Citation: D. Spiteller et G. Spiteller, Identification of toxic 2,4-decadienal in oxidized, low-density lipoprotein by solid-phase microextraction, ANGEW CHEM, 39(3), 2000, pp. 583-585
Citation: D. Spiteller et G. Spiteller, Oxidation of linoleic acid in low-density lipoprotein: An important event in atherogenesis, ANGEW CHEM, 39(3), 2000, pp. 585-589
Authors:
Heinle, H
Gugeler, N
Felde, R
Okech, D
Spiteller, G
Citation: H. Heinle et al., Oxidation of plasmalogens produces highly effective modulators of macrophage function, Z NATURFO C, 55(1-2), 2000, pp. 115-120
Authors:
Adam, P
Hannemann, K
Reiner, J
Spiteller, G
Citation: P. Adam et al., 10-hydroxystearic acid - Identified after homogenization of tissue - Is derived from bacteria, Z NATURFO C, 55(11-12), 2000, pp. 965-970
Citation: A. Mollenberg et G. Spiteller, Transformations of 12,13-epoxy-11-hydroxy-9-octadecenoic acid and 4,5-epoxy-N-acetylsphingosine by incubation with liver homogenate and liver microsomes, Z NATURFO C, 55(11-12), 2000, pp. 981-986
Citation: Baw. Gallasch et G. Spiteller, Synthesis of 9,12-dioxo-10(Z)-dodecenoic acid, a new fatty acid metabolitederived from 9-hydroperoxy-10,12-octadecadienoic acid in lentil seed (Lensculinaris medik.), LIPIDS, 35(9), 2000, pp. 953-960
Citation: Baw. Gallasch et G. Spiteller, Detection of 9,12-dioxo-10(Z)-dodecenoic acid, a new fatty acid metabolitederived from 13-hydroperoxy-9,11-octadecadienoic acid in lentil seed (Lensculinaris Medik.). Synthesis of 9,12-dioxo-10(Z)-dodecenoic acid and 9,12-dioxo-10(E)-dodecenoic acid (vol 35, pg 953, 2000), LIPIDS, 35(11), 2000, pp. 1300-1300
Citation: G. Spiteller et al., Investigation of aldehydic lipid peroxidation products by gas chromatography-mass spectrometry, J CHROMAT A, 843(1-2), 1999, pp. 29-98
Citation: Ct. Fuchs et G. Spiteller, 9-(3,4-dimethyl-5-pentyl-furan-2-yl) nonanoic acid and 9-(3,4-dimethyl-5-propyl-furan-2-yl) nonanoic acid: New naturally occurring peroxidase inhibitors, Z NATURFO C, 54(11), 1999, pp. 932-936
Citation: M. Jahn et al., The reaction of hyaluronic acid and its monomers, glucuronic acid and N-acetylglucosamine, with reactive oxygen species, CARBOHY RES, 321(3-4), 1999, pp. 228-234
Citation: S. Hecht et G. Spiteller, Linoleic acid peroxidation products are metabolized by hydrogenation in porcine liver tissue, EUR MASS SP, 4(5), 1998, pp. 393-399
Citation: W. Jira et al., Increased levels of lipid oxidation products in rheumatically destructed bones of patients suffering from rheumatoid arthritis, Z NATURFO C, 53(11-12), 1998, pp. 1061-1071
Citation: G. Spiteller, Linoleic acid peroxidation - the dominant lipid peroxidation process in low density lipoprotein - and its relationship to chronic diseases, CHEM PHYS L, 95(2), 1998, pp. 105-162