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- Currently displaying 2141 - 2160 of 2506 publications
“The Mechanism of Amyloid Formation and its Links to Human Disease and Biological Evolution”, in Self-Assembling Peptide Systems in Biology, Medicine and Engineering
(2001)
65
Dependence on solution conditions of aggregation and amyloid formation by an SH3 domain11Edited by P. E. Wright
Journal of molecular biology
(2001)
311
325
(doi: 10.1006/jmbi.2001.4858)
Protein folding and its links with human disease.
Biochem Soc Symp
(2001)
68
1
(doi: 10.1042/bss0680001)
Folding and aggregation are selectively influenced by the conformational preferences of the α-helices of muscle acylphosphatase
J Biol Chem
(2001)
276
37149
(doi: 10.1074/jbc.m105720200)
Preparation and characterization of purified amyloid fibrils [13]
Journal of the American Chemical Society
(2001)
123
8141
(doi: 10.1021/ja016229b)
Connectivity of neutral networks and structural conservation in protein evolution
J. Mol. Evol.
(2001)
56
243
Generalized comparative modeling (GENECOMP): A combination of sequence comparison, threading, and lattice modeling for protein structure prediction and refinement
Proteins Structure Function and Genetics
(2001)
44
133
(doi: 10.1002/prot.1080)
How to guarantee optimal stability for most representative structures in the protein data bank
Proteins Structure Function and Genetics
(2001)
44
79
(doi: 10.1002/prot.1075)
Amyloid fibril formation by a helical cytochrome.
FEBS letters
(2001)
495
184
Experimental landscapes for protein folding and misfolding.
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2001)
221
U392
Comparison of the structural and dynamical properties of holo and apo bovine alpha-lactalbumin by NMR spectroscopy.
J Mol Biol
(2001)
307
885
(doi: 10.1006/jmbi.2001.4530)
Detection of two partially structured species in the folding process of the amyloidogenic protein β2-microglobulin11Edited by C. R. Matthews
Journal of molecular biology
(2001)
307
379
(doi: 10.1006/jmbi.2000.4478)
Amyloid fibrils from muscle myoglobin. Even an ordinary globular protein can assume a rogue guise if conditions are right
Nature
(2001)
410
165
(doi: 10.1038/35065514)
From genetics to pathology: tau and alpha-synuclein assemblies in neurodegenerative diseases - Discussion
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
(2001)
356
227
Pathogenesis, diagnosis and treatment of systemic amyloidosis.
Philos Trans R Soc Lond B Biol Sci
(2001)
356
203
(doi: 10.1098/rstb.2000.0766)
The molecular biology of prion propagation
Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences
(2001)
356
185
(doi: 10.1098/rstb.2000.0764)
Investigating protein conformation-based inheritance and disease in yeast - Discussion
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES
(2001)
356
176
Investigating protein conformation-based inheritance and disease in yeast
Philosophical transactions of the Royal Society of London. Series B, Biological sciences
(2001)
356
169
(doi: 10.1098/rstb.2000.0762)
Prions and the lymphoreticular system - Discussion
PHILOS T R SOC B
(2001)
356
184
Pathogenesis, diagnosis and treatment of systemic amyloidosis - Discussion
PHILOS T ROY SOC B
(2001)
356
210
