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 
LibreCat: https://research-explorer.ista.ac.at/record/10282
DOI: 10.1111/nph.17792
WoS: 000714678100001
PMID: 34637542

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 
LibreCat: https://research-explorer.ista.ac.at/record/7582
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WoS: 000525315000035
PMID: 32121542

Fan, L., Zhao, L., Hu, W., Li, W., Novák, O., Strnad, M.,https://doi.org/10.1111/pce.13153__Qiu, Q. (2018). NHX antiporters regulate the pH of endoplasmic reticulum and auxin-mediated development. Plant, Cell and Environment. Wiley-Blackwell.https://doi.org/10.1111/pce.13153 
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PMID: 29360148

Simon, S., Skfpa, P., Viaene, T., Zwiewka, M., Tejos, R., Klíma, P.,https://doi.org/10.1111/nph.14019__Friml, J. (2016). PIN6 auxin transporter at endoplasmic reticulum and plasma membrane mediates auxin homeostasis and organogenesis in Arabidopsis. New Phytologist. Wiley-Blackwell.https://doi.org/10.1111/nph.14019 
LibreCat: https://research-explorer.ista.ac.at/record/1417
DOI: 10.1111/nph.14019

Sasse, J., Simon, S., Gübeli, C., Liu, G., Cheng, X., Friml, J.,https://doi.org/10.1016/j.cub.2015.01.015__Borghi, L. (2015). Asymmetric localizations of the ABC transporter PaPD trace paths of directional strigolactone transport. Current Biology. Cell Press.https://doi.org/10.1016/j.cub.2015.01.015 
LibreCat: https://research-explorer.ista.ac.at/record/1536
DOI: 10.1016/j.cub.2015.01.015

Grones, P., Chen, X., Simon, S., Kaufmann, W., De Rycke, R., Nodzyski, T.,https://doi.org/10.1093/jxb/erv177__Friml, J. (2015). Auxin-binding pocket of AB is crucial for its gain-of-function cellular and developmental roles. Journal of Experimental Botany. Oxford University Press.https://doi.org/10.1093/jxb/erv177 
LibreCat: https://research-explorer.ista.ac.at/record/1562
DOI: 10.1093/jxb/erv177

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 
LibreCat: https://research-explorer.ista.ac.at/record/2245
DOI: 10.1007/978-1-62703-592-7_23

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 
LibreCat: https://research-explorer.ista.ac.at/record/2443
DOI: 10.1111/nph.12437

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 
LibreCat: https://research-explorer.ista.ac.at/record/2472
DOI: 10.1371/journal.pone.0070069

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 
LibreCat: https://research-explorer.ista.ac.at/record/509
DOI: 10.1105/tpc.113.114058
PMID: 23975899

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 
LibreCat: https://research-explorer.ista.ac.at/record/511
DOI: 10.1105/tpc.113.114421
PMID: 24163311

Ding, Z., Wang, B., Moreno, I., Dupláková, N., Simon, S., Carraro, N.,https://doi.org/10.1038/ncomms1941__Friml, J. (2012). ER-localized auxin transporter PIN8 regulates auxin homeostasis and male gametophyte development in Arabidopsis. Nature Communications. Nature Publishing Group.https://doi.org/10.1038/ncomms1941 
LibreCat: https://research-explorer.ista.ac.at/record/3114
DOI: 10.1038/ncomms1941

Robert, S., Kleine Vehn, J., Barbez, E., Sauer, M., Paciorek, T., Baster, P.,https://doi.org/10.1016/j.cell.2010.09.027__Friml, J. (2010). AB mediates auxin inhibition of clathrin-dependent endocytosis in Arabidopsis. Cell. Cell Press.https://doi.org/10.1016/j.cell.2010.09.027 
LibreCat: https://research-explorer.ista.ac.at/record/3075
DOI: 10.1016/j.cell.2010.09.027

Jelínková, A., Malínská, K., Simon, S., Kleine Vehn, J., Paezová, M., Pejchar, P.,https://doi.org/10.1111/j.1365-313X.2009.04102.x__Petrásek, J. (2010). Probing plant membranes with FM dyes: Tracking dragging or blocking? Plant Journal. Wiley-Blackwell.https://doi.org/10.1111/j.1365-313X.2009.04102.x 
LibreCat: https://research-explorer.ista.ac.at/record/3067
DOI: 10.1111/j.1365-313X.2009.04102.x

Rfeidka, K., Simásková, M., Duclercq, J., Petrásek, J., Zaeímalová, E., Simon, S.,https://doi.org/10.1073/pnas.0900060106__Benková, E. (2009). Cytokinin regulates root meristem activity via modulation of the polar auxin transport. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.0900060106 
LibreCat: https://research-explorer.ista.ac.at/record/3050
DOI: 10.1073/pnas.0900060106