About: Opposing activities protect against age-onset proteotoxicity

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scientific article (publication date: 15 September 2006)

Attributes	Values
rdf:type	Item
description	artículu científicu espublizáu en 2006 (ast) 2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված (hy) 2006 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована у вересні 2006 (uk) مقالة علمية (نشرت في 15-9-2006) (ar) wetenschappelijk artikel (gepubliceerd op 2006/09/15) (nl) article publié dans la revue scientifique Science (fr) scientific article (publication date: 15 September 2006) (en) im September 2006 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q29619758-85197C48-E783-4609-B126-1075D106878C
publication date	2006-08-10 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q29619758-A96FCFAD-2F3B-474E-8CE9-0B91844187A8
language of work or name	English
author name string	wds:Q29619758-390DD2F3-965A-41EF-B5B8-2CBAC9E86CE5 wds:Q29619758-B0A32BF6-9764-4FA6-B033-7F9B8775A64D
OpenCitations bibliographic resource ID	wds:Q29619758-62D0FE64-D6CC-4513-9AC5-42D313F929C4
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/1234824
author name string	Andrew Dillin Jan Bieschke
OpenCitations bibliographic resource ID	1234824
rdfs:label	Opposing activities protect against age-onset proteotoxicity (en) Opposing activities protect against age-onset proteotoxicity (ast)
skos:prefLabel	Opposing activities protect against age-onset proteotoxicity (en) Opposing activities protect against age-onset proteotoxicity (ast)
name	Opposing activities protect against age-onset proteotoxicity (en) Opposing activities protect against age-onset proteotoxicity (ast)
author	wds:Q29619758-0D2954B0-82F3-45A6-9E8E-047084A81FD5 wds:Q29619758-2478E5C1-6163-4AAE-941B-C3D8F58D7449 wds:Q29619758-E03F04E6-321B-4665-9144-30F53CC68EA0
author	Jeffery W. Kelly Dr. Rhonda Patrick Ehud Cohen
title	wds:Q29619758-287177A0-F75C-4FE0-8B7B-B82BDF039708
title	Opposing activities protect against age-onset proteotoxicity (en)
page(s)	wds:Q29619758-70BFAA47-F1FC-45EE-A5A7-0171B6C88CA1
page(s)	1604-1610
instance of	wds:Q29619758-3FEFF82E-A3C6-422B-9985-13A778DD1F73
instance of	scholarly article
PubMed ID	wds:Q29619758-71FBD5F3-96FD-4083-B12A-2FA38D4BAD1B
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16902091
PubMed ID	16902091
published in	wds:Q29619758-BB2C9B47-C6BB-4661-AEC0-897B5CAC3A59
published in	Science
issue	wds:Q29619758-E660AA66-6281-4C53-949D-C64640BA5210
volume	wds:Q29619758-F3A2139E-D745-4992-8EAC-0B861D3336D6
issue	5793
volume	313
DOI	wds:Q29619758-D6ADB610-7D56-4B2B-9E38-DD60DFAC9BDB
DOI	http://dx.doi.org/10.1126/SCIENCE.1124646
DOI	10.1126/SCIENCE.1124646
skos:altLabel	Opposing Activities Protect Against Age-Onset Proteotoxicity (en)
ResearchGate publication ID	wds:Q29619758-BD0C1C72-01C0-4045-9B17-1EF86CE942AF
ResearchGate publication ID	6885418
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q29619758
is cites work of	The Wnt receptor Ryk reduces neuronal and cell survival capacity by repressing FOXO activity during the early phases of mutant huntingtin pathogenicity Novel therapeutic strategies for the treatment of protein-misfolding diseases Interplay between protein homeostasis networks in protein aggregation and proteotoxicity Neuronal reprograming of protein homeostasis by calcium-dependent regulation of the heat shock response The unpredictability of prolonged activation of stress response pathways Amyloid-binding compounds maintain protein homeostasis during ageing and extend lifespan Stress proteins in aging and life span Adapting proteostasis for disease intervention Delaying aging and the aging-associated decline in protein homeostasis by inhibition of tryptophan degradation. Sirtuin 2 inhibitors rescue alpha-synuclein-mediated toxicity in models of Parkinson's disease Tissue-specific insulin signaling in the regulation of metabolism and aging Amyloids: friend or foe? Regulation of forkhead transcription factor FoxO3a contributes to calorie restriction-induced prevention of Alzheimer's disease-type amyloid neuropathology and spatial memory deterioration Integrating the stress response: lessons for neurodegenerative diseases from C. elegans Spatial sequestration of misfolded proteins by a dynamic chaperone pathway enhances cellular fitness during stress The new biology of ageing Caenorhabditis elegans 2007: the premier model for the study of aging Mutant TDP-43 and FUS cause age-dependent paralysis and neurodegeneration in C. elegans Establishing a novel C. elegans model to investigate the role of autophagy in amyotrophic lateral sclerosis Polyphenolic glycosides and aglycones utilize opposing pathways to selectively remodel and inactivate toxic oligomers of amyloid β. Insolubility of disrupted-in-schizophrenia 1 disrupts oligomer-dependent interactions with nuclear distribution element 1 and is associated with sporadic mental disease C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation Progeria syndromes and ageing: what is the connection? FOXO/4E-BP signaling in Drosophila muscles regulates organism-wide proteostasis during aging Structural Basis for DNA Recognition by FoxO1 and Its Regulation by Posttranslational Modification Neural mechanisms of ageing and cognitive decline Misfolded proteins partition between two distinct quality control compartments HIF-1 modulates dietary restriction-mediated lifespan extension via IRE-1 in Caenorhabditis elegans Proteotoxic stress and inducible chaperone networks in neurodegenerative disease and aging Proteasomal regulation of the hypoxic response modulates aging in C. elegans Unraveling infectious structures, strain variants and species barriers for the yeast prion [PSI+]. Reduced IGF-1 signaling delays age-associated proteotoxicity in mice Inhibition of GSK-3 ameliorates Abeta pathology in an adult-onset Drosophila model of Alzheimer's disease A molecular mechanism of chronological aging in yeast. A new role for laminins as modulators of protein toxicity in Caenorhabditis elegans The insulin paradox: aging, proteotoxicity and neurodegeneration What have worm models told us about the mechanisms of neuronal dysfunction in human neurodegenerative diseases? Mice fed rapamycin have an increase in lifespan associated with major changes in the liver transcriptome The mammalian disaggregase machinery: Hsp110 synergizes with Hsp70 and Hsp40 to catalyze protein disaggregation and reactivation in a cell-free system The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease. Neuronal production of transthyretin in human and murine Alzheimer's disease: is it protective? Mechanisms of transthyretin inhibition of β-amyloid aggregation in vitro Protein rescue from aggregates by powerful molecular chaperone machines Operational plasticity enables hsp104 to disaggregate diverse amyloid and nonamyloid clients. Differential display of DNA-binding proteins reveals heat-shock factor 1 as a circadian transcription factor

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