BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

272 related articles for article (PubMed ID: 19221580)

  • 21. The protein composition of normal and developmentally defective enamel.
    Wright JT; Hall K; Yamauchi M
    Ciba Found Symp; 1997; 205():85-99; discussion 99-106. PubMed ID: 9189619
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Amelogenesis imperfecta due to a mutation of the enamelin gene: clinical case with genotype-phenotype correlations.
    Lindemeyer RG; Gibson CW; Wright TJ
    Pediatr Dent; 2010; 32(1):56-60. PubMed ID: 20298654
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Phenotype and enamel ultrastructure characteristics in patients with ENAM gene mutations g.13185-13186insAG and 8344delG.
    Pavlic A; Petelin M; Battelino T
    Arch Oral Biol; 2007 Mar; 52(3):209-17. PubMed ID: 17125728
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta.
    Hart PS; Wright JT; Savage M; Kang G; Bensen JT; Gorry MC; Hart TC
    Eur J Oral Sci; 2003 Aug; 111(4):326-31. PubMed ID: 12887398
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular-based phenotype variations in amelogenesis imperfecta.
    Dong J; Ruan W; Duan X
    Oral Dis; 2023 Sep; 29(6):2334-2365. PubMed ID: 37154292
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Gene expression and immunolocalization of amelogenin in enamel hypoplasia induced by successive injections of bisphosphonate in rat incisors.
    Yamada Y; Fuangtharnthip P; Tamura Y; Takagi Y; Ohya K
    Arch Oral Biol; 2000 Mar; 45(3):207-15. PubMed ID: 10761874
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Rat wct mutation induces a hypo-mineralization form of amelogenesis imperfecta and cyst formation in molar teeth.
    Osawa M; Kenmotsu S; Masuyama T; Taniguchi K; Uchida T; Saito C; Ohshima H
    Cell Tissue Res; 2007 Oct; 330(1):97-109. PubMed ID: 17710440
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Simple recessive mutation in ENAM is associated with amelogenesis imperfecta in Italian Greyhounds.
    Gandolfi B; Liu H; Griffioen L; Pedersen NC
    Anim Genet; 2013 Aug; 44(5):569-78. PubMed ID: 23638899
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Amelogenesis imperfecta.
    Crawford PJ; Aldred M; Bloch-Zupan A
    Orphanet J Rare Dis; 2007 Apr; 2():17. PubMed ID: 17408482
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth development.
    Hu CC; Hart TC; Dupont BR; Chen JJ; Sun X; Qian Q; Zhang CH; Jiang H; Mattern VL; Wright JT; Simmer JP
    J Dent Res; 2000 Apr; 79(4):912-9. PubMed ID: 10831092
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Enamel ultrastructure and protein content in X-linked amelogenesis imperfecta.
    Wright JT; Aldred MJ; Crawford PJ; Kirkham J; Robinson C
    Oral Surg Oral Med Oral Pathol; 1993 Aug; 76(2):192-9. PubMed ID: 8361731
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Enamel Hypomineralization and Structural Defects in Amelotin-deficient Mice.
    Nakayama Y; Holcroft J; Ganss B
    J Dent Res; 2015 May; 94(5):697-705. PubMed ID: 25715379
    [TBL] [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; 10(16):1673-7. PubMed ID: 11487571
    [TBL] [Abstract][Full Text] [Related]  

  • 36. An amelogenin gene defect associated with human X-linked amelogenesis imperfecta.
    Collier PM; Sauk JJ; Rosenbloom SJ; Yuan ZA; Gibson CW
    Arch Oral Biol; 1997 Mar; 42(3):235-42. PubMed ID: 9188994
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Splicing mutations in AMELX and ENAM cause amelogenesis imperfecta.
    Zhang Z; Zou X; Feng L; Huang Y; Chen F; Sun K; Song Y; Lv P; Gao X; Dong Y; Tian H
    BMC Oral Health; 2023 Nov; 23(1):893. PubMed ID: 37985977
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary.
    Kida M; Ariga T; Shirakawa T; Oguchi H; Sakiyama Y
    J Dent Res; 2002 Nov; 81(11):738-42. PubMed ID: 12407086
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Reduced amelogenin-MMP20 interactions in amelogenesis imperfecta.
    Tanimoto K; Le T; Zhu L; Witkowska HE; Robinson S; Hall S; Hwang P; Denbesten P; Li W
    J Dent Res; 2008 May; 87(5):451-5. PubMed ID: 18434575
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Alteración del gen AMELX en amelogénesis imperfecta. Una breve revisión].
    Tremillo-Maldonado O; Molina-Frechero N; González-González R; Bologna-Molina R
    Gac Med Mex; 2019; 155(1):101-107. PubMed ID: 30799455
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.