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- W3001622466 abstract "Aim: Characterization of phosphatidylcholines (PCs) and lysophosphatidylcholine in human plasma using LC-IT-MS n . The characterization approach was based on trapping the eluted positive ions and applying low voltage for fragmentation to MS 2 and further fragmentation of the most abundant two peaks to obtain MS 3 . This approach allowed linking the MS 3 data to MS 2 and precursor ion. Methodology: The fatty acid part, at sn-1 and sn-2 of the glycerol backbone, could be identified based on the favored cleavage pathway. Conclusion: The dysregulated PCs and lysophosphatidylcholines in human plasma obtained from acute coronary syndrome cases, and Type 2 diabetes patients suffering no coronary syndromes were estimated and matched versus healthy volunteers. An epoxide form of 16:0–18:2 PC was confirmed, m/z 774.6." @default.
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- W3001622466 date "2020-02-01" @default.
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- W3001622466 title "A new approach for characterization of phosphatidylcholines and <i>lyso</i>phosphatidylcholine in human plasma" @default.
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- W3001622466 doi "https://doi.org/10.4155/bio-2019-0280" @default.
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