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Summary Anatomy Item Literature (1770) Expression Attributions Wiki
XB-ANAT-722

Papers associated with anatomical space (and fgf2)

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BRCA1 and ELK-1 regulate neural progenitor cell fate in the optic tectum in response to visual experience in Xenopus laevis tadpoles., Huang LC., Proc Natl Acad Sci U S A. January 16, 2024; 121 (3): e2316542121.                        


Pinhead signaling regulates mesoderm heterogeneity via the FGF receptor-dependent pathway., Ossipova O., Development. September 11, 2020; 147 (17):                 


Pinhead signaling regulates mesoderm heterogeneity via FGF receptor-dependent pathway., Ossipova O., Development. January 1, 2020;                                       


E-cigarette aerosol exposure can cause craniofacial defects in Xenopus laevis embryos and mammalian neural crest cells., Kennedy AE., PLoS One. September 8, 2017; 12 (9): e0185729.                      


Understanding How the Subcommissural Organ and Other Periventricular Secretory Structures Contribute via the Cerebrospinal Fluid to Neurogenesis., Guerra MM., Front Cell Neurosci. September 23, 2015; 9 480.                


Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.                                  


Insulin-like factor regulates neural induction through an IGF1 receptor-independent mechanism., Haramoto Y., Sci Rep. January 12, 2015; 5 11603.                                  


Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.                                          


Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus., Roberts NA., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.                              


Comparative Functional Analysis of ZFP36 Genes during Xenopus Development., Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.                          


Focal adhesion kinase is essential for cardiac looping and multichamber heart formation., Doherty JT., Genesis. August 1, 2010; 48 (8): 492-504.                  


BMP inhibition initiates neural induction via FGF signaling and Zic genes., Marchal L., Proc Natl Acad Sci U S A. October 13, 2009; 106 (41): 17437-42.        


Temporal and spatial expression of FGF ligands and receptors during Xenopus development., Lea R., Dev Dyn. June 1, 2009; 238 (6): 1467-79.                                                                                                        


Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity., Suga A., Dev Biol. July 1, 2006; 295 (1): 26-39.    


Cold-inducible RNA binding protein is required for the expression of adhesion molecules and embryonic cell movement in Xenopus laevis., Peng Y., Biochem Biophys Res Commun. May 26, 2006; 344 (1): 416-24.        


Matrix metalloproteinases are required for retinal ganglion cell axon guidance at select decision points., Hehr CL., Development. August 1, 2005; 132 (15): 3371-9.            


Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.                          


Fibroblast growth factors redirect retinal axons in vitro and in vivo., Webber CA., Dev Biol. November 1, 2003; 263 (1): 24-34.            


Isolation and growth factor inducibility of the Xenopus laevis Lmx1b gene., Haldin CE., Int J Dev Biol. May 1, 2003; 47 (4): 253-62.            


Using Xenopus as a model system for an undergraduate laboratory course in vertebrate development at the University of Bordeaux, France., Olive M., Int J Dev Biol. January 1, 2003; 47 (2-3): 153-60.          


The role of Xenopus dickkopf1 in prechordal plate specification and neural patterning., Kazanskaya O., Development. November 1, 2000; 127 (22): 4981-92.              


FOG acts as a repressor of red blood cell development in Xenopus., Deconinck AE., Development. May 1, 2000; 127 (10): 2031-40.              


The Xenopus Ets transcription factor XER81 is a target of the FGF signaling pathway., Münchberg SR., Mech Dev. January 1, 1999; 80 (1): 53-65.            


Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K., Development. February 1, 1998; 125 (4): 579-87.              


Loss of cell adhesion in Xenopus laevis embryos mediated by the cytoplasmic domain of XLerk, an erythropoietin-producing hepatocellular ligand., Jones TL., Proc Natl Acad Sci U S A. January 20, 1998; 95 (2): 576-81.            


FGF-8 is associated with anteroposterior patterning and limb regeneration in Xenopus., Christen B., Dev Biol. December 15, 1997; 192 (2): 455-66.        


Wnt and FGF pathways cooperatively pattern anteroposterior neural ectoderm in Xenopus., McGrew LL., Mech Dev. December 1, 1997; 69 (1-2): 105-14.          


Xenopus Pax-2 displays multiple splice forms during embryogenesis and pronephric kidney development., Heller N., Mech Dev. December 1, 1997; 69 (1-2): 83-104.        


PDGF signalling is required for gastrulation of Xenopus laevis., Ataliotis P., Development. September 1, 1995; 121 (9): 3099-110.                  


Induction of the prospective neural crest of Xenopus., Mayor R., Development. March 1, 1995; 121 (3): 767-77.                  


Distinct elements of the xsna promoter are required for mesodermal and ectodermal expression., Mayor R., Development. November 1, 1993; 119 (3): 661-71.                  


GATA-4 is a novel transcription factor expressed in endocardium of the developing heart., Kelley C., Development. July 1, 1993; 118 (3): 817-27.                


The biological effects of XTC-MIF: quantitative comparison with Xenopus bFGF., Green JB., Development. January 1, 1990; 108 (1): 173-83.

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