V. Bilanovidová et al., “The hydrophilic loop of Arabidopsis PIN1 auxin efflux carrier harbors hallmarks of an intrinsically disordered protein,” International Journal of Molecular Sciences, vol. 23, no. 11. MDPI, p. 6352, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/11489
DOI: 10.3390/ijms23116352
WoS: 000808733300001
PMID: 35683031

L. Qi et al., “Adenylate cyclase activity of TI/AFB auxin receptors in plants,” Nature, vol. 611, no. 7934. Springer Nature, pp. 133–138, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/12144
DOI: 10.1038/s41586-022-05369-7
WoS: 000875061600013
PMID: 36289340

H. Xiao et al., “Nitrate availability controls translocation of the transcription factor N for cell-type-specific reprogramming of root growth,” Developmental Cell, vol. 57, no. 23. Elsevier, p. 2638–2651.e6, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/12120
DOI: 10.1016/j.devcel.2022.11.006
WoS: 000919603800005
PMID: 36473460

J. Friml et al., “AB–TMK auxin perception for global phosphorylation and auxin canalization,” Nature, vol. 609, no. 7927. Springer Nature, pp. 575–581, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/12291
DOI: 10.1038/s41586-022-05187-x
WoS: 000851357500002
PMID: 36071161

M. C. Gallei, “Auxin and strigolactone non-canonical signaling regulating development in Arabidopsis thaliana,” Institute of Science and Technology Austria, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/11626
DOI: 10.15479/at:ista:11626

L. Li, M. C. Gallei, and J. Friml, “Bending to auxin: Fast acid growth for tropisms,” Trends in Plant Science, vol. 27, no. 5. Cell Press, pp. 440–449, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/10411
DOI: 10.1016/j.tplants.2021.11.006
WoS: 000793707900005
PMID: 34848141

K. D. Ingole, N. Nagarajan, S. Uhse, C. Giannini, and A. Djamei, “Tetracycline-controlled (TetON) gene expression system for the smut fungus Ustilago maydis,” Frontiers in Fungal Biology, vol. 3. Frontiers Media, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/13240
DOI: 10.3389/ffunb.2022.1029114

J. Friml, “Fourteen stations of auxin,” Cold Spring Harbor Perspectives in Biology, vol. 14, no. 5. Cold Spring Harbor Laboratory, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/10016
DOI: 10.1101/cshperspect.a039859
WoS: 000806563000003
PMID: 34400554

I. Kashkan et al., “Mutually opposing activity of PIN7 splicing isoforms is required for auxin-mediated tropic responses in Arabidopsis thaliana,” New Phytologist, vol. 233, no. 1. Wiley, pp. 329–343, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/10282
DOI: 10.1111/nph.17792
WoS: 000714678100001
PMID: 34637542

J. Floriach-Clark, H. Tang, and V. Willemsen, “Mosses: Accessible Systems for Plant Development Studies,” in Model Organisms in Plant Genetics, I. Y. Abdurakhmonov, Ed. Intech Open, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/17085
DOI: 10.5772/intechopen.100535

S. Zhong et al., “RALF peptide signaling controls the polytubey block in Arabidopsis,” Science, vol. 375, no. 6578. American Association for the Advancement of Science, pp. 290–296, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/17069
DOI: 10.1126/science.abl4683
PMID: 35050671

F. Navarrete et al., “TOPLESS promotes plant immunity by repressing auxin signaling and is targeted by the fungal effector Naked1,” Plant Communications, vol. 3, no. 2. Elsevier, 2022.
LibreCat: https://research-explorer.ista.ac.at/record/17068
DOI: 10.1016/j.xplc.2021.100269
PMID: 35529945

Y. Zhang, L. Li, and J. Friml, “Evaluation of gravitropism in non-seed plants,” in Plant Gravitropism, vol. 2368, E. B. Blancaflor, Ed. Springer Nature, 2021, pp. 43–51.
LibreCat: https://research-explorer.ista.ac.at/record/10267
DOI: 10.1007/978-1-0716-1677-2_2
PMID: 34647246

L. Hörmayer, J. Friml, and M. Glanc, “Automated time-lapse imaging and manipulation of cell divisions in Arabidopsis roots by vertical-stage confocal microscopy,” in Plant Cell Division, vol. 2382, Humana Press, 2021, pp. 105–114.
LibreCat: https://research-explorer.ista.ac.at/record/10268
DOI: 10.1007/978-1-0716-1744-1_6
PMID: 34705235

H. Li et al., “Cellular requirements for PIN polar cargo clustering in Arabidopsis thaliana,” New Phytologist, vol. 229, no. 1. Wiley, pp. 351–369, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/8582
DOI: 10.1111/nph.16887
WoS: 000570187900001

P. He et al., “GhAR-1 modulates leaf development by transcriptionally regulating the GhKNO-1 gene in cotton,” Plant Biotechnology Journal, vol. 19, no. 3. Wiley, pp. 548–562, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/8606
DOI: 10.1111/pbi.13484
WoS: 000577682300001
PMID: 32981232

S. Tan, C. Luschnig, and J. Friml, “Pho-view of auxin: Reversible protein phosphorylation in auxin biosynthesis, transport and signaling,” Molecular Plant, vol. 14, no. 1. Elsevier, pp. 151–165, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/8992
DOI: 10.1016/j.molp.2020.11.004
WoS: 000605359400014
PMID: 33186755

L. Abas et al., “Naphthylphthalamic acid associates with and inhibits PIN auxin transporters,” PNAS, vol. 118, no. 1. National Academy of Sciences, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/8993
DOI: 10.1073/pnas.2020857118
WoS: 000607270100073
PMID: 33443187

Y. Hu et al., “Cell kinetics of auxin transport and activity in Arabidopsis root growth and skewing,” Nature Communications, vol. 12. Springer Nature, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9254
DOI: 10.1038/s41467-021-21802-3
WoS: 000630419400048
PMID: 33712581

N. Ruiz-Lopez et al., “Synaptotagmins at the endoplasmic reticulum-plasma membrane contact sites maintain diacylglycerol homeostasis during abiotic stress,” Plant Cell, vol. 33, no. 7. American Society of Plant Biologists, pp. 2431–2453, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9443
DOI: 10.1093/plcell/koab122
WoS: 000703938100026
PMID: 33944955

Z. Gao et al., “GmPIN-dependent polar auxin transport is involved in soybean nodule development,” Plant Cell, vol. 33, no. 9. American Society of Plant Biologists, pp. 2981–3003, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9657
DOI: 10.1093/plcell/koab183
WoS: 000702165300012
PMID: 34240197

H. Han, M. Adamowski, L. Qi, S. Alotaibi, and J. Friml, “PIN-mediated polar auxin transport regulations in plant tropic responses,” New Phytologist, vol. 232, no. 2. Wiley, pp. 510–522, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9656
DOI: 10.1111/nph.17617
WoS: 000680587100001
PMID: 34254313

Y. Zeng et al., “Arabidopsis hypocotyl adventitious root formation is suppressed by ABA signaling,” Genes, vol. 12, no. 8. MDPI, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9909
DOI: 10.3390/genes12081141
WoS: 000690558000001

E. Xu et al., “Catabolism of strigolactones by a carboxylesterase,” Nature Plants, vol. 7. Springer Nature, pp. 1495–1504, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/10326
DOI: 10.1038/s41477-021-01011-y
WoS: 000717408000002
PMID: 34764442

W. Kong et al., “mRNA surveillance complex PELOTA-HB eegulates phosphoinositide-sependent protein kinase1 and plant growth,” Plant Physiology, vol. 186, no. 4. American Society of Plant Biologists, pp. 2003–2020, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9368
DOI: 10.1093/plphys/kiab199
WoS: 000703922000025
PMID: 33930167

M. Glanc et al., “AGC kinases and MA/MEL proteins maintain PIN polarity by limiting lateral diffusion in plant cells,” Current Biology, vol. 31, no. 9. Elsevier, pp. 1918–1930, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9290
DOI: 10.1016/j.cub.2021.02.028
WoS: 000653077800004
PMID: 33705718

M. Marquès-Bueno et al., “Auxin-regulated reversible inhibition of TMK1 signaling by MAK modulates the dynamics of root gravitropism,” Current Biology, vol. 31, no. 1. Elsevier, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/8824
DOI: 10.1016/j.cub.2020.10.011
WoS: 000614361000039
PMID: 33157019

I. El Houari et al., “Seedling developmental defects upon blocking CINNAMATE-4-HYDROXYLASE are caused by perturbations in auxin transport,” New Phytologist, vol. 230, no. 6. Wiley, pp. 2275–2291, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9288
DOI: 10.1111/nph.17349
WoS: 000639552400001
PMID: 33728703

M. Ke et al., “Salicylic acid regulates PIN2 auxin transporter hyper-clustering and root gravitropic growth via Remorin-dependent lipid nanodomain organization in Arabidopsis thaliana,” New Phytologist, vol. 229, no. 2. Wiley, pp. 963–978, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/8608
DOI: 10.1111/nph.16915
WoS: 000573568000001
PMID: 32901934

D. J. Klionsky et al., “Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition),” Autophagy, vol. 17, no. 1. Taylor &; Francis, pp. 1–382, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9298
DOI: 10.1080/15548627.2020.1797280
WoS: 000636121800001
PMID: 33634751

L. Li et al., “Cell surface and intracellular auxin signalling for H<sup>+</sup> fluxes in root growth,” Nature, vol. 599, no. 7884. Springer Nature, pp. 273–277, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/10223
DOI: 10.1038/s41586-021-04037-6
WoS: 000713338100006
PMID: 34707283

Y. Zhao et al., “INDITTO2 transposon conveys auxin-mediated DRO1 transcription for rice drought avoidance,” Plant, Cell &; Environment, vol. 44, no. 6. Wiley, pp. 1846–1857, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9189
DOI: 10.1111/pce.14029
WoS: 000625398600001
PMID: 33576018

A. J. Johnson et al., “The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis,” Proceedings of the National Academy of Sciences, vol. 118, no. 51. National Academy of Sciences, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9887
DOI: 10.1073/pnas.2113046118
WoS: 000736417600043
PMID: 34907016

A. J. Johnson, “Raw data from Johnson et al, PNAS, 2021.” Zenodo, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/14988
DOI: 10.5281/ZENODO.5747100

F. Navarrete et al., “The Pleiades are a cluster of fungal effectors that inhibit host defenses,” PLOS Pathogens, vol. 17, no. 6. Public Library of Science, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/15276
DOI: 10.1371/journal.ppat.1009641
PMID: 34166468

E. J. R. Overdijk et al., “Phytophthora infestans RXLR effector AV disturbs the growth of Physcomitrium patens without affecting Se localization,” PLoS One, vol. 16, no. 4. Public Library of Science, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/15266
DOI: 10.1371/journal.pone.0249637
PMID: 33831039

L. Hörmayer, “Wound healing in the Arabidopsis root meristem,” Institute of Science and Technology Austria, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9992
DOI: 10.15479/at:ista:9992

K. Ötvös et al., “Modulation of plant root growth by nitrogen source-defined regulation of polar auxin transport,” EMBO Journal, vol. 40, no. 3. Embo Press, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9010
DOI: 10.15252/embj.2020106862
WoS: 000604645600001
PMID:  33399250

Z. Gelová et al., “Developmental roles of auxin binding protein 1 in Arabidopsis thaliana,” Plant Science, vol. 303. Elsevier, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/8931
DOI: 10.1016/j.plantsci.2020.110750
WoS: 000614154500001
PMID: 33487339

M. Narasimhan et al., “Systematic analysis of specific and nonspecific auxin effects on endocytosis and trafficking,” Plant Physiology, vol. 186, no. 2. Oxford University Press, pp. 1122–1142, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/9287
DOI: 10.1093/plphys/kiab134
WoS: 000671555900031
PMID: 33734402

L. Li, “Rapid cell growth regulation in Arabidopsis,” Institute of Science and Technology Austria, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/10083
DOI: 10.15479/at:ista:10083

N. Nikonorova et al., “The Arabidopsis root tip (phospho)proteomes at growth-promoting versus growth-repressing conditions reveal novel root growth regulators,” Cells, vol. 10. MDPI, 2021.
LibreCat: https://research-explorer.ista.ac.at/record/10015
DOI: 10.3390/cells10071665
WoS: 000676604700001
PMID: 34359847

L. Li et al., “Cell surface and intracellular auxin signalling for H+-fluxes in root growth,” Research Square. .
LibreCat: https://research-explorer.ista.ac.at/record/10095
DOI: 10.21203/rs.3.rs-266395/v3

Z. Wei et al., “Plasmodesmata-like intercellular connections by plant remorin in animal cells,” bioRxiv. Cold Spring Harbor Laboratory, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7601
DOI: 10.1101/791137

Y. Zhang and J. Friml, “Auxin guides roots to avoid obstacles during gravitropic growth,” New Phytologist, vol. 225, no. 3. Wiley, pp. 1049–1052, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/6997
DOI: 10.1111/nph.16203
WoS: 000489638800001
PMID: 31603260

Y. Li et al., “Root growth adaptation is mediated by PYLs ABA receptor-PA protein phosphatase complex,” Advanced Science, vol. 7, no. 3. Wiley, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7204
DOI: 10.1002/advs.201901455
WoS: 000501912800001
PMID: 32042554

M. C. Gallei, C. Luschnig, and J. Friml, “Auxin signalling in growth: Schrödinger’s cat out of the bag,” Current Opinion in Plant Biology, vol. 53, no. 2. Elsevier, pp. 43–49, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7142
DOI: 10.1016/j.pbi.2019.10.003
WoS: 000521120600007
PMID: 31760231

G. Xiao and Y. Zhang, “Adaptive growth: Shaping auxin-mediated root system architecture,” Trends in Plant Science, vol. 25, no. 2. Elsevier, pp. 1-123, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7219
DOI: 10.1016/j.tplants.2019.12.001
WoS: 000508637500001
PMID: 31843370

E. Mazur, M. C. Gallei, M. Adamowski, H. Han, H. S. Robert, and J. Friml, “Clathrin-mediated trafficking and PIN trafficking are required for auxin canalization and vascular tissue formation in Arabidopsis,” Plant Science, vol. 293, no. 4. Elsevier, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7465
DOI: 10.1016/j.plantsci.2020.110414
WoS: 000520609800009

M. Narasimhan et al., “Evolutionarily unique mechanistic framework of clathrin-mediated endocytosis in plants,” eLife, vol. 9. eLife Sciences Publications, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7490
DOI: 10.7554/eLife.52067
WoS: 000514104100001
PMID: 31971511

L. Han et al., “Colonization of endophyte Acremonium sp. 2 in Panax notoginseng and rice mediated by auxin and jasmonic acid,” Journal of Integrative Plant Biology, vol. 62, no. 9. Wiley, pp. 1433–1451, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7497
DOI: 10.1111/jipb.12905
WoS: 000515803000001
PMID: 31912615

I. Verstraeten, H. Buyle, S. Werbrouck, M. C. Van Labeke, and D. Geelen, “In vitro shoot growth and adventitious rooting of Wikstroemia gemmata depends on light quality,” Israel Journal of Plant Sciences, vol. 67, no. 1–2. Brill, pp. 16–26, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7540
DOI: 10.1163/22238980-20191110
WoS: 000525343300004

T. R. Moturu et al., “Molecular evolution and diversification of proteins involved in miRNA maturation pathway,” Plants, vol. 9, no. 3. MDPI, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7582
DOI: 10.3390/plants9030299
WoS: 000525315000035
PMID: 32121542

S. Tan et al., “The lipid code-dependent phosphoswitch PDK1–PK activates PIN-mediated auxin efflux in Arabidopsis,” Nature Plants, vol. 6. Springer Nature, pp. 556–569, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7600
DOI: 10.1038/s41477-020-0648-9
WoS: 000531787500006
PMID: 32393881

E. Lee et al., “Rare earth elements induce cytoskeleton-dependent and PP-associated rearrangement of SY/SY ER-PM contact site complexes in Arabidopsis,” Journal of Experimental Botany, vol. 71, no. 14. Oxford University Press, pp. 3986–3998, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7646
DOI: 10.1093/jxb/eraa138
WoS: 000553125400007
PMID: 32179893

H. Xue, Y. Zhang, and G. Xiao, “Neo-gibberellin signaling: Guiding the next generation of the green revolution,” Trends in Plant Science, vol. 25, no. 6. Elsevier, pp. 520–522, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7686
DOI: 10.1016/j.tplants.2020.04.001
WoS: 000533518400003
PMID: 32407691

A. Kuhn et al., “Direct ETTIN-auxin interaction controls chromatin states in gynoecium development,” eLife, vol. 9. eLife Sciences Publications, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7793
DOI: 10.7554/elife.51787
WoS: 000527752200001
PMID: 32267233

J. Zhang et al., “Strigolactones inhibit auxin feedback on PIN-dependent auxin transport canalization,” Nature Communications, vol. 11, no. 1. Springer Nature, p. 3508, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8138
DOI: 10.1038/s41467-020-17252-y
WoS: 000550062200004
PMID: 32665554

P. He, Y. Zhang, and G. Xiao, “Origin of a subgenome and genome evolution of allotetraploid cotton species,” Molecular Plant, vol. 13, no. 9. Elsevier, pp. 1238–1240, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8271
DOI: 10.1016/j.molp.2020.07.006
WoS: 000566895400007
PMID: 32688032

I. Antoniadi et al., “Cell-surface receptors enable perception of extracellular cytokinins,” Nature Communications, vol. 11. Springer Nature, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8337
DOI: 10.1038/s41467-020-17700-9
WoS: 000567931000001

J. Hajny et al., “Receptor kinase module targets PIN-dependent auxin transport during canalization,” Science, vol. 370, no. 6516. American Association for the Advancement of Science, pp. 550–557, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8721
DOI: 10.1126/science.aba3178
WoS: 000583031800041
PMID: 33122378

S. Smith et al., “The CE peptide promotes abiotic stress tolerance, as revealed by quantitative proteomics, and attenuates the AUX/IAA equilibrium in Arabidopsis,” Molecular &; Cellular Proteomics, vol. 19, no. 8. American Society for Biochemistry and Molecular Biology, pp. 1248–1262, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7949
DOI: 10.1074/mcp.ra119.001826
WoS: 000561114000001
PMID: 32404488

X. Zhang et al., “Arabidopsis flippases cooperate with ARF GTPase exchange factors to regulate the trafficking and polarity of PIN auxin transporters,” The Plant Cell, vol. 32, no. 5. American Society of Plant Biologists, pp. 1644–1664, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7619
DOI: 10.1105/tpc.19.00869
WoS: 000545741500030
PMID: 32193204

D. Liu et al., “Endocytosis of BRASSINOSTEROID INSENSITIV is partly driven by a canonical tyrosine-based Motif,” Plant Cell, vol. 32, no. 11. American Society of Plant Biologists, pp. 3598–3612, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8607
DOI: 10.1105/tpc.20.00384
WoS: 000600226800021
PMID: 32958564

J. Wang et al., “High temporal resolution reveals simultaneous plasma membrane recruitment of TPLATE complex subunits,” Plant Physiology, vol. 183, no. 3. American Society of Plant Biologists, pp. 986–997, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7695
DOI: 10.1104/pp.20.00178
WoS: 000550682000018
PMID: 32321842

Y. Zhang, C. Hartinger, X. Wang, and J. Friml, “Directional auxin fluxes in plants by intramolecular domaindomain coevolution of PIN auxin transporters,” New Phytologist, vol. 227, no. 5. Wiley, pp. 1406–1416, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7697
DOI: 10.1111/nph.16629
WoS: 000534092400001
PMID: 32350870

S. A. Sinclair, S. Gille, M. Pauly, and U. Krämer, “Regulation of acetylation of plant cell wall components is complex and responds to external stimuli,” Plant Signaling &; Behavior, vol. 15, no. 1. Informa UK Limited, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7417
DOI: 10.1080/15592324.2019.1687185
WoS: 000494907500001
PMID: 31696770

H. Han, “Novel insights into PIN polarity regulation during Arabidopsis development,” Institute of Science and Technology Austria, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8589
DOI: 10.15479/AT:ISTA:8589

H. Han, H. Rakusova, I. Verstraeten, Y. Zhang, and J. Friml, “SCF TI/AFB auxin signaling for bending termination during shoot gravitropism,” Plant Physiology, vol. 183, no. 5. American Society of Plant Biologists, pp. 37–40, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7643
DOI: 10.1104/pp.20.00212
WoS: 000536641800018
PMID: 32107280

S. A. Sinclair and U. Krämer, “Generation of effective zinc-deficient agar-solidified media allows identification of root morphology changes in response to zinc limitation,” Plant Signaling &; Behavior, vol. 15, no. 1. Taylor &; Francis, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7416
DOI: 10.1080/15592324.2019.1687175
WoS: 000494909300001
PMID: 31696764

S. Tan et al., “Non-steroidal anti-inflammatory drugs target TWISTED DWAR-regulated actin dynamics and auxin transport-mediated plant development,” Cell Reports, vol. 33, no. 9. Elsevier, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8943
DOI: 10.1016/j.celrep.2020.108463
WoS: 000595658100018
PMID: 33264621

L. Hörmayer, J. C. Montesinos López, P. Marhavá, E. Benková, S. Yoshida, and J. Friml, “Wounding-induced changes in cellular pressure and localized auxin signalling spatially coordinate restorative divisions in roots,” Proceedings of the National Academy of Sciences, vol. 117, no. 26. Proceedings of the National Academy of Sciences, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8002
DOI: 10.1073/pnas.2003346117
WoS: 000565729700033
PMID: 32541049

S. Tan et al., “Salicylic acid targets protein phosphatase 2A to attenuate growth in plants,” Current Biology, vol. 30, no. 3. Cell Press, p. 381–395.e8, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7427
DOI: 10.1016/j.cub.2019.11.058
WoS: 000511287900018
PMID: 31956021

E. Mazur, I. Kulik, J. Hajny, and J. Friml, “Auxin canalization and vascular tissue formation by TI/AFB-mediated auxin signaling in arabidopsis,” New Phytologist, vol. 226, no. 5. Wiley, pp. 1375–1383, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/7500
DOI: 10.1111/nph.16446
WoS: 000514939700001
PMID: 31971254

J. Hajny, “Identification and characterization of the molecular machinery of auxin-dependent canalization during vasculature formation and regeneration,” Institute of Science and Technology Austria, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8822
DOI: 10.15479/AT:ISTA:8822

Y. Zhang, L. Rodriguez Solovey, L. Li, X. Zhang, and J. Friml, “Functional innovations of PIN auxin transporters mark crucial evolutionary transitions during rise of flowering plants,” Science Advances, vol. 6, no. 50. AAAS, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8986
DOI: 10.1126/sciadv.abc8895
WoS: 000599903600014
PMID: 33310852

H. Chen et al., “AcoMY, an Ananas comosus L. MYB transcription factor, functions in osmotic stress through negative regulation of ABA signaling,” International Journal of Molecular Sciences, vol. 21, no. 16. MDPI, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8283
DOI: 10.3390/ijms21165727
WoS: 000565090300001
PMID: 32785037

A. J. Johnson et al., “Experimental toolbox for quantitative evaluation of clathrin-mediated endocytosis in the plant model Arabidopsis,” Journal of Cell Science, vol. 133, no. 15. The Company of Biologists, 2020.
LibreCat: https://research-explorer.ista.ac.at/record/8139
DOI: 10.1242/jcs.248062
WoS: 000561047900021
PMID: 32616560

E. Lee et al., “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, vol. 116, no. 4. National Academy of Sciences, pp. 1420–1429, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/5908
DOI: 10.1073/pnas.1818099116
WoS: 000456336100050
PMID: 30610176

S. Yoshida et al., “A SOSEKI-based coordinate system interprets global polarity cues in arabidopsis,” Nature Plants, vol. 5, no. 2. Springer Nature, pp. 160–166, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6023
DOI: 10.1038/s41477-019-0363-6
WoS: 000460479600014

M. Zwiewka et al., “Root adaptation to O2-induced oxidative stress by ARF-GEF BEN1- and cytoskeleton-mediated PIN2 trafficking,” Plant and Cell Physiology, vol. 60, no. 2. Oxford University Press, pp. 255–273, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6104
DOI: 10.1093/pcp/pcz001
WoS: 000459634300002
PMID: 30668780

H. Rakusová, H. Han, P. Valosek, and J. Friml, “Genetic screen for factors mediating PIN polarization in gravistimulated Arabidopsis thaliana hypocotyls,” The Plant Journal, vol. 98, no. 6. Wiley, pp. 1048–1059, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6262
DOI: 10.1111/tpj.14301
WoS: 000473644100008
PMID: 30821050

Y. Wang, Z. Gong, J. Friml, and J. Zhang, “Nitrate modulates the differentiation of root distal stem cells,” Plant Physiology, vol. 180, no. 1. ASPB, pp. 22–25, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6261
DOI: 10.1104/pp.18.01305
WoS: 000466860800010
PMID: 30787134

Y. Zhang et al., “Auxin-mediated statolith production for root gravitropism,” New Phytologist, vol. 224, no. 2. Wiley, pp. 761–774, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6504
DOI: 10.1111/nph.15932
WoS: 000487184200024
PMID: 31111487

M. Glanc, M. Fendrych, and J. Friml, “PIN2 polarity establishment in arabidopsis in the absence of an intact cytoskeleton,” Biomolecules, vol. 9, no. 6. MDPI, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6611
DOI: 10.3390/biom9060222
WoS: 000475301500018
PMID: 31181636

Y. Zhang, G. Xiao, X. Wang, X. Zhang, and J. Friml, “Evolution of fast root gravitropism in seed plants,” Nature Communications, vol. 10. Springer Nature, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6778
DOI: 10.1038/s41467-019-11471-8
WoS: 000478576500012
PMID: 31375675

J. Bellstaedt et al., “A mobile auxin signal connects temperature sensing in cotyledons with growth responses in hypocotyls,” Plant Physiology, vol. 180, no. 2. ASPB, pp. 757–766, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6366
DOI: 10.1104/pp.18.01377
WoS: 000470086100019
PMID: 31000634

M. Cao et al., “TMK1-mediated auxin signalling regulates differential growth of the apical hook,” Nature, vol. 568. Springer Nature, pp. 240–243, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6259
DOI: 10.1038/s41586-019-1069-7
WoS: 000464412700050
PMID: 30944466

R. Skokan et al., “PIN-driven auxin transport emerged early in streptophyte evolution,” Nature Plants, vol. 5, no. 11. Springer Nature, pp. 1114–1119, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/7106
DOI: 10.1038/s41477-019-0542-5
WoS: 000496526100010
PMID: 31712756

S. A. Sinclair and J. Friml, “Defying gravity: a plant’s quest for moisture,” Cell Research, vol. 29. Springer Nature, pp. 965–966, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/7143
DOI: 10.1038/s41422-019-0254-4
WoS: 000500749600001
PMID: 31745287

A. Alcântara et al., “Systematic H screening reveals extensive effector-complex formation,” Frontiers in Plant Science, vol. 10, no. 11. Frontiers, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/7182
DOI: 10.3389/fpls.2019.01437
WoS: 000499821700001
PMID: 31803201

W. Dejonghe et al., “Disruption of endocytosis through chemical inhibition of clathrin heavy chain function,” Nature Chemical Biology, vol. 15, no. 6. Springer Nature, pp. 641–649, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6377
DOI: 10.1038/s41589-019-0262-1
WoS: 000468195600018

M. K. Vasileva, “Molecular mechanisms of endomembrane trafficking in Arabidopsis thaliana,” Institute of Science and Technology Austria, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/7172
DOI: 10.15479/AT:ISTA:7172

D. Huang et al., “Salicylic acid-mediated plasmodesmal closure via Remorin-dependent lipid organization,” Proceedings of the National Academy of Sciences of the United States of America, vol. 116, no. 42. Proceedings of the National Academy of Sciences, pp. 21274–21284, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6999
DOI: 10.1073/pnas.1911892116
WoS: 000490183000068
PMID: 31575745

M. Narasimhan, “Clathrin-Mediated endocytosis, post-endocytic trafficking and their regulatory controls in plants ,” Institute of Science and Technology Austria, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6269
DOI: 10.15479/at:ista:th1075

P. Marhavá, L. Hörmayer, S. Yoshida, P. Marhavý, E. Benková, and J. Friml, “Re-activation of stem cell pathways for pattern restoration in plant wound healing,” Cell, vol. 177, no. 4. Elsevier, p. 957–969.e13, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6351
DOI: 10.1016/j.cell.2019.04.015
WoS: 000466843000015
PMID: 31051107

L. Hörmayer and J. Friml, “Targeted cell ablation-based insights into wound healing and restorative patterning,” Current Opinion in Plant Biology, vol. 52. Elsevier, pp. 124–130, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6943
DOI: 10.1016/j.pbi.2019.08.006
WoS: 000502890600017
PMID: 31585333

A. Oochi et al., “Pinstatic acid promotes auxin transport by inhibiting PIN internalization,” Plant Physiology, vol. 180, no. 2. ASPB, pp. 1152–1165, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6260
DOI: 10.1104/pp.19.00201
WoS: 000470086100045
PMID: 30936248

M. Adamowski, L. Li, and J. Friml, “Reorientation of cortical microtubule arrays in the hypocotyl of arabidopsis thaliana is induced by the cell growth process and independent of auxin signaling,” International Journal of Molecular Sciences, vol. 20, no. 13. MDPI, 2019.
LibreCat: https://research-explorer.ista.ac.at/record/6627
DOI: 10.3390/ijms20133337
WoS: 000477041100221
PMID: 31284661

H. Trinh, I. Verstraeten, and D. Geelen, “In vitro assay for induction of adventitious rooting on intact arabidopsis hypocotyls,” in Root Development , vol. 1761, Springer Nature, 2018, pp. 95–102.
LibreCat: https://research-explorer.ista.ac.at/record/408
DOI: 10.1007/978-1-4939-7747-5_7
PMID: 29525951