Authors:
Lashuel, HA
LaBrenz, SR
Woo, L
Serpell, LC
Kelly, JW
Citation: Ha. Lashuel et al., Protofilaments, filaments, ribbons, and fibrils from peptidomimetic self-assembly: Implications for amyloid fibril formation and materials science, J AM CHEM S, 122(22), 2000, pp. 5262-5277
Authors:
Baures, PW
Oza, VB
Peterson, SA
Kelly, JW
Citation: Pw. Baures et al., Synthesis and evaluation of inhibitors of transthyretin amyloid formation based on the non-steroidal anti-inflammatory drug, flufenamic acid, BIO MED CH, 7(7), 1999, pp. 1339-1347
Authors:
Chitnumsub, P
Fiori, WR
Lashuel, HA
Diaz, H
Kelly, JW
Citation: P. Chitnumsub et al., The nucleation of monomeric parallel beta-sheet-like structures and their self-assembly in aqueous solution, BIO MED CH, 7(1), 1999, pp. 39-59
Authors:
Koepf, EK
Petrassi, HM
Sudol, M
Kelly, JW
Citation: Ek. Koepf et al., WW: An isolated three-stranded antiparallel beta-sheet domain that unfoldsand refolds reversibly; evidence for a structured hydrophobic cluster in urea and GdnHCl and a disordered thermal unfolded state, PROTEIN SCI, 8(4), 1999, pp. 841-853
Authors:
Koepf, EK
Petrassi, HM
Ratnaswamy, G
Huff, ME
Sudol, M
Kelly, JW
Citation: Ek. Koepf et al., Characterization of the structure and function of W -> FWW domain variants: Identification of a natively unfolded protein that folds upon ligand binding, BIOCHEM, 38(43), 1999, pp. 14338-14351
Citation: Ha. Lashuel et al., The most pathogenic transthyretin variant, L55P, forms amyloid fibrils under acidic conditions and protofilaments under physiological conditions, BIOCHEM, 38(41), 1999, pp. 13560-13573
Citation: Ha. Lashuel et al., Characterization of the transthyretin acid denaturation pathways by analytical ultracentrifugation: Implications for wild-type, V30M, and L55P amyloid fibril formation, BIOCHEM, 37(51), 1998, pp. 17851-17864