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Summary Anatomy Item Literature (2164) Expression Attributions Wiki
XB-ANAT-524

Papers associated with posterior (and fgf2)

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The shh limb enhancer is activated in patterned limb regeneration but not in hypomorphic limb regeneration in Xenopus laevis., Tada R., Dev Biol. May 27, 2023; 500 22-30.                        


FGF/MAPK/Ets signaling in Xenopus ectoderm contributes to neural induction and patterning in an autonomous and paracrine manner, respectively., Hongo I., Cells Dev. June 1, 2022; 170 203769.


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


Rspo2 antagonizes FGF signaling during vertebrate mesoderm formation and patterning., Reis AH., Development. May 27, 2020; 147 (10):                   


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


Hyperinnervation improves Xenopus laevis limb regeneration., Mitogawa K., Dev Biol. January 15, 2018; 433 (2): 276-286.                    


Vestigial-like 3 is a novel Ets1 interacting partner and regulates trigeminal nerve formation and cranial neural crest migration., Simon E., Biol Open. October 15, 2017; 6 (10): 1528-1540.                                  


The signalling receptor MCAM coordinates apical-basal polarity and planar cell polarity during morphogenesis., Gao Q., Nat Commun. June 7, 2017; 8 15279.              


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.                                  


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.                                          


Anterior neural development requires Del1, a matrix-associated protein that attenuates canonical Wnt signaling via the Ror2 pathway., Takai A., Development. October 1, 2010; 137 (19): 3293-302.            


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.                                                                                                        


Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H., Development. April 1, 2008; 135 (7): 1283-93.                            


Differential expression of two TEF-1 (TEAD) genes during Xenopus laevis development and in response to inducing factors., Naye F., Int J Dev Biol. January 1, 2007; 51 (8): 745-52.                  


Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T., Development. December 1, 2006; 133 (23): 4643-54.                  


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


Antagonistic interaction between IGF and Wnt/JNK signaling in convergent extension in Xenopus embryo., Carron C., Mech Dev. November 1, 2005; 122 (11): 1234-47.                


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


Shisa promotes head formation through the inhibition of receptor protein maturation for the caudalizing factors, Wnt and FGF., Yamamoto A., Cell. January 28, 2005; 120 (2): 223-35.                      


Integration of multiple signal transducing pathways on Fgf response elements of the Xenopus caudal homologue Xcad3., Haremaki T., Development. October 1, 2003; 130 (20): 4907-17.                  


Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.              


Neural crest induction by paraxial mesoderm in Xenopus embryos requires FGF signals., Monsoro-Burq AH., Development. July 1, 2003; 130 (14): 3111-24.                


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


Essential role of the transcription factor Ets-2 in Xenopus early development., Kawachi K., J Biol Chem. February 14, 2003; 278 (7): 5473-7.            


Initiating Hox gene expression: in the early chick neural tube differential sensitivity to FGF and RA signaling subdivides the HoxB genes in two distinct groups., Bel-Vialar S., Development. November 1, 2002; 129 (22): 5103-15.          


Common and distinct signals specify the distribution of blood and vascular cell lineages in Xenopus laevis embryos., Iraha F., Dev Growth Differ. October 1, 2002; 44 (5): 395-407.            


Endoderm is required for vascular endothelial tube formation, but not for angioblast specification., Vokes SA., Development. February 1, 2002; 129 (3): 775-85.            


Posteriorization by FGF, Wnt, and retinoic acid is required for neural crest induction., Villanueva S., Dev Biol. January 15, 2002; 241 (2): 289-301.


SNT-1/FRS2alpha physically interacts with Laloo and mediates mesoderm induction by fibroblast growth factor., Hama J., Mech Dev. December 1, 2001; 109 (2): 195-204.              


Xenopus Sprouty2 inhibits FGF-mediated gastrulation movements but does not affect mesoderm induction and patterning., Nutt SL., Genes Dev. May 1, 2001; 15 (9): 1152-66.                


Ras-mediated FGF signaling is required for the formation of posterior but not anterior neural tissue in Xenopus laevis., Ribisi S., Dev Biol. November 1, 2000; 227 (1): 183-96.            


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.              


FGF signaling and the anterior neural induction in Xenopus., Hongo I., Dev Biol. December 15, 1999; 216 (2): 561-81.                            


FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.                


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.            


SCL specifies hematopoietic mesoderm in Xenopus embryos., Mead PE., Development. July 1, 1998; 125 (14): 2611-20.        


Postgastrulation effects of fibroblast growth factor on Xenopus development., Lombardo A., Dev Dyn. May 1, 1998; 212 (1): 75-85.


Xenopus eHAND: a marker for the developing cardiovascular system of the embryo that is regulated by bone morphogenetic proteins., Sparrow DB., Mech Dev. February 1, 1998; 71 (1-2): 151-63.            


Neural induction and patterning by fibroblast growth factor, notochord and somite tissue in Xenopus., Barnett MW., Dev Growth Differ. February 1, 1998; 40 (1): 47-57.


Xiro3 encodes a Xenopus homolog of the Drosophila Iroquois genes and functions in neural specification., Bellefroid EJ., EMBO J. January 2, 1998; 17 (1): 191-203.            


Involvement of NF-kappaB associated proteins in FGF-mediated mesoderm induction., Beck CW., Int J Dev Biol. January 1, 1998; 42 (1): 67-77.                  


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.        


Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.              


Studies on the role of fibroblast growth factor signaling in neurogenesis using conjugated/aged animal caps and dorsal ectoderm-grafted embryos., Xu RH., J Neurosci. September 15, 1997; 17 (18): 6892-8.

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