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Summary Anatomy Item Literature (4079) Expression Attributions Wiki
XB-ANAT-86

Papers associated with tail region (and gsc)

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Bestrophin genes are expressed in Xenopus development., Onuma Y., Biochem Biophys Res Commun. July 3, 2009; 384 (3): 290-5.              


Functional dissection of XDppa2/4 structural domains in Xenopus development., Siegel D., Mech Dev. December 1, 2009; 126 (11-12): 974-89.            


Distinct Xenopus Nodal ligands sequentially induce mesendoderm and control gastrulation movements in parallel to the Wnt/PCP pathway., Luxardi G., Development. February 1, 2010; 137 (3): 417-26.          


B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo., Okuda Y., PLoS Genet. May 6, 2010; 6 (5): e1000936.                


Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.                                                


Conservation and diversification of an ancestral chordate gene regulatory network for dorsoventral patterning., Kozmikova I., PLoS One. February 3, 2011; 6 (2): e14650.                  


SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.                              


Use of fully modified 2'-O-methyl antisense oligos for loss-of-function studies in vertebrate embryos., Schneider PN., Genesis. March 1, 2011; 49 (3): 117-23.        


A gene regulatory network controlling hhex transcription in the anterior endoderm of the organizer., Rankin SA, Rankin SA., Dev Biol. March 15, 2011; 351 (2): 297-310.                            


Siamois and Twin are redundant and essential in formation of the Spemann organizer., Bae S., Dev Biol. April 15, 2011; 352 (2): 367-81.                    


Loss of Xenopus tropicalis EMSY causes impairment of gastrulation and upregulation of p53., Rana AA., N Biotechnol. July 1, 2011; 28 (4): 334-41.                


HEB and E2A function as SMAD/FOXH1 cofactors., Yoon SJ., Genes Dev. August 1, 2011; 25 (15): 1654-61.            


Novel functions of Noggin proteins: inhibition of Activin/Nodal and Wnt signaling., Bayramov AV., Development. December 1, 2011; 138 (24): 5345-56.              


Waif1/5T4 inhibits Wnt/β-catenin signaling and activates noncanonical Wnt pathways by modifying LRP6 subcellular localization., Kagermeier-Schenk B., Dev Cell. December 13, 2011; 21 (6): 1129-43.        


Ventx factors function as Nanog-like guardians of developmental potential in Xenopus., Scerbo P., PLoS One. January 1, 2012; 7 (5): e36855.              


High mobility group B proteins regulate mesoderm formation and dorsoventral patterning during zebrafish and Xenopus early development., Cao JM., Mech Dev. January 1, 2012; 129 (9-12): 263-74.    


Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.                          


Toward an unbiased evolutionary platform for unraveling Xenopus developmental gene networks., Beer R., Genesis. March 1, 2012; 50 (3): 186-91.        


The cytoplasmic tyrosine kinase Arg regulates gastrulation via control of actin organization., Bonacci G., Dev Biol. April 1, 2012; 364 (1): 42-55.                                        


Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins., Callery EM., Open Biol. April 1, 2012; 2 (4): 120060.                      


Cadherin-dependent differential cell adhesion in Xenopus causes cell sorting in vitro but not in the embryo., Ninomiya H., J Cell Sci. April 15, 2012; 125 (Pt 8): 1877-83.              


Dynamic in vivo binding of transcription factors to cis-regulatory modules of cer and gsc in the stepwise formation of the Spemann-Mangold organizer., Sudou N., Development. May 1, 2012; 139 (9): 1651-61.                  


Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.                    


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.                                      


Xmab21l3 mediates dorsoventral patterning in Xenopus laevis., Sridharan J., Mech Dev. July 1, 2012; 129 (5-8): 136-46.                      


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.        


Gastrulation and pre-gastrulation morphogenesis, inductions, and gene expression: similarities and dissimilarities between urodelean and anuran embryos., Kaneda T., Dev Biol. September 1, 2012; 369 (1): 1-18.          


Microarray-based identification of Pitx3 targets during Xenopus embryogenesis., Hooker L., Dev Dyn. September 1, 2012; 241 (9): 1487-505.                          


An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.                                      


Transcriptional regulation of mesoderm genes by MEF2D during early Xenopus development., Kolpakova A., PLoS One. January 1, 2013; 8 (7): e69693.                  


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.                                              


The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.                            


FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos., Murgan S., PLoS One. January 1, 2014; 9 (10): e110559.                              


Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification., Yasuoka Y., Nat Commun. July 9, 2014; 5 4322.        


NEDD4L regulates convergent extension movements in Xenopus embryos via Disheveled-mediated non-canonical Wnt signaling., Zhang Y., Dev Biol. August 1, 2014; 392 (1): 15-25.                              


The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish., Young T., Development. September 1, 2014; 141 (18): 3505-16.        


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


Genome-wide view of TGFβ/Foxh1 regulation of the early mesendoderm program., Chiu WT., Development. December 1, 2014; 141 (23): 4537-47.                                  


Fezf2 promotes neuronal differentiation through localised activation of Wnt/β-catenin signalling during forebrain development., Zhang S., Development. December 1, 2014; 141 (24): 4794-805.                            


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.                                          


Direct regulation of siamois by VegT is required for axis formation in Xenopus embryo., Li HY., Int J Dev Biol. January 1, 2015; 59 (10-12): 443-51.                          


The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.                                    


Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.                                  


On the origin of vertebrate somites., Onai T., Zoological Lett. June 15, 2015; 1 33.              


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.                                    


NF2/Merlin is required for the axial pattern formation in the Xenopus laevis embryo., Zhu X., Mech Dev. November 1, 2015; 138 Pt 3 305-12.                


Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.            


The MLL/Setd1b methyltransferase is required for the Spemann's organizer gene activation in Xenopus., Lin H., Mech Dev. November 1, 2016; 142 1-9.              


Functional differences between Tcf1 isoforms in early Xenopus development., Roël G., Int J Dev Biol. January 1, 2017; 61 (1-2): 29-34.          


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.                        

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