about
The role of the cellular prion protein in the immune systemPathogenic protein seeding in Alzheimer disease and other neurodegenerative disordersHumans and cattle: a review of bovine zoonosesPrions adhere to soil minerals and remain infectiousHuman prion diseases in the United States.Interpretation of cerebrospinal fluid protein tests in the diagnosis of sporadic Creutzfeldt-Jakob disease: an evidence-based approach.Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study.Critical factors influencing prion inactivation by sodium hydroxide.Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease.Koch's postulates, carnivorous cows, and tuberculosis today.Variant Creutzfeldt-Jakob disease death, United States.Neuroepidemiology and the epidemiology of viral infections of the nervous systemManagement of neurosurgical instruments and patients exposed to Creutzfeldt-Jakob disease.Absolute quantification of prion protein (90-231) using stable isotope-labeled chymotryptic peptide standards in a LC-MRM AQUA workflowRisk behaviors in a rural community with a known point-source exposure to chronic wasting disease.Prions in the environment: occurrence, fate and mitigationInduction of cerebral beta-amyloidosis: intracerebral versus systemic Abeta inoculationComparative hazard characterization in food toxicology.Facing up to Complexity: Implications for Our Social Experiments.Identification of Anti-prion Compounds using a Novel Cellular Assay.Consumption of bovine spongiform encephalopathy (BSE) contaminated beef and the risk of variant Creutzfeldt-Jakob disease.Strain conformation controls the specificity of cross-species prion transmission in the yeast modelProspective 10-year surveillance of human prion diseases in Japan.A potential blood test for transmissible spongiform encephalopathies by detecting carbohydrate-dependent aggregates of PrPres-like proteins in scrapie-Infected hamster plasma.Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study.A Small-Molecule Inhibitor of Prion Replication and Mutant Prion Protein Toxicity.Ruminant organotypic brain-slice cultures as a model for the investigation of CNS listeriosis.Creutzfeldt-Jakob disease mortality in Canada, 1998 to 2013.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
The public health impact of prion diseases.
@ast
The public health impact of prion diseases.
@en
type
label
The public health impact of prion diseases.
@ast
The public health impact of prion diseases.
@en
prefLabel
The public health impact of prion diseases.
@ast
The public health impact of prion diseases.
@en
P1476
The public health impact of prion diseases.
@en
P2093
Lawrence B Schonberger
P304
P356
10.1146/ANNUREV.PUBLHEALTH.26.021304.144536
P577
2005-01-01T00:00:00Z