Amyloid oligomers: spectroscopic characterization of amyloidogenic protein states.
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The extreme N-terminal region of human apolipoprotein A-I has a strong propensity to form amyloid fibrilsInactivation of VCP/ter94 suppresses retinal pathology caused by misfolded rhodopsin in DrosophilaNon-conjugated small molecule FRET for differentiating monomers from higher molecular weight amyloid beta speciesMethylated BSA mimics amyloid-related proteins and triggers inflammationEarly amyloidogenic oligomerization studied through fluorescence lifetime correlation spectroscopy.Techniques for Monitoring Protein Misfolding and Aggregation in Vitro and in Living CellsEvaluating nuclei concentration in amyloid fibrillation reactions using back-calculation approach.Intrinsically disordered and aggregation prone regions underlie β-aggregation in S100 proteins.Structural transitions and interactions in the early stages of human glucagon amyloid fibrillationThe Toxic Effects of Pathogenic Ataxin-3 Variants in a Yeast Cellular ModelSupramolecular non-amyloid intermediates in the early stages of α-synuclein aggregation.Dual role of an N-terminal amyloidogenic mutation in apolipoprotein A-I: destabilization of helix bundle and enhancement of fibril formation.Protein fibrillation and nanoparticle interactions: opportunities and challenges.Prion protein oligomer and its neurotoxicity.Progress in the treatment of small fiber peripheral neuropathy.Considerably Unfolded Transthyretin Monomers Preceed and Exchange with Dynamically Structured Amyloid Protofibrils.Gold complexes inhibit the aggregation of prion neuropeptides.Nanoscale Structure and Spectroscopic Probing of Aβ1-40 Fibril Bundle FormationUsing molecular rotors to probe gelation.Imaging nanometer-sized α-synuclein aggregates by superresolution fluorescence localization microscopy.Nanoscopic and photonic ultrastructural characterization of two distinct insulin amyloid states.Lysozyme Mutants Accumulate in Cells while Associated at their N-terminal Alpha-domain with the Endoplasmic Reticulum Chaperone GRP78/BiP.The impact of solubility and electrostatics on fibril formation by the H3 and H4 histones.Detection of prion protein oligomers by single molecule fluorescence imaging.Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CII.Pre-aggregation kinetics and intermediates of α-synuclein monitored by the ESIPT probe 7MFE.Anthoxanthin Polyphenols Attenuate Aβ Oligomer-induced Neuronal Responses Associated with Alzheimer's Disease.Specific in situ discrimination of amyloid fibrils versus α-helical fibres by the fluorophore NIAD-4.A peptide probe for detection of various beta-amyloid oligomers.Spectroscopic Investigations of Pentobarbital Interaction with Transthyretin
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Amyloid oligomers: spectroscopic characterization of amyloidogenic protein states.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 09 February 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
Amyloid oligomers: spectroscopic characterization of amyloidogenic protein states.
@en
Amyloid oligomers: spectroscopic characterization of amyloidogenic protein states.
@nl
type
label
Amyloid oligomers: spectroscopic characterization of amyloidogenic protein states.
@en
Amyloid oligomers: spectroscopic characterization of amyloidogenic protein states.
@nl
prefLabel
Amyloid oligomers: spectroscopic characterization of amyloidogenic protein states.
@en
Amyloid oligomers: spectroscopic characterization of amyloidogenic protein states.
@nl
P2860
P1433
P1476
Amyloid oligomers: spectroscopic characterization of amyloidogenic protein states
@en
P2093
Mikael Lindgren
P2860
P304
P356
10.1111/J.1742-4658.2010.07571.X
P407
P577
2010-02-09T00:00:00Z