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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2010
Assuntos:
Research Article
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados