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 

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 

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 

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 

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 

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 

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 

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 

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 

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 

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 

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 

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 

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 

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 

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 

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