3-aminoisobutyric acid has been researched along with Central Nervous System Disease in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abeling, NG; Assmann, B; Dobritzsch, D; Engvall, M; Eto, K; Hennekam, RC; Ito, T; Krumpel, M; Lohkamp, B; Meijer, J; Meinsma, R; Rashed, MS; Saito, K; Selim, LA; Smitka, M; van Kuilenburg, AB; Xu, W; Zhang, C; Zoetekouw, L | 1 |
| Abeling, NG; Assmann, B; Beke, E; Busch, R; Hoffmann, GF; Kulik, W; Lorente, I; Mayatepek, E; Meinsma, R; Ribes, A; Rutsch, F; Stroomer, AE; van Cruchten, A; van Gennip, AH; van Kuilenburg, AB; van Lenthe, H; Voit, T; Wevers, RA; Zoetekouw, L | 1 |
2 other study(ies) available for 3-aminoisobutyric acid and Central Nervous System Disease
| Article | Year |
|---|---|
ß-ureidopropionase deficiency: phenotype, genotype and protein structural consequences in 16 patients.
Topics: Adult; Amidohydrolases; Amino Acid Sequence; Amino Acid Substitution; Aminoisobutyric Acids; Animals; beta-Alanine; Biocatalysis; Catalytic Domain; Central Nervous System Diseases; Child; Child, Preschool; Drosophila melanogaster; Escherichia coli; Female; Genotype; Humans; Infant; Infant, Newborn; Male; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation, Missense; Point Mutation; Protein Conformation; Protein Interaction Domains and Motifs; Purine-Pyrimidine Metabolism, Inborn Errors; Pyrimidines; Racial Groups | 2012 |
beta-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities.
Topics: Amidohydrolases; Aminoisobutyric Acids; beta-Alanine; Central Nervous System Diseases; Female; Humans; Infant; Liver; Male; Mutation; Oxidative Stress; Purine-Pyrimidine Metabolism, Inborn Errors; Pyrimidines | 2004 |