indoleacetic acid has been researched along with Hepatolenticular Degeneration in 2 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indole-3-acetic acid : A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens has been replaced by a 1H-indol-3-yl group.
Hepatolenticular Degeneration: A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (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 |
|---|---|
| SUNDERMAN, FW | 1 |
| SOURKES, TL | 1 |
| MURPHY, GF | 1 |
| SANKOFF, I | 1 |
| WISEMAN-DISTLER, MH | 1 |
| SAINTCYR, S | 1 |
2 other studies available for indoleacetic acid and Hepatolenticular Degeneration
| Article | Year |
|---|---|
DISTURBANCES OF INDOLE METABOLISM IN HEPATOLENTICULAR DEGENERATION.
Topics: Hepatolenticular Degeneration; Indoleacetic Acids; Metabolism | 1963 |
EXCRETION OF DOPAMINE, CATECHOLAMINE METABOLITES AND 5-HYDROXYINDOLEACETIC ACID IN HEPATOLENTICULAR DEGENERATION (WILSON'S DISEASE).
Topics: Adolescent; Child; Chromatography; Creatine; Creatinine; Dopamine; Epinephrine; Hepatolenticular Deg | 1963 |