BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

317 related articles for article (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; 188(2):235-47. PubMed ID: 9268572
    [TBL] [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; 182(1):42-51. PubMed ID: 9073443
    [TBL] [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; 276(2):268-79. PubMed ID: 15581864
    [TBL] [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; 231(1):148-60. PubMed ID: 15305295
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Direct interaction with Hoxd proteins reverses Gli3-repressor function to promote digit formation downstream of Shh.
    Chen Y; Knezevic V; Ervin V; Hutson R; Ward Y; Mackem S
    Development; 2004 May; 131(10):2339-47. PubMed ID: 15102708
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic interaction of Gli3 and Alx4 during limb development.
    Panman L; Drenth T; Tewelscher P; Zuniga A; Zeller R
    Int J Dev Biol; 2005; 49(4):443-8. PubMed ID: 15968591
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A hypermorphic mouse Gli3 allele results in a polydactylous limb phenotype.
    Wang C; Pan Y; Wang B
    Dev Dyn; 2007 Mar; 236(3):769-76. PubMed ID: 17266131
    [TBL] [Abstract][Full Text] [Related]  

  • 8. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.
    Kang S; Graham JM; Olney AH; Biesecker LG
    Nat Genet; 1997 Mar; 15(3):266-8. PubMed ID: 9054938
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 286(1):149-57. PubMed ID: 16122729
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 205(1):145-57. PubMed ID: 9882503
    [TBL] [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; 131(2):413-24. PubMed ID: 14681194
    [TBL] [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; 19(1):43-50. PubMed ID: 8792608
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Skeletal abnormalities in doubly heterozygous Bmp4 and Bmp7 mice.
    Katagiri T; Boorla S; Frendo JL; Hogan BL; Karsenty G
    Dev Genet; 1998; 22(4):340-8. PubMed ID: 9664686
    [TBL] [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; 13(2):159-70. PubMed ID: 18233958
    [TBL] [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; 19(1):33-42. PubMed ID: 8792607
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Smad2 role in mesoderm formation, left-right patterning and craniofacial development.
    Nomura M; Li E
    Nature; 1998 Jun; 393(6687):786-90. PubMed ID: 9655392
    [TBL] [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; 285(2):533-44. PubMed ID: 16039644
    [TBL] [Abstract][Full Text] [Related]  

  • 18. GDF5 coordinates bone and joint formation during digit development.
    Storm EE; Kingsley DM
    Dev Biol; 1999 May; 209(1):11-27. PubMed ID: 10208739
    [TBL] [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; 50(1):1-7. PubMed ID: 20201963
    [TBL] [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; 42(4):367-76. PubMed ID: 10969736
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.