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Summary Anatomy Item Literature (3426) Expression Attributions Wiki
XB-ANAT-726

Papers associated with sensory system (and nodal6)

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Spemann organizer transcriptome induction by early beta-catenin, Wnt, Nodal, and Siamois signals in Xenopus laevis., Ding Y., Proc Natl Acad Sci U S A. April 11, 2017; 114 (15): E3081-E3090.                        


Genome evolution in the allotetraploid frog Xenopus laevis., Session AM., Nature. October 20, 2016; 538 (7625): 336-343.                              


Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development., Owens ND., Cell Rep. January 26, 2016; 14 (3): 632-47.                                                  


Lin28 proteins are required for germ layer specification in Xenopus., Faas L., Development. March 1, 2013; 140 (5): 976-86.                      


beta-Catenin primes organizer gene expression by recruiting a histone H3 arginine 8 methyltransferase, Prmt2., Blythe SA., Dev Cell. August 17, 2010; 19 (2): 220-31.      


Retinoid signaling can repress blastula Wnt signaling and impair dorsal development in Xenopus embryo., Li S., Differentiation. October 1, 2008; 76 (8): 897-907.            


Xnr2 and Xnr5 unprocessed proteins inhibit Wnt signaling upstream of dishevelled., Onuma Y., Dev Dyn. December 1, 2005; 234 (4): 900-10.          


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


Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.            


Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.                

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