These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

320 related items for PubMed ID: 21530942

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Clinical and genetic evaluation of a Chinese family with isolated oligodontia.
    Qin H, Xu HZ, Xuan K.
    Arch Oral Biol; 2013 Sep; 58(9):1180-6. PubMed ID: 23731659
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 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; 155A(7):1616-22. PubMed ID: 21626677
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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; 53(8):773-9. PubMed ID: 18374898
    [Abstract] [Full Text] [Related]

  • 11. 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; 123(2):65-71. PubMed ID: 25683653
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. 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; 59(3):349-53. PubMed ID: 24581859
    [Abstract] [Full Text] [Related]

  • 15. 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; 11(1):24-31. PubMed ID: 18199077
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Axis inhibition protein 2 polymorphisms may be a risk factor for families with isolated oligodontia.
    Qin H, Cai J.
    Mol Med Rep; 2015 Mar; 11(3):1899-904. PubMed ID: 25377791
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. 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; 23(11):4107-4111. PubMed ID: 30809714
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.