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Identification of new molecular alterations in fatal familial insomnia.
Llorens F, Thüne K, Schmitz M, Ansoleaga B, Frau-Méndez MA, Cramm M, Tahir W, Gotzmann N, Berjaoui S, Carmona M, Silva CJ, Fernandez-Vega I, José Zarranz J, Zerr I, Ferrer I. Llorens F, et al. Hum Mol Genet. 2016 Jun 15;25(12):2417-2436. doi: 10.1093/hmg/ddw108. Epub 2016 Apr 7. Hum Mol Genet. 2016. PMID: 27056979
Hereditary Human Prion Diseases: an Update.
Schmitz M, Dittmar K, Llorens F, Gelpi E, Ferrer I, Schulz-Schaeffer WJ, Zerr I. Schmitz M, et al. Among authors: llorens f. Mol Neurobiol. 2017 Aug;54(6):4138-4149. doi: 10.1007/s12035-016-9918-y. Epub 2016 Jun 20. Mol Neurobiol. 2017. PMID: 27324792 Free article. Review.
Molecular Alterations in the Cerebellum of Sporadic Creutzfeldt-Jakob Disease Subtypes with DJ-1 as a Key Regulator of Oxidative Stress.
Tahir W, Zafar S, Llorens F, Arora AS, Thüne K, Schmitz M, Gotzmann N, Kruse N, Mollenhauer B, Torres JM, Andréoletti O, Ferrer I, Zerr I. Tahir W, et al. Among authors: llorens f. Mol Neurobiol. 2018 Jan;55(1):517-537. doi: 10.1007/s12035-016-0294-4. Epub 2016 Dec 14. Mol Neurobiol. 2018. PMID: 27975168 Free article.
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. 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.
134 results