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Items: 1 to 20 of 457

2.

Analytical methods for (oxidized) plasmalogens: Methodological aspects and applications.

Fuchs B.

Free Radic Res. 2015 May;49(5):599-617. doi: 10.3109/10715762.2014.999675. Epub 2015 Apr 3. Review.

PMID:
25536419
3.

HOCl-mediated glycerophosphocholine and glycerophosphoethanolamine generation from plasmalogens in phospholipid mixtures.

Lessig J, Fuchs B.

Lipids. 2010 Jan;45(1):37-51. doi: 10.1007/s11745-009-3365-8. Epub 2009 Nov 25.

PMID:
19937395
4.

Reactive chlorinating species produced by myeloperoxidase target the vinyl ether bond of plasmalogens: identification of 2-chlorohexadecanal.

Albert CJ, Crowley JR, Hsu FF, Thukkani AK, Ford DA.

J Biol Chem. 2001 Jun 29;276(26):23733-41. Epub 2001 Apr 11.

5.

Plasmalogens: targets for oxidants and major lipophilic antioxidants.

Engelmann B.

Biochem Soc Trans. 2004 Feb;32(Pt 1):147-50.

PMID:
14748736
6.

Characteristic oxidation products of choline plasmalogens are detectable in cattle and roe deer spermatozoa by MALDI-TOF mass spectrometry.

Fuchs B, Müller K, Göritz F, Blottner S, Schiller J.

Lipids. 2007 Nov;42(11):991-8. Epub 2007 Aug 24.

PMID:
17717713
7.
8.

Hypochlorous acid-mediated generation of glycerophosphocholine from unsaturated plasmalogen glycerophosphocholine lipids.

Lessig J, Schiller J, Arnhold J, Fuchs B.

J Lipid Res. 2007 Jun;48(6):1316-24. Epub 2007 Mar 29.

9.

Evidence against a major role of plasmalogens in the resistance of astrocytes in lactic acid-induced oxidative stress in vitro.

Fauconneau B, Stadelmann-Ingrand S, Favrelière S, Baudouin J, Renaud L, Piriou A, Tallineau C.

Arch Toxicol. 2001 Jan;74(11):695-701.

PMID:
11218046
10.

Plasmalogen degradation by oxidative stress: production and disappearance of specific fatty aldehydes and fatty alpha-hydroxyaldehydes.

Stadelmann-Ingrand S, Favreliere S, Fauconneau B, Mauco G, Tallineau C.

Free Radic Biol Med. 2001 Nov 15;31(10):1263-71.

PMID:
11705705
11.

The biological significance of plasmalogens in defense against oxidative damage.

Brosche T, Platt D.

Exp Gerontol. 1998 Aug;33(5):363-9. Review.

PMID:
9762517
12.
14.

Mouse brain plasmalogens are targets for hypochlorous acid-mediated modification in vitro and in vivo.

Ullen A, Fauler G, Köfeler H, Waltl S, Nusshold C, Bernhart E, Reicher H, Leis HJ, Wintersperger A, Malle E, Sattler W.

Free Radic Biol Med. 2010 Dec 1;49(11):1655-65. doi: 10.1016/j.freeradbiomed.2010.08.025. Epub 2010 Aug 31. Erratum in: Free Radic Biol Med. 2011 Apr 1;50(7):903.

15.
16.

Selective plasmenylcholine oxidation by hypochlorous acid: formation of lysophosphatidylcholine chlorohydrins.

Messner MC, Albert CJ, Hsu FF, Ford DA.

Chem Phys Lipids. 2006 Oct;144(1):34-44. Epub 2006 Jul 3.

PMID:
16859663
17.
18.

Plasmalogens the neglected regulatory and scavenging lipid species.

Wallner S, Schmitz G.

Chem Phys Lipids. 2011 Sep;164(6):573-89. doi: 10.1016/j.chemphyslip.2011.06.008. Epub 2011 Jun 21. Review.

PMID:
21723266
19.

Oxidation of plasmalogens produces highly effective modulators of macrophage function.

Heinle H, Gugeler N, Felde R, Okech D, Spiteller G.

Z Naturforsch C. 2000 Jan-Feb;55(1-2):115-20.

PMID:
10739110
20.

Reactive chlorinating species produced during neutrophil activation target tissue plasmalogens: production of the chemoattractant, 2-chlorohexadecanal.

Thukkani AK, Hsu FF, Crowley JR, Wysolmerski RB, Albert CJ, Ford DA.

J Biol Chem. 2002 Feb 8;277(6):3842-9. Epub 2001 Nov 27.

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