beta-alanine has been researched along with Mitochondrial Diseases in 1 studies
Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
Excerpt | Relevance | Reference |
---|---|---|
"Taurine treatment limited mitochondrial superoxide generation, supporting a role for taurine in maintaining complex I activity." | 1.43 | Mitochondrial defects associated with β-alanine toxicity: relevance to hyper-beta-alaninemia. ( Alexeyev, M; Jong, CJ; Mehdi, AB; Schaffer, SW; Shetewy, A; Shimada-Takaura, K; Takahashi, K; Warner, D, 2016) |
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 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Shetewy, A | 1 |
Shimada-Takaura, K | 1 |
Warner, D | 1 |
Jong, CJ | 1 |
Mehdi, AB | 1 |
Alexeyev, M | 1 |
Takahashi, K | 1 |
Schaffer, SW | 1 |
1 other study available for beta-alanine and Mitochondrial Diseases
Article | Year |
---|---|
Mitochondrial defects associated with β-alanine toxicity: relevance to hyper-beta-alaninemia.
Topics: Animals; beta-Alanine; Disorders of Excessive Somnolence; Electron Transport Complex I; Embryo, Mamm | 2016 |