isoleucine has been researched along with Mitochondrial Diseases in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Bellar, A; Dasarathy, S; Kumar, A; Mishra, S; Sekar, J; Welch, N | 1 |
| Cleary, S; Cowan, JA; Harvey, SR; Sen, S; Thompson, Z; Wachnowsky, C | 1 |
| Beseler, B; Dalmau, J; García-Silva, MT; García-Villoria, J; Merinero, B; Ofman, R; Perez-Cerda, C; Ramos, J; Ribes, A; Sala, PR; Ugarte, M; Wanders, RJ | 1 |
3 other study(ies) available for isoleucine and Mitochondrial Diseases
| Article | Year |
|---|---|
L-Isoleucine reverses hyperammonemia-induced myotube mitochondrial dysfunction and post-mitotic senescence.
Topics: Amino Acids, Branched-Chain; Ammonia; Animals; Humans; Hyperammonemia; Induced Pluripotent Stem Cells; Isoleucine; Large Neutral Amino Acid-Transporter 1; Mice; Mitochondrial Diseases; Muscle Fibers, Skeletal | 2024 |
Biochemical impact of a disease-causing Ile67Asn substitution on BOLA3 protein.
Topics: Asparagine; Glutaredoxins; Humans; Isoleucine; Mitochondrial Diseases; Mitochondrial Proteins; Mutagenesis, Site-Directed; Mutation; Protein Conformation; Protein Multimerization | 2021 |
2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: an X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Alcohol Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Child; Chromosomes, Human, X; Female; Genetic Linkage; Humans; Infant; Infant, Newborn; Isoleucine; Male; Mitochondrial Diseases | 2005 |