Showing 21 - 40 results of 3,228 for search '"prion"', query time: 0.14s Refine Results
  1. 21

    Etymologia: Prion by Nancy Männikkö

    Published 2012-01-01
    Subjects:
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    Prion replication environment defines the fate of prion strain adaptation. by Elizaveta Katorcha, Nuria Gonzalez-Montalban, Natallia Makarava, Gabor G Kovacs, Ilia V Baskakov

    Published 2018-06-01
    “…The main risk of emergence of prion diseases in humans is associated with a cross-species transmission of prions of zoonotic origin. …”
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    Early preclinical detection of prions in the skin of prion-infected animals by Zerui Wang, Matteo Manca, Aaron Foutz, Manuel V. Camacho, Gregory J. Raymond, Brent Race, Christina D. Orru, Jue Yuan, Pingping Shen, Baiya Li, Yue Lang, Johnny Dang, Alise Adornato, Katie Williams, Nicholas R. Maurer, Pierluigi Gambetti, Bin Xu, Witold Surewicz, Robert B. Petersen, Xiaoping Dong, Brian S. Appleby, Byron Caughey, Li Cui, Qingzhong Kong, Wen-Quan Zou

    Published 2019-01-01
    “…There are currently no validated methods for the diagnosis of prion disease at the preclinical stage. Here the authors show that serial protein misfolding cyclic amplification and real-time quaking-induced conversion can be used to detect prions in the skin of prion-inoculated hamsters and humanized transgenic mice at early preclinical stages.…”
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    Neurotoxic Antibodies against the Prion Protein Do Not Trigger Prion Replication. by Karl Frontzek, Manuela Pfammatter, Silvia Sorce, Assunta Senatore, Petra Schwarz, Rita Moos, Katrin Frauenknecht, Simone Hornemann, Adriano Aguzzi

    Published 2016-01-01
    “…Antibodies targeting the globular domain (GD) of the cellular prion protein PrPC trigger a neurotoxic syndrome morphologically and molecularly similar to prion disease. …”
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    Human prion diseases and the prion protein – what is the current state of knowledge? by Nafe Reinhold, Arendt Christophe T., Hattingen Elke

    Published 2023-10-01
    “…Prion diseases and the prion protein are only partially understood so far in many aspects. …”
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  15. 35

    Glycoform-selective prion formation in sporadic and familial forms of prion disease. by Xiangzhu Xiao, Jue Yuan, Stéphane Haïk, Ignazio Cali, Yian Zhan, Mohammed Moudjou, Baiya Li, Jean-Louis Laplanche, Hubert Laude, Jan Langeveld, Pierluigi Gambetti, Tetsuyuki Kitamoto, Qingzhong Kong, Jean-Philippe Brandel, Brian A Cobb, Robert B Petersen, Wen-Quan Zou

    Published 2013-01-01
    “…The four glycoforms of the cellular prion protein (PrP(C)) variably glycosylated at the two N-linked glycosylation sites are converted into their pathological forms (PrP(Sc)) in most cases of sporadic prion diseases. …”
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