BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

338 related articles for article (PubMed ID: 28040065)

  • 1. 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; 62(13):78-84. PubMed ID: 28040065
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

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

  • 4. A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth.
    Hansen L; Kreiborg S; Jarlov H; Niebuhr E; Eiberg H
    Eur J Oral Sci; 2007 Aug; 115(4):330-3. PubMed ID: 17697174
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 38(5):1338-1348. PubMed ID: 27665865
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. A novel nonsense mutation in PAX9 is associated with sporadic hypodontia.
    Zhu J; Yang X; Zhang C; Ge L; Zheng S
    Mutagenesis; 2012 May; 27(3):313-7. PubMed ID: 22058014
    [TBL] [Abstract][Full Text] [Related]  

  • 9. PAX9 gene mutations and tooth agenesis: A review.
    Bonczek O; Balcar VJ; Šerý O
    Clin Genet; 2017 Nov; 92(5):467-476. PubMed ID: 28155232
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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; 97(2):155-162. PubMed ID: 28910570
    [TBL] [Abstract][Full Text] [Related]  

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

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

  • 14. Mutations in WNT10A are present in more than half of isolated hypodontia cases.
    van den Boogaard MJ; Créton M; Bronkhorst Y; van der Hout A; Hennekam E; Lindhout D; Cune M; Ploos van Amstel HK
    J Med Genet; 2012 May; 49(5):327-31. PubMed ID: 22581971
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

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

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

  • 18. Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia.
    Goldenberg M; Das P; Messersmith M; Stockton DW; Patel PI; D'Souza RN
    J Dent Res; 2000 Jul; 79(7):1469-75. PubMed ID: 11005730
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 19(3):e248-54. PubMed ID: 24316698
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genes affecting tooth morphogenesis.
    Kapadia H; Mues G; D'Souza R
    Orthod Craniofac Res; 2007 Aug; 10(3):105-13. PubMed ID: 17651126
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.