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Journal Abstract Search

311 related items for PubMed ID: 18252720

  • 41. Bmp2 deletion causes an amelogenesis imperfecta phenotype via regulating enamel gene expression.
    Guo F, Feng J, Wang F, Li W, Gao Q, Chen Z, Shoff L, Donly KJ, Gluhak-Heinrich J, Chun YH, Harris SE, MacDougall M, Chen S.
    J Cell Physiol; 2015 Aug; 230(8):1871-82. PubMed ID: 25545831
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  • 42. Overexpression of constitutively active MAP3K7 in ameloblasts causes enamel defects of mouse teeth.
    Jinping Z, Qing C, Wenying S, Chunyan Y, Lili X, Yao S, Yumin W, Zhenzhen X, Li Z, Yuguang G.
    Arch Oral Biol; 2017 Dec; 84():169-175. PubMed ID: 29024853
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  • 43. The Semaphorin 4D-RhoA-Akt Signal Cascade Regulates Enamel Matrix Secretion in Coordination With Cell Polarization During Ameloblast Differentiation.
    Otsu K, Ida-Yonemochi H, Fujiwara N, Harada H.
    J Bone Miner Res; 2016 Nov; 31(11):1943-1954. PubMed ID: 27218883
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  • 44. MMP20-generated amelogenin cleavage products prevent formation of fan-shaped enamel malformations.
    Bartlett JD, Smith CE, Hu Y, Ikeda A, Strauss M, Liang T, Hsu YH, Trout AH, McComb DW, Freeman RC, Simmer JP, Hu JC.
    Sci Rep; 2021 May 19; 11(1):10570. PubMed ID: 34012043
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  • 45. 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 19; 89(7):695-9. PubMed ID: 20439930
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  • 47. 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 Jul 19; 32(1):56-60. PubMed ID: 20298654
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  • 48. Molecular and circadian controls of ameloblasts.
    Athanassiou-Papaefthymiou M, Kim D, Harbron L, Papagerakis S, Schnell S, Harada H, Papagerakis P.
    Eur J Oral Sci; 2011 Dec 19; 119 Suppl 1(Suppl 1):35-40. PubMed ID: 22243224
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  • 49. 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 19; 27(9):2078-94. PubMed ID: 20403965
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  • 50. Enamelin maps to human chromosome 4q21 within the autosomal dominant amelogenesis imperfecta locus.
    Dong J, Gu TT, Simmons D, MacDougall M.
    Eur J Oral Sci; 2000 Oct 19; 108(5):353-8. PubMed ID: 11037750
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  • 54. Enamel Hypomineralization and Structural Defects in Amelotin-deficient Mice.
    Nakayama Y, Holcroft J, Ganss B.
    J Dent Res; 2015 May 19; 94(5):697-705. PubMed ID: 25715379
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  • 60. Epithelial-specific knockout of the Rac1 gene leads to enamel defects.
    Huang Z, Kim J, Lacruz RS, Bringas P, Glogauer M, Bromage TG, Kaartinen VM, Snead ML.
    Eur J Oral Sci; 2011 Dec 19; 119 Suppl 1(0 1):168-76. PubMed ID: 22243243
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