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Pubmed for Handhelds

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Journal Abstract Search

188 related items for PubMed ID: 17913790

  • 21. BMP signaling negatively regulates bone mass through sclerostin by inhibiting the canonical Wnt pathway.
    Kamiya N, Ye L, Kobayashi T, Mochida Y, Yamauchi M, Kronenberg HM, Feng JQ, Mishina Y.
    Development; 2008 Nov; 135(22):3801-11. PubMed ID: 18927151
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  • 25. Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling.
    Roessler E, Hu P, Marino J, Hong S, Hart R, Berger S, Martinez A, Abe Y, Kruszka P, Thomas JW, Mullikin JC, NISC Comparative Sequencing ProgramMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland., Wang Y, Wong WSW, Niederhuber JE, Solomon BD, Richieri-Costa A, Ribeiro-Bicudo LA, Muenke M.
    Hum Mutat; 2018 Oct; 39(10):1416-1427. PubMed ID: 29992659
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  • 29. BMP antagonism protects Nodal signaling in the gastrula to promote the tissue interactions underlying mammalian forebrain and craniofacial patterning.
    Yang YP, Anderson RM, Klingensmith J.
    Hum Mol Genet; 2010 Aug 01; 19(15):3030-42. PubMed ID: 20508035
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  • 31. Genetic analyses demonstrate that bone morphogenetic protein signaling is required for embryonic cerebellar development.
    Qin L, Wine-Lee L, Ahn KJ, Crenshaw EB.
    J Neurosci; 2006 Feb 15; 26(7):1896-905. PubMed ID: 16481421
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  • 36. The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
    Nanni L, Ming JE, Bocian M, Steinhaus K, Bianchi DW, Die-Smulders C, Giannotti A, Imaizumi K, Jones KL, Campo MD, Martin RA, Meinecke P, Pierpont ME, Robin NH, Young ID, Roessler E, Muenke M.
    Hum Mol Genet; 1999 Dec 15; 8(13):2479-88. PubMed ID: 10556296
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  • 37. 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
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  • 38. 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
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