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Summary Anatomy Item Literature (2231) Expression Attributions Wiki
XB-ANAT-3282

Papers associated with posterior hypothalamus (and evx1)

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Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula., Ding Y., Dev Biol. June 15, 2017; 426 (2): 176-187.                                  


Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.                                


Conservation and evolutionary divergence in the activity of receptor-regulated smads., Sorrentino GM., Evodevo. October 1, 2012; 3 (1): 22.              


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


B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo., Okuda Y., PLoS Genet. May 6, 2010; 6 (5): e1000936.                


A microarray screen for direct targets of Zic1 identifies an aquaporin gene, aqp-3b, expressed in the neural folds., Cornish EJ., Dev Dyn. May 1, 2009; 238 (5): 1179-94.                


CDMP1/GDF5 has specific processing requirements that restrict its action to joint surfaces., Thomas JT., J Biol Chem. September 8, 2006; 281 (36): 26725-33.              


BMP-3 is a novel inhibitor of both activin and BMP-4 signaling in Xenopus embryos., Gamer LW., Dev Biol. September 1, 2005; 285 (1): 156-68.              


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


Chordin is required for the Spemann organizer transplantation phenomenon in Xenopus embryos., Oelgeschläger M., Dev Cell. February 1, 2003; 4 (2): 219-30.              


The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling., Domingos PM., Dev Biol. November 1, 2001; 239 (1): 148-60.              


The role of BMP signaling in outgrowth and patterning of the Xenopus tail bud., Beck CW., Dev Biol. October 15, 2001; 238 (2): 303-14.              


Gli2 functions in FGF signaling during antero-posterior patterning., Brewster R., Development. October 1, 2000; 127 (20): 4395-405.            


Requirement for Xvent-1 and Xvent-2 gene function in dorsoventral patterning of Xenopus mesoderm., Onichtchouk D., Development. April 1, 1998; 125 (8): 1447-56.                  


XBMPRII, a novel Xenopus type II receptor mediating BMP signaling in embryonic tissues., Frisch A., Development. February 1, 1998; 125 (3): 431-42.                  


A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation., Horb ME., Development. May 1, 1997; 124 (9): 1689-98.                    


A Xenopus type I activin receptor mediates mesodermal but not neural specification during embryogenesis., Chang C., Development. February 1, 1997; 124 (4): 827-37.                    


The Xvent-2 homeobox gene is part of the BMP-4 signalling pathway controlling [correction of controling] dorsoventral patterning of Xenopus mesoderm., Onichtchouk D., Development. October 1, 1996; 122 (10): 3045-53.                  


Xenopus mothers against decapentaplegic is an embryonic ventralizing agent that acts downstream of the BMP-2/4 receptor., Thomsen GH., Development. August 1, 1996; 122 (8): 2359-66.              


A novel homeobox gene PV.1 mediates induction of ventral mesoderm in Xenopus embryos., Ault KT., Proc Natl Acad Sci U S A. June 25, 1996; 93 (13): 6415-20.          

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