thioctic acid has been researched along with Atrophy in 2 studies
Thioctic Acid: An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
Atrophy: Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Radzki, RP | 1 |
| Bienko, M | 1 |
| Wolski, D | 1 |
| Oniszczuk, T | 1 |
| Radzka-Pogoda, A | 1 |
| Polak, P | 1 |
| Borzecki, A | 1 |
| Stasiak, M | 1 |
| Habarou, F | 1 |
| Hamel, Y | 1 |
| Haack, TB | 1 |
| Feichtinger, RG | 1 |
| Lebigot, E | 1 |
| Marquardt, I | 1 |
| Busiah, K | 1 |
| Laroche, C | 1 |
| Madrange, M | 1 |
| Grisel, C | 1 |
| Pontoizeau, C | 1 |
| Eisermann, M | 1 |
| Boutron, A | 1 |
| Chrétien, D | 1 |
| Chadefaux-Vekemans, B | 1 |
| Barouki, R | 1 |
| Bole-Feysot, C | 1 |
| Nitschke, P | 1 |
| Goudin, N | 1 |
| Boddaert, N | 1 |
| Nemazanyy, I | 1 |
| Delahodde, A | 1 |
| Kölker, S | 1 |
| Rodenburg, RJ | 1 |
| Korenke, GC | 1 |
| Meitinger, T | 1 |
| Strom, TM | 1 |
| Prokisch, H | 1 |
| Rotig, A | 1 |
| Ottolenghi, C | 1 |
| Mayr, JA | 1 |
| de Lonlay, P | 1 |
2 other studies available for thioctic acid and Atrophy
| Article | Year |
|---|---|
Lipoic acid (LA) dose-dependently protects bone losses in the mandible of rats during the development of osteopenia by inhibiting oxidative stress and promoting bone formation.
Topics: Animals; Atrophy; Bone Diseases, Metabolic; Bone Resorption; Dose-Response Relationship, Drug; Femal | 2022 |
Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy.
Topics: Acyltransferases; Amino Acids; Atrophy; Brain; Brain Diseases; Brain Mapping; Cells, Cultured; Energ | 2017 |