BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 12605438)

  • 1. Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia.
    Das P; Hai M; Elcock C; Leal SM; Brown DT; Brook AH; Patel PI
    Am J Med Genet A; 2003 Apr; 118A(1):35-42. PubMed ID: 12605438
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia.
    Jumlongras D; Lin JY; Chapra A; Seidman CE; Seidman JG; Maas RL; Olsen BR
    Hum Genet; 2004 Feb; 114(3):242-9. PubMed ID: 14689302
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia.
    Mendoza-Fandino GA; Gee JM; Ben-Dor S; Gonzalez-Quevedo C; Lee K; Kobayashi Y; Hartiala J; Myers RM; Leal SM; Allayee H; Patel PI
    Clin Genet; 2011 Sep; 80(3):265-72. PubMed ID: 21443745
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia.
    Das P; Stockton DW; Bauer C; Shaffer LG; D'Souza RN; Wright T; Patel PI
    Hum Genet; 2002 Apr; 110(4):371-6. PubMed ID: 11941488
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.
    Nieminen P; Arte S; Tanner D; Paulin L; Alaluusua S; Thesleff I; Pirinen S
    Eur J Hum Genet; 2001 Oct; 9(10):743-6. PubMed ID: 11781684
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation in human PAX9 causes molar oligodontia.
    Frazier-Bowers SA; Guo DC; Cavender A; Xue L; Evans B; King T; Milewicz D; D'Souza RN
    J Dent Res; 2002 Feb; 81(2):129-33. PubMed ID: 11827258
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Novel missense mutation in PAX9 gene associated with familial tooth agenesis.
    Boeira BR; Echeverrigaray S
    J Oral Pathol Med; 2013 Jan; 42(1):99-105. PubMed ID: 22747565
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Functional analysis of a mutation in PAX9 associated with familial tooth agenesis in humans.
    Mensah JK; Ogawa T; Kapadia H; Cavender AC; D'Souza RN
    J Biol Chem; 2004 Feb; 279(7):5924-33. PubMed ID: 14607846
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

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

  • 17. 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]  

  • 18. A novel missense mutation in the paired domain of human PAX9 causes oligodontia.
    Zhao J; Hu Q; Chen Y; Luo S; Bao L; Xu Y
    Am J Med Genet A; 2007 Nov; 143A(21):2592-7. PubMed ID: 17910065
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Identification and functional analysis of two novel PAX9 mutations.
    Wang Y; Wu H; Wu J; Zhao H; Zhang X; Mues G; D'Souza RN; Feng H; Kapadia H
    Cells Tissues Organs; 2009; 189(1-4):80-7. PubMed ID: 18701815
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.