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Centre for Misfolding Diseases

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  • Currently displaying 2661 - 2680 of 3366 publications
Dynamic Visions of Enzymatic Reactions
M Vendruscolo, CM Dobson
– Science (New York, N.Y.)
(2006)
313,
1586
Sequence and structural determinants of amyloid fibril formation.
F Bemporad, G Calloni, S Campioni, G Plakoutsi, N Taddei, F Chiti
– Acc Chem Res
(2006)
39,
620
Ray scattering study of the effect of hydration on the cross-beta structure of amyloid fibrils
AM Squires, GL Devlin, SL Gras, AK Tickler, CE MacPhee, CM Dobson
– J Am Chem Soc
(2006)
128,
11738
Identification of the core structure of lysozyme amyloid fibrils by proteolysis.
E Frare, MF Mossuto, P Polverino de Laureto, M Dumoulin, CM Dobson, A Fontana
– Journal of Molecular Biology
(2006)
361,
551
Prefibrillar Amyloid Aggregates Could Be Generic Toxins in Higher Organisms
S Baglioni, F Casamenti, M Bucciantini, LM Luheshi, N Taddei, F Chiti, CM Dobson, M Stefani
– The Journal of neuroscience : the official journal of the Society for Neuroscience
(2006)
26,
8160
Protein misfolding, functional amyloid, and human disease.
F Chiti, CM Dobson
– Annual Review of Biochemistry
(2006)
75,
333
The native-state ensemble of proteins provides clues for folding, misfolding and function
N Cremades, J Sancho, E Freire
– Trends in biochemical sciences
(2006)
31,
494
Protein unfolding, amyloid fibril formation and configurational energy landscapes under high pressure conditions.
F Meersman, CM Dobson, K Heremans
– Chemical Society reviews
(2006)
35,
908
Characterization of the residual structure in the unfolded state of the Delta131Delta fragment of staphylococcal nuclease.
CJ Francis, K Lindorff-Larsen, RB Best, M Vendruscolo
– Proteins: Structure, Function, and Bioinformatics
(2006)
65,
145
Normal and aberrant biological self-assembly: Insights from studies of human lysozyme and its amyloidogenic variants.
M Dumoulin, JR Kumita, CM Dobson
– Accounts of Chemical Research
(2006)
39,
603
Relation between native ensembles and experimental structures of proteins
RB Best, K Lindorff-Larsen, MA DePristo, M Vendruscolo
– Proceedings of the National Academy of Sciences
(2006)
103,
10901
Absence of p300 induces cellular phenotypic changes characteristic of epithelial to mesenchyme transition
D Krubasik, NG Iyer, WR English, AA Ahmed, M Vias, C Roskelley, JD Brenton, C Caldas, G Murphy
– British Journal of Cancer
(2006)
95,
245
Relation between native ensembles and experimental structures of proteins
RB Best, K Lindorff-Larsen, MA DePristo, M Vendruscolo
– Proceedings of the National Academy of Sciences of the United States of America
(2006)
103,
10901
Loss of the extracellular matrix protein TGFBI induces clinical paclitaxel resistance, mitotic spindle abnormalities and centrosome amplification
AA Ahmed, AD Mills, C Blenkiron, CE Massie, M Vias, N Gopalakrishna, R Crawford, H Earl, R Laskey, C Caldas, JD Brenton
– BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY
(2006)
113,
862
“The Generic Nature of Protein Folding and Misfolding”, in Protein misfolding, aggregation and conformational diseases
CM Dobson
(2006)
21
Spatial persistence of angular correlations in amyloid fibrils
TPJ Knowles, JF Smith, A Craig, CM Dobson, ME Welland
– Phys Rev Lett
(2006)
96,
238301
Enhanced Stability of Human Prion Proteins with Two Disulfide Bridges
TPJ Knowles, R Zahn
– Biophys J
(2006)
91,
1494
The direct formation of glycosyl thiols from reducing sugars allows one-pot protein glycoconjugation.
GJL Bernardes, DP Gamblin, BG Davis
– Angewandte Chemie International Edition
(2006)
45,
4007
Exploring the mechanism of formation of native-like and precursor amyloid oligomers for the native acylphosphatase from Sulfolobus solfataricus.
G Plakoutsi, F Bemporad, M Monti, D Pagnozzi, P Pucci, F Chiti
– Structure
(2006)
14,
993
A protein evolution model with independent sites that reproduces site-specific amino acid distributions from the Protein Data Bank.
U Bastolla, M Porto, HE Roman, M Vendruscolo
– BMC evolutionary biology
(2006)
6,
43