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Journal Abstract Search

315 related items for PubMed ID: 9268572

  • 1. Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4.
    Dunn NR, Winnier GE, Hargett LK, Schrick JJ, Fogo AB, Hogan BL.
    Dev Biol; 1997 Aug 15; 188(2):235-47. PubMed ID: 9268572
    [Abstract] [Full Text] [Related]

  • 2. Multigenic control of the localization of the zone of polarizing activity in limb morphogenesis in the mouse.
    Masuya H, Sagai T, Moriwaki K, Shiroishi T.
    Dev Biol; 1997 Feb 01; 182(1):42-51. PubMed ID: 9073443
    [Abstract] [Full Text] [Related]

  • 3. Bmp4 in limb bud mesoderm regulates digit pattern by controlling AER development.
    Selever J, Liu W, Lu MF, Behringer RR, Martin JF.
    Dev Biol; 2004 Dec 15; 276(2):268-79. PubMed ID: 15581864
    [Abstract] [Full Text] [Related]

  • 4. Levels of Gli3 repressor correlate with Bmp4 expression and apoptosis during limb development.
    Bastida MF, Delgado MD, Wang B, Fallon JF, Fernandez-Teran M, Ros MA.
    Dev Dyn; 2004 Sep 15; 231(1):148-60. PubMed ID: 15305295
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  • 7. A hypermorphic mouse Gli3 allele results in a polydactylous limb phenotype.
    Wang C, Pan Y, Wang B.
    Dev Dyn; 2007 Mar 15; 236(3):769-76. PubMed ID: 17266131
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  • 8. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.
    Kang S, Graham JM, Olney AH, Biesecker LG.
    Nat Genet; 1997 Mar 15; 15(3):266-8. PubMed ID: 9054938
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  • 9. Noggin antagonism of BMP4 signaling controls development of the axial skeleton in the mouse.
    Wijgerde M, Karp S, McMahon J, McMahon AP.
    Dev Biol; 2005 Oct 01; 286(1):149-57. PubMed ID: 16122729
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  • 10. Paired-related homeobox genes cooperate in handplate and hindlimb zeugopod morphogenesis.
    Lu MF, Cheng HT, Lacy AR, Kern MJ, Argao EA, Potter SS, Olson EN, Martin JF.
    Dev Biol; 1999 Jan 01; 205(1):145-57. PubMed ID: 9882503
    [Abstract] [Full Text] [Related]

  • 11. Inactivation of mouse Twisted gastrulation reveals its role in promoting Bmp4 activity during forebrain development.
    Zakin L, De Robertis EM.
    Development; 2004 Jan 01; 131(2):413-24. PubMed ID: 14681194
    [Abstract] [Full Text] [Related]

  • 12. Analysis of limb patterning in BMP-7-deficient mice.
    Hofmann C, Luo G, Balling R, Karsenty G.
    Dev Genet; 1996 Jan 01; 19(1):43-50. PubMed ID: 8792608
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  • 13. Skeletal abnormalities in doubly heterozygous Bmp4 and Bmp7 mice.
    Katagiri T, Boorla S, Frendo JL, Hogan BL, Karsenty G.
    Dev Genet; 1998 Jan 01; 22(4):340-8. PubMed ID: 9664686
    [Abstract] [Full Text] [Related]

  • 14. Reduced BMP4 abundance in Gata2 hypomorphic mutant mice result in uropathies resembling human CAKUT.
    Hoshino T, Shimizu R, Ohmori S, Nagano M, Pan X, Ohneda O, Khandekar M, Yamamoto M, Lim KC, Engel JD.
    Genes Cells; 2008 Feb 01; 13(2):159-70. PubMed ID: 18233958
    [Abstract] [Full Text] [Related]

  • 15. Polydactyly in the Strong's luxoid mouse is suppressed by limb deformity alleles.
    Vogt TF, Leder P.
    Dev Genet; 1996 Feb 01; 19(1):33-42. PubMed ID: 8792607
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  • 16. Smad2 role in mesoderm formation, left-right patterning and craniofacial development.
    Nomura M, Li E.
    Nature; 1998 Jun 25; 393(6687):786-90. PubMed ID: 9655392
    [Abstract] [Full Text] [Related]

  • 17. Function and regulation of Alx4 in limb development: complex genetic interactions with Gli3 and Shh.
    Kuijper S, Feitsma H, Sheth R, Korving J, Reijnen M, Meijlink F.
    Dev Biol; 2005 Sep 15; 285(2):533-44. PubMed ID: 16039644
    [Abstract] [Full Text] [Related]

  • 18. GDF5 coordinates bone and joint formation during digit development.
    Storm EE, Kingsley DM.
    Dev Biol; 1999 May 01; 209(1):11-27. PubMed ID: 10208739
    [Abstract] [Full Text] [Related]

  • 19. Birth defects caused by mutations in human GLI3 and mouse Gli3 genes.
    Naruse I, Ueta E, Sumino Y, Ogawa M, Ishikiriyama S.
    Congenit Anom (Kyoto); 2010 Mar 01; 50(1):1-7. PubMed ID: 20201963
    [Abstract] [Full Text] [Related]

  • 20. Suppression of polydactyly of the Gli3 mutant (extra toes) by deltaEF1 homozygous mutation.
    Moribe H, Takagi T, Kondoh H, Higashi Y.
    Dev Growth Differ; 2000 Aug 01; 42(4):367-76. PubMed ID: 10969736
    [Abstract] [Full Text] [Related]

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