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Systematic in vivo analysis of the intrinsic determinants of amyloid Beta pathogenicityPredicting the conformations of peptides and proteins in early evolution. A review article submitted to Biology DirectNMR derived model of GTPase effector domain (GED) self association: relevance to dynamin assemblyFluorescent Proteins as Biomarkers and Biosensors: Throwing Color Lights on Molecular and Cellular ProcessesDeficiency of disulfide bonds facilitating fibrillogenesis of endostatinStructural features of proinsulin C-peptide oligomeric and amyloid statesLoss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegiaProteins of the endoplasmic-reticulum-associated degradation pathway: domain detection and function predictionValidity of Gō models: comparison with a solvent-shielded empirical energy decomposition.Spatial protein quality control and the evolution of lineage-specific ageingCharacterization of the native and fibrillar conformation of the human Nalpha-acetyltransferase ARD1Amyloid associated with elastin-staining laminar aggregates in the lungs of patients diagnosed with acute respiratory distress syndromeDissection and design of yeast prionsMonitoring protein stability in vivoPrediction of "hot spots" of aggregation in disease-linked polypeptidesMolecular signaling involving intrinsically disordered proteins in prostate cancerProtein Folding and Mechanisms of ProteostasisPhysicochemical properties of cells and their effects on intrinsically disordered proteins (IDPs)Assessing the causes and consequences of co-polymerization in amyloid formationFibrillogenesis of huntingtin and other glutamine containing proteinsLocal order in the unfolded state: conformational biases and nearest neighbor interactionsExploring the accessible conformations of N-terminal acetylated α-synucleinSelf-propagation of pathogenic protein aggregates in neurodegenerative diseasesWrecked regulation of intrinsically disordered proteins in diseases: pathogenicity of deregulated regulatorsThe [RNQ+] prion: a model of both functional and pathological amyloidWhat macromolecular crowding can do to a proteinOligomerization of Peptides LVEALYL and RGFFYT and Their Binding Affinity to InsulinDesigned protein tetramer zipped together with a hydrophobic Alzheimer homology: A structural clue to amyloid assemblyLength-dependent stability and strand length limits in antiparallel -sheet secondary structureAltered Dimer Interface Decreases Stability in an Amyloidogenic ProteinStructural Alterations within Native Amyloidogenic Immunoglobulin Light ChainsAtomic structure and hierarchical assembly of a cross- amyloid fibrilStructural and mutational analysis of a monomeric and dimeric form of a single domain antibody with implications for protein misfoldingRebels with a cause: molecular features and physiological consequences of yeast prionsAn amyloid-forming peptide from the yeast prion Sup35 reveals a dehydrated beta-sheet structure for amyloidInteraction of the molecular chaperone DNAJB6 with growing amyloid-beta 42 (Aβ42) aggregates leads to sub-stoichiometric inhibition of amyloid formationDrugging the cancer kinome: progress and challenges in developing personalized molecular cancer therapeuticsAmyloidogenic hexapeptide fragment of medin: homology to functional islet amyloid polypeptide fragmentsInhibition of amyloid fibril formation by polyphenols: structural similarity and aromatic interactions as a common inhibition mechanismThe roles of turn formation and cross-strand interactions in fibrillization of peptides derived from the OspA single-layer beta-sheet
P2860
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P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Protein misfolding, evolution and disease
@ast
Protein misfolding, evolution and disease
@en
Protein misfolding, evolution and disease
@nl
type
label
Protein misfolding, evolution and disease
@ast
Protein misfolding, evolution and disease
@en
Protein misfolding, evolution and disease
@nl
prefLabel
Protein misfolding, evolution and disease
@ast
Protein misfolding, evolution and disease
@en
Protein misfolding, evolution and disease
@nl
P3181
P1476
Protein misfolding, evolution and disease
@en
P2093
C M Dobson
P304
P3181
P356
10.1016/S0968-0004(99)01445-0
P407
P577
1999-09-01T00:00:00Z