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 *

334 related articles for article (PubMed ID: 20602873)

  • 21. 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]  

  • 22. Dental agenesis: genetic and clinical perspectives.
    De Coster PJ; Marks LA; Martens LC; Huysseune A
    J Oral Pathol Med; 2009 Jan; 38(1):1-17. PubMed ID: 18771513
    [TBL] [Abstract][Full Text] [Related]  

  • 23. WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.
    Mostowska A; Biedziak B; Zadurska M; Matuszewska-Trojan S; Jagodziński PP
    Eur J Oral Sci; 2015 Feb; 123(1):1-8. PubMed ID: 25545742
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Maxillary canine anomalies and tooth agenesis.
    Camilleri S
    Eur J Orthod; 2005 Oct; 27(5):450-6. PubMed ID: 16093260
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Tooth agenesis in a family and homozygous PAX9 mutation in exon 3: a case report.
    Kula K; Trimmell J; Lu Y; Briscoe P; Feng JQ
    World J Orthod; 2008; 9(4):e55-61. PubMed ID: 19641755
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. PAX9 mutations and genetic synergism in familial tooth agenesis.
    Chu KY; Wang YL; Chen JT; Lin CH; Yao CJ; Chen YJ; Chen HW; Simmer JP; Hu JC; Wang SK
    Ann N Y Acad Sci; 2023 Jun; 1524(1):87-96. PubMed ID: 37005710
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Characterization of PAX9 variant P20L identified in a Japanese family with tooth agenesis.
    Murakami A; Yasuhira S; Mayama H; Miura H; Maesawa C; Satoh K
    PLoS One; 2017; 12(10):e0186260. PubMed ID: 29023497
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Tooth dimensions in hypodontia with a known PAX9 mutation.
    Brook AH; Elcock C; Aggarwal M; Lath DL; Russell JM; Patel PI; Smith RN
    Arch Oral Biol; 2009 Dec; 54 Suppl 1():S57-62. PubMed ID: 18653171
    [TBL] [Abstract][Full Text] [Related]  

  • 33. PAX9 polymorphisms and susceptibility to sporadic tooth agenesis: a case-control study in southeast China.
    Pan Y; Wang L; Ma J; Zhang W; Wang M; Zhong W; Huang Y
    Eur J Oral Sci; 2008 Apr; 116(2):98-103. PubMed ID: 18353002
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Agenesis of maxillary lateral incisors and associated dental anomalies.
    Garib DG; Alencar BM; Lauris JR; Baccetti T
    Am J Orthod Dentofacial Orthop; 2010 Jun; 137(6):732.e1-6; discussion 732-3. PubMed ID: 20685523
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis.
    Han D; Gong Y; Wu H; Zhang X; Yan M; Wang X; Qu H; Feng H; Song S
    Eur J Med Genet; 2008; 51(6):536-46. PubMed ID: 18657636
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. Non-syndromic oligodontia with a novel mutation of PAX9.
    Suda N; Ogawa T; Kojima T; Saito C; Moriyama K
    J Dent Res; 2011 Mar; 90(3):382-6. PubMed ID: 21098475
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.