thymine has been researched along with Blood Coagulation Disorders in 1 studies
Blood Coagulation Disorders: Hemorrhagic and thrombotic disorders that occur as a consequence of abnormalities in blood coagulation due to a variety of factors such as COAGULATION PROTEIN DISORDERS; BLOOD PLATELET DISORDERS; BLOOD PROTEIN DISORDERS or nutritional conditions.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The mutation for hypoprothrombinemia was detected by PCR-single-strand conformation polymorphism (PCR-SSCP) with endonuclease digestion in exon 6, near MboII-RFLP and NcoI-RFLP." | 1.28 | Molecular and genetic analysis of a compound heterozygote for dysprothrombinemia of prothrombin Tokushima and hypoprothrombinemia. ( Itakura, M; Iwahana, H; Saito, S; Shigekiyo, T; Shirakami, A; Yoshimoto, K, 1992) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Iwahana, H | 1 |
| Yoshimoto, K | 1 |
| Shigekiyo, T | 1 |
| Shirakami, A | 1 |
| Saito, S | 1 |
| Itakura, M | 1 |
1 other study available for thymine and Blood Coagulation Disorders
| Article | Year |
|---|---|
Molecular and genetic analysis of a compound heterozygote for dysprothrombinemia of prothrombin Tokushima and hypoprothrombinemia.
Topics: Amino Acid Sequence; Base Sequence; Blood Coagulation Disorders; Child; DNA; DNA Mutational Analysis | 1992 |