phenylalanine has been researched along with tetrahydropterin in 9 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (33.33) | 18.7374 |
1990's | 3 (33.33) | 18.2507 |
2000's | 1 (11.11) | 29.6817 |
2010's | 1 (11.11) | 24.3611 |
2020's | 1 (11.11) | 2.80 |
Authors | Studies |
---|---|
Blau, N; Dianzani, I; Endres, W; Ferrero, GB; Guardamagna, O; Ponzone, A | 1 |
Wachtel, U | 1 |
Houst'ková, H; Hyánek, J; Leeming, RJ; Niederwieser, A; Rubín, A; Simková, M; Zeman, J | 1 |
Kapatos, G; Kaufman, S; McInnes, RR; Rizzo, WB; Schulman, JD | 1 |
Mitnaul, LJ; Shiman, R | 1 |
Fitzpatrick, PF; Hillas, PJ | 1 |
Bahrami, S; Heller, R; Werner, ER; Werner-Felmayer, G | 1 |
Bernstein, I; Boland, C; Chikwana, VM; Iwata-Reuyl, D; Kelly, VP; Rakovich, T | 1 |
Aubi, O; Grindheim, AK; Jung-Kc, K; Martinez, A; McCann, A; Prestegård, KS; Scherer, T; Shi, TS; Spriet, E; Thöny, B; Ulvik, A; Ying, M | 1 |
1 review(s) available for phenylalanine and tetrahydropterin
Article | Year |
---|---|
Review of current practices in management of inherited disorders of amino acid metabolism in Western Europe.
Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Biopterins; Diet; Dietary Proteins; Dihydropteridine Reductase; Europe; Female; Glucosephosphate Dehydrogenase Deficiency; Humans; Infant; Infant, Newborn; Intellectual Disability; Liver; Mass Screening; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Pregnancy; Pregnancy Complications; Prognosis; Pterins; Tyrosine | 1986 |
8 other study(ies) available for phenylalanine and tetrahydropterin
Article | Year |
---|---|
Progression of 6-pyruvoyl-tetrahydropterin synthase deficiency from a peripheral into a central phenotype.
Topics: Alcohol Oxidoreductases; Biopterins; Female; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Infant, Newborn; Phenotype; Phenylalanine; Phosphorus-Oxygen Lyases; Pterins | 1990 |
[Transitory hyperphenylalaninemia with a tetrahydrobiopterin synthesis deficiency].
Topics: Female; Humans; Infant, Newborn; Phenylalanine; Pterins | 1987 |
Use of tetrahydropterins in the treatment of hyperphenylalaninemia due to defective synthesis of tetrahydrobiopterin: evidence that peripherally administered tetrahydropterins enter the brain.
Topics: Biopterins; Brain; Child; Child, Preschool; Female; Humans; Male; Neopterin; Phenylalanine; Phenylketonurias; Pteridines; Pterins | 1982 |
Coordinate regulation of tetrahydrobiopterin turnover and phenylalanine hydroxylase activity in rat liver cells.
Topics: Animals; Binding, Competitive; Biopterins; Cells, Cultured; Enzyme Activation; Kinetics; Liver; Phenylalanine; Phenylalanine Hydroxylase; Pterins; Rats; Water | 1995 |
A mechanism for hydroxylation by tyrosine hydroxylase based on partitioning of substituted phenylalanines.
Topics: Animals; Dihydroxyphenylalanine; Fenclonine; Hydroxylation; Kinetics; Models, Chemical; Molecular Structure; Oxygen; p-Fluorophenylalanine; Phenylalanine; Pterins; Rats; Recombinant Proteins; Substrate Specificity; Tyrosine 3-Monooxygenase | 1996 |
Bacterial lipopolysaccharide down-regulates expression of GTP cyclohydrolase I feedback regulatory protein.
Topics: Alanine; Blotting, Northern; Cells, Cultured; Cloning, Molecular; DNA, Complementary; Dose-Response Relationship, Drug; Down-Regulation; Endothelium, Vascular; GTP Cyclohydrolase; Humans; Interferon-gamma; Intracellular Signaling Peptides and Proteins; Lipopolysaccharides; Phenylalanine; Protein Binding; Proteins; Pteridines; Pterins; Recombinant Proteins; RNA, Messenger; Time Factors; Tissue Distribution; Tumor Cells, Cultured; Umbilical Veins; Up-Regulation | 2002 |
Queuosine deficiency in eukaryotes compromises tyrosine production through increased tetrahydrobiopterin oxidation.
Topics: Animals; Hep G2 Cells; Humans; Mice; Nucleoside Q; Oxidation-Reduction; Pentosyltransferases; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Pterins; RNA, Transfer; Tetrahydrofolate Dehydrogenase; Tyrosine | 2011 |
The Pah-R261Q mouse reveals oxidative stress associated with amyloid-like hepatic aggregation of mutant phenylalanine hydroxylase.
Topics: Amyloid; Animals; Autophagy; Biomarkers; Body Weight; Breeding; Female; Gene Expression Regulation; Genotype; Lipid Metabolism; Liver; Male; Metabolome; Mice; Mutant Proteins; Mutation; Neurotransmitter Agents; Oxidative Stress; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Protein Aggregates; Pterins; Respiration; RNA, Messenger; Ubiquitin; Ubiquitination | 2021 |