Biology and genetics of prions causing neurodegeneration
about
Unified theory of Alzheimer's disease (UTAD): implications for prevention and curative therapyMolecular Mechanisms in the Pathogenesis of Alzheimer's disease and Tauopathies-Prion-Like Seeded Aggregation and PhosphorylationSup35 methionine oxidation is a trigger for de novo [PSI(+)] prion formationNeurodegenerative diseases: expanding the prion conceptRepA-WH1, the agent of an amyloid proteinopathy in bacteria, builds oligomeric pores through lipid vesicles.Prenatal transmission of scrapie in sheep and goats: A case study for veterinary public healthThe bowel and beyond: the enteric nervous system in neurological disordersEmerging mechanisms of molecular pathology in ALSEngineering enhanced protein disaggregases for neurodegenerative diseaseTCTP contains a BH3-like domain, which instead of inhibiting, activates Bcl-xLAlzheimer Disease and Its Growing Epidemic: Risk Factors, Biomarkers, and the Urgent Need for Therapeutics.Review: A review on classical and atypical scrapie in caprine: Prion protein gene polymorphisms and their role in the disease.Aβ seeds resist inactivation by formaldehydeFuture Directions in Imaging Neurodegeneration.The Malignant Protein Puzzle.Formation and spreading of TDP-43 aggregates in cultured neuronal and glial cells demonstrated by time-lapse imaging.Genotype-dependent molecular evolution of sheep bovine spongiform encephalopathy (BSE) prions in vitro affects their zoonotic potentialPrion-like nanofibrils of small molecules (PriSM) selectively inhibit cancer cells by impeding cytoskeleton dynamicsNoncerebral Amyloidoses: Aspects on Seeding, Cross-Seeding, and Transmission.Transmission characteristics of variably protease-sensitive prionopathy.Synthetic Aβ peptides acquire prion-like properties in the brain.Glyphosate, pathways to modern diseases III: Manganese, neurological diseases, and associated pathologies.Nonsense codon suppression in fission yeast due to mutations of tRNA(Ser.11) and translation release factor Sup35 (eRF3).Peculiarities of prion diseasesA novel and rapid method for obtaining high titre intact prion strains from mammalian brain.Amyloid polymorphism: structural basis and neurobiological relevance.Functional role of Tia1/Pub1 and Sup35 prion domains: directing protein synthesis machinery to the tubulin cytoskeletonComparative Incidence of Conformational, Neurodegenerative Disorders.Prion-like transmission of neuronal huntingtin aggregates to phagocytic glia in the Drosophila brain.Progression of Seed-Induced Aβ Deposition within the Limbic ConnectomeAggregation of MBP in chronic demyelination.Prion Protein-Antibody Complexes Characterized by Chromatography-Coupled Small-Angle X-Ray Scattering.PrP charge structure encodes interdomain interactionsHsp40 function in yeast prion propagation: Amyloid diversity necessitates chaperone functional complexity.An insight into the complex prion-prion interaction network in the budding yeast Saccharomyces cerevisiaeCellular prion protein: A co-receptor mediating neuronal cofilin-actin rod formation induced by β-amyloid and proinflammatory cytokines.Elucidating the structure of an infectious protein.Swa2, the yeast homolog of mammalian auxilin, is specifically required for the propagation of the prion variant [URE3-1].Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutationShort Fibrils Constitute the Major Species of Seed-Competent Tau in the Brains of Mice Transgenic for Human P301S Tau.
P2860
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P2860
Biology and genetics of prions causing neurodegeneration
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Biology and genetics of prions causing neurodegeneration
@ast
Biology and genetics of prions causing neurodegeneration
@en
Biology and genetics of prions causing neurodegeneration.
@nl
type
label
Biology and genetics of prions causing neurodegeneration
@ast
Biology and genetics of prions causing neurodegeneration
@en
Biology and genetics of prions causing neurodegeneration.
@nl
prefLabel
Biology and genetics of prions causing neurodegeneration
@ast
Biology and genetics of prions causing neurodegeneration
@en
Biology and genetics of prions causing neurodegeneration.
@nl
P2860
P1476
Biology and genetics of prions causing neurodegeneration
@en
P2860
P304
P356
10.1146/ANNUREV-GENET-110711-155524
P577
2013-01-01T00:00:00Z