Structural and Functional Characterization of Recombinant Matrilin-3 A-domain and Implications for Human Genetic Bone Diseases
Open Access
- 1 November 2007
- journal article
- Published by Elsevier BV
- Vol. 282 (48), 34634-34643
- https://doi.org/10.1074/jbc.m705301200
Abstract
No abstract availableThis publication has 48 references indexed in Scilit:
- Decreased chondrocyte proliferation and dysregulated apoptosis in the cartilage growth plate are key features of a murine model of epiphyseal dysplasia caused by a matn3 mutationHuman Molecular Genetics, 2007
- Multiple epiphyseal dysplasia mutations inMATN3 cause misfolding of the A-domain and prevent secretion of mutant matrilin-3Human Mutation, 2005
- Altered Integration of Matrilin-3 into Cartilage Extracellular Matrix in the Absence of Collagen IXMolecular and Cellular Biology, 2005
- The Fibril-associated Collagen IX Provides a Novel Mechanism for Cell Adhesion to Cartilaginous MatrixPublished by Elsevier BV ,2004
- Interactions between the Cartilage Oligomeric Matrix Protein and MatrilinsJournal of Biological Chemistry, 2004
- Metal-dependent conformational changes in a recombinant vWF-A domain from human factor B: A solution study by circular dichroism, fourier transform infrared and 1H NMR spectroscopyJournal of Molecular Biology, 2000
- Splicing mutations in the COL3 domain of collagen IX cause multiple epiphyseal dysplasiaAmerican Journal of Medical Genetics, 2000
- Characterization of Human Matrilin-3 (MATN3)Genomics, 1998
- Collagen IXThe International Journal of Biochemistry & Cell Biology, 1997
- Distribution and expression of cartilage oligomeric matrix protein and bone sialoprotein show marked changes during rat femoral head developmentMatrix Biology, 1995