thymine has been researched along with Muscular Diseases in 3 studies
Muscular Diseases: Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Campos, Y | 1 |
| García, A | 1 |
| del Hoyo, P | 1 |
| Jara, P | 1 |
| Martín, MA | 1 |
| Rubio, JC | 1 |
| Berbel, A | 1 |
| Barberá, JR | 1 |
| Ribacoba, R | 1 |
| Astudillo, A | 1 |
| Cabello, A | 1 |
| Ricoy, JR | 1 |
| Arenas, J | 1 |
| Al-Sanna'a, NA | 1 |
| Van Kuilenburg, AB | 1 |
| Atrak, TM | 1 |
| Abdul-Jabbar, MA | 1 |
| Van Gennip, AH | 1 |
| Gambello, MJ | 1 |
| Bai, RK | 1 |
| Chen, TJ | 1 |
| Dimachkie, M | 1 |
| Wong, LJ | 1 |
3 other studies available for thymine and Muscular Diseases
| Article | Year |
|---|---|
Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypes.
Topics: Acidosis, Lactic; Adenine; Adult; Biopsy; Cardiomyopathies; Cytosine; DNA, Mitochondrial; Female; Gu | 2003 |
Dihydropyrimidine dehydrogenase deficiency presenting at birth.
Topics: Age of Onset; Antimetabolites; Binding Sites; Digestive System Abnormalities; Dihydropyrimidine Dehy | 2005 |
Exercise intolerance associated with a novel 8300T > C mutation in mitochondrial transfer RNAlys.
Topics: Adult; Base Sequence; Cytosine; DNA, Mitochondrial; Electron Transport; Exercise Tolerance; Female; | 2006 |