thymine has been researched along with Porphyrias, Hepatic in 1 studies
Porphyrias, Hepatic: A group of metabolic diseases due to deficiency of one of a number of LIVER enzymes in the biosynthetic pathway of HEME. They are characterized by the accumulation and increased excretion of PORPHYRINS or its precursors. Clinical features include neurological symptoms (PORPHYRIA, ACUTE INTERMITTENT), cutaneous lesions due to photosensitivity (PORPHYRIA CUTANEA TARDA), or both (HEREDITARY COPROPORPHYRIA). Hepatic porphyrias can be hereditary or acquired as a result of toxicity to the hepatic tissues.
| 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 |
|---|---|
| Frank, J | 1 |
| McGrath, JA | 1 |
| Poh-Fitzpatrick, MB | 1 |
| Hawk, JL | 1 |
| Christiano, AM | 1 |
1 other study available for thymine and Porphyrias, Hepatic
| Article | Year |
|---|---|
Mutations in the translation initiation codon of the protoporphyrinogen oxidase gene underlie variegate porphyria.
Topics: Adenosine; Adult; Chromosomes, Human, Pair 1; Codon, Initiator; Cytosine; Female; Flavoproteins; Hum | 1999 |