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Summary Anatomy Item Literature (1547) Expression Attributions Wiki
XB-ANAT-14

Papers associated with diencephalon (and tbxt)

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Nucleotide receptor P2RY4 is required for head formation via induction and maintenance of head organizer in Xenopus laevis., Harata A., Dev Growth Differ. February 1, 2019; 61 (2): 186-197.                                

A novel role of the organizer gene Goosecoid as an inhibitor of Wnt/PCP-mediated convergent extension in Xenopus and mouse., Ulmer B., Sci Rep. February 21, 2017; 7 43010.                  

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.                                    

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.                                    

Direct regulation of siamois by VegT is required for axis formation in Xenopus embryo., Li HY., Int J Dev Biol. January 1, 2015; 59 (10-12): 443-51.                          

An essential role for LPA signalling in telencephalon development., Geach TJ., Development. February 1, 2014; 141 (4): 940-9.                            

Essential role of AWP1 in neural crest specification in Xenopus., Seo JH., Int J Dev Biol. January 1, 2013; 57 (11-12): 829-36.                  

Comparative expression analysis of the H3K27 demethylases, JMJD3 and UTX, with the H3K27 methylase, EZH2, in Xenopus., Kawaguchi A., Int J Dev Biol. January 1, 2012; 56 (4): 295-300.                                          

Cloning and spatiotemporal expression of RIC-8 in Xenopus embryogenesis., Maldonado-Agurto R., Gene Expr Patterns. October 1, 2011; 11 (7): 401-8.          

Siamois and Twin are redundant and essential in formation of the Spemann organizer., Bae S., Dev Biol. April 15, 2011; 352 (2): 367-81.                    

XMeis3 is necessary for mesodermal Hox gene expression and function., In der Rieden PM., PLoS One. March 9, 2011; 6 (3): e18010.            

Tissue-Tissue Interaction-Triggered Calcium Elevation Is Required for Cell Polarization during Xenopus Gastrulation., Shindo A., PLoS One. February 2, 2010; 5 (2): e8897.              

Notch activates Wnt-4 signalling to control medio-lateral patterning of the pronephros., Naylor RW., Development. November 1, 2009; 136 (21): 3585-95.                                  

The mych gene is required for neural crest survival during zebrafish development., Hong SK., PLoS One. April 9, 2008; 3 (4): e2029.                

Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation., Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.                

Determination of the minimal domains of Mix.3/Mixer required for endoderm development., Doherty JR., Mech Dev. January 1, 2006; 123 (1): 56-66.                  

XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B., Development. February 1, 2005; 132 (3): 591-602.                      

Olfactory and lens placode formation is controlled by the hedgehog-interacting protein (Xhip) in Xenopus., Cornesse Y., Dev Biol. January 15, 2005; 277 (2): 296-315.                          

R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis., Kazanskaya O., Dev Cell. October 1, 2004; 7 (4): 525-34.                          

Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways., Moore KB., Dev Cell. January 1, 2004; 6 (1): 55-67.                

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.                    

Evolution of Brachyury proteins: identification of a novel regulatory domain conserved within Bilateria., Marcellini S., Dev Biol. August 15, 2003; 260 (2): 352-61.          

Regulation of nodal and BMP signaling by tomoregulin-1 (X7365) through novel mechanisms., Chang C., Dev Biol. March 1, 2003; 255 (1): 1-11.                    

Temporal and spatial expression patterns of FoxD2 during the early development of Xenopus laevis., Pohl BS., Mech Dev. February 1, 2002; 111 (1-2): 181-4.              

Embryonic XMab21l2 expression is required for gastrulation and subsequent neural development., Lau GT., Biochem Biophys Res Commun. February 9, 2001; 280 (5): 1378-84.              

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

Xenopus Zic3, a primary regulator both in neural and neural crest development., Nakata K., Proc Natl Acad Sci U S A. October 28, 1997; 94 (22): 11980-5.            

Neural induction and patterning in embryos deficient in FGF signaling., Godsave SF., Int J Dev Biol. February 1, 1997; 41 (1): 57-65.        

Dorsal-ventral differences in Xcad-3 expression in response to FGF-mediated induction in Xenopus., Northrop JL., Dev Biol. February 1, 1994; 161 (2): 490-503.                

Xwnt-5A: a maternal Wnt that affects morphogenetic movements after overexpression in embryos of Xenopus laevis., Moon RT., Development. September 1, 1993; 119 (1): 97-111.                  

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