Arabidopsis thaliana transcription factors bZIP19 and bZIP23 regulate the adaptation to zinc deficiency

Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482 · see citing works

Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments

Smyth, G. K. (2004) · Statistical Applications in Genetics and Molecular Biology · doi:10.2202/1544-6115.1027 · Cited by 11,829 · see citing works

Exploration, normalization, and summaries of high density oligonucleotide array probe level data

Irizarry, R. A. (2003) · Biostatistics · doi:10.1093/biostatistics/4.2.249 · Cited by 10,603 · 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

Transformation of yeast by lithium acetate/single-stranded carrier DNA/polyethylene glycol method

Gietz, R. D., & Woods, R. A. (2002) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(02)50957-5 · Cited by 2,890 · see citing works

Genomic Libraries and a Host Strain Designed for Highly Efficient Two-Hybrid Selection in Yeast

James, P. M., Halladay, J. T., & Craig, E. A. (1996) · Genetics · doi:10.1093/genetics/144.4.1425 · Cited by 2,638 · see citing works

bZIP transcription factors in Arabidopsis

Jakoby, M. J., 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 1,862 · see citing works

Zinc coordination, function, and structure of zinc enzymes and other proteins

Vallée, B. L., & Auld, D. S. (1990) · Biochemistry · doi:10.1021/bi00476a001 · Cited by 1,784 · see citing works

Breeding for micronutrients in staple food crops from a human nutrition perspective

Welch, R. M., & Graham, R. D. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh064 · Cited by 1,525 · see citing works

Molecular mechanisms of plant metal tolerance and homeostasis

Clemens, S. (2001) · Planta · doi:10.1007/s004250000458 · Cited by 1,417 · see citing works

A long way ahead: understanding and engineering plant metal accumulation

Clemens, S., Palmgren, M. G., & Krämer, U. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(02)02295-1 · Cited by 1,265 · see citing works

Phylogenetic Relationships within Cation Transporter Families of Arabidopsis

Mäser, P., Thomine, S., Schroeder, J. I., Ward, J. M., Hirschi, K. D., Sze, H., Talke, I. N., Anna Amtmann, A., Maathuis, F. J. M., Sanders, D., et al. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.126.4.1646 · Cited by 1,257 · see citing works

ABFs, a Family of ABA-responsive Element Binding Factors

Choi, H.-I., Hong, J.-H., Ha, J.-O., Kang, J., & Kim, S. Y. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.3.1723 · Cited by 1,212 · see citing works

Scissors-Grip Model for DNA Recognition by a Family of Leucine Zipper Proteins

Vinson, C., Sigler, P. B., & McKnight, S. L. (1989) · Science · doi:10.1126/science.2683088 · Cited by 973 · see citing works

The GCN4 basic region leucine zipper binds DNA as a dimer of uninterrupted α Helices: Crystal structure of the protein-DNA complex

Ellenberger, T. E., Brandl, C. J., Struhl, K., & Harrison, S. C. (1992) · Cell · doi:10.1016/s0092-8674(05)80070-4 · Cited by 972 · see citing works

Zinc transporters and the cellular trafficking of zinc

Eide, D. J. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.03.005 · Cited by 874 · see citing works

The Essential Basic Helix-Loop-Helix Protein FIT1 Is Required for the Iron Deficiency Response

Colangelo, E. P., & Guerinot, M. L. (2004) · The Plant Cell · doi:10.1105/tpc.104.024315 · Cited by 791 · see citing works

Identification of a family of zinc transporter genes from Arabidopsis that respond to zinc deficiency

Grotz, N., Fox, T. C., Connolly, E. L., Park, W. D., Guerinot, M. L., & Eide, D. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.12.7220 · Cited by 735 · see citing works

FIT interacts with AtbHLH38 and AtbHLH39 in regulating iron uptake gene expression for iron homeostasis in Arabidopsis

Yuan, Y., Wu, H., Wang, N., Li, J., Zhao, W., Du, J., Wang, D., & Ling, H. (2008) · Cell Research · doi:10.1038/cr.2008.26 · Cited by 609 · see citing works

The yeast ZRT1 gene encodes the zinc transporter protein of a high-affinity uptake system induced by zinc limitation.

Zhao, H. F., & Eide, D. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.6.2454 · Cited by 566 · see citing works

Zinc biofortification of cereals: problems and solutions

Palmgren, M. B., Clemens, S., Williams, L. E., Krämer, U., Borg, S., Schjoerring, J. K., & Sanders, D. (2008) · Trends in Plant Science · doi:10.1016/j.tplants.2008.06.005 · Cited by 547 · see citing works

Large Expression Differences in Genes for Iron and Zinc Homeostasis, Stress Response, and Lignin Biosynthesis Distinguish Roots of <i>Arabidopsis thaliana</i> and the Related Metal Hyperaccumulator <i>Thlaspi caerulescens</i>

van de Mortel, J. E., Almar Villanueva, L., Schat, H., Kwekkeboom, J., Coughlan, S., Moerland, P. D., Ver Loren van Themaat, E., Koornneef, M., & Aarts, M. G. M. (2006) · Plant Physiology · doi:10.1104/pp.106.082073 · Cited by 547 · see citing works

Zinc-Dependent Global Transcriptional Control, Transcriptional Deregulation, and Higher Gene Copy Number for Genes in Metal Homeostasis of the Hyperaccumulator <i>Arabidopsis halleri</i>

Talke, I. N., Hanikenne, M., & Krämer, U. (2006) · Plant Physiology · doi:10.1104/pp.105.076232 · Cited by 452 · see citing works

Expression Profiles of Arabidopsis thaliana in Mineral Deficiencies Reveal Novel Transporters Involved in Metal Homeostasis

Henri Wintz, A., Fox, T. C., Wu, Y., Feng, V., Chen, W., Chang, H., Zhu, T., & Vulpe, C. D. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m309338200 · Cited by 431 · see citing works

Plant bZIP Protein DNA Binding Specificity

Izawa, T., Foster, R., & Chua, N. (1993) · Journal of Molecular Biology · doi:10.1006/jmbi.1993.1230 · Cited by 409 · see citing works

The Role of bZIP Transcription Factors in Green Plant Evolution: Adaptive Features Emerging from Four Founder Genes

Corrêa, L. G. G., Riaño‐Pachón, D. M., Schrago, C. G., Vicentini, R., Mueller‐Roeber, B., & Vincentz, M. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002944 · Cited by 314 · see citing works

Arabidopsis IRT3 is a zinc‐regulated and plasma membrane localized zinc/iron transporter

Lin, Y., Liang, H., Yang, S., Boch, A., Clemens, S., Chen, C., Wu, J.-F., Huang, J., & Yeh, K. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2009.02766.x · Cited by 292 · see citing works

Differential metal‐specific tolerance and accumulation patterns among Thlaspi caerulescens populations originating from different soil types

Assunção, A. G. L., Bookum, W. M. T., Nelissen, H. J. M., Vooijs, R., Schat, H., & Ernst, W. H. O. (2003) · New Phytologist · doi:10.1046/j.1469-8137.2003.00819.x · Cited by 275 · see citing works

REPRESSION OF SHOOT GROWTH, a bZIP Transcriptional Activator, Regulates Cell Elongation by Controlling the Level of Gibberellins

Fukazawa, J., Sakai, T., Ishida, S., et al. (2000) · The Plant Cell · doi:10.1105/tpc.12.6.901 · Cited by 261 · see citing works

Iron deficiency-mediated stress regulation of four subgroup Ib BHLH genes in Arabidopsis thaliana

Hong-yu, W., Klatte, M., Jakoby, M. J., Bäumlein, H., Weißhaar, B., & Bauer, P. (2007) · Planta · doi:10.1007/s00425-007-0535-x · Cited by 260 · see citing works

The transcription factor IDEF1 regulates the response to and tolerance of iron deficiency in plants

Kobayashi, T., Ogo, Y., Itai, R. N., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707010104 · Cited by 235 · see citing works

A Novel NAC Transcription Factor, IDEF2, That Recognizes the Iron Deficiency-responsive Element 2 Regulates the Genes Involved in Iron Homeostasis in Plants

Ogo, Y., Kobayashi, T., Itai, R. N., et al. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m708732200 · Cited by 233 · see citing works

The Arabidopsis basic leucine zipper transcription factor AtbZIP24 regulates complex transcriptional networks involved in abiotic stress resistance

Yang, O., Popova, O. V., Süthoff, U., Lüking, I., Dietz, K., & Golldack, D. (2009) · Gene · doi:10.1016/j.gene.2009.02.010 · Cited by 201 · see citing works

Structural basis for the diversity of DNA recognition by bZIP transcription factors

Fujii, Y., Shimizu, T., Toda, T., Yanagida, M., & Hakoshima, T. (2000) · Nature Structural Biology · doi:10.1038/82822 · Cited by 198 · see citing works

Plant bZIP G-box binding factors. Modular structure and activation mechanisms.

Sibéril, Y., Doireau, P., & Gantet, P. (2001) · European Journal of Biochemistry · doi:10.1046/j.0014-2956.2001.02552.x · Cited by 189 · see citing works

Regulation of Zinc Homeostasis in Yeast by Binding of the ZAP1 Transcriptional Activator to Zinc-responsive Promoter Elements

Zhao, H. F., Butler, E., Rodgers, J., Spizzo, T., Duesterhoeft, S., & Eide, D. J. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.44.28713 · Cited by 180 · see citing works

The impact of mineral nutrients in food crops on global human health

Welch, R. M. (2002) · Springer eBooks · doi:10.1007/978-94-017-2789-1_6 · Cited by 177 · see citing works

The impact of mineral nutrients in food crops on global human health

Welch, R. M. (2002) · Plant and Soil · doi:10.1023/a:1021140122921 · Cited by 175 · see citing works

Cross-Species Annotation of Basic Leucine Zipper Factor Interactions: Insight into the Evolution of Closed Interaction Networks

Deppmann, C. D., Alvania, R. S., & Taparowsky, E. J. (2006) · Molecular Biology and Evolution · doi:10.1093/molbev/msl022 · Cited by 131 · see citing works

Heavy metal hyperaccumulating plants: how and why do they do it? And what makes them so interesting

Rascio, N., & Navari-Izzo, F. (2011) · Plant Science · doi:10.1016/j.plantsci.2010.08.016 · Cited by 2,012 · see citing works

Heavy metals and metalloids: Sources, risks and strategies to reduce their accumulation in horticultural crops

Edelstein, M., & Ben-Hur, M. (2018) · Scientia Horticulturae · doi:10.1016/j.scienta.2017.12.039 · Cited by 501 · see citing works

Physiological and molecular mechanisms of metal accumulation in hyperaccumulator plants

Sytar, O., Ghosh, S., Malinska, H., Zivcak, M., & Brestic, M. (2020) · Physiologia Plantarum · doi:10.1111/ppl.13285 · Cited by 192 · see citing works

Characterization of the high affinity Zn transporter from <i>Noccaea caerulescens</i>, NcZNT1, and dissection of its promoter for its role in Zn uptake and hyperaccumulation

Milner, M. J., Craft, E., Yamaji, N., Koyama, E., Ma, J. F., & Kochian, L. V. (2012) · New Phytologist · doi:10.1111/j.1469-8137.2012.04144.x · Cited by 73 · see citing works

Plant hyperaccumulators: a state-of-the-art review on mechanism of heavy metal transport and sequestration

Bhat, B. A., Rather, M. A., Bilal, T., Nazir, R., Qadir, R. U., & Mir, R. A. (2025) · Frontiers in Plant Science · doi:10.3389/fpls.2025.1631378 · Cited by 68 · see citing works

Biomolecular approaches to understanding metal tolerance and hyperaccumulation in plants

Corso, M., & García de la Torre, V. S. (2020) · Metallomics · doi:10.1039/d0mt00043d · Cited by 60 · see citing works

The role of ZIP proteins in zinc assimilation and distribution in plants: current challenges

Lira-Morales, J. D., Varela-Bojórquez, N., Montoya-Rojo, M. B., & Sañudo-Barajas, J. A. (2019) · Czech Journal of Genetics and Plant Breeding · doi:10.17221/54/2018-cjgpb · Cited by 21 · see citing works

Heavy metal hyperaccumulation and hypertolerance in Brassicaceae

Dar, M. I., Naikoo, M. I., Green, I. D., Sayeed, N., Ali, B., & Khan, F. A. (2018) · Plants Under Metal and Metalloid Stress · doi:10.1007/978-981-13-2242-6_10 · Cited by 17 · see citing works

Expression of a rice OsARGOS gene in Arabidopsis promotes cell division and expansion and increases organ size

Bao, Wang, Yal�in, et al. (2009) · Acta Scientiarum Naturalium Universitatis Sunyatseni · Cited by 21 · see citing works

Salinity tolerance of Arabidopsis: a good model for cereals?

Møller, I. S., & Tester, M. A. (2007) · Trends in Plant Science · doi:10.1016/j.tplants.2007.09.009 · Cited by 131 · see citing works

HsfAld, a Protein Identified via FOX Hunting Using Thellungiella salsuginea cDNAs Improves Heat Tolerance by Regulating Heat-Stress-Responsive Gene Expression

Yukari, Higashi, Naohiko, et al. (2013) · 分子植物：英文版

Konukçu-Patojen İlişkisinde Model Bir Bitki: Arabidopsis thaliana / A Model Plant In Host-Pathogen Interactıon: Arabidopsis thaliana

Türk, F. M. (2006) · Atatürk University Journal of Agricultural Faculty · doi:10.17097/zfd.73134

Research Article: The effects of aluminum toxicity on the protein expression of Arabidopsis thaliana

Morefield, H., Goodman, T. V., & Hamissou, M. (2005) · BIOS · doi:10.1893/0005-3155(2005)076[0084:rateoa]2.0.co;2 · Cited by 1 · see citing works