Papers associated with muscle (and hoxb9)

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	FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue., Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
	CDC174, a novel component of the exon junction complex whose mutation underlies a syndrome of hypotonia and psychomotor developmental delay., Volodarsky M., Hum Mol Genet. November 15, 2015; 24 (22): 6485-91.
	PV.1 induced by FGF-Xbra functions as a repressor of neurogenesis in Xenopus embryos., Yoon J., BMB Rep. December 1, 2014; 47 (12): 673-8.
	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.
	β-Adrenergic signaling promotes posteriorization in Xenopus early development., Mori S., Dev Growth Differ. April 1, 2013; 55 (3): 350-8.
	Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus., Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.
	A homolog of Subtilisin-like Proprotein Convertase 7 is essential to anterior neural development in Xenopus., Senturker S., PLoS One. January 1, 2012; 7 (6): e39380.
	The forkhead transcription factor FoxB1 regulates the dorsal-ventral and anterior-posterior patterning of the ectoderm during early Xenopus embryogenesis., Takebayashi-Suzuki K., Dev Biol. December 1, 2011; 360 (1): 11-29.
	The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos., Maczkowiak F., Dev Biol. April 15, 2010; 340 (2): 381-96.
	Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
	Xmc mediates Xctr1-independent morphogenesis in Xenopus laevis., Haremaki T., Dev Dyn. September 1, 2009; 238 (9): 2382-7.
	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.
	Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation., Chang C., Development. November 1, 2007; 134 (21): 3861-72.
	FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
	Interaction between X-Delta-2 and Hox genes regulates segmentation and patterning of the anteroposterior axis., Peres JN., Mech Dev. April 1, 2006; 123 (4): 321-33.
	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.
	Isolation and growth factor inducibility of the Xenopus laevis Lmx1b gene., Haldin CE., Int J Dev Biol. May 1, 2003; 47 (4): 253-62.
	Chordin is required for the Spemann organizer transplantation phenomenon in Xenopus embryos., Oelgeschläger M., Dev Cell. February 1, 2003; 4 (2): 219-30.
	Xhex-expressing endodermal tissues are essential for anterior patterning in Xenopus., Smithers LE., Mech Dev. December 1, 2002; 119 (2): 191-200.
	Techniques and probes for the study of Xenopus tropicalis development., Khokha MK., Dev Dyn. December 1, 2002; 225 (4): 499-510.
	Anteroposterior patterning in Xenopus embryos: egg fragment assay system reveals a synergy of dorsalizing and posteriorizing embryonic domains., Fujii H., Dev Biol. December 1, 2002; 252 (1): 15-30.
	The E3 ubiquitin ligase GREUL1 anteriorizes ectoderm during Xenopus development., Borchers AG., Dev Biol. November 15, 2002; 251 (2): 395-408.
	Cloning and developmental expression of Baf57 in Xenopus laevis., Domingos PM., Mech Dev. August 1, 2002; 116 (1-2): 177-81.
	The latent-TGFbeta-binding-protein-1 (LTBP-1) is expressed in the organizer and regulates nodal and activin signaling., Altmann CR., Dev Biol. August 1, 2002; 248 (1): 118-27.
	Xpbx1b and Xmeis1b play a collaborative role in hindbrain and neural crest gene expression in Xenopus embryos., Maeda R., Proc Natl Acad Sci U S A. April 16, 2002; 99 (8): 5448-53.
	The secreted glycoprotein Noelin-1 promotes neurogenesis in Xenopus., Moreno TA., Dev Biol. December 15, 2001; 240 (2): 340-60.
	The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling., Domingos PM., Dev Biol. November 1, 2001; 239 (1): 148-60.
	Siamois functions in the early blastula to induce Spemann's organiser., Kodjabachian L., Mech Dev. October 1, 2001; 108 (1-2): 71-9.
	The orphan receptor ALK7 and the Activin receptor ALK4 mediate signaling by Nodal proteins during vertebrate development., Reissmann E., Genes Dev. August 1, 2001; 15 (15): 2010-22.
	Use of large-scale expression cloning screens in the Xenopus laevis tadpole to identify gene function., Grammer TC., Dev Biol. December 15, 2000; 228 (2): 197-210.
	Ras-mediated FGF signaling is required for the formation of posterior but not anterior neural tissue in Xenopus laevis., Ribisi S., Dev Biol. November 1, 2000; 227 (1): 183-96.
	Different activities of the frizzled-related proteins frzb2 and sizzled2 during Xenopus anteroposterior patterning., Bradley L., Dev Biol. November 1, 2000; 227 (1): 118-32.
	Xenopus embryonic E2F is required for the formation of ventral and posterior cell fates during early embryogenesis., Suzuki A., Mol Cell. February 1, 2000; 5 (2): 217-29.
	Transient depletion of xDnmt1 leads to premature gene activation in Xenopus embryos., Stancheva I., Genes Dev. February 1, 2000; 14 (3): 313-27.
	Requirement of Sox2-mediated signaling for differentiation of early Xenopus neuroectoderm., Kishi M., Development. February 1, 2000; 127 (4): 791-800.
	A role for xGCNF in midbrain-hindbrain patterning in Xenopus laevis., Song K., Dev Biol. September 1, 1999; 213 (1): 170-9.
	Post-transcriptional regulation of Xwnt-8 expression is required for normal myogenesis during vertebrate embryonic development., Tian Q., Development. August 1, 1999; 126 (15): 3371-80.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	Cytochalasin B inhibits morphogenetic movement and muscle differentiation of activin-treated ectoderm in Xenopus., Tamai K., Dev Growth Differ. February 1, 1999; 41 (1): 41-9.
	FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.
	Xenopus Zic family and its role in neural and neural crest development., Nakata K., Mech Dev. July 1, 1998; 75 (1-2): 43-51.
	Xenopus Smad7 inhibits both the activin and BMP pathways and acts as a neural inducer., Casellas R., Dev Biol. June 1, 1998; 198 (1): 1-12.
	Anterior specification of embryonic ectoderm: the role of the Xenopus cement gland-specific gene XAG-2., Aberger F., Mech Dev. March 1, 1998; 72 (1-2): 115-30.
	XBMPRII, a novel Xenopus type II receptor mediating BMP signaling in embryonic tissues., Frisch A., Development. February 1, 1998; 125 (3): 431-42.
	Paraxial-fated mesoderm is required for neural crest induction in Xenopus embryos., Bonstein L., Dev Biol. January 15, 1998; 193 (2): 156-68.
	Wnt and FGF pathways cooperatively pattern anteroposterior neural ectoderm in Xenopus., McGrew LL., Mech Dev. December 1, 1997; 69 (1-2): 105-14.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation., Horb ME., Development. May 1, 1997; 124 (9): 1689-98.
	Caudalization of neural fate by tissue recombination and bFGF., Cox WG., Development. December 1, 1995; 121 (12): 4349-58.
	Disruption of BMP signals in embryonic Xenopus ectoderm leads to direct neural induction., Hawley SH., Genes Dev. December 1, 1995; 9 (23): 2923-35.

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