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Journal of Mass Spectrometry : JMS|March 14, 2009
Hydrogen/deuterium exchange mass spectrometry identifies two highly protected regions in recombinant full-length prion protein amyloid fibrilsAlexis Nazabal, Simone Hornemann, Adriano Aguzzi, et al.
Science (New York, N.Y.)|January 12, 2013
Microglia: scapegoat, saboteur, or something else?Adriano Aguzzi, Ben A Barres, Mariko L Bennett
Journal of Molecular Neuroscience : MN|May 6, 2004
Current concepts and controversies in prion immunopathologyMathias Heikenwalder, Marco Prinz, Frank L Heppner, et al.
The Journal of Experimental Medicine|March 8, 2019
SARM1 deficiency up-regulates XAF1, promotes neuronal apoptosis, and accelerates prion diseaseCaihong Zhu, Bei Li, Karl Frontzek, et al.
Scientific Reports|October 4, 2018
Lymphocyte activation gene 3 (Lag3) expression is increased in prion infections but does not modify disease progressionYingjun Liu, Silvia Sorce, Mario Nuvolone, et al.
Journal of Virology|February 12, 2002
Chronic subclinical prion disease induced by low-dose inoculumAlana M Thackray, Michael A Klein, Adriano Aguzzi, et al.
Archives of Neurology|April 13, 2005
Human prion diseases: molecular and clinical aspectsMarkus Glatzel, Katharina Stoeck, Harald Seeger, et al.
Biological Chemistry|September 12, 2002
Analysis of the prion protein in primates reveals a new polymorphism in codon 226 (Y226F)Markus Glatzel, Vladimir Pekarik, Thorsten Lührs, et al.
Journal of Virology|June 16, 2005
Paracrine inhibition of prion propagation by anti-PrP single-chain Fv miniantibodiesGaetano Donofrio, Frank L Heppner, Magdalini Polymenidou, et al.
Protein Science : a Publication of the Protein Society|October 5, 2019
Transition of the prion protein from a structured cellular form (PrP<sup>C</sup> ) to the infectious scrapie agent (PrP<sup>Sc</sup> )Pravas K Baral, Jiang Yin, Adriano Aguzzi, et al.
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