Visualization of cell-to-cell transmission of mutant huntingtin oligomers
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α-Synuclein modifies huntingtin aggregation in living cellsHuntington's disease cerebrospinal fluid seeds aggregation of mutant huntingtin.Human-to-mouse prion-like propagation of mutant huntingtin protein.Dynamic imaging by fluorescence correlation spectroscopy identifies diverse populations of polyglutamine oligomers formed in vivo.A Novel Microfluidic Cell Co-culture Platform for the Study of the Molecular Mechanisms of Parkinson's Disease and Other SynucleinopathiesRas GTPase activating protein CoIra1 is involved in infection-related morphogenesis by regulating cAMP and MAPK signaling pathways through CoRas2 in Colletotrichum orbiculare.Fragments of HdhQ150 mutant huntingtin form a soluble oligomer pool that declines with aggregate deposition upon agingHsp40 gene therapy exerts therapeutic effects on polyglutamine disease mice via a non-cell autonomous mechanism.α-Synuclein modifies mutant huntingtin aggregation and neurotoxicity in Drosophila.shRNA-Based Screen Identifies Endocytic Recycling Pathway Components That Act as Genetic Modifiers of Alpha-Synuclein Aggregation, Secretion and Toxicity.Glycation potentiates neurodegeneration in models of Huntington's disease.Induced Pluripotent Stem Cells in Huntington's Disease: Disease Modeling and the Potential for Cell-Based Therapy.A deadly spread: cellular mechanisms of α-synuclein transfer.Intercellular (mis)communication in neurodegenerative disease.Prions Ex Vivo: What Cell Culture Models Tell Us about Infectious Proteins.The fate of cell grafts for the treatment of Huntington's disease: the post-mortem evidence.Potential Transfer of Polyglutamine and CAG-Repeat RNA in Extracellular Vesicles in Huntington's Disease: Background and Evaluation in Cell Culture.Binding, internalization and fate of Huntingtin Exon1 fibrillar assemblies in mitotic and nonmitotic neuroblastoma cells.Prion-Like Characteristics of Polyglutamine-Containing Proteins.Detecting soluble polyQ oligomers and investigating their impact on living cells using split-GFPSplit GFP technologies to structurally characterize and quantify functional biomolecular interactions of FTD-related proteinsDJ-1 modulates aggregation and pathogenesis in models of Huntington's disease.Polyglutamine toxicity in yeast uncovers phenotypic variations between different fluorescent protein fusions.Something wicked this way comes: huntingtin.The Evidence for the Spread and Seeding Capacities of the Mutant Huntingtin Protein in in Vitro Systems and Their Therapeutic Implications.Predictive Model of Spread of Progressive Supranuclear Palsy Using Directional Network Diffusion.Flow Cytometric Detection of PrPSc in Neurons and Glial Cells from Prion-Infected Mouse Brains.Amyloidogenesis: FlAsH illuminates Aβ aggregation.Targeting prion-like protein spreading in neurodegenerative diseases
P2860
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P2860
Visualization of cell-to-cell transmission of mutant huntingtin oligomers
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Visualization of cell-to-cell transmission of mutant huntingtin oligomers
@ast
Visualization of cell-to-cell transmission of mutant huntingtin oligomers
@en
type
label
Visualization of cell-to-cell transmission of mutant huntingtin oligomers
@ast
Visualization of cell-to-cell transmission of mutant huntingtin oligomers
@en
prefLabel
Visualization of cell-to-cell transmission of mutant huntingtin oligomers
@ast
Visualization of cell-to-cell transmission of mutant huntingtin oligomers
@en
P50
P356
P1433
P1476
Visualization of cell-to-cell transmission of mutant huntingtin oligomers
@en
P2093
Tiago Fleming Outeiro
P304
P356
10.1371/CURRENTS.RRN1210
P577
2011-02-11T00:00:00Z