The DOI matches its Crossref record; 45 of the 45 references it cites were found in a registry or an index.
Canalization of auxin flow by Aux/IAA-ARF-dependent feedback regulation of PIN polarity
Open accessAbstract
Plant development is characterized by a profound ability to regenerate and form tissues with new axes of polarity. An unsolved question concerns how the position within a tissue and cues from neighboring cells are integrated to specify the polarity of individual cells. The canalization hypothesis proposes a feedback effect of the phytohormone auxin on the directionality of intercellular auxin flow as a means to polarize tissues. Here we identify a cellular and molecular mechanism for canalization. Local auxin application, wounding, or auxin accumulation during de novo organ formation lead to rearrangements in the subcellular polar localization of PIN auxin transport components. This auxin effect on PIN polarity is cell-specific, does not depend on PIN transcription, and involves the Aux/IAA-ARF (indole-3-acetic acid-auxin response factor) signaling pathway. Our data suggest that auxin acts as polarizing cue, which links individual cell polarity with tissue and organ polarity through control of PIN polar targeting. This feedback regulation provides a conceptual framework for polarization during multiple regenerative and patterning processes in plants.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“the expression of PIN proteins precedes vascular development (Sauer et al., 2006; Scarpella et al., 2006; Wenzel et al., 2007)”
From Shaping plant architecture (2015) · cites this paper as Sauer et al., 2006
Citations
Cites
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
Benková, E., Michniewicz, M., Sauer, M., Teichmann, T., Seifertová, D., Jürgens, G., & Friml, J. (2003) · Cell · doi:10.1016/s0092-8674(03)00924-3 · Cited by 2,637
Self-citationAuxin: Regulation, Action, and Interaction
Woodward, A. W. (2005) · Annals of Botany · doi:10.1093/aob/mci083 · Cited by 2,399
The F-box protein TIR1 is an auxin receptor
Dharmasiri, N., Dharmasiri, S., & Estelle, M. (2005) · Nature · doi:10.1038/nature03543 · Cited by 2,083
The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots
Blilou, I., Xu, J., Wildwater, M., Willemsen, V., Paponov, I. A., Friml, J., Heidstra, R., Aida, M., Palme, K. J., & Scheres, B. (2005) · Nature · doi:10.1038/nature03184 · Cited by 2,061
Self-citationEfflux-dependent auxin gradients establish the apical–basal axis of Arabidopsis
Friml, J., Vieten, A., Sauer, M., Weijers, D., Schwarz, H., Hamann, T., Offringa, R., & Jürgens, G. (2003) · Nature · doi:10.1038/nature02085 · Cited by 1,896
Self-citationThe Arabidopsis F-box protein TIR1 is an auxin receptor
Kepinski, S., & Leyser, O. (2005) · Nature · doi:10.1038/nature03542 · Cited by 1,703
Regulation of phyllotaxis by polar auxin transport
Reinhardt, D., Pesce, E.-R., Stieger, P., Mandel, T., Baltensperger, K., Bennett, M., Traas, J., Friml, J., & Kuhlemeier, C. (2003) · Nature · doi:10.1038/nature02081 · Cited by 1,523
Self-citationSteeves, T. A., & Sussex, I. M. (1989) · doi:10.1017/cbo9780511626227 · Cited by 1,334
Auxin transport inhibitors block PIN1 cycling and vesicle trafficking
Geldner, N., Friml, J., Stierhof, Y.-D., Jürgens, G., & Palme, K. J. (2001) · Nature · doi:10.1038/35096571 · Cited by 1,244
Self-citationHeisler, 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
Flagged first, then by citations
Cited by
Sorted by citations
Items 201–300 of 453
Inter‐regulation of the unfolded protein response and auxin signaling
Chen, Y., Aung, K., Rolc̆ı́k, J., Walicki, K., Friml, J., & Brandizzí, F. (2013) · The Plant Journal · doi:10.1111/tpj.12373 · Cited by 48
Self-citationMironova, V., Omelyanchuk, N. A., Novoselova, E. S., Doroshkov, A. V., Владимирович, К. Ф., Kochetov, A. V., Kolchanov, N. A., Mjolsness, E., & Likhoshvai, V. A. (2012) · Annals of Botany · doi:10.1093/aob/mcs069 · Cited by 48
Context, Specificity, and Self-Organization in Auxin ResponsePreprint
Bianco, M. D., & Kepinski, S. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001578 · Cited by 49
Tsugeki, R., Ditengou, F. A., Sumi, Y., Teale, W., Palme, K. J., & Okada, K. (2009) · The Plant Cell · doi:10.1105/tpc.109.068841 · Cited by 45
Prototype cell-to-cell auxin transport mechanism by intracellular auxin compartmentalization
Wabnik, K., Kleine‐Vehn, J., Govaerts, W. J. F., & Friml, J. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2011.05.002 · Cited by 49
Self-citationCvrčková, F., Lipavská, H., & Žárský, V. (2009) · Plant Signaling & Behavior · doi:10.4161/psb.4.5.8276 · Cited by 46
CUC2 as an early marker for regeneration competence in Arabidopsis root explants
Motte, H., Verstraeten, I., Werbrouck, S., & Geelen, D. (2011) · Journal of Plant Physiology · doi:10.1016/j.jplph.2011.02.014 · Cited by 45
Zhou, L., Hou, H., Tao, Y., Lian, Y., Sun, Y., Bian, Z., & Wang, C. (2018) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2018.05.014 · Cited by 45
The canalization hypothesis – challenges and alternatives
Ravichandran, S. J., Linh, N. M., & Scarpella, E. (2020) · New Phytologist · doi:10.1111/nph.16605 · Cited by 42
The carrier AUXIN RESISTANT (AUX1) dominates auxin flux into Arabidopsis protoplasts
Rutschow, H. L., Baskin, T. I., & Kramer, E. M. (2014) · New Phytologist · doi:10.1111/nph.12933 · Cited by 44
Marcos, D., & Berleth, T. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00235 · Cited by 44
Forbidden Fruit: Dominance Relationships and the Control of Shoot Architecture
Walker, C. H., & Bennett, T. (2018) · Wiley eBooks · doi:10.1002/9781119312994.apr0640 · Cited by 43
Polar delivery in plants; commonalities and differences to animal epithelial cells
Kania, U., Fendrych, M., & Friml, J. (2014) · Open Biology · doi:10.1098/rsob.140017 · Cited by 41
Self-citationDevelopmental roles of Auxin Binding Protein 1 in Arabidopsis thaliana
Gelová, Z., Gallei, M., Pernisová, M., Brunoud, G., Zhang, X., Glanc, M., Li, L., Michalko, J., Pavlovičová, Z., Verstraeten, I., et al. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110750 · Cited by 43
Self-citationRegulation of vascular cambium activity
Wang, H. (2019) · Plant Science · doi:10.1016/j.plantsci.2019.110322 · Cited by 41
Feedback models for polarized auxin transport: an emerging trend
Wabnik, K., Govaerts, W. J. F., Friml, J., & Kleine‐Vehn, J. (2011) · Molecular BioSystems · doi:10.1039/c1mb05109a · Cited by 40
Self-citationCell Polarity Signaling: Focus on Polar Auxin Transport
Gao, X., Nagawa, S., Wang, G., & Yang, Z. (2008) · Molecular Plant · doi:10.1093/mp/ssn069 · Cited by 40
Coordination of cell polarity and the patterning of leaf vein networks
Linh, N. M., Verna, C., & Scarpella, E. (2017) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2017.09.009 · Cited by 36
Cellular events during interfascicular cambium ontogenesis in inflorescence stems of Arabidopsis
Mazur, E., Kurczynska, E. U., & Friml, J. (2014) · PROTOPLASMA · doi:10.1007/s00709-014-0620-5 · Cited by 39
Self-citationModulation of Arabidopsis root growth by specialized triterpenes
Bai, Y., Fernández‐Calvo, P., Ritter, A., Huang, A. C., Morales-Herrera, S., Bicalho, K. U., Karády, M., Pauwels, L., Buyst, D., Njo, M. F., et al. (2020) · New Phytologist · doi:10.1111/nph.17144 · Cited by 38
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
Diversity of phyllotaxis in land plants in reference to the shoot apical meristem structure
Gola, E. M., & Banasiak, A. (2016) · Acta Societatis Botanicorum Poloniae · doi:10.5586/asbp.3529 · Cited by 40
Qu, Y., Wang, Q., Guo, J., Wang, P., Song, P., Jia, Q., Zhang, X., Kudla, J., Zhang, W., & Zhang, Q. (2017) · Journal of Experimental Botany · doi:10.1093/jxb/erx290 · Cited by 36
He, Q., Yang, L., Hu, W., Zhang, J., & Xing, Y. (2018) · Scientific Reports · doi:10.1038/s41598-018-32450-x · Cited by 38
Roschzttardtz, H., Paéz-Valencia, J., Dittakavi, T., Jali, S., Reyes, F. C., Baisa, G. A., Anne, P., Gissot, L., Palauqui, J., Masson, P., et al. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.246314 · Cited by 35
Ku, S.-J., Park, J.-Y., Ha, S., & Kim, J. (2008) · Journal of Plant Physiology · doi:10.1016/j.jplph.2008.07.006 · Cited by 35
Cellular requirements for PIN polar cargo clustering in Arabidopsis thaliana
Li, H., von Wangenheim, D., Zhang, X., Tan, S., Darwish, N., Naramoto, S., Wabnik, K., Rycke, R. M. D., Kaufmann, W. A., Gütl, D., et al. (2020) · New Phytologist · doi:10.1111/nph.16887 · Cited by 37
Self-citationCytokinins and polar transport of auxin in axillary pea buds
Kalousek, P., Buchtová, D., Balla, J., Reinöhl, V., & Procházka, S. (2014) · Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis · doi:10.11118/actaun201058040079 · Cited by 40
Self-citationSankaranarayanan, S., & Samuel, M. A. (2015) · Plant Signaling & Behavior · doi:10.4161/15592324.2014.989749 · Cited by 33
Phyllotaxis: from patterns of organogenesis at the meristem to shoot architecture
Galván-Ampudia, C. S., Chaumeret, A., Godin, C., & Vernoux, T. (2016) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.231 · Cited by 35
Cano, A., Sánchez‐García, A. B., Albacete, A. A., González‐Bayón, R., Justamante, M. S., Ibáñez, S., Acosta, M., & Pérez‐Pérez, J. M. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00566 · Cited by 33
Leaf vein patterning is regulated by the aperture of plasmodesmata intercellular channels
Linh, N. M., & Scarpella, E. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001781 · Cited by 32
Planar polarity, tissue polarity and planar morphogenesis in plants
Nakamura, M., Kiefer, C. S., & Grebe, M. (2012) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2012.07.006 · Cited by 33
Analysis of Vascular Development in the hydra Sterol Biosynthetic Mutants of Arabidopsis
Pullen, M., Clark, N. R., Zarinkamar, F., Topping, J. F., & Lindsey, K. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012227 · Cited by 32
CLUMSY VEIN , the Arabidopsis DEAH ‐box Prp16 ortholog, is required for auxin‐mediated development
Tsugeki, R., Tanaka‐Sato, N., Maruyama, N., Terada, S., Kojima, M., Sakakibara, H., & Okada, K. (2014) · The Plant Journal · doi:10.1111/tpj.12721 · Cited by 32
Mazur, E., Gallei, M., Adamowski, M., Han, H., Robert, H. S., & Friml, J. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110414 · Cited by 30
Self-citationBorrell, A. K., Wong, A. C. S., George‐Jaeggli, B., van Oosterom, E. J., Mace, E., Godwin, I. D., Liu, G., Mullet, J. E., Klein, P. G., Hammer, G., et al. (2022) · Journal of Experimental Botany · doi:10.1093/jxb/erac336 · Cited by 31
Interactions between rootstock and scion during grafting and their molecular regulation mechanism
Liu, Y., Liu, H., Zhang, T., Liu, J., Sun, X., Sun, X., Wang, W., & Zheng, C. (2022) · Scientia Horticulturae · doi:10.1016/j.scienta.2022.111554 · Cited by 31
Spicer, R., Tisdale-Orr, T. E., & Talavera, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072499 · Cited by 31
Ye, X., Kang, B.-G., Osburn, L. D., Li, Y., & ZongMing, C. (2009) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-009-9526-x · Cited by 31
Scarpella, E. (2024) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-062923-030348 · Cited by 32
Cell-to-cell communication in vascular morphogenesis
Lehesranta, S. J., Lichtenberger, R., & Helariutta, Y. (2009) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.09.004 · Cited by 30
Wang, Y., Liu, H., Wang, S., & Li, H. (2016) · Plant Growth Regulation · doi:10.1007/s10725-016-0203-x · Cited by 30
Pea (Pisum sativum L.) in biology prior and after Mendel's discovery
Smýkal, P. (2014) · Czech Journal of Genetics and Plant Breeding · doi:10.17221/2/2014-cjgpb · Cited by 30
Advances in Watermelon Grafting to Increase Efficiency and Automation
Devi, P., Lukas, S. B., & Miles, C. A. (2020) · Horticulturae · doi:10.3390/horticulturae6040088 · Cited by 31
Conditional destabilization of the TPLATE complex impairs endocytic internalization
Wang, J., Yperman, K., Grones, P., Jiang, Q., Dragwidge, J. M., Mylle, E., Mor, E., Nolf, J., Eeckhout, D., Jaeger, G. D., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2023456118 · Cited by 27
Polarity, Continuity, and Alignment in Plant Vascular Strands
Sawchuk, M. G., & Scarpella, E. (2013) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12086 · Cited by 29
Built to rebuild: in search of organizing principles in plant regeneration
Sena, G., & Birnbaum, K. D. (2010) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2010.04.011 · Cited by 29
Pavement cells: a model system for non-transcriptional auxin signalling and crosstalks: Fig. 1.
Chen, J., Wang, F., Zheng, S., Xu, T., & Yang, Z. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv266 · Cited by 27
Ca2+ influences heat shock signal transduction in Pyropia haitanensis
Zheng, H., Wang, W., Xu, K., Xu, Y., Ji, D., Chen, C., & Xie, C. (2019) · Aquaculture · doi:10.1016/j.aquaculture.2019.734618 · Cited by 28
Libao, C., Minrong, Z., Hu, Z., huiying, L., & Li, S. (2020) · BMC Genomics · doi:10.1186/s12864-020-07046-3 · Cited by 28
Bantis, F., Panteris, E., Dangitsis, C., Carrera, E., & Κουκουνάρας, Α. (2021) · Scientific Reports · doi:10.1038/s41598-021-01158-w · Cited by 28
Phyllotaxis involves auxin drainage through leaf primordia
Deb, Y., Marti, D., Frenz, M., Kuhlemeier, C. J., & Reinhardt, D. (2015) · Development · doi:10.1242/dev.121244 · Cited by 27
WOX2and polar auxin transport during spruce embryo pattern formation
Palovaara, J., & Hakman, I. (2009) · Plant Signaling & Behavior · doi:10.4161/psb.4.2.7684 · Cited by 27
Pramoolkit, P., Lertpanyasampatha, M., Viboonjun, U., Kongsawadworakul, P., Chrestin, H., & Narangajavana, J. (2014) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2014.09.016 · Cited by 28
Scarpella, E. (2017) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2017.02.009 · Cited by 27
Auxin enhances grafting success in Carya cathayensis (Chinese hickory)
Kumar, R. M. S., Gao, L. X., Yuan, H., Xu, D., Zhao, L., Tao, S., Guo, W. B., Yan, D., Zheng, B., & Edqvist, J. (2017) · Planta · doi:10.1007/s00425-017-2824-3 · Cited by 27
The Auxin Question: A Philosophical Overview
Bennett, T., & Leyser, O. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1526-8_1 · Cited by 26
Modelling polar auxin transport in developmental patterning
Santos, F. C., Teale, W., Fleck, C. C., Volpers, M., Ruperti, B., & Palme, K. J. (2010) · Plant Biology · doi:10.1111/j.1438-8677.2010.00388.x · Cited by 26
Awwad, F., Bertrand, G., Grandbois, M., & Beaudoin, N. (2019) · BMC Plant Biology · doi:10.1186/s12870-019-2130-2 · Cited by 26
Of Cells, Strands, and Networks: Auxin and the Patterned Formation of the Vascular SystemPreprint
Lavania, D., Linh, N. M., & Scarpella, E. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a039958 · Cited by 26
MODULATOR OF PIN genes control steady‐state levels of Arabidopsis PIN proteins
Malenica, N., Abas, L., Benjamins, R., Kitakura, S., Sigmund, H. F., Jun, K. S., Hauser, M., Friml, J., & Luschnig, C. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03158.x · Cited by 25
Self-citationRapid auxin-mediated phosphorylation of Myosin regulates trafficking and polarity in ArabidopsisPreprint
Han, H., Verstraeten, I., Roosjen, M., Mazur, E., Rýdza, N., Hajný, J., Ötvös, K., Weijers, D., & Friml, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.13.439603 · Cited by 25
Self-citationReeger, J. E., Wheatley, M. S., Yang, Y., & Brown, K. M. (2021) · Plant Direct · doi:10.1002/pld3.328 · Cited by 24
A coupled mechano-biochemical model for cell polarity guided anisotropic root growth
Marconi, M., Gallemí, M., Benková, E., & Wabnik, K. (2021) · eLife · doi:10.7554/elife.72132 · Cited by 23
Self-citationXu, Z., Wang, R., Kong, K., Begum, N., Almakas, A., Liu, J., Li, H., Liu, B., Zhao, T., & Zhao, T. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.983650 · Cited by 24
Chen, J., Zhang, J., & He, X. (2013) · Physiologia Plantarum · doi:10.1111/ppl.12112 · Cited by 24
Libao, C., Huiying, L., Yuyan, H., & Li, S. (2019) · Molecular Biology Reports · doi:10.1007/s11033-019-04749-z · Cited by 23
Correlative polar auxin transport to explain the thinning mode of action of benzyladenine on apple
Schröder, M., Link, H., & Bangerth, K. F. (2013) · Scientia Horticulturae · doi:10.1016/j.scienta.2013.02.001 · Cited by 23
Auxin transport and stem vascular reconnection – has our thinking become canalized?
Wulf, K. E., Reid, J. B., & Foo, E. (2018) · Annals of Botany · doi:10.1093/aob/mcy180 · Cited by 23
Short De-Etiolation Increases the Rooting of VC801 Avocado Rootstock
Duman, Z., Hadas-Brandwein, G., Eliyahu, A., Belausov, E., Abu‐Abied, M., Yeselson, Y., Faigenboim, A., Lichter, A., Irihimovitch, V., & Sadot, E. (2020) · Plants · doi:10.3390/plants9111481 · Cited by 22
Auxin redistribution and shifts in PIN gene expression during Arabidopsis grafting
Wang, J., Jin, Z., Yin, H., Yan, B., Ren, Z., Xu, J., Mu, C. J., Zhang, Y., Wang, M. Q., & Liu, H. (2014) · Russian Journal of Plant Physiology · doi:10.1134/s102144371405015x · Cited by 22
Dong, D., Wang, M., Li, Y., Liu, Z., Li, S., Chao, Y., & Han, L. (2021) · Scientific Reports · doi:10.1038/s41598-021-91931-8 · Cited by 21
Fujii, N., Miyabayashi, S., Sugita, T., Kobayashi, A., Yamazaki, C., Miyazawa, Y., Kamada, M., Kasahara, H., Osada, I., Shimazu, T., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0189827 · Cited by 21
Molesini, B., Pandolfini, T., Pii, Y., Korte, A., & Spena, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041327 · Cited by 22
In Silico Roots: Room for Growth
Rutten, J. P., & ten Tusscher, K. (2019) · Trends in Plant Science · doi:10.1016/j.tplants.2018.11.005 · Cited by 20
Deslauriers, S. D., & Spalding, E. P. (2021) · Plant Direct · doi:10.1002/pld3.361 · Cited by 20
Bimodal regulation of ICR1 levels generates self-organizing auxin distribution
Hazak, O., Obolski, U., Prat, T., Friml, J., Hadany, L., & Yalovsky, S. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1413918111 · Cited by 20
Self-citationYan, D., Wang, J., Yuan, T., Hong, L., Gao, X., & Lu, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058103 · Cited by 20
The effect of indole-3-carbinol on PIN1 and PIN2 in Arabidopsis roots
Katz, E., Nisani, S., Sela, M., Behar, H., & Chamovitz, D. (2015) · Plant Signaling & Behavior · doi:10.1080/15592324.2015.1062200 · Cited by 20
Control of lateral root initiation by DA3 in Arabidopsis
Peng, Y., Jiang, S., Wang, J., Xu, X., Gong, X., Jin, W., Song, C., Dong, Z., Siyu, S., Li, Y., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111913 · Cited by 18
Fertilisation and Fruit Initiation
Fuentes, S., & Vivian‐Smith, A. (2009) · Wiley-Blackwell eBooks · doi:10.1002/9781444314557.ch4 · Cited by 18
Alim, K., & Frey, E. (2010) · The European Physical Journal E · doi:10.1140/epje/i2010-10604-5 · Cited by 17
Modelling the dynamics of polar auxin transport in inflorescence stems ofArabidopsis thaliana
Boot, K. J. M., Hille, S. C., Libbenga, K. R., Peletier, L. A., van Spronsen, P. C., van Duijn, B., & Offringa, R. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv471 · Cited by 18
Dhonukshe, P. (2009) · Communicative & Integrative Biology · doi:10.4161/cib.7715 · Cited by 18
Dierck, R., Leus, L., Dhooghe, E., Huylenbroeck, J. V., Riek, J. D., Straeten, D. V. D., & Keyser, E. D. (2018) · Plant Growth Regulation · doi:10.1007/s10725-018-0408-2 · Cited by 19
Hearn, D. J., O’Brien, P., & Poulsen, S. M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0197166 · Cited by 19
Li, X., Zhang, J., Shi, H., Li, B., & Li, J. (2022) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13274 · Cited by 17
Li, P., Ding, L., Zhang, L., He, J., & Huan, Z. (2019) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2019.04.020 · Cited by 17
Identification of MV-generated ROS responsive EST clones in floral buds of Litchi chinensis Sonn.
Liu, W., Kim, H., Chen, H., Lu, X.-Y., & Zhou, B. (2013) · Plant Cell Reports · doi:10.1007/s00299-013-1448-8 · Cited by 17
Unifoliata‐Afila interactions in pea leaf morphogenesis
DeMason, D. A., Chetty, V. J., Barkawi, L. S., Liu, X., & Cohen, J. D. (2013) · American Journal of Botany · doi:10.3732/ajb.1200611 · Cited by 19
Guinel, F. C. (2009) · Botany · doi:10.1139/b09-075 · Cited by 17
Libao, C., Runzhi, J., Jianjun, Y., Xiaoyong, X., Haitao, Z., & Li, S. (2018) · Zeitschrift für Naturforschung C · doi:10.1515/znc-2017-0188 · Cited by 17
TMK-PIN1 drives a short self-organizing circuit for auxin export and signaling in Arabidopsis
Huang, R., Wang, J., Chang, M., Tang, W., Yu, Y., Zhang, Y., Peng, Y., Wang, Y., Guo, Y., Lu, T., et al. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.09.009 · Cited by 18
Self-citationARF4 acting upstream of LBD16 promotes adventitious root formation in peach
Liu, J., Gao, L., Zhang, R., Gao, A., Oginga, Z. K., Zheng, B., & Han, Y. (2023) · Horticultural Plant Journal · doi:10.1016/j.hpj.2023.07.004 · Cited by 16
Nahas, Z., Ticchiarelli, F., van Rongen, M., Dillon, J., & Leyser, O. (2024) · New Phytologist · doi:10.1111/nph.19664 · Cited by 16
Polar expedition: mechanisms for protein polar localization
Raggi, S., Demes, E., Liu, S., Verger, S., & Robert, S. (2020) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2019.12.001 · Cited by 16
Jiu, S., Xu, Y., Wang, J., Haider, M. S., Xu, J., Wang, L., Wang, S., Li, J., Liu, X., Sun, W., et al. (2021) · Scientia Horticulturae · doi:10.1016/j.scienta.2021.110709 · Cited by 16
Tissue specificity and responses to abiotic stresses and hormones of PIN genes in rice
Xu, H., Zhang, Y., Yang, X., Wang, H. H., & Hou, D. (2022) · Biologia · doi:10.1007/s11756-022-01031-9 · Cited by 16
The interplay between extracellular and intracellular auxin signaling in plants
Tang, W., Yu, Y., & Xu, T. (2024) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2024.06.019 · Cited by 17
Metadata
- Authors
- Sauer, M., Balla, J., Luschnig, C., Wiśniewska, J., Reinöhl, V., Friml, J., & Benková, E.
- Affiliations
- University of Tübingen (DE)
- Mendel University in Brno (CZ)
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2006-10-15
- Volume
- 20
- Issue
- 20
- Pages
- 2902-2911
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC1619939
- OpenAlex
- W2105722863
- Cited by
- 453
- References
- 45
- Citations by year
- 2026: 8 · 2025: 13 · 2024: 15 · 2023: 10 · 2022: 20 · 2021: 25 · 2020: 22 · 2019: 19 · 2018: 22 · 2017: 15 · 2016: 26 · 2015: 21 · 2014: 33 · 2013: 37 · 2012: 28
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Volkswagen Foundation
- Grantová Agentura České Republiky
- Fundacja na rzecz Nauki Polskiej
- Austrian Science Fund
- 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 nutrient uptake and metabolism
- Keywords
- auxin transport, PIN auxin efflux carriers, canalization, auxin response factor, auxin response, cell polarity, tissue polarity, wounding, organ formation, plant regeneration, feedback regulation
- MeSH terms
- Indoleacetic Acids, Plant Growth Regulators, Plant Proteins, Transcription, Genetic, Signal Transduction, Arabidopsis, Gene Expression Regulation, Plant, Plant Roots, Plant Physiological Phenomena, Phototropism, Pisum sativum, Arabidopsis Proteins
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