Teplova, A., Pigidanov, A. A., Serebryakova, M. V., Golyshev, S. A., Galiullina, R. A., Chichkova, N. V., &; Vartapetian, A. B. (2023). Phytaspase Is capable of detaching the endoplasmic reticulum retrieval signal from tobacco calreticulin-3. International Journal of Molecular Sciences. MDPI.https://doi.org/10.3390/ijms242216527 

Chen, H., Li, L., Zou, M., Qi, L., &; Friml, J. (2023). Distinct functions of TI and AF receptors in auxin signalling. Molecular Plant. Elsevier .https://doi.org/10.1016/j.molp.2023.06.007 

Qi, L., &; Friml, J. (2023). Tale of cAMP as a second messenger in auxin signaling and beyond. New Phytologist. Wiley.https://doi.org/10.1111/nph.19123 

Xia, J., Kong, M., Yang, Z., Sun, L., Peng, Y., Mao, Y.,https://doi.org/10.1016/j.xplc.2023.100632__Tan, S. (2023). Chemical inhibition of Arabidopsis PIN-FORMED auxin transporters by the anti-inflammatory drug naproxen. Plant Communications. Elsevier .https://doi.org/10.1016/j.xplc.2023.100632 

Gnyliukh, N., Johnson, A. J., Nagel, M.-K., Monzer, A., Hlavata, A., Isono, E.,https://doi.org/10.1101/2023.10.09.561523__Friml, J. (n.d.). Role of dynamin-related proteins 2 and S in clathrin-mediated endocytosis in plants. bioRxiv.https://doi.org/10.1101/2023.10.09.561523 

Wang, Y., Yuan, Z., Wang, J., Xiao, H., Wan, L., Li, L.,https://doi.org/10.1073/pnas.2221313120__Zhang, J. (2023). The nitrate transporter NR.1 directly antagonizes PIN7-mediated auxin transport for root growth adaptation. Proceedings of the National Academy of Sciences of the United States of America. National Academy of Sciences.https://doi.org/10.1073/pnas.2221313120 

Gnyliukh, N. (2023). Mechanism of clathrin-coated vesicle  formation during endocytosis in plants. Institute of Science and Technology Austria.https://doi.org/10.15479/at:ista:14510 

Friml, J. (2022). Fourteen stations of auxin. Cold Spring Harbor Perspectives in Biology. Cold Spring Harbor Laboratory.https://doi.org/10.1101/cshperspect.a039859  

Struk, S., Braem, L., Matthys, C., Walton, A., Vangheluwe, N., Van Praet, S.,https://doi.org/10.1093/pcp/pcab149__Goormachtig, S. (2022). Transcriptional analysis in the Arabidopsis roots reveals new regulators that link rac-G treatment with changes in flavonol accumulation, root hair elongation and lateral root density. Plant &; Cell Physiology. Oxford University Press.https://doi.org/10.1093/pcp/pcab149 

Wang, R., Himschoot, E., Grenzi, M., Chen, J., Safi, A., Krebs, M.,https://doi.org/10.1093/jxb/erac019__Vanneste, S. (2022). Auxin analog-induced C+ signaling is independent of inhibition of endosomal aggregation in Arabidopsis roots. Journal of Experimental Botany. Oxford Academic.https://doi.org/10.1093/jxb/erac019 

Yu, Z., Zhang, F., Friml, J., &; Ding, Z. (2022). Auxin signaling: Research advances over the past 30 years. Journal of Integrative Plant Biology. Wiley.https://doi.org/10.1111/jipb.13225 

Hajny, J., Tan, S., &; Friml, J. (2022). Auxin canalization: From speculative models toward molecular players. Current Opinion in Plant Biology. Elsevier.https://doi.org/10.1016/j.pbi.2022.102174 

Dahhan, D., Reynolds, G., Cárdenas, J., Eeckhout, D., Johnson, A. J., Yperman, K.,https://doi.org/10.1093/plcell/koac071__Bednarek, S. (2022). Proteomic characterization of isolated Arabidopsis clathrin-coated vesicles reveals evolutionarily conserved and plant-specific components. Plant Cell. Oxford Academic.https://doi.org/10.1093/plcell/koac071 

Lu, Q., Zhang, Y., Hellner, J., Giannini, C., Xu, X., Pauwels, J.,https://doi.org/10.1073/pnas.2118220119__Russinova, E. (2022). Proteome-wide cellular thermal shift assay reveals unexpected cross-talk between brassinosteroid and auxin signaling. Proceedings of the National Academy of Sciences of the United States of America. Proceedings of the National Academy of Sciences.https://doi.org/10.1073/pnas.2118220119 

Wang, R., Himschoot, E., Chen, J., Boudsocq, M., Geelen, D., Friml, J.,https://doi.org/10.3389/fpls.2022.862398__Vanneste, S. (2022). Constitutive active CPK30 interferes with root growth and endomembrane trafficking in Arabidopsis thaliana. Frontiers in Plant Science. Frontiers.https://doi.org/10.3389/fpls.2022.862398 

Li, L., Chen, H., Alotaibi, S. S., Pbndík, A., Adamowski, M., Novák, O., &; Friml, J. (2022). RAL peptide triggers biphasic root growth inhibition upstream of auxin biosynthesis. Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences.https://doi.org/10.1073/pnas.2121058119 

Tian, Z., Zhang, Y., Zhu, L., Jiang, B., Wang, H., Gao, R.,https://doi.org/10.1093/plcell/koac270__Xiao, G. (2022). Strigolactones act downstream of gibberellins to regulate fiber cell elongation and cell wall thickness in cotton (Gossypium hirsutum). The Plant Cell. Oxford University Press.https://doi.org/10.1093/plcell/koac270 

Konstantinova, N., Hörmayer, L., Glanc, M., Keshkeih, R., Tan, S., Di Donato, M.,https://doi.org/10.1038/s41467-022-32888-8__Luschnig, C. (2022). WAVY GROWTH Arabidopsishttps://doi.org/10.1038/s41467-022-32888-8__ubiquitin ligases affect apical PIN sorting decisions. Nature Communications. Springer Nature.https://doi.org/10.1038/s41467-022-32888-8 

Yang, Z., Xia, J., Hong, J., Zhang, C., Wei, H., Ying, W.,https://doi.org/10.1038/s41586-022-05143-9__Sun, L. (2022). Structural insights into auxin recognition and efflux by Arabidopsis PIN1. Nature. Springer Nature.https://doi.org/10.1038/s41586-022-05143-9 

Zhao, J., Bui, M. T., Ma, J., Künzl, F., Picchianti, L., De La Concepcion, J. C.,https://doi.org/10.1083/jcb.202203139__Dagdas, Y. (2022). Plant autophagosomes mature into amphisomes prior to their delivery to the central vacuole. Journal of Cell Biology. Rockefeller University Press.https://doi.org/10.1083/jcb.202203139 

Huang, J., Zhao, L., Malik, S., Gentile, B. R., Xiong, V., Arazi, T.,https://doi.org/10.1038/s41467-022-34723-6__Zhao, D. (2022). Specification of female germline by microRNA orchestrated auxin signaling in Arabidopsis. Nature Communications. Springer Nature.https://doi.org/10.1038/s41467-022-34723-6 

Johnson, A. J., Kaufmann, W., Sommer, C. M., Costanzo, T., Dahhan, D. A., Bednarek, S. Y., &; Friml, J. (2022). Three-dimensional visualization of planta clathrin-coated vesicles at ultrastructural resolution. Molecular Plant. Elsevier.https://doi.org/10.1016/j.molp.2022.09.003 

Bilanovidová, V., Rýdza, N., Koczka, L., Hess, M., Feraru, E., Friml, J., &; Nodzyski, T. (2022). The hydrophilic loop of Arabidopsis PIN1 auxin efflux carrier harbors hallmarks of an intrinsically disordered protein. International Journal of Molecular Sciences. MDPI.https://doi.org/10.3390/ijms23116352 

Qi, L., Kwiatkowski, M., Chen, H., Hörmayer, L., Sinclair, S. A., Zou, M.,https://doi.org/10.1038/s41586-022-05369-7__Friml, J. (2022). Adenylate cyclase activity of TI/AFB auxin receptors in plants. Nature. Springer Nature.https://doi.org/10.1038/s41586-022-05369-7 

Xiao, H., Hu, Y., Wang, Y., Cheng, J., Wang, J., Chen, G.,https://doi.org/10.1016/j.devcel.2022.11.006__Zhang, J. (2022). Nitrate availability controls translocation of the transcription factor N for cell-type-specific reprogramming of root growth. Developmental Cell. Elsevier.https://doi.org/10.1016/j.devcel.2022.11.006 

Friml, J., Gallei, M. C., Gelová, Z., Johnson, A. J., Mazur, E., Monzer, A.,https://doi.org/10.1038/s41586-022-05187-x__Rakusová, H. (2022). AB–TMK auxin perception for global phosphorylation and auxin canalization. Nature. Springer Nature.https://doi.org/10.1038/s41586-022-05187-x 

Gallei, M. C. (2022). Auxin and strigolactone non-canonical signaling regulating development in Arabidopsis thaliana. Institute of Science and Technology Austria.https://doi.org/10.15479/at:ista:11626 

Li, L., Gallei, M. C., &; Friml, J. (2022). Bending to auxin: Fast acid growth for tropisms. Trends in Plant Science. Cell Press.https://doi.org/10.1016/j.tplants.2021.11.006 

Ingole, K. D., Nagarajan, N., Uhse, S., Giannini, C., &; Djamei, A. (2022). Tetracycline-controlled (TetON) gene expression system for the smut fungus Ustilago maydis. Frontiers in Fungal Biology. Frontiers Media.https://doi.org/10.3389/ffunb.2022.1029114 

Zhang, Y., Li, L., &; Friml, J. (2021). Evaluation of gravitropism in non-seed plants. In E. B. Blancaflor (Ed.), Plant Gravitropism (Vol. 2368, pp. 43–51). Springer Nature.https://doi.org/10.1007/978-1-0716-1677-2_2 

Hörmayer, L., Friml, J., &; Glanc, M. (2021). Automated time-lapse imaging and manipulation of cell divisions in Arabidopsis roots by vertical-stage confocal microscopy. In Plant Cell Division (Vol. 2382, pp. 105–114). Humana Press.https://doi.org/10.1007/978-1-0716-1744-1_6 

Li, H., von Wangenheim, D., Zhang, X., Tan, S., Darwish-Miranda, N., Naramoto, S.,https://doi.org/10.1111/nph.16887__Friml, J. (2021). Cellular requirements for PIN polar cargo clustering in Arabidopsis thaliana. New Phytologist. Wiley.https://doi.org/10.1111/nph.16887 

He, P., Zhang, Y., Li, H., Fu, X., Shang, H., Zou, C.,https://doi.org/10.1111/pbi.13484__Xiao, G. (2021). GhAR-1 modulates leaf development by transcriptionally regulating the GhKNO-1 gene in cotton. Plant Biotechnology Journal. Wiley.https://doi.org/10.1111/pbi.13484 

Tan, S., Luschnig, C., &; Friml, J. (2021). Pho-view of auxin: Reversible protein phosphorylation in auxin biosynthesis, transport and signaling. Molecular Plant. Elsevier.https://doi.org/10.1016/j.molp.2020.11.004 

Abas, L., Kolb, M., Stadlmann, J., Janacek, D. P., Lukic, K., Schwechheimer, C.,https://doi.org/10.1073/pnas.2020857118__Hammes, U. Z. (2021). Naphthylphthalamic acid associates with and inhibits PIN auxin transporters. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.2020857118 

Hu, Y., Omary, M., Hu, Y., Doron, O., Hörmayer, L., Chen, Q.,https://doi.org/10.1038/s41467-021-21802-3__Shani, E. (2021). Cell kinetics of auxin transport and activity in Arabidopsis root growth and skewing. Nature Communications. Springer Nature.https://doi.org/10.1038/s41467-021-21802-3 

Ruiz-Lopez, N., Pérez-Sancho, J., Esteban Del Valle, A., Haslam, R., Vanneste, S., Catalá, R.,https://doi.org/10.1093/plcell/koab122__Botella, M. (2021). Synaptotagmins at the endoplasmic reticulum-plasma membrane contact sites maintain diacylglycerol homeostasis during abiotic stress. Plant Cell. American Society of Plant Biologists.https://doi.org/10.1093/plcell/koab122 

Gao, Z., Chen, Z., Cui, Y., Ke, M., Xu, H., Xu, Q.,https://doi.org/10.1093/plcell/koab183__Chen, X. (2021). GmPIN-dependent polar auxin transport is involved in soybean nodule development. Plant Cell. American Society of Plant Biologists.https://doi.org/10.1093/plcell/koab183 

Han, H., Adamowski, M., Qi, L., Alotaibi, S., &; Friml, J. (2021). PIN-mediated polar auxin transport regulations in plant tropic responses. New Phytologist. Wiley.https://doi.org/10.1111/nph.17617 

Zeng, Y., Verstraeten, I., Trinh, H. K., Heugebaert, T., Stevens, C. V., Garcia-Maquilon, I.,https://doi.org/10.3390/genes12081141__Geelen, D. (2021). Arabidopsis hypocotyl adventitious root formation is suppressed by ABA signaling. Genes. MDPI.https://doi.org/10.3390/genes12081141 

Kashkan, I., Hrtyan, M., Retzer, K., Humpolídková, J., Jayasree, A., Filepová, R.,https://doi.org/10.1111/nph.17792__Rfeidka, K. (2021). Mutually opposing activity of PIN7 splicing isoforms is required for auxin-mediated tropic responses in Arabidopsis thaliana. New Phytologist. Wiley.https://doi.org/10.1111/nph.17792 

Xu, E., Chai, L., Zhang, S., Yu, R., Zhang, X., Xu, C., &; Hu, Y. (2021). Catabolism of strigolactones by a carboxylesterase. Nature Plants. Springer Nature.https://doi.org/10.1038/s41477-021-01011-y 

Kong, W., Tan, S., Zhao, Q., Lin, D., Xu, Z., Friml, J., &; Xue, H. (2021). mRNA surveillance complex PELOTA-HB eegulates phosphoinositide-sependent protein kinase1 and plant growth. Plant Physiology. American Society of Plant Biologists.https://doi.org/10.1093/plphys/kiab199 

Glanc, M., Van Gelderen, K., Hörmayer, L., Tan, S., Naramoto, S., Zhang, X.,https://doi.org/10.1016/j.cub.2021.02.028__Friml, J. (2021). AGC kinases and MA/MEL proteins maintain PIN polarity by limiting lateral diffusion in plant cells. Current Biology. Elsevier.https://doi.org/10.1016/j.cub.2021.02.028 

Marquès-Bueno, M., Armengot, L., Noack, L., Bareille, J., Rodriguez Solovey, L., Platre, M.,https://doi.org/10.1016/j.cub.2020.10.011__Jaillais, Y. (2021). Auxin-regulated reversible inhibition of TMK1 signaling by MAK modulates the dynamics of root gravitropism. Current Biology. Elsevier.https://doi.org/10.1016/j.cub.2020.10.011 

El Houari, I., Van Beirs, C., Arents, H., Han, H., Chanoca, A., Opdenacker, D.,https://doi.org/10.1111/nph.17349__Vanholme, B. (2021). Seedling developmental defects upon blocking CINNAMATE-4-HYDROXYLASE are caused by perturbations in auxin transport. New Phytologist. Wiley.https://doi.org/10.1111/nph.17349 

Ke, M., Ma, Z., Wang, D., Sun, Y., Wen, C., Huang, D.,https://doi.org/10.1111/nph.16915__Chen, X. (2021). Salicylic acid regulates PIN2 auxin transporter hyper-clustering and root gravitropic growth via Remorin-dependent lipid nanodomain organization in Arabidopsis thaliana. New Phytologist. Wiley.https://doi.org/10.1111/nph.16915 

Klionsky, D. J., Abdel-Aziz, A. K., Abdelfatah, S., Abdellatif, M., Abdoli, A., Abel, S.,https://doi.org/10.1080/15548627.2020.1797280__Tong, C. K. (2021). Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition). Autophagy. Taylor &; Francis.https://doi.org/10.1080/15548627.2020.1797280 

Li, L., Verstraeten, I., Roosjen, M., Takahashi, K., Rodriguez Solovey, L., Merrin, J.,https://doi.org/10.1038/s41586-021-04037-6__Friml, J. (2021). Cell surface and intracellular auxin signalling for H<sup>+</sup> fluxes in root growth. Nature. Springer Nature.https://doi.org/10.1038/s41586-021-04037-6 

Zhao, Y., Wu, L., Fu, Q., Wang, D., Li, J., Yao, B.,https://doi.org/10.1111/pce.14029__Du, Y. (2021). INDITTO2 transposon conveys auxin-mediated DRO1 transcription for rice drought avoidance. Plant, Cell &; Environment. Wiley.https://doi.org/10.1111/pce.14029 

Johnson, A. J., Dahhan, D. A., Gnyliukh, N., Kaufmann, W., Zheden, V., Costanzo, T.,https://doi.org/10.1073/pnas.2113046118__Friml, J. (2021). The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis. Proceedings of the National Academy of Sciences. National Academy of Sciences.https://doi.org/10.1073/pnas.2113046118 

Johnson, A. J. (2021). Raw data from Johnson et al, PNAS, 2021. Zenodo.https://doi.org/10.5281/ZENODO.5747100 

Navarrete, F., Grujic, N., Stirnberg, A., Saado, I., Aleksza, D., Gallei, M. C.,https://doi.org/10.1371/journal.ppat.1009641__Djamei, A. (2021). The Pleiades are a cluster of fungal effectors that inhibit host defenses. PLOS Pathogens. Public Library of Science.https://doi.org/10.1371/journal.ppat.1009641 

Overdijk, E. J. R., Putker, V., Smits, J., Tang, H., Bouwmeester, K., Govers, F., &; Ketelaar, T. (2021). Phytophthora infestans RXLR effector AV disturbs the growth of Physcomitrium patens without affecting Se localization. PLoS One. Public Library of Science.https://doi.org/10.1371/journal.pone.0249637 

Hörmayer, L. (2021). Wound healing in the Arabidopsis root meristem. Institute of Science and Technology Austria.https://doi.org/10.15479/at:ista:9992 

Ötvös, K., Marconi, M., Vega, A., O’Brien, J., Johnson, A. J., Abualia, R.,https://doi.org/10.15252/embj.2020106862__Benková, E. (2021). Modulation of plant root growth by nitrogen source-defined regulation of polar auxin transport. EMBO Journal. Embo Press.https://doi.org/10.15252/embj.2020106862 

Gelová, Z., Gallei, M. C., Pernisová, M., Brunoud, G., Zhang, X., Glanc, M.,https://doi.org/10.1016/j.plantsci.2020.110750__Friml, J. (2021). Developmental roles of auxin binding protein 1 in Arabidopsis thaliana. Plant Science. Elsevier.https://doi.org/10.1016/j.plantsci.2020.110750 

Narasimhan, M., Gallei, M. C., Tan, S., Johnson, A. J., Verstraeten, I., Li, L.,https://doi.org/10.1093/plphys/kiab134__Friml, J. (2021). Systematic analysis of specific and nonspecific auxin effects on endocytosis and trafficking. Plant Physiology. Oxford University Press.https://doi.org/10.1093/plphys/kiab134 

Li, L. (2021). Rapid cell growth regulation in Arabidopsis. Institute of Science and Technology Austria.https://doi.org/10.15479/at:ista:10083 

Nikonorova, N., Murphy, E., Fonseca de Lima, C., Zhu, S., van de Cotte, B., Vu, L.,https://doi.org/10.3390/cells10071665__De Smet, I. (2021). The Arabidopsis root tip (phospho)proteomes at growth-promoting versus growth-repressing conditions reveal novel root growth regulators. Cells. MDPI.https://doi.org/10.3390/cells10071665 

Li, L., Verstraeten, I., Roosjen, M., Takahashi, K., Rodriguez Solovey, L., Merrin, J.,https://doi.org/10.21203/rs.3.rs-266395/v3__Friml, J. (n.d.). Cell surface and intracellular auxin signalling for H+-fluxes in root growth. Research Square.https://doi.org/10.21203/rs.3.rs-266395/v3 

Wei, Z., Tan, S., Liu, T., Wu, Y., Lei, J.-G., Chen, Z.,https://doi.org/10.1101/791137__Liao, K. (2020). Plasmodesmata-like intercellular connections by plant remorin in animal cells. bioRxiv. Cold Spring Harbor Laboratory.https://doi.org/10.1101/791137 

Zhang, Y., &; Friml, J. (2020). Auxin guides roots to avoid obstacles during gravitropic growth. New Phytologist. Wiley.https://doi.org/10.1111/nph.16203 

Li, Y., Wang, Y., Tan, S., Li, Z., Yuan, Z., Glanc, M.,https://doi.org/10.1002/advs.201901455__Zhang, J. (2020). Root growth adaptation is mediated by PYLs ABA receptor-PA protein phosphatase complex. Advanced Science. Wiley.https://doi.org/10.1002/advs.201901455 

Gallei, M. C., Luschnig, C., &; Friml, J. (2020). Auxin signalling in growth: Schrödinger’s cat out of the bag. Current Opinion in Plant Biology. Elsevier.https://doi.org/10.1016/j.pbi.2019.10.003 

Xiao, G., &; Zhang, Y. (2020). Adaptive growth: Shaping auxin-mediated root system architecture. Trends in Plant Science. Elsevier.https://doi.org/10.1016/j.tplants.2019.12.001 

Mazur, E., Gallei, M. C., Adamowski, M., Han, H., Robert, H. S., &; Friml, J. (2020). Clathrin-mediated trafficking and PIN trafficking are required for auxin canalization and vascular tissue formation in Arabidopsis. Plant Science. Elsevier.https://doi.org/10.1016/j.plantsci.2020.110414 

Narasimhan, M., Johnson, A. J., Prizak, R., Kaufmann, W., Tan, S., Casillas Perez, B. E., &; Friml, J. (2020). Evolutionarily unique mechanistic framework of clathrin-mediated endocytosis in plants. ELife. eLife Sciences Publications.https://doi.org/10.7554/eLife.52067 

Han, L., Zhou, X., Zhao, Y., Zhu, S., Wu, L., He, Y.,https://doi.org/10.1111/jipb.12905__Du, Y. (2020). Colonization of endophyte Acremonium sp. 2 in Panax notoginseng and rice mediated by auxin and jasmonic acid. Journal of Integrative Plant Biology. Wiley.https://doi.org/10.1111/jipb.12905 

Verstraeten, I., Buyle, H., Werbrouck, S., Van Labeke, M. C., &; Geelen, D. (2020). In vitro shoot growth and adventitious rooting of Wikstroemia gemmata depends on light quality. Israel Journal of Plant Sciences. Brill.https://doi.org/10.1163/22238980-20191110 

Moturu, T. R., Sinha, S., Salava, H., Thula, S., Nodzyski, T., Vaeková, R. S.,https://doi.org/10.3390/plants9030299__Simon, S. (2020). Molecular evolution and diversification of proteins involved in miRNA maturation pathway. Plants. MDPI.https://doi.org/10.3390/plants9030299 

Tan, S., Zhang, X., Kong, W., Yang, X.-L., Molnar, G., Vondráková, Z.,https://doi.org/10.1038/s41477-020-0648-9__Xue, H.-W. (2020). The lipid code-dependent phosphoswitch PDK1–PK activates PIN-mediated auxin efflux in Arabidopsis. Nature Plants. Springer Nature.https://doi.org/10.1038/s41477-020-0648-9 

Lee, E., Vila Nova Santana, B., Samuels, E., Benitez-Fuente, F., Corsi, E., Botella, M.,https://doi.org/10.1093/jxb/eraa138__Rosado, A. (2020). Rare earth elements induce cytoskeleton-dependent and PP-associated rearrangement of SY/SY ER-PM contact site complexes in Arabidopsis. Journal of Experimental Botany. Oxford University Press.https://doi.org/10.1093/jxb/eraa138 

Xue, H., Zhang, Y., &; Xiao, G. (2020). Neo-gibberellin signaling: Guiding the next generation of the green revolution. Trends in Plant Science. Elsevier.https://doi.org/10.1016/j.tplants.2020.04.001 

Kuhn, A., Ramans Harborough, S., McLaughlin, H. M., Natarajan, B., Verstraeten, I., Friml, J.,https://doi.org/10.7554/elife.51787__Østergaard, L. (2020). Direct ETTIN-auxin interaction controls chromatin states in gynoecium development. ELife. eLife Sciences Publications.https://doi.org/10.7554/elife.51787 

Zhang, J., Mazur, E., Balla, J., Gallei, M. C., Kalousek, P., Medvefová, Z.,https://doi.org/10.1038/s41467-020-17252-y__Friml, J. (2020). Strigolactones inhibit auxin feedback on PIN-dependent auxin transport canalization. Nature Communications. Springer Nature.https://doi.org/10.1038/s41467-020-17252-y 

He, P., Zhang, Y., &; Xiao, G. (2020). Origin of a subgenome and genome evolution of allotetraploid cotton species. Molecular Plant. Elsevier.https://doi.org/10.1016/j.molp.2020.07.006 

Antoniadi, I., Novák, O., Gelová, Z., Johnson, A. J., Plíhal, O., Simerský, R.,https://doi.org/10.1038/s41467-020-17700-9__Turnbull, C. (2020). Cell-surface receptors enable perception of extracellular cytokinins. Nature Communications. Springer Nature.https://doi.org/10.1038/s41467-020-17700-9 

Hajny, J., Prat, T., Rydza, N., Rodriguez Solovey, L., Tan, S., Verstraeten, I.,https://doi.org/10.1126/science.aba3178__Friml, J. (2020). Receptor kinase module targets PIN-dependent auxin transport during canalization. Science. American Association for the Advancement of Science.https://doi.org/10.1126/science.aba3178 

Smith, S., Zhu, S., Joos, L., Roberts, I., Nikonorova, N., Vu, L.,https://doi.org/10.1074/mcp.ra119.001826__De Smet, I. (2020). The CE peptide promotes abiotic stress tolerance, as revealed by quantitative proteomics, and attenuates the AUX/IAA equilibrium in Arabidopsis. Molecular &; Cellular Proteomics. American Society for Biochemistry and Molecular Biology.https://doi.org/10.1074/mcp.ra119.001826 

Zhang, X., Adamowski, M., Marhavá, P., Tan, S., Zhang, Y., Rodriguez Solovey, L.,https://doi.org/10.1105/tpc.19.00869__Friml, J. (2020). Arabidopsis flippases cooperate with ARF GTPase exchange factors to regulate the trafficking and polarity of PIN auxin transporters. The Plant Cell. American Society of Plant Biologists.https://doi.org/10.1105/tpc.19.00869 

Liu, D., Kumar, R., LAN, C., Johnson, A. J., Siao, W., Vanhoutte, I.,https://doi.org/10.1105/tpc.20.00384__Russinova, E. (2020). Endocytosis of BRASSINOSTEROID INSENSITIV is partly driven by a canonical tyrosine-based Motif. Plant Cell. American Society of Plant Biologists.https://doi.org/10.1105/tpc.20.00384 

Wang, J., Mylle, E., Johnson, A. J., Besbrugge, N., De Jaeger, G., Friml, J.,https://doi.org/10.1104/pp.20.00178__van Damme, D. (2020). High temporal resolution reveals simultaneous plasma membrane recruitment of TPLATE complex subunits. Plant Physiology. American Society of Plant Biologists.https://doi.org/10.1104/pp.20.00178 

Zhang, Y., Hartinger, C., Wang, X., &; Friml, J. (2020). Directional auxin fluxes in plants by intramolecular domaindomain coevolution of PIN auxin transporters. New Phytologist. Wiley.https://doi.org/10.1111/nph.16629 

Sinclair, S. A., Gille, S., Pauly, M., &; Krämer, U. (2020). Regulation of acetylation of plant cell wall components is complex and responds to external stimuli. Plant Signaling &; Behavior. Informa UK Limited.https://doi.org/10.1080/15592324.2019.1687185 

Han, H. (2020). Novel insights into PIN polarity regulation during Arabidopsis development. Institute of Science and Technology Austria.https://doi.org/10.15479/AT:ISTA:8589 

Han, H., Rakusova, H., Verstraeten, I., Zhang, Y., &; Friml, J. (2020). SCF TI/AFB auxin signaling for bending termination during shoot gravitropism. Plant Physiology. American Society of Plant Biologists.https://doi.org/10.1104/pp.20.00212 

Sinclair, S. A., &; Krämer, U. (2020). Generation of effective zinc-deficient agar-solidified media allows identification of root morphology changes in response to zinc limitation. Plant Signaling &; Behavior. Taylor &; Francis.https://doi.org/10.1080/15592324.2019.1687175 

Tan, S., Di Donato, M., Glanc, M., Zhang, X., Klíma, P., Liu, J.,https://doi.org/10.1016/j.celrep.2020.108463__Friml, J. (2020). Non-steroidal anti-inflammatory drugs target TWISTED DWAR-regulated actin dynamics and auxin transport-mediated plant development. Cell Reports. Elsevier.https://doi.org/10.1016/j.celrep.2020.108463 

Hörmayer, L., Montesinos López, J. C., Marhavá, P., Benková, E., Yoshida, S., &; Friml, J. (2020). Wounding-induced changes in cellular pressure and localized auxin signalling spatially coordinate restorative divisions in roots. Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences.https://doi.org/10.1073/pnas.2003346117 

Tan, S., Abas, M. F., Verstraeten, I., Glanc, M., Molnar, G., Hajny, J.,https://doi.org/10.1016/j.cub.2019.11.058__Friml, J. (2020). Salicylic acid targets protein phosphatase 2A to attenuate growth in plants. Current Biology. Cell Press.https://doi.org/10.1016/j.cub.2019.11.058 

Mazur, E., Kulik, I., Hajny, J., &; Friml, J. (2020). Auxin canalization and vascular tissue formation by TI/AFB-mediated auxin signaling in arabidopsis. New Phytologist. Wiley.https://doi.org/10.1111/nph.16446 

Hajny, J. (2020). Identification and characterization of the molecular machinery of auxin-dependent canalization during vasculature formation and regeneration. Institute of Science and Technology Austria.https://doi.org/10.15479/AT:ISTA:8822 

Zhang, Y., Rodriguez Solovey, L., Li, L., Zhang, X., &; Friml, J. (2020). Functional innovations of PIN auxin transporters mark crucial evolutionary transitions during rise of flowering plants. Science Advances. AAAS.https://doi.org/10.1126/sciadv.abc8895 

Chen, H., Lai, L., Li, L., Liu, L., Jakada, B. H., Huang, Y.,https://doi.org/10.3390/ijms21165727__Qin, Y. (2020). AcoMY, an Ananas comosus L. MYB transcription factor, functions in osmotic stress through negative regulation of ABA signaling. International Journal of Molecular Sciences. MDPI.https://doi.org/10.3390/ijms21165727 

Johnson, A. J., Gnyliukh, N., Kaufmann, W., Narasimhan, M., Vert, G., Bednarek, S., &; Friml, J. (2020). Experimental toolbox for quantitative evaluation of clathrin-mediated endocytosis in the plant model Arabidopsis. Journal of Cell Science. The Company of Biologists.https://doi.org/10.1242/jcs.248062 

Lee, E., Vanneste, S., Pérez-Sancho, J., Benitez-Fuente, F., Strelau, M., Macho, A. P.,https://doi.org/10.1073/pnas.1818099116__Rosado, A. (2019). Ionic stress enhances ER–PM connectivity via phosphoinositide-associated SY contact site expansion in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America. National Academy of Sciences.https://doi.org/10.1073/pnas.1818099116 

Yoshida, S., Van Der Schuren, A., Van Dop, M., Van Galen, L., Saiga, S., Adibi, M.,https://doi.org/10.1038/s41477-019-0363-6__Weijers, D. (2019). A SOSEKI-based coordinate system interprets global polarity cues in arabidopsis. Nature Plants. Springer Nature.https://doi.org/10.1038/s41477-019-0363-6 

Zwiewka, M., Bielach, A., Tamizhselvan, P., Madhavan, S., Ryad, E. E., Tan, S.,https://doi.org/10.1093/pcp/pcz001__Tognetti, V. B. (2019). Root adaptation to O2-induced oxidative stress by ARF-GEF BEN1- and cytoskeleton-mediated PIN2 trafficking. Plant and Cell Physiology. Oxford University Press.https://doi.org/10.1093/pcp/pcz001 

Rakusová, H., Han, H., Valosek, P., &; Friml, J. (2019). Genetic screen for factors mediating PIN polarization in gravistimulated Arabidopsis thaliana hypocotyls. The Plant Journal. Wiley.https://doi.org/10.1111/tpj.14301