Transcriptional auxin–brassinosteroid crosstalk: Who's talking?

Mechanism of auxin perception by the TIR1 ubiquitin ligase

Tan, X., Calderon-Villalobos, L. I. A., Sharon, M., Zheng, C., Robinson, C. V., Estelle, M., & Zheng, N. (2007) · Nature · doi:10.1038/nature05731 · Cited by 1,688 · see citing works

BES1 Accumulates in the Nucleus in Response to Brassinosteroids to Regulate Gene Expression and Promote Stem Elongation

Yin, Y., Wang, Z., Mora‐García, S., Li, J., Yoshida, S., Asami, T., & Chory, J. (2002) · Cell · doi:10.1016/s0092-8674(02)00721-3 · Cited by 1,287 · see citing works

A Gene Expression Map of the Arabidopsis Root

Birnbaum, K. D., Shasha, D. E., Wang, J. Y., Jung, J. W., Lambert, G. M., Galbraith, D. W., & Benfey, P. N. (2003) · Science · doi:10.1126/science.1090022 · Cited by 1,260 · see citing works

Nuclear-Localized BZR1 Mediates Brassinosteroid-Induced Growth and Feedback Suppression of Brassinosteroid Biosynthesis

Wang, Z., Nakano, T., Gendron, J. M., He, J., Chen, M., Vafeados, D. K., Yang, Y., Fujioka, S., Yoshida, S., Asami, T., et al. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00153-3 · Cited by 1,148 · see citing works

Brassinolide, a plant growth-promoting steroid isolated from Brassica napus pollen

Grove, M. D., Spencer, G. F., Rohwedder, W. K., Mandava, N. B., Worley, J. F., Warthen, J. D., Steffens, G. L., Flippen-Anderson, J. L., & Cook, J. C. (1979) · Nature · doi:10.1038/281216a0 · Cited by 1,024 · see citing works

Plant Development Is Regulated by a Family of Auxin Receptor F Box Proteins

Dharmasiri, N., Dharmasiri, S., Weijers, D., Lechner, E., Yamada, M., Hobbie, L., Ehrismann, J. S., Jürgens, G., & Estelle, M. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.05.014 · Cited by 997 · see citing works

Analysis of Transcription Factor HY5 Genomic Binding Sites Revealed Its Hierarchical Role in Light Regulation of Development

Lee, J., He, K., Štolc, V., Lee, H., Figueroa, P. M., Gao, Y., Tongprasit, W., Zhao, H., Lee, I., & Deng, X. W. (2007) · The Plant Cell · doi:10.1105/tpc.106.047688 · Cited by 981 · see citing works

A Role for Brassinosteroids in Light-Dependent Development of Arabidopsis

Li, J., Nagpal, P., Vitart, V., McMorris, T. C., & Chory, J. (1996) · Science · doi:10.1126/science.272.5260.398 · Cited by 856 · see citing works

A New Class of Transcription Factors Mediates Brassinosteroid-Regulated Gene Expression in Arabidopsis

Yin, Y., Vafeados, D. K., Tao, Y., Yoshida, S., Asami, T., & Chory, J. (2005) · Cell · doi:10.1016/j.cell.2004.11.044 · Cited by 816 · see citing works

Interdependency of Brassinosteroid and Auxin Signaling in Arabidopsis

Nemhauser, J. L., Mockler, T. C., & Chory, J. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020258 · Cited by 590 · see citing works

Comprehensive Comparison of Auxin-Regulated and Brassinosteroid-Regulated Genes in Arabidopsis

Goda, H., Sawa, S., Asami, T., et al. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.034736 · Cited by 500 · see citing works

Early auxin-induced genes encode short-lived nuclear proteins.

Abel, S., Oeller, P. W., & Theologis, A. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.1.326 · Cited by 459 · see citing works

The epidermis both drives and restricts plant shoot growth

Savaldi‐Goldstein, S., Peto, C. A., & Chory, J. (2007) · Nature · doi:10.1038/nature05618 · Cited by 452 · see citing works

Microarray Analysis of Brassinosteroid-Regulated Genes in Arabidopsis

Goda, H., Shimada, Y., Asami, T., Fujioka, S., & Yoshida, S. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.011254 · Cited by 423 · see citing works

Downstream nuclear events in brassinosteroid signalling

Vert, G., & Chory, J. (2006) · Nature · doi:10.1038/nature04681 · Cited by 405 · see citing works

MOLECULAR MECHANISMS OF STEROID HORMONE SIGNALING IN PLANTS

Vert, G., Nemhauser, J. L., Geldner, N., Hong, F., & Chory, J. (2005) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.21.090704.151241 · Cited by 404 · see citing works

Brassinosteroids Interact with Auxin to Promote Lateral Root Development in Arabidopsis

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

Genetic evidence for an essential role of brassinosteroids in plant development

Kauschmann, A., Jessop, A. C., Koncz, C., Szekeres, M., Willmitzer, L., & Altmann, T. (1996) · The Plant Journal · doi:10.1046/j.1365-313x.1996.9050701.x · Cited by 353 · see citing works

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

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

Brassinosteroid-Regulated Gene Expression

Müssig, C., Fischer, S., & Altmann, T. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.011003 · Cited by 286 · see citing works

Molecular genetic studies confirm the role of brassinosteroids in plant growth and development

Clouse, S. D. (1996) · The Plant Journal · doi:10.1046/j.1365-313x.1996.10010001.x · Cited by 281 · see citing works

Dynamic Integration of Auxin Transport and Signalling

Leyser, O. (2006) · Current Biology · doi:10.1016/j.cub.2006.05.014 · Cited by 280 · see citing works

Organ-Specific Expression of Brassinosteroid-Biosynthetic Genes and Distribution of Endogenous Brassinosteroids in Arabidopsis

Shimada, Y., Goda, H., Nakamura, A., et al. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.013029 · Cited by 252 · see citing works

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

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

Plant heterotrimeric G protein function: insights from Arabidopsis and rice mutants

Perfus‐Barbeoch, L., Jones, A. M., & Assmann, S. M. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.09.013 · Cited by 240 · see citing works

Brassinosteroids Stimulate Plant Tropisms through Modulation of Polar Auxin Transport in Brassica and Arabidopsis

Li, L., Xu, J., Xu, Z. H., et al. (2005) · The Plant Cell · doi:10.1105/tpc.105.034397 · Cited by 238 · see citing works

Brassinolide Induces IAA5, IAA19 , and DR5, a Synthetic Auxin Response Element in Arabidopsis, Implying a Cross Talk Point of Brassinosteroid and Auxin Signaling

Nakamura, A., Higuchi, K., Goda, H., FUJIWARA, M. T., Sawa, S., Koshiba, T., Shimada, Y., & Yoshida, S. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.030031 · Cited by 234 · see citing works

Cross-talk in Plant Hormone Signalling: What Arabidopsis Mutants Are Telling Us

Gazzarrini, S. (2003) · Annals of Botany · doi:10.1093/aob/mcg064 · Cited by 227 · see citing works

Transcription of the Arabidopsis CPD gene, encoding a steroidogenic cytochrome P450, is negatively controlled by brassinosteroids

Mathur, J., Molnár, G., Fujioka, S., Takatsuto, S., Sakurai, A., Yokota, T., Adam, G., Voigt, B., Nagy, F., Maas, C., et al. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00158.x · Cited by 223 · see citing works

Molecular Cloning and Characterization of a Brassinosteroid-Regulated Gene from Elongating Soybean (Glycine max L.) Epicotyls

Zurek, D. M., & Clouse, S. D. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.1.161 · Cited by 218 · see citing works

The Role of OsBRI1 and Its Homologous Genes, OsBRL1 and OsBRL3 , in Rice

Nakamura, A., Fujioka, S., Sunohara, H., Kamiya, N., Hong, Z., Inukai, Y., Miura, K., Takatsuto, S., Yoshida, S., Ueguchi‐Tanaka, M., et al. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.072330 · Cited by 214 · see citing works

Blockage of Brassinosteroid Biosynthesis and Sensitivity Causes Dwarfism in Garden Pea

Nomura, T., Nakayama, M., Reid, J. B., et al. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.1.31 · Cited by 202 · see citing works

Opposite Root Growth Phenotypes of hy5 versus hy5 hyh Mutants Correlate with Increased Constitutive Auxin Signaling

Sibout, R., Sukumar, P., Hettiarachchi, C. M., Holm, M., Muday, G. K., & Hardtke, C. S. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020202 · Cited by 194 · see citing works

Brassinosteroids Do Not Undergo Long-Distance Transport in Pea. Implications for the Regulation of Endogenous Brassinosteroid Levels

Symons, G. M., & Reid, J. B. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.043034 · Cited by 191 · see citing works

AUXIN RESPONSE FACTOR7 Restores the Expression of Auxin-Responsive Genes in Mutant Arabidopsis Leaf Mesophyll Protoplasts

Wang, S., Tiwari, S. B., Hagen, G., et al. (2005) · The Plant Cell · doi:10.1105/tpc.105.031096 · Cited by 189 · see citing works

The Regulation of DWARF4 Expression Is Likely a Critical Mechanism in Maintaining the Homeostasis of Bioactive Brassinosteroids in Arabidopsis

Kim, H. B., Kwon, M. J., Ryu, H., et al. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.067918 · Cited by 154 · see citing works

Investigation of Gene Expression, Growth Kinetics, and Wall Extensibility during Brassinosteroid-Regulated Stem Elongation

Zurek, D. M., Rayle, D. L., McMorris, T. C., & Clouse, S. D. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.2.505 · Cited by 152 · see citing works

Characterization of the Auxin-Inducible SAUR-AC1 Gene for Use as a Molecular Genetic Tool in Arabidopsis

Gil, P., Liu, Y., Orbović, V., Verkamp, E., Poff, K. L., & Green, P. J. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.2.777 · Cited by 151 · see citing works

Involvement of Brassinosteroids in the Gravitropic Response of Primary Root of Maize

Kim, S., Chang, S. C., Lee, E. J., et al. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.123.3.997 · Cited by 141 · see citing works

Brassinosteroid‐Promoted Growth

Müssig, C. (2005) · Plant Biology · doi:10.1055/s-2005-837493 · Cited by 133 · see citing works

Auxin and brassinosteroid differentially regulate the expression of three members of the 1-aminocyclopropane-1-carboxylate synthase gene family in mung bean (Vigna radiata L.)

Yi, H. C., Joo, S., Nam, K. H., et al. (1999) · Plant Molecular Biology · doi:10.1023/a:1006372612574 · Cited by 127 · see citing works

Heterotrimeric G protein α subunit is involved in rice brassinosteroid response

Wang, L., Xu, Y., Ma, Q., et al. (2006) · Cell Research · doi:10.1038/sj.cr.7310111 · Cited by 126 · see citing works

Auxin and embryo axis formation: the ends in sight?

Weijers, D., & Jürgens, G. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.11.001 · Cited by 117 · see citing works

Arabidopsis Aux/IAA genes are involved in brassinosteroid‐mediated growth responses in a manner dependent on organ type

Nakamura, A., Nakajima, N., Goda, H., Shimada, Y., Hayashi, K., Nozaki, H., Asami, T., Yoshida, S., & Fujioka, S. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02582.x · Cited by 109 · see citing works

Physiological and molecular effects of brassinosteroids on Arabidopsis thaliana

Clouse, S. D., Hall, A. F., Langford, M., McMorris, T. C., & Baker, M. E. (1993) · Journal of Plant Growth Regulation · doi:10.1007/bf00193234 · Cited by 105 · see citing works

Elongation and gravitropic responses of Arabidopsis roots are regulated by brassinolide and IAA

Kim, T., Lee, S. M., Joo, S., Yun, H. S., Lee, Y., Kaufman, P. B., Kirakosyan, A., Kim, S.-H., Nam, K. H., Lee, J. S., et al. (2007) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2007.01659.x · Cited by 101 · see citing works

The effect of brassinosteroid on auxin‐induced ethylene production by etiolated mung bean segments

Arteca, R. N., Tsai, D., Schlagnhaufer, C. D., et al. (1983) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1983.tb06277.x · Cited by 83 · see citing works

Brassinosteroid Signals Control Expression of theAXR3/IAA17Gene in the Cross-Talk Point with Auxin in Root Development

Kim, H., Pil-Joon, P. A. R. K., Hwang, H., So-Young, L. E. E., Oh, M., & Kim, S. (2006) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.70.768 · Cited by 82 · see citing works

Brassinolide affects the rate of cell division in isolated leaf protoplasts of Petunia hybrida

Oh, M., & Clouse, S. D. (1998) · Plant Cell Reports · doi:10.1007/s002990050510 · Cited by 80 · see citing works

Molecular Analysis of Brassinolide Action in Plant Growth and Development

Clouse, S. D., & Zurek, D. M. (1991) · ACS symposium series · doi:10.1021/bk-1991-0474.ch011 · Cited by 78 · see citing works

Acceleration of Aux/IAA proteolysis is specific for auxin and independent of AXR1

Zenser, N., Dreher, K. A., Edwards, S. R., & Callis, J. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01801.x · Cited by 61 · see citing works

Control of Internode Length in Pisum sativum (Further Evidence for the Involvement of Indole-3-Acetic Acid)

McKay, M. J., Ross, J. J., Lawrence, N. L., Cramp, R. E., Beveridge, C. A., & Reid, J. B. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.4.1521 · Cited by 57 · see citing works

Molecular genetic analysis of brassinosteroid action

Clouse, S. D. (1997) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1997.tb03077.x · Cited by 56 · see citing works

Sticking with auxin

Guilfoyle, T. J. (2007) · Nature · doi:10.1038/446621a · Cited by 55 · see citing works

Inhibition of Brassinosteroid Biosynthesis by Either a dwarf4 Mutation or a Brassinosteroid Biosynthesis Inhibitor Rescues Defects in Tropic Responses of Hypocotyls in the Arabidopsis Mutant nonphototropic hypocotyl 4

Nakamoto, D., Ikeura, A., Asami, T., & Yamamoto, K. T. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.076273 · Cited by 51 · see citing works

Effects of Brassin‐Complex on Auxin and Gibberellin Mediated Events in the Morphogenesis of the Etiolated Bean Hypocotyl

Yopp, J. H., Colclasure, G. C., & Mandava, N. B. (1979) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1979.tb06530.x · Cited by 47 · see citing works

Brassinosteroid Selectively RegulatesPINGene Expression in Arabidopsis

Nakamura, A., Goda, H., Shimada, Y., et al. (2004) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.68.952 · Cited by 46 · see citing works

AXR1 is involved in BR‐mediated elongation and SAUR‐AC1 gene expression in Arabidopsis

Nakamura, A., Shimada, Y., Goda, H., FUJIWARA, M. T., Asami, T., & Yoshida, S. (2003) · FEBS Letters · doi:10.1016/s0014-5793(03)00945-1 · Cited by 45 · see citing works

A novel brassinolide-enhanced gene identified by cDNA microarray is involved in the growth of rice

Yang, G., Matsuoka, M., Iwasaki, Y., et al. (2003) · Plant Molecular Biology · doi:10.1023/a:1025001304994 · Cited by 44 · see citing works

Investigations on the Mechanism of the Brassinosteroid Response

Meudt, W. J. (1987) · PLANT PHYSIOLOGY · doi:10.1104/pp.83.1.195 · Cited by 40 · see citing works

Brassinosteroid induction of AtACS4 encoding an auxin‐responsive 1‐aminocyclopropane‐1‐carboxylate synthase 4 in Arabidopsis seedlings

Joo, S., Seo, Y. S., Kim, S. M., et al. (2005) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2005.00602.x · Cited by 37 · see citing works

Evidence that brassinosteroid stimulates auxin‐induced ethylene synthesis in mung bean hypocotyls between S‐adenosylmethionine and 1‐aminocyclopropane‐1‐carboxylic acid

Schlagnhaufer, C. D., Arteca, R. N., & Yopp, J. H. (1984) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1984.tb05169.x · Cited by 36 · see citing works

Effect of epibrassinolide on hypocotyl growth of the tomato mutant diageotropica

Park, W. J. (1998) · Planta · doi:10.1007/s004250050463 · Cited by 28 · see citing works

A molecular basis for auxin action

Leyser, O., & Berleth, T. (1999) · Seminars in Cell and Developmental Biology · doi:10.1006/scdb.1999.0288 · Cited by 28 · see citing works

OsBLE3, a brassinolide-enhanced gene, is involved in the growth of rice

Yang, G., Nakamura, H., Ichikawa, H., et al. (2006) · Phytochemistry · doi:10.1016/j.phytochem.2006.05.026 · Cited by 26 · see citing works

Crosstalk

Mundy, J., Nielsen, H. B., & Brodersen, P. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2005.12.003 · Cited by 26 · see citing works

Differential IAA dose response relations of the axr1 and axr2 mutants of Arabidopsis

Knee, E. M., & Hangarter, R. P. (1996) · Physiologia Plantarum · doi:10.1034/j.1399-3054.1996.980213.x · Cited by 17 · see citing works

A brassinosteroid transcriptional network revealed by genome‐wide identification of BESI target genes in Arabidopsis thaliana

Yu, X., Li, L., Żola, J., Aluru, M. R., Ye, H., Foudree, A., Guo, H., Anderson, S. N., Aluru, S., Liu, P., et al. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04449.x · Cited by 660 · see citing works

Hormone signalling crosstalk in plant growth regulation.

Depuydt, S., & Hardtke, C. (2011) · Current Biology · doi:10.1016/j.cub.2011.03.013 · Cited by 523 · see citing works

Target Genes of the MADS Transcription Factor SEPALLATA3: Integration of Developmental and Hormonal Pathways in the Arabidopsis Flower

Kaufmann, K., Muiño, J. M., Jáuregui, R., Airoldi, C. A., Smaczniak, C., Krajewski, P., & Angenent, G. C. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000090 · Cited by 458 · see citing works

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

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

Integration of auxin and brassinosteroid pathways by Auxin Response Factor 2

Vert, G., Walcher, C. L., Chory, J., & Nemhauser, J. L. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803996105 · Cited by 407 · see citing works

Three related receptor-like kinases are required for optimal cell elongation in Arabidopsis thaliana

Guo, H., Li, L., Ye, H., Yu, X., Algreen, A., & Yin, Y. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812346106 · Cited by 371 · see citing works

Arabidopsis Class I and Class II TCP Transcription Factors Regulate Jasmonic Acid Metabolism and Leaf Development Antagonistically

Danisman, S., van der Wal, F., Dhondt, S., et al. (2012) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.200303 · Cited by 338 · see citing works

From dwarves to giants? Plant height manipulation for biomass yield

Fernandez, M. G. S., Becraft, P. W., Yin, Y., et al. (2009) · Trends in Plant Science · doi:10.1016/j.tplants.2009.06.005 · Cited by 258 · see citing works

Cytokinins modulate auxin-induced organogenesis in plants via regulation of the auxin efflux

Pernisová, M., Klíma, P., Horák, J., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811539106 · Cited by 253 · see citing works

Shaping plant architecture

Teichmann, T., & Muhr, M. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00233 · Cited by 228 · see citing works

Regulation and processing of a plant peptide hormone, AtRALF23, in Arabidopsis

Srivastava, R., Liu, J., Guo, H., et al. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03926.x · Cited by 241 · see citing works

Brassinosteroids Dominate Hormonal Regulation of Plant Thermomorphogenesis via BZR1

Ibañez, C., Delker, C., Martínez, C., et al. (2018) · Current Biology · doi:10.1016/j.cub.2017.11.077 · Cited by 218 · see citing works

From Squalene to Brassinolide: The Steroid Metabolic and Signaling Pathways across the Plant Kingdom

Vriet, C., Russinova, E., & Reuzeau, C. (2013) · Molecular Plant · doi:10.1093/mp/sst096 · Cited by 202 · see citing works

SMALL ORGAN SIZE 1 and SMALL ORGAN SIZE 2/DWARF AND LOW-TILLERING Form a Complex to Integrate Auxin and Brassinosteroid Signaling in Rice

Hirano, K., Yoshida, H., Aya, K., Kawamura, M., Hayashi, M., Hobo, T., Sato‐Izawa, K., Kitano, H., Ueguchi‐Tanaka, M., & Matsuoka, M. (2017) · Molecular Plant · doi:10.1016/j.molp.2016.12.013 · Cited by 153 · see citing works

Brassinosteroids in growth control: How, when and where

Fridman, Y., & Savaldi‐Goldstein, S. (2013) · Plant Science · doi:10.1016/j.plantsci.2013.04.002 · Cited by 150 · see citing works

Recent Advances in the Regulation of Brassinosteroid Signaling and Biosynthesis PathwaysF

Ye, H., Li, L., & Yin, Y. (2011) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2011.01046.x · Cited by 137 · see citing works

Elongation‐related functions of LEAFY COTYLEDON1 during the development of Arabidopsis thaliana

Junker, A., Mönke, G., Rutten, T. L. M., Keilwagen, J., Seifert, M., Thi, T. M. N., Renou, J., Balzergue, S., Viehöver, P., Hähnel, U., et al. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.04999.x · Cited by 134 · see citing works

The Basic Leucine Zipper Transcription Factor ABSCISIC ACID RESPONSE ELEMENT-BINDING FACTOR2 Is an Important Transcriptional Regulator of Abscisic Acid-Dependent Grape Berry Ripening Processes

Nicolas, P., Lecourieux, D., Kappel, C., Cluzet, S., Cramer, G. R., Delrot, S., & Lecourieux, F. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.231977 · Cited by 133 · see citing works

Role of Actin Cytoskeleton in Brassinosteroid Signaling and in Its Integration with the Auxin Response in Plants

Lanza, M., García‐Ponce, B., Castrillo, G., Catarecha, P., Sauer, M., Rodríguez‐Serrano, M., Páez-García, A., Sánchez-Bermejo, E., Mohan, T. C., del Puerto, Y. L., et al. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.04.008 · Cited by 131 · see citing works

Spatio-temporal sequence of cross-regulatory events in root meristem growth

Scacchi, E., Salinas, P., Gujas, B., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1014716108 · Cited by 130 · see citing works

PIF4 Integrates Multiple Environmental and Hormonal Signals for Plant Growth Regulation in Arabidopsis

Choi, H., & Oh, E. (2016) · Molecules and Cells · doi:10.14348/molcells.2016.0126 · Cited by 130 · see citing works

New auxin analogs with growth-promoting effects in intact plants reveal a chemical strategy to improve hormone delivery

Savaldi‐Goldstein, S., Baiga, T. J., Pojer, F., Dabi, T., Butterfield, C. N., Parry, G., Santner, A. A., Dharmasiri, N., Tao, Y., Estelle, M. A., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806324105 · Cited by 126 · see citing works

Making bigger plants: key regulators of final organ size

Krizek, B. A. (2008) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2008.09.006 · Cited by 125 · see citing works

Auxin signal transcription factor regulates expression of the brassinosteroid receptor gene in rice

Sakamoto, T., Morinaka, Y., Inukai, Y., et al. (2012) · The Plant Journal · doi:10.1111/tpj.12071 · Cited by 117 · see citing works

Recent Advances in Hormonal Regulation and Cross-Talk during Non-Climacteric Fruit Development and Ripening

Fuentes, L., Figueroa, C. R., & Valdenegro, M. (2019) · Horticulturae · doi:10.3390/horticulturae5020045 · Cited by 109 · see citing works

MADS: the missing link between identity and growth?

Dornelas, M. C., Patreze, C. M., Angenent, G. C., et al. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.11.003 · Cited by 102 · see citing works

Phytohormone collaboration: zooming in on auxin–brassinosteroid interactions

Hardtke, C. S., Dorcey, E., Sanguinet, K. A., & Sibout, R. (2007) · Trends in Cell Biology · doi:10.1016/j.tcb.2007.08.003 · Cited by 102 · see citing works

Bipartite Promoter Element Required for Auxin Response

Walcher, C. L., & Nemhauser, J. L. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.187559 · Cited by 99 · see citing works

Dynamic, auxin-responsive plasma membrane-to-nucleus movement of Arabidopsis BRX

Scacchi, E., Sanguinet, K. A., Beuchat, J., Salinas, P., Navarrete‐Gómez, M., Trigueros, M., Ferrándiz, C., & Hardtke, C. S. (2009) · Development · doi:10.1242/dev.035444 · Cited by 97 · see citing works

BIM1, a bHLH protein involved in brassinosteroid signalling, controls Arabidopsis embryonic patterning via interaction with DORNRÖSCHEN and DORNRÖSCHEN-LIKE

Chandler, J., Cole, M., Flier, A., & Werr, W. (2008) · Plant Molecular Biology · doi:10.1007/s11103-008-9405-6 · Cited by 93 · see citing works

Auxin as compère in plant hormone crosstalk

Chandler, J. (2009) · Planta · doi:10.1007/s00425-009-1036-x · Cited by 90 · see citing works

Hormone mediated regulation of the shoot apical meristem

Veit, B. E. (2008) · Plant Molecular Biology · doi:10.1007/s11103-008-9396-3 · Cited by 85 · see citing works

Auxin as a Model for the Integration of Hormonal Signal Processing and Transduction

Teale, W., Ditengou, F. A., Dovzhenko, A., Li, X., Molendijk, A. J., Ruperti, B., Paponov, I. A., & Palme, K. J. (2008) · Molecular Plant · doi:10.1093/mp/ssn006 · Cited by 75 · see citing works

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

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

Geminivirus C4 protein alters Arabidopsis development

Mills-Lujan, K., & Deom, C. M. (2009) · PROTOPLASMA · doi:10.1007/s00709-009-0086-z · Cited by 71 · see citing works

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

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

Somatic Embryogenesis Receptor Kinases Control Root Development Mainly via Brassinosteroid‐Independent Actions in Arabidopsis thaliana

Du, J., Yin, H., Zhang, S., Wei, Z., Zhao, B., Zhang, J., Gou, X., Lin, H., & Li, J. (2012) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2012.01124.x · Cited by 65 · see citing works

The Microtubule-Associated Protein CLASP Sustains Cell Proliferation through a Brassinosteroid Signaling Negative Feedback Loop

Ruan, Y., Halat, L., Khan, D., et al. (2018) · Current Biology · doi:10.1016/j.cub.2018.06.048 · Cited by 66 · see citing works

Mechanisms of brassinosteroids interacting with multiple hormones

Zhang, S., Wei, Y., Lu, Y., et al. (2009) · Plant Signaling & Behavior · doi:10.4161/psb.4.12.9903 · Cited by 57 · see citing works

Interactive effects of CO2 enrichment and brassinosteroid on CO2 assimilation and photosynthetic electron transport in Cucumis sativus

Jiang, Y., Cheng, F., Zhou, Y., et al. (2011) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2011.09.002 · Cited by 53 · see citing works

Loss-of-Function Mutations in the Arabidopsis Heterotrimeric G-protein α Subunit Enhance the Developmental Defects of Brassinosteroid Signaling and Biosynthesis Mutants

Gao, Y., Wang, S., Asami, T., et al. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn078 · Cited by 53 · see citing works

Synergistic disruptions in seuss cyp85A2 double mutants reveal a role for brassinolide synthesis during gynoecium and ovule development

Nole-Wilson, S., Rueschhoff, E. E., Bhatti, H., et al. (2010) · BMC Plant Biology · doi:10.1186/1471-2229-10-198 · Cited by 52 · see citing works

Arabidopsis MSBP1 Is Activated by HY5 and HYH and Is Involved in Photomorphogenesis and Brassinosteroid Sensitivity Regulation

Shi, Q.-M., Yang, X., Song, L., et al. (2011) · Molecular Plant · doi:10.1093/mp/ssr049 · Cited by 51 · see citing works

Brassinosteroid signaling converges with SUPPRESSOR OF PHYTOCHROME B4‐#3 to influence the expression of SMALL AUXIN UP RNA genes and hypocotyl growth

Favero, D. S., Le, K. N., & Neff, M. M. (2016) · The Plant Journal · doi:10.1111/tpj.13451 · Cited by 47 · see citing works

BRX promotes Arabidopsis shoot growth

Beuchat, J., Scacchi, E., Tarkowská, D., et al. (2010) · New Phytologist · doi:10.1111/j.1469-8137.2010.03387.x · Cited by 44 · see citing works

Asynchrony of ovule primordia initiation in Arabidopsis

Yu, S., Zhou, L.-W., Hu, L.-Q., et al. (2020) · Development · doi:10.1242/dev.196618 · Cited by 44 · see citing works

DIMINUTO 1 affects the lignin profile and secondary cell wall formation in Arabidopsis

Hossain, Z., McGarvey, B. D., Amyot, L., et al. (2011) · Planta · doi:10.1007/s00425-011-1519-4 · Cited by 43 · see citing works

A qualitative continuous model of cellular auxin and brassinosteroid signaling and their crosstalk

Sankar, M., Sanguinet, K. A., Rolc̆ı́k, J., Gujas, B., Tarkowská, D., Strnad, M., Xénarios, I., & Hardtke, C. S. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr158 · Cited by 37 · see citing works

Brassinosteroids Confer Stress Tolerance

Divi, U. K., & Krishna, P. (2009) · doi:10.1002/9783527628964.ch6 · Cited by 37 · see citing works

Impact of Climate Change on Altered Fruit Quality with Organoleptic, Health Benefit, and Nutritional Attributes

Kishor, P. B. K., Rajasheker, G., Kulkarni, J., Singam, P., Somanaboina, A. K., Tejaswi, N., Patil, S. A., Polavarapu, R., Suravajhala, P., Sreenivasulu, N., et al. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c03312 · Cited by 36 · see citing works

Membrane Steroid Binding Protein 1 (MSBP1) Stimulates Tropism by Regulating Vesicle Trafficking and Auxin Redistribution

Yang, X., Song, L., & Xue, H. (2008) · Molecular Plant · doi:10.1093/mp/ssn071 · Cited by 34 · see citing works

Auxin promotion of seedling growth via ARF5 is dependent on the brassinosteroid‐regulated transcription factors BES1 and BEH4

Galstyan, A., & Nemhauser, J. L. (2019) · Plant Direct · doi:10.1002/pld3.166 · Cited by 31 · see citing works

Multifunctionality of the LEC1 transcription factor during plant development

Junker, A., & Bäumlein, H. (2012) · Plant Signaling & Behavior · doi:10.4161/psb.22365 · Cited by 26 · see citing works

A strain of Bacillus subtilis stimulates sunflower growth (Helianthus annuus L.) temporarily

López-Valdez, F., Fernández-Luqueño, F., Ceballos-Ramirez, J. M., Marsch, R., Olalde‐Portugal, V., & Dendooven, L. (2011) · Scientia Horticulturae · doi:10.1016/j.scienta.2011.02.006 · Cited by 26 · see citing works

Auxin–brassinosteroid crosstalk: Regulating rice plant architecture and grain shape

Wu, M., Zhou, J., Li, Q., et al. (2024) · The Crop Journal · doi:10.1016/j.cj.2024.06.003 · Cited by 25 · see citing works

Activation-Tagged Suppressors of a Weak Brassinosteroid Receptor Mutant

Kang, B. G., Wang, H., Nam, K. H., et al. (2009) · Molecular Plant · doi:10.1093/mp/ssp099 · Cited by 25 · see citing works

Brassinosteroids: Physiological Roles and its Signalling in Plants

Yusuf, M., Khan, T. A., & Fariduddin, Q. (2016) · Springer eBooks · doi:10.1007/978-3-319-42183-4_10 · Cited by 20 · see citing works

Advances in the regulation and crosstalks of phytohormones

Xiong, G., Li, J., & Wang, Y. (2009) · Chinese Science Bulletin · doi:10.1007/s11434-009-0629-x · Cited by 19 · see citing works

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

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

Indole-3-acetic acid-induced oxidative burst and an increase in cytosolic calcium ion concentration in rice suspension culture

Nguyen, H. T. H., Umemura, K., & Kawano, T. (2016) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2016.1179094 · Cited by 12 · see citing works

Brassinosteroid Signaling Converges With Auxin-Mediated C3H17 to Regulate Xylem Formation in Populus

Tang, X., Wang, C., Liu, Y., He, G. Q., Ma, N., Chai, G., Li, S., Xu, H., & Zhou, G. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.586014 · Cited by 12 · see citing works

The mechanism and network of BES1 mediated transcriptional regulation in Brassinosteroids (BR) pathway in Arabidopsis

Li, L. (2010) · doi:10.31274/etd-180810-352 · Cited by 9 · see citing works

Glycosyltransferase UGT76F1 is involved in the temperature-mediated petiole elongation and the BR-mediated hypocotyl growth in Arabidopsis

Chen, L., Huang, X., Li, Y., et al. (2020) · Plant Signaling & Behavior · doi:10.1080/15592324.2020.1777377 · Cited by 8 · see citing works

Computational modelling of the BRI1 receptor system

van Esse, G. W., Harter, K., & de Vries, S. C. (2013) · Plant Cell & Environment · doi:10.1111/pce.12077 · Cited by 7 · see citing works

Molecular dynamics simulations of the auxin-binding protein 1 in complex with indole-3-acetic acid and naphthalen-1-acetic acid

Grandits, M., & Oostenbrink, C. (2014) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.24639 · Cited by 5 · see citing works

植物激素调控研究进展

熊, 国., 李, 家., & 王, 永. (2009) · Chinese Science Bulletin (Chinese Version) · doi:10.1360/csb2009-54-18-2718 · Cited by 2 · see citing works

Lateral/Secondary Roots

Guyomarc’h, S., Lucas, M., & Laplaze, L. (2010) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0002060.pub2 · Cited by 3 · see citing works

The Transcriptional Regulatory Mechanism of CYP72B1 and AUR3 in Response to Light, Auxin and Brassinosteroid*

Zhang, C., Wang, J., Zhu, H., et al. (2010) · PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS · doi:10.3724/sp.j.1206.2009.00088 · Cited by 2 · see citing works

Boron Toxicity Modulates Hypocotyl Growth Through Brassinosteroid and Thermomorphogenic‐Like Mechanisms

Hassinger‐Lino, G. R., Bolaños, L., García‐Mina, J. M., et al. (2025) · Plant Cell & Environment · doi:10.1111/pce.70173 · Cited by 1 · see citing works

Ultrafine polystyrene nanoplastics penetrate roots and induce organelle damage and extensive transcriptomic reprogramming in Arabidopsis thaliana

Hassinger‐Lino, G. R., García, J., Maestro‐Gaitán, I., Muñoz, M., & Reguera, M. (2026) · Environmental Pollution · doi:10.1016/j.envpol.2026.128382 · Cited by 1 · see citing works

Does the brassinosteroid signal pathway in photomorphogenesis overlap with the gravitropic response caused by auxin?

Jaroensanti, N., Yoon, J., Nakai, Y., et al. (2014) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2014.925783 · Cited by 1 · see citing works

Characterising the cellulose synthase complexes of cell walls

Zangir, N. M. (2012) · doi:10.18174/212979 · Cited by 1 · see citing works

Morphogenesis at the shoot Apical Meristem

Vivero, U. C. A. (2017) · doi:10.70675/07054c68z0638z4978za21ezc9b9fcda305d · Cited by 1 · see citing works

Análisis funcional de los factores de trascripción Tower-of-Pisa1 y Tower-of-Pisa2 y su implicación en el desarrollo del gineceo de Arabidopsis.

GONZÁLEZ, M. T. (2008) · doi:10.4995/thesis/10251/2669

Mechanisms of BES1-regulated gene expression downstream of brassinosteroid signaling in Arabidopsis thaliana

Yu, X. (2008) · doi:10.31274/rtd-180813-3117

Differential expression of the brassinosteroid receptor-encoding BRI1 gene in Arabidopsis thaliana

Haţegan, L. (2014) · doi:10.14232/phd.2149

Growth Enhancement Effect of Gene Expression of Plants Induced by Active Oxygen Species in Oxygen Plasma

Hayashi, N. (2022) · Springer eBooks · doi:10.1007/978-981-16-3891-6_12

Auxin signal transcription factor regulates expression of the brassinosteroid receptor gene in rice

Sakamoto, T., Morinaka, Y., Inukai, Y., et al. (2012) · The Plant Journal · doi:10.1111/tpj.12071 · Cited by 117 · see citing works

Molecular actions of two synthetic brassinosteroids, iso-carbaBL and 6-deoxoBL, which cause altered physiological activities between Arabidopsis and rice

Nakamura, A., Tochio, N., Fujioka, S., Ito, S., Kigawa, T., Shimada, Y., Matsuoka, M., Yoshida, S., Kinoshita, T., Asami, T., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0174015 · Cited by 11 · see citing works

Rice CYP734A cytochrome P450s inactivate brassinosteroids in Arabidopsis

Thornton, L. E., Peng, H. F., & Neff, M. M. (2011) · Planta · doi:10.1007/s00425-011-1464-2 · Cited by 36 · see citing works

Characterization of OsIAA1 gene, a member of rice Aux/IAA family involved in auxin and brassinosteroid hormone responses and plant morphogenesis

Song, Y., You, J., & Xiong, L. (2009) · Plant Molecular Biology · doi:10.1007/s11103-009-9474-1 · Cited by 203 · see citing works

Brassinosteroid induction of AtACS4 encoding an auxin‐responsive 1‐aminocyclopropane‐1‐carboxylate synthase 4 in Arabidopsis seedlings

Joo, S., Seo, Y. S., Kim, S. M., et al. (2005) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2005.00602.x · Cited by 37 · see citing works