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Tanaka, H., Nodzyski, T., Kitakura, S., Feraru, M., Sasabe, M., Ishikawa, T.,https://doi.org/10.1093/pcp/pct196__Friml, J. (2014). BE/ARC is required for BFA-sensitive recycling of PIN auxin transporters and auxin-mediated development in arabidopsis. Plant and Cell Physiology. Oxford University Press.https://doi.org/10.1093/pcp/pct196 
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Naramoto, S., Nodzyski, T., Dainobu, T., Takatsuka, H., Okada, T., Friml, J., &; Fukuda, H. (2014). VAN4 encodes a putative T that is required for normal cell growth and vein development in arabidopsis. Plant and Cell Physiology. Oxford University Press.https://doi.org/10.1093/pcp/pcu012 
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Cires Rodriguez, E., Baltisberger, M., Cuesta, C., Vargas, P., &; Prieto, J. (2014). Allopolyploid origin of the Balkan endemic Ranunculus wettsteinii (Ranunculaceae) inferred from nuclear and plastid DNA sequences. Organisms Diversity and Evolution. Springer.https://doi.org/10.1007/s13127-013-0150-6 
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Gadeyne, A., Sánchez Rodríguez, C., Vanneste, S., Di Rubbo, S., Zauber, H., Vanneste, K.,https://doi.org/10.1016/j.cell.2014.01.039__Van Damme, D. (2014). The TPLATE adaptor complex drives clathrin-mediated endocytosis in plants. Cell. Cell Press.https://doi.org/10.1016/j.cell.2014.01.039 
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Simon, S., Skfpa, P., Dobrev, P., Petrásek, J., Zaeímalová, E., &; Friml, J. (2014). Analyzing the in vivo status of exogenously applied auxins: A HPLC-based method to characterize the intracellularly localized auxin transporters. In G. Hicks &; S. Robert (Eds.), Plant Chemical Genomics (Vol. 1056, pp. 255–264). Springer.https://doi.org/10.1007/978-1-62703-592-7_23 
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Bailly, A., Wang, B., Zwiewka, M., Pollmann, S., Schenck, D., Lüthen, H.,https://doi.org/10.1111/tpj.12369__Geisler, M. (2014). Expression of TWISTED DWAR lacking its in-plane membrane anchor leads to increased cell elongation and hypermorphic growth. Plant Journal. Wiley-Blackwell.https://doi.org/10.1111/tpj.12369 
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Chen, Y., Aung, K., Roldík, J., Walicki, K., Friml, J., &; Brandizzí, F. (2014). Inter-regulation of the unfolded protein response and auxin signaling. Plant Journal. Wiley-Blackwell.https://doi.org/10.1111/tpj.12373 
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Marhavá, P. (2014). Molecular mechanisms of patterning and subcellular trafficking in Arabidopsis thaliana. Institute of Science and Technology Austria.
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Vanneste, S., &; Friml, J. (2013). Calcium: The missing link in auxin action. Plants. MDPI.https://doi.org/10.3390/plants2040650 
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Boutté, Y., Jonsson, K., Mcfarlane, H., Johnson, E., Gendre, D., Swarup, R.,https://doi.org/10.1073/pnas.1309057110__Bhalerao, R. (2013). ECHIDNA mediated post Golgi trafficking of auxin carriers for differential cell elongation. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.1309057110 
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Simon, S., Kubes, M., Baster, P., Robert, S., Dobrev, P., Friml, J.,https://doi.org/10.1111/nph.12437__Zaeímalová, E. (2013). Defining the selectivity of processes along the auxin response chain: A study using auxin analogues. New Phytologist. Wiley.https://doi.org/10.1111/nph.12437 
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Nodzyski, T., Feraru, M., Hirsch, S., De Rycke, R., Nicuales, C., Van Leene, J.,https://doi.org/10.1093/mp/sst044__Friml, J. (2013). Retromer subunits VPA and VP mediate prevacuolar compartment (PVC) function in Arabidopsis. Molecular Plant. Cell Press.https://doi.org/10.1093/mp/sst044 
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Cazzonelli, C., Vanstraelen, M., Simon, S., Yin, K., Carron Arthur, A., Nisar, N.,https://doi.org/10.1371/journal.pone.0070069__Pogson, B. (2013). Role of the Arabidopsis PIN6 auxin transporter in auxin homeostasis and auxin-mediated development. PLoS One. Public Library of Science.https://doi.org/10.1371/journal.pone.0070069 
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covanová, M., Sauer, M., Rychtá, J., Friml, J., Petrásek, J., &; Zaeímalová, E. (2013). Overexpression of the auxin binding PROTEIN1 modulates PIN-dependent auxin transport in tobacco cells. PLoS One. Public Library of Science.https://doi.org/10.1371/journal.pone.0070050 
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Landberg, K., Pederson, E., Viaene, T., Bozorg, B., Friml, J., Jönsson, H.,https://doi.org/10.1104/pp.113.214023__Sundberg, E. (2013). The moss physcomitrella patens reproductive organ development is highly organized, affected by the two SHI/STY genes and by the level of active auxin in the SHI/STY expression domain. Plant Physiology. American Society of Plant Biologists.https://doi.org/10.1104/pp.113.214023 
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Remy, E., Cabrito, T., Baster, P., Batista, R., Teixeira, M., Friml, J.,https://doi.org/10.1105/tpc.113.110353__Duque, P. (2013). A major facilitator superfamily transporter plays a dual role in polar auxin transport and drought stress tolerance in Arabidopsis. Plant Cell. American Society of Plant Biologists.https://doi.org/10.1105/tpc.113.110353 
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Du, Y., Tejos, R., Beck, M., Himschoot, E., Li, H., Robatzek, S.,https://doi.org/10.1073/pnas.1220205110__Friml, J. (2013). Salicylic acid interferes with clathrin-mediated endocytic protein trafficking. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.1220205110 
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Tanaka, H., Kitakura, S., Rakusová, H., Uemura, T., Feraru, M., De Rycke, R.,https://doi.org/10.1371/journal.pgen.1003540__Friml, J. (2013). Cell polarity and patterning by PIN trafficking through early endosomal compartments in arabidopsis thaliana. PLoS Genetics. Public Library of Science.https://doi.org/10.1371/journal.pgen.1003540 
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Yu, H., Karampelias, M., Robert, S., Peer, W., Swarup, R., Ye, S.,https://doi.org/10.1104/pp.113.217018__Estelle, M. (2013). Root ultraviolet b-sensitive1/weak auxin response3 is essential for polar auxin transport in arabidopsis. Plant Physiology. American Society of Plant Biologists.https://doi.org/10.1104/pp.113.217018 
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Rosquete, M., von Wangenheim, D., Marhavý, P., Barbez, E., Stelzer, E., Benková, E.,https://doi.org/10.1016/j.cub.2013.03.064__Kleine Vehn, J. (2013). An auxin transport mechanism restricts positive orthogravitropism in lateral roots. Current Biology. Cell Press.https://doi.org/10.1016/j.cub.2013.03.064 
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Wang, B., Bailly, A., Zwiewk, M., Henrichs, S., Azzarello, E., Mancuso, S.,https://doi.org/10.1105/tpc.112.105999__Geisler, M. (2013). Arabidopsis TWISTED DWAR functionally interacts with auxin exporter ABC on the root plasma membrane. Plant Cell. American Society of Plant Biologists.https://doi.org/10.1105/tpc.112.105999 
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Löfke, C., Zwiewka, M., Heilmann, I., Van Montagu, M., Teichmann, T., &; Friml, J. (2013). Asymmetric gibberellin signaling regulates vacuolar trafficking of PIN auxin transporters during root gravitropism. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.1300107110 
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Baster, P., Robert, S., Kleine Vehn, J., Vanneste, S., Kania, U., Grunewald, W.,https://doi.org/10.1038/emboj.2012.310__Friml, J. (2013). SCF^TI AFB-auxin signalling regulates PIN vacuolar trafficking and auxin fluxes during root gravitropism. EMBO Journal. Wiley-Blackwell.https://doi.org/10.1038/emboj.2012.310 
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Di Rubbo, S., Irani, N., Kim, S., Xu, Z., Gadeyne, A., Dejonghe, W.,https://doi.org/10.1105/tpc.113.114058__Russinova, E. (2013). The clathrin adaptor complex AP-2 mediates endocytosis of brassinosteroid INSENSITIV in arabidopsis. Plant Cell. American Society of Plant Biologists.https://doi.org/10.1105/tpc.113.114058 
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Kim, S., Xu, Z., Song, K., Kim, D., Kang, H., Reichardt, I.,https://doi.org/10.1105/tpc.113.114264__Hwang, I. (2013). Adaptor protein complex 2-mediated endocytosis is crucial for male reproductive organ development in arabidopsis. Plant Cell. American Society of Plant Biologists.https://doi.org/10.1105/tpc.113.114264 
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PMID: 23975898

Pbndík, A., Simonovik, B., Petersson, S., Henyková, E., Simon, S., Greenham, K.,https://doi.org/10.1105/tpc.113.114421__Ljung, K. (2013). Regulation of auxin homeostasis and gradients in Arabidopsis roots through the formation of the indole-3-acetic acid catabolite 2-oxindole-3-acetic acid. Plant Cell. American Society of Plant Biologists.https://doi.org/10.1105/tpc.113.114421 
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Bargmann, B., Vanneste, S., Krouk, G., Nawy, T., Efroni, I., Shani, E.,https://doi.org/10.1038/msb.2013.40__Birnbaum, K. (2013). A map of cell typespecific auxin responses. Molecular Systems Biology. Nature Publishing Group.https://doi.org/10.1038/msb.2013.40 
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Robert, H., Grones, P., Stepanova, A., Robles, L., Lokerse, A., Alonso, J.,https://doi.org/10.1016/j.cub.2013.09.039__Friml, J. (2013). Local auxin sources orient the apical basal axis in arabidopsis embryos. Current Biology. Cell Press.https://doi.org/10.1016/j.cub.2013.09.039 
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Wabnik, K. T., Robert, H., Smith, R., &; Friml, J. (2013). Modeling framework for the establishment of the apical-basal embryonic axis in plants. Current Biology. Cell Press.https://doi.org/10.1016/j.cub.2013.10.038 
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Remy, E., Baster, P., Friml, J., &; Duque, P. (2013). ZIFL1.1 transporter modulates polar auxin transport by stabilizing membrane abundance of multiple PINs in Arabidopsis root tip. Plant Signaling &; Behavior. Taylor &; Francis.https://doi.org/10.4161/psb.25688 
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PMID: 23857365