Papers associated with marginal zone (and en2)

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	PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J., Development. December 1, 2003; 130 (23): 5569-78.
	Timed interactions between the Hox expressing non-organiser mesoderm and the Spemann organiser generate positional information during vertebrate gastrulation., Wacker SA., Dev Biol. April 1, 2004; 268 (1): 207-19.
	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.
	XIdax, an inhibitor of the canonical Wnt pathway, is required for anterior neural structure formation in Xenopus., Michiue T., Dev Dyn. May 1, 2004; 230 (1): 79-90.
	R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis., Kazanskaya O., Dev Cell. October 1, 2004; 7 (4): 525-34.
	Ethanol exposure affects gene expression in the embryonic organizer and reduces retinoic acid levels., Yelin R., Dev Biol. March 1, 2005; 279 (1): 193-204.
	Xenopus hairy2b specifies anterior prechordal mesoderm identity within Spemann's organizer., Yamaguti M., Dev Dyn. September 1, 2005; 234 (1): 102-13.
	The assembly of POSH-JNK regulates Xenopus anterior neural development., Kim GH., Dev Biol. October 1, 2005; 286 (1): 256-69.
	The Ca2+-induced methyltransferase xPRMT1b controls neural fate in amphibian embryo., Batut J., Proc Natl Acad Sci U S A. October 18, 2005; 102 (42): 15128-33.
	Regulation of ADMP and BMP2/4/7 at opposite embryonic poles generates a self-regulating morphogenetic field., Reversade B., Cell. December 16, 2005; 123 (6): 1147-60.
	Regulation of early Xenopus development by ErbB signaling., Nie S., Dev Dyn. February 1, 2006; 235 (2): 301-14.
	FGF8, Wnt8 and Myf5 are target genes of Tbx6 during anteroposterior specification in Xenopus embryo., Li HY., Dev Biol. February 15, 2006; 290 (2): 470-81.
	FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
	Tes regulates neural crest migration and axial elongation in Xenopus., Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
	Combined ectopic expression of Pdx1 and Ptf1a/p48 results in the stable conversion of posterior endoderm into endocrine and exocrine pancreatic tissue., Afelik S., Genes Dev. June 1, 2006; 20 (11): 1441-6.
	Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
	Metastasis-associated kinase modulates Wnt signaling to regulate brain patterning and morphogenesis., Kibardin A., Development. August 1, 2006; 133 (15): 2845-54.
	Cholesterol homeostasis in development: the role of Xenopus 7-dehydrocholesterol reductase (Xdhcr7) in neural development., Tadjuidje E., Dev Dyn. August 1, 2006; 235 (8): 2095-110.
	Xenopus Xotx2 and Drosophila otd share similar activities in anterior patterning of the frog embryo., Lunardi A., Dev Genes Evol. September 1, 2006; 216 (9): 511-21.
	Smurf1 regulates neural patterning and folding in Xenopus embryos by antagonizing the BMP/Smad1 pathway., Alexandrova EM., Dev Biol. November 15, 2006; 299 (2): 398-410.
	Early molecular effects of ethanol during vertebrate embryogenesis., Yelin R., Differentiation. June 1, 2007; 75 (5): 393-403.
	The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
	The secreted serine protease xHtrA1 stimulates long-range FGF signaling in the early Xenopus embryo., Hou S., Dev Cell. August 1, 2007; 13 (2): 226-41.
	Wise retained in the endoplasmic reticulum inhibits Wnt signaling by reducing cell surface LRP6., Guidato S., Dev Biol. October 15, 2007; 310 (2): 250-63.
	Retinoic acid metabolizing factor xCyp26c is specifically expressed in neuroectoderm and regulates anterior neural patterning in Xenopus laevis., Tanibe M., Int J Dev Biol. January 1, 2008; 52 (7): 893-901.
	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.
	Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.
	Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal., Rhinn M., Neural Dev. April 2, 2009; 4 12.
	Dazap2 is required for FGF-mediated posterior neural patterning, independent of Wnt and Cdx function., Roche DD., Dev Biol. September 1, 2009; 333 (1): 26-36.
	BMP antagonists and FGF signaling contribute to different domains of the neural plate in Xenopus., Wills AE., Dev Biol. January 15, 2010; 337 (2): 335-50.
	FMR1/FXR1 and the miRNA pathway are required for eye and neural crest development., Gessert S., Dev Biol. May 1, 2010; 341 (1): 222-35.
	Anterior neural development requires Del1, a matrix-associated protein that attenuates canonical Wnt signaling via the Ror2 pathway., Takai A., Development. October 1, 2010; 137 (19): 3293-302.
	Peter Pan functions independently of its role in ribosome biogenesis during early eye and craniofacial cartilage development in Xenopus laevis., Bugner V., Development. June 1, 2011; 138 (11): 2369-78.
	Xenopus laevis insulin receptor substrate IRS-1 is important for eye development., Bugner V., Dev Dyn. July 1, 2011; 240 (7): 1705-15.
	A novel mechanism for the transcriptional regulation of Wnt signaling in development., Vacik T., Genes Dev. September 1, 2011; 25 (17): 1783-95.
	The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.
	Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
	ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P., Cell Rep. May 31, 2012; 1 (5): 516-27.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Subfunctionalization and neofunctionalization of vertebrate Lef/Tcf transcription factors., Klingel S., Dev Biol. August 1, 2012; 368 (1): 44-53.
	An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
	Xnr3 affects brain patterning via cell migration in the neural-epidermal tissue boundary during early Xenopus embryogenesis., Morita M., Int J Dev Biol. January 1, 2013; 57 (9-10): 779-86.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Xenopus Nkx6.1 and Nkx6.2 are required for mid-hindbrain boundary development., Ma P., Dev Genes Evol. July 1, 2013; 223 (4): 253-9.
	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.
	Loss of Xenopus cadherin-11 leads to increased Wnt/β-catenin signaling and up-regulation of target genes c-myc and cyclin D1 in neural crest., Koehler A., Dev Biol. November 1, 2013; 383 (1): 132-45.
	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.
	An essential role for LPA signalling in telencephalon development., Geach TJ., Development. February 1, 2014; 141 (4): 940-9.
	The Prdm13 histone methyltransferase encoding gene is a Ptf1a-Rbpj downstream target that suppresses glutamatergic and promotes GABAergic neuronal fate in the dorsal neural tube., Hanotel J., Dev Biol. February 15, 2014; 386 (2): 340-57.
	Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus., Young JJ., Development. April 1, 2014; 141 (8): 1683-93.

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