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Journal Abstract Search

361 related items for PubMed ID: 31667691

  • 1. FAM20A is essential for amelogenesis, but is dispensable for dentinogenesis.
    Li L, Saiyin W, Zhang H, Wang S, Xu Q, Qin C, Lu Y.
    J Mol Histol; 2019 Dec; 50(6):581-591. PubMed ID: 31667691
    [Abstract] [Full Text] [Related]

  • 2. The specific role of FAM20C in amelogenesis.
    Wang X, Jung J, Liu Y, Yuan B, Lu Y, Feng JQ, Qin C.
    J Dent Res; 2013 Nov; 92(11):995-9. PubMed ID: 24026952
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  • 3. Amelogenesis imperfecta and other biomineralization defects in Fam20a and Fam20c null mice.
    Vogel P, Hansen GM, Read RW, Vance RB, Thiel M, Liu J, Wronski TJ, Smith DD, Jeter-Jones S, Brommage R.
    Vet Pathol; 2012 Nov; 49(6):998-1017. PubMed ID: 22732358
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  • 4. Loss of epithelial FAM20A in mice causes amelogenesis imperfecta, tooth eruption delay and gingival overgrowth.
    Li LL, Liu PH, Xie XH, Ma S, Liu C, Chen L, Qin CL.
    Int J Oral Sci; 2016 Jun 30; 8(2):98-109. PubMed ID: 27281036
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  • 5. The specific role of FAM20C in dentinogenesis.
    Wang X, Wang J, Liu Y, Yuan B, Ruest LB, Feng JQ, Qin C.
    J Dent Res; 2015 Feb 30; 94(2):330-6. PubMed ID: 25515778
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  • 6. Ablation of Fam20c causes amelogenesis imperfecta via inhibiting Smad dependent BMP signaling pathway.
    Liu J, Saiyin W, Xie X, Mao L, Li L.
    Biol Direct; 2020 Oct 07; 15(1):16. PubMed ID: 33028367
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  • 7. FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome.
    Wang SK, Zhang H, Wang YL, Lin HY, Seymen F, Koruyucu M, Wright JT, Kim JW, Simmer JP, Hu JC.
    Int Endod J; 2023 Aug 07; 56(8):943-954. PubMed ID: 37159186
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  • 8. Enamel formation and amelogenesis imperfecta.
    Hu JC, Chun YH, Al Hazzazzi T, Simmer JP.
    Cells Tissues Organs; 2007 Aug 07; 186(1):78-85. PubMed ID: 17627121
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  • 15. 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 07; 58(9):1148-54. PubMed ID: 23545224
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  • 16. Nephrocalcinosis in Amelogenesis Imperfecta Caused by the FAM20A Mutation.
    Koruyucu M, Seymen F, Gencay G, Gencay K, Tuna EB, Shin TJ, Hyun HK, Kim YJ, Kim JW.
    Nephron; 2018 Sep 07; 139(2):189-196. PubMed ID: 29439260
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  • 17. Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome.
    O'Sullivan J, Bitu CC, Daly SB, Urquhart JE, Barron MJ, Bhaskar SS, Martelli-Júnior H, dos Santos Neto PE, Mansilla MA, Murray JC, Coletta RD, Black GC, Dixon MJ.
    Am J Hum Genet; 2011 May 13; 88(5):616-20. PubMed ID: 21549343
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