thymidine has been researched along with Genetic Diseases, Inborn in 5 studies
Genetic Diseases, Inborn: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yoshinaga, H | 1 |
| Nakahara, M | 1 |
| Koyama, T | 1 |
| Shibamiya, A | 1 |
| Nakazawa, F | 1 |
| Miles, LA | 1 |
| Hirosawa, S | 1 |
| Aoki, N | 1 |
| Ghosal, G | 1 |
| Muniyappa, K | 1 |
| Iurov, IuB | 1 |
| Vorsanova, SG | 1 |
| Jaspers, NG | 1 |
| Zdzienicka, MZ | 1 |
| Siminovitch, L | 1 |
1 review available for thymidine and Genetic Diseases, Inborn
| Article | Year |
|---|---|
Hoogsteen base-pairing revisited: resolving a role in normal biological processes and human diseases.
Topics: Adenine; Base Pairing; DNA; DNA Replication; G-Quadruplexes; Gene Expression Regulation; Genetic Dis | 2006 |
4 other studies available for thymidine and Genetic Diseases, Inborn
| Article | Year |
|---|---|
A single thymine nucleotide deletion responsible for congenital deficiency of plasmin inhibitor.
Topics: alpha-2-Antiplasmin; Cloning, Molecular; DNA Mutational Analysis; DNA, Complementary; Family Health; | 2002 |
[DNA replication in cultured amniotic fluid cells].
Topics: Amniotic Fluid; Autoradiography; Cells, Cultured; DNA Replication; Female; Genetic Diseases, Inborn; | 1981 |
Inhibition of DNA synthesis by ionizing radiation.
Topics: Animals; Carbon Radioisotopes; Cell Culture Techniques; Cells, Cultured; DNA Replication; Genetic Di | 1999 |
Temperature-sensitive conditional lethal mutants of somatic cells.
Topics: Animals; Clone Cells; Culture Techniques; Cytogenetics; DNA; Genes, Lethal; Genetic Diseases, Inborn | 1970 |