These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


159 related items for PubMed ID: 7554922

  • 21. PCR detection of the human amelogenin gene and its application to the diagnosis of amelogenesis imperfecta.
    Sekiguchi H, Minaguchi K, Machida Y, Yakushiji M.
    Bull Tokyo Dent Coll; 1998 Nov; 39(4):275-85. PubMed ID: 10218009
    [Abstract] [Full Text] [Related]

  • 22. SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1).
    Lench NJ, Brook AH, Winter GB.
    Hum Mol Genet; 1994 May; 3(5):827-8. PubMed ID: 8081371
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. X-linked amelogenesis imperfecta may result from decreased formation of tyrosine rich amelogenin peptide (TRAP).
    Li W, Gao C, Yan Y, DenBesten P.
    Arch Oral Biol; 2003 Mar; 48(3):177-83. PubMed ID: 12648554
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Dental enamel formation and its impact on clinical dentistry.
    Simmer JP, Hu JC.
    J Dent Educ; 2001 Sep; 65(9):896-905. PubMed ID: 11569606
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Amelogenin-deficient mice display an amelogenesis imperfecta phenotype.
    Gibson CW, Yuan ZA, Hall B, Longenecker G, Chen E, Thyagarajan T, Sreenath T, Wright JT, Decker S, Piddington R, Harrison G, Kulkarni AB.
    J Biol Chem; 2001 Aug 24; 276(34):31871-5. PubMed ID: 11406633
    [Abstract] [Full Text] [Related]

  • 33. Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta.
    Santos MC, Hart PS, Ramaswami M, Kanno CM, Hart TC, Line SR.
    Head Face Med; 2007 Jan 31; 3():8. PubMed ID: 17266769
    [Abstract] [Full Text] [Related]

  • 34. Enamelin and autosomal-dominant amelogenesis imperfecta.
    Hu JC, Yamakoshi Y.
    Crit Rev Oral Biol Med; 2003 Jan 31; 14(6):387-98. PubMed ID: 14656895
    [Abstract] [Full Text] [Related]

  • 35. Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta.
    Rajpar MH, Harley K, Laing C, Davies RM, Dixon MJ.
    Hum Mol Genet; 2001 Aug 01; 10(16):1673-7. PubMed ID: 11487571
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI).
    Masuya H, Shimizu K, Sezutsu H, Sakuraba Y, Nagano J, Shimizu A, Fujimoto N, Kawai A, Miura I, Kaneda H, Kobayashi K, Ishijima J, Maeda T, Gondo Y, Noda T, Wakana S, Shiroishi T.
    Hum Mol Genet; 2005 Mar 01; 14(5):575-83. PubMed ID: 15649948
    [Abstract] [Full Text] [Related]

  • 38. Evidence for regulation of amelogenin gene expression by 1,25-dihydroxyvitamin D(3) in vivo.
    Papagerakis P, Hotton D, Lezot F, Brookes S, Bonass W, Robinson C, Forest N, Berdal A.
    J Cell Biochem; 1999 Dec 01; 76(2):194-205. PubMed ID: 10618637
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Analysis of human enamel genes: insights into genetic disorders of enamel.
    Lau EC, Slavkin HC, Snead ML.
    Cleft Palate J; 1990 Apr 01; 27(2):121-30. PubMed ID: 2187631
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 8.