Generalized Connective Tissue Disease in Crtap-/- Mouse

Mutations in CRTAP (coding for cartilage-associated protein), LEPRE1 (coding for prolyl 3-hydroxylase 1 [P3H1]) or PPIB (coding for Cyclophilin B [CYPB]) cause recessive forms of osteogenesis imperfecta and loss or decrease of type I collagen prolyl 3-hydroxylation. A comprehensive analysis of the p...

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Bibliografische gegevens
Hoofdauteurs: Baldridge, Dustin, Lennington, Jennifer, Weis, MaryAnn, Homan, Erica P., Jiang, Ming-Ming, Munivez, Elda, Keene, Douglas R., Hogue, William R., Pyott, Shawna, Byers, Peter H., Krakow, Deborah, Cohn, Daniel H., Eyre, David R., Lee, Brendan, Morello, Roy
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Public Library of Science 2010
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2868021/
https://ncbi.nlm.nih.gov/pubmed/20485499
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0010560
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