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Journal Abstract Search

292 related items for PubMed ID: 24554542

  • 21. Novel PAX9 mutations cause non-syndromic tooth agenesis.
    Mitsui SN, Yasue A, Masuda K, Watanabe K, Horiuchi S, Imoto I, Tanaka E.
    J Dent Res; 2014 Mar; 93(3):245-9. PubMed ID: 24436340
    [Abstract] [Full Text] [Related]

  • 22. Familial human hypodontia--is it all in the genes?
    Cobourne MT.
    Br Dent J; 2007 Aug 25; 203(4):203-8. PubMed ID: 17721480
    [Abstract] [Full Text] [Related]

  • 23. Tooth agenesis association with self-reported family history of cancer.
    Küchler EC, Lips A, Tannure PN, Ho B, Costa MC, Granjeiro JM, Vieira AR.
    J Dent Res; 2013 Feb 25; 92(2):149-55. PubMed ID: 23169889
    [Abstract] [Full Text] [Related]

  • 24. MSX1, PAX9, and TGFA contribute to tooth agenesis in humans.
    Vieira AR, Meira R, Modesto A, Murray JC.
    J Dent Res; 2004 Sep 25; 83(9):723-7. PubMed ID: 15329380
    [Abstract] [Full Text] [Related]

  • 25. De novo EDA mutations: Variable expression in two Egyptian families.
    Gaczkowska A, Abdalla EM, Dowidar KM, Elhady GM, Jagodzinski PP, Mostowska A.
    Arch Oral Biol; 2016 Aug 25; 68():21-8. PubMed ID: 27054699
    [Abstract] [Full Text] [Related]

  • 26. Absence of association between transforming growth factor-beta1 promoter polymorphisms and hypodontia.
    Peres RC, Scarel-Caminaga RM, Silva ER, De Conto F, Line SR.
    Angle Orthod; 2004 Oct 25; 74(5):665-71. PubMed ID: 15529502
    [Abstract] [Full Text] [Related]

  • 27. PAX9 polymorphisms and susceptibility to sporadic tooth agenesis: a case-control study in southeast China.
    Pan Y, Wang L, Ma J, Zhang W, Wang M, Zhong W, Huang Y.
    Eur J Oral Sci; 2008 Apr 25; 116(2):98-103. PubMed ID: 18353002
    [Abstract] [Full Text] [Related]

  • 28. 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 25; 83(6):1036-42. PubMed ID: 23718693
    [Abstract] [Full Text] [Related]

  • 29. Tooth agenesis: What do we know and is there a connection to cancer?
    Bonczek O, Krejci P, Izakovicova-Holla L, Cernochova P, Kiss I, Vojtesek B.
    Clin Genet; 2021 Apr 25; 99(4):493-502. PubMed ID: 33249565
    [Abstract] [Full Text] [Related]

  • 30. Polymorphism in the MSX1 gene in a family with upper lateral incisor agenesis.
    Boeira Junior BR, Echeverrigaray S.
    Arch Oral Biol; 2012 Oct 25; 57(10):1423-8. PubMed ID: 22591773
    [Abstract] [Full Text] [Related]

  • 31. [Msh homebox-1 polymorphisms and susceptibility to 198 sporadic tooth agenesis: a case-control study].
    Wang H, Wang L, Pan YC, Ma JQ, Zhang WB.
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2010 Mar 25; 45(3):135-40. PubMed ID: 20450679
    [Abstract] [Full Text] [Related]

  • 32. Novel PAX9 mutation associated with syndromic tooth agenesis.
    Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP.
    Eur J Oral Sci; 2013 Oct 25; 121(5):403-11. PubMed ID: 24028587
    [Abstract] [Full Text] [Related]

  • 33. 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 25; 122(1):15-20. PubMed ID: 24329876
    [Abstract] [Full Text] [Related]

  • 34. Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis.
    Salvi A, Giacopuzzi E, Bardellini E, Amadori F, Ferrari L, De Petro G, Borsani G, Majorana A.
    Int J Mol Med; 2016 Nov 25; 38(5):1338-1348. PubMed ID: 27665865
    [Abstract] [Full Text] [Related]

  • 35. 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 25; 59(8):377-85. PubMed ID: 27365112
    [Abstract] [Full Text] [Related]

  • 36. Effects of PAX9 and MSX1 gene variants to hypodontia, tooth size and the type of congenitally missing teeth.
    Kirac D, Eraydin F, Avcilar T, Ulucan K, Özdemir F, Guney AI, Kaspar EÇ, Keshi E, Isbir T.
    Cell Mol Biol (Noisy-le-grand); 2016 Nov 30; 62(13):78-84. PubMed ID: 28040065
    [Abstract] [Full Text] [Related]

  • 37. Msx1 mutations: how do they cause tooth agenesis?
    Wang Y, Kong H, Mues G, D'Souza R.
    J Dent Res; 2011 Mar 30; 90(3):311-6. PubMed ID: 21297014
    [Abstract] [Full Text] [Related]

  • 38. Novel EDA p.Ile260Ser mutation linked to non-syndromic hypodontia.
    Yang Y, Luo L, Xu J, Zhu P, Xue W, Wang J, Li W, Wang M, Cheng K, Liu S, Tang Z, Ring BZ, Su L.
    J Dent Res; 2013 Jun 30; 92(6):500-6. PubMed ID: 23625373
    [Abstract] [Full Text] [Related]

  • 39. A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
    Abdalla EM, Mostowska A, Jagodziński PP, Dwidar K, Ismail SR.
    Arch Oral Biol; 2014 Jul 30; 59(7):722-8. PubMed ID: 24798981
    [Abstract] [Full Text] [Related]

  • 40. Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.
    Arte S, Parmanen S, Pirinen S, Alaluusua S, Nieminen P.
    PLoS One; 2013 Jul 30; 8(8):e73705. PubMed ID: 23991204
    [Abstract] [Full Text] [Related]

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