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Infectious Disorders Drug Targets|February 10, 2009
Therapy in prion diseases: from molecular and cellular biology to therapeutic targetsCarmen Krammer, Ina Vorberg, Hermann M Schätzl, et al.Journal of Virology|January 15, 2003
Multiple amino acid residues within the rabbit prion protein inhibit formation of its abnormal isoformIna Vorberg, Martin H Groschup, Eberhard Pfaff, et al.Viruses|January 24, 2013
Cellular aspects of prion replication in vitroAndrea Grassmann, Hanna Wolf, Julia Hofmann, et al.Cellular and Molecular Life Sciences : CMLS|October 14, 2009
Inhibition of cholesterol recycling impairs cellular PrP(Sc) propagationSabine Gilch, Christian Bach, Gloria Lutzny, et al.Plos One|September 13, 2011
Effect of hydrophobic mutations in the H2-H3 subdomain of prion protein on stability and conversion in vitro and in vivoIva Hafner-Bratkovič, Lars Gaedtke, Andrej Ondracka, et al.The FEBS Journal|March 30, 2010
Tetracysteine-tagged prion protein allows discrimination between the native and converted formsJernej Gaspersic, Iva Hafner-Bratkovic, Michel Stephan, et al.The Biochemical Journal|August 18, 2017
Genetic human prion disease modelled in PrP transgenic <i>Drosophila</i>Alana M Thackray, Alzbeta Cardova, Hanna Wolf, et al.The Biochemical Journal|July 8, 2014
Prion-induced and spontaneous formation of transmissible toxicity in PrP transgenic DrosophilaAlana M Thackray, Ying Di, Chang Zhang, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 12, 2007
Prion protein/protein interactions: fusion with yeast Sup35p-NM modulates cytosolic PrP aggregation in mammalian cellsCarmen Krammer, Michael H Suhre, Elisabeth Kremmer, et al.Molecular Neurobiology|March 17, 2018
Endoplasmic Reticulum Stress Induces Myostatin High Molecular Weight Aggregates and Impairs Mature Myostatin SecretionRishibha Sachdev, Karin Kappes-Horn, Lydia Paulsen, et al.Pageof 4