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Summary Anatomy Item Literature (547) Expression Attributions Wiki
XB-ANAT-510

Papers associated with mesenchyme (and myod1)

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Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):                                           


Xenopus Pkdcc1 and Pkdcc2 Are Two New Tyrosine Kinases Involved in the Regulation of JNK Dependent Wnt/PCP Signaling Pathway., Vitorino M., PLoS One. August 13, 2015; 10 (8): e0135504.                                    


The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.                                            


Expression pattern of zcchc24 during early Xenopus development., Vitorino M., Int J Dev Biol. January 1, 2014; 58 (1): 45-50.                    


The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.                            


Lin28 proteins are required for germ layer specification in Xenopus., Faas L., Development. March 1, 2013; 140 (5): 976-86.                      


Cardiac neural crest is dispensable for outflow tract septation in Xenopus., Lee YH., Development. May 1, 2011; 138 (10): 2025-34.                  


Lhx1 is required for specification of the renal progenitor cell field., Cirio MC., PLoS One. April 15, 2011; 6 (4): e18858.                          


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


Tissue-specific expression of Sarcoplasmic/Endoplasmic Reticulum Calcium ATPases (ATP2A/SERCA) 1, 2, 3 during Xenopus laevis development., Pegoraro C., Gene Expr Patterns. January 1, 2011; 11 (1-2): 122-8.    


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.                  


Vestigial like gene family expression in Xenopus: common and divergent features with other vertebrates., Faucheux C., Int J Dev Biol. January 1, 2010; 54 (8-9): 1375-82.                            


Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size., Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.                                          


Muscular dystrophy candidate gene FRG1 is critical for muscle development., Hanel ML., Dev Dyn. June 1, 2009; 238 (6): 1502-12.        


Two Hoxc6 transcripts are differentially expressed and regulate primary neurogenesis in Xenopus laevis., Bardine N., Dev Dyn. March 1, 2009; 238 (3): 755-65.              


Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction., Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.            


Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation., Chang C., Development. November 1, 2007; 134 (21): 3861-72.                


Pescadillo is required for Xenopus laevis eye development and neural crest migration., Gessert S., Dev Biol. October 1, 2007; 310 (1): 99-112.                  


Foxc2 induces expression of MyoD and differentiation of the mouse myoblast cell line C2C12., Omoteyama K., Biochem Biophys Res Commun. July 6, 2007; 358 (3): 885-9.


Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T., Development. December 1, 2006; 133 (23): 4643-54.                  


ADMP2 is essential for primitive blood and heart development in Xenopus., Kumano G., Dev Biol. November 15, 2006; 299 (2): 411-23.                


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.                    


Limb regeneration in Xenopus laevis froglet., Suzuki M, Suzuki M., ScientificWorldJournal. May 12, 2006; 6 Suppl 1 26-37.        


Characteristics of initiation and early events for muscle development in the Xenopus limb bud., Satoh A., Dev Dyn. December 1, 2005; 234 (4): 846-57.            


Differential regulation of avian pelvic girdle development by the limb field ectoderm., Malashichev Y., Anat Embryol (Berl). October 1, 2005; 210 (3): 187-97.


Regulated gene expression of hyaluronan synthases during Xenopus laevis development., Nardini M., Gene Expr Patterns. May 1, 2004; 4 (3): 303-8.        


Cloning and characterization of Xenopus Id4 reveals differing roles for Id genes., Liu KJ, Liu KJ., Dev Biol. December 15, 2003; 264 (2): 339-51.                      


Cloning and characterization of Xenopus laevis drg2, a member of the developmentally regulated GTP-binding protein subfamily., Ishikawa K., Gene. December 11, 2003; 322 105-12.                  


Xenopus Cdc42 regulates convergent extension movements during gastrulation through Wnt/Ca2+ signaling pathway., Choi SC., Dev Biol. April 15, 2002; 244 (2): 342-57.                  


Xenopus marginal coil (Xmc), a novel FGF inducible cytosolic coiled-coil protein regulating gastrulation movements., Frazzetto G., Mech Dev. April 1, 2002; 113 (1): 3-14.            


Expression of the RNA recognition motif-containing protein SEB-4 during Xenopus embryonic development., Fetka I., Mech Dev. June 1, 2000; 94 (1-2): 283-6.  


Cytochalasin B inhibits morphogenetic movement and muscle differentiation of activin-treated ectoderm in Xenopus., Tamai K., Dev Growth Differ. February 1, 1999; 41 (1): 41-9.            


XIdx, a dominant negative regulator of bHLH function in early Xenopus embryos., Wilson R., Mech Dev. February 1, 1995; 49 (3): 211-22.          

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