BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 17652207)

  • 1. A mutation in the enamelin gene in a mouse model.
    Seedorf H; Klaften M; Eke F; Fuchs H; Seedorf U; Hrabe de Angelis M
    J Dent Res; 2007 Aug; 86(8):764-8. PubMed ID: 17652207
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 14(5):575-83. PubMed ID: 15649948
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).
    Mårdh CK; Bäckman B; Holmgren G; Hu JC; Simmer JP; Forsman-Semb K
    Hum Mol Genet; 2002 May; 11(9):1069-74. PubMed ID: 11978766
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families.
    Dashash M; Bazrafshani MR; Poulton K; Jaber S; Naeem E; Blinkhorn AS
    J Investig Clin Dent; 2011 Feb; 2(1):16-22. PubMed ID: 25427323
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

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

  • 8. Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines.
    Fuchs H; Sabrautzki S; Seedorf H; Rathkolb B; Rozman J; Hans W; Schneider R; Klaften M; Hölter SM; Becker L; Klempt M; Elvert R; Wurst W; Klopstock T; Klingenspor M; Wolf E; Gailus-Durner V; de Angelis MH
    Eur J Oral Sci; 2012 Aug; 120(4):269-77. PubMed ID: 22813216
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Enamelin maps to human chromosome 4q21 within the autosomal dominant amelogenesis imperfecta locus.
    Dong J; Gu TT; Simmons D; MacDougall M
    Eur J Oral Sci; 2000 Oct; 108(5):353-8. PubMed ID: 11037750
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Amelogenesis imperfecta in a new animal model--a mutation in chromosome 5 (human 4q21).
    Seedorf H; Springer IN; Grundner-Culemann E; Albers HK; Reis A; Fuchs H; Hrabe de Angelis M; Açil Y
    J Dent Res; 2004 Aug; 83(8):608-12. PubMed ID: 15271968
    [TBL] [Abstract][Full Text] [Related]  

  • 11. ENAM mutations in autosomal-dominant amelogenesis imperfecta.
    Kim JW; Seymen F; Lin BP; Kiziltan B; Gencay K; Simmer JP; Hu JC
    J Dent Res; 2005 Mar; 84(3):278-82. PubMed ID: 15723871
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta.
    Gutierrez SJ; Chaves M; Torres DM; Briceño I
    Arch Oral Biol; 2007 May; 52(5):503-6. PubMed ID: 17316551
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21.
    MacDougall M; DuPont BR; Simmons D; Reus B; Krebsbach P; Kärrman C; Holmgren G; Leach RJ; Forsman K
    Genomics; 1997 Apr; 41(1):115-8. PubMed ID: 9126491
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects.
    Hart TC; Hart PS; Gorry MC; Michalec MD; Ryu OH; Uygur C; Ozdemir D; Firatli S; Aren G; Firatli E
    J Med Genet; 2003 Dec; 40(12):900-6. PubMed ID: 14684688
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients.
    Mårdh CK; Bäckman B; Simmons D; Golovleva I; Gu TT; Holmgren G; MacDougall M; Forsman-Semb K
    Eur J Oral Sci; 2001 Feb; 109(1):8-13. PubMed ID: 11330937
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cloning and characterization of the mouse and human enamelin genes.
    Hu JC; Zhang CH; Yang Y; Kärrman-Mårdh C; Forsman-Semb K; Simmer JP
    J Dent Res; 2001 Mar; 80(3):898-902. PubMed ID: 11379892
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Genes and related proteins involved in amelogenesis imperfecta.
    Stephanopoulos G; Garefalaki ME; Lyroudia K
    J Dent Res; 2005 Dec; 84(12):1117-26. PubMed ID: 16304440
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identifying polymorphism in enamelin gene in amelogenesis imperfecta (AI).
    Gopinath VK; Yoong TP; Yean CY; Ravichandran M
    Arch Oral Biol; 2008 Oct; 53(10):937-40. PubMed ID: 18466877
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.