2,8-dihydroxyadenine has been researched along with Lesch-Nyhan Syndrome in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 1 (50.00) | 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 |
---|---|
Melton, DW; Redhead, NJ; Selfridge, J; Wu, CL | 1 |
Akaoka, I; Enomoto, S; Fujimori, S; Kamatani, N; Matsuta, K; Miyamoto, T; Nishioka, K; Takeuchi, F | 1 |
2 other study(ies) available for 2,8-dihydroxyadenine and Lesch-Nyhan Syndrome
Article | Year |
---|---|
Mice with adenine phosphoribosyltransferase deficiency develop fatal 2,8-dihydroxyadenine lithiasis.
Topics: Adenine; Adenine Phosphoribosyltransferase; Alleles; Allopurinol; Animals; Blotting, Southern; Chromatography, High Pressure Liquid; Cloning, Molecular; Crystallization; Disease Models, Animal; Genotype; Humans; Hypoxanthine; Kidney; Lesch-Nyhan Syndrome; Mice; Mice, Transgenic; Polymerase Chain Reaction; Purines | 1996 |
Rapid method for the diagnosis of partial adenine phosphoribosyltransferase deficiencies causing 2,8-dihydroxyadenine urolithiasis.
Topics: Adenine; Adenine Phosphoribosyltransferase; Clinical Enzyme Tests; Erythrocytes; Humans; Japan; Lesch-Nyhan Syndrome; Pentosyltransferases; Urinary Calculi | 1985 |