Abscisic Acid Synthesis and Response

MYB transcription factors in Arabidopsis

Dubos, C., Stracke, R., Grotewold, E., Weisshaar, B., Martin, C., & Lepiniec, L. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.06.005 · Cited by 4,865

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

PLANT COLD ACCLIMATION: Freezing Tolerance Genes and Regulatory Mechanisms

Thomashow, M. F. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.571 · Cited by 3,551

Abscisic Acid: Emergence of a Core Signaling Network

Cutler, S. R., Rodriguez, P. L., Finkelstein, R. R., & Abrams, S. R. (2010) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042809-112122 · Cited by 3,151

Abscisic Acid Inhibits Type 2C Protein Phosphatases via the PYR/PYL Family of START Proteins

Park, S.-Y., Fung, P., Nishimura, N., Jensen, D. R., Fujii, H., Zhao, Y., Lumba, S., Santiago, J., Rodrigues, A., Chow, T.-F. F., et al. (2009) · Science · doi:10.1126/science.1173041 · Cited by 2,974

TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES

Yamaguchi-Shinozaki, K., & Shinozaki, K. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105444 · Cited by 2,950

Arabidopsis Transcription Factors: Genome-Wide Comparative Analysis Among Eukaryotes

Riechmann, J. L., Heard, J., Martin, G., Reuber, L., Jiang, C.-Z., Keddie, J., Adam, L., Pineda, O., Ratcliffe, O. J., Samaha, R. R., et al. (2000) · Science · doi:10.1126/science.290.5499.2105 · Cited by 2,807

An “Electronic Fluorescent Pictograph” Browser for Exploring and Analyzing Large-Scale Biological Data Sets

Winter, D., Vinegar, B., Nahal, H., Ammar, R., Wilson, G. V., & Provart, N. J. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000718 · Cited by 2,558

A gene expression map of Arabidopsis thaliana development

Schmid, M., Davison, T. S., Henz, S. R., Pape, U. J., Demar, M., Vingron, M., Schölkopf, B., Weigel, D., & Lohmann, J. U. (2005) · Nature Genetics · doi:10.1038/ng1543 · Cited by 2,523

Regulators of PP2C Phosphatase Activity Function as Abscisic Acid Sensors

Ma, Y., Szostkiewicz, I., Korte, A., Moes, D., Yang, Y., Christmann, A., & Grill, E. (2009) · Science · doi:10.1126/science.1172408 · Cited by 2,459

ABSCISIC ACID BIOSYNTHESIS AND CATABOLISM

Nambara, E., & Marion-Poll, A. (2005) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.56.032604.144046 · Cited by 2,237

Abscisic Acid Signaling in Seeds and Seedlings

Finkelstein, R. R., Gampala, S. S. L., & Rock, C. D. (2002) · The Plant Cell · doi:10.1105/tpc.010441 · Cited by 2,232

THE MOLECULAR BASIS OF DEHYDRATION TOLERANCE IN PLANTS

Ingram, J., & Bartels, D. (1996) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.47.1.377 · Cited by 2,191

Leaf Senescence

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

CTR1, a negative regulator of the ethylene response pathway in arabidopsis, encodes a member of the Raf family of protein kinases

Kieber, J. J., Rothenberg, M., Roman, G., Feldmann, K. A., & Ecker, J. R. (1993) · Cell · doi:10.1016/0092-8674(93)90119-b · Cited by 1,923

bZIP transcription factors in Arabidopsis

Jakoby, M., Weisshaar, B., Dröge-Laser, W., Vicente-Carbajosa, J., Tiedemann, J., Kroj, T., & Parcy, F. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(01)02223-3 · Cited by 1,849

ROS and redox signalling in the response of plants to abiotic stress

SUZUKI, N., KOUSSEVITZKY, S., MITTLER, R., & MILLER, G. (2012) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2011.02336.x · Cited by 1,694

Recent advances in engineering plant tolerance to abiotic stress: achievements and limitations

Vinocur, B., & Altman, A. (2005) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2005.02.001 · Cited by 1,565

Functional analysis of oxidative stress-activated mitogen-activated protein kinase cascade in plants

Kovtun, Y., Chiu, W.-L., Tena, G., & Sheen, J. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.6.2940 · Cited by 1,530

Isolation and Functional Analysis of Arabidopsis Stress-Inducible NAC Transcription Factors That Bind to a Drought-Responsive cis-Element in the early responsive to dehydration stress 1 Promoter[W]

Tran, L.-S. P., Nakashima, K., Sakuma, Y., Simpson, S. D., Fujita, Y., Maruyama, K., Fujita, M., Seki, M., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2004) · The Plant Cell · doi:10.1105/tpc.104.022699 · Cited by 1,511

Metabolism And Physiology Of Abscisic Acid

Zeevaart, J. (1988) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.39.1.439 · Cited by 1,463

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., Batistic, 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 1,417

Arabidopsis basic leucine zipper transcription factors involved in an abscisic acid-dependent signal transduction pathway under drought and high-salinity conditions

Uno, Y., Furihata, T., Abe, H., Yoshida, R., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.190309197 · Cited by 1,365

Guard Cell Signal Transduction Network: Advances in Understanding Abscisic Acid, CO2, and Ca2+Signaling

Kim, T.-H., Böhmer, M., Hu, H., Nishimura, N., & Schroeder, J. I. (2010) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042809-112226 · Cited by 1,357

EIN2, a Bifunctional Transducer of Ethylene and Stress Responses in Arabidopsis

Alonso, J. M., Hirayama, T., Roman, G., Nourizadeh, S., & Ecker, J. R. (1999) · Science · doi:10.1126/science.284.5423.2148 · Cited by 1,312

Plant Aquaporins: Membrane Channels with Multiple Integrated Functions

Maurel, C., Verdoucq, L., Luu, D.-T., & Santoni, V. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092734 · Cited by 1,280

Transcriptional Regulatory Networks in Response to Abiotic Stresses in Arabidopsis and Grasses

Nakashima, K., Ito, Y., & Yamaguchi-Shinozaki, K. (2009) · Plant Physiology · doi:10.1104/pp.108.129791 · Cited by 1,250

Regulation of SOS1, a plasma membrane Na + /H + exchanger in Arabidopsis thaliana , by SOS2 and SOS3

Qiu, Q.-S., Guo, Y., Dietrich, M. A., Schumaker, K. S., & Zhu, J.-K. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.122224699 · Cited by 1,241

Arabidopsis OST1 Protein Kinase Mediates the Regulation of Stomatal Aperture by Abscisic Acid and Acts Upstream of Reactive Oxygen Species Production

Mustilli, A.-C., Merlot, S., Vavasseur, A., Fenzi, F., & Giraudat, J. (2002) · The Plant Cell · doi:10.1105/tpc.007906 · Cited by 1,231

ABFs, a Family of ABA-responsive Element Binding Factors

Choi, H.-I., Hong, J.-H., Ha, J.-O., Kang, J.-Y., & Kim, S. Y. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.3.1723 · Cited by 1,218

The Arabidopsis Abscisic Acid Response Gene ABI5 Encodes a Basic Leucine Zipper Transcription Factor

Finkelstein, R. R., & Lynch, T. J. (2000) · The Plant Cell · doi:10.1105/tpc.12.4.599 · Cited by 1,143

AREB1, AREB2, and ABF3 are master transcription factors that cooperatively regulate ABRE-dependent ABA signaling involved in drought stress tolerance and require ABA for full activation

Yoshida, T., Fujita, Y., Sayama, H., Kidokoro, S., Maruyama, K., Mizoi, J., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2009.04092.x · Cited by 1,119

Arabidopsis LEAFY COTYLEDON1 Is Sufficient to Induce Embryo Development in Vegetative Cells

Lotan, T., Ohto, M.-A., Yee, K. M., West, M. A. L., Lo, R., Kwong, R. W., Yamagishi, K., Fischer, R. L., Goldberg, R. B., & Harada, J. J. (1998) · Cell · doi:10.1016/s0092-8674(00)81463-4 · Cited by 1,070

Role of arabidopsis MYC and MYB homologs in drought- and abscisic acid-regulated gene expression.

Abe, H., Yamaguchi-Shinozaki, K., Urao, T., Iwasaki, T., Hosokawa, D., & Shinozaki, K. (1997) · The Plant Cell · doi:10.1105/tpc.9.10.1859 · Cited by 1,049

Isolation of the Arabidopsis ABI3 gene by positional cloning.

Giraudat, J., Hauge, B. M., Valon, C., Smalle, J., Parcy, F., & Goodman, H. M. (1992) · The Plant Cell · doi:10.1105/tpc.4.10.1251 · Cited by 1,029

ABA-mediated transcriptional regulation in response to osmotic stress in plants

Fujita, Y., Fujita, M., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2011) · Journal of Plant Research · doi:10.1007/s10265-011-0412-3 · Cited by 1,028

The Arabidopsis cytochrome P450 CYP707A encodes ABA 8′‐hydroxylases: key enzymes in ABA catabolism

Kushiro, T., Okamoto, M., Nakabayashi, K., Yamagishi, K., Kitamura, S., Asami, T., Hirai, N., Koshiba, T., Kamiya, Y., & Nambara, E. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600121 · Cited by 1,019

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., Gil, E., et al. (2010) · Nature · doi:10.1038/nature08854 · Cited by 1,018

Role of DREBs in regulation of abiotic stress responses in plants

Lata, C., & Prasad, M. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err210 · Cited by 1,016

Arabidopsis Mutants Define a Central Role for the Xanthophyll Cycle in the Regulation of Photosynthetic Energy Conversion

Niyogi, K. K., Grossman, A. R., & Björkman, O. (1998) · The Plant Cell · doi:10.1105/tpc.10.7.1121 · Cited by 968

Molecular networks regulating Arabidopsis seed maturation, after‐ripening, dormancy and germination

Holdsworth, M. J., Bentsink, L., & Soppe, W. J. J. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02437.x · Cited by 964

ROOT SIGNALS AND THE REGULATION OF GROWTH AND DEVELOPMENT OF PLANTS IN DRYING SOIL

Zhang, L. (2002) · Cited by 964

Recent advances and emerging trends in plant hormone signalling

Santner, A., & Estelle, M. (2009) · Nature · doi:10.1038/nature08122 · Cited by 960

Different Plant Hormones Regulate Similar Processes through Largely Nonoverlapping Transcriptional Responses

Nemhauser, J. L., Hong, F., & Chory, J. (2006) · Cell · doi:10.1016/j.cell.2006.05.050 · Cited by 947

A postgermination developmental arrest checkpoint is mediated by abscisic acid and requires the ABI5 transcription factor in Arabidopsis

Lopez-Molina, L., Mongrand, S., & Chua, N.-H. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081594298 · Cited by 938

The isolation and characterization of abscisic acid‐insensitive mutants of Arabidopsis thaliana

Koornneef, M., Reuling, G., & Karssen, C. M. (1984) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1984.tb06343.x · Cited by 925

Specific Oxidative Cleavage of Carotenoids by VP14 of Maize

Schwartz, S. H., Tan, B. C., Gage, D. A., Zeevaart, J. A. D., & McCarty, D. R. (1997) · Science · doi:10.1126/science.276.5320.1872 · Cited by 917

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 880

Signal transduction during cold, salt, and drought stresses in plants

Huang, G.-T., Ma, S.-L., Bai, L.-P., Zhang, L., Ma, H., Jia, P., Liu, J., Zhong, M., & Guo, Z.-F. (2012) · Molecular Biology Reports · doi:10.1007/s11033-011-0823-1 · Cited by 866

Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant.

Staswick, P. E., Su, W., & Howell, S. H. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.15.6837 · Cited by 864

SLAC1 is required for plant guard cell S-type anion channel function in stomatal signalling

Vahisalu, T., Kollist, H., Wang, Y.-F., Nishimura, N., Chan, W.-Y., Valerio, G., Lamminmäki, A., Brosché, M., Moldau, H., Desikan, R., et al. (2008) · Nature · doi:10.1038/nature06608 · Cited by 853

AtNAP, a NAC family transcription factor, has an important role in leaf senescence

Guo, Y., & Gan, S. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02723.x · Cited by 850

Molecular characterization of the Arabidopsis 9‐cis epoxycarotenoid dioxygenase gene family

Tan, B., Joseph, L. M., Deng, W., Liu, L., Li, Q., Cline, K., & McCarty, D. R. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01786.x · Cited by 825

Regulation of Abscisic Acid Biosynthesis

Xiong, L., & Zhu, J.-K. (2003) · Plant Physiology · doi:10.1104/pp.103.025395 · Cited by 820

A Brassinosteroid-Insensitive Mutant in Arabidopsis thaliana Exhibits Multiple Defects in Growth and Development

Clouse, S. D., Langford, M., & McMorris, T. C. (1996) · Plant Physiology · doi:10.1104/pp.111.3.671 · Cited by 819

Three Arabidopsis SnRK2 Protein Kinases, SRK2D/SnRK2.2, SRK2E/SnRK2.6/OST1 and SRK2I/SnRK2.3, Involved in ABA Signaling are Essential for the Control of Seed Development and Dormancy

Nakashima, K., Fujita, Y., Kanamori, N., Katagiri, T., Umezawa, T., Kidokoro, S., Maruyama, K., Yoshida, T., Ishiyama, K., Kobayashi, M., et al. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp083 · Cited by 797

Analysis of Cytokinin Mutants and Regulation of Cytokinin Metabolic Genes Reveals Important Regulatory Roles of Cytokinins in Drought, Salt and Abscisic Acid Responses, and Abscisic Acid Biosynthesis

Nishiyama, R., Watanabe, Y., Fujita, Y., Le, D. T., Kojima, M., Werner, T., Vankova, R., Yamaguchi-Shinozaki, K., Shinozaki, K., Kakimoto, T., et al. (2011) · The Plant Cell · doi:10.1105/tpc.111.087395 · Cited by 796

LEAFY COTYLEDON2 encodes a B3 domain transcription factor that induces embryo development

Stone, S. L., Kwong, L. W., Yee, K. M., Pelletier, J., Lepiniec, L., Fischer, R. L., Goldberg, R. B., & Harada, J. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.201413498 · Cited by 786

Arabidopsis ABA Response Gene ABI1 : Features of a Calcium-Modulated Protein Phosphatase

Leung, J., Bouvier-Durand, M., Morris, P.-C., Guerrier, D., Chefdor, F., & Giraudat, J. (1994) · Science · doi:10.1126/science.7910981 · Cited by 767

PDR-type ABC transporter mediates cellular uptake of the phytohormone abscisic acid

Kang, J., Hwang, J.-U., Lee, M., Kim, Y.-Y., Assmann, S. M., Martinoia, E., & Lee, Y. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909222107 · Cited by 764

The Arabidopsis ABSCISIC ACID-INSENSITIVE2 (ABI2) and ABI1 genes encode homologous protein phosphatases 2C involved in abscisic acid signal transduction.

Leung, J., Merlot, S., & Giraudat, J. (1997) · The Plant Cell · doi:10.1105/tpc.9.5.759 · Cited by 755

Nitric oxide, stomatal closure, and abiotic stress

Neill, S., Barros, R., Bright, J., Desikan, R., Hancock, J., Harrison, J., Morris, P., Ribeiro, D., & Wilson, I. (2008) · Journal of Experimental Botany · doi:10.1093/jxb/erm293 · Cited by 741

Three SnRK2 Protein Kinases are the Main Positive Regulators of Abscisic Acid Signaling in Response to Water Stress in Arabidopsis

Fujita, Y., Nakashima, K., Yoshida, T., Katagiri, T., Kidokoro, S., Kanamori, N., Umezawa, T., Fujita, M., Maruyama, K., Ishiyama, K., et al. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp147 · Cited by 730

A Protein Phosphatase 2C Involved in ABA Signal Transduction in Arabidopsis thaliana

Meyer, K., Leube, M. P., & Grill, E. (1994) · Science · doi:10.1126/science.8197457 · Cited by 729

Control of plant development and gene expression by sugar signaling

Gibson, S. I. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.11.003 · Cited by 694

Activation of Glucosidase via Stress-Induced Polymerization Rapidly Increases Active Pools of Abscisic Acid

Lee, K. H., Piao, H. L., Kim, H.-Y., Choi, S. M., Jiang, F., Hartung, W., Hwang, I., Kwak, J. M., Lee, I.-J., & Hwang, I. (2006) · Cell · doi:10.1016/j.cell.2006.07.034 · Cited by 690

ABI5 acts downstream of ABI3 to execute an ABA‐dependent growth arrest during germination

Lopez‐Molina, L., Mongrand, S., McLachlin, D. T., Chait, B. T., & Chua, N. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01430.x · Cited by 686

Arabidopsis MYC2 Interacts with DELLA Proteins in Regulating Sesquiterpene Synthase Gene Expression

Hong, G.-J., Xue, X.-Y., Mao, Y.-B., Wang, L.-J., & Chen, X.-Y. (2012) · The Plant Cell · doi:10.1105/tpc.112.098749 · Cited by 680

Engineering Cold Stress Tolerance in Crop Plants

S. Sanghera, G., H. Wani, S., Hussain, W., & B. Singh, N. (2011) · Current Genomics · doi:10.2174/138920211794520178 · Cited by 640

WRKY transcription factors: key components in abscisic acid signalling

Rushton, D. L., Tripathi, P., Rabara, R. C., Lin, J., Ringler, P., Boken, A. K., Langum, T. J., Smidt, L., Boomsma, D. D., Emme, N. J., et al. (2012) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2011.00634.x · Cited by 638

The Arabidopsis Abscisic Acid Response Locus ABI4 Encodes an APETALA2 Domain Protein

Finkelstein, R. R., Li Wang, M., Lynch, T. J., Rao, S., & Goodman, H. M. (1998) · The Plant Cell · doi:10.1105/tpc.10.6.1043 · Cited by 635

CDPKs CPK6 and CPK3 Function in ABA Regulation of Guard Cell S-Type Anion- and Ca2+- Permeable Channels and Stomatal Closure

Mori, I. C., Murata, Y., Yang, Y., Munemasa, S., Wang, Y.-F., Andreoli, S., Tiriac, H., Alonso, J. M., Harper, J. F., Ecker, J. R., et al. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040327 · Cited by 635

CO2 regulator SLAC1 and its homologues are essential for anion homeostasis in plant cells

Negi, J., Matsuda, O., Nagasawa, T., Oba, Y., Takahashi, H., Kawai-Yamada, M., Uchimiya, H., Hashimoto, M., & Iba, K. (2008) · Nature · doi:10.1038/nature06720 · Cited by 632

Two Calcium-Dependent Protein Kinases, CPK4 and CPK11, Regulate Abscisic Acid Signal Transduction in Arabidopsis

Zhu, S.-Y., Yu, X.-C., Wang, X.-J., Zhao, R., Li, Y., Fan, R.-C., Shang, Y., Du, S.-Y., Wang, X.-F., Wu, F.-Q., et al. (2007) · The Plant Cell · doi:10.1105/tpc.107.050666 · Cited by 632

Pivotal role of the AREB/ABF‐SnRK2 pathway in ABRE‐mediated transcription in response to osmotic stress in plants

Fujita, Y., Yoshida, T., & Yamaguchi‐Shinozaki, K. (2013) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2012.01635.x · Cited by 623

The isolation of abscisic acid (ABA) deficient mutants by selection of induced revertants in non-germinating gibberellin sensitive lines of Arabidopsis thaliana (L.) heynh.

Koornneef, M., Jorna, M. L., Brinkhorst-van der Swan, D. L. C., & Karssen, C. M. (1982) · Theoretical and Applied Genetics · doi:10.1007/bf00272861 · Cited by 623

Repression of AUXIN RESPONSE FACTOR10 by microRNA160 is critical for seed germination and post‐germination stages

Liu, P., Montgomery, T. A., Fahlgren, N., Kasschau, K. D., Nonogaki, H., & Carrington, J. C. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03218.x · Cited by 621

Interactions between Abscisic Acid and Ethylene Signaling Cascades

Beaudoin, N., Serizet, C., Gosti, F., & Giraudat, J. (2000) · The Plant Cell · doi:10.1105/tpc.12.7.1103 · Cited by 621

ABC transporter AtABCG25 is involved in abscisic acid transport and responses

Kuromori, T., Miyaji, T., Yabuuchi, H., Shimizu, H., Sugimoto, E., Kamiya, A., Moriyama, Y., & Shinozaki, K. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912516107 · Cited by 618

ABI1 Protein Phosphatase 2C Is a Negative Regulator of Abscisic Acid Signaling

Gosti, F., Beaudoin, N., Serizet, C., Webb, A. A. R., Vartanian, N., & Giraudat, J. (1999) · The Plant Cell · doi:10.1105/tpc.11.10.1897 · Cited by 613

CYP707A1 and CYP707A2, Which Encode Abscisic Acid 8′-Hydroxylases, Are Indispensable for Proper Control of Seed Dormancy and Germination in Arabidopsis

Okamoto, M., Kuwahara, A., Seo, M., Kushiro, T., Asami, T., Hirai, N., Kamiya, Y., Koshiba, T., & Nambara, E. (2006) · Plant Physiology · doi:10.1104/pp.106.079475 · Cited by 611

Induction of dormancy during seed development by endogenous abscisic acid: studies on abscisic acid deficient genotypes of Arabidopsis thaliana (L.) Heynh.

Karssen, C. M., Brinkhorst-van der Swan, D. L. C., Breekland, A. E., & Koornneef, M. (1983) · Planta · doi:10.1007/bf00393650 · Cited by 609

Gibberellins Promote Flowering of Arabidopsis by Activating the LEAFY Promoter

Blázquez, M. A., Green, R., Nilsson, O., Sussman, M. R., & Weigel, D. (1998) · The Plant Cell · doi:10.1105/tpc.10.5.791 · Cited by 606

Carotenoid Biosynthesis in Arabidopsis: A Colorful Pathway

Ruiz-Sola, M. Á., & Rodríguez-Concepción, M. (2012) · The Arabidopsis Book · doi:10.1199/tab.0158 · Cited by 605

Regulation of Abscisic Acid Signaling by the Ethylene Response Pathway in Arabidopsis

Ghassemian, M., Nambara, E., Cutler, S., Kawaide, H., Kamiya, Y., & McCourt, P. (2000) · The Plant Cell · doi:10.1105/tpc.12.7.1117 · Cited by 595

Molecular Mimicry Regulates ABA Signaling by SnRK2 Kinases and PP2C Phosphatases

Soon, F.-F., Ng, L.-M., Zhou, X. E., West, G. M., Kovach, A., Tan, M. H. E., Suino-Powell, K. M., He, Y., Xu, Y., Chalmers, M. J., et al. (2012) · Science · doi:10.1126/science.1215106 · Cited by 587

Phospholipase Dα1 and Phosphatidic Acid Regulate NADPH Oxidase Activity and Production of Reactive Oxygen Species in ABA-Mediated Stomatal Closure in Arabidopsis

Zhang, Y., Zhu, H., Zhang, Q., Li, M., Yan, M., Wang, R., Wang, L., Welti, R., Zhang, W., & Wang, X. (2009) · The Plant Cell · doi:10.1105/tpc.108.062992 · Cited by 580

The CBL–CIPK network in plant calcium signaling

Luan, S. (2009) · Trends in Plant Science · doi:10.1016/j.tplants.2008.10.005 · Cited by 579

Arabidopsis PYR/PYL/RCAR Receptors Play a Major Role in Quantitative Regulation of Stomatal Aperture and Transcriptional Response to Abscisic Acid

Gonzalez-Guzman, M., Pizzio, G. A., Antoni, R., Vera-Sirera, F., Merilo, E., Bassel, G. W., Fernández, M. A., Holdsworth, M. J., Perez-Amador, M. A., Kollist, H., et al. (2012) · The Plant Cell · doi:10.1105/tpc.112.098574 · Cited by 579

A defined range of guard cell calcium oscillation parameters encodes stomatal movements

Allen, G. J., Chu, S. P., Harrington, C. L., Schumacher, K., Hoffmann, T., Tang, Y. Y., Grill, E., & Schroeder, J. I. (2001) · Nature · doi:10.1038/35082575 · Cited by 578

An Arabidopsis myb homolog is induced by dehydration stress and its gene product binds to the conserved MYB recognition sequence.

Urao, T., Yamaguchi-Shinozaki, K., Urao, S., & Shinozaki, K. (1993) · The Plant Cell · doi:10.1105/tpc.5.11.1529 · Cited by 574

Arabidopsis CYP707A s Encode (+)-Abscisic Acid 8′-Hydroxylase, a Key Enzyme in the Oxidative Catabolism of Abscisic Acid

Saito, S., Hirai, N., Matsumoto, C., Ohigashi, H., Ohta, D., Sakata, K., & Mizutani, M. (2004) · Plant Physiology · doi:10.1104/pp.103.037614 · Cited by 565

Regulation of gene expression programs during Arabidopsis seed development: roles of the ABI3 locus and of endogenous abscisic acid.

Parcy, F., Valon, C., Raynal, M., Gaubier-Comella, P., Delseny, M., & Giraudat, J. (1994) · The Plant Cell · doi:10.1105/tpc.6.11.1567 · Cited by 563

Global analysis of gene activity during Arabidopsis seed development and identification of seed-specific transcription factors

Le, B. H., Cheng, C., Bui, A. Q., Wagmaister, J. A., Henry, K. F., Pelletier, J., Kwong, L., Belmonte, M., Kirkbride, R., Horvath, S., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003530107 · Cited by 562

Genome‐wide profiling of stored mRNA in Arabidopsis thaliana seed germination: epigenetic and genetic regulation of transcription in seed

Nakabayashi, K., Okamoto, M., Koshiba, T., Kamiya, Y., & Nambara, E. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02337.x · Cited by 560

The Mg-Chelatase H Subunit of Arabidopsis Antagonizes a Group of WRKY Transcription Repressors to Relieve ABA-Responsive Genes of Inhibition

Shang, Y., Yan, L., Liu, Z.-Q., Cao, Z., Mei, C., Xin, Q., Wu, F.-Q., Wang, X.-F., Du, S.-Y., Jiang, T., et al. (2010) · The Plant Cell · doi:10.1105/tpc.110.073874 · Cited by 556

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

de Torres‐Zabala, M., Truman, W., Bennett, M. H., Lafforgue, G., Mansfield, J. W., Rodriguez Egea, P., Bögre, L., & Grant, M. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601575 · Cited by 554

The Arabidopsis LOS5/ABA3 Locus Encodes a Molybdenum Cofactor Sulfurase and Modulates Cold Stress– and Osmotic Stress–Responsive Gene Expression

Xiong, L., Ishitani, M., Lee, H., & Zhu, J.-K. (2001) · The Plant Cell · doi:10.1105/tpc.010101 · Cited by 552

Molecular identification of zeaxanthin epoxidase of Nicotiana plumbaginifolia, a gene involved in abscisic acid biosynthesis and corresponding to the ABA locus of Arabidopsis thaliana.

Marin, E., Nussaume, L., Quesada, A., Gonneau, M., Sotta, B., Hugueney, P., Frey, A., & Marion-Poll, A. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00589.x · Cited by 550

A hydraulic signal in root‐to‐shoot signalling of water shortage

Christmann, A., Weiler, E. W., Steudle, E., & Grill, E. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03234.x · Cited by 546

The Mg-chelatase H subunit is an abscisic acid receptor

Shen, Y.-Y., Wang, X.-F., Wu, F.-Q., Du, S.-Y., Cao, Z., Shang, Y., Wang, X.-L., Peng, C.-C., Yu, X.-C., Zhu, S.-Y., et al. (2006) · Nature · doi:10.1038/nature05176 · Cited by 538

Hormone Signalling Crosstalk in Plant Growth Regulation

Depuydt, S., & Hardtke, C. S. (2011) · Current Biology · doi:10.1016/j.cub.2011.03.013 · Cited by 535

Genetic analysis of osmotic and cold stress signal transduction in Arabidopsis: interactions and convergence of abscisic acid-dependent and abscisic acid-independent pathways.

Ishitani, M., Xiong, L., Stevenson, B., & Zhu, J. K. (1997) · The Plant Cell · doi:10.1105/tpc.9.11.1935 · Cited by 531

The Arabidopsis double-stranded RNA-binding protein HYL1 plays a role in microRNA-mediated gene regulation

Han, M.-H., Goud, S., Song, L., & Fedoroff, N. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307969100 · Cited by 525

‘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 516

G Protein Regulation of Ion Channels and Abscisic Acid Signaling in Arabidopsis Guard Cells

Wang, Q., Ullah, H., Jones, A. M., & Assmann, S. M. (2001) · Science · doi:10.1126/science.1059046 · Cited by 514

Whole Gene Family Expression and Drought Stress Regulation of Aquaporins

Alexandersson, E., Fraysse, L., Sjövall-Larsen, S., Gustavsson, S., Fellert, M., Karlsson, M., Johanson, U., & Kjellbom, P. (2005) · Plant Molecular Biology · doi:10.1007/s11103-005-0352-1 · Cited by 512

The AtGenExpress hormone and chemical treatment data set: experimental design, data evaluation, model data analysis and data access

Goda, H., Sasaki, E., Akiyama, K., Maruyama‐Nakashita, A., Nakabayashi, K., Li, W., Ogawa, M., Yamauchi, Y., Preston, J., Aoki, K., et al. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03510.x · Cited by 509

Arabidopsis Transcriptome Analysis under Drought, Cold, High-Salinity and ABA Treatment Conditions using a Tiling Array

Matsui, A., Ishida, J., Morosawa, T., Mochizuki, Y., Kaminuma, E., Endo, T. A., Okamoto, M., Nambara, E., Nakajima, M., Kawashima, M., et al. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn101 · Cited by 509

PYR/PYL/RCAR family members are major in‐vivo ABI1 protein phosphatase 2C‐interacting proteins in Arabidopsis

Nishimura, N., Sarkeshik, A., Nito, K., Park, S., Wang, A., Carvalho, P. C., Lee, S., Caddell, D. F., Cutler, S. R., Chory, J., et al. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2009.04054.x · Cited by 505

Achievements and Challenges in Understanding Plant Abiotic Stress Responses and Tolerance

Qin, F., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2011) · Plant and Cell Physiology · doi:10.1093/pcp/pcr106 · Cited by 500

An Update on Abscisic Acid Signaling in Plants and More …

Wasilewska, A., Vlad, F., Sirichandra, C., Redko, Y., Jammes, F., Valon, C., Frey, N. F. D., & Leung, J. (2008) · Molecular Plant · doi:10.1093/mp/ssm022 · Cited by 499

Identification of an abscisic acid transporter by functional screening using the receptor complex as a sensor

Kanno, Y., Hanada, A., Chiba, Y., Ichikawa, T., Nakazawa, M., Matsui, M., Koshiba, T., Kamiya, Y., & Seo, M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1203567109 · Cited by 498

The interaction between DCL1 and HYL1 is important for efficient and precise processing of pri-miRNA in plant microRNA biogenesis

KURIHARA, Y., TAKASHI, Y., & WATANABE, Y. (2006) · RNA · doi:10.1261/rna.2146906 · Cited by 495

A Mutation in the Arabidopsis HYL1 Gene Encoding a dsRNA Binding Protein Affects Responses to Abscisic Acid, Auxin, and Cytokinin

Lu, C., & Fedoroff, N. (2000) · The Plant Cell · doi:10.1105/tpc.12.12.2351 · Cited by 489

The Stomatal Response to Reduced Relative Humidity Requires Guard Cell-Autonomous ABA Synthesis

Bauer, H., Ache, P., Lautner, S., Fromm, J., Hartung, W., Al-Rasheid, K. A. S., Sonnewald, S., Sonnewald, U., Kneitz, S., Lachmann, N., et al. (2013) · Current Biology · doi:10.1016/j.cub.2012.11.022 · Cited by 485

Alteration of Stimulus-Specific Guard Cell Calcium Oscillations and Stomatal Closing in Arabidopsis det3 Mutant

Allen, G. J., Chu, S. P., Schumacher, K., Shimazaki, C. T., Vafeados, D., Kemper, A., Hawke, S. D., Tallman, G., Tsien, R. Y., Harper, J. F., et al. (2000) · Science · doi:10.1126/science.289.5488.2338 · Cited by 481

An Expression Analysis of a Gene Family Encoding Plasma Membrane Aquaporins in Response to Abiotic Stresses in Arabidopsis Thaliana

Jang, J. Y., Kim, D. G., Kim, Y. O., Kim, J. S., & Kang, H. (2004) · Plant Molecular Biology · doi:10.1023/b:plan.0000040900.61345.a6 · Cited by 480

Biosynthesis of Plant Isoprenoids: Perspectives for Microbial Engineering

Kirby, J., & Keasling, J. D. (2009) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.043008.091955 · Cited by 478

Interaction with ethylene: changing views on the role of abscisic acid in root and shoot growth responses to water stress

Sharp, R. E. (2002) · Plant, Cell & Environment · doi:10.1046/j.1365-3040.2002.00798.x · Cited by 478

BIN2, a New Brassinosteroid-Insensitive Locus in Arabidopsis

Li, J., Nam, K. H., Vafeados, D., & Chory, J. (2001) · Plant Physiology · doi:10.1104/pp.127.1.14 · Cited by 474

MAPK target networks in Arabidopsis thaliana revealed using functional protein microarrays

Popescu, S. C., Popescu, G. V., Bachan, S., Zhang, Z., Gerstein, M., Snyder, M., & Dinesh-Kumar, S. P. (2009) · Genes & Development · doi:10.1101/gad.1740009 · Cited by 472

A Role for Brassinosteroids in Germination in Arabidopsis

Steber, C. M., & McCourt, P. (2001) · Plant Physiology · doi:10.1104/pp.125.2.763 · Cited by 461

Two Novel GPCR-Type G Proteins Are Abscisic Acid Receptors in Arabidopsis

Pandey, S., Nelson, D. C., & Assmann, S. M. (2009) · Cell · doi:10.1016/j.cell.2008.12.026 · Cited by 461

Analysis of Arabidopsis glucose insensitive mutants, gin5 and gin6, reveals a central role of the plant hormone ABA in the regulation of plant vegetative development by sugar.

Arenas‐Huertero, F., Arroyo-Becerra, A., Zhou, L., Sheen, J., & León, P. (2000) · PubMed Central · Cited by 456

The Arabidopsis LOS5/ABA3 Locus Encodes a Molybdenum Cofactor Sulfurase and Modulates Cold Stress- and Osmotic Stress-Responsive Gene Expression

Xiong, L. (2001) · THE PLANT CELL ONLINE · doi:10.1105/tpc.13.9.2063 · Cited by 454

Reconstitution of abscisic acid activation of SLAC1 anion channel by CPK6 and OST1 kinases and branched ABI1 PP2C phosphatase action

Brandt, B., Brodsky, D. E., Xue, S., Negi, J., Iba, K., Kangasjärvi, J., Ghassemian, M., Stephan, A. B., Hu, H., & Schroeder, J. I. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1116590109 · Cited by 447

A dominant mutation inArabidopsis confers resistance to auxin, ethylene and abscisic acid

Wilson, A. K., Pickett, F. B., Turner, J. C., & Estelle, M. (1990) · Molecular and General Genetics MGG · doi:10.1007/bf00633843 · Cited by 446

The Arabidopsis HOS1 gene negatively regulates cold signal transduction and encodes a RING finger protein that displays cold-regulated nucleo–cytoplasmic partitioning

Lee, H., Xiong, L., Gong, Z., Ishitani, M., Stevenson, B., & Zhu, J.-K. (2001) · Genes & Development · doi:10.1101/gad.866801 · Cited by 446

The Arabidopsis aldehyde oxidase 3 ( AAO3 ) gene product catalyzes the final step in abscisic acid biosynthesis in leaves

Seo, M., Peeters, A. J. M., Koiwai, H., Oritani, T., Marion-Poll, A., Zeevaart, J. A. D., Koornneef, M., Kamiya, Y., & Koshiba, T. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.220426197 · Cited by 439

An mRNA Cap Binding Protein, ABH1, Modulates Early Abscisic Acid Signal Transduction in Arabidopsis

Hugouvieux, V., Kwak, J. M., & Schroeder, J. I. (2001) · Cell · doi:10.1016/s0092-8674(01)00460-3 · Cited by 435

Genetics and Phosphoproteomics Reveal a Protein Phosphorylation Network in the Abscisic Acid Signaling Pathway in Arabidopsis thaliana

Umezawa, T., Sugiyama, N., Takahashi, F., Anderson, J. C., Ishihama, Y., Peck, S. C., & Shinozaki, K. (2013) · Science Signaling · doi:10.1126/scisignal.2003509 · Cited by 433

Leafy Cotyledon Mutants of Arabidopsis.

Meinke, D. W., Franzmann, L. H., Nickle, T. C., & Yeung, E. C. (1994) · The Plant Cell · doi:10.1105/tpc.6.8.1049 · Cited by 429

Mutations at two new Arabidopsis ABA response loci are similar to the abi3 mutations

Finkelstein, R. R. (1994) · The Plant Journal · doi:10.1046/j.1365-313x.1994.5060765.x · Cited by 429

The roles of ABA in plant–pathogen interactions

Cao, F. Y., Yoshioka, K., & Desveaux, D. (2011) · Journal of Plant Research · doi:10.1007/s10265-011-0409-y · Cited by 427

The AIP2 E3 ligase acts as a novel negative regulator of ABA signaling by promoting ABI3 degradation

Zhang, X., Garreton, V., & Chua, N.-H. (2005) · Genes & Development · doi:10.1101/gad.1318705 · Cited by 427

Regulation of Osmotic Stress-responsive Gene Expression by theLOS6/ABA1 Locus inArabidopsis

Xiong, L., Lee, H., Ishitani, M., & Zhu, J.-K. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m109275200 · Cited by 424

ICK1, a cyclin‐dependent protein kinase inhibitor fromArabidopsis thalianainteracts with both Cdc2a and CycD3, and its expression is induced by abscisic acid

Wang, H., Qi, Q., Schorr, P., Cutler, A. J., Crosby, W. L., & Fowke, L. C. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00231.x · Cited by 423

The CBL–CIPK Ca2+‐decoding signaling network: function and perspectives

Weinl, S., & Kudla, J. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2009.02938.x · Cited by 421

Impaired sucrose‐induction mutants reveal the modulation of sugar‐induced starch biosynthetic gene expression by abscisic acid signalling

Rook, F., Corke, F., Card, R., Munz, G., Smith, C., & Bevan, M. W. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.2641043.x · Cited by 421

Predicting Essential Components of Signal Transduction Networks: A Dynamic Model of Guard Cell Abscisic Acid Signaling

Li, S., Assmann, S. M., & Albert, R. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040312 · Cited by 418

A Protein Farnesyl Transferase Involved in Abscisic Acid Signal Transduction in Arabidopsis

Cutler, S., Ghassemian, M., Bonetta, D., Cooney, S., & McCourt, P. (1996) · Science · doi:10.1126/science.273.5279.1239 · Cited by 414

The Arabidopsis sugar‐insensitive mutants sis4 and sis5 are defective in abscisic acid synthesis and response

Laby, R. J., Kincaid, M. S., Kim, D., & Gibson, S. I. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00833.x · Cited by 406

The Arabidopsis thaliana NAC transcription factor family: structure–function relationships and determinants of ANAC019 stress signalling

Jensen, M. K., Kjaersgaard, T., Nielsen, M. M., Galberg, P., Petersen, K., O'Shea, C., & Skriver, K. (2010) · Biochemical Journal · doi:10.1042/bj20091234 · Cited by 405

ABA plays a central role in mediating the regulatory effects of nitrate on root branching in Arabidopsis

Signora, L., De Smet, I., Foyer, C. H., & Zhang, H. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.01185.x · Cited by 403

Analysis of Arabidopsis glucose insensitive mutants,gin5 and gin6, reveals a central role of the plant hormone ABA in the regulation of plant vegetative development by sugar

Arenas-Huertero, F., Arroyo, A., Zhou, L., Sheen, J., & León, P. (2000) · Genes & Development · doi:10.1101/gad.14.16.2085 · Cited by 403

Signals from Chloroplasts Converge to Regulate Nuclear Gene Expression

Koussevitzky, S., Nott, A., Mockler, T. C., Hong, F., Sachetto-Martins, G., Surpin, M., Lim, J., Mittler, R., & Chory, J. (2007) · Science · doi:10.1126/science.1140516 · Cited by 400

The Arabidopsis NAC Transcription Factor VNI2 Integrates Abscisic Acid Signals into Leaf Senescence via the COR/RD Genes

Yang, S.-D., Seo, P. J., Yoon, H.-K., & Park, C.-M. (2011) · The Plant Cell · doi:10.1105/tpc.111.084913 · Cited by 399

Stomatal Closure by Fast Abscisic Acid Signaling Is Mediated by the Guard Cell Anion Channel SLAH3 and the Receptor RCAR1

Geiger, D., Maierhofer, T., AL-Rasheid, K. A. S., Scherzer, S., Mumm, P., Liese, A., Ache, P., Wellmann, C., Marten, I., Grill, E., et al. (2011) · Science Signaling · doi:10.1126/scisignal.2001346 · Cited by 399

Drought and Abscisic Acid Effects on Aquaporin Content Translate into Changes in Hydraulic Conductivity and Leaf Growth Rate: A Trans-Scale Approach

Parent, B., Hachez, C., Redondo, E., Simonneau, T., Chaumont, F., & Tardieu, F. (2009) · Plant Physiology · doi:10.1104/pp.108.130682 · Cited by 396

Abscisic Acid Accumulation Maintains Maize Primary Root Elongation at Low Water Potentials by Restricting Ethylene Production

Spollen, W. G., LeNoble, M. E., Samuels, T. D., Bernstein, N., & Sharp, R. E. (2000) · Plant Physiology · doi:10.1104/pp.122.3.967 · Cited by 395

A bZIP factor, TRAB1, interacts with VP1 and mediates abscisic acid-induced transcription

Hobo, T., Kowyama, Y., & Hattori, T. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.26.15348 · Cited by 386

AtALMT12 represents an R-type anion channel required for stomatal movement in Arabidopsis guard cells: AtALMT12-mediated release of anions in guard cells

Meyer, S., Mumm, P., Imes, D., Endler, A., Weder, B., Al-Rasheid, K. A. S., Geiger, D., Marten, I., Martinoia, E., & Hedrich, R. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04302.x · Cited by 385

Interaction of light and hormone signals in germinating seeds

Seo, M., Nambara, E., Choi, G., & Yamaguchi, S. (2009) · Plant Molecular Biology · doi:10.1007/s11103-008-9429-y · Cited by 381

MOTHER OF FT AND TFL1 Regulates Seed Germination through a Negative Feedback Loop Modulating ABA Signaling in Arabidopsis

Xi, W., Liu, C., Hou, X., & Yu, H. (2010) · The Plant Cell · doi:10.1105/tpc.109.073072 · Cited by 376

Changes in cytosolic pH and calcium of guard cells precede stomatal movements.

Irving, H. R., Gehring, C. A., & Parish, R. W. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.5.1790 · Cited by 374

FIERY1 encoding an inositol polyphosphate 1-phosphatase is a negative regulator of abscisic acid and stress signaling in Arabidopsis

Xiong, L., Lee, B.-H., Ishitani, M., Lee, H., Zhang, C., & Zhu, J.-K. (2001) · Genes & Development · doi:10.1101/gad.891901 · Cited by 370

ABA-Hypersensitive Germination3 Encodes a Protein Phosphatase 2C (AtPP2CA) That Strongly Regulates Abscisic Acid Signaling during Germination among Arabidopsis Protein Phosphatase 2Cs

Yoshida, T., Nishimura, N., Kitahata, N., Kuromori, T., Ito, T., Asami, T., Shinozaki, K., & Hirayama, T. (2006) · Plant Physiology · doi:10.1104/pp.105.070128 · Cited by 370

FUSCA3encodes a protein with a conserved VP1/ABI3‐like B3 domain which is of functional importance for the regulation of seed maturation inArabidopsis thaliana

Luerßen, H., Kirik, V., Herrmann, P., & Miséra, S. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00259.x · Cited by 369

Drought Induction of Arabidopsis 9-cis-Epoxycarotenoid Dioxygenase Occurs in Vascular Parenchyma Cells

Endo, A., Sawada, Y., Takahashi, H., Okamoto, M., Ikegami, K., Koiwai, H., Seo, M., Toyomasu, T., Mitsuhashi, W., Shinozaki, K., et al. (2008) · Plant Physiology · doi:10.1104/pp.108.116632 · Cited by 369

The ABSCISIC ACID INSENSITIVE 3 ( ABI3 ) gene is modulated by farnesylation and is involved in auxin signaling and lateral root development in Arabidopsis

Brady, S. M., Sarkar, S. F., Bonetta, D. T., & McCourt, P. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01707.x · Cited by 367

Use of infrared thermal imaging to isolate Arabidopsis mutants defective in stomatal regulation

Merlot, S., Mustilli, A., Genty, B., North, H., Lefebvre, V., Sotta, B., Vavasseur, A., & Giraudat, J. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01322.x · Cited by 366

Oligogalacturonic Acid and Chitosan Reduce Stomatal Aperture by Inducing the Evolution of Reactive Oxygen Species from Guard Cells of Tomato and Commelina communis

Lee, S., Choi, H., Suh, S., Doo, I.-S., Oh, K.-Y., Jeong Choi, E., Schroeder Taylor, A. T., Low, P. S., & Lee, Y. (1999) · Plant Physiology · doi:10.1104/pp.121.1.147 · Cited by 362

Homeodomain protein ATHB6 is a target of the protein phosphatase ABI1 and regulates hormone responses in Arabidopsis

Himmelbach, A. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf316 · Cited by 359

A DEAD Box RNA Helicase Is Essential for mRNA Export and Important for Development and Stress Responses in Arabidopsis

Gong, Z., Dong, C.-H., Lee, H., Zhu, J., Xiong, L., Gong, D., Stevenson, B., & Zhu, J.-K. (2005) · The Plant Cell · doi:10.1105/tpc.104.027557 · Cited by 358

The aba mutant of Arabidopsis thaliana is impaired in epoxy-carotenoid biosynthesis.

Rock, C. D., & Zeevaart, J. A. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.17.7496 · Cited by 355

Arabidopsis Calcium-Dependent Protein Kinase AtCPK32 Interacts with ABF4, a Transcriptional Regulator of Abscisic Acid-Responsive Gene Expression, and Modulates Its Activity

Choi, H.-I., Park, H.-J., Park, J. H., Kim, S., Im, M.-Y., Seo, H.-H., Kim, Y.-W., Hwang, I., & Kim, S. Y. (2005) · Plant Physiology · doi:10.1104/pp.105.069757 · Cited by 353

Constitutive activation of a plasma membrane H+‐ATPase prevents abscisic acid‐mediated stomatal closure

Merlot, S., Leonhardt, N., Fenzi, F., Valon, C., Costa, M., Piette, L., Vavasseur, A., Genty, B., Boivin, K., Müller, A., et al. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601750 · Cited by 353

A Stress-Inducible Gene for 9-cis-Epoxycarotenoid Dioxygenase Involved in Abscisic Acid Biosynthesis under Water Stress in Drought-Tolerant Cowpea

Iuchi, S., Kobayashi, M., Yamaguchi-Shinozaki, K., & Shinozaki, K. (2000) · Plant Physiology · doi:10.1104/pp.123.2.553 · Cited by 353

Isolation of a strong Arabidopsis guard cell promoter and its potential as a research tool

Yang, Y., Costa, A., Leonhardt, N., Siegel, R. S., & Schroeder, J. I. (2008) · Plant Methods · doi:10.1186/1746-4811-4-6 · Cited by 352

Epoxycarotenoid cleavage by NCED5 fine‐tunes ABA accumulation and affects seed dormancy and drought tolerance with other NCED family members

Frey, A., Effroy, D., Lefebvre, V., Seo, M., Perreau, F., Berger, A., Sechet, J., To, A., North, H. M., & Marion‐Poll, A. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04887.x · Cited by 350

Leucine-Rich Repeat Receptor-Like Kinase1 Is a Key Membrane-Bound Regulator of Abscisic Acid Early Signaling in Arabidopsis

Osakabe, Y., Maruyama, K., Seki, M., Satou, M., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2005) · The Plant Cell · doi:10.1105/tpc.104.027474 · Cited by 348

AFP is a novel negative regulator of ABA signaling that promotes ABI5 protein degradation

Lopez-Molina, L., Mongrand, S., Kinoshita, N., & Chua, N.-H. (2003) · Genes & Development · doi:10.1101/gad.1055803 · Cited by 344

LOS2, a genetic locus required for cold-responsive gene transcription encodes a bi-functional enolase

Lee, H. (2002) · The EMBO Journal · doi:10.1093/emboj/21.11.2692 · Cited by 343

Arabidopsis decuple mutant reveals the importance of SnRK2 kinases in osmotic stress responses in vivo

Fujii, H., Verslues, P. E., & Zhu, J.-K. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018367108 · Cited by 341

GORK, a delayed outward rectifier expressed in guard cells of Arabidopsis thaliana, is a K+‐selective, K+‐sensing ion channel

Ache, P., Becker, D., Ivashikina, N., Dietrich, P., Roelfsema, M. R. G., & Hedrich, R. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)02248-1 · Cited by 338

The dual effect of abscisic acid on stomata

Pantin, F., Monnet, F., Jannaud, D., Costa, J. M., Renaud, J., Muller, B., Simonneau, T., & Genty, B. (2013) · New Phytologist · doi:10.1111/nph.12013 · Cited by 338

Modulation of Abscisic Acid Signal Transduction and Biosynthesis by an Sm-like Protein in Arabidopsis

Xiong, L., Gong, Z., Rock, C. D., Subramanian, S., Guo, Y., Xu, W., Galbraith, D., & Zhu, J.-K. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00087-9 · Cited by 331

Triple Loss of Function of Protein Phosphatases Type 2C Leads to Partial Constitutive Response to Endogenous Abscisic Acid

Rubio, S., Rodrigues, A., Saez, A., Dizon, M. B., Galle, A., Kim, T.-H., Santiago, J., Flexas, J., Schroeder, J. I., & Rodriguez, P. L. (2009) · Plant Physiology · doi:10.1104/pp.109.137174 · Cited by 326

The ABSCISIC ACID-INSENSITIVE3, FUSCA3, and LEAFY COTYLEDON1 loci act in concert to control multiple aspects of Arabidopsis seed development.

Parcy, F., Valon, C., Kohara, A., Miséra, S., & Giraudat, J. (1997) · The Plant Cell · doi:10.1105/tpc.9.8.1265 · Cited by 325

Endogenous ABA maintains shoot growth in tomato independently of effects on plant water balance: evidence for an interaction with ethylene

Sharp, R. E., LeNoble, M. E., Else, M. A., Thorne, E. T., & Gherardi, F. (2000) · Journal of Experimental Botany · doi:10.1093/jexbot/51.350.1575 · Cited by 316

Postgerminative growth and lipid catabolism in oilseeds lacking the glyoxylate cycle

Eastmond, P. J., Germain, V., Lange, P. R., Bryce, J. H., Smith, S. M., & Graham, I. A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.10.5669 · Cited by 314

A Vacuolar β-Glucosidase Homolog That Possesses Glucose-Conjugated Abscisic Acid Hydrolyzing Activity Plays an Important Role in Osmotic Stress Responses in Arabidopsis

Xu, Z.-Y., Lee, K. H., Dong, T., Jeong, J. C., Jin, J. B., Kanno, Y., Kim, D. H., Kim, S. Y., Seo, M., Bressan, R. A., et al. (2012) · The Plant Cell · doi:10.1105/tpc.112.095935 · Cited by 314

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

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

Carbon and nitrogen nutrient balance signaling in plants

Zheng, Z.-L. (2009) · Plant Signaling & Behavior · doi:10.4161/psb.4.7.8540 · Cited by 308

Stress‐induced changes in the Arabidopsis thaliana transcriptome analyzed using whole‐genome tiling arrays

Zeller, G., Henz, S. R., Widmer, C. K., Sachsenberg, T., Rätsch, G., Weigel, D., & Laubinger, S. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03835.x · Cited by 306

Involvement of Arabidopsis HOS15 in histone deacetylation and cold tolerance

Zhu, J., Jeong, J. C., Zhu, Y., Sokolchik, I., Miyazaki, S., Zhu, J.-K., Hasegawa, P. M., Bohnert, H. J., Shi, H., Yun, D.-J., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801029105 · Cited by 306

Physical interactions between ABA response loci of Arabidopsis

Nakamura, S., Lynch, T. J., & Finkelstein, R. R. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.01069.x · Cited by 305

Dormancy cycling in Arabidopsis seeds is controlled by seasonally distinct hormone-signaling pathways

Footitt, S., Douterelo-Soler, I., Clay, H., & Finch-Savage, W. E. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1116325108 · Cited by 304

The Molecular Basis of ABA-Independent Inhibition of PP2Cs by a Subclass of PYL Proteins

Hao, Q., Yin, P., Li, W., Wang, L., Yan, C., Lin, Z., Wu, J. Z., Wang, J., Yan, S. F., & Yan, N. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.05.011 · Cited by 304

Abscisic Acid‐mediated Epigenetic Processes in Plant Development and Stress Responses

Chinnusamy, V., Gong, Z., & Zhu, J. (2008) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2008.00727.x · Cited by 303

Unique Drought Resistance Functions of the Highly ABA-Induced Clade A Protein Phosphatase 2Cs

Bhaskara, G. B., Nguyen, T. T., & Verslues, P. E. (2012) · Plant Physiology · doi:10.1104/pp.112.202408 · Cited by 299

ABI4 Mediates Abscisic Acid and Cytokinin Inhibition of Lateral Root Formation by Reducing Polar Auxin Transport in Arabidopsis

Shkolnik‐Inbar, D., & Bar‐Zvi, D. (2010) · The Plant Cell · doi:10.1105/tpc.110.074641 · Cited by 298

Mutational analysis of protein phosphatase 2C involved in abscisic acid signal transduction in higher plants

Sheen, J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.3.975 · Cited by 297

Ethylene Interacts with Abscisic Acid to Regulate Endosperm Rupture during Germination: A Comparative Approach Using Lepidium sativum and Arabidopsis thaliana

Linkies, A., Müller, K., Morris, K., Turečková, V., Wenk, M., Cadman, C. S. C., Corbineau, F., Strnad, M., Lynn, J. R., Finch-Savage, W. E., et al. (2010) · The Plant Cell · doi:10.1105/tpc.109.070201 · Cited by 297

A Null Mutation in a bZIP Factor Confers ABA-Insensitivity in Arabidopsis thaliana

Lopez-Molina, L., & Chua, N.-H. (2000) · Plant and Cell Physiology · doi:10.1093/pcp/41.5.541 · Cited by 297

A framework integrating plant growth with hormones and nutrients

Krouk, G., Ruffel, S., Gutiérrez, R. A., Gojon, A., Crawford, N. M., Coruzzi, G. M., & Lacombe, B. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2011.02.004 · Cited by 292

Major flowering time gene, FLOWERING LOCUS C , regulates seed germination in Arabidopsis thaliana

Chiang, G. C. K., Barua, D., Kramer, E. M., Amasino, R. M., & Donohue, K. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901367106 · Cited by 292

Bundle‐sheath cell regulation of xylem‐mesophyll water transport via aquaporins under drought stress: a target of xylem‐borne ABA?

Shatil‐Cohen, A., Attia, Z., & Moshelion, M. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04576.x · Cited by 288

Carotenoid Metabolism in Plants: The Role of Plastids

Sun, T., Yuan, H., Cao, H., Yazdani, M., Tadmor, Y., & Li, L. (2018) · Molecular Plant · doi:10.1016/j.molp.2017.09.010 · Cited by 685

Mechanisms of abscisic acid-mediated control of stomatal aperture

Munemasa, S., Hauser, F., Park, J., Waadt, R., Brandt, B., & Schroeder, J. I. (2015) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2015.10.010 · Cited by 567

Crosstalk between phytohormones and secondary metabolites in the drought stress tolerance of crop plants: A review

Jogawat, A., Yadav, B., Chhaya, Lakra, N., Singh, A. K., & Narayan, O. P. (2021) · Physiologia Plantarum · doi:10.1111/ppl.13328 · Cited by 429

Degradation of the ABA co-receptor ABI1 by PUB12/13 U-box E3 ligases

Kong, L., Cheng, J., Zhu, Y., Ding, Y., Meng, J., Chen, Z., Xie, Q., Guo, Y., Li, J., Yang, S., et al. (2015) · Nature Communications · doi:10.1038/ncomms9630 · Cited by 316

Regulatory networks in plant responses to drought and cold stress

Kim, J.-S., Kidokoro, S., Yamaguchi-Shinozaki, K., & Shinozaki, K. (2024) · Plant Physiology · doi:10.1093/plphys/kiae105 · Cited by 303