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Items: 12

1.

Fibril-induced glutamine-/asparagine-rich prions recruit stress granule proteins in mammalian cells.

Riemschoss K, Arndt V, Bolognesi B, von Eisenhart-Rothe P, Liu S, Buravlova O, Duernberger Y, Paulsen L, Hornberger A, Hossinger A, Lorenzo-Gotor N, Hogl S, Müller SA, Tartaglia G, Lichtenthaler SF, Vorberg IM.

Life Sci Alliance. 2019 Jul 2;2(4). pii: e201800280. doi: 10.26508/lsa.201800280. Print 2019 Aug.

2.

Editorial overview: Prion disease: From drug discovery tools to clinical trials.

Chiesa R, Vorberg IM.

Curr Opin Pharmacol. 2019 Feb;44:iii-v. doi: 10.1016/j.coph.2019.05.002. No abstract available.

PMID:
31186145
3.

All the Same? The Secret Life of Prion Strains within Their Target Cells.

Vorberg IM.

Viruses. 2019 Apr 9;11(4). pii: E334. doi: 10.3390/v11040334. Review.

4.

Mammalian amyloidogenic proteins promote prion nucleation in yeast.

Chandramowlishwaran P, Sun M, Casey KL, Romanyuk AV, Grizel AV, Sopova JV, Rubel AA, Nussbaum-Krammer C, Vorberg IM, Chernoff YO.

J Biol Chem. 2018 Mar 2;293(9):3436-3450. doi: 10.1074/jbc.M117.809004. Epub 2018 Jan 12.

5.

YKL-40 in the brain and cerebrospinal fluid of neurodegenerative dementias.

Llorens F, Thüne K, Tahir W, Kanata E, Diaz-Lucena D, Xanthopoulos K, Kovatsi E, Pleschka C, Garcia-Esparcia P, Schmitz M, Ozbay D, Correia S, Correia Â, Milosevic I, Andréoletti O, Fernández-Borges N, Vorberg IM, Glatzel M, Sklaviadis T, Torres JM, Krasemann S, Sánchez-Valle R, Ferrer I, Zerr I.

Mol Neurodegener. 2017 Nov 10;12(1):83. doi: 10.1186/s13024-017-0226-4.

6.

Prion strains depend on different endocytic routes for productive infection.

Fehlinger A, Wolf H, Hossinger A, Duernberger Y, Pleschka C, Riemschoss K, Liu S, Bester R, Paulsen L, Priola SA, Groschup MH, Schätzl HM, Vorberg IM.

Sci Rep. 2017 Jul 31;7(1):6923. doi: 10.1038/s41598-017-07260-2.

7.

Prions on the run: How extracellular vesicles serve as delivery vehicles for self-templating protein aggregates.

Liu S, Hossinger A, Göbbels S, Vorberg IM.

Prion. 2017 Mar 4;11(2):98-112. doi: 10.1080/19336896.2017.1306162. Review.

8.

Horizontal Transmission of Cytosolic Sup35 Prions by Extracellular Vesicles.

Liu S, Hossinger A, Hofmann JP, Denner P, Vorberg IM.

MBio. 2016 Jul 12;7(4). pii: e00915-16. doi: 10.1128/mBio.00915-16.

9.

Deposition pattern and subcellular distribution of disease-associated prion protein in cerebellar organotypic slice cultures infected with scrapie.

Wolf H, Hossinger A, Fehlinger A, Büttner S, Sim V, McKenzie D, Vorberg IM.

Front Neurosci. 2015 Nov 4;9:410. doi: 10.3389/fnins.2015.00410. eCollection 2015.

10.

Cell-to-cell propagation of infectious cytosolic protein aggregates.

Hofmann JP, Denner P, Nussbaum-Krammer C, Kuhn PH, Suhre MH, Scheibel T, Lichtenthaler SF, Schätzl HM, Bano D, Vorberg IM.

Proc Natl Acad Sci U S A. 2013 Apr 9;110(15):5951-6. doi: 10.1073/pnas.1217321110. Epub 2013 Mar 18.

11.

Acute cellular uptake of abnormal prion protein is cell type and scrapie-strain independent.

Greil CS, Vorberg IM, Ward AE, Meade-White KD, Harris DA, Priola SA.

Virology. 2008 Sep 30;379(2):284-93. doi: 10.1016/j.virol.2008.07.006. Epub 2008 Aug 8.

12.

Scrapie infection of prion protein-deficient cell line upon ectopic expression of mutant prion proteins.

Maas E, Geissen M, Groschup MH, Rost R, Onodera T, Schätzl H, Vorberg IM.

J Biol Chem. 2007 Jun 29;282(26):18702-10. Epub 2007 Apr 27.

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