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Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17

Bruck syndrome is characterized by the presence of osteoporosis, joint contractures, fragile bones, and short stature. We report that lysine residues within the telopeptides of collagen type I in bone are underhydroxylated, leading to aberrant crosslinking, but that the lysine residues in the triple...

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Gorde:
Argitaratua izan da:Proc Natl Acad Sci U S A
Egile Nagusiak: Bank, Ruud A., Robins, Simon P., Wijmenga, Cisca, Breslau-Siderius, Liesbeth J., Bardoel, Alfons F. J., Van der Sluijs, Hans A., Pruijs, Hans E. H., TeKoppele, Johan M.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: National Academy of Sciences 1999
Gaiak:
Biological Sciences
Sarrera elektronikoa:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC15349/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9927692/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.96.3.1054
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