Papers associated with upper blastopore lip (and vegt)

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	Activation of a T-box-Otx2-Gsc gene network independent of TBP and TBP-related factors., Gazdag E., Development. April 15, 2016; 143 (8): 1340-50.
	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	Direct regulation of siamois by VegT is required for axis formation in Xenopus embryo., Li HY., Int J Dev Biol. January 1, 2015; 59 (10-12): 443-51.
	The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.
	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.
	Maternal Dead-End1 is required for vegetal cortical microtubule assembly during Xenopus axis specification., Mei W., Development. June 1, 2013; 140 (11): 2334-44.
	Transcriptional regulation of mesoderm genes by MEF2D during early Xenopus development., Kolpakova A., PLoS One. January 1, 2013; 8 (7): e69693.
	Dynamic in vivo binding of transcription factors to cis-regulatory modules of cer and gsc in the stepwise formation of the Spemann-Mangold organizer., Sudou N., Development. May 1, 2012; 139 (9): 1651-61.
	The functions of maternal Dishevelled 2 and 3 in the early Xenopus embryo., Tadjuidje E., Dev Dyn. July 1, 2011; 240 (7): 1727-36.
	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.
	Bestrophin genes are expressed in Xenopus development., Onuma Y., Biochem Biophys Res Commun. July 3, 2009; 384 (3): 290-5.
	The role of FGF signaling in the establishment and maintenance of mesodermal gene expression in Xenopus., Fletcher RB., Dev Dyn. May 1, 2008; 237 (5): 1243-54.
	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.
	The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm., Spagnoli FM., Development. February 1, 2008; 135 (3): 451-61.
	Expression of Siamois and Twin in the blastula Chordin/Noggin signaling center is required for brain formation in Xenopus laevis embryos., Ishibashi H., Mech Dev. January 1, 2008; 125 (1-2): 58-66.
	FoxD3 regulation of Nodal in the Spemann organizer is essential for Xenopus dorsal mesoderm development., Steiner AB., Development. December 1, 2006; 133 (24): 4827-38.
	Status of RNAs, localized in Xenopus laevis oocytes, in the frogs Rana pipiens and Eleutherodactylus coqui., Nath K., J Exp Zool B Mol Dev Evol. January 15, 2005; 304 (1): 28-39.
	New roles for FoxH1 in patterning the early embryo., Kofron M., Development. October 1, 2004; 131 (20): 5065-78.
	Cytoplasmic and molecular reconstruction of Xenopus embryos: synergy of dorsalizing and endo-mesodermalizing determinants drives early axial patterning., Katsumoto K., Development. March 1, 2004; 131 (5): 1135-44.
	Cell fate specification and competence by Coco, a maternal BMP, TGFbeta and Wnt inhibitor., Bell E., Development. April 1, 2003; 130 (7): 1381-9.
	Early embryonic expression of ion channels and pumps in chick and Xenopus development., Rutenberg J., Dev Dyn. December 1, 2002; 225 (4): 469-84.
	Zygotic Wnt activity is required for Brachyury expression in the early Xenopus laevis embryo., Vonica A., Dev Biol. October 1, 2002; 250 (1): 112-27.
	Molecular regulation of vertebrate early endoderm development., Shivdasani RA., Dev Biol. September 15, 2002; 249 (2): 191-203.
	The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.
	Repression of organizer genes in dorsal and ventral Xenopus cells mediated by maternal XTcf3., Houston DW., Development. September 1, 2002; 129 (17): 4015-25.
	Effects of heterodimerization and proteolytic processing on Derrière and Nodal activity: implications for mesoderm induction in Xenopus., Eimon PM., Development. July 1, 2002; 129 (13): 3089-103.
	VegT activation of Sox17 at the midblastula transition alters the response to nodal signals in the vegetal endoderm domain., Engleka MJ., Dev Biol. September 1, 2001; 237 (1): 159-72.
	Maternal VegT is the initiator of a molecular network specifying endoderm in Xenopus laevis., Xanthos JB., Development. January 1, 2001; 128 (2): 167-80.
	Bottle cell formation in relation to mesodermal patterning in the Xenopus embryo., Kurth T., Mech Dev. October 1, 2000; 97 (1-2): 117-31.
	HNF1(beta) is required for mesoderm induction in the Xenopus embryo., Vignali R., Development. April 1, 2000; 127 (7): 1455-65.
	Endodermal Nodal-related signals and mesoderm induction in Xenopus., Agius E., Development. March 1, 2000; 127 (6): 1173-83.
	In Xenopus embryos, BMP heterodimers are not required for mesoderm induction, but BMP activity is necessary for dorsal/ventral patterning., Eimon PM., Dev Biol. December 1, 1999; 216 (1): 29-40.
	The role of paraxial protocadherin in selective adhesion and cell movements of the mesoderm during Xenopus gastrulation., Kim SH., Development. December 1, 1998; 125 (23): 4681-90.
	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.

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