The interaction of plant biotic and abiotic stresses: from genes to the field

Climate change 2007: the physical science basis

Solomon, S., Qin, D., Manning, M., Marquis, M. C., Averyt, K. B., Tignor, M., Miller, H. L., & Chen, Z. (2007) · Cited by 23,398 · see citing works

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

Apel, K., & Hirt, H. (2004) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.55.031903.141701 · Cited by 11,723 · see citing works

MYB transcription factors in Arabidopsis

Dubos, C., Stracke, R., Erich Grotewold, A., Weißhaar, B., Martin, C. R., & Lepiniec, L. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.06.005 · Cited by 4,885 · see citing works

Climate Extremes: Observations, Modeling, and Impacts

Easterling, D. R., Meehl, G. A., Parmesan, C., Changnon, S. A., Karl, T. R., & Mearns, L. O. (2000) · Science · doi:10.1126/science.289.5487.2068 · Cited by 4,855 · see citing works

The Dilemma of Plants: To Grow or Defend

Herms, D. A., & Mattson, W. J. (1992) · The Quarterly Review of Biology · doi:10.1086/417659 · Cited by 4,287 · see citing works

Plant productivity and environment

Boyer, J. S. (1982) · Science · doi:10.1126/science.218.4571.443 · Cited by 3,959 · see citing works

Reactive oxygen species homeostasis and signalling during drought and salinity stresses

MILLER, G., SUZUKI, N., CIFTCI‐YILMAZ, S., & MITTLER, R. (2010) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2009.02041.x · Cited by 3,945 · see citing works

Understanding plant responses to drought—from genes to the whole plant.

Chaves, M. M., Maroco, J. P., & Pereira, J. S. (2003) · Functional Plant Biology · doi:10.1071/fp02076 · Cited by 3,845 · see citing works

Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance

Wang, W., Vinocur, B. J., & Altman, A. (2003) · Planta · doi:10.1007/s00425-003-1105-5 · Cited by 3,676 · see citing works

Abiotic stress, the field environment and stress combination

Mittler, R. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2005.11.002 · Cited by 3,083 · see citing works

Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought-and low-temperature-responsive gene expression, respectively, in Arabidopsis

Liu, Q., Kasuga, M., Sakuma, Y., Abe, H., Miura, S., Yamaguchi-Shinozaki, K., & Shinozaki, K. (1998) · The Plant Cell · doi:10.1105/tpc.10.8.1391 · Cited by 3,044 · see citing works

Biochemistry & molecular biology of plants

(2001) · Choice Reviews Online · doi:10.5860/choice.38-3895 · Cited by 2,980 · see citing works

Herbivory in global climate change research: direct effects of rising temperature on insect herbivores

Bale, J. S., Masters, G. J., Hodkinson, I. D., Awmack, C., Bezemer, T. M., Brown, V. K., Butterfield, J., Buse, A., Coulson, J. C., Farrar, J., et al. (2002) · Global Change Biology · doi:10.1046/j.1365-2486.2002.00451.x · Cited by 2,775 · see citing works

Climate change and water.

Bates, B. C., Kundzewicz, Z. W., & Wu, S. (2008) · TaCCIRe Repository (Sokoine University of Agriculture) · Cited by 2,641 · see citing works

Gene networks involved in drought stress response and tolerance

Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl164 · Cited by 2,641 · see citing works

Drought and Salt Tolerance in Plants

Bartels, D., & Sunkar, R. (2005) · Critical Reviews in Plant Sciences · doi:10.1080/07352680590910410 · Cited by 2,611 · see citing works

Networking by small-molecule hormones in plant immunity

Pieterse, C. M. J., León-Reyes, A., der Ent, S. V., & Wees, S. C. M. V. (2009) · Nature Chemical Biology · doi:10.1038/nchembio.164 · Cited by 2,334 · see citing works

Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) Function as Transcriptional Activators in Abscisic Acid Signaling

Abe, H., Urao, T., Ito, T., Seki, M., Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2002) · The Plant Cell · doi:10.1105/tpc.006130 · Cited by 2,272 · see citing works

The effect of drought and heat stress on reproductive processes in cereals

Barnabás, B., Jäger, K., & Fehér, A. (2007) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2007.01727.x · Cited by 2,113 · see citing works

Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor

Kasuga, M., Liu, Q., Miura, S., Yamaguchi‐Shinozaki, K., & Shinozaki, K. (1999) · Nature Biotechnology · doi:10.1038/7036 · Cited by 2,105 · see citing works

Plant Stomata Function in Innate Immunity against Bacterial Invasion

Melotto, M., Underwood, W. R., Koczan, J. M., Nomura, K., & He, S. Y. (2006) · Cell · doi:10.1016/j.cell.2006.06.054 · Cited by 1,988 · see citing works

Novel and Stress-Regulated MicroRNAs and Other Small RNAs from Arabidopsis[W]

Sunkar, R., & Zhu, J. (2004) · The Plant Cell · doi:10.1105/tpc.104.022830 · Cited by 1,936 · see citing works

Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high‐salinity stresses using a full‐length cDNA microarray

Seki, M., Narusaka, M., Ishida, J., Nanjo, T., Fujita, M., Oono, Y., Kamiya, A., Nakajima, M., Enju, A., Sakurai, T., et al. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01359.x · Cited by 1,924 · see citing works

A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence

Chinchilla, D., Zipfel, C., Robatzek, S., Kemmerling, B., Nürnberger, T., Jones, J. D. G., Felix, G., & Boller, T. (2007) · Nature · doi:10.1038/nature05999 · Cited by 1,923 · see citing works

Crosstalk between abiotic and biotic stress responses: a current view from the points of convergence in the stress signaling networks

Fujita, M., Fujita, Y., Noutoshi, Y., Takahashi, F., Narusaka, Y., Yamaguchi‐Shinozaki, K., & Shinozaki, K. (2006) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2006.05.014 · Cited by 1,834 · see citing works

When Defense Pathways Collide. The Response of Arabidopsis to a Combination of Drought and Heat Stress

Rizhsky, L., Liang, H., Shuman, J. L., Shulaev, V., Davletova, S., & Mittler, R. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.033431 · Cited by 1,724 · see citing works

OsDREB genes in rice, Oryza sativa L., encode transcription activators that function in drought‐, high‐salt‐ and cold‐responsive gene expression

Dubouzet, J. G., Sakuma, Y., Ito, Y., Kasuga, M., Dubouzet, E. G., Miura, S., Seki, M., Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01661.x · Cited by 1,660 · see citing works

Transcriptome Changes for Arabidopsis in Response to Salt, Osmotic, and Cold Stress,

Kreps, J. A., Wu, Y., Chang, H., Zhu, T., Wang, X., & Harper, J. F. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.008532 · Cited by 1,576 · see citing works

The AtGenExpress global stress expression data set: protocols, evaluation and model data analysis of UV‐B light, drought and cold stress responses

Kilian, J., Whitehead, D., Horak, J., Wanke, D., Weinl, S., Batistič, O., D’Angelo, C., Bornberg‐Bauer, E., Kudla, J., & Harter, K. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03052.x · Cited by 1,420 · see citing works

Overexpression of [delta]-Pyrroline-5-Carboxylate Synthetase Increases Proline Production and Confers Osmotolerance in Transgenic Plants

Kishor, P., Hong, Z., Miao, G.-H., Hu, C. ‐., & Verma, D. P. S. (1995) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.4.1387 · Cited by 1,355 · see citing works

Posttranscriptional Induction of Two Cu/Zn Superoxide Dismutase Genes in Arabidopsis Is Mediated by Downregulation of miR398 and Important for Oxidative Stress Tolerance

Sunkar, R., Kapoor, A., & Zhu, J. (2006) · The Plant Cell · doi:10.1105/tpc.106.041673 · Cited by 1,316 · see citing works

Significance of flavonoids in plant resistance: a review

Treutter, D. (2006) · Environmental Chemistry Letters · doi:10.1007/s10311-006-0068-8 · Cited by 1,260 · 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

High-Throughput Sequencing of Arabidopsis microRNAs: Evidence for Frequent Birth and Death of MIRNA Genes

Fahlgren, N., Howell, M. D., Kasschau, K. D., Chapman, E. J., Sullivan, C. M., Cumbie, J. S., Givan, S. A., Law, T. F., Grant, S. R., Dangl, J. L., et al. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000219 · Cited by 1,200 · see citing works

Antagonistic Interaction between Abscisic Acid and Jasmonate-Ethylene Signaling Pathways Modulates Defense Gene Expression and Disease Resistance in Arabidopsis

Anderson, J. P., Badruzsaufari, B., Schenk, P. M., Manners, J. M., Desmond, O. J., Ehlert, C., Maclean, D. J., Ebert, P. R., & Kazan, K. (2004) · The Plant Cell · doi:10.1105/tpc.104.025833 · Cited by 1,197 · see citing works

Functional analysis of a NAC‐type transcription factor OsNAC6 involved in abiotic and biotic stress‐responsive gene expression in rice

Nakashima, K., Tran, L. P., Nguyen, D. V., Fujita, M., Maruyama, K., Todaka, D., Ito, Y., Hayashi, N., Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03168.x · Cited by 1,155 · see citing works

Genetic Engineering for Modern Agriculture: Challenges and Perspectives

Mittler, R., & Blumwald, E. (2010) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042809-112116 · Cited by 1,140 · see citing works

The Combined Effect of Drought Stress and Heat Shock on Gene Expression in Tobacco

Rizhsky, L., Liang, H., & Mittler, R. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.006858 · Cited by 1,135 · see citing works

Endogenous siRNAs Derived from a Pair of Natural cis-Antisense Transcripts Regulate Salt Tolerance in Arabidopsis

Borsani, O., Zhu, J., Verslues, P. E., Sunkar, R., & Zhu, J. (2005) · Cell · doi:10.1016/j.cell.2005.11.035 · Cited by 1,125 · see citing works

Mitogen-Activated Protein Kinase Signaling in Plants

Cristina, M., Petersen, M., & Mundy, J. (2010) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042809-112252 · Cited by 1,107 · see citing works

TT2, TT8, and TTG1 synergistically specify the expression of BANYULS and proanthocyanidin biosynthesis in Arabidopsis thaliana

Baudry, A., Heim, M. A., Dubreucq, B., Caboche, M. M., Weißhaar, B., & Lepiniec, L. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02138.x · Cited by 1,053 · see citing works

Crop responses to climatic variation

Porter, J. R., & Semenov, M. A. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1752 · Cited by 1,034 · see citing works

Coordination of carbon supply and plant growth

Smith, A. M., & Stitt, M. (2007) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2007.01708.x · Cited by 1,028 · see citing works

Water-deficit stress-induced anatomical changes in higher plants

Shao, H., Chu, L.-Y., Jaleel, C. A., & Zhao, C. (2008) · Comptes Rendus Biologies · doi:10.1016/j.crvi.2008.01.002 · Cited by 1,009 · see citing works

The MKK2 Pathway Mediates Cold and Salt Stress Signaling in Arabidopsis

Teige, M., Scheikl, E., Eulgem, T., Dóczi, R., Ichimura, K., Shinozaki, K., Dangl, J. L., & Hirt, H. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.06.023 · Cited by 1,002 · see citing works

MicroRNA Directs mRNA Cleavage of the Transcription Factor NAC1 to Downregulate Auxin Signals for Arabidopsis Lateral Root Development

Guo, H., Xie, Q., Fei, J., & Chua, N. (2005) · The Plant Cell · doi:10.1105/tpc.105.030841 · Cited by 995 · see citing works

Signal Signature and Transcriptome Changes of Arabidopsis During Pathogen and Insect Attack

de Vos, M., van Oosten, V. R., Poecke, R. M. P. V., van Pelt, J. A., Pozo, M. J., Mueller, M. J., Buchala, A. J., Métraux, J., van Loon, L. C., Dicke, M., et al. (2005) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-18-0923 · Cited by 974 · see citing works

Transcriptional repression by AtMYB4 controls production of UV‐protecting sunscreens in Arabidopsis

Jin, H., Cominelli, E., Bailey, P., Parr, A., Mehrtens, F., Jones, J., Tonelli, C., Weißhaar, B., & Martin, C. (2000) · The EMBO Journal · doi:10.1093/emboj/19.22.6150 · Cited by 943 · see citing works

A dehydration‐induced NAC protein, RD26, is involved in a novel ABA‐dependent stress‐signaling pathway

Fujita, M., Fujita, Y., Maruyama, K., Seki, M., Hiratsu, K., Ohme‐Takagi, M., Tran, L. P., Yamaguchi‐Shinozaki, K., & Shinozaki, K. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02171.x · Cited by 937 · see citing works

Small RNAs as big players in plant abiotic stress responses and nutrient deprivation

Sunkar, R., Chinnusamy, V., Zhu, J., & Zhu, J.-K. (2007) · Trends in Plant Science · doi:10.1016/j.tplants.2007.05.001 · Cited by 930 · see citing works

The multifaceted role of ABA in disease resistance

Ton, J., Flors, V., & Mauch‐Mani, B. (2009) · Trends in Plant Science · doi:10.1016/j.tplants.2009.03.006 · Cited by 914 · see citing works

ROS in biotic interactions

Torres, M. Á. M. (2009) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2009.01326.x · Cited by 903 · see citing works

Regulation of Phosphate Homeostasis by MicroRNA in Arabidopsis

Chiou, T., Aung, K., Lin, S.-I., Wu, C.-C., Chiang, S., & Su, C.-L. (2005) · The Plant Cell · doi:10.1105/tpc.105.038943 · Cited by 873 · see citing works

A miRNA Involved in Phosphate-Starvation Response in Arabidopsis

Fujii, H., Chiou, T., Lin, S.-I., Aung, K., & Zhu, J. (2005) · Current Biology · doi:10.1016/j.cub.2005.10.016 · Cited by 854 · see citing works

The role of abscisic acid in plant–pathogen interactions

Mauch‐Mani, B., & Mauch, F. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.05.015 · Cited by 839 · see citing works

ABA Is an Essential Signal for Plant Resistance to Pathogens Affecting JA Biosynthesis and the Activation of Defenses in Arabidopsis

Adie, B. A. T., Pérez‐Pérez, J., Pérez‐Pérez, M. M., Godoy, M., Sánchez‐Serrano, J. J., Schmelz, E. A., & Solano, R. (2007) · The Plant Cell · doi:10.1105/tpc.106.048041 · Cited by 839 · see citing works

Hydrogen peroxide is generated systemically in plant leaves by wounding and systemin via the octadecanoid pathway

Orozco-Cárdenas, M. L., & Ryan, C. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.11.6553 · Cited by 837 · see citing works

Disease Resistance and Abiotic Stress Tolerance in Rice Are Inversely Modulated by an Abscisic Acid–Inducible Mitogen-Activated Protein Kinase[W]

Xiong, L., & Yang, Y. (2003) · The Plant Cell · doi:10.1105/tpc.008714 · Cited by 830 · see citing works

Modulation of floral development by a gibberellin-regulated microRNA

Achard, P., Herr, A. J., Baulcombe, D. C., & Harberd, N. P. (2004) · Development · doi:10.1242/dev.01206 · Cited by 822 · see citing works

Functions of microRNAs and related small RNAs in plants

Mallory, A. C., & Vaucheret, H. (2006) · Nature Genetics · doi:10.1038/ng1791 · Cited by 816 · see citing works

Responses of forest trees to single and multiple environmental stresses from seedlings to mature plants: Past stress history, stress interactions, tolerance and acclimation

Niinemets, Ü. (2010) · Forest Ecology and Management · doi:10.1016/j.foreco.2010.07.054 · Cited by 811 · see citing works

Fitness costs of R-gene-mediated resistance in Arabidopsis thaliana

Tian, D., Traw, M. B., Chen, J., et al. (2003) · Nature · doi:10.1038/nature01588 · Cited by 810 · see citing works

Engineering drought tolerance in plants: discovering and tailoring genes to unlock the future

Umezawa, T., Fujita, M., Fujita, Y., Yamaguchi-Shinozaki, K., & Shinozaki, K. (2006) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2006.02.002 · Cited by 802 · see citing works

Roles of the CBF2 and ZAT12 transcription factors in configuring the low temperature transcriptome of Arabidopsis

Vogel, J. T., Zarka, D. G., Buskirk, H. A. V., Fowler, S., & Thomashow, M. F. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02288.x · Cited by 779 · see citing works

Current Nematode Threats to World Agriculture

Nıcol, J. M., Turner, S., Coyne, D., et al. (2011) · Springer eBooks · doi:10.1007/978-94-007-0434-3_2 · Cited by 768 · see citing works

Callose Deposition: A Multifaceted Plant Defense Response

Luna, E., Pastor, V., Robert, J., Flors, V., Mauch‐Mani, B., & Ton, J. (2010) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-07-10-0149 · Cited by 767 · see citing works

Responses to Abiotic Stresses

Dracup, M., Turner, N. C., Tang, C., Reader, M. A., & Palta, J. A. (1998) · UWA Profiles and Research Repository (University of Western Australia) · Cited by 753 · see citing works

Jasmonate-induced responses are costly but benefit plants under attack in native populations

Baldwin, I. T. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.14.8113 · Cited by 743 · see citing works

Transcriptomic Footprints Disclose Specificity of Reactive Oxygen Species Signaling in Arabidopsis

Gadjev, I., Vanderauwera, S., Gechev, T. S., Laloi, C., Minkov, I. N., Shulaev, V., Apel, K., Inzé, D., Mittler, R., & Breusegem, F. V. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.078717 · Cited by 729 · see citing works

Metabolomics for plant stress response

Shulaev, V., Cortes, D., Miller, G., & Mittler, R. (2008) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2007.01025.x · Cited by 728 · see citing works

Common Components, Networks, and Pathways of Cross-Tolerance to Stress. The Central Role of “Redox” and Abscisic Acid-Mediated Controls

Pastori, G. M., & Foyer, C. H. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.011021 · Cited by 716 · see citing works

The MYB96 Transcription Factor Regulates Cuticular Wax Biosynthesis under Drought Conditions inArabidopsis

Seo, P. J., Lee, S. B., Suh, M. C., Park, M., Go, Y. S., & Park, C. (2011) · The Plant Cell · doi:10.1105/tpc.111.083485 · Cited by 700 · see citing works

MicroRNA Regulation of NAC-Domain Targets Is Required for Proper Formation and Separation of Adjacent Embryonic, Vegetative, and Floral Organs

Mallory, A. C., Dugas, D. V., Bartel, D. P., & Bartel, B. (2004) · Current Biology · doi:10.1016/j.cub.2004.06.022 · Cited by 697 · see citing works

The Zinc-Finger Protein Zat12 Plays a Central Role in Reactive Oxygen and Abiotic Stress Signaling in Arabidopsis

Davletova, S., Schlauch, K. A., Coutu, J., & Mittler, R. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.068254 · Cited by 690 · see citing works

Role of microorganisms in adaptation of agriculture crops to abiotic stresses

Grover, M., Ali, S. Z., Sandhya, V., Rasul, A., & Venkateswarlu, B. (2010) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-010-0572-7 · Cited by 684 · see citing works

Roles of Plant Small RNAs in Biotic Stress Responses

Ruíz‐Ferrer, V., & Voinnet, O. (2009) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.043008.092111 · Cited by 647 · see citing works

Rice WRKY45 Plays a Crucial Role in Benzothiadiazole-Inducible Blast Resistance

Shimono, M., Sugano, S., Nakayama, A., Jiang, C., Ono, K., Toki, S., & Takatsuji, H. (2007) · The Plant Cell · doi:10.1105/tpc.106.046250 · Cited by 635 · see citing works

β‐amino‐butyric acid‐induced resistance against necrotrophic pathogens is based on ABA‐dependent priming for callose

Ton, J., & Mauch‐Mani, B. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02028.x · Cited by 629 · see citing works

Surveying Patterns in the Cost of Resistance in Plants

Bergelson, J. M., & Purrington, C. B. (1996) · The American Naturalist · doi:10.1086/285938 · Cited by 622 · see citing works

Convergent energy and stress signaling

Gonzalez, E. B., & Sheen, J. (2008) · Trends in Plant Science · doi:10.1016/j.tplants.2008.06.006 · Cited by 610 · see citing works

Improving water use in crop production

Morison, J. I. L., Baker, N. R., Mullineaux, P. M., & Davies, W. J. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2175 · Cited by 609 · see citing works

Transgenic approaches for abiotic stress tolerance in plants: retrospect and prospects

Bhatnagar‐Mathur, P., Vadez, V., & Sharma, K. K. (2007) · Plant Cell Reports · doi:10.1007/s00299-007-0474-9 · Cited by 606 · see citing works

Overexpression of the soybean GmERF3 gene, an AP2/ERF type transcription factor for increased tolerances to salt, drought, and diseases in transgenic tobacco

Zhang, G., Chen, M., Li, L., Xu, Z., Chen, X., Guo, J., & Ma, Y. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp214 · Cited by 599 · see citing works

Arabidopsis heat shock transcription factor A2 as a key regulator in response to several types of environmental stress

Nishizawa‐Yokoi, A., Yabuta, Y., Yoshida, E., et al. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02889.x · Cited by 595 · see citing works

Characterization of the ABA‐regulated global responses to dehydration in Arabidopsis by metabolomics

Urano, K., Maruyama, K., Ogata, Y., Morishita, Y., Takeda, M., Sakurai, N., Suzuki, H., Saito, K., Shibata, D., Kobayashi, M., et al. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03748.x · Cited by 593 · see citing works

Antagonistic Interaction between Systemic Acquired Resistance and the Abscisic Acid–Mediated Abiotic Stress Response in Arabidopsis

Yasuda, M., Ishikawa, A., Jikumaru, Y., Seki, M., Umezawa, T., Asami, T., Maruyama, A., Kudo, T., Shinozaki, K., Yoshida, S., et al. (2008) · The Plant Cell · doi:10.1105/tpc.107.054296 · Cited by 566 · see citing works

A Transmembrane Hybrid-Type Histidine Kinase in Arabidopsis Functions as an Osmosensor

Urao, T., Yakubov, B., Satoh, R., Yamaguchi‐Shinozaki, K., Seki, M., Hirayama, T., & Shinozaki, K. (1999) · The Plant Cell · doi:10.1105/tpc.11.9.1743 · Cited by 564 · see citing works

The Plant-Growth-Promoting Rhizobacterium Paenibacillus polymyxa Induces Changes in Arabidopsis thaliana Gene Expression: A Possible Connection Between Biotic and Abiotic Stress Responses

Timmusk, S., & Wagner, E. G. H. (1999) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1999.12.11.951 · Cited by 562 · see citing works

Quantitative Trait Loci and Crop Performance under Abiotic Stress: Where Do We Stand?: Table I.

Collins, N. C., Tardieu, F., & Tuberosa, R. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.118117 · Cited by 559 · see citing works

WRKY70 modulates the selection of signaling pathways in plant defense

Li, J., Brader, G., Kariola, T., & Palva, E. T. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02712.x · Cited by 559 · see citing works

The BOTRYTIS SUSCEPTIBLE1 Gene Encodes an R2R3MYB Transcription Factor Protein That Is Required for Biotic and Abiotic Stress Responses in Arabidopsis

Mengiste, T. D., Chen, X., Salmeron, J. M., & Dietrich, R. A. (2003) · The Plant Cell · doi:10.1105/tpc.014167 · Cited by 553 · see citing works

The role of class A1 heat shock factors (HSFA1s) in response to heat and other stresses in Arabidopsis

Liu, H., Liao, H.-T., & Charng, Y. (2011) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2011.02278.x · Cited by 552 · see citing works

Pseudomonas syringae pv. tomato hijacks the Arabidopsis abscisic acid signalling pathway to cause disease

Zabala, M. D. T., Truman, W., Bennett, M. H., Lafforgue, G., Mansfıeld, J. W., Rodrı́guez, P. L., Bögre, L., & Grant, M. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601575 · Cited by 544 · see citing works

The diversity of plant heat stress transcription factors

von Koskull‐Döring, P., Scharf, K., & Nover, L. (2007) · Trends in Plant Science · doi:10.1016/j.tplants.2007.08.014 · Cited by 541 · see citing works

The effect of potassium nutrition on pest and disease resistance in plants

Amtmann, A., Troufflard, S., & Armengaud, P. (2008) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2008.01075.x · Cited by 535 · see citing works

Abscisic Acid Determines Basal Susceptibility of Tomato toBotrytis cinereaand Suppresses Salicylic Acid-Dependent Signaling Mechanisms

Audenaert, K., Meyer, G. D., & Höfte, M. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.010605 · Cited by 529 · see citing works

A pathogen-inducible endogenous siRNA in plant immunity

Katiyar‐Agarwal, S., Morgan, R., Dahlbeck, D., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608258103 · Cited by 522 · see citing works

‘Omics’ analyses of regulatory networks in plant abiotic stress responses

Urano, K., Kurihara, Y., Seki, M., & Shinozaki, K. (2010) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.12.006 · Cited by 518 · see citing works

Genes commonly regulated by water-deficit stress in Arabidopsis thaliana

Bray, E. A. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh270 · Cited by 510 · see citing works

The relationship of drought-related gene expression in Arabidopsis thaliana to hormonal and environmental factors

Huang, D., Wu, W., Abrams, S. R., & Cutler, A. J. (2008) · Journal of Experimental Botany · doi:10.1093/jxb/ern155 · Cited by 508 · see citing works

Overexpression of the Tobacco Tsi1 Gene Encoding an EREBP/AP2-Type Transcription Factor Enhances Resistance against Pathogen Attack and Osmotic Stress in Tobacco

Park, J. M., Park, C.-J., Lee, S.-B., Ham, B., Shin, R., & Paek, K.-H. (2001) · The Plant Cell · doi:10.1105/tpc.13.5.1035 · Cited by 507 · see citing works

Arabidopsis HsfA1 transcription factors function as the main positive regulators in heat shock-responsive gene expression

Yoshida, T., Ohama, N., Nakajima, J., et al. (2011) · Molecular Genetics and Genomics · doi:10.1007/s00438-011-0647-7 · Cited by 501 · see citing works

ACC deaminase from Pseudomonas fluorescens mediated saline resistance in groundnut (Arachis hypogea) plants

Saravanakumar, D., & Samiyappan, R. (2006) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2006.03179.x · Cited by 500 · see citing works

Diverse set of microRNAs are responsive to powdery mildew infection and heat stress in wheat (Triticum aestivum L.)

Xin, M., Wang, Y., Yao, Y., Xie, C., Peng, H., Ni, Z., & Sun, Q. (2010) · BMC Plant Biology · doi:10.1186/1471-2229-10-123 · Cited by 497 · see citing works

Could Heat Shock Transcription Factors Function as Hydrogen Peroxide Sensors in Plants?

Miller, G., & Mittler, R. (2006) · Annals of Botany · doi:10.1093/aob/mcl107 · Cited by 484 · see citing works

Global Switches and Fine-Tuning—ABA Modulates Plant Pathogen Defense

Asselbergh, B., Vleesschauwer, D. D., & Höfte, M. (2008) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-21-6-0709 · Cited by 465 · see citing works

The Zinc Finger Protein Zat12 Is Required for Cytosolic Ascorbate Peroxidase 1 Expression during Oxidative Stress in Arabidopsis

Rizhsky, L., Davletova, S., Liang, H., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313350200 · Cited by 465 · see citing works

Rhizosphere Soil Aggregation and Plant Growth Promotion of Sunflowers by an Exopolysaccharide-Producing Rhizobium sp. Strain Isolated from Sunflower Roots

Alami, Y., Achouak, W., Marol, C., et al. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.8.3393-3398.2000 · Cited by 464 · see citing works

Genetic approaches to crop improvement: responding to environmental and population changes

Takeda, S., & Matsuoka, M. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2342 · Cited by 463 · see citing works

HISTONE DEACETYLASE19 Is Involved in Jasmonic Acid and Ethylene Signaling of Pathogen Response in Arabidopsis

Zhou, C., Zhang, L., Duan, J., Miki, B. L. A., & Wu, K. (2005) · The Plant Cell · doi:10.1105/tpc.104.028514 · Cited by 449 · see citing works

Functions and Application of the AP2/ERF Transcription Factor Family in Crop Improvement F

Xu, Z., Chen, M., Li, L., & Ma, Y. (2011) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2011.01062.x · Cited by 438 · see citing works

Genomics and Molecular Genetics of Plant-Nematode Interactions

Jones, J. T., Gheysen, G., & Fenoll, C. (2011) · Springer eBooks · doi:10.1007/978-94-007-0434-3 · Cited by 424 · see citing works

Virus infection improves drought tolerance

Xu, P., Chen, F., Mannas, J. P., et al. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02627.x · Cited by 418 · see citing works

Gene stacking in transgenic plants – the challenge for 21st century plant biotechnology

Halpin, C. (2005) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2004.00113.x · Cited by 413 · see citing works

Ascorbate Peroxidase 1 Plays a Key Role in the Response of Arabidopsis thaliana to Stress Combination

Koussevitzky, S., Suzuki, N., Huntington, S., Armijo, L., Sha, W., Cortes, D., Shulaev, V., & Mittler, R. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m806337200 · Cited by 413 · see citing works

The antioxidant systems vis-à-vis reactive oxygen species during plant–pathogen interaction

Gara, L. D., de Pinto, M. C., & Tommasi, F. (2003) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(03)00135-9 · Cited by 411 · see citing works

Over-expression of the stress-induced OsWRKY45 enhances disease resistance and drought tolerance in Arabidopsis

QIU, Y., & YU, D. (2008) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2008.07.002 · Cited by 393 · see citing works

Resistance to Botrytis cinerea in sitiens, an Abscisic Acid-Deficient Tomato Mutant, Involves Timely Production of Hydrogen Peroxide and Cell Wall Modifications in the Epidermis

Asselbergh, B., Curvers, K., França, S. C., et al. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.099226 · Cited by 373 · see citing works

Climate change and diseases of food crops

Luck, J., Spackman, M., Freeman, A. J., Trębicki, P., Griffiths, W., Finlay, K. J., & Chakraborty, S. (2011) · Plant Pathology · doi:10.1111/j.1365-3059.2010.02414.x · Cited by 365 · see citing works

Identification of novel soybean microRNAs involved in abiotic and biotic stresses

Kulcheski, F. R., de Oliveira, L. F., Molina, L. G., Almerão, M. P., Rodrigues, F. A., Marcolino, J., Barbosa, J. F., Stolf-Moreira, R., Nepomuceno, A. L., Marcelino‐Guimarães, F. C., et al. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-307 · Cited by 355 · see citing works

Overexpression of the rice Osmyb4 gene increases chilling and freezing tolerance of Arabidopsis thaliana plants

Vannini, C., Locatelli, F., Bracale, M., Magnani, E., Marsoni, M., Osnato, M., Mattana, M., Baldoni, E., & Coraggio, I. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01938.x · Cited by 352 · see citing works

MYB96‐mediated abscisic acid signals induce pathogen resistance response by promoting salicylic acid biosynthesis in Arabidopsis

Seo, P. J., & Park, C. (2010) · New Phytologist · doi:10.1111/j.1469-8137.2010.03183.x · Cited by 346 · see citing works

Cold activation of a plasma membrane-tethered NAC transcription factor induces a pathogen resistance response in Arabidopsis

Seo, P. J., Kim, M. J., Park, J. Y., Kim, S., Jeon, J., Lee, Y., Kim, J., & Park, C. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.04091.x · Cited by 333 · see citing works

Plant-growth-promoting rhizobacteria and arbuscular mycorrhizal fungi modify alleviation biochemical mechanisms in water-stressed plants

Kohler, J., Hernández, J. A., Caravaca, F., & Roldán, A. (2008) · Functional Plant Biology · doi:10.1071/fp07218 · Cited by 330 · 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

The transcription factor ATAF2 represses the expression of pathogenesis‐related genes in Arabidopsis

Delessert, C., Kazan, K., Wilson, I. W., Straeten, D. V. D., Manners, J. M., Dennis, E. S., & Dolferus, R. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02488.x · Cited by 321 · see citing works

Calmodulin-Dependent Activation of MAP Kinase for ROS Homeostasis in Arabidopsis

Takahashi, F., Mizoguchi, T., Yoshida, R., et al. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.02.029 · Cited by 313 · see citing works

Genome-wide survey and expression profiling of heat shock proteins and heat shock factors revealed overlapped and stress specific response under abiotic stresses in rice

Hu, W., Hu, G., & Han, B. (2009) · Plant Science · doi:10.1016/j.plantsci.2009.01.016 · Cited by 313 · see citing works

Deep sequencing of Brachypodium small RNAs at the global genome level identifies microRNAs involved in cold stress response

Zhang, J., Xu, Y., Huan, Q., & Chong, K. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-449 · Cited by 311 · see citing works

Breeding for improved abiotic stress tolerance in maize adapted to southern Africa

Bänziger, M., Setimela, P. S., Hodson, D., & Vivek, B. (2005) · Agricultural Water Management · doi:10.1016/j.agwat.2005.07.014 · Cited by 300 · see citing works

Abscisic Acid Interacts Antagonistically with Salicylic Acid Signaling Pathway in Rice–Magnaporthe griseaInteraction

Jiang, C., Shimono, M., Sugano, S., et al. (2010) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-23-6-0791 · Cited by 296 · see citing works

Estimating accuracy of RNA-Seq and microarrays with proteomics

Fu, X., Fu, N., Guo, S., Yan, Z., Xu, Y., Hu, H., Menzel, C., Chen, W., Li, Y., Zeng, R., et al. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-161 · Cited by 292 · see citing works

Breeding for abiotic stresses for sustainable agriculture

Witcombe, J. R., Hollington, P. A., Howarth, C. J., Reader, S., & Steele, K. A. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2179 · Cited by 287 · see citing works

The transcription factor SlAREB1 confers drought, salt stress tolerance and regulates biotic and abiotic stress‐related genes in tomato

Orellana, S., Yáñez, M., ESPINOZA, A., Verdugo, I., GONZÁLEZ, E., Ruíz-Lara, S., & Casaretto, J. A. (2010) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2010.02220.x · Cited by 287 · see citing works

Analysis of Temperature Modulation of Plant Defense Against Biotrophic Microbes

Wang, Y., Bao, Z., Zhu, Y., & Hua, J. (2009) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-22-5-0498 · Cited by 283 · see citing works

Identification of AtHD2C as a novel regulator of abscisic acid responses in Arabidopsis

Sridha, S., & Wu, K. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02678.x · Cited by 282 · see citing works

Exogenous salicylic acid increases polyamine content but may decrease drought tolerance in maize

Németh, M., Janda, T., Horváth, E., et al. (2002) · Plant Science · doi:10.1016/s0168-9452(01)00593-3 · Cited by 275 · see citing works

Suppression by ABA of salicylic acid and lignin accumulation and the expression of multiple genes, in Arabidopsis infected with Pseudomonas syringae pv. tomato

Mohr, P. G., & Cahill, D. M. (2006) · Functional & Integrative Genomics · doi:10.1007/s10142-006-0041-4 · Cited by 272 · see citing works

Implications of climate change for diseases, crop yields and food security

Newton, A. C., Johnson, S. N., & Gregory, P. J. (2011) · Euphytica · doi:10.1007/s10681-011-0359-4 · Cited by 269 · see citing works

Ascorbate Deficiency Can Limit Violaxanthin De-Epoxidase Activity in Vivo

Müller-Moulé, P., Conklin, P. L., & Niyogi, K. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.010924 · Cited by 262 · see citing works

Abscisic acid influences the susceptibility of Arabidopsis thaliana to Pseudomonas syringae pv. tomato and Peronospora parasitica

Mohr, P. G., & Cahill, D. M. (2003) · Functional Plant Biology · doi:10.1071/fp02231 · Cited by 261 · see citing works

Convergence and specificity in the Arabidopsis MAPK nexus

Andréasson, E., & Ellis, B. E. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2009.12.001 · Cited by 261 · see citing works

necrotic reaction of tomatoes and other hosts resistant to Meloidogyne: reversal by temperature

Dropkin, V. H. (1969) · Phytopathology · Cited by 252 · see citing works

The Arabidopsis thaliana JASMONATE INSENSITIVE 1 Gene Is Required for Suppression of Salicylic Acid-Dependent Defenses During Infection by Pseudomonas syringae

Laurie-Berry, N., Joardar, V., Street, I. H., et al. (2006) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-19-0789 · Cited by 245 · see citing works

Crosstalk in the responses to abiotic and biotic stresses in Arabidopsis: Analysis of gene expression in cytochrome P450 gene superfamily by cDNA microarray

Narusaka, Y., Narusaka, M., Seki, M., et al. (2004) · Plant Molecular Biology · doi:10.1007/s11103-004-0685-1 · Cited by 245 · see citing works

Nematode resistance

Fuller, V. L., Lilley, C. J., & Urwin, P. E. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02508.x · Cited by 238 · see citing works

Combinatorial control of Arabidopsis proline dehydrogenase transcription by specific heterodimerisation of bZIP transcription factors

Weltmeier, F., Ehlert, A., Mayer, C. S., Dietrich, K., Wang, X., Schütze, K., Alonso, R., Harter, K., Vicente‐Carbajosa, J., & Dröge‐Laser, W. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601206 · Cited by 237 · see citing works

Identification and analysis of seven H2O2-responsive miRNAs and 32 new miRNAs in the seedlings of rice (Oryza sativa L. ssp. indica)

Li, T., Li, H., Zhang, Y.-X., & Liu, J. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq1047 · Cited by 233 · see citing works

Influence of drought, salt stress and abscisic acid on the resistance of tomato to Botrytis cinerea and Oidium neolycopersici

Achuo, E. A., Prinsen, E., & Höfte, M. (2006) · Plant Pathology · doi:10.1111/j.1365-3059.2006.01340.x · Cited by 227 · see citing works

Mycorrhizal and non-mycorrhizal Lactuca sativa plants exhibit contrasting responses to exogenous ABA during drought stress and recovery

Aroca, R., Vernieri, P., & Ruíz-Lozano, J. M. (2008) · Journal of Experimental Botany · doi:10.1093/jxb/ern057 · Cited by 227 · see citing works

Biotechnology of water and salinity stress tolerance

Pardo, J. M. (2010) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2010.02.005 · Cited by 224 · see citing works

Winter Survival of Transgenic Alfalfa Overexpressing Superoxide Dismutase1

McKersie, B. D., Bowley, S. R., & Jones, K. S. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.119.3.839 · Cited by 223 · see citing works

Water Relations in the Interaction of Foliar Bacterial Pathogens with Plants

Beattie, G. A. (2011) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-073009-114436 · Cited by 222 · see citing works

Transcriptional regulation by an NAC (NAM–ATAF1,2–CUC2) transcription factor attenuates ABA signalling for efficient basal defence towards Blumeria graminis f. sp. hordei in Arabidopsis

Jensen, M. K., Hagedorn, P., Zabala, M. D. T., Grant, M., Rung, J. H., Collinge, D. B., & Lyngkjær, M. F. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03646.x · Cited by 218 · see citing works

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

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

Semiarid Crop Production from a Hydrological Perspective: Gap between Potential and Actual Yields

Rockström, J., & Falkenmark, M. (2000) · Critical Reviews in Plant Sciences · doi:10.1080/07352680091139259 · Cited by 214 · see citing works

Crosstalk between biotic and abiotic stress responses in tomato is mediated by the AIM1 transcription factor

AbuQamar, S. F., Luo, H., Laluk, K., et al. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03783.x · Cited by 210 · see citing works

Modulation of chlorogenic acid biosynthesis in Solanum lycopersicum; consequences for phenolic accumulation and UV-tolerance

Clé, C., Hill, L. M., Niggeweg, R., Martin, C. R., Guisez, Y., Prinsen, E., & Jansen, M. A. K. (2008) · Phytochemistry · doi:10.1016/j.phytochem.2008.04.024 · Cited by 207 · see citing works

Semiarid Crop Production from a Hydrological Perspective: Gap between Potential and Actual Yields

Rockström, J. (2000) · Critical Reviews in Plant Sciences · doi:10.1016/s0735-2689(00)80007-6 · Cited by 203 · see citing works

The Arabidopsis Mitochondria-Localized Pentatricopeptide Repeat Protein PGN Functions in Defense against Necrotrophic Fungi and Abiotic Stress Tolerance

Laluk, K., AbuQamar, S. F., & Mengiste, T. D. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.177501 · Cited by 202 · see citing works

Characterization of a novel wheat NAC transcription factor gene involved in defense response against stripe rust pathogen infection and abiotic stresses

Ning, X., Zhang, G., Liu, X., Deng, L., Cai, G., Zhang, Y., Wang, X., Zhao, J., Huang, L., & Kang, Z. (2010) · Molecular Biology Reports · doi:10.1007/s11033-010-0023-4 · Cited by 194 · see citing works

Metabolic profiling reveals local and systemic responses of host plants to nematode parasitism

Hofmann, J. P., Ashry, A. E., Anwar, S., et al. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04217.x · Cited by 192 · see citing works

Convergence of Signaling Pathways Induced by Systemin, Oligosaccharide Elicitors, and Ultraviolet-B Radiation at the Level of Mitogen-Activated Protein Kinases in Lycopersicon peruvianum Suspension-Cultured Cells

Holley, S. R., Yalamanchili, R., de Moura, D. S., et al. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.024414 · Cited by 179 · see citing works

Water relations, histopathology and growth of common bean (Phaseolus vulgaris L.) during pathogenesis of Macrophomina phaseolina under drought stress

Mayek-Pérez, N., García-Espinosa, R., López-Castañeda, C., et al. (2002) · Physiological and Molecular Plant Pathology · doi:10.1006/pmpp.2001.0388 · Cited by 171 · see citing works

Herbivore‐induced plant vaccination. Part II. Array‐studies reveal the transience of herbivore‐specific transcriptional imprints and a distinct imprint from stress combinations

Voelckel, C., & Baldwin, I. T. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02077.x · Cited by 170 · see citing works

Ethylene Induces Antifreeze Activity in Winter Rye Leaves

Yu, X.-M., Griffith, M., & Wiseman, S. B. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.126.3.1232 · Cited by 170 · see citing works

EARLY RESPONSIVE TO DEHYDRATION 15, a Negative Regulator of Abscisic Acid Responses in Arabidopsis

Kariola, T., Brader, G., Helenius, E., et al. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.086223 · Cited by 169 · see citing works

Variability of Endotoxin Expression in Bt Transgenic Cotton

Dong, H., & Li, W. J. (2006) · Journal of Agronomy and Crop Science · doi:10.1111/j.1439-037x.2006.00240.x · Cited by 168 · see citing works

Diverse signals converge at MAPK cascades in plant

Zhang, T., Liu, Y., Yang, T., et al. (2006) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2006.06.004 · Cited by 165 · see citing works

DEAR1, a transcriptional repressor of DREB protein that mediates plant defense and freezing stress responses in Arabidopsis

Tsutsui, T., Kato, W., Asada, Y., Sako, K., Sato, T., Sonoda, Y., Kidokoro, S., Yamaguchi‐Shinozaki, K., Tamaoki, M., Arakawa, K., et al. (2009) · Journal of Plant Research · doi:10.1007/s10265-009-0252-6 · Cited by 165 · see citing works

Overexpression of the AP2/EREBP transcription factor OPBP1 enhances disease resistance and salt tolerance in tobacco

Guo, Z., Chen, X., Wu, X., Ling, J., & Xu, P. (2004) · Plant Molecular Biology · doi:10.1007/s11103-004-1521-3 · Cited by 158 · see citing works

Abscisic acid and low temperatures suppress the whole plant-specific resistance reaction of rice plants to the infection of Magnaporthe grisea

Koga, H., Dohi, K., & Mori, M. (2004) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2004.11.002 · Cited by 158 · see citing works

Impacts of climate change on wheat anthesis and fusarium ear blight in the UK

Madgwick, J. W., West, J. S., White, R. P., Semenov, M. A., Townsend, J. A., Turner, J. A., & Fitt, B. D. L. (2011) · European Journal of Plant Pathology · doi:10.1007/s10658-010-9739-1 · Cited by 157 · see citing works

The Pseudomonas syringae Type III Effector HopAM1 Enhances Virulence on Water-Stressed Plants

Goel, A. K., Lundberg, D. S., Torres, M. Á. M., et al. (2008) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-21-3-0361 · Cited by 155 · see citing works

Molecular characterization of four rice genes encoding ethylene-responsive transcriptional factors and their expressions in response to biotic and abiotic stress

Cao, Y., Song, F., Goodman, R. M., et al. (2006) · Journal of Plant Physiology · doi:10.1016/j.jplph.2005.11.004 · Cited by 153 · see citing works

Heat shock protein 70 regulates the abscisic acid-induced antioxidant response of maize to combined drought and heat stress

Hu, X., Liu, R., Li, Y., Wang, W., Tai, F., Xue, R., & Chao-hai, L. (2009) · Plant Growth Regulation · doi:10.1007/s10725-009-9436-2 · Cited by 152 · see citing works

Elevated atmospheric carbon dioxide and ozone alter soybean diseases at SoyFACE

EASTBURN, D. M., DEGENNARO, M. M., DELUCIA, E. H., DERMODY, O., & MCELRONE, A. J. (2010) · Global Change Biology · doi:10.1111/j.1365-2486.2009.01978.x · Cited by 150 · see citing works

Engineering drought and salinity tolerance in plants: lessons from genome-wide expression profiling in Arabidopsis

Denby, K., & Gehring, C. (2005) · Trends in biotechnology · doi:10.1016/j.tibtech.2005.09.001 · Cited by 150 · see citing works

OMTK1, a Novel MAPKKK, Channels Oxidative Stress Signaling through Direct MAPK Interaction

Nakagami, H., Kiegerl, S., & Heribert Hirt, A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m312662200 · Cited by 149 · see citing works

Abscisic acid deficiency leads to rapid activation of tomato defence responses upon infection with Erwinia chrysanthemi

Asselbergh, B., Achuo, A. E., Höfte, M., & Gijsegem, F. V. (2007) · Molecular Plant Pathology · doi:10.1111/j.1364-3703.2007.00437.x · Cited by 148 · see citing works

Crosstalk between abiotic ultraviolet‐B stress and biotic (flg22) stress signalling in Arabidopsis prevents flavonol accumulation in favor of pathogen defence compound production

Schenke, D., Böttcher, C., & Scheel, D. (2011) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2011.02381.x · Cited by 145 · see citing works

The ethylene-responsive factor like protein 1 (CaERFLP1) of hot pepper (Capsicum annuum L.) interacts in vitro with both GCC and DRE/CRT sequences with different binding affinities: Possible biological roles of CaERFLP1 in response to pathogen infection and high salinity conditions in transgenic tobacco plants

Lee, J. H., Hong, J.-P., Oh, S., Lee, S., Choi, D., & Kim, W. S. (2004) · Plant Molecular Biology · doi:10.1007/s11103-004-0417-6 · Cited by 138 · see citing works

Induction of Pathogen Resistance in Barley by Abiotic Stress

Wiese, J., Kranz, T., & Schubert, S. (2004) · Plant Biology · doi:10.1055/s-2004-821176 · Cited by 132 · see citing works

Drought Stress in Tomatoes: Changes in Plant Chemistry and Potential Nonlinear Consequences for Insect Herbivores

English‐Loeb, G. M., Stout, M. J., & Duffey, S. S. (1997) · Oikos · doi:10.2307/3546888 · Cited by 132 · see citing works

Expression of a wheat MYB gene in transgenic tobacco enhances resistance to Ralstonia solanacearum, and to drought and salt stresses

Liu, H., Zhou, X., Dong, N., Liu, X., Zhang, H., & Zhang, Z. (2011) · Functional & Integrative Genomics · doi:10.1007/s10142-011-0228-1 · Cited by 128 · see citing works

The Association Among Gene Expression Responses to Nine Abiotic Stress Treatments inArabidopsis thaliana

Swindell, W. R. (2006) · Genetics · doi:10.1534/genetics.106.061374 · Cited by 126 · see citing works

GhMPK16, a novel stress-responsive group D MAPK gene from cotton, is involved in disease resistance and drought sensitivity

Shi, J., Zhang, L., An, H., et al. (2011) · BMC Molecular Biology · doi:10.1186/1471-2199-12-22 · Cited by 125 · see citing works

Making the most of drought and salinity transcriptomics

Deyholos, M. K. (2009) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2009.02092.x · Cited by 124 · see citing works

The effect of high temperature on the insecticidal properties of Bt Cotton

CHEN, D., Ye, G., YANG, C., CHEN, Y., & Wu, Y. (2004) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2004.04.004 · Cited by 123 · see citing works

The ectopic expression of the rice Osmyb4 gene in Arabidopsis increases tolerance to abiotic, environmental and biotic stresses

Vannini, C., Iriti, M., Bracale, M., et al. (2006) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2006.12.005 · Cited by 121 · see citing works

Two Cysteines in Plant R2R3 MYB Domains Participate in REDOX-dependent DNA Binding

Heine, G. F., Hernandez, J. M., & Grotewold, E. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m405166200 · Cited by 118 · see citing works

Progress and challenge towards reducing wheat spot blotch threat in the Eastern Gangetic Plains of South Asia: Is climate change already taking its toll?

Sharma, R. C., Duveiller, E., & Ortiz‐Ferrara, G. (2007) · Field Crops Research · doi:10.1016/j.fcr.2007.05.004 · Cited by 117 · see citing works

Influence of Combined Biotic and Abiotic Stress on Nutritional Quality Parameters in Tomato (Solanum lycopersicum)

Atkinson, N. J., Dew, T. P., Orfila, C., & Urwin, P. E. (2011) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf202081t · Cited by 117 · see citing works

Rice Mitogen‐activated Protein Kinase Gene Family and Its Role in Biotic and Abiotic Stress Response

Rohila, J. S., & Yang, Y. (2007) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2007.00501.x · Cited by 116 · see citing works

Reconciling Gene Expression Data With Known Genome-Scale Regulatory Network StructuresPreprint

Herrgård, M. J., Covert, M. W., & Palsson, B. Ø. (2003) · Genome Research · doi:10.1101/gr.1330003 · Cited by 115 · see citing works

Improvement of heat and drought photosynthetic tolerance in wheat by overaccumulation of glycinebetaine

Wang, G., Hui, Z., Li, F., Zhao, M., Zhang, J., & Wang, W. (2010) · Plant Biotechnology Reports · doi:10.1007/s11816-010-0139-y · Cited by 110 · see citing works

Plant Response to Root-Knot Nematode

Bird, A. F. (1974) · Annual Review of Phytopathology · doi:10.1146/annurev.py.12.090174.000441 · Cited by 110 · see citing works

Theory and Limitations of Genetic Network Inference from Microarray Data

Margolin, A. A., & Califano, A. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1407.019 · Cited by 107 · see citing works

Effects of Water Stress on Symptomatology and Growth of Parthenocissus quinquefolia Infected by Xylella fastidiosa

McElrone, A. J., Sherald, J. L., & Forseth, I. N. (2001) · Plant Disease · doi:10.1094/pdis.2001.85.11.1160 · Cited by 105 · see citing works

Combined drought and heat stress in wheat: changes in some heat shock proteins

Grigorova, B., Vaseva, I., Demirevska, K., et al. (2011) · Biologia Plantarum · doi:10.1007/s10535-011-0014-x · Cited by 104 · see citing works

Abiotic and biotic stress combinations

Suzuki, N., Rivero, R. M., Shulaev, V., Blumwald, E., & Mittler, R. (2014) · New Phytologist · doi:10.1111/nph.12797 · Cited by 2,153 · see citing works

Plant immune system: Crosstalk between responses to biotic and abiotic stresses the missing link in understanding plant defence

Nejat, N., & Mantri, N. (2017) · Current Issues in Molecular Biology · doi:10.21775/cimb.023.001 · Cited by 287 · see citing works

The effects of climate change associated abiotic stresses on maize phytochemical defenses

Vaughan, M. M., Block, A., Christensen, S. A., Allen, L. H., & Schmelz, E. A. (2018) · Phytochemistry Reviews · doi:10.1007/s11101-017-9508-2 · Cited by 179 · see citing works

Barley Genes as Tools to Confer Abiotic Stress Tolerance in Crops

Gürel, F., Öztürk, Z. N., Uçarlı, C., & Rosellini, D. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01137 · Cited by 130 · see citing works

Genome-wide association analysis of seedling traits in diverse Sorghum germplasm under thermal stress

Chopra, R., Burow, G., Burke, J. J., Gladman, N., & Xin, Z. (2017) · BMC Plant Biology · doi:10.1186/s12870-016-0966-2 · Cited by 113 · see citing works

Abiotic Stress Responses in Plants: Unraveling the Complexity of Genes and Networks to Survive

Sofia, A., de Almeida, A. M., da Silva, A. B., da Silva, J. M., Paula, A., Santos, D., Fevereiro, P., & Sousa Araujo, S. D. (2013) · Abiotic Stress - Plant Responses and Applications in Agriculture · doi:10.5772/52779 · Cited by 106 · see citing works

Genetic approaches to enhance multiple stress tolerance in maize

Malenica, N., Dunić, J. A., Vukadinović, L., Cesar, V., & Šimić, D. (2021) · Genes · doi:10.3390/genes12111760 · Cited by 48 · see citing works

Genetic response of growth phases for abiotic environmental stress tolerance in cereal crop plants

Ali, Q., & Malik, A. (2021) · Genetika · doi:10.2298/gensr2101419a · Cited by 28 · see citing works

Genetic resources and precise gene editing for targeted improvement of barley abiotic stress tolerance

Karunarathne, S., Walker, E., Sharma, D., Li, C., & Han, Y. (2023) · Journal of Zhejiang University-SCIENCE B · doi:10.1631/jzus.b2200552 · Cited by 18 · see citing works

Research Progress on Abscisic Acid and Plant Abiotic Stress Tolerance

Lu, M. (2014) · Northern Horticulture

A novel ABA-insensitive mutant in Arabidopsis reveals molecular network of ABA-induced anthocyanin accumulation and abiotic stress tolerance

Shi, W., Wang, X., Liu, H., et al. (2022) · Journal of Plant Physiology · doi:10.1016/j.jplph.2022.153810 · Cited by 21 · see citing works

In vivo role of nitric oxide in plant response to abiotic and biotic stress

Shi, H., Li, R., Cai, W., Liu, W., Fu, Z.-W., & Lu, Y. (2012) · Plant Signaling & Behavior · doi:10.4161/psb.19219 · Cited by 40 · see citing works

Role of Ethylene in Combating Biotic Stress

Jasrotia, S., & Jasrotia, R. (2022) · doi:10.1002/9781119744719.ch18 · Cited by 20 · see citing works

Quantitative patterns between plant volatile emissions induced by biotic stresses and the degree of damage

Niinemets, Ü., Kännaste, A., & Copolovici, L. O. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00262 · Cited by 282 · see citing works