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Journal Abstract Search

155 related items for PubMed ID: 21821669

  • 1. Noggin null allele mice exhibit a microform of holoprosencephaly.
    Lana-Elola E, Tylzanowski P, Takatalo M, Alakurtti K, Veistinen L, Mitsiadis TA, Graf D, Rice R, Luyten FP, Rice DP.
    Hum Mol Genet; 2011 Oct 15; 20(20):4005-15. PubMed ID: 21821669
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  • 6. Rescue of holoprosencephaly in fetal alcohol-exposed Cdon mutant mice by reduced gene dosage of Ptch1.
    Hong M, Krauss RS.
    PLoS One; 2013 Oct 15; 8(11):e79269. PubMed ID: 24244464
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  • 7. Expression of Indian Hedgehog, BMP-4 and Noggin in craniosynostosis induced by fetal constraint.
    Jacob S, Wu C, Freeman TA, Koyama E, Kirschner RE.
    Ann Plast Surg; 2007 Feb 15; 58(2):215-21. PubMed ID: 17245153
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  • 8. Roles of bone morphogenetic protein signaling and its antagonism in holoprosencephaly.
    Klingensmith J, Matsui M, Yang YP, Anderson RM.
    Am J Med Genet C Semin Med Genet; 2010 Feb 15; 154C(1):43-51. PubMed ID: 20104603
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  • 10. Loss of Tgif function causes holoprosencephaly by disrupting the SHH signaling pathway.
    Taniguchi K, Anderson AE, Sutherland AE, Wotton D.
    PLoS Genet; 2012 Feb 15; 8(2):e1002524. PubMed ID: 22383895
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  • 13. Chordin and noggin promote organizing centers of forebrain development in the mouse.
    Anderson RM, Lawrence AR, Stottmann RW, Bachiller D, Klingensmith J.
    Development; 2002 Nov 15; 129(21):4975-87. PubMed ID: 12397106
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  • 14. Signaling by bone morphogenetic proteins directs formation of an ectodermal signaling center that regulates craniofacial development.
    Foppiano S, Hu D, Marcucio RS.
    Dev Biol; 2007 Dec 01; 312(1):103-14. PubMed ID: 18028903
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  • 15. Mutations in the BMP pathway in mice support the existence of two molecular classes of holoprosencephaly.
    Fernandes M, Gutin G, Alcorn H, McConnell SK, Hébert JM.
    Development; 2007 Nov 01; 134(21):3789-94. PubMed ID: 17913790
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