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Summary Anatomy Item Literature (1713) Expression Attributions Wiki
XB-ANAT-106

Papers associated with tail bud (and eomes)

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Combinatorial transcription factor activities on open chromatin induce embryonic heterogeneity in vertebrates., Bright AR., EMBO J. May 3, 2021; 40 (9): e104913.                        

Hes5.9 Coordinate FGF and Notch Signaling to Modulate Gastrulation via Regulating Cell Fate Specification and Cell Migration in Xenopus tropicalis., Huang X., Genes (Basel). November 18, 2020; 11 (11):                   

Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endoderm gene regulatory network., Mukherjee S., Elife. September 7, 2020; 9                           

Skeletal muscle differentiation drives a dramatic downregulation of RNA polymerase III activity and differential expression of Polr3g isoforms., McQueen C., Dev Biol. October 1, 2019; 454 (1): 74-84.                        

Maternal pluripotency factors initiate extensive chromatin remodelling to predefine first response to inductive signals., Gentsch GE., Nat Commun. September 19, 2019; 10 (1): 4269.                                        

Nucleotide receptor P2RY4 is required for head formation via induction and maintenance of head organizer in Xenopus laevis., Harata A., Dev Growth Differ. February 1, 2019; 61 (2): 186-197.                                

The Xenopus animal cap transcriptome: building a mucociliary epithelium., Angerilli A., Nucleic Acids Res. September 28, 2018; 46 (17): 8772-8787.                          

Tbx2 is required for the suppression of mesendoderm during early Xenopus development., Teegala S., Dev Dyn. July 1, 2018; 247 (7): 903-913.                

Id genes are essential for early heart formation., Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.                

Conservatism and variability of gene expression profiles among homeologous transcription factors in Xenopus laevis., Watanabe M., Dev Biol. June 15, 2017; 426 (2): 301-324.                          

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.                              

Optimal histone H3 to linker histone H1 chromatin ratio is vital for mesodermal competence in Xenopus., Lim CY., Development. February 1, 2013; 140 (4): 853-60.                                              

A developmental requirement for HIRA-dependent H3.3 deposition revealed at gastrulation in Xenopus., Szenker E., Cell Rep. June 28, 2012; 1 (6): 730-40.                                      

Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.                                    

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

Twisted gastrulation is required for forebrain specification and cooperates with Chordin to inhibit BMP signaling during X. tropicalis gastrulation., Wills A., Dev Biol. January 1, 2006; 289 (1): 166-78.                                  

Maternal Xenopus Zic2 negatively regulates Nodal-related gene expression during anteroposterior patterning., Houston DW., Development. November 1, 2005; 132 (21): 4845-55.              

Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.                                  

The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos., Callery EM., Dev Biol. February 15, 2005; 278 (2): 542-59.                              

Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.                  

Induction of cardiomyocytes by GATA4 in Xenopus ectodermal explants., Latinkić BV., Development. August 1, 2003; 130 (16): 3865-76.              

Links between tumor suppressors: p53 is required for TGF-beta gene responses by cooperating with Smads., Cordenonsi M., Cell. May 2, 2003; 113 (3): 301-14.  

Redundant early and overlapping larval roles of Xsox17 subgroup genes in Xenopus endoderm development., Clements D., Mech Dev. March 1, 2003; 120 (3): 337-48.            

The nodal target gene Xmenf is a component of an FGF-independent pathway of ventral mesoderm induction in Xenopus., Kumano G., Mech Dev. October 1, 2002; 118 (1-2): 45-56.    

Cloning and characterization of the T-box gene Tbx6 in Xenopus laevis., Uchiyama H., Dev Growth Differ. December 1, 2001; 43 (6): 657-69.            

Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.                    

In synergy with noggin and follistatin, Xenopus nodal-related gene induces sonic hedgehog on notochord and floor plate., Ito Y., Biochem Biophys Res Commun. March 2, 2001; 281 (3): 714-9.      

The bHLH class protein pMesogenin1 can specify paraxial mesoderm phenotypes., Yoon JK., Dev Biol. June 15, 2000; 222 (2): 376-91.            

derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.                    

Xenopus eomesodermin is expressed in neural differentiation., Ryan K., Mech Dev. July 1, 1998; 75 (1-2): 155-8.    

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