Microglial activation varies in different models of Creutzfeldt-Jakob disease.
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Blood borne transit of CJD from brain to gut at early stages of infectionGenetic and Transcriptomic Profiles of Inflammation in Neurodegenerative Diseases: Alzheimer, Parkinson, Creutzfeldt-Jakob and TauopathiesPrion pathogenesis in the absence of NLRP3/ASC inflammasomesComprehensive transcriptional profiling of prion infection in mouse models reveals networks of responsive genesAltered Ca2+ homeostasis induces Calpain-Cathepsin axis activation in sporadic Creutzfeldt-Jakob diseaseGenes contributing to prion pathogenesisNeuroinvasion by a Creutzfeldt-Jakob disease agent in the absence of B cells and follicular dendritic cellsUnique inflammatory RNA profiles of microglia in Creutzfeldt-Jakob disease.Replication and spread of CJD, kuru and scrapie agents in vivo and in cell culturePrion disease induced alterations in gene expression in spleen and brain prior to clinical symptoms.Cystatin F is a biomarker of prion pathogenesis in mice.Prion pathogenesis is unaltered in the absence of SIRPα-mediated "don't-eat-me" signaling.Microglia in the degenerating brain are capable of phagocytosis of beads and of apoptotic cells, but do not efficiently remove PrPSc, even upon LPS stimulation.Defining the Microglia Response during the Time Course of Chronic NeurodegenerationBrain microglia were activated in sporadic CJD but almost unchanged in fatal familial insomnia and G114V genetic CJD.Accelerated prion disease in the absence of interleukin-10.Prion disease and the innate immune system.Identification of upregulated genes in scrapie-infected brain tissueFollicular dendritic cells and dissemination of Creutzfeldt-Jakob disease.Microglia from Creutzfeldt-Jakob disease-infected brains are infectious and show specific mRNA activation profiles.Microglia in prion diseases.Differential expression of interferon responsive genes in rodent models of transmissible spongiform encephalopathy disease.The NLRP3-Caspase 1 Inflammasome Negatively Regulates Autophagy via TLR4-TRIF in Prion Peptide-Infected Microglia.
P2860
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P2860
Microglial activation varies in different models of Creutzfeldt-Jakob disease.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Microglial activation varies in different models of Creutzfeldt-Jakob disease.
@en
Microglial activation varies in different models of Creutzfeldt-Jakob disease.
@nl
type
label
Microglial activation varies in different models of Creutzfeldt-Jakob disease.
@en
Microglial activation varies in different models of Creutzfeldt-Jakob disease.
@nl
prefLabel
Microglial activation varies in different models of Creutzfeldt-Jakob disease.
@en
Microglial activation varies in different models of Creutzfeldt-Jakob disease.
@nl
P2093
P2860
P1433
P1476
Microglial activation varies in different models of Creutzfeldt-Jakob disease
@en
P2093
P2860
P304
P407
P577
1999-06-01T00:00:00Z