Papers associated with ventral (and foxa4)

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	Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G., PLoS Genet. May 12, 2017; 13 (5): e1006757.
	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
	Early neural ectodermal genes are activated by Siamois and Twin during blastula stages., Klein SL., Genesis. May 1, 2015; 53 (5): 308-20.
	E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation., Wills AE., Dev Cell. February 9, 2015; 32 (3): 345-57.
	Variable combinations of specific ephrin ligand/Eph receptor pairs control embryonic tissue separation., Rohani N., PLoS Biol. September 23, 2014; 12 (9): e1001955.
	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.
	Inference of the Xenopus tropicalis embryonic regulatory network and spatial gene expression patterns., Zheng Z., BMC Syst Biol. January 8, 2014; 8 3.
	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.
	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.
	An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
	Cadherin-dependent differential cell adhesion in Xenopus causes cell sorting in vitro but not in the embryo., Ninomiya H., J Cell Sci. April 15, 2012; 125 (Pt 8): 1877-83.
	A revised model of Xenopus dorsal midline development: differential and separable requirements for Notch and Shh signaling., Peyrot SM., Dev Biol. April 15, 2011; 352 (2): 254-66.
	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.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	Identification of novel transcripts with differential dorso-ventral expression in Xenopus gastrula using serial analysis of gene expression., Faunes F., Genome Biol. February 11, 2009; 10 (2): R15.
	Concentrations of TATA box-binding protein (TBP)-type genes affect chordamesodermal gene expression., Goto T., Int J Dev Biol. January 1, 2008; 52 (4): 371-5.
	Early molecular effects of ethanol during vertebrate embryogenesis., Yelin R., Differentiation. June 1, 2007; 75 (5): 393-403.
	Genomic analysis of Xenopus organizer function., Hufton AL., BMC Dev Biol. June 6, 2006; 6 27.
	Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.
	Identification of novel genes affecting mesoderm formation and morphogenesis through an enhanced large scale functional screen in Xenopus., Chen JA., Mech Dev. March 1, 2005; 122 (3): 307-31.
	The Notch-target gene hairy2a impedes the involution of notochordal cells by promoting floor plate fates in Xenopus embryos., López SL., Development. March 1, 2005; 132 (5): 1035-46.
	The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos., Callery EM., Dev Biol. February 15, 2005; 278 (2): 542-59.
	Smad2 and Smad3 coordinately regulate craniofacial and endodermal development., Liu Y., Dev Biol. June 15, 2004; 270 (2): 411-26.
	Analysis of Spemann organizer formation in Xenopus embryos by cDNA macroarrays., Wessely O., Dev Biol. May 15, 2004; 269 (2): 552-66.
	Inhibition of mesodermal fate by Xenopus HNF3beta/FoxA2., Suri C., Dev Biol. January 1, 2004; 265 (1): 90-104.
	Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.
	Notch activates sonic hedgehog and both are involved in the specification of dorsal midline cell-fates in Xenopus., López SL., Development. May 1, 2003; 130 (10): 2225-38.
	Role of Goosecoid, Xnot and Wnt antagonists in the maintenance of the notochord genetic programme in Xenopus gastrulae., Yasuo H., Development. October 1, 2001; 128 (19): 3783-93.
	Determinants of T box protein specificity., Conlon FL., Development. October 1, 2001; 128 (19): 3749-58.
	Fox (forkhead) genes are involved in the dorso-ventral patterning of the Xenopus mesoderm., El-Hodiri H., Int J Dev Biol. January 1, 2001; 45 (1): 265-71.
	A screen for targets of the Xenopus T-box gene Xbra., Saka Y., Mech Dev. May 1, 2000; 93 (1-2): 27-39.
	Characterization of a subfamily of related winged helix genes, XFD-12/12'/12" (XFLIP), during Xenopus embryogenesis., Sölter M., Mech Dev. December 1, 1999; 89 (1-2): 161-5.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
	The Xcad-2 gene can provide a ventral signal independent of BMP-4., Pillemer G., Mech Dev. June 1, 1998; 74 (1-2): 133-43.
	The ALK-2 and ALK-4 activin receptors transduce distinct mesoderm-inducing signals during early Xenopus development but do not co-operate to establish thresholds., Armes NA., Development. October 1, 1997; 124 (19): 3797-804.
	Gli1 is a target of Sonic hedgehog that induces ventral neural tube development., Lee J., Development. July 1, 1997; 124 (13): 2537-52.
	Inhibition of Xbra transcription activation causes defects in mesodermal patterning and reveals autoregulation of Xbra in dorsal mesoderm., Conlon FL., Development. August 1, 1996; 122 (8): 2427-35.
	Bone morphogenetic protein-4 (BMP-4) acts during gastrula stages to cause ventralization of Xenopus embryos., Jones CM., Development. May 1, 1996; 122 (5): 1545-54.
	Overexpression of the homeobox gene Xnot-2 leads to notochord formation in Xenopus., Gont LK., Dev Biol. February 25, 1996; 174 (1): 174-8.
	A fork head related multigene family is transcribed in Xenopus laevis embryos., Lef J., Int J Dev Biol. February 1, 1996; 40 (1): 245-53.
	Bone morphogenetic protein 2 in the early development of Xenopus laevis., Clement JH., Mech Dev. August 1, 1995; 52 (2-3): 357-70.
	Patterning of the mesoderm in Xenopus: dose-dependent and synergistic effects of Brachyury and Pintallavis., O'Reilly MA., Development. May 1, 1995; 121 (5): 1351-9.
	Expression of the LIM class homeobox gene Xlim-1 in pronephros and CNS cell lineages of Xenopus embryos is affected by retinoic acid and exogastrulation., Taira M., Development. June 1, 1994; 120 (6): 1525-36.
	Sequential expression of HNF-3 beta and HNF-3 alpha by embryonic organizing centers: the dorsal lip/node, notochord and floor plate., Ruiz i Altaba A., Mech Dev. December 1, 1993; 44 (2-3): 91-108.
	Ectopic neural expression of a floor plate marker in frog embryos injected with the midline transcription factor Pintallavis., Ruiz i Altaba A., Proc Natl Acad Sci U S A. September 1, 1993; 90 (17): 8268-72.
	A novel, activin-inducible, blastopore lip-specific gene of Xenopus laevis contains a fork head DNA-binding domain., Dirksen ML., Genes Dev. April 1, 1992; 6 (4): 599-608.

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