These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

367 related articles for article (PubMed ID: 15111628)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta.
    Kida M; Sakiyama Y; Matsuda A; Takabayashi S; Ochi H; Sekiguchi H; Minamitake S; Ariga T
    J Dent Res; 2007 Jan; 86(1):69-72. PubMed ID: 17189466
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Detection of a novel mutation in X-linked amelogenesis imperfecta.
    Kindelan SA; Brook AH; Gangemi L; Lench N; Wong FS; Fearne J; Jackson Z; Foster G; Stringer BM
    J Dent Res; 2000 Dec; 79(12):1978-82. PubMed ID: 11201048
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta.
    Lagerström-Fermér M; Nilsson M; Bäckman B; Salido E; Shapiro L; Pettersson U; Landegren U
    Genomics; 1995 Mar; 26(1):159-62. PubMed ID: 7782077
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [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]  

  • 14. Novel missense mutation of the FAM83H gene causes retention of amelogenin and a mild clinical phenotype of hypocalcified enamel.
    Urzúa B; Martínez C; Ortega-Pinto A; Adorno D; Morales-Bozo I; Riadi G; Jara L; Plaza A; Lefimil C; Lozano C; Reyes M
    Arch Oral Biol; 2015 Sep; 60(9):1356-67. PubMed ID: 26142250
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17.
    Wang SK; Zhang H; Lin HC; Wang YL; Lin SC; Seymen F; Koruyucu M; Simmer JP; Hu JC
    Int J Mol Sci; 2024 Jun; 25(11):. PubMed ID: 38892321
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. A new frameshift mutation encoding a truncated amelogenin leads to X-linked amelogenesis imperfecta.
    Greene SR; Yuan ZA; Wright JT; Amjad H; Abrams WR; Buchanan JA; Trachtenberg DI; Gibson CW
    Arch Oral Biol; 2002 Mar; 47(3):211-7. PubMed ID: 11839357
    [TBL] [Abstract][Full Text] [Related]  

  • 20. PCR detection of the human amelogenin gene and its application to the diagnosis of amelogenesis imperfecta.
    Sekiguchi H; Minaguchi K; Machida Y; Yakushiji M
    Bull Tokyo Dent Coll; 1998 Nov; 39(4):275-85. PubMed ID: 10218009
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.