These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 10452854)

  • 1. A role for xGCNF in midbrain-hindbrain patterning in Xenopus laevis.
    Song K; Takemaru KI; Moon RT
    Dev Biol; 1999 Sep; 213(1):170-9. PubMed ID: 10452854
    [TBL] [Abstract][Full Text] [Related]  

  • 2. FGF is required for posterior neural patterning but not for neural induction.
    Holowacz T; Sokol S
    Dev Biol; 1999 Jan; 205(2):296-308. PubMed ID: 9917365
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Meis3 protein and retinoid signaling interact to pattern the Xenopus hindbrain.
    Dibner C; Elias S; Ofir R; Souopgui J; Kolm PJ; Sive H; Pieler T; Frank D
    Dev Biol; 2004 Jul; 271(1):75-86. PubMed ID: 15196951
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Xenopus Meis3 protein forms a hindbrain-inducing center by activating FGF/MAP kinase and PCP pathways.
    Aamar E; Frank D
    Development; 2004 Jan; 131(1):153-63. PubMed ID: 14660437
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The pro-apoptotic activity of a vertebrate Bar-like homeobox gene plays a key role in patterning the Xenopus neural plate by limiting the number of chordin- and shh-expressing cells.
    Offner N; Duval N; Jamrich M; Durand B
    Development; 2005 Apr; 132(8):1807-18. PubMed ID: 15772136
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Syndecan-1 regulates BMP signaling and dorso-ventral patterning of the ectoderm during early Xenopus development.
    Olivares GH; Carrasco H; Aroca F; Carvallo L; Segovia F; LarraĆ­n J
    Dev Biol; 2009 May; 329(2):338-49. PubMed ID: 19303002
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Flik, a chick follistatin-related gene, functions in gastrular dorsalisation/neural induction and in subsequent maintenance of midline Sonic hedgehog signalling.
    Towers P; Patel K; Withington S; Isaac A; Cooke J
    Dev Biol; 1999 Oct; 214(2):298-317. PubMed ID: 10525336
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Differential display of genes expressed at the midbrain - hindbrain junction identifies sprouty2: an FGF8-inducible member of a family of intracellular FGF antagonists.
    Chambers D; Medhurst AD; Walsh FS; Price J; Mason I
    Mol Cell Neurosci; 2000 Jan; 15(1):22-35. PubMed ID: 10662503
    [TBL] [Abstract][Full Text] [Related]  

  • 9. xGCNF, a nuclear orphan receptor is expressed during neurulation in Xenopus laevis.
    Joos TO; David R; Dreyer C
    Mech Dev; 1996 Nov; 60(1):45-57. PubMed ID: 9025060
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Anteroposterior patterning and organogenesis of Xenopus laevis require a correct dose of germ cell nuclear factor (xGCNF).
    David R; Joos TO; Dreyer C
    Mech Dev; 1998 Dec; 79(1-2):137-52. PubMed ID: 10349627
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Specific induction of cranial placode cells from Xenopus ectoderm by modulating the levels of BMP, Wnt, and FGF signaling.
    Watanabe T; Kanai Y; Matsukawa S; Michiue T
    Genesis; 2015 Oct; 53(10):652-9. PubMed ID: 26249012
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ras-mediated FGF signaling is required for the formation of posterior but not anterior neural tissue in Xenopus laevis.
    Ribisi S; Mariani FV; Aamar E; Lamb TM; Frank D; Harland RM
    Dev Biol; 2000 Nov; 227(1):183-96. PubMed ID: 11076686
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Loss of orphan nuclear receptor GCNF function disrupts forebrain development and the establishment of the isthmic organizer.
    Chung AC; Xu X; Niederreither KA; Cooney AJ
    Dev Biol; 2006 May; 293(1):13-24. PubMed ID: 16530751
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expression patterns of Hoxb genes in the Xenopus embryo suggest roles in anteroposterior specification of the hindbrain and in dorsoventral patterning of the mesoderm.
    Godsave S; Dekker EJ; Holling T; Pannese M; Boncinelli E; Durston A
    Dev Biol; 1994 Dec; 166(2):465-76. PubMed ID: 7813770
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neural induction requires BMP inhibition only as a late step, and involves signals other than FGF and Wnt antagonists.
    Linker C; Stern CD
    Development; 2004 Nov; 131(22):5671-81. PubMed ID: 15509767
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Refinement of gene expression patterns in the early Xenopus embryo.
    Wardle FC; Smith JC
    Development; 2004 Oct; 131(19):4687-96. PubMed ID: 15329341
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Xenopus Zic4: conservation and diversification of expression profiles and protein function among the Xenopus Zic family.
    Fujimi TJ; Mikoshiba K; Aruga J
    Dev Dyn; 2006 Dec; 235(12):3379-86. PubMed ID: 16871625
    [TBL] [Abstract][Full Text] [Related]  

  • 18. foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain.
    Sullivan SA; Akers L; Moody SA
    Dev Biol; 2001 Apr; 232(2):439-57. PubMed ID: 11401404
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Shh/BMP-4 signaling pathway is essential for intestinal epithelial development during Xenopus larval-to-adult remodeling.
    Ishizuya-Oka A; Hasebe T; Shimizu K; Suzuki K; Ueda S
    Dev Dyn; 2006 Dec; 235(12):3240-9. PubMed ID: 17016847
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Knockdown of the complete Hox paralogous group 1 leads to dramatic hindbrain and neural crest defects.
    McNulty CL; Peres JN; Bardine N; van den Akker WM; Durston AJ
    Development; 2005 Jun; 132(12):2861-71. PubMed ID: 15930115
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.