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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

225 related items for PubMed ID: 19429910

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  • 23. 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; 122(1):15-20. PubMed ID: 24329876
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  • 24. Associations between the risk of tooth agenesis and single-nucleotide polymorphisms of MSX1 and PAX9 genes in nonsyndromic cleft patients.
    Seo YJ, Park JW, Kim YH, Baek SH.
    Angle Orthod; 2013 Nov; 83(6):1036-42. PubMed ID: 23718693
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  • 25. Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
    Yu M, Wong SW, Han D, Cai T.
    Oral Dis; 2019 Apr; 25(3):646-651. PubMed ID: 29969831
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  • 26. Natural selection and molecular evolution in primate PAX9 gene, a major determinant of tooth development.
    Pereira TV, Salzano FM, Mostowska A, Trzeciak WH, Ruiz-Linares A, Chies JA, Saavedra C, Nagamachi C, Hurtado AM, Hill K, Castro-de-Guerra D, Silva-Júnior WA, Bortolini MC.
    Proc Natl Acad Sci U S A; 2006 Apr 11; 103(15):5676-81. PubMed ID: 16585527
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  • 27. Non-syndromic oligodontia with a novel mutation of PAX9.
    Suda N, Ogawa T, Kojima T, Saito C, Moriyama K.
    J Dent Res; 2011 Mar 11; 90(3):382-6. PubMed ID: 21098475
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  • 33. 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 11; 9(3):129-36. PubMed ID: 16918677
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  • 36. An inclusive study of deleterious missense PAX9 variants using user-friendly tools reveals structural, functional alterations, as well as potential therapeutic targets.
    Ranjan P, Das P.
    Int J Biol Macromol; 2023 Apr 01; 233():123375. PubMed ID: 36702222
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  • 38. Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities.
    Wang SK, Chan HC, Makovey I, Simmer JP, Hu JC.
    PLoS One; 2012 Apr 01; 7(12):e51533. PubMed ID: 23227268
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  • 39. Msx1 deficiency interacts with hypoxia and induces a morphogenetic regulation during mouse lip development.
    Nakatomi M, Ludwig KU, Knapp M, Kist R, Lisgo S, Ohshima H, Mangold E, Peters H.
    Development; 2020 Jun 24; 147(21):. PubMed ID: 32467233
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  • 40. [Correlation between the phenotype and genotype of tooth agenesis patients by tooth agenesis code].
    Gong Y, Feng HL, He HY, Ge YJ.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2010 Jun 24; 32(3):254-9. PubMed ID: 20602873
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