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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 33078491)

  • 21. 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]  

  • 22. 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]  

  • 23. Novel mutation of the initiation codon of PAX9 causes oligodontia.
    Klein ML; Nieminen P; Lammi L; Niebuhr E; Kreiborg S
    J Dent Res; 2005 Jan; 84(1):43-7. PubMed ID: 15615874
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. [Novel mutations of PAX9 gene in Chinese patients with oligodontia].
    Zhao JL; Chen YX; Bao L; Xia QJ; Wu TJ; Zhou L
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2005 Jul; 40(4):266-70. PubMed ID: 16191360
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel G to A transition at initiation codon and exon-intron boundary of PAX9 identified in association with familial isolated oligodontia.
    Sarkar T; Bansal R; Das P
    Gene; 2017 Nov; 635():69-76. PubMed ID: 28847717
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia.
    Mostowska A; Kobielak A; Biedziak B; Trzeciak WH
    Eur J Oral Sci; 2003 Jun; 111(3):272-6. PubMed ID: 12786960
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Novel missense mutations in PAX9 causing oligodontia.
    Liang J; Song G; Li Q; Bian Z
    Arch Oral Biol; 2012 Jun; 57(6):784-9. PubMed ID: 22277187
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing.
    Zhao K; Lian M; Zou D; Huang W; Zhou W; Shen Y; Wang F; Wu Y
    Oral Dis; 2019 Mar; 25(2):523-534. PubMed ID: 30417976
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9.
    Wang Y; Groppe JC; Wu J; Ogawa T; Mues G; D'Souza RN; Kapadia H
    Hum Mol Genet; 2009 Aug; 18(15):2863-74. PubMed ID: 19429910
    [TBL] [Abstract][Full Text] [Related]  

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

  • 37. 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]  

  • 38. 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]  

  • 39. A missense mutation in PAX9 in a family with distinct phenotype of oligodontia.
    Lammi L; Halonen K; Pirinen S; Thesleff I; Arte S; Nieminen P
    Eur J Hum Genet; 2003 Nov; 11(11):866-71. PubMed ID: 14571272
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.