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   Abnormalities    Amelogenesis Imperfecta
  • Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects.
    >Abstract >Full Text   (J Med Genet.)

  • Restoring function and esthetics in a patient with amelogenesis imperfecta: a clinical report.
    >Abstract >Full Text   (J Prosthet Dent.)

  • Enamelin and autosomal-dominant amelogenesis imperfecta
    >Abstract >Full Text   (Crit Rev Oral Biol Med.)

  • Evaluation of oral and systemic manifestations in an amelogenesis imperfecta population.
    >Abstract >Full Text   (J Dent.)

  • Oral and dental manifestations of vitamin D-dependent rickets type I: report of a pediatric case
    >Abstract >Full Text   (Oral Surg Oral Med Oral Pathol Oral Radiol Endod.)

  • Amelogenin interacts with cytokeratin-5 in ameloblasts during enamel growth.
    >Abstract >Full Text   (J Biol Chem.)

  • X-linked amelogenesis imperfecta may result from decreased formation of tyrosine rich amelogenin peptide (TRAP).
    >Abstract >Full Text   (Arch Oral Biol.)

  • Amelogenesis imperfecta: a classification and catalogue for the 21st century
    >Abstract >Full Text   (Oral Dis.)

  • Inheritance pattern and elemental composition of enamel affected by hypomaturation amelogenesis imperfecta.
    >Abstract   (Connect Tissue Res.)

  • Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate.
    >Abstract >Full Text   (Eur J Hum Genet.)

  • Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary.
    >Abstract >Full Text   (J Dent Res.)

  • Enamelysin (matrix metalloproteinase 20)-deficient mice display an amelogenesis imperfecta phenotype.
    >Abstract >Full Text   (J Biol Chem.)

  • Molecular analysis for genetic counselling in amelogenesis imperfecta.
    >Abstract >Full Text   (Oral Dis.)

  • An atomic force microscopic study of the ultrastructure of dental enamel afflicted with amelogenesis imperfecta..
    >Abstract   (J Biomater Sci Polym Ed.)

  • A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).
    >Abstract >Free Full Text   (Hum Mol Genet.)

  • Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontism.
    >Abstract >Full Text   (Oral Dis.)

  • A nomenclature for X-linked amelogenesis imperfecta.
    >Abstract >Full Text   (Arch Oral Biol.)

  • Altered amelogenin self-assembly based on mutations observed in human X-linked amelogenesis imperfecta (AIH1)
    >Abstract >Full Text   (J Biol Chem.)

  • A new frameshift mutation encoding a truncated amelogenin leads to X-linked amelogenesis imperfecta.
    >Abstract >Full Text   (Arch Oral Biol.)

  • A detailed study of enamel hypoplasia in a post-medieval adolescent of known age and sex.
    >Abstract >Full Text   (Arch Oral Biol.)

  • Enamel hypoplasia in the deciduous teeth of great apes: variation in prevalence and timing of defects.
    >Abstract >Full Text   (Am J Phys Anthropol.)

  • Dental enamel formation and its impact on clinical dentistry.
    >Abstract   (J Dent Educ.)

  • Amelogenin-cytokeratin 14 interaction in ameloblasts during enamel formation.
    >Free Full Text

  • Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients.
    >Abstract >Full Text   (Eur J Oral Sci.)


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