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Journal Abstract Search

236 related items for PubMed ID: 24222224

  • 1. Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families.
    Mu YD, Xu Z, Contreras CI, McDaniel JS, Donly KJ, Chen S.
    Genet Mol Res; 2013 Oct 10; 12(4):4446-58. PubMed ID: 24222224
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  • 5. Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype.
    Gerits A, Nieminen P, De Muynck S, Carels C.
    Orthod Craniofac Res; 2006 Aug 10; 9(3):129-36. PubMed ID: 16918677
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  • 6. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes.
    Bergendal B, Klar J, Stecksén-Blicks C, Norderyd J, Dahl N.
    Am J Med Genet A; 2011 Jul 10; 155A(7):1616-22. PubMed ID: 21626677
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  • 7. Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.
    Shahid M, Balto HA, Al-Hammad N, Joshi S, Khalil HS, Somily AM, Sinjilawi NA, Al-Ghamdi S, Faiyaz-Ul-Haque M, Dhillon VS.
    Eur J Med Genet; 2016 Aug 10; 59(8):377-85. PubMed ID: 27365112
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  • 8. Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series.
    Haddaji Mastouri M, De Coster P, Zaghabani A, Jammali F, Raouahi N, Ben Salem A, Saad A, Coucke P, H'mida Ben Brahim D.
    Eur J Oral Sci; 2018 Feb 10; 126(1):24-32. PubMed ID: 29114927
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  • 9. Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein 2 (AXIN2) Genes in Nonsyndromic Hypodontia.
    Mártha K, Kerekes Máthé B, Moldovan VG, Bănescu C.
    Biomed Res Int; 2019 Feb 10; 2019():2183720. PubMed ID: 31781599
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  • 10. Investigating the etiology of multiple tooth agenesis in three sisters with severe oligodontia.
    Swinnen S, Bailleul-Forestier I, Arte S, Nieminen P, Devriendt K, Carels C.
    Orthod Craniofac Res; 2008 Feb 10; 11(1):24-31. PubMed ID: 18199077
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  • 11. A novel initiation codon mutation of PAX9 in a family with oligodontia.
    Liang J, Qin C, Yue H, He H, Bian Z.
    Arch Oral Biol; 2016 Jan 10; 61():144-8. PubMed ID: 26571067
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  • 12. Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation?
    Bock NC, Lenz S, Ruiz-Heiland G, Ruf S.
    J Orofac Orthop; 2017 Mar 10; 78(2):112-120. PubMed ID: 28204848
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  • 13. Axis inhibition protein 2 polymorphisms may be a risk factor for families with isolated oligodontia.
    Qin H, Cai J.
    Mol Med Rep; 2015 Mar 10; 11(3):1899-904. PubMed ID: 25377791
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  • 14. Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4.
    Kimura M, Machida J, Yamaguchi S, Shibata A, Tatematsu T, Miyachi H, Jezewski PA, Nakayama A, Higashi Y, Shimozato K, Tokita Y.
    Eur J Oral Sci; 2014 Feb 10; 122(1):15-20. PubMed ID: 24329876
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  • 15. A screen of a large Czech cohort of oligodontia patients implicates a novel mutation in the PAX9 gene.
    Šerý O, Bonczek O, Hloušková A, Černochová P, Vaněk J, Míšek I, Krejčí P, Izakovičová Hollá L.
    Eur J Oral Sci; 2015 Apr 10; 123(2):65-71. PubMed ID: 25683653
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  • 16. A novel PAX9 mutation causing oligodontia.
    Daw EM, Saliba C, Grech G, Camilleri S.
    Arch Oral Biol; 2017 Dec 10; 84():100-105. PubMed ID: 28965043
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  • 17. Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia.
    Wong S, Liu H, Bai B, Chang H, Zhao H, Wang Y, Han D, Feng H.
    Arch Oral Biol; 2014 Mar 10; 59(3):349-53. PubMed ID: 24581859
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  • 18. What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndromic hypodontia? A case-control study in orthodontically treated patients.
    Alhazmi N, Alaqla A, Almuzzaini B, Aldrees M, Alnaqa G, Almasoud F, Aldibasi O, Alshamlan H.
    Prog Orthod; 2024 Aug 26; 25(1):31. PubMed ID: 39183201
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  • 19. Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia.
    Xuan K, Jin F, Liu YL, Yuan LT, Wen LY, Yang FS, Wang XJ, Wang GH, Jin Y.
    Arch Oral Biol; 2008 Aug 26; 53(8):773-9. PubMed ID: 18374898
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  • 20. Familial oligodontia and regional odontodysplasia associated with a PAX9 initiation codon mutation.
    Koskinen S, Keski-Filppula R, Alapulli H, Nieminen P, Anttonen V.
    Clin Oral Investig; 2019 Nov 26; 23(11):4107-4111. PubMed ID: 30809714
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