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Scientific Reports|May 7, 2016
Rational design of mutations that change the aggregation rate of a protein while maintaining its native structure and stabilityCarlo Camilloni, Benedetta Maria Sala, Pietro Sormanni, et al.
Gastroenterology|May 8, 2004
Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian familiesLaura Obici, Giovanni Palladini, Sofia Giorgetti, et al.
Journal of Medicinal Chemistry|August 9, 2019
Binding of Monovalent and Bivalent Ligands by Transthyretin Causes Different Short- and Long-Distance Conformational ChangesAlessandra Corazza, Guglielmo Verona, Christopher A Waudby, et al.
Cells|March 11, 2023
The Protein Network in Subcutaneous Fat Biopsies from Patients with AL Amyloidosis: More Than Diagnosis?Dario Di Silvestre, Francesca Brambilla, Francesca Lavatelli, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|November 12, 2010
Embryonic stem and haematopoietic progenitor cells resist to Aβ oligomer toxicity and maintain the differentiation potency in cultureTui Neri, Monica Bucciantini, Vittorio Rosti, et al.
The Journal of Biological Chemistry|December 24, 2009
Native-unlike long-lived intermediates along the folding pathway of the amyloidogenic protein beta2-microglobulin revealed by real-time two-dimensional NMRAlessandra Corazza, Enrico Rennella, Paul Schanda, et al.
Molecular & Cellular Proteomics : MCP|May 14, 2008
Amyloidogenic and associated proteins in systemic amyloidosis proteome of adipose tissueFrancesca Lavatelli, David H Perlman, Brian Spencer, et al.
The Journal of Biological Chemistry|February 28, 2016
Co-fibrillogenesis of Wild-type and D76N β2-Microglobulin: THE CRUCIAL ROLE OF FIBRILLAR SEEDSAntonino Natalello, P Patrizia Mangione, Sofia Giorgetti, et al.
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