Impaired heat shock response in cells expressing full-length polyglutamine-expanded huntingtin.
about
Targeting New Candidate Genes by Small Molecules Approaching Neurodegenerative DiseasesHuntington's disease: underlying molecular mechanisms and emerging conceptsCharacterizing the altered cellular proteome induced by the stress-independent activation of heat shock factor 1.The biology of proteostasis in aging and disease.Aqueous Extract of Paeonia lactiflora and Paeoniflorin as Aggregation Reducers Targeting Chaperones in Cell Models of Spinocerebellar Ataxia 3Heat shock response activation exacerbates inclusion body formation in a cellular model of Huntington disease.Unreported intrinsic disorder in proteins: Building connections to the literature on IDPs.Abnormal degradation of the neuronal stress-protective transcription factor HSF1 in Huntington's disease.The de-ubiquitinating enzyme ataxin-3 does not modulate disease progression in a knock-in mouse model of Huntington disease.The role of amyloidogenic protein oligomerization in neurodegenerative disease.Opportunities and challenges for molecular chaperone modulation to treat protein-conformational brain diseasesPharmacological protein targets in polyglutamine diseases: mutant polypeptides and their interactors.Association of heat-shock proteins in various neurodegenerative disorders: is it a master key to open the therapeutic door?Polyglutamine (PolyQ) diseases: genetics to treatments.Modulation of Molecular Chaperones in Huntington's Disease and Other Polyglutamine Disorders.Metabolic control of the proteotoxic stress response: implications in diabetes mellitus and neurodegenerative disorders.Dexamethasone induces heat shock response and slows down disease progression in mouse and fly models of Huntington's disease.Proteins Containing Expanded Polyglutamine Tracts and Neurodegenerative Disease.The heat shock response in neurons and astroglia and its role in neurodegenerative diseases.Causes and consequences of protein folding stress in aneuploid cells.Azadiradione Restores Protein Quality Control and Ameliorates the Disease Pathogenesis in a Mouse Model of Huntington's Disease.Regulation of heat shock transcription factors and their roles in physiology and disease.Deciphering the roles of trehalose and Hsp104 in the inhibition of aggregation of mutant huntingtin in a yeast model of Huntington's disease.
P2860
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P2860
Impaired heat shock response in cells expressing full-length polyglutamine-expanded huntingtin.
description
2012 nî lūn-bûn
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2012 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2012年の論文
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2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
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name
Impaired heat shock response i ...... glutamine-expanded huntingtin.
@ast
Impaired heat shock response i ...... glutamine-expanded huntingtin.
@en
Impaired heat shock response i ...... glutamine-expanded huntingtin.
@nl
type
label
Impaired heat shock response i ...... glutamine-expanded huntingtin.
@ast
Impaired heat shock response i ...... glutamine-expanded huntingtin.
@en
Impaired heat shock response i ...... glutamine-expanded huntingtin.
@nl
prefLabel
Impaired heat shock response i ...... glutamine-expanded huntingtin.
@ast
Impaired heat shock response i ...... glutamine-expanded huntingtin.
@en
Impaired heat shock response i ...... glutamine-expanded huntingtin.
@nl
P2860
P1433
P1476
Impaired heat shock response i ...... glutamine-expanded huntingtin.
@en
P2093
Martin L Duennwald
Sidhartha M Chafekar
P2860
P304
P356
10.1371/JOURNAL.PONE.0037929
P407
P577
2012-05-23T00:00:00Z