PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.
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Epidemiological characteristics of human prion diseasesAn overview of human prion diseasesAll clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJDLoss of Octarepeats in two processed prion pseudogenes in the red squirrel, Sciurus vulgarisHuman prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.Epidemiological mechanisms of genetic resistance to kuru.The molecular epidemiology of variant CJD.Age at Death of Creutzfeldt-Jakob disease in subsequent family generation carrying the E200K mutation of the prion protein gene.Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease.A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk.Protective V127 prion variant prevents prion disease by interrupting the formation of dimer and fibril from molecular dynamics simulations.Quantifying prion disease penetrance using large population control cohortsGenotype patterns and characteristics of PRNP in the Korean population.Prion diseases as transmissible zoonotic diseases.UK Iatrogenic Creutzfeldt-Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approachesEstimation of variant Creutzfeldt-Jakob disease infectivity titers in human blood.The contribution of different prion protein types and host polymorphisms to clinicopathological variations in Creutzfeldt-Jakob disease.Exploring the zoonotic potential of animal prion diseases: in vivo and in vitro approaches.Review of studies that have used knockout mice to assess normal function of prion protein under immunological or pathophysiological stress.Creutzfeldt-Jakob disease and blood transfusion: updated results of the UK Transfusion Medicine Epidemiology Review Study.Endogenous prion protein attenuates experimentally induced colitis.Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.No evidence of asymptomatic variant CJD infection in immunodeficiency patients treated with UK-sourced immunoglobulin.Dominant-negative effects in prion diseases: insights from molecular dynamics simulations on mouse prion protein chimeras.Codon 129 polymorphism of prion protein gene in is not a risk factor for Alzheimer's disease.Creutzfeldt-Jakob disease: recent developments.Human embryonic stem cells rapidly take up and then clear exogenous human and animal prions in vitro.Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases
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P2860
PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
PRNP variation in UK sporadic ...... l non-synonymous polymorphism.
@ast
PRNP variation in UK sporadic ...... l non-synonymous polymorphism.
@en
PRNP variation in UK sporadic ...... l non-synonymous polymorphism.
@nl
type
label
PRNP variation in UK sporadic ...... l non-synonymous polymorphism.
@ast
PRNP variation in UK sporadic ...... l non-synonymous polymorphism.
@en
PRNP variation in UK sporadic ...... l non-synonymous polymorphism.
@nl
prefLabel
PRNP variation in UK sporadic ...... l non-synonymous polymorphism.
@ast
PRNP variation in UK sporadic ...... l non-synonymous polymorphism.
@en
PRNP variation in UK sporadic ...... l non-synonymous polymorphism.
@nl
P2093
P2860
P356
P1433
P1476
PRNP variation in UK sporadic ...... l non-synonymous polymorphism.
@en
P2093
Catherine Pennington
Craig A Heath
Matthew T Bishop
Richard S G Knight
Robert G Will
P2860
P2888
P356
10.1186/1471-2350-10-146
P577
2009-12-26T00:00:00Z
P5875
P6179
1004632403