tyrosine and 4-hydroxyphenylacetaldehyde

tyrosine has been researched along with 4-hydroxyphenylacetaldehyde in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (42.86)18.2507
2000's3 (42.86)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hazen, SL; Heinecke, JW; Hsu, FF1
Crowley, JR; d'Avignon, A; Gaut, JP; Hazen, SL; Heinecke, JW; Hsu, FF1
Hazen, SL; Hegele, RA; Heinecke, JW; Huff, MW; Miller, DB; Whitman, SC1
Crowley, JR; Hazen, SL; Heinecke, JW; Heller, JI; Pennathur, S; Salvay, DM; Wagner, P1
Crowley, JR; Gaut, JP; Hazen, SL; Heinecke, JW; Hsu, FF1
Alt, E; Exner, M; Gmeiner, B; Hermann, M; Hofbauer, R; Kapiotis, S; Minar, E; Quehenberger, P; Speiser, W1
Gillaspy, G; Harich, K; Li, J; Torrens-Spence, MP; White, RH; Zhao, B1

Other Studies

7 other study(ies) available for tyrosine and 4-hydroxyphenylacetaldehyde

ArticleYear
p-Hydroxyphenylacetaldehyde is the major product of L-tyrosine oxidation by activated human phagocytes. A chloride-dependent mechanism for the conversion of free amino acids into reactive aldehydes by myeloperoxidase.
    The Journal of biological chemistry, 1996, Jan-26, Volume: 271, Issue:4

    Topics: Acetaldehyde; Cells, Cultured; Chlorides; Chromatography, High Pressure Liquid; Fourier Analysis; Humans; Magnetic Resonance Spectroscopy; Neutrophils; Oxidation-Reduction; Peroxidase; Phagocytes; Phenol; Superoxides; Tyrosine

1996
p-Hydroxyphenylacetaldehyde, the major product of L-tyrosine oxidation by the myeloperoxidase-H2O2-chloride system of phagocytes, covalently modifies epsilon-amino groups of protein lysine residues.
    The Journal of biological chemistry, 1997, Jul-04, Volume: 272, Issue:27

    Topics: Acetaldehyde; Amino Acids; Animals; Cattle; Chlorides; Chromatography, High Pressure Liquid; Humans; Hydrogen Peroxide; Inflammation; Lysine; Magnetic Resonance Spectroscopy; Neutrophils; Peroxidase; Phagocytes; Phenol; Proteins; Schiff Bases; Serum Albumin, Bovine; Tyrosine

1997
Modification of type III VLDL, their remnants, and VLDL from ApoE-knockout mice by p-hydroxyphenylacetaldehyde, a product of myeloperoxidase activity, causes marked cholesteryl ester accumulation in macrophages.
    Arteriosclerosis, thrombosis, and vascular biology, 1999, Volume: 19, Issue:5

    Topics: Acetaldehyde; Animals; Apolipoproteins E; Arteriosclerosis; Cell Line; Cholesterol Esters; Esterification; Humans; Hyperlipoproteinemia Type III; Hypochlorous Acid; Interferon-gamma; Lipoprotein Lipase; Lipoproteins, VLDL; Macrophages; Membrane Proteins; Mice; Mice, Inbred C57BL; Mice, Knockout; Oxidation-Reduction; Peroxidase; Phenol; Poly I; Receptors, Immunologic; Receptors, Lipoprotein; Receptors, Scavenger; Scavenger Receptors, Class A; Scavenger Receptors, Class B; Sterol O-Acyltransferase; Triglycerides; Tyrosine

1999
p-hydroxyphenylacetaldehyde, an aldehyde generated by myeloperoxidase, modifies phospholipid amino groups of low density lipoprotein in human atherosclerotic intima.
    The Journal of biological chemistry, 2000, Apr-07, Volume: 275, Issue:14

    Topics: Acetaldehyde; Arteriosclerosis; Humans; Hydrogen Peroxide; Kinetics; Lipoproteins, LDL; Neutrophils; Peroxidase; Phenol; Phosphatidylethanolamines; Phospholipids; Tunica Intima; Tyrosine

2000
Elevated levels of protein-bound p-hydroxyphenylacetaldehyde, an amino-acid-derived aldehyde generated by myeloperoxidase, are present in human fatty streaks, intermediate lesions and advanced atherosclerotic lesions.
    The Biochemical journal, 2000, Dec-15, Volume: 352 Pt 3

    Topics: Acetaldehyde; Antioxidants; Aorta; Arteriosclerosis; Chlorides; Gas Chromatography-Mass Spectrometry; Humans; Lipid Metabolism; Lipoproteins, LDL; Lysine; Peroxidase; Phenol; Schiff Bases; Solubility; Tunica Intima; Tyrosine; Water

2000
p-Hydroxyphenylacetaldehyde, the major product of tyrosine oxidation by the activated myeloperoxidase system can act as an antioxidant in LDL.
    FEBS letters, 2001, Feb-09, Volume: 490, Issue:1-2

    Topics: Acetaldehyde; Antioxidants; Dose-Response Relationship, Drug; Electrophoresis, Agar Gel; Endothelium, Vascular; Free Radical Scavengers; Humans; Hydrogen-Ion Concentration; Hypochlorous Acid; Ions; Lipid Metabolism; Lipoproteins, LDL; Neutrophils; Oxygen; Peroxidase; Phenol; Protein Binding; Thiobarbituric Acid Reactive Substances; Time Factors; Tyrosine; Umbilical Veins

2001
Biochemical evaluation of a parsley tyrosine decarboxylase results in a novel 4-hydroxyphenylacetaldehyde synthase enzyme.
    Biochemical and biophysical research communications, 2012, Feb-10, Volume: 418, Issue:2

    Topics: Acetaldehyde; Aromatic-L-Amino-Acid Decarboxylases; Dihydroxyphenylalanine; Petroselinum; Phenol; Thalictrum; Tyrosine; Tyrosine Decarboxylase

2012