Prolyl 3-Hydroxylase 1 Null Mice Display Abnormalities in Fibrillar Collagen-rich Tissues Such as Tendons, Skin, and Bones

Osteogenesis imperfecta (OI) is a skeletal disorder primarily caused by mutations in the type I collagen genes. However, recent investigations have revealed that mutations in the genes encoding for cartilage-associated protein (CRTAP) or prolyl 3-hydroxylase 1 (P3H1) can cause a severe, recessive fo...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Vranka, Janice A., Pokidysheva, Elena, Hayashi, Lauren, Zientek, Keith, Mizuno, Kazunori, Ishikawa, Yoshihiro, Maddox, Kerry, Tufa, Sara, Keene, Douglas R., Klein, Robert, Bächinger, Hans Peter
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society for Biochemistry and Molecular Biology 2010
Aiheet:
Glycobiology and Extracellular Matrices
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2878055/
https://ncbi.nlm.nih.gov/pubmed/20363744
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M110.102228
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia