Selective protein arylation and acetaminophen-induced hepatotoxicity.
about
Mechanisms of acetaminophen-induced liver necrosisCREBH determines the severity of sulpyrine-induced fatal shockProtein targets of monocrotaline pyrrole in pulmonary artery endothelial cells.The hepatic stem cell niche: identification by label-retaining cell assay.Lysosomal iron mobilization and induction of the mitochondrial permeability transition in acetaminophen-induced toxicity to mouse hepatocytes.Ringer's lactate improves liver recovery in a murine model of acetaminophen toxicity.JS-K has potent anti-angiogenic activity in vitro and inhibits tumour angiogenesis in a multiple myeloma model in vivo.Challenges and limitations of gene expression profiling in mechanistic and predictive toxicology.High mobility group B1 impairs hepatocyte regeneration in acetaminophen hepatotoxicityAlteration of liver cell function and proliferation: differentiation between adaptation and toxicity.Proteomic analysis of acetaminophen-induced changes in mitochondrial protein expression using spectral countingAge-related changes in the hepatic pharmacology and toxicology of paracetamol.HMGB1 neutralization is associated with bacterial translocation during acetaminophen hepatotoxicity.Nrf2-mediated liver protection by sauchinone, an antioxidant lignan, from acetaminophen toxicity through the PKCδ-GSK3β pathway.S-adenosyl-l-methionine protection of acetaminophen mediated oxidative stress and identification of hepatic 4-hydroxynonenal protein adducts by mass spectrometryIRE1α activation protects mice against acetaminophen-induced hepatotoxicityAcetaminophen-induced hepatotoxicity: role of metabolic activation, reactive oxygen/nitrogen species, and mitochondrial permeability transition.Regulation of alternative macrophage activation in the liver following acetaminophen intoxication by stem cell-derived tyrosine kinase.Drug bioactivation, covalent binding to target proteins and toxicity relevance.Enhanced Production of Adenosine Triphosphate by Pharmacological Activation of Adenosine Monophosphate-Activated Protein Kinase Ameliorates Acetaminophen-Induced Liver Injury.Functional role of monocytes and macrophages for the inflammatory response in acute liver injury.Classical and alternative activation of rat hepatic sinusoidal endothelial cells by inflammatory stimuliGlycocapture-assisted global quantitative proteomics (gagQP) reveals multiorgan responses in serum toxicoproteome.Protein targets of reactive metabolites of thiobenzamide in rat liver in vivoRobust protein nitration contributes to acetaminophen-induced mitochondrial dysfunction and acute liver injuryProlonged treatment with N-acetylcystine delays liver recovery from acetaminophen hepatotoxicity.Effects of acetaminophen on mitochondrial complex I activity in the rat liver and kidney: a PET study with 18F-BCPP-BF.Role of cytochrome P450 2E1 in protein nitration and ubiquitin-mediated degradation during acetaminophen toxicity.Mechanism of protection by metallothionein against acetaminophen hepatotoxicity.Acylcarnitine profiles in acetaminophen toxicity in the mouse: comparison to toxicity, metabolism and hepatocyte regeneration.TRPM2 channels mediate acetaminophen-induced liver damageMechanistic biomarkers in acetaminophen-induced hepatotoxicity and acute liver failure: from preclinical models to patients.Extracorporeal treatment for acetaminophen poisoning: recommendations from the EXTRIP workgroup.Removal of acetaminophen protein adducts by autophagy protects against acetaminophen-induced liver injury in mice.NQO2 is a reactive oxygen species generating off-target for acetaminophen.Extensive protein carbonylation precedes acrolein-mediated cell death in mouse hepatocytes.The protective role of NAD(P)H:quinone oxidoreductase 1 on acetaminophen-induced liver injury is associated with prevention of adenosine triphosphate depletion and improvement of mitochondrial dysfunction.rhIL-1Ra reduces hepatocellular apoptosis in mice with acetaminophen-induced acute liver failure.Attenuation of Acetaminophen-Induced Hepatotoxicity In Vivo and In Vitro by a 43-kD Protein Isolated from the Herb Cajanus indicus L.Reduced acetaminophen-induced liver injury in mice by genetic disruption of IL-1 receptor antagonist.
P2860
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P2860
Selective protein arylation and acetaminophen-induced hepatotoxicity.
description
1997 nî lūn-bûn
@nan
1997 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Selective protein arylation and acetaminophen-induced hepatotoxicity.
@ast
Selective protein arylation and acetaminophen-induced hepatotoxicity.
@en
type
label
Selective protein arylation and acetaminophen-induced hepatotoxicity.
@ast
Selective protein arylation and acetaminophen-induced hepatotoxicity.
@en
prefLabel
Selective protein arylation and acetaminophen-induced hepatotoxicity.
@ast
Selective protein arylation and acetaminophen-induced hepatotoxicity.
@en
P2860
P1476
Selective protein arylation and acetaminophen-induced hepatotoxicity.
@en
P2093
E A Khairallah
P2860
P356
10.3109/03602539709037573
P407
P577
1997-02-01T00:00:00Z