adenosine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Blum, D; Galas, MC; Hourez, R; Popoli, P; Schiffmann, SN | 1 |
| Belguith, N; Charfeddine, I; Fakhfakh, F; Masmoudi, S; Mkaouar-Rebai, E; Mnif, M; Tlili, A; Triki, C | 1 |
1 review(s) available for adenosine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Adenosine receptors and Huntington's disease: implications for pathogenesis and therapeutics.
Topics: Adenosine; Adenosine A1 Receptor Agonists; Adenosine A2 Receptor Antagonists; Animals; Corpus Striatum; Disease Models, Animal; Humans; Huntington Disease; Mitochondrial Diseases; Models, Molecular; Models, Neurological; Mutation; Neural Networks, Computer; Neuroprotective Agents; Receptor, Adenosine A1; Receptor, Adenosine A2A; Receptors, Dopamine | 2003 |
1 other study(ies) available for adenosine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases.
Topics: Adenosine; Base Sequence; DNA Mutational Analysis; Female; Guanosine; Humans; Male; Mitochondrial Diseases; Molecular Sequence Data; Mutation; Nucleic Acid Conformation; Pedigree; RNA, Transfer, Leu; Tunisia | 2007 |