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Summary Anatomy Item Literature (10392) Expression Attributions Wiki
XB-ANAT-111

Papers associated with embryo (and grem1)

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Heparan sulfate proteoglycans regulate BMP signalling during neural crest induction., Pegge J., Dev Biol. April 15, 2020; 460 (2): 108-114.        


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


Role of remodeling and spacing factor 1 in histone H2A ubiquitination-mediated gene silencing., Zhang Z, Zhang Z., Proc Natl Acad Sci U S A. September 19, 2017; 114 (38): E7949-E7958.                          


Proper Notch activity is necessary for the establishment of proximal cells and differentiation of intermediate, distal, and connecting tubule in Xenopus pronephros development., Katada T., Dev Dyn. April 1, 2016; 245 (4): 472-82.                  


Gremlin1 induces anterior-posterior limb bifurcations in developing Xenopus limbs but does not enhance limb regeneration., Wang YH., Mech Dev. November 1, 2015; 138 Pt 3 256-67.                


The neural crest is a powerful regulator of pre-otic brain development., Le Douarin NM., Dev Biol. June 1, 2012; 366 (1): 74-82.


Evolution of development: diversified dorsoventral patterning., Bier E., Curr Biol. August 9, 2011; 21 (15): R591-4.  


Role of Tbx2 in defining the territory of the pronephric nephron., Cho GS., Development. February 1, 2011; 138 (3): 465-74.                        


XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis., Lee SJ., Mech Dev. January 1, 2010; 127 (1-2): 49-61.                  


Identification of genes associated with regenerative success of Xenopus laevis hindlimbs., Pearl EJ., BMC Dev Biol. June 23, 2008; 8 66.              


FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.                    


Molecular evidence for deep evolutionary roots of bilaterality in animal development., Matus DQ., Proc Natl Acad Sci U S A. July 25, 2006; 103 (30): 11195-200.            


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.                


XHas2 activity is required during somitogenesis and precursor cell migration in Xenopus development., Ori M., Development. February 1, 2006; 133 (4): 631-40.                        


Regulated expression pattern of gremlin during zebrafish development., Nicoli S., Gene Expr Patterns. April 1, 2005; 5 (4): 539-44.                


Gremlin is the BMP antagonist required for maintenance of Shh and Fgf signals during limb patterning., Khokha MK., Nat Genet. July 1, 2003; 34 (3): 303-7.


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


Mouse GLI3 regulates Fgf8 expression and apoptosis in the developing neural tube, face, and limb bud., Aoto K., Dev Biol. November 15, 2002; 251 (2): 320-32.


Cloning and expression analysis of the chick DAN gene, an antagonist of the BMP family of growth factors., Gerlach-Bank LM., Dev Dyn. May 1, 2002; 224 (1): 109-15.


In vitro induction of the pronephric duct in Xenopus explants., Osafune K., Dev Growth Differ. April 1, 2002; 44 (2): 161-7.      


Mutual genetic antagonism involving GLI3 and dHAND prepatterns the vertebrate limb bud mesenchyme prior to SHH signaling., te Welscher P., Genes Dev. February 15, 2002; 16 (4): 421-6.


The Xenopus pronephros as a model system for the study of kidney development and pathophysiology., Hensey C., Nephrol Dial Transplant. January 1, 2002; 17 Suppl 9 73-4.


Expression of the Dan gene during chicken embryonic development., Ogita J., Mech Dev. December 1, 2001; 109 (2): 363-5.


Xenopus Dan, a member of the Dan gene family of BMP antagonists, is expressed in derivatives of the cranial and trunk neural crest., Eimon PM., Mech Dev. September 1, 2001; 107 (1-2): 187-9.    


Conserved cellular and molecular mechanisms in development., Giudice G., Cell Biol Int. January 1, 2001; 25 (11): 1081-90.


In Xenopus embryos, BMP heterodimers are not required for mesoderm induction, but BMP activity is necessary for dorsal/ventral patterning., Eimon PM., Dev Biol. December 1, 1999; 216 (1): 29-40.          


XBF-2 is a transcriptional repressor that converts ectoderm into neural tissue., Mariani FV., Development. December 1, 1998; 125 (24): 5019-31.


The Xenopus dorsalizing factor Gremlin identifies a novel family of secreted proteins that antagonize BMP activities., Hsu DR., Mol Cell. April 1, 1998; 1 (5): 673-83.                  

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