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	Quantitative analysis of transcriptome dynamics provides novel insights into developmental state transitions., Johnson K, Freedman S, Braun R, LaBonne C., BMC Genomics. October 23, 2022; 23 (1): 723.
	Exportins can inhibit major mitotic assembly events in vitro: membrane fusion, nuclear pore formation, and spindle assembly., Nord MS, Bernis C, Carmona S, Garland DC, Travesa A, Forbes DJ., Nucleus. December 1, 2020; 11 (1): 178-193.
	Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G, Singhal N, Nicetto D, Straub T, Kremmer E, Rupp RAW., PLoS Genet. May 12, 2017; 13 (5): e1006757.
	Ubiquitin C-terminal hydrolase37 regulates Tcf7 DNA binding for the activation of Wnt signalling., Han W, Lee H, Lee H, Han JK., Sci Rep. February 15, 2017; 7 42590.
	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A, Gillis WQ, Zhu H, Thomsen GH., Dev Biol. August 15, 2014; 392 (2): 358-67.
	Regulation of primitive hematopoiesis by class I histone deacetylases., Shah RR, Koniski A, Shinde M, Blythe SA, Fass DM, Haggarty SJ, Palis J, Klein PS., Dev Dyn. February 1, 2013; 242 (2): 108-21.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ, Latinkić BV., PLoS One. October 28, 2009; 4 (10): e7650.
	Microarray-based identification of VegT targets in Xenopus., Taverner NV, Kofron M, Kofron M, Shin Y, Kabitschke C, Gilchrist MJ, Wylie C, Cho KW, Heasman J, Smith JC., Mech Dev. March 1, 2005; 122 (3): 333-54.
	Ectopic EphA4 receptor induces posterior protrusions via FGF signaling in Xenopus embryos., Park EK, Warner N, Bong YS, Stapleton D, Maeda R, Pawson T, Daar IO., Mol Biol Cell. April 1, 2004; 15 (4): 1647-55.
	In situ analysis of gene expression in Xenopus embryos., Pollet N, Delius H, Niehrs C., C R Biol. January 1, 2003; 326 (10-11): 1011-7.
	Steady-state nuclear localization of exportin-t involves RanGTP binding and two distinct nuclear pore complex interaction domains., Kuersten S, Arts GJ, Walther TC, Englmeier L, Mattaj IW., Mol Cell Biol. August 1, 2002; 22 (16): 5708-20.
	The competence of marginal zone cells to become Spemann's organizer is controlled by Xcad2., Levy V, Marom K, Zins S, Koutsia N, Yelin R, Fainsod A., Dev Biol. August 1, 2002; 248 (1): 40-51.
	Difference in XTcf-3 dependency accounts for change in response to beta-catenin-mediated Wnt signalling in Xenopus blastula., Hamilton FS, Wheeler GN, Hoppler S., Development. June 1, 2001; 128 (11): 2063-73.
	Recognition of engineered tRNAs with an extended 3' end by Exportin-t (Xpo-t) and transport of tRNA-attached ribozymes to the cytoplasm in somatic cells., Kuwabara T, Warashina M, Sano M, Tang H, Wong-Staal F, Munekata E, Taira K., Biomacromolecules. January 1, 2001; 2 (4): 1229-42.
	HNF1(beta) is required for mesoderm induction in the Xenopus embryo., Vignali R, Poggi L, Madeddu F, Barsacchi G., Development. April 1, 2000; 127 (7): 1455-65.
	Spatial and temporal properties of ventral blood island induction in Xenopus laevis., Kumano G, Belluzzi L, Smith WC., Development. December 1, 1999; 126 (23): 5327-37.
	The role of exportin-t in selective nuclear export of mature tRNAs., Arts GJ, Kuersten S, Romby P, Ehresmann B, Mattaj IW., EMBO J. December 15, 1998; 17 (24): 7430-41.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V, Pollet N, Delius H, Vingron M, Pfister R, Nitsch R, Blumenstock C, Niehrs C., Mech Dev. October 1, 1998; 77 (2): 95-141.
	Sizzled: a secreted Xwnt8 antagonist expressed in the ventral marginal zone of Xenopus embryos., Salic AN, Kroll KL, Evans LM, Kirschner MW., Development. December 1, 1997; 124 (23): 4739-48.
	Frzb, a secreted protein expressed in the Spemann organizer, binds and inhibits Wnt-8., Wang S, Krinks M, Lin K, Luyten FP, Moos M., Cell. March 21, 1997; 88 (6): 757-66.
	eFGF, Xcad3 and Hox genes form a molecular pathway that establishes the anteroposterior axis in Xenopus., Pownall ME, Tucker AS, Slack JM, Isaacs HV., Development. December 1, 1996; 122 (12): 3881-92.
	Expression of a dominant-negative Wnt blocks induction of MyoD in Xenopus embryos., Hoppler S, Brown JD, Moon RT., Genes Dev. November 1, 1996; 10 (21): 2805-17.
	An experimental system for analyzing response to a morphogen gradient., Gurdon JB, Mitchell A, Ryan K., Proc Natl Acad Sci U S A. September 3, 1996; 93 (18): 9334-8.
	Competition between noggin and bone morphogenetic protein 4 activities may regulate dorsalization during Xenopus development., Re'em-Kalma Y, Lamb T, Frank D., Proc Natl Acad Sci U S A. December 19, 1995; 92 (26): 12141-5.
	Tail bud determination in the vertebrate embryo., Tucker AS, Slack JM., Curr Biol. July 1, 1995; 5 (7): 807-13.
	A truncated bone morphogenetic protein receptor affects dorsal-ventral patterning in the early Xenopus embryo., Suzuki A, Thies RS, Yamaji N, Song JJ, Wozney JM, Murakami K, Ueno N., Proc Natl Acad Sci U S A. October 25, 1994; 91 (22): 10255-9.
	FGF signalling in the early specification of mesoderm in Xenopus., Amaya E, Stein PA, Musci TJ, Kirschner MW., Development. June 1, 1993; 118 (2): 477-87.
	Localized and inducible expression of Xenopus-posterior (Xpo), a novel gene active in early frog embryos, encoding a protein with a 'CCHC' finger domain., Sato SM, Sargent TD., Development. July 1, 1991; 112 (3): 747-53.

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