Low serum vitamin K in PXE results in defective carboxylation of mineralization inhibitors similar to the GGCX mutations in the PXE-like syndrome
- 1 June 2010
- journal article
- research article
- Published by Elsevier in Laboratory Investigation
- Vol. 90 (6) , 895-905
- https://doi.org/10.1038/labinvest.2010.68
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Mutations in the GGCX and ABCC6 Genes in a Family with Pseudoxanthoma Elasticum-Like PhenotypesJournal of Investigative Dermatology, 2009
- The Circulating Inactive Form of Matrix Gla Protein (ucMGP) as a Biomarker for Cardiovascular CalcificationJournal of Vascular Research, 2008
- Metabolism and cell biology of vitamin KThrombosis and Haemostasis, 2008
- Pharmacogenomics of 4-Hydroxycoumarin AnticoagulantsDrug Metabolism Reviews, 2008
- Pseudoxanthoma elasticum: Reduced γ-glutamyl carboxylation of matrix gla protein in a mouse model (Abcc6−/−)Biochemical and Biophysical Research Communications, 2007
- Emerging role for fetuin-A as contributor to morbidity and mortality in chronic kidney diseaseKidney International, 2007
- Immunohistochemical characterization of elastofibroma and exclusion of ABCC6 as a predisposing geneBritish Journal of Dermatology, 2007
- Vascular smooth muscle cells and calcification in atherosclerosisAmerican Heart Journal, 2004
- Extracutaneous Ultrastructural Alterations in Pseudoxanthoma ElasticumUltrastructural Pathology, 2003
- Spontaneous calcification of arteries and cartilage in mice lacking matrix GLA proteinNature, 1997