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Summary Anatomy Item Literature (3673) Expression Attributions Wiki
XB-ANAT-490

Papers associated with tail (and eomes)

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Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.                                            

Tril dampens Nodal signaling through Pellino2- and Traf6-mediated activation of Nedd4l., Kim HS., Proc Natl Acad Sci U S A. September 7, 2021; 118 (36):                       

FAM46B is a prokaryotic-like cytoplasmic poly(A) polymerase essential in human embryonic stem cells., Hu JL., Nucleic Acids Res. March 18, 2020; 48 (5): 2733-2748.                

The Spatiotemporal Control of Zygotic Genome Activation., Gentsch GE., iScience. June 28, 2019; 16 485-498.                          

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

High-resolution analysis of gene activity during the Xenopus mid-blastula transition., Collart C., Development. May 1, 2014; 141 (9): 1927-39.                  

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.                              

The Mix family of homeobox genes--key regulators of mesendoderm formation during vertebrate development., Pereira LA., Dev Biol. July 15, 2012; 367 (2): 163-77.        

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.                                      

fus/TLS orchestrates splicing of developmental regulators during gastrulation., Dichmann DS., Genes Dev. June 15, 2012; 26 (12): 1351-63.                        

Zygotic VegT is required for Xenopus paraxial mesoderm formation and is regulated by Nodal signaling and Eomesodermin., Fukuda M., Int J Dev Biol. January 1, 2010; 54 (1): 81-92.              

The role of FGF signaling in the establishment and maintenance of mesodermal gene expression in Xenopus., Fletcher RB., Dev Dyn. May 1, 2008; 237 (5): 1243-54.            

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

Emilin1 links TGF-beta maturation to blood pressure homeostasis., Zacchigna L., Cell. March 10, 2006; 124 (5): 929-42.    

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.                  

FGF signaling restricts the primary blood islands to ventral mesoderm., Kumano G., Dev Biol. December 15, 2000; 228 (2): 304-14.            

Xbra3 induces mesoderm and neural tissue in Xenopus laevis., Strong CF., Dev Biol. June 15, 2000; 222 (2): 405-19.                  

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

An indelible lineage marker for Xenopus using a mutated green fluorescent protein., Zernicka-Goetz M., Development. December 1, 1996; 122 (12): 3719-24.        

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