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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900401/
https://www.ncbi.nlm.nih.gov/pubmed/24465224
http://dx.doi.org/10.1371/journal.pgen.1004121

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900401/
https://www.ncbi.nlm.nih.gov/pubmed/24465224
http://dx.doi.org/10.1371/journal.pgen.1004121

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