Compounds > tyrosine

tyrosine and Hyperlipoproteinemia Type II

tyrosine has been researched along with Hyperlipoproteinemia Type II in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Allen, TJ; Calkin, AC; Cooper, ME; de Haan, JB; Giunti, S; Jandeleit-Dahm, KA; Kola, I; Lewis, P; Pete, J; Stefanovic, N; Thallas-Bonke, V1
Allende, H; Boix-Ochoa, J; Infante, D; Margarit, C; Martínez Ibáñez, V; Sanchís, L; Tormo, R1
Anderson, RG; Brown, MS; Davis, CG; Goldstein, JL; Lehrman, MA; Russell, DW1

Other Studies

3 other study(ies) available for tyrosine and Hyperlipoproteinemia Type II

ArticleYear
Lack of the antioxidant enzyme glutathione peroxidase-1 accelerates atherosclerosis in diabetic apolipoprotein E-deficient mice.
    Circulation, 2007, Apr-24, Volume: 115, Issue:16

    Topics: Animals; Aorta; Aortic Diseases; Apolipoproteins E; Atherosclerosis; Connective Tissue Growth Factor; Diabetes Mellitus, Experimental; Diabetic Angiopathies; Fibrosis; Gene Expression Regulation; Glutathione; Glutathione Peroxidase; Glutathione Peroxidase GPX1; Hyperlipoproteinemia Type II; Immediate-Early Proteins; Inflammation; Intercellular Signaling Peptides and Proteins; Isoenzymes; Macrophages; Male; Membrane Glycoproteins; Mice; Mice, Inbred C57BL; Mice, Knockout; NADPH Oxidase 2; NADPH Oxidases; NF-kappa B; Oxidation-Reduction; Receptor for Advanced Glycation End Products; Receptors, Immunologic; Sinus of Valsalva; Streptozocin; Superoxide Dismutase; Tyrosine; Vascular Cell Adhesion Molecule-1; Vascular Endothelial Growth Factor A

2007
[New perspectives in liver-based metabolic errors: liver transplantation].
    Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica, 1989, Volume: 2, Issue:3

    Topics: alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Child; Female; Glycogen Storage Disease Type II; Humans; Hyperlipoproteinemia Type II; Infant, Newborn; Liver; Liver Cirrhosis; Liver Transplantation; Male; Metabolism, Inborn Errors; Tyrosine

1989
The J.D. mutation in familial hypercholesterolemia: amino acid substitution in cytoplasmic domain impedes internalization of LDL receptors.
    Cell, 1986, Apr-11, Volume: 45, Issue:1

    Topics: Alleles; Amino Acid Sequence; Base Sequence; Cell Compartmentation; Cloning, Molecular; Cysteine; Endocytosis; Humans; Hyperlipoproteinemia Type II; Mutation; Receptors, LDL; Structure-Activity Relationship; Transfection; Tyrosine

1986