Formation of Aldehydic Phosphatidylcholines during the Anaerobic Decomposition of a Phosphatidylcholine Bearing the 9-Hydroperoxide of Linoleic Acid.

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The Contribution of Singlet Oxygen to Insulin Resistance.

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P2860

Formation of Aldehydic Phosphatidylcholines during the Anaerobic Decomposition of a Phosphatidylcholine Bearing the 9-Hydroperoxide of Linoleic Acid.

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http://www.wikidata.org/entity/Q42178262

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2016 nî lūn-bûn

@nan

2016年の論文

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2016年論文

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2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Formation of Aldehydic Phospha ...... ydroperoxide of Linoleic Acid.

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Formation of Aldehydic Phospha ...... ydroperoxide of Linoleic Acid.

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type

Item

label

Formation of Aldehydic Phospha ...... ydroperoxide of Linoleic Acid.

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Formation of Aldehydic Phospha ...... ydroperoxide of Linoleic Acid.

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prefLabel

Formation of Aldehydic Phospha ...... ydroperoxide of Linoleic Acid.

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Formation of Aldehydic Phospha ...... ydroperoxide of Linoleic Acid.

@nl

P1476

Formation of Aldehydic Phospha ...... Hydroperoxide of Linoleic Acid

@en

P2093

Arnold N Onyango

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P2860

The formation of threo-11-hydroxy-trans-12: 13-epoxy-9-cis-octadecenoic acid by enzymic isomerisation of 13-L-hydroperoxy-9-cis, 11-transoctadecadienoic acid by soybean lipoxygenase-1

Aldehydic lipid peroxidation products derived from linoleic acid.

An ancient relative of cyclooxygenase in cyanobacteria is a linoleate 10S-dioxygenase that works in tandem with a catalase-related protein with specific 10S-hydroperoxide lyase activity.

Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal

A lipid peroxidation product 9-oxononanoic acid induces phospholipase A2 activity and thromboxane A2 production in human blood.

The lipid peroxidation product 4-hydroxy-2-nonenal: Advances in chemistry and analysis

Organ-Protective Effects of Red Wine Extract, Resveratrol, in Oxidative Stress-Mediated Reperfusion Injury

Phospholipase A2, reactive oxygen species, and lipid peroxidation in cerebral ischemia.

Fragmentation of a linoleate-derived γ-hydroperoxy-α,β-unsaturated epoxide to γ-hydroxy- and γ-oxo-alkenals involves a unique pseudo-symmetrical diepoxycarbinyl radical.

Routes to 4-hydroxynonenal: fundamental issues in the mechanisms of lipid peroxidation

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8218439

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scholarly article

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10.1155/2016/8218439

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English

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2016

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Arnold N Onyango

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2016-06-05T00:00:00Z

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27366754

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phosphatidylcholines

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4913024

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Formation of Aldehydic Phosphatidylcholines during the Anaerobic Decomposition of a Phosphatidylcholine Bearing the 9-Hydroperoxide of Linoleic Acid.

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P2860

P2860

Formation of Aldehydic Phosphatidylcholines during the Anaerobic Decomposition of a Phosphatidylcholine Bearing the 9-Hydroperoxide of Linoleic Acid.

description

name

type

label

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P50

P577

P698

P921

P932