thymine has been researched along with Thalassemia in 3 studies
Thalassemia: A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Zarkada, E | 1 |
| Yfanti, E | 1 |
| Teli, A | 1 |
| Balassopoulou, A | 1 |
| Sinopoulou, K | 1 |
| Theodoridou, S | 1 |
| Guida, S | 1 |
| Giglioni, B | 1 |
| Comi, P | 1 |
| Ottolenghi, S | 1 |
| Camaschella, C | 1 |
| Saglio, G | 1 |
| Naritomi, Y | 1 |
| Naito, Y | 1 |
| Nakashima, H | 1 |
| Yokota, E | 1 |
| Imamura, T | 1 |
3 other studies available for thymine and Thalassemia
| Article | Year |
|---|---|
Rare Pathogenic β
Topics: beta-Globins; beta-Thalassemia; Codon, Terminator; DNA Mutational Analysis; Emigrants and Immigrants | 2022 |
The beta-globin gene in Sardinian delta beta 0-thalassemia carries a C----T nonsense mutation at codon 39.
Topics: Base Sequence; Codon; Cytosine; DNA Restriction Enzymes; Genes; Globins; Humans; Mutation; RNA, Mess | 1984 |
A substitution of cytosine for thymine in codon 110 of the human beta-globin gene is a novel cause of beta-thalassemia phenotypes.
Topics: Amino Acid Sequence; Base Sequence; Codon; Cytosine; Genes; Globins; Humans; Molecular Sequence Data | 1988 |