BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

403 related articles for article (PubMed ID: 7935794)

  • 1. A positive feedback loop coordinates growth and patterning in the vertebrate limb.
    Niswander L; Jeffrey S; Martin GR; Tickle C
    Nature; 1994 Oct; 371(6498):609-12. PubMed ID: 7935794
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Expression of genes encoding bone morphogenetic proteins and sonic hedgehog in talpid (ta3) limb buds: their relationships in the signalling cascade involved in limb patterning.
    Francis-West PH; Robertson KE; Ede DA; Rodriguez C; Izpisúa-Belmonte JC; Houston B; Burt DW; Gribbin C; Brickell PM; Tickle C
    Dev Dyn; 1995 Jun; 203(2):187-97. PubMed ID: 7655081
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Constitutive activation of sonic hedgehog signaling in the chicken mutant talpid(2): Shh-independent outgrowth and polarizing activity.
    Caruccio NC; Martinez-Lopez A; Harris M; Dvorak L; Bitgood J; Simandl BK; Fallon JF
    Dev Biol; 1999 Aug; 212(1):137-49. PubMed ID: 10419691
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Manifestation of the limb prepattern: limb development in the absence of sonic hedgehog function.
    Chiang C; Litingtung Y; Harris MP; Simandl BK; Li Y; Beachy PA; Fallon JF
    Dev Biol; 2001 Aug; 236(2):421-35. PubMed ID: 11476582
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The limb bud Shh-Fgf feedback loop is terminated by expansion of former ZPA cells.
    Scherz PJ; Harfe BD; McMahon AP; Tabin CJ
    Science; 2004 Jul; 305(5682):396-9. PubMed ID: 15256670
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fgf8 signalling from the AER is essential for normal limb development.
    Lewandoski M; Sun X; Martin GR
    Nat Genet; 2000 Dec; 26(4):460-3. PubMed ID: 11101846
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Differential response of Shh expression between chick forelimb and hindlimb buds by FGF-4.
    Wada N; Nohno T
    Dev Dyn; 2001 Aug; 221(4):402-11. PubMed ID: 11500977
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Signal relay by BMP antagonism controls the SHH/FGF4 feedback loop in vertebrate limb buds.
    Zúñiga A; Haramis AP; McMahon AP; Zeller R
    Nature; 1999 Oct; 401(6753):598-602. PubMed ID: 10524628
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A BMP-Shh negative-feedback loop restricts Shh expression during limb development.
    Bastida MF; Sheth R; Ros MA
    Development; 2009 Nov; 136(22):3779-89. PubMed ID: 19855020
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gremlin is the BMP antagonist required for maintenance of Shh and Fgf signals during limb patterning.
    Khokha MK; Hsu D; Brunet LJ; Dionne MS; Harland RM
    Nat Genet; 2003 Jul; 34(3):303-7. PubMed ID: 12808456
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Conditional inactivation of Fgf4 reveals complexity of signalling during limb bud development.
    Sun X; Lewandoski M; Meyers EN; Liu YH; Maxson RE; Martin GR
    Nat Genet; 2000 May; 25(1):83-6. PubMed ID: 10802662
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Activation of fgf4 gene expression in the myotomes is regulated by myogenic bHLH factors and by sonic hedgehog.
    Fraidenraich D; Iwahori A; Rudnicki M; Basilico C
    Dev Biol; 2000 Sep; 225(2):392-406. PubMed ID: 10985858
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Distance between AER and ZPA is defined by feed-forward loop and is stabilized by their feedback loop in vertebrate limb bud.
    Hirashima T; Iwasa Y; Morishita Y
    Bull Math Biol; 2008 Feb; 70(2):438-59. PubMed ID: 17994267
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sef is synexpressed with FGFs during chick embryogenesis and its expression is differentially regulated by FGFs in the developing limb.
    Harduf H; Halperin E; Reshef R; Ron D
    Dev Dyn; 2005 Jun; 233(2):301-12. PubMed ID: 15844098
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Early chick limb cartilaginous elements possess polarizing activity and express hedgehog-related morphogenetic factors.
    Koyama E; Leatherman JL; Noji S; Pacifici M
    Dev Dyn; 1996 Nov; 207(3):344-54. PubMed ID: 8922533
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The mouse polydactylous mutation, luxate (lx), causes anterior shift of the anteroposterior border in the developing hindlimb bud.
    Yada Y; Makino S; Chigusa-Ishiwa S; Shiroishi T
    Int J Dev Biol; 2002; 46(7):975-82. PubMed ID: 12455637
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pbx1/Pbx2 requirement for distal limb patterning is mediated by the hierarchical control of Hox gene spatial distribution and Shh expression.
    Capellini TD; Di Giacomo G; Salsi V; Brendolan A; Ferretti E; Srivastava D; Zappavigna V; Selleri L
    Development; 2006 Jun; 133(11):2263-73. PubMed ID: 16672333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Control of the positioning of the vertebrate limb axes during development].
    Catala M
    Morphologie; 2000 Jun; 84(265):17-23. PubMed ID: 11048294
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Shh expression in developing and regenerating limb buds of Xenopus laevis.
    Endo T; Yokoyama H; Tamura K; Ide H
    Dev Dyn; 1997 Jun; 209(2):227-32. PubMed ID: 9186057
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dorsalizing signal Wnt-7a required for normal polarity of D-V and A-P axes of mouse limb.
    Parr BA; McMahon AP
    Nature; 1995 Mar; 374(6520):350-3. PubMed ID: 7885472
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.