Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease.
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Prion uptake in the gut: identification of the first uptake and replication sitesDistinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.Repetitive immunization enhances the susceptibility of mice to peripherally administered prions.B cells and platelets harbor prion infectivity in the blood of deer infected with chronic wasting diseaseEfficient lymphoreticular prion propagation requires PrP(c) in stromal and hematopoietic cells.Deletion of beta-strand and alpha-helix secondary structure in normal prion protein inhibits formation of its protease-resistant isoform.Grafting mouse brains: from neurocarcinogenesis to neurodegeneration.Neuroinvasion by a Creutzfeldt-Jakob disease agent in the absence of B cells and follicular dendritic cellsBiological network inferences for a protection mechanism against familial Creutzfeldt-Jakob disease with E200K pathogenic mutation.Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie.Infectious particles, stress, and induced prion amyloids: a unifying perspective.Retrograde transport of transmissible mink encephalopathy within descending motor tracts.Lymphotoxin, but not TNF, is required for prion invasion of lymph nodes.Rapid prion neuroinvasion following tongue infection.Immunomodulation for prion and prion-related diseases.Human prions and plasma lipoproteins.B lymphocyte-restricted expression of prion protein does not enable prion replication in prion protein knockout mice.Orally administered prion protein is incorporated by m cells and spreads into lymphoid tissues with macrophages in prion protein knockout mice.Recent developments in the pathogenesis, diagnosis, and therapy of prion diseases.Accumulation of proteinase K-resistant prion protein (PrP) is restricted by the expression level of normal PrP in mice inoculated with a mouse-adapted strain of the Creutzfeldt-Jakob disease agent.Immune system-dependent and -independent replication of the scrapie agent.Prion infection of muscle cells in vitroThe nasal cavity is a route for prion infection in hamstersCould immunomodulation be used to prevent prion diseases?Oral infection by the bovine spongiform encephalopathy prion.How do follicular dendritic cells interact intimately with B cells in the germinal centre?Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders.Prion diseases and the gastrointestinal tract.Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replication.Immunohistochemical detection of prion protein in lymphoid tissues of sheep with natural scrapie.Species barrier prevents an abnormal isoform of prion protein from accumulating in follicular dendritic cells of mice with Creutzfeldt-Jakob diseasePrions and lymphoid organs: solved and remaining mysteries.Detection and control of prion diseases in food animals.Epithelial and endothelial expression of the green fluorescent protein reporter gene under the control of bovine prion protein (PrP) gene regulatory sequences in transgenic mice.Characterization of variant Creutzfeldt-Jakob disease prions in prion protein-humanized mice carrying distinct codon 129 genotypes.PrP antibody binding-induced epitope modulation evokes immunocooperativityFollicular dendritic cell disruption as a novel mechanism of virus-induced immunosuppressionTunnelling nanotubes: a highway for prion spreading?Complement protein C3 exacerbates prion disease in a mouse model of chronic wasting disease.Tumor necrosis factor alpha-deficient, but not interleukin-6-deficient, mice resist peripheral infection with scrapie.
P2860
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P2860
Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年学术文章
@wuu
1991年学术文章
@zh-cn
1991年学术文章
@zh-hans
1991年学术文章
@zh-my
1991年学术文章
@zh-sg
1991年學術文章
@yue
1991年學術文章
@zh
1991年學術文章
@zh-hant
name
Abnormal isoform of prion prot ...... ith Creutzfeldt-Jakob disease.
@en
type
label
Abnormal isoform of prion prot ...... ith Creutzfeldt-Jakob disease.
@en
prefLabel
Abnormal isoform of prion prot ...... ith Creutzfeldt-Jakob disease.
@en
P2093
P2860
P1433
P1476
Abnormal isoform of prion prot ...... ith Creutzfeldt-Jakob disease.
@en
P2093
P2860
P304
P407
P577
1991-11-01T00:00:00Z