These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

347 related items for PubMed ID: 23071453

  • 1. 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; 8(10):e1002999. PubMed ID: 23071453
    [Abstract] [Full Text] [Related]

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

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Modeling the complex etiology of holoprosencephaly in mice.
    Hong M, Krauss RS.
    Am J Med Genet C Semin Med Genet; 2018 Jun 02; 178(2):140-150. PubMed ID: 29749693
    [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 02; 4(3):368-80. PubMed ID: 21183473
    [Abstract] [Full Text] [Related]

  • 6. 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 May 02; 8(10):e1002927. PubMed ID: 23055936
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Loss of Tgif function causes holoprosencephaly by disrupting the SHH signaling pathway.
    Taniguchi K, Anderson AE, Sutherland AE, Wotton D.
    PLoS Genet; 2012 Aug 12; 8(2):e1002524. PubMed ID: 22383895
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. The teratogenic effects of prenatal ethanol exposure are exacerbated by Sonic Hedgehog or GLI2 haploinsufficiency in the mouse.
    Kietzman HW, Everson JL, Sulik KK, Lipinski RJ.
    PLoS One; 2014 Jun 15; 9(2):e89448. PubMed ID: 24586787
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Holoprosencephaly: signaling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans.
    Petryk A, Graf D, Marcucio R.
    Wiley Interdiscip Rev Dev Biol; 2015 Jun 15; 4(1):17-32. PubMed ID: 25339593
    [Abstract] [Full Text] [Related]

  • 18. Microform holoprosencephaly in mice that lack the Ig superfamily member Cdon.
    Cole F, Krauss RS.
    Curr Biol; 2003 Mar 04; 13(5):411-5. PubMed ID: 12620190
    [Abstract] [Full Text] [Related]

  • 19. Gli2 gene-environment interactions contribute to the etiological complexity of holoprosencephaly: evidence from a mouse model.
    Heyne GW, Everson JL, Ansen-Wilson LJ, Melberg CG, Fink DM, Parins KF, Doroodchi P, Ulschmid CM, Lipinski RJ.
    Dis Model Mech; 2016 Nov 01; 9(11):1307-1315. PubMed ID: 27585885
    [Abstract] [Full Text] [Related]

  • 20. Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects.
    Paulo SS, Fernandes-Rosa FL, Turatti W, Coeli-Lacchini FB, Martinelli CE, Nakiri GS, Moreira AC, Santos AC, de Castro M, Antonini SR.
    Clin Endocrinol (Oxf); 2015 Apr 01; 82(4):562-9. PubMed ID: 25056824
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 18.