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Summary Anatomy Item Literature (2349) Expression Attributions Wiki
XB-ANAT-4083

Papers associated with tadpole (and vegt)

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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.                                            


Normal Table of Xenopus development: a new graphical resource., Zahn N., Development. July 15, 2022; 149 (14):                         


Chromatin accessibility and histone acetylation in the regulation of competence in early development., Esmaeili M., Dev Biol. June 1, 2020; 462 (1): 20-35.                


BAP1 regulates epigenetic switch from pluripotency to differentiation in developmental lineages giving rise to BAP1-mutant cancers., Kuznetsov JN., Sci Adv. September 18, 2019; 5 (9): eaax1738.        


Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.                                    


Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.                                          


The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.                                          


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.                              


Maternal Dead-End1 is required for vegetal cortical microtubule assembly during Xenopus axis specification., Mei W., Development. June 1, 2013; 140 (11): 2334-44.                          


The RNA-binding protein XSeb4R regulates maternal Sox3 at the posttranscriptional level during maternal-zygotic transition in Xenopus., Bentaya S., Dev Biol. March 15, 2012; 363 (2): 362-72.                      


The homeobox leucine zipper gene Homez plays a role in Xenopus laevis neurogenesis., Ghimouz R., Biochem Biophys Res Commun. November 11, 2011; 415 (1): 11-6.            


Deficient induction response in a Xenopus nucleocytoplasmic hybrid., Narbonne P., PLoS Biol. November 1, 2011; 9 (11): e1001197.              


The roles of maternal Vangl2 and aPKC in Xenopus oocyte and embryo patterning., Cha SW., Development. September 1, 2011; 138 (18): 3989-4000.                  


Programming pluripotent precursor cells derived from Xenopus embryos to generate specific tissues and organs., Borchers A., Genes (Basel). November 18, 2010; 1 (3): 413-26.      


XsFRP5 modulates endodermal organogenesis in Xenopus laevis., Damianitsch K., Dev Biol. May 15, 2009; 329 (2): 327-37.      


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.                                                    


FoxD3 regulation of Nodal in the Spemann organizer is essential for Xenopus dorsal mesoderm development., Steiner AB., Development. December 1, 2006; 133 (24): 4827-38.                    


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


The RNA-binding protein, Vg1RBP, is required for pancreatic fate specification., Spagnoli FM., Dev Biol. April 15, 2006; 292 (2): 442-56.                      


Microarray-based identification of VegT targets in Xenopus., Taverner NV., Mech Dev. March 1, 2005; 122 (3): 333-54.                                          


New roles for FoxH1 in patterning the early embryo., Kofron M., Development. October 1, 2004; 131 (20): 5065-78.              


PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J., Development. December 1, 2003; 130 (23): 5569-78.            


Cell fate specification and competence by Coco, a maternal BMP, TGFbeta and Wnt inhibitor., Bell E., Development. April 1, 2003; 130 (7): 1381-9.    


Localization of RNAs in oocytes of Eleutherodactylus coqui, a direct developing frog, differs from Xenopus laevis., Beckham YM., Evol Dev. January 1, 2003; 5 (6): 562-71.


Molecular cloning and developmental expression of Par-1/MARK homologues XPar-1A and XPar-1B from Xenopus laevis., Ossipova O., Mech Dev. December 1, 2002; 119 Suppl 1 S143-8.    


Repression of organizer genes in dorsal and ventral Xenopus cells mediated by maternal XTcf3., Houston DW., Development. September 1, 2002; 129 (17): 4015-25.          


From intestine to muscle: nuclear reprogramming through defective cloned embryos., Byrne JA., Proc Natl Acad Sci U S A. April 30, 2002; 99 (9): 6059-63.            


Mesendoderm induction and reversal of left-right pattern by mouse Gdf1, a Vg1-related gene., Wall NA., Dev Biol. November 15, 2000; 227 (2): 495-509.              


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


Tbx5 is essential for heart development., Horb ME., Development. April 1, 1999; 126 (8): 1739-51.              


A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation., Horb ME., Development. May 1, 1997; 124 (9): 1689-98.                    


Xenopus VegT RNA is localized to the vegetal cortex during oogenesis and encodes a novel T-box transcription factor involved in mesodermal patterning., Zhang J., Development. December 1, 1996; 122 (12): 4119-29.                  

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