arginine has been researched along with Bessel-Hagen Disease in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alimsardjono, H; Fujii, S; Matsuo, M; Pokharel, RK; Shiba, R; Uno, K | 1 |
| Ala-Kokko, L; Fertala, A; Prockop, DJ; Wiaderkiewicz, R | 1 |
| Lee, CC; Shi, YR; Tsai, CH; Tsai, FJ; Wu, JY | 1 |
3 other study(ies) available for arginine and Bessel-Hagen Disease
| Article | Year |
|---|---|
A novel mutation substituting tryptophan with arginine in the carboxyl-terminal, non-collagenous domain of collagen X in a case of Schmid metaphyseal chondrodysplasia.
Topics: Amino Acid Sequence; Arginine; Base Sequence; Child, Preschool; Collagen; Exostoses, Multiple Hereditary; Female; Humans; Male; Molecular Sequence Data; Pedigree; Point Mutation; Tryptophan | 1995 |
Collagen II containing a Cys substitution for arg-alpha1-519. Homotrimeric monomers containing the mutation do not assemble into fibrils but alter the self-assembly of the normal protein.
Topics: Amino Acid Sequence; Arginine; Collagen; Computer Simulation; Cysteine; Exostoses, Multiple Hereditary; Humans; Macromolecular Substances; Microscopy, Electron; Molecular Sequence Data; Osteoarthritis; Point Mutation; Protein Binding; Protein Denaturation; Protein Structure, Tertiary; Structure-Activity Relationship | 1997 |
An R223P mutation in EXT2 gene causes hereditary multiple exostoses.
Topics: Amino Acid Substitution; Arginine; Asian People; China; Chromosomes, Human, Pair 11; DNA Mutational Analysis; Exostoses, Multiple Hereditary; Female; Genes, Dominant; Humans; Mutation, Missense; N-Acetylglucosaminyltransferases; Proline; Proteins; Taiwan | 2000 |