lysine has been researched along with Amyoplasia Congenita in 3 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 | 3 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Coucke, PJ; De Paepe, A; Dierick, M; Eyre, DR; Gistelinck, C; Huysseune, A; Kwon, RY; Larionova, D; Malfait, F; Simoens, P; Symoens, S; Van Hoorebeke, L; Weis, M; Willaert, A; Witten, PE | 1 |
| Bank, RA; Gjaltema, RA | 1 |
| Aftimos, S; Al-Aqeel, A; Ankala, A; Anyane-Yeboa, K; Babovic-Vuksanovic, D; Bank, RA; Ben-Neriah, Z; Byers, PH; Chong, K; Christiansen, HE; Clemens, M; Conneely, K; Cundy, T; Davis, EC; Eyre, D; Hannibal, M; Hegde, MR; Hudgins, L; Kim, LS; Lieberman, S; Mahan, J; McPherson, E; Pals, G; Pyott, SM; Raney, E; Schwarze, U; Seaver, L; Segel, R; Siderius, L; Smith, R; Steiner, RD; Stoler, J; Sussman, MD; Sutton, VR; Uster, T; Weis, MA; Wynn, J; Yandow, SM | 1 |
1 review(s) available for lysine and Amyoplasia Congenita
| Article | Year |
|---|---|
Molecular insights into prolyl and lysyl hydroxylation of fibrillar collagens in health and disease.
Topics: Animals; Arthrogryposis; Connective Tissue Diseases; Ehlers-Danlos Syndrome; Fibrillar Collagens; Glycosylation; Humans; Hydroxylation; Hydroxylysine; Hydroxyproline; Lysine; Osteogenesis Imperfecta; Proline; Protein Folding | 2017 |
2 other study(ies) available for lysine and Amyoplasia Congenita
| Article | Year |
|---|---|
Loss of Type I Collagen Telopeptide Lysyl Hydroxylation Causes Musculoskeletal Abnormalities in a Zebrafish Model of Bruck Syndrome.
Topics: Amino Acid Sequence; Animals; Arthrogryposis; Bone and Bones; Calcification, Physiologic; Catalytic Domain; Codon, Nonsense; Collagen Type I; Conserved Sequence; Cross-Linking Reagents; Evolution, Molecular; Hydroxylation; Larva; Lysine; Mass Spectrometry; Musculoskeletal Abnormalities; Notochord; Osteogenesis Imperfecta; Peptides; Phenotype; X-Ray Microtomography; Zebrafish; Zebrafish Proteins | 2016 |
Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen.
Topics: Arthrogryposis; Collagen Type I; Female; Genes, Recessive; Humans; Hydroxylation; Lysine; Male; Mutation; Osteogenesis Imperfecta; Protein Processing, Post-Translational; Tacrolimus Binding Proteins | 2013 |