taurine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 10 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Taurine is a naturally occurring sulfur-containing amino acid that is found abundantly in excitatory tissues, such as the heart, brain, retina and skeletal muscles." | 2.72 | The Role of Taurine in Mitochondria Health: More Than Just an Antioxidant. ( Jong, CJ; Sandal, P; Schaffer, SW, 2021) |
| "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 | 4 (40.00) | 29.6817 |
| 2010's | 3 (30.00) | 24.3611 |
| 2020's | 3 (30.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ueda, S | 1 |
| Yagi, M | 1 |
| Tomoda, E | 1 |
| Matsumoto, S | 1 |
| Ueyanagi, Y | 1 |
| Do, Y | 1 |
| Setoyama, D | 1 |
| Matsushima, Y | 1 |
| Nagao, A | 1 |
| Suzuki, T | 9 |
| Ide, T | 1 |
| Mori, Y | 1 |
| Oyama, N | 1 |
| Kang, D | 1 |
| Uchiumi, T | 1 |
| Kazuhito, T | 1 |
| Wei, FY | 3 |
| Jong, CJ | 2 |
| Sandal, P | 1 |
| Schaffer, SW | 2 |
| Fakruddin, M | 1 |
| Asano, K | 2 |
| Kaieda, T | 1 |
| Omori, A | 1 |
| Izumi, R | 1 |
| Fujimura, A | 1 |
| Kaitsuka, T | 1 |
| Miyata, K | 1 |
| Araki, K | 1 |
| Oike, Y | 1 |
| Scorrano, L | 1 |
| Tomizawa, K | 2 |
| Saito, A | 1 |
| Ikeuchi, Y | 1 |
| Numata, T | 1 |
| Tanaka, R | 1 |
| Yamane, Y | 1 |
| Yamamoto, T | 1 |
| Goto, T | 1 |
| Kishita, Y | 1 |
| Murayama, K | 1 |
| Ohtake, A | 1 |
| Okazaki, Y | 1 |
| Sakaguchi, Y | 1 |
| Shetewy, A | 1 |
| Shimada-Takaura, K | 1 |
| Warner, D | 1 |
| Mehdi, AB | 1 |
| Alexeyev, M | 1 |
| Takahashi, K | 1 |
| Wada, T | 1 |
| Saigo, K | 1 |
| Watanabe, K | 2 |
| Ohta, S | 1 |
| Umeda, N | 1 |
| Yukawa, M | 1 |
| Ohya, Y | 1 |
| Shindo, H | 1 |
| Palmi, M | 1 |
| Davey, G | 1 |
| Tipton, KF | 1 |
| Meini, A | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Taurine Supplementation and Physical Training Effects on Adipose Tissue Mitochondrial Energy Metabolism, and Blood Inflammation and Oxidative Stress in Obese Women[NCT04279600] | 24 participants (Actual) | Interventional | 2017-05-01 | Completed | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
3 reviews available for taurine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Posttranscriptional modifications in mitochondrial tRNA and its implication in mitochondrial translation and disease.
Topics: Animals; Humans; Mitochondria; Mitochondrial Diseases; RNA Processing, Post-Transcriptional; RNA, Tr | 2020 |
The Role of Taurine in Mitochondria Health: More Than Just an Antioxidant.
Topics: Animals; Antioxidants; Apoptosis; Clinical Trials as Topic; Humans; Mitochondria; Mitochondrial Dise | 2021 |
[Mitochondrial tRNA diseases: defect of modification in anticodon in mutant tRNA molecules].
Topics: Animals; Anticodon; Codon, Terminator; Humans; Mice; Mitochondrial Diseases; Mutation; RNA; RNA, Mit | 2003 |
7 other studies available for taurine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Mitochondrial haplotype mutation alleviates respiratory defect of MELAS by restoring taurine modification in tRNA with 3243A > G mutation.
Topics: DNA, Mitochondrial; Haplotypes; Humans; MELAS Syndrome; Mitochondrial Diseases; Mutation; RNA, Trans | 2023 |
Defective Mitochondrial tRNA Taurine Modification Activates Global Proteostress and Leads to Mitochondrial Disease.
Topics: Humans; Mitochondrial Diseases; RNA, Transfer; Taurine | 2018 |
Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease.
Topics: Animals; Carrier Proteins; Cats; Child, Preschool; Female; GTP-Binding Proteins; HEK293 Cells; HeLa | 2018 |
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 |
Taurine as a constituent of mitochondrial tRNAs: new insights into the functions of taurine and human mitochondrial diseases.
Topics: Anticodon; Humans; Mass Spectrometry; Mitochondria; Mitochondrial Diseases; RNA, Transfer; Sequence | 2002 |
Mitochondria-specific RNA-modifying enzymes responsible for the biosynthesis of the wobble base in mitochondrial tRNAs. Implications for the molecular pathogenesis of human mitochondrial diseases.
Topics: Amino Acid Sequence; Carrier Proteins; Cell Respiration; GTP Phosphohydrolases; GTP-Binding Proteins | 2005 |
Taurine, taurine analogues, and mitochondrial function and dysfuntion.
Topics: Animals; Calcium; Cytochromes c; Male; Membrane Potentials; Mitochondria; Mitochondrial Diseases; Mo | 2006 |