Dianalee A McKnight

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. pmc Molecular evolution of dentin phosphoprotein among toothed and toothless animals
    Dianalee A McKnight
    Craniofacial and Skeletal Diseases Branch, NIDCR, NIH, DHHS, Bethesda MD 20892, USA
    BMC Evol Biol 9:299. 2009
  2. pmc Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP
    Zofia Von Marschall
    Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health DHHS, 9000 Rockville Pike, Bethesda, MD, USA 20892 4320, USA
    J Bone Miner Res 27:1309-21. 2012
  3. ncbi request reprint TM14 is a new member of the fibulin family (fibulin-7) that interacts with extracellular matrix molecules and is active for cell binding
    Susana de Vega
    Laboratory of Cell and Developmental Biology, NIDCR, National Institutes of Health, Bethesda, Maryland 20892 4370, USA
    J Biol Chem 282:30878-88. 2007
  4. doi request reprint A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene
    Dianalee A McKnight
    Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research NIDCR, National Institutes of Health NIH, Department of Health and Human Services DHHS, Bethesda, Maryland 20892, USA
    Hum Mutat 29:1392-404. 2008

Collaborators

  • Thomas C Hart
  • Satoshi Fukumoto
  • Zofia Von Marschall
  • Larry W Fisher
  • Susana de Vega
  • Seeun Mok
  • Matthew D Phillips
  • Kentaro Hozumi
  • Tsutomu Iwamoto
  • Takashi Nakamura
  • Yoshihiko Yamada

Detail Information

Publications4

  1. pmc Molecular evolution of dentin phosphoprotein among toothed and toothless animals
    Dianalee A McKnight
    Craniofacial and Skeletal Diseases Branch, NIDCR, NIH, DHHS, Bethesda MD 20892, USA
    BMC Evol Biol 9:299. 2009
    ....
  2. pmc Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP
    Zofia Von Marschall
    Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health DHHS, 9000 Rockville Pike, Bethesda, MD, USA 20892 4320, USA
    J Bone Miner Res 27:1309-21. 2012
    ..Evidence is also presented that many acidic, Ca2+-binding proteins may use the same IPV-like receptor/pathway for exiting the rER...
  3. ncbi request reprint TM14 is a new member of the fibulin family (fibulin-7) that interacts with extracellular matrix molecules and is active for cell binding
    Susana de Vega
    Laboratory of Cell and Developmental Biology, NIDCR, National Institutes of Health, Bethesda, Maryland 20892 4370, USA
    J Biol Chem 282:30878-88. 2007
    ..Because of its protein characteristics, TM14 can be classified as a new member of the fibulin family: fibulin-7...
  4. doi request reprint A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene
    Dianalee A McKnight
    Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research NIDCR, National Institutes of Health NIH, Department of Health and Human Services DHHS, Bethesda, Maryland 20892, USA
    Hum Mutat 29:1392-404. 2008
    ..Analysis of 37 haplotypes of the highly variable DSPP gene from geographically diverse people suggests it may be a useful autosomal marker in human migration studies...