BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

347 related articles for article (PubMed ID: 20067920)

  • 1. A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta.
    Barron MJ; Brookes SJ; Kirkham J; Shore RC; Hunt C; Mironov A; Kingswell NJ; Maycock J; Shuttleworth CA; Dixon MJ
    Hum Mol Genet; 2010 Apr; 19(7):1230-47. PubMed ID: 20067920
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta.
    Kim JW; Simmer JP; Hu YY; Lin BP; Boyd C; Wright JT; Yamada CJ; Rayes SK; Feigal RJ; Hu JC
    J Dent Res; 2004 May; 83(5):378-83. PubMed ID: 15111628
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation.
    Ravassipour DB; Hart PS; Hart TC; Ritter AV; Yamauchi M; Gibson C; Wright JT
    J Dent Res; 2000 Jul; 79(7):1476-81. PubMed ID: 11005731
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations.
    Hart PS; Aldred MJ; Crawford PJ; Wright NJ; Hart TC; Wright JT
    Arch Oral Biol; 2002 Apr; 47(4):261-5. PubMed ID: 11922869
    [TBL] [Abstract][Full Text] [Related]  

  • 5. AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout-NLS-lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue-specificity.
    Liang T; Hu Y; Smith CE; Richardson AS; Zhang H; Yang J; Lin B; Wang SK; Kim JW; Chun YH; Simmer JP; Hu JC
    Mol Genet Genomic Med; 2019 Sep; 7(9):e929. PubMed ID: 31402633
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.
    Hu JC; Chan HC; Simmer SG; Seymen F; Richardson AS; Hu Y; Milkovich RN; Estrella NM; Yildirim M; Bayram M; Chen CF; Simmer JP
    PLoS One; 2012; 7(12):e52052. PubMed ID: 23251683
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
    Wright JT; Hart PS; Aldred MJ; Seow K; Crawford PJ; Hong SP; Gibson CW; Hart TC
    Connect Tissue Res; 2003; 44 Suppl 1():72-8. PubMed ID: 12952177
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Mouse genetic background influences the dental phenotype.
    Li Y; Konicki WS; Wright JT; Suggs C; Xue H; Kuehl MA; Kulkarni AB; Gibson CW
    Cells Tissues Organs; 2013; 198(6):448-56. PubMed ID: 24732779
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Amelogenin phosphorylation regulates tooth enamel formation by stabilizing a transient amorphous mineral precursor.
    Shin NY; Yamazaki H; Beniash E; Yang X; Margolis SS; Pugach MK; Simmer JP; Margolis HC
    J Biol Chem; 2020 Feb; 295(7):1943-1959. PubMed ID: 31919099
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel AMELX mutation causes hypoplastic amelogenesis imperfecta.
    Kim YJ; Kim YJ; Kang J; Shin TJ; Hyun HK; Lee SH; Lee ZH; Kim JW
    Arch Oral Biol; 2017 Apr; 76():61-65. PubMed ID: 28130977
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations Causing X-Linked Amelogenesis Imperfecta Alter miRNA Formation from Amelogenin Exon4.
    Shemirani R; Le MH; Nakano Y
    J Dent Res; 2023 Oct; 102(11):1210-1219. PubMed ID: 37563801
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations.
    Coxon TL; Brook AH; Barron MJ; Smith RN
    Cells Tissues Organs; 2012; 196(5):420-30. PubMed ID: 22759786
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Alteration of conserved alternative splicing in AMELX causes enamel defects.
    Cho ES; Kim KJ; Lee KE; Lee EJ; Yun CY; Lee MJ; Shin TJ; Hyun HK; Kim YJ; Lee SH; Jung HS; Lee ZH; Kim JW
    J Dent Res; 2014 Oct; 93(10):980-7. PubMed ID: 25117480
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Transgenic mice that express normal and mutated amelogenins.
    Gibson CW; Yuan ZA; Li Y; Daly B; Suggs C; Aragon MA; Alawi F; Kulkarni AB; Wright JT
    J Dent Res; 2007 Apr; 86(4):331-5. PubMed ID: 17384027
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synergistic roles of amelogenin and ameloblastin.
    Hatakeyama J; Fukumoto S; Nakamura T; Haruyama N; Suzuki S; Hatakeyama Y; Shum L; Gibson CW; Yamada Y; Kulkarni AB
    J Dent Res; 2009 Apr; 88(4):318-22. PubMed ID: 19407150
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.