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 *

144 related articles for article (PubMed ID: 29932061)

  • 1. Novel
    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
    [No 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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Novel
    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
    [No 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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a Novel Variant of
    Tang JX; Xiao XS; Wang K; Jin JY; Fan LL; Xiang R
    Biomed Res Int; 2020; 2020():8790531. PubMed ID: 33150183
    [TBL] [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; 11(22):2793-804. PubMed ID: 12374769
    [TBL] [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; 29(2):179-83. PubMed ID: 11559848
    [TBL] [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; 55(7):449-458. PubMed ID: 29500247
    [TBL] [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; 22(7):420-424. PubMed ID: 29932736
    [TBL] [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; 41(1):68-74. PubMed ID: 14729838
    [No Abstract]   [Full Text] [Related]  

  • 17. PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese: population-based and family-based candidate gene analyses.
    Ichikawa E; Watanabe A; Nakano Y; Akita S; Hirano A; Kinoshita A; Kondo S; Kishino T; Uchiyama T; Niikawa N; Yoshiura KI
    J Hum Genet; 2006; 51(1):38-46. PubMed ID: 16247549
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort.
    Wang Y; Sun Y; Huang Y; Pan Y; Jia Z; Ma L; Ma L; Lan F; Zhou Y; Shi J; Yang X; Zhang L; Jiang H; Jiang M; Yin A; Cheng J; Wang L; Yang Y; Shi B
    Gene; 2016 Aug; 588(1):69-73. PubMed ID: 27129939
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 100(9):679-85. PubMed ID: 25163644
    [TBL] [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; 49(2):240-4. PubMed ID: 21375406
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.