相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Convergent Replication of Mouse Synthetic Prion Strains
Sina Ghaemmaghami et al.
AMERICAN JOURNAL OF PATHOLOGY (2013)
Selective Amplification of Classical and Atypical Prions Using Modified Protein Misfolding Cyclic Amplification
Natallia Makarava et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Acquisition of Drug Resistance and Dependence by Prions
Anja M. Oelschlegel et al.
PLOS PATHOGENS (2013)
Sporadic human prion diseases: molecular insights and diagnosis
Gianfranco Puoti et al.
LANCET NEUROLOGY (2012)
Molecular pathogenesis of sporadic prion diseases in man
Jiri G. Safar
PRION (2012)
Small Protease Sensitive Oligomers of PrPSc in Distinct Human Prions Determine Conversion Rate of PrPC
Chae Kim et al.
PLOS PATHOGENS (2012)
Co-Occurrence of Types 1 and 2 PrPres in Sporadic Creutzfeldt-Jakob Disease MM1
Atsushi Kobayashi et al.
AMERICAN JOURNAL OF PATHOLOGY (2011)
Comparison of the level, distribution and form of disease-associated prion protein in variant and sporadic Creutzfeldt-Jakob diseased brain using conformation-dependent immunoassay and Western blot
Young Pyo Choi et al.
JOURNAL OF GENERAL VIROLOGY (2011)
Protease-Sensitive Conformers in Broad Spectrum of Distinct PrPSc Structures in Sporadic Creutzfeldt-Jakob Disease Are Indicator of Progression Rate
Chae Kim et al.
PLOS PATHOGENS (2011)
Coinfecting Prion Strains Compete for a Limiting Cellular Resource
Ronald A. Shikiya et al.
JOURNAL OF VIROLOGY (2010)
Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties
Matthew T. Bishop et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Darwinian Evolution of Prions in Cell Culture
Jiali Li et al.
SCIENCE (2010)
Generating a Prion with Bacterially Expressed Recombinant Prion Protein
Fei Wang et al.
SCIENCE (2010)
Protease-Sensitive Synthetic Prions
David W. Colby et al.
PLOS PATHOGENS (2010)
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics
Ignazio Cali et al.
BRAIN (2009)
Prion Protein Glycosylation Is Not Required for Strain-Specific Neurotropism
Justin R. Piro et al.
JOURNAL OF VIROLOGY (2009)
Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease
Ed M. Choi et al.
LABORATORY INVESTIGATION (2009)
Rapidly progressive dementia
Michael D. Geschwind et al.
ANNALS OF NEUROLOGY (2008)
Cell-free propagation of prion strains
Joaquin Castilla et al.
EMBO JOURNAL (2008)
Transmission and detection of prions in feces
Jiri G. Safar et al.
JOURNAL OF INFECTIOUS DISEASES (2008)
Beyond PrPres type 1/Type 2 dichotomy in Creutzfeldt-Jakob disease
Emmanuelle Uro-Coste et al.
PLOS PATHOGENS (2008)
A refined method for molecular typing reveals that co-occurrence of PrPSc types in Creutzfeldt-Jakob disease is not the rule
Silvio Notari et al.
LABORATORY INVESTIGATION (2007)
Formation of native prions from minimal components in vitro
Nathan R. Deleault et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Proteinase K-sensitive disease-associated ovine prion protein revealed by conformation-dependent immunoassay
Alana M. Thackray et al.
BIOCHEMICAL JOURNAL (2007)
Prion interference is due to a reduction in strain-specific PrPSc levels
Jason C. Bartz et al.
JOURNAL OF VIROLOGY (2007)
Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains
Jue Yuan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease
S. J. Collins et al.
BRAIN (2006)
Human prions and plasma lipoproteins
Jiri G. Safar et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease
G Schoch et al.
PLOS MEDICINE (2006)
Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease
HM Yull et al.
AMERICAN JOURNAL OF PATHOLOGY (2006)
Chronic wasting disease of elk: Transmissibility to humans examined by transgenic mouse models
QZ Kong et al.
JOURNAL OF NEUROSCIENCE (2005)
Transmission barriers for bovine ovine, and human prions in transgenic mice
MR Scott et al.
JOURNAL OF VIROLOGY (2005)
Diagnosis of human prion disease
JG Safar et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Use of a new immunoassay to measure PrPSc levels in scrapie-infected sheep brains reveals PrP genotype-specific differences
S McCutcheon et al.
JOURNAL OF IMMUNOLOGICAL METHODS (2005)
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies
M Pocchiari et al.
BRAIN (2004)
Improved conformation-dependent immunoassay:: suitability for human prion detection with enhanced sensitivity
A Bellon et al.
JOURNAL OF GENERAL VIROLOGY (2003)
Virus-like interference in the latency and prevention of Creutzfeldt-Jakob disease
L Manuelidis et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene
C Korth et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Sporadic and familial CJD: classification and characterisation
P Gambetti et al.
BRITISH MEDICAL BULLETIN (2003)
Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice
JG Safar et al.
NATURE BIOTECHNOLOGY (2002)
Shattuck lecture - Neurodegenerative diseases and prions.
SB Prusiner
NEW ENGLAND JOURNAL OF MEDICINE (2001)
Genetic influence on the structural variations of the abnormal prion protein
P Parchi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Aggregation and fibrillization of the recombinant human prion protein huPrP90-231
W Swietnicki et al.
BIOCHEMISTRY (2000)
分享论文
