Papers associated with urogenital system (and gsc)

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	Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.
	TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9
	Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
	The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus., Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.
	Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.
	The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish., Young T., Development. September 1, 2014; 141 (18): 3505-16.
	Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.
	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.
	Microarray-based identification of Pitx3 targets during Xenopus embryogenesis., Hooker L., Dev Dyn. September 1, 2012; 241 (9): 1487-505.
	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.
	Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins., Callery EM., Open Biol. April 1, 2012; 2 (4): 120060.
	Use of fully modified 2'-O-methyl antisense oligos for loss-of-function studies in vertebrate embryos., Schneider PN., Genesis. March 1, 2011; 49 (3): 117-23.
	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.
	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.
	Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.
	Xenopus ADAM19 is involved in neural, neural crest and muscle development., Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
	Chordin affects pronephros development in Xenopus embryos by anteriorizing presomitic mesoderm., Mitchell T., Dev Dyn. January 1, 2007; 236 (1): 251-61.
	Kermit 2/XGIPC, an IGF1 receptor interacting protein, is required for IGF signaling in Xenopus eye development., Wu J., Development. September 1, 2006; 133 (18): 3651-60.
	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.
	Genomic profiling of mixer and Sox17beta targets during Xenopus endoderm development., Dickinson K., Dev Dyn. February 1, 2006; 235 (2): 368-81.
	Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.
	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.
	Smad10 is required for formation of the frog nervous system., LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.
	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.
	A direct screen for secreted proteins in Xenopus embryos identifies distinct activities for the Wnt antagonists Crescent and Frzb-1., Pera EM., Mech Dev. September 1, 2000; 96 (2): 183-95.
	The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.
	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.
	Characterization of the Ets-type protein ER81 in Xenopus embryos., Chen Y, Chen Y., Mech Dev. January 1, 1999; 80 (1): 67-76.
	Xenopus brain factor-2 controls mesoderm, forebrain and neural crest development., Gómez-Skarmeta JL., Mech Dev. January 1, 1999; 80 (1): 15-27.
	Expression of Xfz3, a Xenopus frizzled family member, is restricted to the early nervous system., Shi DL., Mech Dev. January 1, 1998; 70 (1-2): 35-47.
	p53 activity is essential for normal development in Xenopus., Wallingford JB., Curr Biol. October 1, 1997; 7 (10): 747-57.
	Frzb-1 is a secreted antagonist of Wnt signaling expressed in the Spemann organizer., Leyns L., Cell. March 21, 1997; 88 (6): 747-56.
	XIPOU 2, a noggin-inducible gene, has direct neuralizing activity., Witta SE., Development. March 1, 1995; 121 (3): 721-30.
	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.
	Mesodermal patterning by a gradient of the vertebrate homeobox gene goosecoid., Niehrs C., Science. February 11, 1994; 263 (5148): 817-20.

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