Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein.
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Isoprostanes and neuroprostanes as biomarkers of oxidative stress in neurodegenerative diseasesThe ubiquitin-proteasome system in spongiform degenerative disordersExpression of prion protein increases cellular copper binding and antioxidant enzyme activities but not copper deliveryFunctions of the cellular prion protein, the end of Moore's law, and Ockham's razor theoryComparison of brain transcriptome of the greater horseshoe bats (Rhinolophus ferrumequinum) in active and torpid episodesRole of the cellular prion protein in oligodendrocyte precursor cell proliferation and differentiation in the developing and adult mouse CNS.Redox control of prion and disease pathogenesis.To develop with or without the prion protein.What is the basis of transmissible spongiform encephalopathy induced neurodegeneration and can it be repaired?Detection of new quantitative trait Loci for susceptibility to transmissible spongiform encephalopathies in mice.The transmissible spongiform encephalopathies: pathogenic mechanisms and strategies for therapeutic intervention.Prion protein accumulation and neuroprotection in hypoxic brain damage.The pathophysiology of variant Creutzfeldt-Jacob disease: the hypotheses behind concerns for blood components and products.Prion protein expression and functional importance in skeletal muscle.Prion Protein Does Not Confer Resistance to Hippocampus-Derived Zpl Cells against the Toxic Effects of Cu2+, Mn2+, Zn2+ and Co2+ Not Supporting a General Protective Role for PrP in Transition Metal Induced Toxicity.Modulation of proteinase K-resistant prion protein in cells and infectious brain homogenate by redox iron: implications for prion replication and disease pathogenesisThe cellular prion protein (PrP(C)): its physiological function and role in diseaseMethionine oxidation perturbs the structural core of the prion protein and suggests a generic misfolding pathwayBovine spongiform encephalopathy in Japan: history and recent studies on oxidative stress in prion diseases.Identification of a novel endoplasmic reticulum stress response element regulated by XBP1.The prion protein knockout mouse: a phenotype under challenge.Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide geneMetal Dyshomeostasis and Their Pathological Role in Prion and Prion-Like Diseases: The Basis for a Nutritional Approach.Protein oxidative modifications in the ageing brain: consequence for the onset of neurodegenerative disease.Nanoparticles and colloids as contributing factors in neurodegenerative disease.Metal attenuating therapies in neurodegenerative disease.Review of studies that have used knockout mice to assess normal function of prion protein under immunological or pathophysiological stress.Prion protein and aging.Neuroprotective role of PrPC against kainate-induced epileptic seizures and cell death depends on the modulation of JNK3 activation by GluR6/7-PSD-95 bindingAltered prion protein glycosylation in the aging mouse brain.Dual role of cellular prion protein in normal host and Alzheimer's disease.Unraveling the neuroprotective mechanisms of PrP (C) in excitotoxicity.Retinal function and morphology are altered in cattle infected with the prion disease transmissible mink encephalopathy.Resistance of cell lines to prion toxicity aided by phospho-ERK expression.Absence of the cellular prion protein exacerbates and prolongs neuroinflammation in experimental autoimmune encephalomyelitis.Affinity, speciation, and molecular features of copper(II) complexes with a prion tetraoctarepeat domain in aqueous solution: insights into old and new results.Aberrant metal binding by prion protein in human prion disease.Oxidative impairment in scrapie-infected mice is associated with brain metals perturbations and altered antioxidant activities.Tethering the N-terminus of the prion protein compromises the cellular response to oxidative stress.Prion Protein Family Contributes to Tumorigenesis via Multiple Pathways.
P2860
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P2860
Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein.
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին 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
Increased levels of oxidative ...... mice devoid of prion protein.
@ast
Increased levels of oxidative ...... mice devoid of prion protein.
@en
type
label
Increased levels of oxidative ...... mice devoid of prion protein.
@ast
Increased levels of oxidative ...... mice devoid of prion protein.
@en
prefLabel
Increased levels of oxidative ...... mice devoid of prion protein.
@ast
Increased levels of oxidative ...... mice devoid of prion protein.
@en
P2093
P2860
P1476
Increased levels of oxidative ...... mice devoid of prion protein.
@en
P2093
Gambetti P
Petersen RB
P2860
P304
P356
10.1046/J.1471-4159.2001.00028.X
P407
P50
P577
2001-01-01T00:00:00Z