BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

237 related articles for article (PubMed ID: 18714142)

  • 1. Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4.
    Wright JT; Hart TC; Hart PS; Simmons D; Suggs C; Daley B; Simmer J; Hu J; Bartlett JD; Li Y; Yuan ZA; Seow WK; Gibson CW
    Cells Tissues Organs; 2009; 189(1-4):224-9. PubMed ID: 18714142
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Enamel proteins and proteases in Mmp20 and Klk4 null and double-null mice.
    Yamakoshi Y; Richardson AS; Nunez SM; Yamakoshi F; Milkovich RN; Hu JC; Bartlett JD; Simmer JP
    Eur J Oral Sci; 2011 Dec; 119 Suppl 1(Suppl 1):206-16. PubMed ID: 22243248
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Kallikrein-related peptidase 4, matrix metalloproteinase 20, and the maturation of murine and porcine enamel.
    Hu Y; Hu JC; Smith CE; Bartlett JD; Simmer JP
    Eur J Oral Sci; 2011 Dec; 119 Suppl 1(Suppl 1):217-25. PubMed ID: 22243249
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Target gene analyses of 39 amelogenesis imperfecta kindreds.
    Chan HC; Estrella NM; Milkovich RN; Kim JW; Simmer JP; Hu JC
    Eur J Oral Sci; 2011 Dec; 119 Suppl 1(Suppl 1):311-23. PubMed ID: 22243262
    [TBL] [Abstract][Full Text] [Related]  

  • 5. M180 amelogenin processed by MMP20 is sufficient for decussating murine enamel.
    Pugach MK; Suggs C; Li Y; Wright JT; Kulkarni AB; Bartlett JD; Gibson CW
    J Dent Res; 2013 Dec; 92(12):1118-22. PubMed ID: 24072097
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Amelogenesis imperfecta: an introduction.
    Gadhia K; McDonald S; Arkutu N; Malik K
    Br Dent J; 2012 Apr; 212(8):377-9. PubMed ID: 22538897
    [TBL] [Abstract][Full Text] [Related]  

  • 9. MMP20 hemopexin domain mutation in amelogenesis imperfecta.
    Lee SK; Seymen F; Kang HY; Lee KE; Gencay K; Tuna B; Kim JW
    J Dent Res; 2010 Jan; 89(1):46-50. PubMed ID: 19966041
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exclusion of candidate genes in seven Turkish families with autosomal recessive amelogenesis imperfecta.
    Becerik S; Cogulu D; Emingil G; Han T; Hart PS; Hart TC
    Am J Med Genet A; 2009 Jul; 149A(7):1392-8. PubMed ID: 19530186
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Novel KLK4 and MMP20 mutations discovered by whole-exome sequencing.
    Wang SK; Hu Y; Simmer JP; Seymen F; Estrella NM; Pal S; Reid BM; Yildirim M; Bayram M; Bartlett JD; Hu JC
    J Dent Res; 2013 Mar; 92(3):266-71. PubMed ID: 23355523
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The molecular etiologies and associated phenotypes of amelogenesis imperfecta.
    Wright JT
    Am J Med Genet A; 2006 Dec; 140(23):2547-55. PubMed ID: 16838342
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15.
    Wang YL; Lin HC; Liang T; Lin JC; Simmer JP; Hu JC; Wang SK
    J Dent Res; 2024 Jun; 103(6):662-671. PubMed ID: 38716742
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MMP20 active-site mutation in hypomaturation amelogenesis imperfecta.
    Ozdemir D; Hart PS; Ryu OH; Choi SJ; Ozdemir-Karatas M; Firatli E; Piesco N; Hart TC
    J Dent Res; 2005 Nov; 84(11):1031-5. PubMed ID: 16246936
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta.
    Seymen F; Park JC; Lee KE; Lee HK; Lee DS; Koruyucu M; Gencay K; Bayram M; Tuna EB; Lee ZH; Kim YJ; Kim JW
    J Dent Res; 2015 Aug; 94(8):1063-9. PubMed ID: 26124219
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Abrogation of epithelial BMP2 and BMP4 causes Amelogenesis Imperfecta by reducing MMP20 and KLK4 expression.
    Xie X; Liu C; Zhang H; Jani PH; Lu Y; Wang X; Zhang B; Qin C
    Sci Rep; 2016 May; 6():25364. PubMed ID: 27146352
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.