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RNA editing alterations define manifestation of prion diseases.
Kanata E, Llorens F, Dafou D, Dimitriadis A, Thüne K, Xanthopoulos K, Bekas N, Espinosa JC, Schmitz M, Marín-Moreno A, Capece V, Shormoni O, Andréoletti O, Bonn S, Torres JM, Ferrer I, Zerr I, Sklaviadis T. Kanata E, et al. Among authors: zerr i. Proc Natl Acad Sci U S A. 2019 Sep 24;116(39):19727-19735. doi: 10.1073/pnas.1803521116. Epub 2019 Sep 6. Proc Natl Acad Sci U S A. 2019. PMID: 31492812 Free PMC article.
Molecular subtype-specific clinical diagnosis of prion diseases.
Heinemann U, Krasnianski A, Meissner B, Gloeckner SF, Kretzschmar HA, Zerr I. Heinemann U, et al. Among authors: zerr i. Vet Microbiol. 2007 Aug 31;123(4):328-35. doi: 10.1016/j.vetmic.2007.04.002. Epub 2007 Apr 7. Vet Microbiol. 2007. PMID: 17513070
Similarities between forms of sheep scrapie and Creutzfeldt-Jakob disease are encoded by distinct prion types.
Wemheuer WM, Benestad SL, Wrede A, Schulze-Sturm U, Wemheuer WE, Hahmann U, Gawinecka J, Schütz E, Zerr I, Brenig B, Bratberg B, Andréoletti O, Schulz-Schaeffer WJ. Wemheuer WM, et al. Among authors: zerr i. Am J Pathol. 2009 Dec;175(6):2566-73. doi: 10.2353/ajpath.2009.090623. Epub 2009 Oct 22. Am J Pathol. 2009. PMID: 19850886 Free PMC article.
Codon 129 polymorphism and the E200K mutation do not affect the cellular prion protein isoform composition in the cerebrospinal fluid from patients with Creutzfeldt-Jakob disease.
Schmitz M, Schlomm M, Hasan B, Beekes M, Mitrova E, Korth C, Breil A, Carimalo J, Gawinecka J, Varges D, Zerr I. Schmitz M, et al. Among authors: zerr i. Eur J Neurosci. 2010 Jun;31(11):2024-31. doi: 10.1111/j.1460-9568.2010.07224.x. Epub 2010 May 31. Eur J Neurosci. 2010. PMID: 20529115
Immunotherapy in prion disease.
Roettger Y, Du Y, Bacher M, Zerr I, Dodel R, Bach JP. Roettger Y, et al. Among authors: zerr i. Nat Rev Neurol. 2013 Feb;9(2):98-105. doi: 10.1038/nrneurol.2012.258. Epub 2012 Dec 18. Nat Rev Neurol. 2013. PMID: 23247613 Review.
409 results