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Journal Abstract Search

241 related items for PubMed ID: 24103583

  • 1. MSX1 and PAX9 investigation in monozygotic twins with variable expression of tooth agenesis.
    Lopez SI, Mundstock KS, Paixão-Côrtes VR, Schüler-Faccini L, Mundstock CA, Bortolini MC, Salzano FM.
    Twin Res Hum Genet; 2013 Dec; 16(6):1112-6. PubMed ID: 24103583
    [Abstract] [Full Text] [Related]

  • 2. PAX9 and MSX1 transcription factor genes in non-syndromic dental agenesis.
    Paixão-Côrtes VR, Braga T, Salzano FM, Mundstock K, Mundstock CA, Bortolini MC.
    Arch Oral Biol; 2011 Apr; 56(4):337-44. PubMed ID: 21111400
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  • 4. [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; 32(3):254-9. PubMed ID: 20602873
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  • 6. 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; 59(8):377-85. PubMed ID: 27365112
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  • 8. 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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  • 9. Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.
    Mostowska A, Biedziak B, Jagodzinski PP.
    Arch Oral Biol; 2012 Jun; 57(6):790-5. PubMed ID: 22297032
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  • 10. PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China.
    Wang J, Xu Y, Chen J, Wang F, Huang R, Wu S, Shu L, Qiu J, Yang Z, Xue J, Wang R, Zhao J, Lai W.
    J Appl Oral Sci; 2013 Jun; 21(3):256-64. PubMed ID: 23857653
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  • 12. Sequence analysis of PAX9, MSX1 and AXIN2 genes in a Chinese oligodontia family.
    Wang J, Jian F, Chen J, Wang H, Lin Y, Yang Z, Pan X, Lai W.
    Arch Oral Biol; 2011 Oct; 56(10):1027-34. PubMed ID: 21530942
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  • 13. Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review.
    Tallón-Walton V, Manzanares-Céspedes MC, Carvalho-Lobato P, Valdivia-Gandur I, Arte S, Nieminen P.
    Med Oral Patol Oral Cir Bucal; 2014 May 01; 19(3):e248-54. PubMed ID: 24316698
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  • 15. Msx1 mutations: how do they cause tooth agenesis?
    Wang Y, Kong H, Mues G, D'Souza R.
    J Dent Res; 2011 Mar 01; 90(3):311-6. PubMed ID: 21297014
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  • 16. Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype.
    Wong SW, Han D, Zhang H, Liu Y, Zhang X, Miao MZ, Wang Y, Zhao N, Zeng L, Bai B, Wang YX, Liu H, Frazier-Bowers SA, Feng H.
    J Dent Res; 2018 Feb 01; 97(2):155-162. PubMed ID: 28910570
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  • 17. The genetic basis of tooth agenesis: basic concepts and genes involved.
    Pani SC.
    J Indian Soc Pedod Prev Dent; 2011 Feb 01; 29(2):84-9. PubMed ID: 21911943
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  • 18. 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 01; 126(1):24-32. PubMed ID: 29114927
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  • 19. Dental agenesis: genetic and clinical perspectives.
    De Coster PJ, Marks LA, Martens LC, Huysseune A.
    J Oral Pathol Med; 2009 Jan 01; 38(1):1-17. PubMed ID: 18771513
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  • 20. Novel PAX9 mutation associated with syndromic tooth agenesis.
    Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP.
    Eur J Oral Sci; 2013 Oct 01; 121(5):403-11. PubMed ID: 24028587
    [Abstract] [Full Text] [Related]

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