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Journal Abstract Search


271 related items for PubMed ID: 30375332

  • 1. Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome.
    Teng CS, Ting MC, Farmer DT, Brockop M, Maxson RE, Crump JG.
    Elife; 2018 Oct 25; 7():. PubMed ID: 30375332
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  • 2. Embryonic requirements for Tcf12 in the development of the mouse coronal suture.
    Ting MC, Farmer DT, Teng CS, He J, Chai Y, Crump JG, Maxson RE.
    Development; 2022 Jan 01; 149(1):. PubMed ID: 34878091
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  • 3. Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
    Sharma VP, Fenwick AL, Brockop MS, McGowan SJ, Goos JA, Hoogeboom AJ, Brady AF, Jeelani NO, Lynch SA, Mulliken JB, Murray DJ, Phipps JM, Sweeney E, Tomkins SE, Wilson LC, Bennett S, Cornall RJ, Broxholme J, Kanapin A, 500 Whole-Genome Sequences (WGS500) Consortium, Johnson D, Wall SA, van der Spek PJ, Mathijssen IM, Maxson RE, Twigg SR, Wilkie AO.
    Nat Genet; 2013 Mar 01; 45(3):304-7. PubMed ID: 23354436
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  • 4. The developing mouse coronal suture at single-cell resolution.
    Farmer DT, Mlcochova H, Zhou Y, Koelling N, Wang G, Ashley N, Bugacov H, Chen HJ, Parvez R, Tseng KC, Merrill AE, Maxson RE, Wilkie AOM, Crump JG, Twigg SRF.
    Nat Commun; 2021 Aug 10; 12(1):4797. PubMed ID: 34376651
    [Abstract] [Full Text] [Related]

  • 5. EphA4 as an effector of Twist1 in the guidance of osteogenic precursor cells during calvarial bone growth and in craniosynostosis.
    Ting MC, Wu NL, Roybal PG, Sun J, Liu L, Yen Y, Maxson RE.
    Development; 2009 Mar 10; 136(5):855-64. PubMed ID: 19201948
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  • 8. Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome.
    Carver EA, Oram KF, Gridley T.
    Anat Rec; 2002 Oct 01; 268(2):90-2. PubMed ID: 12221714
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  • 10. Recombinant mouse periostin ameliorates coronal sutures fusion in Twist1+/- mice.
    Bai S, Li D, Xu L, Duan H, Yuan J, Wei M.
    J Transl Med; 2018 Apr 17; 16(1):103. PubMed ID: 29665811
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  • 12. Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis.
    Merrill AE, Bochukova EG, Brugger SM, Ishii M, Pilz DT, Wall SA, Lyons KM, Wilkie AO, Maxson RE.
    Hum Mol Genet; 2006 Apr 15; 15(8):1319-28. PubMed ID: 16540516
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  • 15. Mutations in snail family genes enhance craniosynostosis of Twist1 haplo-insufficient mice: implications for Saethre-Chotzen Syndrome.
    Oram KF, Gridley T.
    Genetics; 2005 Jun 15; 170(2):971-4. PubMed ID: 15802514
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  • 18. Clinical spectrum and outcomes in families with coronal synostosis and TCF12 mutations.
    di Rocco F, Baujat G, Arnaud E, Rénier D, Laplanche JL, Daire VC, Collet C.
    Eur J Hum Genet; 2014 Dec 15; 22(12):1413-6. PubMed ID: 24736737
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