Isoketals form cytotoxic phosphatidylethanolamine adducts in cells - Wikidata - awgldk - TriplyDB

Isoketals form cytotoxic phosphatidylethanolamine adducts in cells

Isoketals form cytotoxic phosphatidylethanolamine adducts in cells

http://www.wikidata.org/entity/Q33784657

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Lipid peroxidation generates biologically active phospholipids including oxidatively N-modified phospholipids The effect of oxidized phospholipids on phenotypic polarization and function of macrophages.A liquid chromatography-tandem mass spectrometry method for measurement of N-modified phosphatidylethanolamines.Phosphatidylethanolamines modified by γ-ketoaldehyde (γKA) induce endoplasmic reticulum stress and endothelial activation.Isolevuglandins and mitochondrial enzymes in the retina: mass spectrometry detection of post-translational modification of sterol-metabolizing CYP27A1 Determination of the Pharmacokinetics and Oral Bioavailability of Salicylamine, a Potent γ-Ketoaldehyde Scavenger, by LC/MS/MS.Isoprostane generation and function.Isolevuglandin adducts in disease Isolevuglandin-type lipid aldehydes induce the inflammatory response of macrophages by modifying phosphatidylethanolamines and activating the receptor for advanced glycation endproducts.Identification of novel bioactive aldehyde-modified phosphatidylethanolamines formed by lipid peroxidation.Novel phosphatidylethanolamine derivatives accumulate in circulation in hyperlipidemic ApoE-/- mice and activate platelets via TLR2.Isolevuglandin-modified phosphatidylethanolamine is metabolized by NAPE-hydrolyzing phospholipase D.Pretreatment with pyridoxamine mitigates isolevuglandin-associated retinal effects in mice exposed to bright light.Scavenging of highly reactive gamma-ketoaldehydes attenuates cognitive dysfunction associated with epileptogenesis.Identification of novel oxidized levuglandin D2 in marine red alga and mouse tissue.Efficient Quantitative Analysis of Carboxyalkylpyrrole Ethanolamine Phospholipids: Elevated Levels in Sickle Cell Disease Blood.Covalent modification of lipids and proteins in rat hepatocytes and in vitro by thioacetamide metabolites.Detection and biological activities of carboxyethylpyrrole ethanolamine phospholipids (CEP-EPs).Bioactive 4-Oxoheptanedioic Monoamide Derivatives of Proteins and Ethanolaminephospholipids: Products of Docosahexaenoate Oxidation.The anticancer natural product ophiobolin A induces cytotoxicity by covalent modification of phosphatidylethanolamine.Isolevuglandins as a gauge of lipid peroxidation in human tumors.

P2860

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P2860

Isoketals form cytotoxic phosphatidylethanolamine adducts in cells

http://www.wikidata.org/entity/Q33784657

description

2009 nî lūn-bûn

@nan

2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Isoketals form cytotoxic phosphatidylethanolamine adducts in cells

@ast

Isoketals form cytotoxic phosphatidylethanolamine adducts in cells

@en

type

label

Isoketals form cytotoxic phosphatidylethanolamine adducts in cells

@ast

Isoketals form cytotoxic phosphatidylethanolamine adducts in cells

@en

prefLabel

Isoketals form cytotoxic phosphatidylethanolamine adducts in cells

@ast

Isoketals form cytotoxic phosphatidylethanolamine adducts in cells

@en

P1433

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P2860

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P1433

Journal of Lipid Research

P1476

Isoketals form cytotoxic phosphatidylethanolamine adducts in cells

@en

P2093

C Blake Sullivan

http://www.w3.org/2001/XMLSchema#string

Elena Matafonova

http://www.w3.org/2001/XMLSchema#string

L Jackson Roberts

http://www.w3.org/2001/XMLSchema#string

Sean S Davies

http://www.w3.org/2001/XMLSchema#string

Venkataraman Amarnath

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P2860

Molecular characterization of a phospholipase D generating anandamide and its congeners

Prostaglandin endoperoxides. 14. Solvent-induced fragmentation of prostaglandin endoperoxides. New aldehyde products from PGH2 and a novel intramolecular 1,2-hydride shift during endoperoxide fragmentation in aqueous solution

Pyridoxamine analogues scavenge lipid-derived gamma-ketoaldehydes and protect against H2O2-mediated cytotoxicity.

Localization of isoketal adducts in vivo using a single-chain antibody.

Modulation of protein function by isoketals and levuglandins.

Isolevuglandins covalently modify phosphatidylethanolamines in vivo: detection and quantitative analysis of hydroxylactam adducts.

Oxidative mediated lipid peroxidation recapitulates proarrhythmic effects on cardiac sodium channels.

Effects of reactive gamma-ketoaldehydes formed by the isoprostane pathway (isoketals) and cyclooxygenase pathway (levuglandins) on proteasome function.

Endocannabinoid biosynthesis proceeding through glycerophospho-N-acyl ethanolamine and a role for alpha/beta-hydrolase 4 in this pathway.

Characterization of covalent adducts of nucleosides and DNA formed by reaction with levuglandin.

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999-1009

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scholarly article

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10.1194/JLR.M001040

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5

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51

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19965577

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P932

2853468

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