indoleacetic acid has been researched along with Phenylketonurias in 8 studies
indoleacetic acid: RN given refers to unlabeled parent cpd; structure in Merck Index, 9th ed, #4841
auxin : Any of a group of compounds, both naturally occurring and synthetic, that induce cell elongation in plant stems (from Greek alphaupsilonxialphanuomega, "to grow").
indole-3-acetic acid : A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens has been replaced by a 1H-indol-3-yl group.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 | 8 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| HSIA, DY | 1 |
| ROWLEY, WA | 1 |
| HUANG, I | 1 |
| BOGGS, DE | 1 |
| MCLAY, D | 1 |
| KAPPY, M | 1 |
| WAISMAN, HA | 1 |
| PERRY, TL | 1 |
| HANSEN, S | 1 |
| TISCHLER, B | 1 |
| HESTRIN, M | 1 |
| FISCHL, J | 1 |
| RABIAH, S | 1 |
| MURTAGH, JJ | 1 |
| RAPPALLINI, C | 1 |
| BESSMAN, SP | 1 |
| ALLEGRANZA, A | 1 |
| ALDEGHI, E | 1 |
| CANEVINI, P | 1 |
| DEVITO, C | 1 |
| Antoshechkin, AG | 1 |
| Zuyeva, LA | 1 |
| Maximova, LA | 1 |
8 other studies available for indoleacetic acid and Phenylketonurias
| Article | Year |
|---|---|
The excretion of 5-hydroxyindoleacetic acid in the heterozygous carrier for phenylketonuria.
Topics: Biological Transport; Humans; Hydroxyindoleacetic Acid; Indoleacetic Acids; Intellectual Disability; | 1961 |
EXCRETION OF INDOLYL ACIDS IN PHENYLKETONURIC MONKEYS.
Topics: Animals; Body Fluids; Haplorhini; Humans; Indoleacetic Acids; Indoles; Lactates; Metabolism; Phenyla | 1963 |
DEFECTIVE 5-HYDROXYLATION OF TRYPTOPHAN IN PHENYLKETONURIA.
Topics: Blood Chemical Analysis; Body Fluids; Humans; Hydroxyindoleacetic Acid; Hydroxylation; Indoleacetic | 1964 |
DETERMINATION OF FREE AND TOTAL INDOLE-3-ACETIC ACID AND OF THE INDOLE INDEX.
Topics: Friedreich Ataxia; Humans; Indoleacetic Acids; Indoles; Intestines; Kynurenine; Metabolism; Myotonia | 1964 |
[SEROTONIN AND 5-HYDROXYINDOLACETIC ACID IN THE NEWBORN INFANT].
Topics: Anemia; Anemia, Aplastic; Cardiovascular System; Gastrointestinal Tract; Humans; Hydroxyindoleacetic | 1964 |
SOME BIOCHEMICAL LESSONS TO BE LEARNED FROM PHENYLKETONURIA.
Topics: Glutamates; Humans; Indican; Indoleacetic Acids; Indoles; Learning; Metabolism; Phenylacetates; Phen | 1964 |
[METABOLIC ASPECTS OF PHENYLKETONURIA WITH PARTICULAR ATTENTION TO URINARY ELIMINATION OF SOME PHENOLIC ACIDS].
Topics: Adolescent; Attention; Biomedical Research; Child; Humans; Hydroxybenzoates; Indoleacetic Acids; Man | 1964 |
Excretion of phenylpyruvic, 4-hydroxyphenylpyruvic and indolyl-3-acetic acids by the skin fibroblasts from a phenylketonuric child.
Topics: Adult; Child, Preschool; Epidermis; Female; Fibroblasts; Humans; Indoleacetic Acids; Phenylketonuria | 1988 |