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EMBO Molecular Medicine|July 22, 2021
Loss of PIKfyve drives the spongiform degeneration in prion diseasesAsvin K K Lakkaraju, Karl Frontzek, Emina Lemes, et al.Stroke|March 16, 2021
Observation of Collagen-Containing Lesions After Hematoma Resolution in Intracerebral HemorrhageChristopher J Love, Daniel Kirschenbaum, Magdy Selim, et al.Nature|February 14, 2024
A model of human neural networks reveals NPTX2 pathology in ALS and FTLDMarian Hruska-Plochan, Vera I Wiersma, Katharina M Betz, et al.Journal of Proteome Research|August 24, 2018
Biology/Disease-Driven Initiative on Protein-Aggregation Diseases of the Human Proteome Project: Goals and Progress to DatePaul J Boersema, Andre Melnik, Bouke P C Hazenberg, et al.The EMBO Journal|July 12, 2002
Absence of the prion protein homologue Doppel causes male sterilityAxel Behrens, Nicolas Genoud, Heike Naumann, et al.Journal of Neurochemistry|May 13, 2020
The uptake of tau amyloid fibrils is facilitated by the cellular prion protein and hampers prion propagation in cultured cellsElena De Cecco, Luigi Celauro, Silvia Vanni, et al.Prion|December 5, 2015
Iatrogenic and sporadic Creutzfeldt-Jakob disease in 2 sisters without mutation in the prion protein geneKarl Frontzek, Rita Moos, Elke Schaper, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 13, 2005
Truncated prion protein and Doppel are myelinotoxic in the absence of oligodendrocytic PrPCIvan Radovanovic, Nathalie Braun, Olivier T Giger, et al.Plos Pathogens|March 26, 2011
The strain-encoded relationship between PrP replication, stability and processing in neurons is predictive of the incubation period of diseaseJacob I Ayers, Charles R Schutt, Ronald A Shikiya, et al.Oncogene|April 6, 2004
IL-6 is required for glioma development in a mouse modelJakob Weissenberger, Sébastien Loeffler, Andreas Kappeler, et al.Pageof 39