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Altered Ca2+ homeostasis induces Calpain-Cathepsin axis activation in sporadic Creutzfeldt-Jakob disease.
Llorens F, Thüne K, Sikorska B, Schmitz M, Tahir W, Fernández-Borges N, Cramm M, Gotzmann N, Carmona M, Streichenberger N, Michel U, Zafar S, Schuetz AL, Rajput A, Andréoletti O, Bonn S, Fischer A, Liberski PP, Torres JM, Ferrer I, Zerr I. Llorens F, et al. Among authors: zafar s. Acta Neuropathol Commun. 2017 Apr 27;5(1):35. doi: 10.1186/s40478-017-0431-y. Acta Neuropathol Commun. 2017. PMID: 28449707 Free PMC article.
Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Schmitz M, Lüllmann K, Zafar S, Ebert E, Wohlhage M, Oikonomou P, Schlomm M, Mitrova E, Beekes M, Zerr I. Schmitz M, et al. Among authors: zafar s. Neurobiol Aging. 2014 May;35(5):1177-88. doi: 10.1016/j.neurobiolaging.2013.11.010. Epub 2013 Nov 16. Neurobiol Aging. 2014. PMID: 24360565
Characteristic CSF prion seeding efficiency in humans with prion diseases.
Cramm M, Schmitz M, Karch A, Zafar S, Varges D, Mitrova E, Schroeder B, Raeber A, Kuhn F, Zerr I. Cramm M, et al. Among authors: zafar s. Mol Neurobiol. 2015 Feb;51(1):396-405. doi: 10.1007/s12035-014-8709-6. Epub 2014 May 9. Mol Neurobiol. 2015. PMID: 24809690 Free PMC article.
1,180 results