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Summary Anatomy Item Literature (2703) Expression Attributions Wiki
XB-ANAT-3657

Papers associated with neural nucleus (and gsc)

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NSrp70 is significant for embryonic growth and development, being a crucial factor for gastrulation and mesoderm induction., Lee SH., Biochem Biophys Res Commun. October 14, 2016; 479 (2): 238-244.        


Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.                                    


JmjC Domain-containing Protein 6 (Jmjd6) Derepresses the Transcriptional Repressor Transcription Factor 7-like 1 (Tcf7l1) and Is Required for Body Axis Patterning during Xenopus Embryogenesis., Zhang X., J Biol Chem. August 14, 2015; 290 (33): 20273-83.                      


The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.                                    


Custos controls β-catenin to regulate head development during vertebrate embryogenesis., Komiya Y., Proc Natl Acad Sci U S A. September 9, 2014; 111 (36): 13099-104.                                


Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling., Bates TJ., Development. October 1, 2013; 140 (20): 4177-81.              


Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins., Callery EM., Open Biol. April 1, 2012; 2 (4): 120060.                      


Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.                  


Homeodomain-interacting protein kinase 2 (HIPK2) targets beta-catenin for phosphorylation and proteasomal degradation., Kim EA., Biochem Biophys Res Commun. April 16, 2010; 394 (4): 966-71.  


Functional dissection of XDppa2/4 structural domains in Xenopus development., Siegel D., Mech Dev. December 1, 2009; 126 (11-12): 974-89.            


Non-redundant roles for Profilin2 and Profilin1 during vertebrate gastrulation., Khadka DK., Dev Biol. August 15, 2009; 332 (2): 396-406.          


Identification of a novel negative regulator of activin/nodal signaling in mesendodermal formation of Xenopus embryos., Cheong SM., J Biol Chem. June 19, 2009; 284 (25): 17052-60.                        


Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.                


Crossveinless-2 Is a BMP feedback inhibitor that binds Chordin/BMP to regulate Xenopus embryonic patterning., Ambrosio AL., Dev Cell. August 1, 2008; 15 (2): 248-60.                            


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


Nuclear accumulation of Smad complexes occurs only after the midblastula transition in Xenopus., Saka Y., Development. December 1, 2007; 134 (23): 4209-18.


Interpretation of BMP signaling in early Xenopus development., Simeoni I., Dev Biol. August 1, 2007; 308 (1): 82-92.                  


Kinesin-mediated transport of Smad2 is required for signaling in response to TGF-beta ligands., Batut J., Dev Cell. February 1, 2007; 12 (2): 261-74.  


Jun NH2-terminal kinase (JNK) prevents nuclear beta-catenin accumulation and regulates axis formation in Xenopus embryos., Liao G., Proc Natl Acad Sci U S A. October 31, 2006; 103 (44): 16313-8.                    


XGAP, an ArfGAP, is required for polarized localization of PAR proteins and cell polarity in Xenopus gastrulation., Hyodo-Miura J., Dev Cell. July 1, 2006; 11 (1): 69-79.                                


Notch signaling modulates the nuclear localization of carboxy-terminal-phosphorylated smad2 and controls the competence of ectodermal cells for activin A., Abe T., Mech Dev. May 1, 2005; 122 (5): 671-80.            


Visualizing long-range movement of the morphogen Xnr2 in the Xenopus embryo., Williams PH., Curr Biol. November 9, 2004; 14 (21): 1916-23.      


Analysis of Spemann organizer formation in Xenopus embryos by cDNA macroarrays., Wessely O., Dev Biol. May 15, 2004; 269 (2): 552-66.        


Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.                    


Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway., Zhao H., Dev Biol. May 15, 2003; 257 (2): 278-91.          


A role for biliverdin IXalpha in dorsal axis development of Xenopus laevis embryos., Falchuk KH., Proc Natl Acad Sci U S A. January 8, 2002; 99 (1): 251-6.                


Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.                    


Bottle cell formation in relation to mesodermal patterning in the Xenopus embryo., Kurth T., Mech Dev. October 1, 2000; 97 (1-2): 117-31.  


A beta-catenin/engrailed chimera selectively suppresses Wnt signaling., Montross WT., J Cell Sci. May 1, 2000; 113 ( Pt 10) 1759-70.


Homeodomain and winged-helix transcription factors recruit activated Smads to distinct promoter elements via a common Smad interaction motif., Germain S., Genes Dev. February 15, 2000; 14 (4): 435-51.                


A quantitative analysis of signal transduction from activin receptor to nucleus and its relevance to morphogen gradient interpretation., Shimizu K., Proc Natl Acad Sci U S A. June 8, 1999; 96 (12): 6791-6.


Characterization of the Ets-type protein ER81 in Xenopus embryos., Chen Y, Chen Y., Mech Dev. January 1, 1999; 80 (1): 67-76.                    


Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor., Hata A., Genes Dev. January 15, 1998; 12 (2): 186-97.          


Analysis of HIV-1 Tat effects in Xenopus laevis embryos., Venanzi S., J Biomed Sci. January 1, 1998; 5 (3): 211-20.


The KH domain protein encoded by quaking functions as a dimer and is essential for notochord development in Xenopus embryos., Zorn AM., Genes Dev. September 1, 1997; 11 (17): 2176-90.                  


Xwnt-8 and lithium can act upon either dorsal mesodermal or neurectodermal cells to cause a loss of forebrain in Xenopus embryos., Fredieu JR., Dev Biol. June 1, 1997; 186 (1): 100-14.                


Xbap, a vertebrate gene related to bagpipe, is expressed in developing craniofacial structures and in anterior gut muscle., Newman CS., Dev Biol. January 15, 1997; 181 (2): 223-33.            


Nuclear transplantation from stably transfected cultured cells of Xenopus., Chan AP., Int J Dev Biol. April 1, 1996; 40 (2): 441-51.                


Localized BMP-4 mediates dorsal/ventral patterning in the early Xenopus embryo., Schmidt JE., Dev Biol. May 1, 1995; 169 (1): 37-50.              


Competence prepattern in the animal hemisphere of the 8-cell-stage Xenopus embryo., Kinoshita K., Dev Biol. November 1, 1993; 160 (1): 276-84.        


Interactions between Xwnt-8 and Spemann organizer signaling pathways generate dorsoventral pattern in the embryonic mesoderm of Xenopus., Christian JL., Genes Dev. January 1, 1993; 7 (1): 13-28.              

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