The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease.
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Intracerebral administration of interleukin-12 (IL-12) and IL-18 modifies the course of mouse scrapieQuantitative and qualitative analysis of cellular prion protein (PrP(C)) expression in bovine somatic tissues.Transmission of scrapie and sheep-passaged bovine spongiform encephalopathy prions to transgenic mice expressing elk prion protein.Transmission barriers for bovine, ovine, and human prions in transgenic mice.B cells and platelets harbor prion infectivity in the blood of deer infected with chronic wasting diseaseIdentification of two prion protein regions that modify scrapie incubation time.Strain-specified characteristics of mouse synthetic prions.Accelerated, spleen-based titration of variant Creutzfeldt-Jakob disease infectivity in transgenic mice expressing human prion protein with sensitivity comparable to that of survival time bioassay.Dominant-negative inhibition of prion replication in transgenic mice.T cells infiltrate the brain in murine and human transmissible spongiform encephalopathies.Transmission of elk and deer prions to transgenic miceB lymphocyte-restricted expression of prion protein does not enable prion replication in prion protein knockout mice.Chronic wasting disease prion trafficking via the autonomic nervous system.Continuum of prion protein structures enciphers a multitude of prion isolate-specified phenotypes.Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion proteinEtiology and pathogenesis of prion diseases.Immune system-dependent and -independent replication of the scrapie agent.Intracerebral Infusion of Antisense Oligonucleotides Into Prion-infected Mice.Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replication.Species barrier prevents an abnormal isoform of prion protein from accumulating in follicular dendritic cells of mice with Creutzfeldt-Jakob diseaseCompelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans.Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice.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.Identification of clinical target areas in the brainstem of prion-infected mice.A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformationPrion diseases: what will be next?Role of the lymphoreticular system in prion neuroinvasion from the oral and nasal mucosaCryo-immunogold electron microscopy for prions: toward identification of a conversion site.Accumulation of abnormal prion protein in mice infected with Creutzfeldt-Jakob disease via intraperitoneal route: a sequential study.The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system.PrP-dependent association of prions with splenic but not circulating lymphocytes of scrapie-infected mice.
P2860
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P2860
The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
The sequential development of ...... ith Creutzfeldt-Jakob disease.
@en
The sequential development of ...... ith Creutzfeldt-Jakob disease.
@nl
type
label
The sequential development of ...... ith Creutzfeldt-Jakob disease.
@en
The sequential development of ...... ith Creutzfeldt-Jakob disease.
@nl
prefLabel
The sequential development of ...... ith Creutzfeldt-Jakob disease.
@en
The sequential development of ...... ith Creutzfeldt-Jakob disease.
@nl
P2093
P2860
P1476
The sequential development of ...... ith Creutzfeldt-Jakob disease.
@en
P2093
P2860
P304
P407
P577
1992-06-01T00:00:00Z