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Journal Abstract Search

155 related items for PubMed ID: 29932061

  • 1. 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; 97(2):411-417. PubMed ID: 29932061
    [Abstract] [Full Text] [Related]

  • 2. 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; 81(4):700-12. PubMed ID: 17846996
    [Abstract] [Full Text] [Related]

  • 3. 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; 134(2):147-58. PubMed ID: 25373698
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Interaction between interferon regulatory factor 6 and glycine receptor beta shows a protective effect on developing nonsyndromic cleft lip with or without cleft palate in the Han Chinese population.
    Wu D, Wang M, Wang X, Zhang YB, Song T, Yin N, Zhao Z.
    Eur J Oral Sci; 2019 Feb; 127(1):27-32. PubMed ID: 30462859
    [Abstract] [Full Text] [Related]

  • 6. A Novel CDH1 Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft Palate.
    Du S, Yang Y, Yi P, Luo J, Liu T, Chen R, Liu CJ, Ma T, Li Y, Wang C, Weng J, Liu M, Zhang L, Yang B, Zeng X, Liu JY.
    Genet Test Mol Biomarkers; 2019 Nov; 23(11):759-765. PubMed ID: 31638429
    [Abstract] [Full Text] [Related]

  • 7. Three GLI2 mutations combined potentially underlie non-syndromic cleft lip with or without cleft palate in a Chinese pedigree.
    Meng P, Zhao H, Huang W, Zhang Y, Zhong W, Zhang M, Jia P, Zhou Z, Maimaitili G, Chen F, Zhang J, Lin J.
    Mol Genet Genomic Med; 2019 Sep; 7(9):e714. PubMed ID: 31386309
    [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. 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]

  • 10. Association between single-nucleotide polymorphisms on chromosome 1p22 and 20q12 and nonsyndromic cleft lip with or without cleft palate: new data in Han Chinese and meta-analysis.
    Huang E, Cheng H, Xu M, Shu S, Tang S.
    Birth Defects Res A Clin Mol Teratol; 2012 Jun; 94(6):469-76. PubMed ID: 22522387
    [Abstract] [Full Text] [Related]

  • 11. Identification of a Novel Variant of ARHGAP29 in a Chinese Family with Nonsyndromic Cleft Lip and Palate.
    Tang JX, Xiao XS, Wang K, Jin JY, Fan LL, Xiang R.
    Biomed Res Int; 2020 Jun; 2020():8790531. PubMed ID: 33150183
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. 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 15; 29(2):179-83. PubMed ID: 11559848
    [Abstract] [Full Text] [Related]

  • 14. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes.
    Basha M, Demeer B, Revencu N, Helaers R, Theys S, Bou Saba S, Boute O, Devauchelle B, Francois G, Bayet B, Vikkula M.
    J Med Genet; 2018 Jul 15; 55(7):449-458. PubMed ID: 29500247
    [Abstract] [Full Text] [Related]

  • 15. Association of EPHA3 Gene Polymorphisms with Nonsyndromic Cleft Lip With or Without Cleft Palate.
    Chen R, Guo S, Wang X, Mu Y, Duan E, Xu Y.
    Genet Test Mol Biomarkers; 2018 Jul 15; 22(7):420-424. PubMed ID: 29932736
    [Abstract] [Full Text] [Related]

  • 16. TBX22 mutations are a frequent cause of cleft palate.
    Marçano AC, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P.
    J Med Genet; 2004 Jan 15; 41(1):68-74. PubMed ID: 14729838
    [No Abstract] [Full Text] [Related]

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  • 19. Further evidence suggesting a role for variation in ARHGAP29 variants in nonsyndromic cleft lip/palate.
    Letra A, Maili L, Mulliken JB, Buchanan E, Blanton SH, Hecht JT.
    Birth Defects Res A Clin Mol Teratol; 2014 Sep 15; 100(9):679-85. PubMed ID: 25163644
    [Abstract] [Full Text] [Related]

  • 20. TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly.
    Kaewkhampa A, Jotikasthira D, Malaivijitnond S, Kantaputra P.
    Cleft Palate Craniofac J; 2012 Mar 15; 49(2):240-4. PubMed ID: 21375406
    [Abstract] [Full Text] [Related]

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