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Summary Anatomy Item Literature (716) Expression Attributions Wiki
XB-ANAT-3561

Papers associated with coelom (and myod1)

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


Differential regulation of chordin expression domains in mutant zebrafish., Miller-Bertoglio VE., Dev Biol. December 15, 1997; 192 (2): 537-50.      


Frizzled-8 is expressed in the Spemann organizer and plays a role in early morphogenesis., Deardorff MA., Development. July 1, 1998; 125 (14): 2687-700.                  


The role of paraxial protocadherin in selective adhesion and cell movements of the mesoderm during Xenopus gastrulation., Kim SH., Development. December 1, 1998; 125 (23): 4681-90.                      


XTIF2, a Xenopus homologue of the human transcription intermediary factor, is required for a nuclear receptor pathway that also interacts with CBP to suppress Brachyury and XMyoD., de la Calle-Mustienes E., Mech Dev. March 1, 2000; 91 (1-2): 119-29.  


Use of large-scale expression cloning screens in the Xenopus laevis tadpole to identify gene function., Grammer TC., Dev Biol. December 15, 2000; 228 (2): 197-210.              


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.                  


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.                      


An atlas of differential gene expression during early Xenopus embryogenesis., Pollet N., Mech Dev. March 1, 2005; 122 (3): 365-439.                                                                                                                                                        


A novel role for lbx1 in Xenopus hypaxial myogenesis., Martin BL., Development. January 1, 2006; 133 (2): 195-208.                                


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.                    


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


Hedgehog signaling regulates the amount of hypaxial muscle development during Xenopus myogenesis., Martin BL., Dev Biol. April 15, 2007; 304 (2): 722-34.                


The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros., Wingert RA., PLoS Genet. October 1, 2007; 3 (10): 1922-38.                


Characterization of a novel Xenopus SH3 domain binding protein 5 like (xSH3BP5L) gene., Hu ZG., Biochem Biophys Res Commun. January 11, 2008; 365 (2): 214-20.            


The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm., Spagnoli FM., Development. February 1, 2008; 135 (3): 451-61.                                                    


Binding of sFRP-3 to EGF in the extra-cellular space affects proliferation, differentiation and morphogenetic events regulated by the two molecules., Scardigli R., PLoS One. June 18, 2008; 3 (6): e2471.                    


Extracellular regulation of developmental cell signaling by XtSulf1., Freeman SD., Dev Biol. August 15, 2008; 320 (2): 436-45.            


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.                  


Fli1 acts at the top of the transcriptional network driving blood and endothelial development., Liu F., Curr Biol. August 26, 2008; 18 (16): 1234-40.                              


An increase in intracellular Ca2+ is involved in pronephric tubule differentiation in the amphibian Xenopus laevis., Leclerc C., Dev Biol. September 15, 2008; 321 (2): 357-67.        


Xenopus ADAM19 is involved in neural, neural crest and muscle development., Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.                      


Expression patterns of Src-family tyrosine kinases during Xenopus laevis development., Ferjentsik Z., Int J Dev Biol. January 1, 2009; 53 (1): 163-8.                


Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis., Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.          


Loss of REEP4 causes paralysis of the Xenopus embryo., Argasinska J., Int J Dev Biol. January 1, 2009; 53 (1): 37-43.          


Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.                    


In vivo analyzes of dystroglycan function during somitogenesis in Xenopus laevis., Hidalgo M., Dev Dyn. June 1, 2009; 238 (6): 1332-45.          


Dazap2 is required for FGF-mediated posterior neural patterning, independent of Wnt and Cdx function., Roche DD., Dev Biol. September 1, 2009; 333 (1): 26-36.                              


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


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.                  


Lymph heart musculature is under distinct developmental control from lymphatic endothelium., Peyrot SM., Dev Biol. March 15, 2010; 339 (2): 429-38.        


Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.                              


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.    


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


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


EBF proteins participate in transcriptional regulation of Xenopus muscle development., Green YS., Dev Biol. October 1, 2011; 358 (1): 240-50.                    


Involvement of the eukaryotic initiation factor 6 and kermit2/gipc2 in Xenopus laevis pronephros formation., Tussellino M., Int J Dev Biol. January 1, 2012; 56 (5): 357-62.          


sizzled function and secreted factor network dynamics., Shi J., Biol Open. March 15, 2012; 1 (3): 286-94.            


Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B., Dev Dyn. May 1, 2012; 241 (5): 995-1007.                                    


Retinoic acid-dependent control of MAP kinase phosphatase-3 is necessary for early kidney development in Xenopus., Le Bouffant R., Biol Cell. September 1, 2012; 104 (9): 516-32.


Comparative Functional Analysis of ZFP36 Genes during Xenopus Development., Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.                          


Regulation of primitive hematopoiesis by class I histone deacetylases., Shah RR., Dev Dyn. February 1, 2013; 242 (2): 108-21.              


Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton., Ioannou A., Dev Biol. August 15, 2013; 380 (2): 243-58.                                  


In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.                              


Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.                    


Circadian genes, xBmal1 and xNocturnin, modulate the timing and differentiation of somites in Xenopus laevis., Curran KL., PLoS One. January 1, 2014; 9 (9): e108266.                            


The Wnt/JNK signaling target gene alcam is required for embryonic kidney development., Cizelsky W., Development. May 1, 2014; 141 (10): 2064-74.          


The alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform., Dichmann DS., Cell Rep. February 3, 2015; 10 (4): 527-36.                    


Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.                      


Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus., Gentsch GE., Dev Cell. March 12, 2018; 44 (5): 597-610.e10.                                            

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