The DOI matches its Crossref record; 48 of the 48 references it cites were found in a registry or an index.
Brassinosteroids regulate organ boundary formation in the shoot apical meristem of Arabidopsis
Open accessAbstract
Spatiotemporal control of the formation of organ primordia and organ boundaries from the stem cell niche in the shoot apical meristem (SAM) determines the patterning and architecture of plants, but the underlying signaling mechanisms remain poorly understood. Here we show that brassinosteroids (BRs) play a key role in organ boundary formation by repressing organ boundary identity genes. BR-hypersensitive mutants display organ-fusion phenotypes, whereas BR-insensitive mutants show enhanced organ boundaries. The BR-activated transcription factor BZR1 directly represses the CUP-SHAPED COTYLEDON ( CUC ) family of organ boundary identity genes. In WT plants, BZR1 accumulates at high levels in the nuclei of central meristem and organ primordia but at a low level in organ boundary cells to allow CUC gene expression. Activation of BR signaling represses CUC gene expression and causes organ fusion phenotypes. This study uncovers a role for BR in the spatiotemporal control of organ boundary formation and morphogenesis in the SAM.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The LOB1-mediated decrease of brassinosteroid activity causes a reduction of cell size and cell division rate in the boundary zone compared to neighboring zones (Bell et al., 2012; Gendron et al., 2012).”
From Shaping plant architecture (2015) · cites this paper as Gendron et al., 2012
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In addition, LOF1 and CUC genes show complex interactions, regulating each other's expression (Lee et al., 2009;Gendron et al., 2012; Fig. 3).”
From Divide et impera: boundaries shape the plant body and initiate new meristems (2016) · cites this paper as Gendron et al., 2012
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“CUC genes are down-regulated by brassinosteroids.”
From Shaping plant architecture (2015) · cites this paper as Gendron et al., 2012
The cited source says what the claim attributes to it.
In the citing paper
“Thus, low brassinosteroid activity in the boundary zone not only reduces cell expansion and division as described above, but also allows the induction of CUC genes (Bell et al., 2012; Gendron et al., 2012).”
From Shaping plant architecture (2015) · cites this paper as Gendron et al., 2012
The cited source says what the claim attributes to it.
In the citing paper
“In wild type, BZR1 proteins accumulate to high levels in the central meristem and organ primordia, limiting the expression of a specific set of genes, including CUC genes, to the boundary (Gendron et al., 2012).”
From Divide et impera: boundaries shape the plant body and initiate new meristems (2016) · cites this paper as Gendron et al., 2012
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant.
Aida, M., Ishida, T., Fukaki, H., Fujisawa, H., & Tasaka, M. (1997) · The Plant Cell · doi:10.1105/tpc.9.6.841 · Cited by 1,486
BRASSINOSTEROIDS: Essential Regulators of Plant Growth and Development
Clouse, S. D., & Sasse, J. M. (1998) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.49.1.427 · Cited by 1,462
Heisler, M. G., Ohno, C., Das, P., Sieber, P., Reddy, G. V., Long, J. A., & Meyerowitz, E. M. (2005) · Current Biology · doi:10.1016/j.cub.2005.09.052 · Cited by 1,189
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
Self-citationSun, Y., Fan, X.-Y., Cao, D.-M., Tang, W., He, K., Zhu, J.-Y., He, J.-X., Bai, M., Zhu, S., Oh, E., et al. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.10.010 · Cited by 1,002
Self-citationSzekeres, M., Németh, K., Koncz–Kálmán, Z., Mathur, J., Kauschmann, A., Altmann, T., Rédei, G. P., Nagy, F., Schell, J., & Koncz, C. (1996) · Cell · doi:10.1016/s0092-8674(00)81094-6 · Cited by 998
Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses
Oh, E., Zhu, J.-Y., & Wang, Z. (2012) · Nature Cell Biology · doi:10.1038/ncb2545 · Cited by 886
Self-citationHe, J., Gendron, J. M., Sun, Y., Gampala, S. S. L., Gendron, N., Sun, C. Q., & Wang, Z. (2005) · Science · doi:10.1126/science.1107580 · Cited by 868
Self-citationA 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
Yamamuro, C., Ihara, Y., Wu, X., Noguchi, T., Fujioka, S., Takatsuto, S., Ashikari, M., Kitano, H., & Matsuoka, M. (2000) · The Plant Cell · doi:10.1105/tpc.12.9.1591 · Cited by 758
Cited by
Sorted by citations
Items 101–200 of 205
Li, M., Li, P., Wang, C., Xu, H., Wang, M., Wang, Y., Niu, X., Xu, M., Hong, W., Qin, Y., et al. (2022) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiac327 · Cited by 24
Self-citationRegulatory variation controlling architectural pleiotropy in maize
Bertolini, E., Rice, B. R., Braud, M., Yang, J., Hake, S., Strable, J., Lipka, A. E., & Eveland, A. L. (2025) · Nature Communications · doi:10.1038/s41467-025-56884-w · Cited by 24
Tai, H., Opitz, N., Lithio, A., Lu, X., Nettleton, D. S., & Hochholdinger, F. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw422 · Cited by 21
Ruan, Y., & Wasteneys, G. O. (2014) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2014.11.003 · Cited by 21
Xu, W., Zhu, W., Liu, Y., Liang, W., Li, H., Yang, L. C., Chen, M., Luo, Z., Huang, G., Duan, L., et al. (2021) · New Phytologist · doi:10.1111/nph.17849 · Cited by 21
Molecular Mechanisms of Floral Boundary Formation in Arabidopsis
Yu, H., & Huang, T. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17030317 · Cited by 19
Brassinosteroids in plant developmental signaling networks
Ryu, H., & Hwang, I. (2013) · Journal of Plant Biology · doi:10.1007/s12374-013-0298-9 · Cited by 17
The vascular plants: open system of growth
Basile, A., Fambrini, M., & Pugliesi, C. (2017) · Development Genes and Evolution · doi:10.1007/s00427-016-0572-1 · Cited by 18
Plant Development: Brassinosteroids Go Out of Bounds
Arnaud, N., & Laufs, P. (2013) · Current Biology · doi:10.1016/j.cub.2013.01.001 · Cited by 16
The whole and its parts: cell-specific functions of brassinosteroids
Aardening, Z., Khandal, H., Erlichman, O. A., & Savaldi‐Goldstein, S. (2024) · Trends in Plant Science · doi:10.1016/j.tplants.2024.10.015 · Cited by 15
Manipulating brassinosteroid signaling pathway to genetically improve horticultural plants
Li, X. S., Li, J., Zabed, H. M., Li, J., Xiong, M., Shi, H., & Li, J. (2025) · aBIOTECH · doi:10.1007/s42994-025-00201-y · Cited by 15
Feng, Z., Shi, H., Lv, M., Ma, Y., & Li, J. (2021) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13093 · Cited by 15
He, J., Li, Q., Liang, C., Wang, N., Wang, J., Jiang, C., Kang, Z., Tang, C., & Wang, X. (2025) · Molecular Plant · doi:10.1016/j.molp.2025.08.012 · Cited by 14
Research Progress and Application of Plant Branching
Yang, Y., Hu, Y., Li, P., Hancock, J. T., & Hu, X. (2022) · Phyton · doi:10.32604/phyton.2023.024904 · Cited by 16
Chen, Y., Vermeersch, M., Leene, J. V., Jaeger, G. D., Li, Y., & Vanhaeren, H. (2024) · Science Advances · doi:10.1126/sciadv.adj2570 · Cited by 14
Unraveling the molecular mechanisms governing axillary meristem initiation in plants
Yuan, Y., Du, Y., & Delaplace, P. (2024) · Planta · doi:10.1007/s00425-024-04370-w · Cited by 13
Zhao, W., Bai, Q., Zhao, B., Wu, Q. Y., Wang, C., Liu, Y., Yang, T., Liu, Y., He, H., Du, S., et al. (2021) · New Phytologist · doi:10.1111/nph.17198 · Cited by 13
Transcriptome analysis revealed hormone signaling response of grapevine buds to strigolactones
Min, Z., Li, Z., Chen, L., Zhang, Y., Liu, M., Yan, X., & Fang, Y. (2021) · Scientia Horticulturae · doi:10.1016/j.scienta.2021.109936 · Cited by 12
Colling, J., Tohge, T., Clercq, R. D., Brunoud, G., Vernoux, T., Fernie, A. R., Makunga, N. P., Goossens, A., & Pauwels, L. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv291 · Cited by 13
Xu, L., Fang, N., Lu, T., Tameshige, T., Nakata, M. T., Jiang, Y., Tan, L., He, H. Y., Zhang, X., Huang, Y., et al. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae443 · Cited by 12
The Secrets of Meristems Initiation: Axillary Meristem Initiation and Floral Meristem Initiation
Yang, Q., Yuan, C., Cong, T., & Zhang, Q. (2023) · Plants · doi:10.3390/plants12091879 · Cited by 11
Riekötter, J., Oklešťková, J., Muth, J. R., Twyman, R. M., & Epping, J. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1112793 · Cited by 11
HISTONE DEACETYLASE19 Controls Ovule Number Determination and Transmitting Tract Differentiation
Manrique, S., Cavalleri, A., Guazzotti, A., Villarino, G., Simonini, S., Bombarely, A., Higashiyama, T., Grossniklaus, U., Mizzotti, C., Pereira, A. M., et al. (2023) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiad629 · Cited by 10
Zhang, Z., Zhang, H., Feng, L., Wang, A., Lin, Z., Tan, C., Gonzalez, E., Grismer, T. S., Xu, S., & Wang, Z. (2025) · Plant Communications · doi:10.1016/j.xplc.2025.101389 · Cited by 11
Self-citationA recessive high-density pod mutant resource of Brassica napus
Tang, M., Tong, C., Liang, L., Du, C., Zhao, J., Xiao, L., Tong, J., Dai, X., Helal, M., Dai, W., et al. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110411 · Cited by 11
Spatial control of plant steroid signaling
Caño‐Delgado, A. I., & Blázquez, M. A. (2013) · Trends in Plant Science · doi:10.1016/j.tplants.2013.01.005 · Cited by 11
Over-expression of GhDWF4 gene improved tomato fruit quality and accelerated fruit ripening
Ye, S., Fang, L. I., Li, X., Hong, Q., Zhai, Y., Hu, M., Wei, T., Deng, S., Pei, Y., & Luo, M. (2015) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(15)61059-0 · Cited by 11
Wang, X., Liu, J., Shang, E., Hawar, A., Ito, T., & Sun, B. (2024) · The Plant Cell · doi:10.1093/plcell/koae273 · Cited by 10
Self-citationHuixiao, Y., Liao, H., Xu, F., Zhang, W., Xu, B., Chen, X., Zhu, B., Pan, W., & Yang, X. (2022) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2022.05.034 · Cited by 11
Brassinosteroid homeostasis is critical for the functionality of the Medicago truncatula pulvinus
Kong, Y., Meng, Z., Wang, H., Wang, Y., Zhang, Y., Hong, L., Liu, R., Wang, M., Zhang, J., Han, L., et al. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab008 · Cited by 10
Self-citationLardon, R., Trinh, H. K., Xu, X., Vu, L. D., van de Cotte, B., Pernisová, M., Vanneste, S., Smet, I. D., & Geelen, D. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.894208 · Cited by 10
Putting heads together: Developmental genetics of the Asteraceae capitulum
Gurung, V., Muñoz-Gómez, S., & Jones, D. S. (2024) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2024.102589 · Cited by 9
Ammitsøe, T. J., Ebstrup, E. N., Blanco‐Touriñán, N., Hansen, J., Hardtke, C. S., Petersen, M., & Rodriguez, E. (2025) · EMBO Reports · doi:10.1038/s44319-025-00433-5 · Cited by 9
Neher, W., Rasmussen, C. G., Braybrook, S. A., Lažetić, V., Stowers, C. E., Mooney, P. T., Sylvester, A. W., & Springer, P. S. (2023) · Development · doi:10.1242/dev.201608 · Cited by 10
Self-citationStem Cell Basis for Fractal Patterns: Axillary Meristem Initiation
Wang, Y. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.805434 · Cited by 8
Kramer, E. M., & Li, W. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00869 · Cited by 8
A cell wall-associated gene network shapes leaf boundary domains
Bouré, N., Peaucelle, A., Goussot, M., Adroher, B., Soubigou‐Taconnat, L., Borrega, N., Biot, E., Tariq, Z., Martin‐Magniette, M., Pautot, V., et al. (2022) · Development · doi:10.1242/dev.200359 · Cited by 8
Delineating a New Class of Membrane-Bound Guanylate Cyclases
Muleya, V., & Irving, H. R. (2016) · Springer Science Reviews · doi:10.1007/s40362-015-0037-3 · Cited by 7
Dong, H., Smith, C., Prior, R., Carter, R., Dumenil, J., Saalbach, G., McKenzie, N., & Bevan, M. W. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.15.098178 · Cited by 7
Basso, M. F., Girardin, G., Vergata, C., Buti, M., & Martinelli, F. (2024) · Frontiers in Plant Science · doi:10.3389/fpls.2024.1384237 · Cited by 6
Brassinosteroid Regulated Physiological Process: An Omics Perspective
Siddiqui, H., Sami, F., Juan, H., & Hayat, S. (2019) · Springer eBooks · doi:10.1007/978-981-13-6058-9_10 · Cited by 6
Transcription Factor RhCUC3 Regulates Petal Numbers in Rose Flowers
Fang, Y. M., Zhao, Z., Shen, Y., Ding, Z., Cui, Y., & Chen, W. (2025) · Horticulturae · doi:10.3390/horticulturae11020170 · Cited by 5
Brassinosteroids in Cucurbits: Modulators of Plant Growth Architecture and Stress Response
Słomnicka, R., Cieplak, M., Martín‐Hernández, A. M., & Bartoszewski, G. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157234 · Cited by 5
Male Germ Cell Specification in Plants
Chen, W., Wang, P., Liu, C., Han, Y., & Zhao, F. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126643 · Cited by 5
Diversity of flowers in basic structure and its underlying molecular mechanisms
Wang, H., ZHANG, R., Cheng, J., Duan, X., Zhao, H., HongYan, S. H. A. N., & Kong, H. (2019) · Scientia Sinica Vitae · doi:10.1360/n052018-00219 · Cited by 4
Emerging Dynamics of Brassinosteroids Research
Sharma, I., Kaur, N., Saini, S., & Pati, P. K. (2013) · Springer eBooks · doi:10.1007/978-81-322-1683-4_1 · Cited by 4
CUC genes control boundary domains for shoot meristem maintenance and organ initiation in maize
Zhong, W., Dong, L., Zhang, G., Li, Z., Wang, Q., Jackson, D. P., & Yang, F. (2025) · New Phytologist · doi:10.1111/nph.70441 · Cited by 3
The Formation of Shapes: Interplay of Genes during Leaf Development Processes
Ma, J., & Li, H. (2022) · Forests · doi:10.3390/f13101726 · Cited by 3
Role of somatic embryogenesis receptor-like kinase family in plants
Madhu, M., Kaur, A., Sharma, A., & Upadhyay, S. K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90594-7.00015-6 · Cited by 3
Brassinosteroids in Lowering Abiotic Stress‐mediated Damages
Sirohi, G., & Kapoor, M. (2020) · doi:10.1002/9781119552154.ch15 · Cited by 3
Hasegawa, R., Ikeda, M., Fujita, K., Tanaka, Y., Takasaki, H., Kinugasa, Y., Tachibana, R., Yamagami, A., Nomura, T., Yano, T., et al. (2025) · Journal of Experimental Botany · doi:10.1093/jxb/eraf233 · Cited by 2
Brassinosteroid-modified crops: key players for a modern Green Revolution
Ahmar, S., Rapacz, M., Wattoo, F. M., & Pociecha, E. (2026) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2025.2610339 · Cited by 2
Brassinosteroids control cell proliferation in the lateral root cap of the Arabidopsis root
Unterholzner, S. J., Svolacchia, N., Mimmo, T., Cesco, S., Mambro, R. D., Sabatini, S., & Ioio, R. D. (2026) · EMBO Reports · doi:10.1038/s44319-026-00737-0 · Cited by 2
Li, Z. Y., Wang, S., Zeng, L., Zhong, W., Yang, R., Zhang, G., He, B., Wang, T., Liao, Z., Tang, X., et al. (2026) · The Plant Cell · doi:10.1093/plcell/koag152 · Cited by 2
Brassinolide and BZR1 are up-regulated in a parthenocarpic mutant of prickly pear
Ramakrishnan, R., Zurgil, U., Tarkowská, D., Novák, O., Strnad, M., Tel‐Zur, N., & Sitrit, Y. (2025) · Plant Cell Reports · doi:10.1007/s00299-025-03514-w · Cited by 2
Brassinosteroids' regulation of plant architecture
Song, X., Qi, Z., Ahammed, G. J., Yu, J., & Xia, X. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-813227-2.00016-3 · Cited by 2
Characterization of a new leaf-compound radish mutant (Raphanus sativus L.)
Wang, F., Li, G., Chen, S., Jiang, Y., & Wang, S. (2015) · Journal of Applied Horticulture · doi:10.37855/jah.2015.v17i02.23 · Cited by 2
ERECTA family signaling controls cell fate specification during ovule initiation in ArabidopsisPreprint
Overholt, A. M., Pierce, C. E., Paleologos, C. S., & Shpak, E. D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.10.617662 · Cited by 2
Morphogenesis at the shoot meristem
Traas, J. A. (2022) · Comptes Rendus Biologies · doi:10.5802/crbiol.98 · Cited by 1
WOX out, those teeth are sharp!
Drieberg, H. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae485 · Cited by 1
miR164-targets involved in plant biological processes and stress response: A review
Wang, Y., Ruan, Q., Qiu, X., Wang, X., Chen, L., Liu, H., Wang, T., Zhang, D., Wang, B., Zhao, Y. Y., et al. (2025) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2025.110508 · Cited by 2
Hu, X., Kang, X., Ding, C., & Du, L. (2025) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-025-10581-x · Cited by 1
Wang, M., Guo, L., Wang, H., Wu, Y., Zhao, S., Song, W., Li, J., & Wang, J. (2025) · Horticulturae · doi:10.3390/horticulturae11121429 · Cited by 1
Ye, Y., Liu, D.-D., Tang, R.-J., Gong, Y., Zhang, C., Mei, P., Ma, C.-L., & Chen, J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084549 · Cited by 1
Dynamic Transcriptome Analysis Uncovers Key Regulatory Genes During Stem Elongation Stages in Wheat
Cao, R. F., Chen, Y., Dai, H., Xie, Z., Wu, L., Li, Z., Yang, Y., Zhang, L., Liu, X., Kong, X., et al. (2025) · Journal of Plant Growth Regulation · doi:10.1007/s00344-025-11734-3 · Cited by 1
Francis, D. A. (2015) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0020111.pub2 · Cited by 1
Morphogenesis at the shoot Apical Meristem
Vivero, U. C. A. (2017) · theses.fr (ABES) · doi:10.70675/07054c68z0638z4978za21ezc9b9fcda305d · Cited by 1
Mechanistic modulation of a bifunctional GC-linked receptor kinase, PSKR1
Muleya, V. (2017) · Figshare · doi:10.4225/03/58b647a0ade11
Cellular Dynamics of the Primary Shoot and Root Meristem
Vu, L. D., & Smet, I. D. (2016) · CRC Press eBooks · doi:10.1201/b20316-16
Paleochronic reversion in Psophocarpus: Dynamics II, rhizogeny on floral anatomic fieldsPreprint
Benya, E. G. F. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/253955
Regulation of shoot apical meristem activity
Venn, P. J. H. (2017) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)
Xiong, K. (2019) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2019-13691
A Simplified Thermal Circuit of Permanent Magnet Machine Part II: Experiment and Calibration
Fan, T., Sun, W., & Wen, X. (2012) · PubMed Central · doi:10.1109/mace.2012.372
Guthrie, K. A. (2021) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/90997
Gibberellins and ovule number: a molecular mechanism
Barro‐Trastoy, D. (2022) · doi:10.4995/thesis/10251/187756
Manrique, S., Cavalleri, A., Guazzotti, A., Villarino, G., Simonini, S., Bombarely, A., Higashiyama, T., Grossniklaus, U., Mizzotti, C., Pereira, A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.08.537343
SWI/SNF chromatin remodeling determines brassinosteroid-induced transcriptional activationPreprint
Zhu, T., Wei, C., Yu, Y., Zhu, J., Liang, Z., Cui, Y., Wang, Z., & Li, C. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.23.544932
Self-citationRNA-based disease control of citrus canker caused by Xanthomonas: challenges and perspectives
Gaffar, F. Y. (2023) · Journal of Plant Diseases and Protection · doi:10.1007/s41348-023-00770-4
An interview with Joshua Gendron
(2023) · Development · doi:10.1242/dev.202268
Ebstrup, E. N., Ammitsøe, T. J., Blanco‐Touriñán, N., Hansen, J., Hardtke, C. S., Rodriguez, E., & Petersen, M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.22.586258
Zhang, X., & Liu, T. (2024) · South African Journal of Botany · doi:10.1016/j.sajb.2024.07.029
Brassinosteroids mediate proper coordination of sepal elongationPreprint
Rusnak, B., Oliver, L. S., Procopio, K., & Roeder, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.13.664398
Antirrhinum flower shape: unravelling gene expression across developmental axes and boundariesPreprint
Cunha, A. M., Raimundo, J., Verweij, A., Bradley, D. J., Coen, E., & Costa, M. M. R. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.10.687484
Kapoor, S., Babanjeet, Talwar, D., & Patel, S. A. H. (2026) · Journal of Plant Growth Regulation · doi:10.1007/s00344-026-12105-2
The FUL-SHP-AP2 module regulates fruit development in petuniaPreprint
Bemer, M., Chambrier, P., Ciro, N. H., Morel, P., Thoris, K., An, E., Bento, S. R., & Vandenbussche, M. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.04.709543
EMF2b-1 regulates endosperm cell cycling through PRC2 recruitment in maize
Xu, J., Zhang, Y., Qing, K., Xue, N., Chen, J., Zhang, X. H., Zhao, W., Tian, X., Yan, H., Li, Y. F., et al. (2026) · Genome biology · doi:10.1186/s13059-026-04049-3
Moreau, F. (2014) · theses.fr (ABES) · doi:10.70675/cb0a4af7z4d8ez4760z9986z3b5530e59a09
Maugarny-Calès, A. (2017) · theses.fr (ABES) · doi:10.70675/a450e4dazc92cz43e6z9d73z98a77e17322a
Multi-Scale Analysis of CUP-SHAPED COTYLEDON Transcription Factors Function
Bouré, N. (2021) · theses.fr (ABES) · doi:10.70675/8b6527a9z9a38z4813z97eez18b5f9d3f357
Su, Y. H., Tang, L. P., & Zhang, X. S. (2026) · Springer eBooks · doi:10.1007/978-981-95-7033-1_2
González‐Suárez, P., & Song, Y. (2026) · The Plant Cell · doi:10.1093/plcell/koag157
Zhang, J., Wang, F., Zhang, S., Yu, Q., Dong, Q., Li, J., Wei, X., Du, H., Shen, Y., Mu, R., et al. (2026) · New Phytologist · doi:10.1111/nph.71320
Wang, X., Liu, J., Zhao, H., Tang, Y., Jiang, Y., Zhu, T., Tian, X., Chen, D., Lin, W., & Sun, B. (2026) · Science Advances · doi:10.1126/sciadv.aed5120
Self-citation
Metadata
- Authors
- Gendron, J. M., Liu, J.-S., Fan, M., Bai, M.-Y., Wenkel, S., Springer, P. S., Barton, M. K., & Wang, Z.-Y.
- Affiliations
- Carnegie Institution for Science (US)
- Department of Plant Biology, Carnegie Institution for Science, Stanford, CA 94305; and
- University of California, Riverside (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2012-12-04
- Volume
- 109
- Issue
- 51
- Pages
- 21152-21157
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3529081
- OpenAlex
- W2141148584
- Cited by
- 205
- References
- 48
- Citations by year
- 2026: 14 · 2025: 17 · 2024: 14 · 2023: 8 · 2022: 11 · 2021: 15 · 2020: 15 · 2019: 14 · 2018: 11 · 2017: 19 · 2016: 10 · 2015: 26 · 2014: 12 · 2013: 17 · 2012: 2
- FWCI
- 20.84
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM066258)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Parasitism and Resistance
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant tissue culture and regeneration
- Keywords
- brassinosteroids, shoot apical meristem, BZR1, organ primordia, transcriptional repression, plant morphogenesis
- MeSH terms
- Cell Nucleus, Microscopy, Electron, Scanning, Mutation, Phenotype, Signal Transduction, Genes, Plant, Arabidopsis, Gene Expression Regulation, Plant, Meristem, Plant Shoots, Microscopy, Confocal, Arabidopsis Proteins, Chromatin Immunoprecipitation, Brassinosteroids
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review