Papers associated with blastopore (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.
	JmjC Domain-containing Protein 6 (Jmjd6) Derepresses the Transcriptional Repressor Transcription Factor 7-like 1 (Tcf7l1) and Is Required for Body Axis Patterning during Xenopus Embryogenesis., Zhang X., J Biol Chem. August 14, 2015; 290 (33): 20273-83.
	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.
	Genome-wide view of TGFβ/Foxh1 regulation of the early mesendoderm program., Chiu WT., Development. December 1, 2014; 141 (23): 4537-47.
	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.
	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.
	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.
	Evolutionary origin of the Otx2 enhancer for its expression in visceral endoderm., Kurokawa D., Dev Biol. June 1, 2010; 342 (1): 110-20.
	Highly conserved functions of the Brachyury gene on morphogenetic movements: insight from the early-diverging phylum Ctenophora., Yamada A., Dev Biol. March 1, 2010; 339 (1): 212-22.
	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.
	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.
	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.
	Systematic screening for genes specifically expressed in the anterior neuroectoderm during early Xenopus development., Takahashi N., Int J Dev Biol. January 1, 2005; 49 (8): 939-51.
	Analysis of Spemann organizer formation in Xenopus embryos by cDNA macroarrays., Wessely O., Dev Biol. May 15, 2004; 269 (2): 552-66.
	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.
	A novel Xenopus Smad-interacting forkhead transcription factor (XFast-3) cooperates with XFast-1 in regulating gastrulation movements., Howell M., Development. June 1, 2002; 129 (12): 2823-34.
	Antisense inhibition of Xbrachyury impairs mesoderm formation in Xenopus embryos., Giovannini N., Dev Growth Differ. April 1, 2002; 44 (2): 147-59.
	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.
	Neuroectodermal specification and regionalization of the Spemann organizer in Xenopus., Fetka I., Mech Dev. May 1, 2000; 93 (1-2): 49-58.
	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.
	Gli1 is a target of Sonic hedgehog that induces ventral neural tube development., Lee J., Development. July 1, 1997; 124 (13): 2537-52.
	Expression pattern of an axolotl floor plate-specific fork head gene reflects early developmental differences between frogs and salamanders., Whiteley M., Dev Genet. January 1, 1997; 20 (2): 145-51.
	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.
	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.
	Pintallavis, a gene expressed in the organizer and midline cells of frog embryos: involvement in the development of the neural axis., Ruiz i Altaba A., Development. September 1, 1992; 116 (1): 81-93.
	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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