HECTD2 is associated with susceptibility to mouse and human prion disease - Wikidata - awgldk - TriplyDB

HECTD2 is associated with susceptibility to mouse and human prion disease

HECTD2 is associated with susceptibility to mouse and human prion disease

http://www.wikidata.org/entity/Q33408776

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The ubiquitin proteasome system in neuropathology The proinflammatory role of HECTD2 in innate immunity and experimental lung injury Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP Identification of a gene regulatory network associated with prion replication.Genomic and post-genomic analyses of human prion diseases HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q.Genetic studies in human prion diseases.The retinoic acid receptor beta (Rarb) region of Mmu14 is associated with prion disease incubation time in mouse.Transcriptional analysis implicates endoplasmic reticulum stress in bovine spongiform encephalopathy Evidence for varied aetiologies regulating the transmission of prion disease: implications for understanding the heritable basis of prion incubation times.Sex effects in mouse prion disease incubation time.Population screening for variant Creutzfeldt-Jakob disease using a novel blood test: diagnostic accuracy and feasibility study.A common BACE1 polymorphism is a risk factor for sporadic Creutzfeldt-Jakob disease Molecular pathology of human prion disease.Review: contribution of transgenic models to understanding human prion disease.Sod1 deficiency reduces incubation time in mouse models of prion disease Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein.Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry Genome wide association studies and prion disease.Contrasting genetic architectures in different mouse reference populations used for studying complex traits.Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice.Prion diseases as transmissible zoonotic diseases.Interaction between misfolded PrP and the ubiquitin-proteasome system in prion-mediated neurodegeneration.Genetics of prion diseases Regulation of proteasomes in prion disease.In vitro screen of prion disease susceptibility genes using the scrapie cell assay.Misfolding leads the way to unraveling signaling pathways in the pathophysiology of prion diseases.Neurodegenerative Disease Transmission and Transgenesis in Mice.Early Origin and Evolution of the Angelman Syndrome Ubiquitin Ligase Gene Ube3a.A genomic survey of HECT ubiquitin ligases in eukaryotes reveals independent expansions of the HECT system in several lineages.Functional genomics approach for identification of molecular processes underlying neurodegenerative disorders in prion diseases.A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse.Deubiquitinating enzyme VCIP135 dictates the duration of botulinum neurotoxin type A intoxication.What's next for genomics and prion diseases?A polymorphism in the YWHAH gene encoding 14-3-3 eta that is not associated with sporadic Creutzfeldt-Jakob disease (CJD).

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HECTD2 is associated with susceptibility to mouse and human prion disease

http://www.wikidata.org/entity/Q33408776

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2009 nî lūn-bûn

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2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2009 թվականի փետրվարին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

HECTD2 is associated with susceptibility to mouse and human prion disease

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HECTD2 is associated with susceptibility to mouse and human prion disease

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HECTD2 is associated with susceptibility to mouse and human prion disease

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HECTD2 is associated with susceptibility to mouse and human prion disease

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HECTD2 is associated with susceptibility to mouse and human prion disease

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HECTD2 is associated with susceptibility to mouse and human prion disease

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HECTD2 is associated with susceptibility to mouse and human prion disease

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Eleni Molou

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Emma G Maytham

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Hirva Pota

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Holger Hummerich

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James Uphill

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Jerome Whitfield

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John Collinge

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Julia Grizenkova

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Michael P Alpers

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Sarah E Lloyd

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P2860

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea

Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice

The International HapMap Project

Principal components analysis corrects for stratification in genome-wide association studies

Spongiform degeneration in mahoganoid mutant mice

How to improve the clinical diagnosis of Creutzfeldt-Jakob disease.

Variant Creutzfeldt-Jakob disease.

Kuru in the 21st century--an acquired human prion disease with very long incubation periods.

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics.

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2

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19214206

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Prion protein family

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2633041

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