BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 24631698)

  • 1. Is there a link between ovarian cancer and tooth agenesis?
    Bonds J; Pollan-White S; Xiang L; Mues G; D'Souza R
    Eur J Med Genet; 2014 Apr; 57(5):235-9. PubMed ID: 24631698
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 99(4):493-502. PubMed ID: 33249565
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Coexistence of tooth agenesis and ovarian cancer - a systematic literature review.
    Gawron-Jakubek W; Spaczynska J; Pitynski K; Loster BW
    Ginekol Pol; 2019; 90(12):707-710. PubMed ID: 31909464
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Novel PAX9 gene polymorphisms and mutations and susceptibility to tooth agenesis in the Czech population.
    Hlousková A; Bonczek O; Izakovicová-Hollá L; Lochman J; Soukalová J; Stembírek J; Mísek I; Cernochová P; Krejcí P; Vanek J; Šerý O
    Neuro Endocrinol Lett; 2015; 36(5):452-7. PubMed ID: 26707046
    [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. Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis.
    Callahan N; Modesto A; Meira R; Seymen F; Patir A; Vieira AR
    Arch Oral Biol; 2009 Jan; 54(1):45-9. PubMed ID: 18790474
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese family.
    Tatematsu T; Kimura M; Nakashima M; Machida J; Yamaguchi S; Shibata A; Goto H; Nakayama A; Higashi Y; Miyachi H; Shimozato K; Matsumoto N; Tokita Y
    PLoS One; 2015; 10(6):e0128227. PubMed ID: 26030286
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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; 8(8):e73705. PubMed ID: 23991204
    [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. Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis.
    Yue H; Liang J; Yang K; Hua B; Bian Z
    Eur J Oral Sci; 2016 Jun; 124(3):228-33. PubMed ID: 27090353
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.
    Mostowska A; Biedziak B; Zadurska M; Dunin-Wilczynska I; Lianeri M; Jagodzinski PP
    Clin Genet; 2013 Nov; 84(5):429-40. PubMed ID: 23167694
    [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. Hypodontia, a prospective predictive marker for tumor?
    Yin W; Bian Z
    Oral Dis; 2016 May; 22(4):265-73. PubMed ID: 26600092
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis.
    Haddaji Mastouri M; De Coster P; Zaghabani A; Trabelsi S; May Y; Saad A; Coucke P; H'mida Ben Brahim D
    Arch Oral Biol; 2016 Nov; 71():110-116. PubMed ID: 27491081
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of genetic risk factors for maxillary lateral incisor agenesis.
    Alves-Ferreira M; Pinho T; Sousa A; Sequeiros J; Lemos C; Alonso I
    J Dent Res; 2014 May; 93(5):452-8. PubMed ID: 24554542
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.