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Journal Abstract Search

227 related items for PubMed ID: 18617531

  • 1. Zic2-associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation.
    Warr N, Powles-Glover N, Chappell A, Robson J, Norris D, Arkell RM.
    Hum Mol Genet; 2008 Oct 01; 17(19):2986-96. PubMed ID: 18617531
    [Abstract] [Full Text] [Related]

  • 2. New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
    Mercier S, Dubourg C, Garcelon N, Campillo-Gimenez B, Gicquel I, Belleguic M, Ratié L, Pasquier L, Loget P, Bendavid C, Jaillard S, Rochard L, Quélin C, Dupé V, David V, Odent S.
    J Med Genet; 2011 Nov 01; 48(11):752-60. PubMed ID: 21940735
    [Abstract] [Full Text] [Related]

  • 3. ZIC2 in Holoprosencephaly.
    Barratt KS, Arkell RM.
    Adv Exp Med Biol; 2018 Nov 01; 1046():269-299. PubMed ID: 29442327
    [Abstract] [Full Text] [Related]

  • 4. Zic2 mutation causes holoprosencephaly via disruption of NODAL signalling.
    Houtmeyers R, Tchouate Gainkam O, Glanville-Jones HA, Van den Bosch B, Chappell A, Barratt KS, Souopgui J, Tejpar S, Arkell RM.
    Hum Mol Genet; 2016 Sep 15; 25(18):3946-3959. PubMed ID: 27466203
    [Abstract] [Full Text] [Related]

  • 5. Boc modifies the holoprosencephaly spectrum of Cdo mutant mice.
    Zhang W, Hong M, Bae GU, Kang JS, Krauss RS.
    Dis Model Mech; 2011 May 15; 4(3):368-80. PubMed ID: 21183473
    [Abstract] [Full Text] [Related]

  • 6. Zic-associated holoprosencephaly: zebrafish Zic1 controls midline formation and forebrain patterning by regulating Nodal, Hedgehog, and retinoic acid signaling.
    Maurus D, Harris WA.
    Genes Dev; 2009 Jun 15; 23(12):1461-73. PubMed ID: 19528322
    [Abstract] [Full Text] [Related]

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

  • 8. NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos.
    Mercier S, David V, Ratié L, Gicquel I, Odent S, Dupé V.
    Dis Model Mech; 2013 Mar 15; 6(2):537-43. PubMed ID: 23264560
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Link between the causative genes of holoprosencephaly: Zic2 directly regulates Tgif1 expression.
    Ishiguro A, Hatayama M, Otsuka MI, Aruga J.
    Sci Rep; 2018 Feb 01; 8(1):2140. PubMed ID: 29391420
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Rescue of holoprosencephaly in fetal alcohol-exposed Cdon mutant mice by reduced gene dosage of Ptch1.
    Hong M, Krauss RS.
    PLoS One; 2013 Jun 15; 8(11):e79269. PubMed ID: 24244464
    [Abstract] [Full Text] [Related]

  • 13. SHH signaling mediated by a prechordal and brain enhancer controls forebrain organization.
    Sagai T, Amano T, Maeno A, Ajima R, Shiroishi T.
    Proc Natl Acad Sci U S A; 2019 Nov 19; 116(47):23636-23642. PubMed ID: 31685615
    [Abstract] [Full Text] [Related]

  • 14. Fetal ethanol exposure activates protein kinase A and impairs Shh expression in prechordal mesendoderm cells in the pathogenesis of holoprosencephaly.
    Aoto K, Shikata Y, Higashiyama D, Shiota K, Motoyama J.
    Birth Defects Res A Clin Mol Teratol; 2008 Apr 19; 82(4):224-31. PubMed ID: 18338389
    [Abstract] [Full Text] [Related]

  • 15. 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 Apr 19; 8(10):e1002927. PubMed ID: 23055936
    [Abstract] [Full Text] [Related]

  • 16. Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
    Gripp KW, Wotton D, Edwards MC, Roessler E, Ades L, Meinecke P, Richieri-Costa A, Zackai EH, Massagué J, Muenke M, Elledge SJ.
    Nat Genet; 2000 Jun 19; 25(2):205-8. PubMed ID: 10835638
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  • 19. The ups and downs of holoprosencephaly: dorsal versus ventral patterning forces.
    Fernandes M, Hébert JM.
    Clin Genet; 2008 May 19; 73(5):413-23. PubMed ID: 18394003
    [Abstract] [Full Text] [Related]

  • 20. 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]

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