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Eiki Koyama, DDS, PhD

Contact Dr. Koyama

Children's Hospital of Philadelphia
3400 Civic Center Blvd.
Philadelphia, PA 19104


Most Recent Peer-reviewed Publications

  1. Biomechanical properties of murine TMJ articular disc and condyle cartilage via AFM-nanoindentation
  2. Cell origin, volume and arrangement are drivers of articular cartilage formation, morphogenesis and response to injury in mouse limbs
  3. Unsuspected osteochondroma-like outgrowths in the cranial base of Hereditary Multiple Exostoses patients and modeling and treatment with a BMP antagonist in mice
  4. Epiprofin Regulates Enamel Formation and Tooth Morphogenesis by Controlling Epithelial-Mesenchymal Interactions During Tooth Development
  5. Osteophyte formation and matrix mineralization in a TMJ osteoarthritis mouse model are associated with ectopic hedgehog signaling
  6. Excess BMP Signaling in Heterotopic Cartilage Forming in Prg4 -null TMJ Discs
  7. Mouse limb skeletal growth and synovial joint development are coordinately enhanced by Kartogenin
  8. Genesis and morphogenesis of limb synovial joints and articular cartilage
  9. TMJ degeneration in SAMP8 mice is accompanied by deranged ihh signaling
  10. Lubricin is required for the structural integrity and post-natal maintenance of TMJ
  11. Expression and roles of CCN2 in dental mesenchymal cells in primary culture-With findings in a case of odontogenic myxofibroma
  12. Epidermal growth factor receptor (EGFR) signaling regulates epiphyseal cartilage development through β-catenin-dependent and -independent pathways
  13. Epiphyseal abnormalities, trabecular bone loss and articular chondrocyte hypertrophy develop in the long bones of postnatal Ext1-deficient mice
  14. Regulation of CCN2 gene expression and possible roles in developing tooth germs
  15. Heparan sulfate in skeletal development, growth, and pathology: The case of hereditary multiple exostoses
  16. Perichondrium phenotype and border function are regulated by Ext1 and heparan sulfate in developing long bones: A mechanism likely deranged in Hereditary Multiple Exostoses
  17. Distinct spatiotemporal roles of hedgehog signalling during chick and mouse cranial base and axial skeleton development
  18. Phenotype profile of a genetic mouse model for Muenke syndrome
  19. Muenke syndrome mutation, FgfR3 P244R, Causes TMJ Defects
  20. The Muenke syndrome mutation (FgfR3 P244R) causes cranial base shortening associated with growth plate dysfunction and premature perichondrial ossification in murine basicranial synchondroses