Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia
- 29 September 2009
- Vol. 46 (2) , 402-409
- https://doi.org/10.1016/j.bone.2009.09.016
Abstract
No abstract availableKeywords
Funding Information
- National Institutes of Health (R21 DK075856-01)
This publication has 40 references indexed in Scilit:
- Studies of the DMP1 57-kDa Functional Domain both in vivo and in vitroCells Tissues Organs, 2008
- Distinct roles for intrinsic osteocyte abnormalities and systemic factors in regulation of FGF23 and bone mineralization in Hyp miceAmerican Journal of Physiology-Endocrinology and Metabolism, 2007
- Hereditary Dentin DefectsJournal of Dental Research, 2007
- Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolismNature Genetics, 2006
- DMP1 Depletion Decreases Bone Mineralization In Vivo: An FTIR Imaging AnalysisJournal of Bone and Mineral Research, 2005
- Dentin matrix protein 1 expression during osteoblastic differentiation, generation of an osteocyte GFP-transgeneBone, 2004
- Deletion of Dentin Matrix Protein-1 Leads to a Partial Failure of Maturation of Predentin into Dentin, Hypomineralization, and Expanded Cavities of Pulp and Root Canal during Postnatal Tooth DevelopmentJournal of Biological Chemistry, 2004
- Three small integrin‐binding ligand N‐linked glycoproteins (SIBLINGs) bind and activate specific matrix metalloproteinasesThe FASEB Journal, 2004
- Fibroblast Growth Factor 23 in Oncogenic Osteomalacia and X-Linked HypophosphatemiaNew England Journal of Medicine, 2003
- Six Genes Expressed in Bones and Teeth Encode the Current Members of the SIBLING Family of ProteinsConnective Tissue Research, 2003