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Summary Anatomy Item Literature (1723) Expression Attributions Wiki
XB-ANAT-233

Papers associated with cardiac mesoderm (and twist1)

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The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus., Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.                              


5-Mehtyltetrahydrofolate rescues alcohol-induced neural crest cell migration abnormalities., Shi Y, Shi Y., Mol Brain. September 16, 2014; 7 67.        


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


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.                                  


Calponin 2 acts as an effector of noncanonical Wnt-mediated cell polarization during neural crest cell migration., Ulmer B., Cell Rep. March 28, 2013; 3 (3): 615-21.              


ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P., Cell Rep. May 31, 2012; 1 (5): 516-27.                              


Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1., Bonnard C., Nat Genet. May 13, 2012; 44 (6): 709-13.    


Plakophilin-3 is required for late embryonic amphibian development, exhibiting roles in ectodermal and neural tissues., Munoz WA., PLoS One. January 1, 2012; 7 (4): e34342.              


ARVCF depletion cooperates with Tbx1 deficiency in the development of 22q11.2DS-like phenotypes in Xenopus., Tran HT., Dev Dyn. December 1, 2011; 240 (12): 2680-7.                


Xenopus reduced folate carrier regulates neural crest development epigenetically., Li J., PLoS One. January 1, 2011; 6 (11): e27198.                            


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


Systematic discovery of nonobvious human disease models through orthologous phenotypes., McGary KL., Proc Natl Acad Sci U S A. April 6, 2010; 107 (14): 6544-9.                                    


CHD7 cooperates with PBAF to control multipotent neural crest formation., Bajpai R., Nature. February 18, 2010; 463 (7283): 958-62.      


Diversification of the expression patterns and developmental functions of the dishevelled gene family during chordate evolution., Gray RS., Dev Dyn. August 1, 2009; 238 (8): 2044-57.            


Semaphorin and neuropilin expression during early morphogenesis of Xenopus laevis., Koestner U., Dev Dyn. December 1, 2008; 237 (12): 3853-63.                                                                                              


A Myc-Slug (Snail2)/Twist regulatory circuit directs vascular development., Rodrigues CO., Development. June 1, 2008; 135 (11): 1903-11.              


Genomic profiling of mixer and Sox17beta targets during Xenopus endoderm development., Dickinson K., Dev Dyn. February 1, 2006; 235 (2): 368-81.                        


DRAGON, a bone morphogenetic protein co-receptor., Samad TA., J Biol Chem. April 8, 2005; 280 (14): 14122-9.                  


Gene profiling during neural induction in Xenopus laevis: regulation of BMP signaling by post-transcriptional mechanisms and TAB3, a novel TAK1-binding protein., Muñoz-Sanjuán I., Development. December 1, 2002; 129 (23): 5529-40.    


The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.              


Genomic organization, expression, and chromosome location of the human SNAIL gene (SNAI1) and a related processed pseudogene (SNAI1P)., Paznekas WA., Genomics. November 15, 1999; 62 (1): 42-9.


X-twi is expressed prior to gastrulation in presumptive neurectodermal and mesodermal cells in dorsalized and ventralized Xenopus laevis embryos., Stoetzel C., Int J Dev Biol. September 1, 1998; 42 (6): 747-56.                


Xenopus Smad7 inhibits both the activin and BMP pathways and acts as a neural inducer., Casellas R., Dev Biol. June 1, 1998; 198 (1): 1-12.                


tinman, a Drosophila homeobox gene required for heart and visceral mesoderm specification, may be represented by a family of genes in vertebrates: XNkx-2.3, a second vertebrate homologue of tinman., Evans SM., Development. November 1, 1995; 121 (11): 3889-99.                


v-erbA and citral reduce the teratogenic effects of all-trans retinoic acid and retinol, respectively, in Xenopus embryogenesis., Schuh TJ., Development. November 1, 1993; 119 (3): 785-98.                  

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