tyrosine has been researched along with Brittle Bone Disease in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 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 | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Atkinson, M; Byers, PH; Chitayat, D; Pace, JM; Schwarze, U; Wilcox, WR | 1 |
| Francis, MJ; Macmillan, DC; Smith, R | 1 |
2 other study(ies) available for tyrosine and Brittle Bone Disease
| Article | Year |
|---|---|
A single amino acid substitution (D1441Y) in the carboxyl-terminal propeptide of the proalpha1(I) chain of type I collagen results in a lethal variant of osteogenesis imperfecta with features of dense bone diseases.
Topics: Amino Acid Substitution; Aspartic Acid; Bone Density; Bone Diseases; Cell Line; Cells, Cultured; Collagen Type I; Female; Genes, Lethal; Humans; Infant, Newborn; Mutation; Osteogenesis Imperfecta; Peptide Fragments; Procollagen; Protein Processing, Post-Translational; Tyrosine | 2002 |
Polymeric collagen of skin in normal sunjects and in patients with inherited connective tissue disorders.
Topics: Acromegaly; Adolescent; Adult; Aged; Child; Child, Preschool; Collagen; Collagen Diseases; Female; Hexosamines; Homocystinuria; Hot Temperature; Humans; Hyperparathyroidism; Male; Microscopy, Electron; Middle Aged; Myositis Ossificans; Osteitis Deformans; Osteogenesis Imperfecta; Osteopetrosis; Pseudoxanthoma Elasticum; Skin; Tyrosine; Werner Syndrome | 1973 |