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Summary Anatomy Item Literature (13748) Expression Attributions Wiki
XB-ANAT-505

Papers associated with compound organ (and furin)

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R-Spondin 2 governs Xenopus left-right body axis formation by establishing an FGF signaling gradient., Lee H, Lee H., Nat Commun. February 2, 2024; 15 (1): 1003.                                                                  


R-spondins are BMP receptor antagonists in Xenopus early embryonic development., Lee H, Lee H., Nat Commun. November 4, 2020; 11 (1): 5570.                                            


Plasmin improves blood-gas barrier function in oedematous lungs by cleaving epithelial sodium channels., Zhao R., Br J Pharmacol. July 1, 2020; 177 (13): 3091-3106.


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


The NOTCH signaling pathway in normal and malignant blood cell production., Suresh S., J Cell Commun Signal. March 1, 2015; 9 (1): 5-13.      


The R-spondin/Lgr5/Rnf43 module: regulator of Wnt signal strength., de Lau W., Genes Dev. February 15, 2014; 28 (4): 305-16.          


Characterization of the molecular structure, expression and bioactivity of the TNFSF13B (BAFF) gene of the South African clawed frog, Xenopus laevis., Yang L., Int Immunopharmacol. March 1, 2013; 15 (3): 478-87.


A homolog of Subtilisin-like Proprotein Convertase 7 is essential to anterior neural development in Xenopus., Senturker S., PLoS One. January 1, 2012; 7 (6): e39380.                


Inhibition of lung fluid clearance and epithelial Na+ channels by chlorine, hypochlorous acid, and chloramines., Song W., J Biol Chem. March 26, 2010; 285 (13): 9716-9728.


The role and regulation of GDF11 in Smad2 activation during tailbud formation in the Xenopus embryo., Ho DM., Mech Dev. January 1, 2010; 127 (9-12): 485-95.                  


Single-channel analysis of functional epithelial sodium channel (ENaC) stability at the apical membrane of A6 distal kidney cells., Yu L., Am J Physiol Renal Physiol. November 1, 2008; 295 (5): F1519-27.


Vg1 has specific processing requirements that restrict its action to body axis patterning centers., Thomas JT., Dev Biol. October 1, 2007; 310 (1): 129-39.          


Subtilisin-like proprotein convertase activity is necessary for left-right axis determination in Xenopus neurula embryos., Toyoizumi R., Dev Genes Evol. October 1, 2006; 216 (10): 607-22.


Furin cleavage activates the epithelial Na+ channel by relieving Na+ self-inhibition., Sheng S., Am J Physiol Renal Physiol. June 1, 2006; 290 (6): F1488-96.


Proprotein convertase genes in Xenopus development., Nelsen S., Dev Dyn. July 1, 2005; 233 (3): 1038-44.    


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.                      


Distinct pools of epithelial sodium channels are expressed at the plasma membrane., Hughey RP., J Biol Chem. November 19, 2004; 279 (47): 48491-4.


Matrix metalloproteinase-21, the human orthologue for XMMP, is expressed during fetal development and in cancer., Ahokas K., Gene. November 13, 2002; 301 (1-2): 31-41.


A hatching enzyme substrate in the Xenopus laevis egg envelope is a high molecular weight ZPA homolog., Lindsay LL., Dev Growth Differ. June 1, 2001; 43 (3): 305-13.            


Failure of ventral closure and axial rotation in embryos lacking the proprotein convertase Furin., Roebroek AJ., Development. December 1, 1998; 125 (24): 4863-76.


cDNA cloning and sequence analysis of the Xenopus laevis egg envelope glycoprotein gp43., Yang JC., Dev Growth Differ. August 1, 1997; 39 (4): 457-67.        

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