Papers associated with animal hemisphere (and pax2)

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	Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.
	Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.
	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.
	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.
	Differential distribution of competence for panplacodal and neural crest induction to non-neural and neural ectoderm., Pieper M., Development. March 1, 2012; 139 (6): 1175-87.
	Xenopus as a model system for the study of GOLPH2/GP73 function: Xenopus GOLPH2 is required for pronephros development., Li L., PLoS One. January 1, 2012; 7 (6): e38939.
	PAPC and the Wnt5a/Ror2 pathway control the invagination of the otic placode in Xenopus., Jung B., BMC Dev Biol. June 10, 2011; 11 36.
	Role of Tbx2 in defining the territory of the pronephric nephron., Cho GS., Development. February 1, 2011; 138 (3): 465-74.
	The nephrogenic potential of the transcription factors osr1, osr2, hnf1b, lhx1 and pax8 assessed in Xenopus animal caps., Drews C., BMC Dev Biol. January 31, 2011; 11 5.
	Polypyrimidine tract-binding protein is required for the repression of gene expression by all-trans retinoic acid., Tamanoue Y., Dev Growth Differ. June 1, 2010; 52 (5): 469-79.
	The role of miR-124a in early development of the Xenopus eye., Qiu R., Mech Dev. October 1, 2009; 126 (10): 804-16.
	Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal., Rhinn M., Neural Dev. April 2, 2009; 4 12.
	PP2A:B56epsilon is required for eye induction and eye field separation., Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
	FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.
	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.
	Xenopus XsalF: anterior neuroectodermal specification by attenuating cellular responsiveness to Wnt signaling., Onai T., Dev Cell. July 1, 2004; 7 (1): 95-106.
	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.
	Conserved expression control and shared activity between cognate T-box genes Tbx2 and Tbx3 in connection with Sonic hedgehog signaling during Xenopus eye development., Takabatake Y., Dev Growth Differ. August 1, 2002; 44 (4): 257-71.
	Differential regulation of chordin expression domains in mutant zebrafish., Miller-Bertoglio VE., Dev Biol. December 15, 1997; 192 (2): 537-50.
	Xenopus Pax-2 displays multiple splice forms during embryogenesis and pronephric kidney development., Heller N., Mech Dev. December 1, 1997; 69 (1-2): 83-104.

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