arginine has been researched along with Factor XIII Deficiency in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 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 |
|---|---|
| Castaman, G; Ichinose, A; Rodeghiero, F; Takahashi, N; Tsukamoto, H; Umeyama, H | 1 |
| Ichinose, A; Izumi, T; Saito, H; Takamatsu, J; Togashi, M; Tsukamoto, H; Umeyama, H; Yamazaki, T | 1 |
2 other study(ies) available for arginine and Factor XIII Deficiency
| Article | Year |
|---|---|
Molecular mechanisms of type II factor XIII deficiency: novel Gly562-Arg mutation and C-terminal truncation of the A subunit cause factor XIII deficiency as characterized in a mammalian expression system.
Topics: Arginine; Factor XIII; Factor XIII Deficiency; Glycine; Humans; Point Mutation; Protein Conformation; Recombination, Genetic; Sequence Deletion; Structure-Activity Relationship | 1998 |
Arg260-Cys mutation in severe factor XIII deficiency: conformational change of the A subunit is predicted by molecular modelling and mechanics.
Topics: Amino Acid Substitution; Arginine; Cysteine; Factor XIII Deficiency; Female; Humans; Models, Molecular; Point Mutation; Polymerase Chain Reaction; Sequence Analysis, DNA; Sequence Analysis, RNA | 1998 |