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Biorxiv : the Preprint Server for Biology|January 7, 2026
Lysosomal escape and TMEM106B fibrillar core determine TDP-43 seeding outcomesWeijia Zhong, Carlo Scialò, Beatrice Gatta, 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.
Scientific Reports|October 27, 2017
Split GFP technologies to structurally characterize and quantify functional biomolecular interactions of FTD-related proteinsChiara Foglieni, Stéphanie Papin, Agnese Salvadè, et al.
Protein Science : a Publication of the Protein Society|October 5, 2019
Transition of the prion protein from a structured cellular form (PrPC ) to the infectious scrapie agent (PrPSc )Pravas K Baral, Jiang Yin, Adriano Aguzzi, et al.
The FEBS Journal|March 24, 2018
Structural characterization of POM6 Fab and mouse prion protein complex identifies key regions for prions conformational conversionPravas Kumar Baral, Mridula Swayampakula, Adriano Aguzzi, et al.
HFSP Journal|May 14, 2009
Chemical and biophysical insights into the propagation of prion strainsJeppe Falsig, K Peterr Nilsson, Tuomas P J Knowles, et al.
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