pyridinoline has been researched along with Amyoplasia Congenita 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 | 0 (0.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 1 (50.00) | 2.80 |
Authors | Studies |
---|---|
Callewaert, B; Coucke, PJ; Essawi, OH; Essawi, T; Eyre, DR; Gistelinck C, C; Malfait, F; Symoens, S; Tapaneeyaphan, P | 1 |
Bank, RA; Boersema, M; Gjaltema, RA; van der Stoel, MM | 1 |
2 other study(ies) available for pyridinoline and Amyoplasia Congenita
Article | Year |
---|---|
New insights on the clinical variability of FKBP10 mutations.
Topics: Adolescent; Adult; Amino Acids; Arthrogryposis; Cells, Cultured; Child; Female; Homozygote; Humans; Male; Mutation; Osteogenesis Imperfecta; Pedigree; Phenotype; RNA Splice Sites; Tacrolimus Binding Proteins | 2020 |
Disentangling mechanisms involved in collagen pyridinoline cross-linking: The immunophilin FKBP65 is critical for dimerization of lysyl hydroxylase 2.
Topics: Amino Acids; Arthrogryposis; Collagen; Collagen Type I; Collagen Type I, alpha 1 Chain; Cross-Linking Reagents; Dimerization; Humans; Osteogenesis Imperfecta; Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase; Protein Binding; Protein Processing, Post-Translational; Tacrolimus Binding Proteins | 2016 |