Papers associated with urogenital system (and tbxt)

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	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.
	Induction of the prospective neural crest of Xenopus., Mayor R., Development. March 1, 1995; 121 (3): 767-77.
	p53 activity is essential for normal development in Xenopus., Wallingford JB., Curr Biol. October 1, 1997; 7 (10): 747-57.
	Xsox17alpha and -beta mediate endoderm formation in Xenopus., Hudson C., Cell. October 31, 1997; 91 (3): 397-405.
	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 dorsalizing factor Gremlin identifies a novel family of secreted proteins that antagonize BMP activities., Hsu DR., Mol Cell. April 1, 1998; 1 (5): 673-83.
	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 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.
	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.
	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.
	The POU domain gene, XlPOU 2 is an essential downstream determinant of neural induction., Matsuo-Takasaki M., Mech Dev. December 1, 1999; 89 (1-2): 75-85.
	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.
	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.
	Participation of transcription elongation factor XSII-K1 in mesoderm-derived tissue development in Xenopus laevis., Taira Y., J Biol Chem. October 13, 2000; 275 (41): 32011-5.
	XCL-2 is a novel m-type calpain and disrupts morphogenetic movements during embryogenesis in Xenopus laevis., Cao Y., Dev Growth Differ. October 1, 2001; 43 (5): 563-71.
	Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.
	Smad10 is required for formation of the frog nervous system., LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.
	Isolation and growth factor inducibility of the Xenopus laevis Lmx1b gene., Haldin CE., Int J Dev Biol. May 1, 2003; 47 (4): 253-62.
	Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway., Zhao H., Dev Biol. May 15, 2003; 257 (2): 278-91.
	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.
	Xenopus tropicalis peroxidasin gene is expressed within the developing neural tube and pronephric kidney., Tindall AJ., Dev Dyn. February 1, 2005; 232 (2): 377-84.
	Genomic profiling of mixer and Sox17beta targets during Xenopus endoderm development., Dickinson K., Dev Dyn. February 1, 2006; 235 (2): 368-81.
	Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation., Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.
	XGAP, an ArfGAP, is required for polarized localization of PAR proteins and cell polarity in Xenopus gastrulation., Hyodo-Miura J., Dev Cell. July 1, 2006; 11 (1): 69-79.
	Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity., Suga A., Dev Biol. July 1, 2006; 295 (1): 26-39.
	Heading in a new direction: implications of the revised fate map for understanding Xenopus laevis development., Lane MC., Dev Biol. August 1, 2006; 296 (1): 12-28.
	ADMP2 is essential for primitive blood and heart development in Xenopus., Kumano G., Dev Biol. November 15, 2006; 299 (2): 411-23.
	IRE1beta is required for mesoderm formation in Xenopus embryos., Yuan L., Mech Dev. January 1, 2008; 125 (3-4): 207-22.
	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.
	Extracellular regulation of developmental cell signaling by XtSulf1., Freeman SD., Dev Biol. August 15, 2008; 320 (2): 436-45.
	Mix.1/2-dependent control of FGF availability during gastrulation is essential for pronephros development in Xenopus., Colas A., Dev Biol. August 15, 2008; 320 (2): 351-65.
	Xenopus ADAM19 is involved in neural, neural crest and muscle development., Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
	Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis., Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.
	Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
	Xenopus Wntless and the retromer complex cooperate to regulate XWnt4 secretion., Kim H., Mol Cell Biol. April 1, 2009; 29 (8): 2118-28.
	Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus., Thomas JT., J Biol Chem. July 10, 2009; 284 (28): 18994-9005.
	Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size., Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.
	Notch activates Wnt-4 signalling to control medio-lateral patterning of the pronephros., Naylor RW., Development. November 1, 2009; 136 (21): 3585-95.
	PRDC regulates placode neurogenesis in chick by modulating BMP signalling., Kriebitz NN., Dev Biol. December 15, 2009; 336 (2): 280-92.
	Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus., Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.
	EBF proteins participate in transcriptional regulation of Xenopus muscle development., Green YS., Dev Biol. October 1, 2011; 358 (1): 240-50.
	sizzled function and secreted factor network dynamics., Shi J., Biol Open. March 15, 2012; 1 (3): 286-94.
	Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins., Callery EM., Open Biol. April 1, 2012; 2 (4): 120060.
	Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/β-catenin-mediated lung specification in Xenopus., Rankin SA, Rankin SA., Development. August 1, 2012; 139 (16): 3010-20.
	Comparative Functional Analysis of ZFP36 Genes during Xenopus Development., Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.
	Essential role of AWP1 in neural crest specification in Xenopus., Seo JH., Int J Dev Biol. January 1, 2013; 57 (11-12): 829-36.
	Regulation of primitive hematopoiesis by class I histone deacetylases., Shah RR., Dev Dyn. February 1, 2013; 242 (2): 108-21.
	In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.
	Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.

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