Boytsov, D., Madej, G. M., Horn, G., Blaha, N., Köcher, T., Sitte, H. H.,https://doi.org/10.1073/pnas.2319686121__Roblek, M. (2024). Orphan lysosomal solute carrier MFS facilitates highly selective dipeptide transport. 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.2319686121 

Nagano, M., Aoshima, K., Shimamura, H., Siekhaus, D. E., Toshima, J. Y., &; Toshima, J. (2023). Distinct role of TGN-resident clathrin adaptors for Vpp activation in the TGN-endosome trafficking pathway. Journal of Cell Science. The Company of Biologists.https://doi.org/10.1242/jcs.261448 

Toshima, J. Y., Tsukahara, A., Nagano, M., Tojima, T., Siekhaus, D. E., Nakano, A., &; Toshima, J. (2023). The yeast endocytic early/sorting compartment exists as an independent sub-compartment within the trans-Golgi network. ELife. eLife Sciences Publications.https://doi.org/10.7554/eLife.84850 

Roblek, M., Bicher, J., van Gogh, M., György, A., Seeböck, R., Szulc, B.,https://doi.org/10.3389/fonc.2022.777634__Siekhaus, D. E. (2022). The solute carrier MFS decreases ;21 integrin’s activation status and thus tumor metastasis. Frontiers in Oncology. Frontiers.https://doi.org/10.3389/fonc.2022.777634 

Martin, E. T., Blatt, P., Ngyuen, E., Lahr, R., Selvam, S., Yoon, H. A. M.,https://doi.org/10.1016/j.devcel.2022.03.005__Rangan, P. (2022). A translation control module coordinates germline stem cell differentiation with ribosome biogenesis during Drosophila oogenesis. Developmental Cell. Elsevier.https://doi.org/10.1016/j.devcel.2022.03.005 

Akhmanova, M., Emtenani, S., Krueger, D., György, A., Pereira Guarda, M., Vlasov, M.,https://doi.org/10.1126/science.abj0425__Siekhaus, D. E. (2022). Cell division in tissues enables macrophage infiltration. Science. American Association for the Advancement of Science.https://doi.org/10.1126/science.abj0425 

Emtenani, S., Martin, E. T., György, A., Bicher, J., Genger, J.-W., Köcher, T.,https://doi.org/10.15252/embj.2021109049__Siekhaus, D. E. (2022). Macrophage mitochondrial bioenergetics and tissue invasion are boosted by an Atossa-Porthos axis in Drosophila. The Embo Journal. Embo Press.https://doi.org/10.15252/embj.2021109049 

Enshoji, M., Miyano, Y., Yoshida, N., Nagano, M., Watanabe, M., Kunihiro, M.,https://doi.org/10.1083/jcb.202112138__Toshima, J. (2022). Ep/Pan1p is a master regulator of the late stages of the endocytic pathway. Journal of Cell Biology. Rockefeller University Press.https://doi.org/10.1083/jcb.202112138 

Belyaeva, V., Wachner, S., György, A., Emtenani, S., Gridchyn, I., Akhmanova, M.,https://doi.org/10.1371/journal.pbio.3001494__Siekhaus, D. E. (2022). Fos regulates macrophage infiltration against surrounding tissue resistance by a cortical actin-based mechanism in Drosophila. PLoS Biology. Public Library of Science.https://doi.org/10.1371/journal.pbio.3001494 

Inglés Prieto, Á., Furthmann, N., Crossman, S. H., Tichy, A. M., Hoyer, N., Petersen, M.,https://doi.org/10.1371/journal.pgen.1009479__Janovjak, H. L. (2021). Optogenetic delivery of trophic signals in a genetic model of Parkinson’s disease. PLoS Genetics. Public Library of Science.https://doi.org/10.1371/journal.pgen.1009479 

Kierdorf, K., Hersperger, F., Sharrock, J., Vincent, C. M., Ustaoglu, P., Dou, J.,https://doi.org/10.7554/eLife.51595__Dionne, M. S. (2020). Muscle function and homeostasis require cytokine inhibition of AKT activity in Drosophila. ELife. eLife Sciences Publications.https://doi.org/10.7554/eLife.51595 

Belyaeva, V., Wachner, S., Gridchyn, I., Linder, M., Emtenani, S., György, A.,https://doi.org/10.1101/2020.09.18.301481__Siekhaus, D. E. (n.d.). Cortical actin properties controlled by Drosophila Fos aid macrophage infiltration against surrounding tissue resistance. bioRxiv.https://doi.org/10.1101/2020.09.18.301481 

Nagano, M., Toshima, J. Y., Siekhaus, D. E., &; Toshima, J. (2019). Rab5-mediated endosome formation is regulated at the trans-Golgi network. Communications Biology. Springer Nature.https://doi.org/10.1038/s42003-019-0670-5 

Trébuchet, G., Cattenoz, P. B., Zsámboki, J., Mazaud, D., Siekhaus, D. E., Fanto, M., &; Giangrande, A. (2019). The Repo homeodomain transcription factor suppresses hematopoiesis in Drosophila and preserves the glial fate. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.1059-18.2018 

Valosková, K., Bicher, J., Roblek, M., Emtenani, S., György, A., Misova, M.,https://doi.org/10.7554/elife.41801__Siekhaus, D. E. (2019). A conserved major facilitator superfamily member orchestrates a subset of O-glycosylation to aid macrophage tissue invasion. ELife. eLife Sciences Publications.https://doi.org/10.7554/elife.41801 

Ratheesh, A., Bicher, J., Smutny, M., Veselá, J., Papusheva, E., Krens, G.,https://doi.org/10.1016/j.devcel.2018.04.002__Siekhaus, D. E. (2018). Drosophila TNF modulates tissue tension in the embryo to facilitate macrophage invasive migration. Developmental Cell. Elsevier.https://doi.org/10.1016/j.devcel.2018.04.002 

Yamamoto, W., Wada, S., Nagano, M., Aoshima, K., Siekhaus, D. E., Toshima, J., &; Toshima, J. (2018). Distinct roles for plasma membrane PtdIns 4 P and PtdIns 4 5https://doi.org/10.1242/jcs.207696__during yeast receptor mediated endocytosis. Journal of Cell Science. Company of Biologists.https://doi.org/10.1242/jcs.207696 

György, A., Roblek, M., Ratheesh, A., Valosková, K., Belyaeva, V., Wachner, S.,https://doi.org/10.1534/g3.117.300452__Siekhaus, D. E. (2018). Tools allowing independent visualization and genetic manipulation of Drosophila melanogaster macrophages and surrounding tissues. : Genes, Genomes, Genetics. Genetics Society of America.https://doi.org/10.1534/g3.117.300452 

Matsubayashi, Y., Louani, A., Dragu, A., Sanchez Sanchez, B., Serna Morales, E., Yolland, L.,https://doi.org/10.1016/j.cub.2017.10.001__Stramer, B. (2017). A moving source of matrix components is essential for De Novo basement membrane formation. Current Biology. Cell Press.https://doi.org/10.1016/j.cub.2017.10.001 

Toshima, J., Horikomi, C., Okada, A., Hatori, M., Nagano, M., Masuda, A.,https://doi.org/10.1242/jcs.176651__Toshima, J. (2016). Sr/CAP is required for polarized actin cable assembly and patch internalization during clathrin-mediated endocytosis. Journal of Cell Science. Company of Biologists.https://doi.org/10.1242/jcs.176651 

Toshima, J., Furuya, E., Nagano, M., Kanno, C., Sakamoto, Y., Ebihara, M.,https://doi.org/10.7554/eLife.10276__Toshima, J. (2016). Yeast Ep-like endocytic protein Pan1p regulates the interaction between endocytic vesicles, endosomes and the actin cytoskeleton. ELife. eLife Sciences Publications.https://doi.org/10.7554/eLife.10276 

Ratheesh, A., Belyaeva, V., &; Siekhaus, D. E. (2015). Drosophila immune cell migration and adhesion during embryonic development and larval immune responses. Current Opinion in Cell Biology. Elsevier.https://doi.org/10.1016/j.ceb.2015.07.003 

Kawada, D., Kobayashi, H., Tomita, T., Nakata, E., Nagano, M., Siekhaus, D. E.,https://doi.org/10.1016/j.bbamcr.2014.10.009__Toshimaa, J. (2015). The yeast Arf-GAP Glo3p is required for the endocytic recycling of cell surface proteins. Biochimica et Biophysica Acta - Molecular Cell Research. Elsevier.https://doi.org/10.1016/j.bbamcr.2014.10.009 

Toshima, J., Nishinoaki, S., Sato, Y., Yamamoto, W., Furukawa, D., Siekhaus, D. E.,https://doi.org/10.1038/ncomms4498__Toshima, J. (2014). Bifurcation of the endocytic pathway into Rab5-dependent and -independent transport to the vacuole. Nature Communications. Nature Publishing Group.https://doi.org/10.1038/ncomms4498 

Degennaro, M., Hurd, T., Siekhaus, D. E., Biteau, B., Jasper, H., &; Lehmann, R. (2011). Peroxiredoxin stabilization of DE-cadherin promotes primordial germ cell adhesion. Developmental Cell. Cell Press.https://doi.org/10.1016/j.devcel.2010.12.007 

Siekhaus, D. E., Haesemeyer, M., Moffitt, O., &; Lehmann, R. (2010). RhoL controls invasion and Ra localization during immune cell transmigration in Drosophila. Nature Cell Biology. Nature Publishing Group.

Kunwar, P., Siekhaus, D. E., &; Lehmann, R. (2006). In vivo migration A germ cell perspective. Annual Review of Cell and Developmental Biology. Annual Reviews.https://doi.org/10.1146/annurev.cellbio.22.010305.103337 

Rayburn, L., Gooding, H., Choksi, S., Maloney, D., Kidd, A., Siekhaus, D. E., &; Bender, M. (2003). Amontillado, the Drosophila homolog of the prohormone processing protease P, is required during embryogenesis and early larval development. Genetics. Genetics Society of America.

Siekhaus, D. E., &; Drubin, D. (2003). Spontaneous receptor-independent heterotrimeric G-protein signalling in an RGS mutant. Nature Cell Biology. Nature Publishing Group.https://doi.org/10.1038/ncb941 

Hwang, J., Siekhaus, D. E., Fuller, R., Taghert, P., &; Lindberg, I. (2000). Interaction of Drosophila melanogaster prohormone convertase 2 and 7: Insect cell specific processing and secretion. Journal of Biological Chemistry. American Society for Biochemistry and Molecular Biology.https://doi.org/10.1074/jbc.M000032200  

Siekhaus, D. E., &; Fuller, R. (1999). A role for amontillado the Drosophila homolog of the neuropeptide precursor processing protease P in triggering hatching behavior. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/jneurosci.19-16-06942.1999