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EMBO Molecular Medicine|August 20, 2015
A novel mechano-enzymatic cleavage mechanism underlies transthyretin amyloidogenesisJulien Marcoux, P Patrizia Mangione, Riccardo Porcari, et al.Journal of Molecular Biology|February 8, 2011
Effects of the known pathogenic mutations on the aggregation pathway of the amyloidogenic peptide of apolipoprotein A-ISara Raimondi, Fulvio Guglielmi, Sofia Giorgetti, et al.The Journal of Biological Chemistry|September 10, 2013
Structure, folding dynamics, and amyloidogenesis of D76N β2-microglobulin: roles of shear flow, hydrophobic surfaces, and α-crystallinP Patrizia Mangione, Gennaro Esposito, Annalisa Relini, et al.Proceedings of the National Academy of Sciences of the United States of America|January 30, 2014
Proteolytic cleavage of Ser52Pro variant transthyretin triggers its amyloid fibrillogenesisP Patrizia Mangione, Riccardo Porcari, Julian D Gillmore, et al.Scientific Reports|April 22, 2017
A specific nanobody prevents amyloidogenesis of D76N β<sub>2</sub>-microglobulin in vitro and modifies its tissue distribution in vivoSara Raimondi, Riccardo Porcari, P Patrizia Mangione, et al.The New England Journal of Medicine|June 15, 2012
Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulinSophie Valleix, Julian D Gillmore, Frank Bridoux, et al.Nature Communications|January 22, 2016
D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profileSophie Valleix, Guglielmo Verona, Noémie Jourde-Chiche, et al.Journal of the American Chemical Society|August 8, 2014
Rapid proton-detected NMR assignment for proteins with fast magic angle spinningEmeline Barbet-Massin, Andrew J Pell, Joren S Retel, et al.Pageof 5