Papers associated with blastopore (and tbxt)

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	Neuroectodermal specification and regionalization of the Spemann organizer in Xenopus., Fetka I., Mech Dev. May 1, 2000; 93 (1-2): 49-58.
	goosecoid expression represses Brachyury in embryonic stem cells and affects craniofacial development in chimeric mice., Boucher DM., Int J Dev Biol. April 1, 2000; 44 (3): 279-88.
	Xenopus frizzled 7 can act in canonical and non-canonical Wnt signaling pathways: implications on early patterning and morphogenesis., Medina A., Mech Dev. April 1, 2000; 92 (2): 227-37.
	HNF1(beta) is required for mesoderm induction in the Xenopus embryo., Vignali R., Development. April 1, 2000; 127 (7): 1455-65.
	Regulation of early expression of Dlx3, a Xenopus anti-neural factor, by beta-catenin signaling., Beanan MJ., Mech Dev. March 1, 2000; 91 (1-2): 227-35.
	XTIF2, a Xenopus homologue of the human transcription intermediary factor, is required for a nuclear receptor pathway that also interacts with CBP to suppress Brachyury and XMyoD., de la Calle-Mustienes E., Mech Dev. March 1, 2000; 91 (1-2): 119-29.
	Regulation of the early expression of the Xenopus nodal-related 1 gene, Xnr1., Hyde CE., Development. March 1, 2000; 127 (6): 1221-9.
	Endodermal Nodal-related signals and mesoderm induction in Xenopus., Agius E., Development. March 1, 2000; 127 (6): 1173-83.
	The lefty-related factor Xatv acts as a feedback inhibitor of nodal signaling in mesoderm induction and L-R axis development in xenopus., Cheng AM., Development. March 1, 2000; 127 (5): 1049-61.
	Xenopus embryonic E2F is required for the formation of ventral and posterior cell fates during early embryogenesis., Suzuki A., Mol Cell. February 1, 2000; 5 (2): 217-29.
	Transient depletion of xDnmt1 leads to premature gene activation in Xenopus embryos., Stancheva I., Genes Dev. February 1, 2000; 14 (3): 313-27.
	Wnt signaling in Xenopus embryos inhibits bmp4 expression and activates neural development., Baker JC., Genes Dev. December 1, 1999; 13 (23): 3149-59.
	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.
	Neuralization of the Xenopus embryo by inhibition of p300/ CREB-binding protein function., Kato Y., J Neurosci. November 1, 1999; 19 (21): 9364-73.
	An anterior signalling centre in Xenopus revealed by the homeobox gene XHex., Jones CM., Curr Biol. September 9, 1999; 9 (17): 946-54.
	Inhibitory patterning of the anterior neural plate in Xenopus by homeodomain factors Dlx3 and Msx1., Feledy JA., Dev Biol. August 15, 1999; 212 (2): 455-64.
	Xenopus GDF6, a new antagonist of noggin and a partner of BMPs., Chang C., Development. August 1, 1999; 126 (15): 3347-57.
	Amphibian embryos as a model system for organ engineering: in vitro induction and rescue of the heart anlage., Grunz H., Int J Dev Biol. July 1, 1999; 43 (4): 361-4.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.
	A developmental pathway controlling outgrowth of the Xenopus tail bud., Beck CW., Development. April 1, 1999; 126 (8): 1611-20.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	Misexpression of the catenin p120(ctn)1A perturbs Xenopus gastrulation but does not elicit Wnt-directed axis specification., Paulson AF., Dev Biol. March 15, 1999; 207 (2): 350-63.
	FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.
	Anteroposterior patterning by mutual repression of orthodenticle and caudal-type transcription factors., Isaacs HV., Evol Dev. January 1, 1999; 1 (3): 143-52.
	Characterization of the Ets-type protein ER81 in Xenopus embryos., Chen Y, Chen Y., Mech Dev. January 1, 1999; 80 (1): 67-76.
	The Xenopus Ets transcription factor XER81 is a target of the FGF signaling pathway., Münchberg SR., Mech Dev. January 1, 1999; 80 (1): 53-65.
	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.
	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.
	Evidence for non-axial A/P patterning in the nonneural ectoderm of Xenopus and zebrafish pregastrula embryos., Read EM., Int J Dev Biol. September 1, 1998; 42 (6): 763-74.
	The Spemann organizer-expressed zinc finger gene Xegr-1 responds to the MAP kinase/Ets-SRF signal transduction pathway., Panitz F., EMBO J. August 3, 1998; 17 (15): 4414-25.
	Geminin, a neuralizing molecule that demarcates the future neural plate at the onset of gastrulation., Kroll KL., Development. August 1, 1998; 125 (16): 3247-58.
	Xenopus Smad7 inhibits both the activin and BMP pathways and acts as a neural inducer., Casellas R., Dev Biol. June 1, 1998; 198 (1): 1-12.
	Two phases of Hox gene regulation during early Xenopus development., Pownall ME., Curr Biol. May 21, 1998; 8 (11): 673-6.
	Cooperation between the activin and Wnt pathways in the spatial control of organizer gene expression., Crease DJ., Proc Natl Acad Sci U S A. April 14, 1998; 95 (8): 4398-403.
	Anterior specification of embryonic ectoderm: the role of the Xenopus cement gland-specific gene XAG-2., Aberger F., Mech Dev. March 1, 1998; 72 (1-2): 115-30.
	Analysis of the developing Xenopus tail bud reveals separate phases of gene expression during determination and outgrowth., Beck CW., Mech Dev. March 1, 1998; 72 (1-2): 41-52.
	Xenopus Smad8 acts downstream of BMP-4 to modulate its activity during vertebrate embryonic patterning., Nakayama T., Development. March 1, 1998; 125 (5): 857-67.
	A POU protein regulates mesodermal competence to FGF in Xenopus., Henig C., Mech Dev. February 1, 1998; 71 (1-2): 131-42.
	Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K., Development. February 1, 1998; 125 (4): 579-87.
	XBMPRII, a novel Xenopus type II receptor mediating BMP signaling in embryonic tissues., Frisch A., Development. February 1, 1998; 125 (3): 431-42.
	Mesoderm induction by heterodimeric AP-1 (c-Jun and c-Fos) and its involvement in mesoderm formation through the embryonic fibroblast growth factor/Xbra autocatalytic loop during the early development of Xenopus embryos., Kim J., J Biol Chem. January 16, 1998; 273 (3): 1542-50.
	Differential regulation of chordin expression domains in mutant zebrafish., Miller-Bertoglio VE., Dev Biol. December 15, 1997; 192 (2): 537-50.
	The Spemann organizer of Xenopus is patterned along its anteroposterior axis at the earliest gastrula stage., Zoltewicz JS., Dev Biol. December 15, 1997; 192 (2): 482-91.
	FGF-8 is associated with anteroposterior patterning and limb regeneration in Xenopus., Christen B., Dev Biol. December 15, 1997; 192 (2): 455-66.
	The Xenopus Brachyury promoter is activated by FGF and low concentrations of activin and suppressed by high concentrations of activin and by paired-type homeodomain proteins., Latinkić BV., Genes Dev. December 1, 1997; 11 (23): 3265-76.
	Sizzled: a secreted Xwnt8 antagonist expressed in the ventral marginal zone of Xenopus embryos., Salic AN., Development. December 1, 1997; 124 (23): 4739-48.
	Misexpression of chick Vg1 in the marginal zone induces primitive streak formation., Shah SB., Development. December 1, 1997; 124 (24): 5127-38.
	Siamois is required for formation of Spemann's organizer., Kessler DS., Proc Natl Acad Sci U S A. November 25, 1997; 94 (24): 13017-22.
	Epidermal induction and inhibition of neural fate by translation initiation factor 4AIII., Weinstein DC., Development. November 1, 1997; 124 (21): 4235-42.
	Cleavage of Chordin by Xolloid metalloprotease suggests a role for proteolytic processing in the regulation of Spemann organizer activity., Piccolo S., Cell. October 31, 1997; 91 (3): 407-16.

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