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 *

151 related articles for article (PubMed ID: 21118793)

  • 21. Amelogenesis imperfecta: A novel FAM83H mutation and characteristics of periodontal ligament cells.
    Nowwarote N; Theerapanon T; Osathanon T; Pavasant P; Porntaveetus T; Shotelersuk V
    Oral Dis; 2018 Nov; 24(8):1522-1531. PubMed ID: 29949226
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular characterization of amelogenesis imperfecta in Chinese patients.
    Song YL; Wang CN; Zhang CZ; Yang K; Bian Z
    Cells Tissues Organs; 2012; 196(3):271-9. PubMed ID: 22414746
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.
    Hart PS; Becerik S; Cogulu D; Emingil G; Ozdemir-Ozenen D; Han ST; Sulima PP; Firatli E; Hart TC
    Clin Genet; 2009 Apr; 75(4):401-4. PubMed ID: 19220331
    [No Abstract]   [Full Text] [Related]  

  • 24. A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetrance.
    Bai RQ; He WB; Peng Q; Shen SH; Yu QQ; Du J; Tan YQ; Wang YH; Liu BJ
    Mol Genet Genomic Med; 2022 Apr; 10(4):e1902. PubMed ID: 35212465
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Characterisation of the biochemical and cellular roles of native and pathogenic amelogenesis imperfecta mutants of FAM83H.
    Tachie-Menson T; Gázquez-Gutiérrez A; Fulcher LJ; Macartney TJ; Wood NT; Varghese J; Gourlay R; Soares RF; Sapkota GP
    Cell Signal; 2020 Aug; 72():109632. PubMed ID: 32289446
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Evolutionary analysis of FAM83H in vertebrates.
    Huang W; Yang M; Wang C; Song Y
    PLoS One; 2017; 12(7):e0180360. PubMed ID: 28683132
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Novel WDR72 mutation and cytoplasmic localization.
    Lee SK; Seymen F; Lee KE; Kang HY; Yildirim M; Tuna EB; Gencay K; Hwang YH; Nam KH; De La Garza RJ; Hu JC; Simmer JP; Kim JW
    J Dent Res; 2010 Dec; 89(12):1378-82. PubMed ID: 20938048
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. 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]  

  • 31. 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]  

  • 32. 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]  

  • 33. Novel FAM20A mutations in hypoplastic amelogenesis imperfecta.
    Cho SH; Seymen F; Lee KE; Lee SK; Kweon YS; Kim KJ; Jung SE; Song SJ; Yildirim M; Bayram M; Tuna EB; Gencay K; Kim JW
    Hum Mutat; 2012 Jan; 33(1):91-4. PubMed ID: 21990045
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. 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]  

  • 36. Phenotype of ENAM mutations is dosage-dependent.
    Ozdemir D; Hart PS; Firatli E; Aren G; Ryu OH; Hart TC
    J Dent Res; 2005 Nov; 84(11):1036-41. PubMed ID: 16246937
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Effects of Fam83h overexpression on enamel and dentine formation.
    Kweon YS; Lee KE; Ko J; Hu JC; Simmer JP; Kim JW
    Arch Oral Biol; 2013 Sep; 58(9):1148-54. PubMed ID: 23545224
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fam83h mutation inhibits the mineralization in ameloblasts by activating Wnt/β-catenin signaling pathway.
    Yang M; Huang W; Yang F; Zhang T; Wang C; Song Y
    Biochem Biophys Res Commun; 2018 Jun; 501(1):206-211. PubMed ID: 29709481
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.