arginine has been researched along with ALDOB Deficiency 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 | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Esposito, G; Salvatore, F; Santamaria, R; Viola, A; Vitagliano, L; Zagari, A | 1 |
| Esposito, G; Paglionico, I; Race, V; Salvatore, F; Santamaria, R; Vitagliano, L; Zagari, A; Zancan, L | 1 |
2 other study(ies) available for arginine and ALDOB Deficiency
| Article | Year |
|---|---|
Structural and functional analysis of aldolase B mutants related to hereditary fructose intolerance.
Topics: Arginine; Catalysis; Fructose Intolerance; Fructose-Bisphosphate Aldolase; Humans; Kinetics; Models, Molecular; Mutation; Mutation, Missense; Recombinant Proteins; Structure-Activity Relationship | 2002 |
Functional and molecular modelling studies of two hereditary fructose intolerance-causing mutations at arginine 303 in human liver aldolase.
Topics: Amino Acid Substitution; Arginine; Base Sequence; DNA Mutational Analysis; DNA Primers; Female; Fructose Intolerance; Fructose-Bisphosphate Aldolase; Humans; Infant; Kinetics; Liver; Male; Models, Molecular; Mutation; Pedigree; Protein Conformation; Recombinant Proteins | 2000 |