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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Homan, Erica P., Lietman, Caressa, Grafe, Ingo, Lennington, Jennifer, Morello, Roy, Napierala, Dobrawa, Jiang, Ming-Ming, Munivez, Elda M., Dawson, Brian, Bertin, Terry K., Chen, Yuqing, Lua, Rhonald, Lichtarge, Olivier, Hicks, John, Weis, Mary Ann, Eyre, David, Lee, Brendan H. L.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Public Library of Science 2014
विषय:
Research Article
ऑनलाइन पहुंच: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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