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Differential Effects of Collagen Prolyl 3-Hydroxylation on Skeletal Tissues
Mutations in the genes encoding cartilage associated protein (CRTAP) and prolyl 3-hydroxylase 1 (P3H1 encoded by LEPRE1) were the first identified causes of recessive Osteogenesis Imperfecta (OI). These proteins, together with cyclophilin B (encoded by PPIB), form a complex that 3-hydroxylates a sin...
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| Autors principals: | , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Public Library of Science
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3900401/ https://ncbi.nlm.nih.gov/pubmed/24465224 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1004121 |
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