Analysis of Covalent Modifications of Proteins by Oxidized Phospholipids Using a Novel Method of Peptide Enrichment
Author:
Affiliation:
1. Department of Molecular Cardiology, Cleveland Clinic, Lerner Research Institute, Cleveland, Ohio 44195, United States
2. Proteomics Core, Cleveland Clinic, Lerner Research Institute, Cleveland, Ohio 44195, United States
Funder
National Heart, Lung, and Blood Institute
National Center for Research Resources
Publisher
American Chemical Society (ACS)
Subject
Analytical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ac4035949
Reference32 articles.
1. Generation and Biological Activities of Oxidized Phospholipids
2. Identification of a Novel Family of Oxidized Phospholipids That Serve as Ligands for the Macrophage Scavenger Receptor CD36
3. A Novel Family of Atherogenic Oxidized Phospholipids Promotes Macrophage Foam Cell Formation via the Scavenger Receptor CD36 and Is Enriched in Atherosclerotic Lesions
4. Molecular and mechanistic characterization of platelet-activating factor-like bioactivity produced upon LDL oxidation
5. Identification of Prostaglandin E2 Receptor Subtype 2 As a Receptor Activated by OxPAPC
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