A defect in the structure of type I procollagen in a patient who had osteogenesis imperfecta: excess mannose in the COOH-terminal propeptide.
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Cited by 70 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. The triple helix of collagens – an ancient protein structure that enabled animal multicellularity and tissue evolution;Journal of Cell Science;2018-04-01
2. Osteogenesis imperfecta mutations lead to local tropocollagen unfolding and disruption of H-bond network;RSC Advances;2012
3. Computational multiscale studies of collagen tissues in the context of brittle bone disease osteogenesis imperfecta;MRS Proceedings;2010
4. Molecular and Mesoscale Mechanisms of Osteogenesis Imperfecta Disease in Collagen Fibrils;Biophysical Journal;2009-08
5. Altered collagen metabolism in osteogenesis imperfecta fibroblasts: a study on 33 patients with diverse forms;European Journal of Clinical Investigation;2008-06-28
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