serine has been researched along with Phenylketonurias in 7 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
Phenylketonurias: A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (71.43) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Leandro, J | 1 |
| Simonsen, N | 1 |
| Saraste, J | 1 |
| Leandro, P | 1 |
| Flatmark, T | 1 |
| Liang, L | 1 |
| Gu, X | 1 |
| Li, D | 1 |
| Lu, L | 1 |
| Benevenga, NJ | 1 |
| Steele, RD | 1 |
| Shaw, KN | 1 |
| Lieberman, E | 1 |
| Koch, R | 1 |
| Donnell, GN | 1 |
| Kerr, GR | 1 |
| Chamove, AS | 1 |
| Harlow, HF | 1 |
| Waisman, HA | 1 |
| Levy, HL | 1 |
| Barkin, E | 1 |
| McKean, CM | 1 |
| Peterson, NA | 1 |
1 review available for serine and Phenylketonurias
| Article | Year |
|---|---|
Adverse effects of excessive consumption of amino acids.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Brain; Cattle; Diet; Disease Models, Ani | 1984 |
6 other studies available for serine and Phenylketonurias
| Article | Year |
|---|---|
Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation.
Topics: Amino Acid Substitution; Biocatalysis; Heat-Shock Proteins; Humans; Hydrogen-Ion Concentration; Isoq | 2011 |
The expression and phosphorylation of acid sensing ion channel 1a in the brain of a mouse model of phenylketonuria.
Topics: Acid Sensing Ion Channels; Animals; Blotting, Western; Brain Chemistry; Cerebral Cortex; Female; Gen | 2011 |
Cystathioninuria.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carcinoma, Hepatocellular; Child, Preschoo | 1967 |
"Fetal PKU:" the effect of maternal hyperphenylalaninemia during pregnancy in the rhesus monkey (Macaca mulatta).
Topics: Amino Acids; Animals; Animals, Newborn; Birth Weight; Diet; Female; Fetal Diseases; Haplorhini; Huma | 1968 |
Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Aspartic Acid; Biological Transp | 1971 |
Glutamine in the phenylketonuric central nervous system.
Topics: Adolescent; Adult; Amino Acids; Biological Transport, Active; Brain; Brain Chemistry; Child; Female; | 1970 |