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Journal Abstract Search

214 related items for PubMed ID: 25063195

  • 1. Boc modifies the spectrum of holoprosencephaly in the absence of Gas1 function.
    Seppala M, Xavier GM, Fan CM, Cobourne MT.
    Biol Open; 2014 Jul 25; 3(8):728-40. PubMed ID: 25063195
    [Abstract] [Full Text] [Related]

  • 2. Gas1 is a modifier for holoprosencephaly and genetically interacts with sonic hedgehog.
    Seppala M, Depew MJ, Martinelli DC, Fan CM, Sharpe PT, Cobourne MT.
    J Clin Invest; 2007 Jun 25; 117(6):1575-84. PubMed ID: 17525797
    [Abstract] [Full Text] [Related]

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

  • 4. Genetic interactions between the hedgehog co-receptors Gas1 and Boc regulate cell proliferation during murine palatogenesis.
    Xavier GM, Seppala M, Papageorgiou SN, Fan CM, Cobourne MT.
    Oncotarget; 2016 Nov 29; 7(48):79233-79246. PubMed ID: 27811357
    [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 29; 4(3):368-80. PubMed ID: 21183473
    [Abstract] [Full Text] [Related]

  • 6. Vax1 Plays an Indirect Role in the Etiology of Murine Cleft Palate.
    Geoghegan F, Xavier GM, Birjandi AA, Seppala M, Cobourne MT.
    J Dent Res; 2017 Dec 29; 96(13):1555-1562. PubMed ID: 28771384
    [Abstract] [Full Text] [Related]

  • 7. Gas1 Regulates Patterning of the Murine and Human Dentitions through Sonic Hedgehog.
    Seppala M, Thivichon-Prince B, Xavier GM, Shaffie N, Sangani I, Birjandi AA, Rooney J, Lau JNS, Dhaliwal R, Rossi O, Riaz MA, Stonehouse-Smith D, Wang Y, Papageorgiou SN, Viriot L, Cobourne MT.
    J Dent Res; 2022 Apr 29; 101(4):473-482. PubMed ID: 34796774
    [Abstract] [Full Text] [Related]

  • 8. Hedgehog receptor function during craniofacial development.
    Xavier GM, Seppala M, Barrell W, Birjandi AA, Geoghegan F, Cobourne MT.
    Dev Biol; 2016 Jul 15; 415(2):198-215. PubMed ID: 26875496
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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]

  • 11. A sonic hedgehog missense mutation associated with holoprosencephaly causes defective binding to GAS1.
    Martinelli DC, Fan CM.
    J Biol Chem; 2009 Jul 17; 284(29):19169-72. PubMed ID: 19478089
    [Abstract] [Full Text] [Related]

  • 12. GAS1 is required for NOTCH-dependent facilitation of SHH signaling in the ventral forebrain neuroepithelium.
    Marczenke M, Sunaga-Franze DY, Popp O, Althaus IW, Sauer S, Mertins P, Christ A, Allen BL, Willnow TE.
    Development; 2021 Nov 01; 148(21):. PubMed ID: 34698766
    [Abstract] [Full Text] [Related]

  • 13. Holoprosencephaly.
    Dubourg C, Bendavid C, Pasquier L, Henry C, Odent S, David V.
    Orphanet J Rare Dis; 2007 Feb 02; 2():8. PubMed ID: 17274816
    [Abstract] [Full Text] [Related]

  • 14. DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations.
    Lavillaureix A, Rollier P, Kim A, Panasenkava V, De Tayrac M, Carré W, Guyodo H, Faoucher M, Poirel E, Akloul L, Quélin C, Whalen S, Bos J, Broekema M, van Hagen JM, Grand K, Allen-Sharpley M, Magness E, McLean SD, Kayserili H, Altunoglu U, En Qi Chong A, Xue S, Jeanne M, Almontashiri N, Habhab W, Vanlerberghe C, Faivre L, Viora-Dupont E, Philippe C, Safraou H, Laffargue F, Mittendorf L, Abou Jamra R, Patil SJ, Dalal A, Sarma AS, Keren B, Reversade B, Dubourg C, Odent S, Dupé V.
    Genet Med; 2024 Jul 02; 26(7):101126. PubMed ID: 38529886
    [Abstract] [Full Text] [Related]

  • 15. Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH.
    Pineda-Alvarez DE, Roessler E, Hu P, Srivastava K, Solomon BD, Siple CE, Fan CM, Muenke M.
    Hum Genet; 2012 Feb 02; 131(2):301-10. PubMed ID: 21842183
    [Abstract] [Full Text] [Related]

  • 16. 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 02; 8(10):e1002927. PubMed ID: 23055936
    [Abstract] [Full Text] [Related]

  • 17. Definition of critical periods for Hedgehog pathway antagonist-induced holoprosencephaly, cleft lip, and cleft palate.
    Heyne GW, Melberg CG, Doroodchi P, Parins KF, Kietzman HW, Everson JL, Ansen-Wilson LJ, Lipinski RJ.
    PLoS One; 2015 Feb 02; 10(3):e0120517. PubMed ID: 25793997
    [Abstract] [Full Text] [Related]

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