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Journal Abstract Search

266 related items for PubMed ID: 24785830

  • 21. MEMO1 drives cranial endochondral ossification and palatogenesis.
    Van Otterloo E, Feng W, Jones KL, Hynes NE, Clouthier DE, Niswander L, Williams T.
    Dev Biol; 2016 Jul 15; 415(2):278-295. PubMed ID: 26746790
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  • 22. ALK5-mediated transforming growth factor β signaling in neural crest cells controls craniofacial muscle development via tissue-tissue interactions.
    Han A, Zhao H, Li J, Pelikan R, Chai Y.
    Mol Cell Biol; 2014 Aug 15; 34(16):3120-31. PubMed ID: 24912677
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  • 23. Msx1 and Dlx5 act independently in development of craniofacial skeleton, but converge on the regulation of Bmp signaling in palate formation.
    Levi G, Mantero S, Barbieri O, Cantatore D, Paleari L, Beverdam A, Genova F, Robert B, Merlo GR.
    Mech Dev; 2006 Jan 15; 123(1):3-16. PubMed ID: 16330189
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  • 24. Complete congenital bony syngnathia in a case of oromandibular limb hypogenesis syndrome.
    Knoll B, Karas D, Persing JA, Shin J.
    J Craniofac Surg; 2000 Jul 15; 11(4):398-404. PubMed ID: 11314391
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  • 25. Congenital bony syngnathia: a proposed classification.
    Dawson KH, Gruss JS, Myall RW.
    Cleft Palate Craniofac J; 1997 Mar 15; 34(2):141-6. PubMed ID: 9138509
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  • 26. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development.
    Satokata I, Maas R.
    Nat Genet; 1994 Apr 15; 6(4):348-56. PubMed ID: 7914451
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  • 28. Mice with Tak1 deficiency in neural crest lineage exhibit cleft palate associated with abnormal tongue development.
    Song Z, Liu C, Iwata J, Gu S, Suzuki A, Sun C, He W, Shu R, Li L, Chai Y, Chen Y.
    J Biol Chem; 2013 Apr 12; 288(15):10440-50. PubMed ID: 23460641
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  • 29. Congenital maxillomandibular syngnathia: case report.
    Parkins GE, Boamah MO.
    J Craniomaxillofac Surg; 2009 Jul 12; 37(5):276-8. PubMed ID: 19231229
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  • 31. RERE deficiency contributes to the development of orofacial clefts in humans and mice.
    Kim BJ, Zaveri HP, Kundert PN, Jordan VK, Scott TM, Carmichael J, Scott DA.
    Hum Mol Genet; 2021 May 12; 30(7):595-602. PubMed ID: 33772547
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  • 33. Crucial and Overlapping Roles of Six1 and Six2 in Craniofacial Development.
    Liu Z, Li C, Xu J, Lan Y, Liu H, Li X, Maire P, Wang X, Jiang R.
    J Dent Res; 2019 May 12; 98(5):572-579. PubMed ID: 30905259
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  • 37. Pdgfra and Pdgfrb genetically interact during craniofacial development.
    McCarthy N, Liu JS, Richarte AM, Eskiocak B, Lovely CB, Tallquist MD, Eberhart JK.
    Dev Dyn; 2016 Jun 12; 245(6):641-52. PubMed ID: 26971580
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  • 40. Facial clefting in Tp63 deficient mice results from altered Bmp4, Fgf8 and Shh signaling.
    Thomason HA, Dixon MJ, Dixon J.
    Dev Biol; 2008 Sep 01; 321(1):273-82. PubMed ID: 18634775
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