Papers associated with blastopore (and wnt11b)

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	Dorsal lip maturation and initial archenteron extension depend on Wnt11 family ligands., Van Itallie ES., Dev Biol. January 1, 2023; 493 67-79.
	Maternal Huluwa dictates the embryonic body axis through β-catenin in vertebrates., Yan L., Science. November 23, 2018; 362 (6417):
	A Conserved Role of the Unconventional Myosin 1d in Laterality Determination., Tingler M., Curr Biol. March 5, 2018; 28 (5): 810-816.e3.
	Regulation of distinct branches of the non-canonical Wnt-signaling network in Xenopus dorsal marginal zone explants., Wallkamm V., BMC Biol. July 5, 2016; 14 55.
	A gradient of maternal Bicaudal-C controls vertebrate embryogenesis via translational repression of mRNAs encoding cell fate regulators., Park S., Development. March 1, 2016; 143 (5): 864-71.
	A novel role for Ascl1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT., Gao L., Development. February 1, 2016; 143 (3): 492-503.
	Sulf1 has ligand-dependent effects on canonical and non-canonical Wnt signalling., Fellgett SW., J Cell Sci. April 1, 2015; 128 (7): 1408-21.
	The alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform., Dichmann DS., Cell Rep. February 3, 2015; 10 (4): 527-36.
	Genome-wide view of TGFβ/Foxh1 regulation of the early mesendoderm program., Chiu WT., Development. December 1, 2014; 141 (23): 4537-47.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Functional conservation of Nematostella Wnts in canonical and noncanonical Wnt-signaling., Rigo-Watermeier T., Biol Open. January 15, 2012; 1 (1): 43-51.
	Agonistic and antagonistic roles for TNIK and MINK in non-canonical and canonical Wnt signalling., Mikryukov A., PLoS One. January 1, 2012; 7 (9): e43330.
	Cortical rotation and messenger RNA localization in Xenopus axis formation., Houston DW., Wiley Interdiscip Rev Dev Biol. January 1, 2012; 1 (3): 371-88.
	Highly conserved functions of the Brachyury gene on morphogenetic movements: insight from the early-diverging phylum Ctenophora., Yamada A., Dev Biol. March 1, 2010; 339 (1): 212-22.
	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.
	The non-methylated DNA-binding function of Kaiso is not required in early Xenopus laevis development., Ruzov A., Development. March 1, 2009; 136 (5): 729-38.
	Sfrp5 coordinates foregut specification and morphogenesis by antagonizing both canonical and noncanonical Wnt11 signaling., Li Y., Genes Dev. November 1, 2008; 22 (21): 3050-63.
	Mechanism of activation of the Formin protein Daam1., Liu W., Proc Natl Acad Sci U S A. January 8, 2008; 105 (1): 210-5.
	ANR5, an FGF target gene product, regulates gastrulation in Xenopus., Chung HA., Curr Biol. June 5, 2007; 17 (11): 932-9.
	Wnt11/beta-catenin signaling in both oocytes and early embryos acts through LRP6-mediated regulation of axin., Kofron M., Development. February 1, 2007; 134 (3): 503-13.
	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.
	Role of crescent in convergent extension movements by modulating Wnt signaling in early Xenopus embryogenesis., Shibata M., Mech Dev. December 1, 2005; 122 (12): 1322-39.
	Antagonistic interaction between IGF and Wnt/JNK signaling in convergent extension in Xenopus embryo., Carron C., Mech Dev. November 1, 2005; 122 (11): 1234-47.
	Maternal wnt11 activates the canonical wnt signaling pathway required for axis formation in Xenopus embryos., Tao Q, Tao Q., Cell. March 25, 2005; 120 (6): 857-71.
	Screening of FGF target genes in Xenopus by microarray: temporal dissection of the signalling pathway using a chemical inhibitor., Chung HA., Genes Cells. August 1, 2004; 9 (8): 749-61.
	Activation of Gbetagamma signaling downstream of Wnt-11/Xfz7 regulates Cdc42 activity during Xenopus gastrulation., Penzo-Mendèz A., Dev Biol. May 15, 2003; 257 (2): 302-14.
	The prickle-related gene in vertebrates is essential for gastrulation cell movements., Takeuchi M., Curr Biol. April 15, 2003; 13 (8): 674-9.
	The secreted Frizzled-related protein Sizzled functions as a negative feedback regulator of extreme ventral mesoderm., Collavin L., Development. February 1, 2003; 130 (4): 805-16.
	The Xenopus receptor tyrosine kinase Xror2 modulates morphogenetic movements of the axial mesoderm and neuroectoderm via Wnt signaling., Hikasa H., Development. November 1, 2002; 129 (22): 5227-39.
	Xenopus Sprouty2 inhibits FGF-mediated gastrulation movements but does not affect mesoderm induction and patterning., Nutt SL., Genes Dev. May 1, 2001; 15 (9): 1152-66.
	Role of frizzled 7 in the regulation of convergent extension movements during gastrulation in Xenopus laevis., Djiane A., Development. July 1, 2000; 127 (14): 3091-100.
	Contribution of METRO pathway localized molecules to the organization of the germ cell lineage., Kloc M., Mech Dev. July 1, 1998; 75 (1-2): 81-93.
	Apparent continuity between the messenger transport organizer and late RNA localization pathways during oogenesis in Xenopus., Kloc M., Mech Dev. April 1, 1998; 73 (1): 95-106.
	Combinatorial signalling by Xwnt-11 and Xnr3 in the organizer epithelium., Glinka A., Mech Dev. December 1, 1996; 60 (2): 221-31.
	Elaboration of the messenger transport organizer pathway for localization of RNA to the vegetal cortex of Xenopus oocytes., Kloc M., Dev Biol. November 25, 1996; 180 (1): 119-30.
	Two distinct pathways for the localization of RNAs at the vegetal cortex in Xenopus oocytes., Kloc M., Development. February 1, 1995; 121 (2): 287-97.
	Inducing factors in Xenopus early embryos., Slack JM., Curr Biol. February 1, 1994; 4 (2): 116-26.
	Xwnt-11: a maternally expressed Xenopus wnt gene., Ku M., Development. December 1, 1993; 119 (4): 1161-73.

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