BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 23731659)

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

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 12(4):4446-58. PubMed ID: 24222224
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 61():144-8. PubMed ID: 26571067
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 21(3):256-64. PubMed ID: 23857653
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 126(1):24-32. PubMed ID: 29114927
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 78(2):112-120. PubMed ID: 28204848
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 9(3):129-36. PubMed ID: 16918677
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel PAX9 mutation causing oligodontia.
    Daw EM; Saliba C; Grech G; Camilleri S
    Arch Oral Biol; 2017 Dec; 84():100-105. PubMed ID: 28965043
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family.
    Liang J; Zhu L; Meng L; Chen D; Bian Z
    Eur J Oral Sci; 2012 Aug; 120(4):278-82. PubMed ID: 22813217
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in the PAX9 gene in sporadic oligodontia.
    Pawlowska E; Janik-Papis K; Poplawski T; Blasiak J; Szczepanska J
    Orthod Craniofac Res; 2010 Aug; 13(3):142-52. PubMed ID: 20618716
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.