cytosine has been researched along with Alkaptonuria in 1 studies
Alkaptonuria: An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS.
| 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 |
|---|---|
| Beltrán-Valero de Bernabé, D | 1 |
| Jimenez, FJ | 1 |
| Aquaron, R | 1 |
| Rodríguez de Córdoba, S | 1 |
1 other study available for cytosine and Alkaptonuria
| Article | Year |
|---|---|
Analysis of alkaptonuria (AKU) mutations and polymorphisms reveals that the CCC sequence motif is a mutational hot spot in the homogentisate 1,2 dioxygenase gene (HGO).
Topics: Alkaptonuria; Base Sequence; Cytosine; Dioxygenases; Founder Effect; Genetic Markers; Homogentisate | 1999 |