Inhibition of heparin-induced tau filament formation by phenothiazines, polyphenols, and porphyrins.
about
Alzheimer mechanisms and therapeutic strategiesGSPE interferes with tau aggregation in vivo: implication for treating tauopathyEffects of grape seed-derived polyphenols on amyloid beta-protein self-assembly and cytotoxicityTau-Centric Targets and Drugs in Clinical Development for the Treatment of Alzheimer's DiseaseNMR Meets Tau: Insights into Its Function and PathologyMolecular Mechanisms in the Pathogenesis of Alzheimer's disease and Tauopathies-Prion-Like Seeded Aggregation and PhosphorylationDiverse molecular targets for therapeutic strategies in Alzheimer's diseaseDye-binding assays for evaluation of the effects of small molecule inhibitors on amyloid (aβ) self-assemblyThe Role of MAPT in Neurodegenerative Diseases: Genetics, Mechanisms and TherapyModulating self-assembly of amyloidogenic proteins as a therapeutic approach for neurodegenerative diseases: strategies and mechanismsMethylene blue reduced abnormal tau accumulation in P301L tau transgenic miceIdentification of Small Molecule Inhibitors of Tau Aggregation by Targeting Monomeric Tau As a Potential Therapeutic Approach for TauopathiesSecondary Metabolites in Ramalina terebrata Detected by UHPLC/ESI/MS/MS and Identification of Parietin as Tau Protein InhibitorMethylene Blue (Tetramethylthionine Chloride) Influences the Mobility of Adult Neural Stem Cells: A Potentially Novel Therapeutic Mechanism of a Therapeutic Approach in the Treatment of Alzheimer's Disease.Structural determinants of Tau aggregation inhibitor potencyNucleation-dependent tau filament formation: the importance of dimerization and an estimation of elementary rate constantsPhenothiazine-mediated rescue of cognition in tau transgenic mice requires neuroprotection and reduced soluble tau burden.Preventive methylene blue treatment preserves cognition in mice expressing full-length pro-aggregant human Tau.Molecular mechanisms for Alzheimer's disease: implications for neuroimaging and therapeutics.High throughput screening for small molecule inhibitors of heparin-induced tau fibril formation.In silico theoretical molecular modeling for Alzheimer's disease: the nicotine-curcumin paradigm in neuroprotection and neurotherapy.Tau-directed drug discovery for Alzheimer's disease and related tauopathies: a focus on tau assembly inhibitors.Discovery of brain-penetrant, orally bioavailable aminothienopyridazine inhibitors of tau aggregation.cis-Glyco-fused benzopyran compounds as new amyloid-β peptide ligands.Structure activity relationship of phenolic acid inhibitors of α-synuclein fibril formation and toxicityAn aggregation sensing reporter identifies leflunomide and teriflunomide as polyglutamine aggregate inhibitors.Sodium selenate mitigates tau pathology, neurodegeneration, and functional deficits in Alzheimer's disease modelsDevelopment of a grape seed polyphenolic extract with anti-oligomeric activity as a novel treatment in progressive supranuclear palsy and other tauopathiesDefective protein folding and aggregation as the basis of neurodegenerative diseases: the darker aspect of proteins.Effects of Various Flavonoids on the α-Synuclein Fibrillation Process.Structure of core domain of fibril-forming PHF/Tau fragments.Cellular and molecular actions of Methylene Blue in the nervous systemMethylene blue modulates β-secretase, reverses cerebral amyloidosis, and improves cognition in transgenic mice.Microtubule-associated protein tau as a therapeutic target in neurodegenerative disease.Naturally occurring multipotent anti-Alzheimer's agents.Resveratrol inhibits the formation of multiple-layered β-sheet oligomers of the human islet amyloid polypeptide segment 22-27Structure and mechanism of action of tau aggregation inhibitors.Simultaneous quantification of methylene blue and its major metabolite, azure B, in plasma by LC-MS/MS and its application for a pharmacokinetic study.PE859, a novel tau aggregation inhibitor, reduces aggregated tau and prevents onset and progression of neural dysfunction in vivo.Promoting autophagic clearance: viable therapeutic targets in Alzheimer's disease.
P2860
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P2860
Inhibition of heparin-induced tau filament formation by phenothiazines, polyphenols, and porphyrins.
description
2004 nî lūn-bûn
@nan
2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Inhibition of heparin-induced ...... , polyphenols, and porphyrins.
@ast
Inhibition of heparin-induced ...... , polyphenols, and porphyrins.
@en
Inhibition of heparin-induced ...... , polyphenols, and porphyrins.
@nl
type
label
Inhibition of heparin-induced ...... , polyphenols, and porphyrins.
@ast
Inhibition of heparin-induced ...... , polyphenols, and porphyrins.
@en
Inhibition of heparin-induced ...... , polyphenols, and porphyrins.
@nl
prefLabel
Inhibition of heparin-induced ...... , polyphenols, and porphyrins.
@ast
Inhibition of heparin-induced ...... , polyphenols, and porphyrins.
@en
Inhibition of heparin-induced ...... , polyphenols, and porphyrins.
@nl
P2093
P2860
P356
P1476
Inhibition of heparin-induced ...... , polyphenols, and porphyrins.
@en
P2093
Masami Masuda
Masato Hasegawa
Michel Goedert
Nobuyuki Suzuki
Sayuri Taniguchi
Shin-ichi Hisanaga
Takeshi Iwatsubo
P2860
P304
P356
10.1074/JBC.M408714200
P407
P577
2004-12-17T00:00:00Z