BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 23251683)

  • 1. 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]  

  • 2. 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]  

  • 3. [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]  

  • 4. Tooth enamel defects in mice with a deletion at the Arhgap 6/Amel X locus.
    Prakash SK; Gibson CW; Wright JT; Boyd C; Cormier T; Sierra R; Li Y; Abrams WR; Aragon MA; Yuan ZA; van den Veyver IB
    Calcif Tissue Int; 2005 Jul; 77(1):23-9. PubMed ID: 16007484
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 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. 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]  

  • 11. An Intron c.103-3T>C Variant of the AMELX Gene Causes Combined Hypomineralized and Hypoplastic Type of Amelogenesis Imperfecta: Case Series and Review of the Literature.
    Leban T; Trebušak Podkrajšek K; Kovač J; Fidler A; Pavlič A
    Genes (Basel); 2022 Jul; 13(7):. PubMed ID: 35886055
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Imaging RNA polymerase-amelogenin gene complexes with single molecule resolution using atomic force microscopy.
    Crampton N; Thomson NH; Kirkham J; Gibson CW; Bonass WA
    Eur J Oral Sci; 2006 May; 114 Suppl 1():133-8; discussion 164-5, 380-1. PubMed ID: 16674675
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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; 3():8. PubMed ID: 17266769
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion of amelotin exons 3-6 is associated with amelogenesis imperfecta.
    Smith CE; Murillo G; Brookes SJ; Poulter JA; Silva S; Kirkham J; Inglehearn CF; Mighell AJ
    Hum Mol Genet; 2016 Aug; 25(16):3578-3587. PubMed ID: 27412008
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Mutational analysis of candidate genes in 24 amelogenesis imperfecta families.
    Kim JW; Simmer JP; Lin BP; Seymen F; Bartlett JD; Hu JC
    Eur J Oral Sci; 2006 May; 114 Suppl 1():3-12; discussion 39-41, 379. PubMed ID: 16674655
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.