xanthine has been researched along with Metal Metabolism, Inborn Errors in 2 studies
7H-xanthine : An oxopurine in which the purine ring is substituted by oxo groups at positions 2 and 6 and N-7 is protonated.
9H-xanthine : An oxopurine in which the purine ring is substituted by oxo groups at positions 2 and 6 and N-9 is protonated.
Metal Metabolism, Inborn Errors: Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Jakubiczka-Smorag, J | 1 |
Santamaria-Araujo, JA | 1 |
Metz, I | 1 |
Kumar, A | 1 |
Hakroush, S | 1 |
Brueck, W | 1 |
Schwarz, G | 1 |
Burfeind, P | 1 |
Reiss, J | 1 |
Smorag, L | 1 |
Matsuishi, T | 1 |
Ishibashi, S | 1 |
Nakashima, M | 1 |
Satoi, M | 1 |
1 review available for xanthine and Metal Metabolism, Inborn Errors
Article | Year |
---|---|
[Molybdenum cofactor deficiency].
Topics: Biomarkers; Coenzymes; Cysteine; Diagnosis, Differential; Female; Humans; Infant; Infant, Newborn; M | 1998 |
1 other study available for xanthine and Metal Metabolism, Inborn Errors
Article | Year |
---|---|
Mouse model for molybdenum cofactor deficiency type B recapitulates the phenotype observed in molybdenum cofactor deficient patients.
Topics: Animals; Apoptosis; Carbon-Carbon Lyases; Coenzymes; Cysteine; Disease Models, Animal; Gene Expressi | 2016 |