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The American Journal of Pathology|March 26, 2003
Oral prion infection requires normal numbers of Peyer's patches but not of enteric lymphocytesMarco Prinz, Gerhard Huber, Andrew J S Macpherson, et al.Plos One|November 19, 2010
Preclinical deposition of pathological prion protein in muscle of experimentally infected primatesSusanne Krasemann, Melanie Neumann, Markus Geissen, et al.Brain Pathology (Zurich, Switzerland)|November 4, 2022
Rapid ex vivo reverse genetics identifies the essential determinants of prion protein toxicityRegina R Reimann, Martina Puzio, Antonella Rosati, et al.Plos Pathogens|November 8, 2012
Prion pathogenesis is faithfully reproduced in cerebellar organotypic slice culturesJeppe Falsig, Tiziana Sonati, Uli S Herrmann, et al.Journal of the American Chemical Society|November 15, 2024
Structural Insights into the Mechanism of a Polyketide Synthase Thiocysteine Lyase DomainAndrew D Steele, Song Meng, Gengnan Li, et al.Cell Reports|January 12, 2022
Mice hypomorphic for Pitx3 show robust entrainment of circadian behavioral and metabolic rhythms to scheduled feedingLori L Scarpa, Brad Wanken, Marten Smidt, et al.Plos One|February 8, 2021
Type 1 dopamine receptor (D1R)-independent circadian food anticipatory activity in miceDina R Assali, Michael Sidikpramana, Andrew P Villa, et al.Haematologica|August 3, 2019
Prion protein deficiency impairs hematopoietic stem cell determination and sensitizes myeloid progenitors to irradiationCapucine Siberchicot, Nathalie Gault, Nathalie Déchamps, et al.The EMBO Journal|January 25, 2007
Lethal recessive myelin toxicity of prion protein lacking its central domainFrank Baumann, Markus Tolnay, Christine Brabeck, et al.Bio-Protocol|September 20, 2021
Efficient Generation of Multi-gene Knockout Cell Lines and Patient-derived Xenografts Using Multi-colored Lenti-CRISPR-Cas9Lena Behrmann, Scott McComb, Júlia Aguadé-Gorgorió, et al.Pageof 41