Human apolipoprotein A-I natural variants: molecular mechanisms underlying amyloidogenic propensity

Human apolipoprotein A-I natural variants: molecular mechanisms underlying amyloidogenic propensity

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http://www.wikidata.org/entity/Q28482893
Amyloidogenic mutations in human apolipoprotein A-I are not necessarily destabilizing - a common mechanism of apolipoprotein A-I misfolding in familial amyloidosis and atherosclerosisAmyloidogenic propensity of a natural variant of human apolipoprotein A-I: stability and interaction with ligandsStructural and Functional Analysis of the ApolipoproteinA-I A164S VariantInsight into the Protein Composition of Immunoglobulin Light Chain Deposits of Eyelid, Orbital and Conjunctival Amyloidosis.Binding of human apoA-I[K107del] variant to TG-rich particles: implications for mechanisms underlying hypertriglyceridemia.Structural Stability and Local Dynamics in Disease-Causing Mutants of Human Apolipoprotein A-I: What Makes the Protein Amyloidogenic?Dual role of an N-terminal amyloidogenic mutation in apolipoprotein A-I: destabilization of helix bundle and enhancement of fibril formation.Amyloid-Forming Properties of Human Apolipoproteins: Sequence Analyses and Structural InsightsCharacterization of a human apolipoprotein a-I construct expressed in a bacterial system.Effects of the Iowa and Milano mutations on apolipoprotein A-I structure and dynamics determined by hydrogen exchange and mass spectrometry.Renal ApoA-1 amyloidosis with Glu34Lys mutation and intra-amyloid lipid accumulation.Learning from Synthetic Models of Extracellular Matrix; Differential Binding of Wild Type and Amyloidogenic Human Apolipoprotein A-I to Hydrogels Formed from Molecules Having Charges Similar to Those Found in Natural GAGs.Triglyceride increase in the core of high-density lipoproteins augments apolipoprotein dissociation from the surface: Potential implications for treatment of apolipoprotein deposition diseases.Epigallocatechin-3-gallate remodels apolipoprotein A-I amyloid fibrils into soluble oligomers in the presence of heparin
P2860

Human apolipoprotein A-I natural variants: molecular mechanisms underlying amyloidogenic propensity

Item
http://www.wikidata.org/entity/Q28482893
description
2012 nî lūn-bûn
@nan
2012 թուականին հրատարակուած գիտական յօդուած
@hyw
2012 թվականին հրատարակված գիտական հոդված
@hy
2012年の論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年论文
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name
Human apolipoprotein A-I natur ...... lying amyloidogenic propensity
@ast
Human apolipoprotein A-I natur ...... lying amyloidogenic propensity
@en
Human apolipoprotein A-I natur ...... lying amyloidogenic propensity
@nl
type
label
Human apolipoprotein A-I natur ...... lying amyloidogenic propensity
@ast
Human apolipoprotein A-I natur ...... lying amyloidogenic propensity
@en
Human apolipoprotein A-I natur ...... lying amyloidogenic propensity
@nl
prefLabel
Human apolipoprotein A-I natur ...... lying amyloidogenic propensity
@ast
Human apolipoprotein A-I natur ...... lying amyloidogenic propensity
@en
Human apolipoprotein A-I natur ...... lying amyloidogenic propensity
@nl
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Human apolipoprotein A-I natur ...... lying amyloidogenic propensity
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P2860
P304
P31
P356
10.1371/JOURNAL.PONE.0043755
P407
P433
P478
P50
P577
P5875
P698
P932