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Journal Abstract Search

196 related items for PubMed ID: 33864320

  • 1. A novel ENAM mutation causes hypoplastic amelogenesis imperfecta.
    Yu S, Zhang C, Zhu C, Quan J, Liu D, Wang X, Zheng S.
    Oral Dis; 2022 Sep; 28(6):1610-1619. PubMed ID: 33864320
    [Abstract] [Full Text] [Related]

  • 2. Hypoplastic AI with Highly Variable Expressivity Caused by ENAM Mutations.
    Koruyucu M, Kang J, Kim YJ, Seymen F, Kasimoglu Y, Lee ZH, Shin TJ, Hyun HK, Kim YJ, Lee SH, Hu JCC, Simmer JP, Kim JW.
    J Dent Res; 2018 Aug; 97(9):1064-1069. PubMed ID: 29554435
    [Abstract] [Full Text] [Related]

  • 3. 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 20; 23(1):893. PubMed ID: 37985977
    [Abstract] [Full Text] [Related]

  • 4. Novel ENAM and LAMB3 mutations in Chinese families with hypoplastic amelogenesis imperfecta.
    Wang X, Zhao Y, Yang Y, Qin M.
    PLoS One; 2015 Nov 20; 10(3):e0116514. PubMed ID: 25769099
    [Abstract] [Full Text] [Related]

  • 5. 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 20; 52(3):209-17. PubMed ID: 17125728
    [Abstract] [Full Text] [Related]

  • 6. ENAM Mutations Can Cause Hypomaturation Amelogenesis Imperfecta.
    Wang YL, Lin HC, Liang T, Lin JC, Simmer JP, Hu JC, Wang SK.
    J Dent Res; 2024 Jun 20; 103(6):662-671. PubMed ID: 38716742
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 14(5):575-83. PubMed ID: 15649948
    [Abstract] [Full Text] [Related]

  • 8. The structure and composition of deciduous enamel affected by local hypoplastic autosomal dominant amelogenesis imperfecta resulting from an ENAM mutation.
    Shore RC, Bäckman B, Elcock C, Brook AH, Brookes SJ, Kirkham J.
    Cells Tissues Organs; 2010 Mar 01; 191(4):301-6. PubMed ID: 19923784
    [Abstract] [Full Text] [Related]

  • 9. Phenotype of ENAM mutations is dosage-dependent.
    Ozdemir D, Hart PS, Firatli E, Aren G, Ryu OH, Hart TC.
    J Dent Res; 2005 Nov 01; 84(11):1036-41. PubMed ID: 16246937
    [Abstract] [Full Text] [Related]

  • 10. 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 01; 40(12):900-6. PubMed ID: 14684688
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 84(3):278-82. PubMed ID: 15723871
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 11(9):1069-74. PubMed ID: 11978766
    [Abstract] [Full Text] [Related]

  • 13. ENAM mutations and digenic inheritance.
    Zhang H, Hu Y, Seymen F, Koruyucu M, Kasimoglu Y, Wang SK, Wright JT, Havel MW, Zhang C, Kim JW, Simmer JP, Hu JC.
    Mol Genet Genomic Med; 2019 Oct 01; 7(10):e00928. PubMed ID: 31478359
    [Abstract] [Full Text] [Related]

  • 14. Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta.
    Gutierrez SJ, Chaves M, Torres DM, Briceño I.
    Arch Oral Biol; 2007 May 01; 52(5):503-6. PubMed ID: 17316551
    [Abstract] [Full Text] [Related]

  • 15. ENAM mutations with incomplete penetrance.
    Seymen F, Lee KE, Koruyucu M, Gencay K, Bayram M, Tuna EB, Lee ZH, Kim JW.
    J Dent Res; 2014 Oct 01; 93(10):988-92. PubMed ID: 25143514
    [Abstract] [Full Text] [Related]

  • 16. A novel mutation in GPR68 causes hypomaturation amelogenesis imperfecta.
    Yu S, Liu D, Yan C, Yuan C, Zhang C, Zheng S.
    Arch Oral Biol; 2024 Aug 01; 164():105991. PubMed ID: 38761453
    [Abstract] [Full Text] [Related]

  • 17. Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families.
    Dashash M, Bazrafshani MR, Poulton K, Jaber S, Naeem E, Blinkhorn AS.
    J Investig Clin Dent; 2011 Feb 01; 2(1):16-22. PubMed ID: 25427323
    [Abstract] [Full Text] [Related]

  • 18. 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 Feb 01; 32(1):56-60. PubMed ID: 20298654
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 81(11):738-42. PubMed ID: 12407086
    [Abstract] [Full Text] [Related]

  • 20. Craniofacial characteristics and genotypes of amelogenesis imperfecta patients.
    Pavlic A, Battelino T, Trebusak Podkrajsek K, Ovsenik M.
    Eur J Orthod; 2011 Jun 01; 33(3):325-31. PubMed ID: 21068190
    [Abstract] [Full Text] [Related]

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