Kinetic theory of fibrillogenesis of amyloid beta-protein.
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Vitamin A and Alzheimer's diseaseAmyloid beta-protein monomer folding: free-energy surfaces reveal alloform-specific differencesDementia of the eye: the role of amyloid beta in retinal degenerationDynamics of the formation of a hydrogel by a pathogenic amyloid peptide: islet amyloid polypeptide.The rate and equilibrium constants for a multistep reaction sequence for the aggregation of superoxide dismutase in amyotrophic lateral sclerosisA mathematical model of the kinetics of beta-amyloid fibril growth from the denatured stateIn vitro studies of amyloid beta-protein fibril assembly and toxicity provide clues to the aetiology of Flemish variant (Ala692-->Gly) Alzheimer's diseaseStepwise dynamics of epitaxially growing single amyloid fibrils.Contrasting effects of nanoparticle-protein attraction on amyloid aggregationRole of phosphatidylinositol clathrin assembly lymphoid-myeloid leukemia (PICALM) in intracellular amyloid precursor protein (APP) processing and amyloid plaque pathogenesisCharacterization of oligomers of heterogeneous size as precursors of amyloid fibril nucleation of an SH3 domain: an experimental kinetics study.Induced beta-barrel formation of the Alzheimer's Abeta25-35 oligomers on carbon nanotube surfaces: implication for amyloid fibril inhibitionA single mutation in an SH3 domain increases amyloid aggregation by accelerating nucleation, but not by destabilizing thermodynamically the native state.Self-assembly of human latexin into amyloid-like oligomers.Ultrafast colorimetric determination of predominant protein structure evolution with gold nanoplasmonic particles.Structural differences between Abeta(1-40) intermediate oligomers and fibrils elucidated by proteolytic fragmentation and hydrogen/deuterium exchange.Role of aggregation conditions in structure, stability, and toxicity of intermediates in the Abeta fibril formation pathwayUltrasonic force microscopy for nanomechanical characterization of early and late-stage amyloid-β peptide aggregation.Structural classification of toxic amyloid oligomersMechanism of amyloid plaque formation suggests an intracellular basis of Abeta pathogenicity.Concentration effect on the aggregation of a self-assembling oligopeptide.Dynamic imaging by fluorescence correlation spectroscopy identifies diverse populations of polyglutamine oligomers formed in vivo.Simulation study of the structure and dynamics of the Alzheimer's amyloid peptide congener in solution.Kinetic control of dimer structure formation in amyloid fibrillogenesisA kinetic study of beta-lactoglobulin amyloid fibril formation promoted by urea.Biophysical studies of the development of amyloid fibrils from a peptide fragment of cold shock protein B.Polymorphic fibril formation by residues 10-40 of the Alzheimer's beta-amyloid peptide.Benchmarking implicit solvent folding simulations of the amyloid beta(10-35) fragmentAmyloid seeds formed by cellular uptake, concentration, and aggregation of the amyloid-beta peptide.Role of small oligomers on the amyloidogenic aggregation free-energy landscapeDynamics of protofibril elongation and association involved in Aβ42 peptide aggregation in Alzheimer's disease.In vitro polymerization of a functional Escherichia coli amyloid protein.Mathematical modeling for the pathogenesis of Alzheimer's disease.Simultaneous single-molecule fluorescence and conductivity studies reveal distinct classes of Abeta species on lipid bilayersAmyloid β Protein and Alzheimer's Disease: When Computer Simulations Complement Experimental Studies.Structure determination of micelle-like intermediates in amyloid beta -protein fibril assembly by using small angle neutron scatteringEnhancing astrocytic lysosome biogenesis facilitates Aβ clearance and attenuates amyloid plaque pathogenesisInsulin glycation by methylglyoxal results in native-like aggregation and inhibition of fibril formationEffects of the English (H6R) and Tottori (D7N) familial Alzheimer disease mutations on amyloid beta-protein assembly and toxicity.Therapeutic protein aggregation: mechanisms, design, and control.
P2860
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P2860
Kinetic theory of fibrillogenesis of amyloid beta-protein.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh
1997年學術文章
@zh-hant
name
Kinetic theory of fibrillogenesis of amyloid beta-protein.
@ast
Kinetic theory of fibrillogenesis of amyloid beta-protein.
@en
type
label
Kinetic theory of fibrillogenesis of amyloid beta-protein.
@ast
Kinetic theory of fibrillogenesis of amyloid beta-protein.
@en
prefLabel
Kinetic theory of fibrillogenesis of amyloid beta-protein.
@ast
Kinetic theory of fibrillogenesis of amyloid beta-protein.
@en
P2093
P2860
P356
P1476
Kinetic theory of fibrillogenesis of amyloid beta-protein.
@en
P2093
D A Kirschner
D B Teplow
G B Benedek
P2860
P304
P356
10.1073/PNAS.94.15.7942
P407
P577
1997-07-01T00:00:00Z