Papers associated with animal pole (and sox3)

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	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.
	NEURODEVELOPMENT. Shared regulatory programs suggest retention of blastula-stage potential in neural crest cells., Buitrago-Delgado E., Science. June 19, 2015; 348 (6241): 1332-5.
	Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm., Nordin K., Dev Cell. November 10, 2014; 31 (3): 374-382.
	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.
	The Xenopus homologue of Down syndrome critical region protein 6 drives dorsoanterior gene expression and embryonic axis formation by antagonising polycomb group proteins., Li HY., Development. December 1, 2013; 140 (24): 4903-13.
	Suv4-20h histone methyltransferases promote neuroectodermal differentiation by silencing the pluripotency-associated Oct-25 gene., Nicetto D., PLoS Genet. January 1, 2013; 9 (1): e1003188.
	Pou-V factor Oct25 regulates early morphogenesis in Xenopus laevis., Julier A., Dev Growth Differ. September 1, 2012; 54 (7): 702-16.
	Xmab21l3 mediates dorsoventral patterning in Xenopus laevis., Sridharan J., Mech Dev. July 1, 2012; 129 (5-8): 136-46.
	The RNA-binding protein XSeb4R regulates maternal Sox3 at the posttranscriptional level during maternal-zygotic transition in Xenopus., Bentaya S., Dev Biol. March 15, 2012; 363 (2): 362-72.
	High mobility group B proteins regulate mesoderm formation and dorsoventral patterning during zebrafish and Xenopus early development., Cao JM., Mech Dev. January 1, 2012; 129 (9-12): 263-74.
	The homeobox leucine zipper gene Homez plays a role in Xenopus laevis neurogenesis., Ghimouz R., Biochem Biophys Res Commun. November 11, 2011; 415 (1): 11-6.
	The response of early neural genes to FGF signaling or inhibition of BMP indicate the absence of a conserved neural induction module., Rogers CD., BMC Dev Biol. January 26, 2011; 11 74.
	Histone XH2AX is required for Xenopus anterior neural development: critical role of threonine 16 phosphorylation., Lee SY., J Biol Chem. September 17, 2010; 285 (38): 29525-34.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	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.
	A role for Syndecan-4 in neural induction involving ERK- and PKC-dependent pathways., Kuriyama S., Development. February 1, 2009; 136 (4): 575-84.
	Samba, a Xenopus hnRNP expressed in neural and neural crest tissues., Yan CY., Dev Dyn. January 1, 2009; 238 (1): 204-9.
	Xenopus Sox3 activates sox2 and geminin and indirectly represses Xvent2 expression to induce neural progenitor formation at the expense of non-neural ectodermal derivatives., Rogers CD., Mech Dev. January 1, 2009; 126 (1-2): 42-55.
	Hairy2 functions through both DNA-binding and non DNA-binding mechanisms at the neural plate border in Xenopus., Nichane M., Dev Biol. October 15, 2008; 322 (2): 368-80.
	Hairy2-Id3 interactions play an essential role in Xenopus neural crest progenitor specification., Nichane M., Dev Biol. October 15, 2008; 322 (2): 355-67.
	Sox3 expression is maintained by FGF signaling and restricted to the neural plate by Vent proteins in the Xenopus embryo., Rogers CD., Dev Biol. January 1, 2008; 313 (1): 307-19.
	PP2A:B56epsilon is required for eye induction and eye field separation., Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
	Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures., Khokha MK., Dev Cell. March 1, 2005; 8 (3): 401-11.
	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.
	A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system., Saka Y., Dev Biol. September 15, 2004; 273 (2): 210-25.
	Repression of nodal expression by maternal B1-type SOXs regulates germ layer formation in Xenopus and zebrafish., Zhang C., Dev Biol. September 1, 2004; 273 (1): 23-37.
	Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways., Moore KB., Dev Cell. January 1, 2004; 6 (1): 55-67.
	Transcription factors of the anterior neural plate alter cell movements of epidermal progenitors to specify a retinal fate., Kenyon KL., Dev Biol. December 1, 2001; 240 (1): 77-91.
	Neuralization of the Xenopus embryo by inhibition of p300/ CREB-binding protein function., Kato Y., J Neurosci. November 1, 1999; 19 (21): 9364-73.
	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.

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