about
Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale surveyKuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type miceRapid folding of the prion protein captured by pressure-jumpNeuroserpin binds Abeta and is a neuroprotective component of amyloid plaques in Alzheimer diseaseIsolation of proteinase K-sensitive prions using pronase E and phosphotungstic acidPhysical, chemical and kinetic factors affecting prion infectivityGenome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPIdentification of a gene regulatory network associated with prion replication.Nosocomial transmission of sporadic Creutzfeldt-Jakob disease: results from a risk-based assessment of surgical interventions.From high-throughput cell culture screening to mouse model: identification of new inhibitor classes against prion disease.Scrapie infectivity is quickly cleared in tissues of orally-infected farmed fish.Repetitive immunization enhances the susceptibility of mice to peripherally administered prions.The retinoic acid receptor beta (Rarb) region of Mmu14 is associated with prion disease incubation time in mouse.Manganese upregulates cellular prion protein and contributes to altered stabilization and proteolysis: relevance to role of metals in pathogenesis of prion diseaseAbsence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteinsVariant Creutzfeldt-Jakob disease with extremely low lymphoreticular deposition of prion protein.Population screening for variant Creutzfeldt-Jakob disease using a novel blood test: diagnostic accuracy and feasibility study.Pharmacological chaperone for the structured domain of human prion protein.Searching for reliable premortem protein biomarkers for prion diseases: progress and challenges to date.Molecular pathology of human prion disease.Review: contribution of transgenic models to understanding human prion disease.A naturally occurring variant of the human prion protein completely prevents prion disease.Sod1 deficiency reduces incubation time in mouse models of prion diseaseImmunomodulation for prion and prion-related diseases.Assessing proteinase K resistance of fish prion proteins in a scrapie-infected mouse neuroblastoma cell line.Solid-state NMR studies of amyloid fibril structureMRI detection of prion protein plaques in variant Creutzfeldt-Jakob disease.Infectious prion protein alters manganese transport and neurotoxicity in a cell culture model of prion disease.Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice.Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein genePrion Type-Dependent Deposition of PRNP Allelic Products in Heterozygous Sheep.Protective V127 prion variant prevents prion disease by interrupting the formation of dimer and fibril from molecular dynamics simulations.Low activity of complement in the cerebrospinal fluid of the patients with various prion diseases.Cerebrospinal fluid markers in Creutzfeldt-Jakob disease.Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.Review. The origin of the prion agent of kuru: molecular and biological strain typing.Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease.Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysin.Discovery and Preliminary SAR of Arylpiperazines as Novel, Brainpenetrant Antiprion Compounds.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
name
Molecular neurology of prion disease.
@ast
Molecular neurology of prion disease.
@en
type
label
Molecular neurology of prion disease.
@ast
Molecular neurology of prion disease.
@en
prefLabel
Molecular neurology of prion disease.
@ast
Molecular neurology of prion disease.
@en
P2860
P356
P1476
Molecular neurology of prion disease.
@en
P2093
Collinge J
P2860
P304
P356
10.1136/JNNP.2004.048660
P407
P577
2005-07-01T00:00:00Z