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Summary Anatomy Item Literature (19) Expression Attributions Wiki
XB-ANAT-240

Papers associated with mesonephric duct

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A polycystin-2 protein with modified channel properties leads to an increased diameter of renal tubules and to renal cysts., Grosch M., J Cell Sci. August 15, 2021; 134 (16):                 


Expression analysis of the peroxiredoxin gene family during early development in Xenopus laevis., Shafer ME., Gene Expr Patterns. December 1, 2011; 11 (8): 511-6.      


Non-canonical wnt signals antagonize and canonical wnt signals promote cell proliferation in early kidney development., McCoy KE., Dev Dyn. June 1, 2011; 240 (6): 1558-66.          


Mix.1/2-dependent control of FGF availability during gastrulation is essential for pronephros development in Xenopus., Colas A., Dev Biol. August 15, 2008; 320 (2): 351-65.                  


Collectrin/tmem27 is expressed at high levels in all segments of the developing Xenopus pronephric nephron and in the Wolffian duct., McCoy KE., Gene Expr Patterns. April 1, 2008; 8 (4): 271-4.        


Beta-catenin is necessary to keep cells of ureteric bud/Wolffian duct epithelium in a precursor state., Marose TD., Dev Biol. February 1, 2008; 314 (1): 112-26.    


Ectopic germline cells in embryos of Xenopus laevis., Ikenishi K., Dev Growth Differ. September 1, 2007; 49 (7): 561-70.      


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.                    


Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system., Carroll TJ., Dev Cell. August 1, 2005; 9 (2): 283-92.


Sprouty1 is a critical regulator of GDNF/RET-mediated kidney induction., Basson MA., Dev Cell. February 1, 2005; 8 (2): 229-39.


A trial for induction of supernumerary primordial germ cells in Xenopus tadpoles by injecting RNA of Xenopus vasa homologue into germline cells of 32-cell embryos., Ikenishi K., Dev Growth Differ. January 1, 2003; 45 (5-6): 417-26.                  


The vegetally localized mRNA fatvg is associated with the germ plasm in the early embryo and is later expressed in the fat body., Chan AP., Mech Dev. January 1, 2001; 100 (1): 137-40.          


Expression of the Xenopus laevis metallothionein gene during ontogeny., Durliat M., Int J Dev Biol. September 1, 1999; 43 (6): 575-8.            


Involvement of the protein of Xenopus vasa homolog (Xenopus vasa-like gene 1, XVLG1) in the differentiation of primordial germ cells., Ikenishi K., Dev Growth Differ. October 1, 1997; 39 (5): 625-33.            


Ets-1 and Ets-2 proto-oncogenes exhibit differential and restricted expression patterns during Xenopus laevis oogenesis and embryogenesis., Meyer D., Int J Dev Biol. August 1, 1997; 41 (4): 607-20.                                      


Cloning and developmental expression of LFB3/HNF1 beta transcription factor in Xenopus laevis., Demartis A., Mech Dev. July 1, 1994; 47 (1): 19-28.        


Xlcaax-1 is localized to the basolateral membrane of kidney tubule and other polarized epithelia during Xenopus development., Cornish JA., Dev Biol. March 1, 1992; 150 (1): 108-20.                  


The distribution of E-cadherin during Xenopus laevis development., Levi G., Development. January 1, 1991; 111 (1): 159-69.                


Ontogeny and tissue distribution of leukocyte-common antigen bearing cells during early development of Xenopus laevis., Ohinata H., Development. November 1, 1989; 107 (3): 445-52.              

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