thymidine has been researched along with Inborn Errors of Metabolism in 6 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| ") with the cobalamin D variant of congenital methylmalonic aciduria-homocystinuria, whose previously reported lack of megaloblastic anemia conflicted with current concepts of cobalamin's role in DNA synthesis and the "methyltetrahydrofolate (MTHF) trap" hypothesis." | 7.66 | Abnormal deoxyuridine suppression test in congenital methylmalonic aciduria-homocystinuria without megaloblastic anemia: divergent biochemical and morphological bone marrow manifestations of disordered cobalamin metabolism in man. ( Carmel, R; Goodman, SI, 1982) |
| ") with the cobalamin D variant of congenital methylmalonic aciduria-homocystinuria, whose previously reported lack of megaloblastic anemia conflicted with current concepts of cobalamin's role in DNA synthesis and the "methyltetrahydrofolate (MTHF) trap" hypothesis." | 3.66 | Abnormal deoxyuridine suppression test in congenital methylmalonic aciduria-homocystinuria without megaloblastic anemia: divergent biochemical and morphological bone marrow manifestations of disordered cobalamin metabolism in man. ( Carmel, R; Goodman, SI, 1982) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (83.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lopez-Gomez, C | 1 |
| Levy, RJ | 1 |
| Sanchez-Quintero, MJ | 1 |
| Juanola-Falgarona, M | 1 |
| Barca, E | 1 |
| Garcia-Diaz, B | 1 |
| Tadesse, S | 1 |
| Garone, C | 1 |
| Hirano, M | 1 |
| Carmel, R | 1 |
| Goodman, SI | 1 |
| Osterman, JV | 1 |
| Waddell, A | 1 |
| Aposhian, HV | 1 |
| Zink, HA | 1 |
| Palmberg, PF | 1 |
| Bigger, JF | 1 |
| Cline, MJ | 1 |
| Jung, EG | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Deoxythymidine and Deoxycytidine Treatment for Thymidine Kinase 2 (TK2) Deficiency[NCT03639701] | Phase 1/Phase 2 | 23 participants (Actual) | Interventional | 2017-05-16 | Active, not recruiting | ||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
1 trial available for thymidine and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Increased sensitivity to theophylline associated with primary open-angle glaucoma.
Topics: Clinical Trials as Topic; Cyclic AMP; Dexamethasone; DNA; Dose-Response Relationship, Drug; Drug Hyp | 1973 |
5 other studies available for thymidine and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency.
Topics: Animals; Antimetabolites; Deoxycytidine Monophosphate; Disease Models, Animal; DNA, Mitochondrial; D | 2017 |
Abnormal deoxyuridine suppression test in congenital methylmalonic aciduria-homocystinuria without megaloblastic anemia: divergent biochemical and morphological bone marrow manifestations of disordered cobalamin metabolism in man.
Topics: Adolescent; Adult; Anemia, Megaloblastic; Bone Marrow; Deoxyuridine; Homocystinuria; Humans; Male; M | 1982 |
Gene therapy systems: the need, experimental approach, and implications.
Topics: Animals; Cell Line; Centrifugation, Density Gradient; Deoxyribonucleases; DNA, Bacterial; Embryo, Ma | 1971 |
Microbicidal activity of human eosinophils.
Topics: ABO Blood-Group System; Autoradiography; Blood Bactericidal Activity; Cell Adhesion; Eosinophils; Hu | 1972 |
New form of molecular defect in xeroderma pigmentosum.
Topics: Adult; Autoradiography; Deoxyribonucleases; DNA; DNA Nucleotidyltransferases; DNA Replication; Human | 1970 |