Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease.
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Techniques to elucidate the conformation of prionsGenesis of mammalian prions: from non-infectious amyloid fibrils to a transmissible prion diseaseRecombinant prion protein refolded with lipid and RNA has the biochemical hallmarks of a prion but lacks in vivo infectivityThe structure of the infectious prion protein: experimental data and molecular models.A C-terminal protease-resistant prion fragment distinguishes ovine "CH1641-like" scrapie from bovine classical and L-Type BSE in ovine transgenic miceBiochemical characterization of prion strains in bank volesMultiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States.Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate.Atypical scrapie isolates involve a uniform prion species with a complex molecular signature.Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.Characterization of the prion protein in human urine.Allelic origin of protease-sensitive and protease-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease with the P102L mutation.Regional distribution of anchorless prion protein, PrP226*, in the human brainCalcium binding promotes prion protein fragment 90-231 conformational change toward a membrane destabilizing and cytotoxic structure.Identifying critical sites of PrP(c)-PrP(Sc) interaction in prion-infected cells by dominant-negative inhibition.Structural organization of mammalian prions as probed by limited proteolysis.Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease.Detection of the GPI-anchorless prion protein fragment PrP226* in human brain.Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.Beta-sheet core of human prion protein amyloid fibrils as determined by hydrogen/deuterium exchangeChronic wasting disease of elk and deer and Creutzfeldt-Jakob disease: comparative analysis of the scrapie prion proteinMolecular pathogenesis of sporadic prion diseases in man.A new mechanism for transmissible prion diseasesAntibody to DNA detects scrapie but not normal prion protein.Role of prion protein aggregation in neurotoxicity.Two alternative pathways for generating transmissible prion disease de novo.Sialylation of the prion protein glycans controls prion replication rate and glycoform ratioSelective amplification of classical and atypical prions using modified protein misfolding cyclic amplification.Investigation of a possible iatrogenic case of Creutzfeldt-Jakob disease after a neurosurgical procedure.The reconstitution of mammalian prion infectivity de novo.H-type bovine spongiform encephalopathy: complex molecular features and similarities with human prion diseasesCharacterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease.Coexistence of two forms of disease-associated prion protein in extracerebral tissues of cattle infected with H-type bovine spongiform encephalopathy.Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prionsAtypical and classical forms of the disease-associated state of the prion protein exhibit distinct neuronal tropism, deposition patterns, and lesion profiles.Similar biochemical signatures and prion protein genotypes in atypical scrapie and Nor98 cases, France and NorwayCo-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristicsGerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.A closer look at prion strains: characterization and important implications.The diversity and relationship of prion protein self-replicating states.
P2860
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P2860
Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Identification of novel protei ...... in Creutzfeldt-Jakob disease.
@en
Identification of novel protei ...... in Creutzfeldt-Jakob disease.
@nl
type
label
Identification of novel protei ...... in Creutzfeldt-Jakob disease.
@en
Identification of novel protei ...... in Creutzfeldt-Jakob disease.
@nl
prefLabel
Identification of novel protei ...... in Creutzfeldt-Jakob disease.
@en
Identification of novel protei ...... in Creutzfeldt-Jakob disease.
@nl
P2093
P2860
P356
P1476
Identification of novel protei ...... in Creutzfeldt-Jakob disease.
@en
P2093
Man-Sun Sy
Pierluigi Gambetti
Sabina Capellari
Wen-Quan Zou
P2860
P304
40429-40436
P356
10.1074/JBC.M308550200
P407
P577
2003-08-12T00:00:00Z