tryptophan has been researched along with Brittle Bone 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 | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chlebna-Sokół, D; Gach, A; Jakubowska-Pietkiewicz, E; Kępczyński, Ł; Michałus, I; Pinkier, I; Rutkowska, L; Salachna, D; Sałacińska, K | 1 |
| Apak, MY; De Paepe, A; Kayserili, H; Nuytinck, L; Tükel, T | 1 |
2 other study(ies) available for tryptophan and Brittle Bone Disease
| Article | Year |
|---|---|
The first glycine-to-tryptophan substitution in the COL1A1 gene identified in a patient with progressively-deforming Osteogenesis imperfecta.
Topics: Collagen Type I; Collagen Type I, alpha 1 Chain; Glycine; Humans; Osteogenesis Imperfecta; Tryptophan | 2022 |
Glycine to tryptophan substitution in type I collagen in a patient with OI type III: a unique collagen mutation.
Topics: Adult; Amino Acid Substitution; Child; Collagen; Female; Glycine; Humans; Male; Osteogenesis Imperfecta; Point Mutation; Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; Tryptophan | 2000 |