about
Towards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson's, Huntington's, Alzheimer's, prions, bactericides, chemical toxicology and others as examplesSilencing prion protein in MDA-MB-435 breast cancer cells leads to pleiotropic cellular responses to cytotoxic stimuliPrion protein regulates iron transport by functioning as a ferrireductase.Copper redox cycling in the prion protein depends critically on binding modeGene regulatory network analysis supports inflammation as a key neurodegeneration process in prion disease.Exposure of RML scrapie agent to a sodium percarbonate-based product and sodium dodecyl sulfate renders PrPSc protease sensitive but does not eliminate infectivity.Analyses of the mitochondrial mutations in the Chinese patients with sporadic Creutzfeldt-Jakob diseaseChange in the characteristics of ferritin induces iron imbalance in prion disease affected brains.Pathogenic prions deviate PrP(C) signaling in neuronal cells and impair A-beta clearanceCytosolic caspases mediate mislocalised SOD2 depletion in an in vitro model of chronic prion infection.A low-molecular-weight ferroxidase is increased in the CSF of sCJD cases: CSF ferroxidase and transferrin as diagnostic biomarkers for sCJD.Up-regulation of mRNA ventricular PRNP prion protein gene expression in air pollution highly exposed young urbanites: endoplasmic reticulum stress, glucose regulated protein 78, and nanosized particles.Brain iron homeostasis: from molecular mechanisms to clinical significance and therapeutic opportunitiesIron in neurodegenerative disorders of protein misfolding: a case of prion disorders and Parkinson's disease.Multitarget ligands and theranostics: sharpening the medicinal chemistry sword against prion diseases.Cellular prion protein (PrP(C)) in the development of Merlin-deficient tumours.Rational approach to an antiprion compound with a multiple mechanism of action.The olfactory bulb as the entry site for prion-like propagation in neurodegenerative diseases.LIV-1 ZIP ectodomain shedding in prion-infected mice resembles cellular response to transition metal starvation.Hybrid lipoic acid derivatives to attack prion disease on multiple fronts.The Rich Electrochemistry and Redox Reactions of the Copper Sites in the Cellular Prion Protein.Affinity, speciation, and molecular features of copper(II) complexes with a prion tetraoctarepeat domain in aqueous solution: insights into old and new results.Aromatase expression in cultured fetal sheep astrocytes after nitrosative/oxidative damage.
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Redox control of prion and disease pathogenesis.
@ast
Redox control of prion and disease pathogenesis.
@en
type
label
Redox control of prion and disease pathogenesis.
@ast
Redox control of prion and disease pathogenesis.
@en
prefLabel
Redox control of prion and disease pathogenesis.
@ast
Redox control of prion and disease pathogenesis.
@en
P2093
P2860
P356
P1476
Redox control of prion and disease pathogenesis.
@en
P2093
Ajay Singh
Maradumane L Mohan
Neena Singh
P2860
P304
P356
10.1089/ARS.2009.2628
P577
2010-06-01T00:00:00Z