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dc.date.accessioned2013-03-12T08:35:14Z
dc.date.available2013-03-12T08:35:14Z
dc.date.issued2008en_US
dc.date.submitted2009-01-22en_US
dc.identifier.citationSkånland, Sigrid. Mechanisms in Intracellular Transport of Toxins. Doktoravhandling, University of Oslo, 2008en_US
dc.identifier.urihttp://hdl.handle.net/10852/11339
dc.description.abstractRicin and Shiga toxin are protein toxins able to enter target cells by endocytosis. They can be transported via early endosomes to the Golgi apparatus and the endoplasmic reticulum. From this compartment, they are translocated to the cytosol where they inactivate ribosomes and thus kill the cell. We have studied mechanisms involved in endosome to Golgi transport of ricin and Shiga toxin. We have found that Shiga toxin can induce signaling events which promote the toxin transport, and identified effectors of this pathway. When it comes to ricin, we have characterized several proteins important for its endosome to Golgi transport, and show how they act together to regulate endosome motility. These findings provide new knowledge on how molecules travel inside cells.eng
dc.language.isoengen_US
dc.relation.haspartI Skånland SS, Wälchli S, Utskarpen A, Wandinger-Ness A, Sandvig K (2007): Phosphoinositide-regulated retrograde transport of ricin: crosstalk between hVps34 and sorting nexins. Traffic, 8, 297-309. (2007). The paper is removed from the thesis in DUO. The published version is available at: http://dx.doi.org/10.1111/j.1600-0854.2006.00527.x
dc.relation.haspartII Wälchli S, Skånland SS, Gregers TF, Lauvrak SU, Torgersen ML, Ying M, Kuroda S, Maturana A, Sandvig K (2008): The Mitogen-activated Protein Kinase p38 Links Shiga Toxin-dependent Signaling and Trafficking. Mol Biol Cell, 19, 95-104. (2008). http://dx.doi.org/10.1091/mbc.E07-06-0565
dc.relation.haspartIII Skånland SS, Wälchli S, Brech A, Sandvig K: SNX4 in complex with and dynein: implications for endosome movement. PLoS ONE, 4, e5935. (2009). The paper is removed from the thesis in DUO. The published version is available at: http://dx.doi.org/10.1371/journal.pone.0005935
dc.relation.haspartIV Skånland SS, Wälchli S, Sandvig K: beta-arrestins attenuate p38 mediated endosome to Golgi transport. Cell Microbiol, 11, 796-807. (2009). The paper is removed from the thesis in DUO. The published version is available at: http://dx.doi.org/10.1111/j.1462-5822.2009.01292.x
dc.relation.urihttp://dx.doi.org/10.1111/j.1600-0854.2006.00527.x
dc.relation.urihttp://dx.doi.org/10.1091/mbc.E07-06-0565
dc.relation.urihttp://dx.doi.org/10.1371/journal.pone.0005935
dc.relation.urihttp://dx.doi.org/10.1111/j.1462-5822.2009.01292.x
dc.titleMechanisms in Intracellular Transport of Toxinsen_US
dc.typeDoctoral thesisen_US
dc.date.updated2009-07-28en_US
dc.creator.authorSkånland, Sigriden_US
dc.subject.nsiVDP::473en_US
cristin.unitcode152000en_US
cristin.unitnameMolekylær biovitenskapen_US
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft.au=Skånland, Sigrid&rft.title=Mechanisms in Intracellular Transport of Toxins&rft.inst=University of Oslo&rft.date=2008&rft.degree=Doktoravhandlingen_US
dc.identifier.urnURN:NBN:no-22029en_US
dc.type.documentDoktoravhandlingen_US
dc.identifier.duo88811en_US
dc.contributor.supervisorKirsten Sandvigen_US
dc.identifier.bibsys092844030en_US
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/11339/1/88811_Skaanland_DUO_Publ.pdf


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