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251 related items for PubMed ID: 20012271

  • 1. Evolutionary analysis of mammalian enamelin, the largest enamel protein, supports a crucial role for the 32-kDa peptide and reveals selective adaptation in rodents and primates.
    Al-Hashimi N, Sire JY, Delgado S.
    J Mol Evol; 2009 Dec; 69(6):635-56. PubMed ID: 20012271
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Evolutionary analysis of selective constraints identifies ameloblastin (AMBN) as a potential candidate for amelogenesis imperfecta.
    Delsuc F, Gasse B, Sire JY.
    BMC Evol Biol; 2015 Jul 30; 15():148. PubMed ID: 26223266
    [Abstract] [Full Text] [Related]

  • 4. The phosphorylation of serine55 in enamelin is essential for murine amelogenesis.
    Dong C, Lamichhane B, Yamazaki H, Vasquez B, Wang J, Zhang Y, Feng JQ, Margolis HC, Beniash E, Wang X.
    Matrix Biol; 2022 Aug 30; 111():245-263. PubMed ID: 35820561
    [Abstract] [Full Text] [Related]

  • 5. Enamelin and autosomal-dominant amelogenesis imperfecta.
    Hu JC, Yamakoshi Y.
    Crit Rev Oral Biol Med; 2003 Aug 30; 14(6):387-98. PubMed ID: 14656895
    [Abstract] [Full Text] [Related]

  • 6. Enamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in mice.
    Hu JC, Hu Y, Smith CE, McKee MD, Wright JT, Yamakoshi Y, Papagerakis P, Hunter GK, Feng JQ, Yamakoshi F, Simmer JP.
    J Biol Chem; 2008 Apr 18; 283(16):10858-71. PubMed ID: 18252720
    [Abstract] [Full Text] [Related]

  • 7. Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.
    Hart PS, Michalec MD, Seow WK, Hart TC, Wright JT.
    Arch Oral Biol; 2003 Aug 18; 48(8):589-96. PubMed ID: 12828988
    [Abstract] [Full Text] [Related]

  • 8. 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 18; 103(6):662-671. PubMed ID: 38716742
    [Abstract] [Full Text] [Related]

  • 9. 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 18; 2(1):16-22. PubMed ID: 25427323
    [Abstract] [Full Text] [Related]

  • 10. 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 18; 52(3):209-17. PubMed ID: 17125728
    [Abstract] [Full Text] [Related]

  • 11. 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 18; 191(4):301-6. PubMed ID: 19923784
    [Abstract] [Full Text] [Related]

  • 12. Evolutionary analysis suggests that AMTN is enamel-specific and a candidate for AI.
    Gasse B, Silvent J, Sire JY.
    J Dent Res; 2012 Nov 18; 91(11):1085-9. PubMed ID: 22968158
    [Abstract] [Full Text] [Related]

  • 13. The enamelin genes in lizard, crocodile, and frog and the pseudogene in the chicken provide new insights on enamelin evolution in tetrapods.
    Al-Hashimi N, Lafont AG, Delgado S, Kawasaki K, Sire JY.
    Mol Biol Evol; 2010 Sep 18; 27(9):2078-94. PubMed ID: 20403965
    [Abstract] [Full Text] [Related]

  • 14. 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 18; 84(3):278-82. PubMed ID: 15723871
    [Abstract] [Full Text] [Related]

  • 15. 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 18; 28(6):1610-1619. PubMed ID: 33864320
    [Abstract] [Full Text] [Related]

  • 16. Altered enamelin phosphorylation site causes amelogenesis imperfecta.
    Chan HC, Mai L, Oikonomopoulou A, Chan HL, Richardson AS, Wang SK, Simmer JP, Hu JC.
    J Dent Res; 2010 Jul 18; 89(7):695-9. PubMed ID: 20439930
    [Abstract] [Full Text] [Related]

  • 17. Simple recessive mutation in ENAM is associated with amelogenesis imperfecta in Italian Greyhounds.
    Gandolfi B, Liu H, Griffioen L, Pedersen NC.
    Anim Genet; 2013 Aug 18; 44(5):569-78. PubMed ID: 23638899
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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 Nov 20; 32(1):56-60. PubMed ID: 20298654
    [Abstract] [Full Text] [Related]

  • 20. 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 Nov 20; 196(5):420-30. PubMed ID: 22759786
    [Abstract] [Full Text] [Related]

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