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191 related items for PubMed ID: 11559848

  • 1. The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.
    Braybrook C, Doudney K, Marçano AC, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P.
    Nat Genet; 2001 Oct; 29(2):179-83. PubMed ID: 11559848
    [Abstract] [Full Text] [Related]

  • 2. A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia.
    Pauws E, Moore GE, Stanier P.
    J Med Genet; 2009 Aug; 46(8):555-61. PubMed ID: 19648124
    [Abstract] [Full Text] [Related]

  • 3. Isolation and developmental expression analysis of Tbx22, the mouse homolog of the human X-linked cleft palate gene.
    Bush JO, Lan Y, Maltby KM, Jiang R.
    Dev Dyn; 2002 Nov; 225(3):322-6. PubMed ID: 12412015
    [Abstract] [Full Text] [Related]

  • 4. Expression of mouse Tbx22 supports its role in palatogenesis and glossogenesis.
    Herr A, Meunier D, Müller I, Rump A, Fundele R, Ropers HH, Nuber UA.
    Dev Dyn; 2003 Apr; 226(4):579-86. PubMed ID: 12666195
    [Abstract] [Full Text] [Related]

  • 5. Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations.
    Kantaputra PN, Paramee M, Kaewkhampa A, Hoshino A, Lees M, McEntagart M, Masrour N, Moore GE, Pauws E, Stanier P.
    J Dent Res; 2011 Apr; 90(4):450-5. PubMed ID: 21248356
    [Abstract] [Full Text] [Related]

  • 6. X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations.
    Pauws E, Peskett E, Boissin C, Hoshino A, Mengrelis K, Carta E, Abruzzo MA, Lees M, Moore GE, Erickson RP, Stanier P.
    Clin Genet; 2013 Apr; 83(4):352-8. PubMed ID: 22784330
    [Abstract] [Full Text] [Related]

  • 7. TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population.
    Suphapeetiporn K, Tongkobpetch S, Siriwan P, Shotelersuk V.
    Clin Genet; 2007 Nov; 72(5):478-83. PubMed ID: 17868388
    [Abstract] [Full Text] [Related]

  • 8. Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.
    Braybrook C, Lisgo S, Doudney K, Henderson D, Marçano AC, Strachan T, Patton MA, Villard L, Moore GE, Stanier P, Lindsay S.
    Hum Mol Genet; 2002 Oct 15; 11(22):2793-804. PubMed ID: 12374769
    [Abstract] [Full Text] [Related]

  • 9. TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression.
    Andreou AM, Pauws E, Jones MC, Singh MK, Bussen M, Doudney K, Moore GE, Kispert A, Brosens JJ, Stanier P.
    Am J Hum Genet; 2007 Oct 15; 81(4):700-12. PubMed ID: 17846996
    [Abstract] [Full Text] [Related]

  • 10. Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and Ankyloglossia (CPX) critical region.
    Braybrook C, Warry G, Howell G, Arnason A, Bjornsson A, Moore GE, Ross MT, Stanier P.
    Genomics; 2001 Mar 01; 72(2):128-36. PubMed ID: 11401425
    [Abstract] [Full Text] [Related]

  • 11. Cloning and expression analysis of the chick ortholog of TBX22, the gene mutated in X-linked cleft palate and ankyloglossia.
    Haenig B, Schmidt C, Kraus F, Pfordt M, Kispert A.
    Mech Dev; 2002 Sep 01; 117(1-2):321-5. PubMed ID: 12204278
    [Abstract] [Full Text] [Related]

  • 12. Localization of a mutant gene for cleft palate and ankyloglossia in an X-linked Icelandic family.
    Moore GE, Williamson R, Jensson O, Chambers J, Takakubo F, Newton R, Balacs MA, Ivens A.
    J Craniofac Genet Dev Biol; 1991 Sep 01; 11(4):372-6. PubMed ID: 1687471
    [Abstract] [Full Text] [Related]

  • 13. Tbx22 expressions during palatal development in fetuses with glucocorticoid-/alcohol-induced C57BL/6N cleft palates.
    Kim SM, Lee JH, Jabaiti S, Lee SK, Choi JY.
    J Craniofac Surg; 2009 Sep 01; 20(5):1316-26. PubMed ID: 19816249
    [Abstract] [Full Text] [Related]

  • 14. Time for T.
    Murray JC.
    Nat Genet; 2001 Oct 01; 29(2):107-9. PubMed ID: 11586288
    [Abstract] [Full Text] [Related]

  • 15. Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.
    Forbes SA, Brennan L, Richardson M, Coffey A, Cole CG, Gregory SG, Bentley DR, Mumm S, Moore GE, Stanier P.
    Genomics; 1996 Jan 01; 31(1):36-43. PubMed ID: 8808277
    [Abstract] [Full Text] [Related]

  • 16. The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X.
    Stanier P, Forbes SA, Arnason A, Bjornsson A, Sveinbjornsdottir E, Williamson R, Moore G.
    Genomics; 1993 Sep 01; 17(3):549-55. PubMed ID: 8244369
    [Abstract] [Full Text] [Related]

  • 17. Loss-of-function mutation in the X-linked TBX22 promoter disrupts an ETS-1 binding site and leads to cleft palate.
    Fu X, Cheng Y, Yuan J, Huang C, Cheng H, Zhou R.
    Hum Genet; 2015 Feb 01; 134(2):147-58. PubMed ID: 25373698
    [Abstract] [Full Text] [Related]

  • 18. Novel TBX22 mutations in Chinese nonsyndromic cleft lip/palate families.
    Dai J, Xu C, Wang G, Liang Y, Wan T, Zhang Y, Xu X, Yu L, Che Z, Han Q, Wu D, Yang Y.
    J Genet; 2018 Jun 01; 97(2):411-417. PubMed ID: 29932061
    [Abstract] [Full Text] [Related]

  • 19. Mutation analysis of TBX22 reveals new mutation in Tunisian CPX family.
    Chaabouni M, Smaoui N, Benneji N, M'rad R, Jemaa LB, Hachicha S, Chaabouni H.
    Clin Dysmorphol; 2005 Jan 01; 14(1):23-25. PubMed ID: 15602089
    [Abstract] [Full Text] [Related]

  • 20. X-linked cleft palate and ankyloglossia in an Icelandic family.
    Björnsson A, Arnason A, Tippet P.
    Cleft Palate J; 1989 Jan 01; 26(1):3-8. PubMed ID: 2563678
    [Abstract] [Full Text] [Related]

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