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Journal Abstract Search

152 related items for PubMed ID: 12412015

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. 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; 20(5):1316-26. PubMed ID: 19816249
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 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. 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]

  • 9. 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]

  • 10. 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 15; 117(1-2):321-5. PubMed ID: 12204278
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Molecular cloning and characterization of a gene expressed in mouse developing tongue, mDscr5 gene, a homolog of human DSCR5 (Down syndrome Critical Region gene 5).
    Choi DK, Suzuki Y, Yoshimura S, Togashi T, Hida M, Taylor TD, Wang Y, Sugano S, Hattori M, Sakaki Y.
    Mamm Genome; 2001 May 15; 12(5):347-51. PubMed ID: 11331941
    [Abstract] [Full Text] [Related]

  • 13. Expression and requirement of T-box transcription factors Tbx2 and Tbx3 during secondary palate development in the mouse.
    Zirzow S, Lüdtke TH, Brons JF, Petry M, Christoffels VM, Kispert A.
    Dev Biol; 2009 Dec 15; 336(2):145-55. PubMed ID: 19769959
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 134(2):147-58. PubMed ID: 25373698
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. 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]

  • 17. Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes.
    Pauws E, Hoshino A, Bentley L, Prajapati S, Keller C, Hammond P, Martinez-Barbera JP, Moore GE, Stanier P.
    Hum Mol Genet; 2009 Nov 01; 18(21):4171-9. PubMed ID: 19648291
    [Abstract] [Full Text] [Related]

  • 18. Identification of SATB2 as the cleft palate gene on 2q32-q33.
    FitzPatrick DR, Carr IM, McLaren L, Leek JP, Wightman P, Williamson K, Gautier P, McGill N, Hayward C, Firth H, Markham AF, Fantes JA, Bonthron DT.
    Hum Mol Genet; 2003 Oct 01; 12(19):2491-501. PubMed ID: 12915443
    [Abstract] [Full Text] [Related]

  • 19. The Mn1 transcription factor acts upstream of Tbx22 and preferentially regulates posterior palate growth in mice.
    Liu W, Lan Y, Pauws E, Meester-Smoor MA, Stanier P, Zwarthoff EC, Jiang R.
    Development; 2008 Dec 01; 135(23):3959-68. PubMed ID: 18948418
    [Abstract] [Full Text] [Related]

  • 20. Position-dependent correlation between TBX22 exon 5 methylation and palatal shelf fusion in the development of cleft palate.
    Li KE, Shu X, Gong H, Cheng L, Dong Z, Shu S.
    An Acad Bras Cienc; 2019 Jun 19; 91(2):e20180945. PubMed ID: 31241704
    [Abstract] [Full Text] [Related]

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