Seddig, S., Peters, R., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22116123 · Cited by 21 · see citing works

Genome-wide association study of yield components in spring wheat collection harvested under two water regimes in Northern Kazakhstan

Amalova, A., Абугалиева, С., Babkenov, A., Babkenova, S., & Turuspekov, Y. (2021) · PeerJ · doi:10.7717/peerj.11857 · Cited by 21 · see citing works

Overexpression of TaSIM provides increased drought stress tolerance in transgenic Arabidopsis

Yu, Y., Bi, C., Qing, W., & Ni, Z. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.03.007 · Cited by 21 · see citing works

Some Mechanisms Modulating the Root Growth of Various Wheat Species under Osmotic-Stress Conditions

Terletskaya, N. V., Lee, T. E., Altayeva, N. A., Kudrina, N. O., Blavachinskaya, I. V., & Erezhetova, U. (2020) · Plants · doi:10.3390/plants9111545 · Cited by 20 · see citing works

Diurnal and Seasonal Mapping of Water Deficit Index and Evapotranspiration by an Unmanned Aerial System: A Case Study for Winter Wheat in Denmark

Antoniuk, V., Manevski, K., Sørensen, K. K., Larsen, R., Sandholt, I., Zhang, X., & Andersen, M. N. (2021) · Remote Sensing · doi:10.3390/rs13152998 · Cited by 20 · see citing works

Selection and Validation of Reference Genes for RT-qPCR Analysis in Aegilops tauschii (Coss.) under Different Abiotic Stresses

Abbas, A., Yu, H., Li, X., Cui, H., Chen, J., & Huang, P. C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011017 · Cited by 20 · see citing works

Characteristics and Regulating Roles of Wheat TaHsfA2-13 in Abiotic Stresses

Meng, X., Zhao, B., Li, M., Liu, R., Ren, Q., Li, G., & Guo, X. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.922561 · Cited by 20 · see citing works

Assessment of genetic variation among wheat genotypes for drought tolerance utilizing microsatellite markers and morpho-physiological characteristics

Ahmed, S. F., Ahmed, J. U., Hasan, M., & Mohi-Ud-Din, M. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e21629 · Cited by 21 · see citing works

Effects of drought and high temperature on physiological and biochemical processes, and productivity of plants nanochelates

Kiriziy, D. A., & Стасик, О. О. (2022) · Fiziologia rastenij i genetika · doi:10.15407/frg2022.02.095 · Cited by 27 · see citing works

Drought Stress Tolerance and Photosynthetic Activity of Alloplasmic Lines T. dicoccum x T. aestivum

Terletskaya, N. V., Shcherban, A. B., Nesterov, M. A., Perfil’ev, R. N., Salina, E. A., Altayeva, N. A., & Blavachinskaya, I. V. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21093356 · Cited by 20 · see citing works

Breaking Yield Ceiling in Wheat: Progress and Future Prospects

Pal, N., Saini, D. K., & Kumar, S. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.102919 · Cited by 19 · see citing works

Identification of Wheat Ideotype under Multiple Abiotic Stresses and Complex Environmental Interplays by Multivariate Analysis Techniques

Al-Ashkar, I. M., Sallam, M., Ibrahim, A. A., Ghazy, A. I., Al-Suhaibani, N., Romdhane, W. B., & Al-Doss, A. (2023) · Plants · doi:10.3390/plants12203540 · Cited by 19 · see citing works

Stress-Responsive Gene Expression, Metabolic, Physiological, and Agronomic Responses by Consortium Nano-Silica with Trichoderma against Drought Stress in Bread Wheat

Aljeddani, G. S., Hamouda, R. A., Abdelsattar, A. M., & Heikal, Y. M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252010954 · Cited by 18 · see citing works

Functional characterization of wheat myo-inositol oxygenase promoter under different abiotic stress conditions in Arabidopsis thaliana

Alok, A., Kaur, J., & Tiwari, S. (2020) · Biotechnology Letters · doi:10.1007/s10529-020-02967-1 · Cited by 18 · see citing works

Pertinent Water-Saving Management Strategies for Sustainable Turfgrass in the Desert U.S. Southwest

Serba, D. D., Hejl, R. W., Burayu, W., Umeda, K., Bushman, B. S., & Williams, C. F. (2022) · Sustainability · doi:10.3390/su141912722 · Cited by 17 · see citing works

Genome-wide analysis for root and leaf architecture traits associated with drought tolerance at the seedling stage in a highly ecologically diverse wheat population

Sallam, A., Awadalla, R. A., Elshamy, M. M., Börner, A., & Heikal, Y. M. (2024) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2024.01.020 · Cited by 17 · see citing works

Breeding for water-use efficiency in wheat: progress, challenges and prospects

Hafeez, A., Ali, S., Javed, M. A., Iqbal, R., Khan, M. N., Çığ, F., Sabagh, A. E., Abujamel, T. S., Harakeh, S., Erċışlı, S., et al. (2024) · Molecular Biology Reports · doi:10.1007/s11033-024-09345-4 · Cited by 17 · see citing works

Ectopic expression of a Musa acuminata root hair defective 3 (MaRHD3) in Arabidopsis enhances drought tolerance

Wong, G. R., Mazumdar, P., Lau, S.-E., & Harikrishna, J. A. (2018) · Journal of Plant Physiology · doi:10.1016/j.jplph.2018.09.018 · Cited by 17 · see citing works

Expression profiling of DREB1 and evaluation of vegetation indices in contrasting wheat genotypes exposed to drought stress

Rustamova, S. M., Shrestha, A., Naz, A. A., & Huseynova, I. M. (2020) · Plant Gene · doi:10.1016/j.plgene.2020.100266 · Cited by 16 · see citing works

IMPACT OF GLOBAL CLIMATE CHANGE ON MAIZE (ZEA MAYS): PHYSIOLOGICAL RESPONSES AND MODERN BREEDING TECHNIQUES

(2024) · Trends in Biotechnology and Plant Sciences · doi:10.62460/tbps/2023.010 · Cited by 16 · see citing works

Recognizing the hidden half in wheat: root system attributes associated with drought tolerance

Li, C., Li, L., Reynolds, M. P., Wang, J., Chang, X., Mao, X., & Jing, R. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab124 · Cited by 114 · see citing works

Root-Related Genes in Crops and Their Application under Drought Stress Resistance—A Review

Qin, T., Ali, K., Wang, Y., Dormatey, R., Yao, P., Bi, Z., Liu, Y., Sun, C., & Bai, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911477 · Cited by 24 · see citing works

Genetics of Drought Stress Tolerance in Crop Plants

Oosten, M. J. V., Costa, A., Punzo, P., Landi, S., Ruggiero, A., Batelli, G., & Grillo, S. (2016) · Springer eBooks · doi:10.1007/978-3-319-32423-4_2 · Cited by 42 · see citing works

Genetic diversity as a paramount factor determining wheat adaptation to drought stress

Georgieva, M. S., Dimitrova, A., & Vassileva, V. (2022) · ARPHA Conference Abstracts · doi:10.3897/aca.5.e89829

Drought Tolerance in Wheat

Nezhadahmadi, A., Prodhan, Z. H., & Faruq, G. (2013) · The Scientific World JOURNAL · doi:10.1155/2013/610721 · Cited by 474 · see citing works