Papers associated with blastopore (and not)

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	Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):
	Furry is required for cell movements during gastrulation and functionally interacts with NDR1., Cervino AS., Sci Rep. March 23, 2021; 11 (1): 6607.
	TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9
	Natural size variation among embryos leads to the corresponding scaling in gene expression., Leibovich A., Dev Biol. June 15, 2020; 462 (2): 165-179.
	The tumor suppressor PTPRK promotes ZNRF3 internalization and is required for Wnt inhibition in the Spemann organizer., Chang LS., Elife. January 14, 2020; 9
	RAPGEF5 Regulates Nuclear Translocation of β-Catenin., Griffin JN., Dev Cell. January 22, 2018; 44 (2): 248-260.e4.
	A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates., Plouhinec JL., PLoS Biol. October 19, 2017; 15 (10): e2004045.
	Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates., Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.
	sall1 and sall4 repress pou5f3 family expression to allow neural patterning, differentiation, and morphogenesis in Xenopus laevis., Exner CRT., Dev Biol. May 1, 2017; 425 (1): 33-43.
	Activation of a T-box-Otx2-Gsc gene network independent of TBP and TBP-related factors., Gazdag E., Development. April 15, 2016; 143 (8): 1340-50.
	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	Identification of microRNAs and microRNA targets in Xenopus gastrulae: The role of miR-26 in the regulation of Smad1., Liu C., Dev Biol. January 1, 2016; 409 (1): 26-38.
	Early neural ectodermal genes are activated by Siamois and Twin during blastula stages., Klein SL., Genesis. May 1, 2015; 53 (5): 308-20.
	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.
	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.
	Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus., Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
	Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.
	A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance., Livigni A., Curr Biol. November 18, 2013; 23 (22): 2233-2244.
	Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.
	Directional migration of leading-edge mesoderm generates physical forces: Implication in Xenopus notochord formation during gastrulation., Hara Y., Dev Biol. October 15, 2013; 382 (2): 482-95.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
	Essential role of AWP1 in neural crest specification in Xenopus., Seo JH., Int J Dev Biol. January 1, 2013; 57 (11-12): 829-36.
	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.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	TAK1 promotes BMP4/Smad1 signaling via inhibition of erk MAPK: a new link in the FGF/BMP regulatory network., Liu C., Differentiation. April 1, 2012; 83 (4): 210-9.
	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.
	Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.
	Xenopus furry contributes to release of microRNA gene silencing., Goto T., Proc Natl Acad Sci U S A. November 9, 2010; 107 (45): 19344-9.
	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.
	Comparison of Lim1 expression in embryos of frogs with different modes of reproduction., Venegas-Ferrín M., Int J Dev Biol. January 1, 2010; 54 (1): 195-202.
	Bestrophin genes are expressed in Xenopus development., Onuma Y., Biochem Biophys Res Commun. July 3, 2009; 384 (3): 290-5.
	Unc5B interacts with FLRT3 and Rnd1 to modulate cell adhesion in Xenopus embryos., Karaulanov E., PLoS One. May 29, 2009; 4 (5): e5742.
	Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
	VegT, eFGF and Xbra cause overall posteriorization while Xwnt8 causes eye-level restricted posteriorization in synergy with chordin in early Xenopus development., Fujii H., Dev Growth Differ. March 1, 2008; 50 (3): 169-80.
	Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction., Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.
	The mouse homeobox gene Noto regulates node morphogenesis, notochordal ciliogenesis, and left right patterning., Beckers A., Proc Natl Acad Sci U S A. October 2, 2007; 104 (40): 15765-70.
	TGF-beta signaling-mediated morphogenesis: modulation of cell adhesion via cadherin endocytosis., Ogata S., Genes Dev. July 15, 2007; 21 (14): 1817-31.
	ANR5, an FGF target gene product, regulates gastrulation in Xenopus., Chung HA., Curr Biol. June 5, 2007; 17 (11): 932-9.
	Early molecular effects of ethanol during vertebrate embryogenesis., Yelin R., Differentiation. June 1, 2007; 75 (5): 393-403.
	Evolution of axis specification mechanisms in jawed vertebrates: insights from a chondrichthyan., Coolen M., PLoS One. April 18, 2007; 2 (4): e374.
	Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
	New tools for visualization and analysis of morphogenesis in spherical embryos., Tyszka JM., Dev Dyn. December 1, 2005; 234 (4): 974-83.
	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.
	XBtg2 is required for notochord differentiation during early Xenopus development., Sugimoto K., Dev Growth Differ. September 1, 2005; 47 (7): 435-43.
	Xenopus hairy2b specifies anterior prechordal mesoderm identity within Spemann's organizer., Yamaguti M., Dev Dyn. September 1, 2005; 234 (1): 102-13.
	Temporal analysis of the early BMP functions identifies distinct anti-organizer and mesoderm patterning phases., Marom K., Dev Biol. June 15, 2005; 282 (2): 442-54.
	XIC is required for Siamois activity and dorsoanterior development., Snider L., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.
	JNK and ROKalpha function in the noncanonical Wnt/RhoA signaling pathway to regulate Xenopus convergent extension movements., Kim GH., Dev Dyn. April 1, 2005; 232 (4): 958-68.
	Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures., Khokha MK., Dev Cell. March 1, 2005; 8 (3): 401-11.

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