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Journal Abstract Search

321 related items for PubMed ID: 21183473

  • 1. Boc modifies the holoprosencephaly spectrum of Cdo mutant mice.
    Zhang W, Hong M, Bae GU, Kang JS, Krauss RS.
    Dis Model Mech; 2011 May; 4(3):368-80. PubMed ID: 21183473
    [Abstract] [Full Text] [Related]

  • 2. Cdo functions at multiple points in the Sonic Hedgehog pathway, and Cdo-deficient mice accurately model human holoprosencephaly.
    Zhang W, Kang JS, Cole F, Yi MJ, Krauss RS.
    Dev Cell; 2006 May; 10(5):657-65. PubMed ID: 16647303
    [Abstract] [Full Text] [Related]

  • 3. BOC is a modifier gene in holoprosencephaly.
    Hong M, Srivastava K, Kim S, Allen BL, Leahy DJ, Hu P, Roessler E, Krauss RS, Muenke M.
    Hum Mutat; 2017 Nov; 38(11):1464-1470. PubMed ID: 28677295
    [Abstract] [Full Text] [Related]

  • 4. Cdon mutation and fetal ethanol exposure synergize to produce midline signaling defects and holoprosencephaly spectrum disorders in mice.
    Hong M, Krauss RS.
    PLoS Genet; 2012 Nov; 8(10):e1002999. PubMed ID: 23071453
    [Abstract] [Full Text] [Related]

  • 5. Rescue of holoprosencephaly in fetal alcohol-exposed Cdon mutant mice by reduced gene dosage of Ptch1.
    Hong M, Krauss RS.
    PLoS One; 2013 Nov; 8(11):e79269. PubMed ID: 24244464
    [Abstract] [Full Text] [Related]

  • 6. Mutations in CDON, encoding a hedgehog receptor, result in holoprosencephaly and defective interactions with other hedgehog receptors.
    Bae GU, Domené S, Roessler E, Schachter K, Kang JS, Muenke M, Krauss RS.
    Am J Hum Genet; 2011 Aug 12; 89(2):231-40. PubMed ID: 21802063
    [Abstract] [Full Text] [Related]

  • 7. Ectopic sonic hedgehog signaling impairs telencephalic dorsal midline development: implication for human holoprosencephaly.
    Huang X, Litingtung Y, Chiang C.
    Hum Mol Genet; 2007 Jun 15; 16(12):1454-68. PubMed ID: 17468181
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  • 10. Modeling the complex etiology of holoprosencephaly in mice.
    Hong M, Krauss RS.
    Am J Med Genet C Semin Med Genet; 2018 Jun 15; 178(2):140-150. PubMed ID: 29749693
    [Abstract] [Full Text] [Related]

  • 11. The hedgehog co-receptor BOC differentially regulates SHH signaling during craniofacial development.
    Echevarría-Andino ML, Allen BL.
    Development; 2020 Dec 14; 147(23):. PubMed ID: 33060130
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  • 13. The mode of Hedgehog binding to Ihog homologues is not conserved across different phyla.
    McLellan JS, Zheng X, Hauk G, Ghirlando R, Beachy PA, Leahy DJ.
    Nature; 2008 Oct 16; 455(7215):979-83. PubMed ID: 18794898
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  • 15. Cdon mutation and fetal alcohol converge on Nodal signaling in a mouse model of holoprosencephaly.
    Hong M, Christ A, Christa A, Willnow TE, Krauss RS.
    Elife; 2020 Sep 02; 9():. PubMed ID: 32876567
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  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. Loss of Tgif function causes holoprosencephaly by disrupting the SHH signaling pathway.
    Taniguchi K, Anderson AE, Sutherland AE, Wotton D.
    PLoS Genet; 2012 Oct 15; 8(2):e1002524. PubMed ID: 22383895
    [Abstract] [Full Text] [Related]

  • 18. Shh and Gli3 regulate formation of the telencephalic-diencephalic junction and suppress an isthmus-like signaling source in the forebrain.
    Rash BG, Grove EA.
    Dev Biol; 2011 Nov 15; 359(2):242-50. PubMed ID: 21925158
    [Abstract] [Full Text] [Related]

  • 19. Cytoneme delivery of Sonic Hedgehog from ligand-producing cells requires Myosin 10 and a Dispatched-BOC/CDON co-receptor complex.
    Hall ET, Dillard ME, Stewart DP, Zhang Y, Wagner B, Levine RM, Pruett-Miller SM, Sykes A, Temirov J, Cheney RE, Mori M, Robinson CG, Ogden SK.
    Elife; 2021 Feb 11; 10():. PubMed ID: 33570491
    [Abstract] [Full Text] [Related]

  • 20. Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects.
    Dennis JF, Kurosaka H, Iulianella A, Pace J, Thomas N, Beckham S, Williams T, Trainor PA.
    PLoS Genet; 2012 Feb 11; 8(10):e1002927. PubMed ID: 23055936
    [Abstract] [Full Text] [Related]

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