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Role of microglia in central nervous system infectionsA systems approach to prion diseaseAnti-prion activity of Brilliant Blue GCharacterization of Novel Src Family Kinase Inhibitors to Attenuate MicrogliosisIn Vivo NMR Studies of the Brain with Hereditary or Acquired Metabolic Disorders.Phagocytosis of microglia in the central nervous system diseasesPresence of an acute phase response in sheep with clinical classical scrapie.Involvement of endogenous retroviruses in prion diseases.What is the basis of transmissible spongiform encephalopathy induced neurodegeneration and can it be repaired?The intricate mechanisms of neurodegeneration in prion diseases.Differences in scrapie-induced pathology of the retina and brain in transgenic mice that express hamster prion protein in neurons, astrocytes, or multiple cell typesIdentification of Major Signaling Pathways in Prion Disease Progression Using Network Analysis.Brain microglia were activated in sporadic CJD but almost unchanged in fatal familial insomnia and G114V genetic CJD.Analysis of protein levels of 24 cytokines in scrapie agent-infected brain and glial cell cultures from mice differing in prion protein expression levelsMetalloproteins and neuronal death.The role of regulatory T cells in neurodegenerative diseases.Gene regulation as a potential avenue for the treatment of neurodegenerative disorders.Prion protein (PrP) gene-knockout cell lines: insight into functions of the PrP.C-Abl tyrosine kinase mediates neurotoxic prion peptide-induced neuronal apoptosis via regulating mitochondrial homeostasis.Pathological prion protein exposure switches on neuronal mitogen-activated protein kinase pathway resulting in microglia recruitment.Chronic Progressive Neurodegeneration in a Transgenic Mouse Model of Prion Disease.A roadmap for investigating the role of the prion protein in depression associated with neurodegenerative diseaseFundamental paradox of survival determinism: the ur-etiology disease paradigm.Expression of excitatory amino acid transporter-1 (EAAT-1) in brain macrophages and microglia of patients with prion diseases.Excitotoxic and apoptotic neuronal death induce different patterns of glial activation in vitro.Simplified Murine 3D Neuronal Cultures for Investigating Neuronal Activity and Neurodegeneration.Glial alterations in human prion diseases: A correlative study of astroglia, reactive microglia, protein deposition, and neuropathological lesions.
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Microglia and prion disease.
@ast
Microglia and prion disease.
@en
Microglia and prion disease.
@nl
type
label
Microglia and prion disease.
@ast
Microglia and prion disease.
@en
Microglia and prion disease.
@nl
prefLabel
Microglia and prion disease.
@ast
Microglia and prion disease.
@en
Microglia and prion disease.
@nl
P2860
P356
P1476
Microglia and prion disease.
@en
P2093
P2860
P356
10.1002/JEMT.1122
P577
2001-07-01T00:00:00Z