Papers associated with urogenital system (and sox2)

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	Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;
	Retinoic acid control of pax8 during renal specification of Xenopus pronephros involves hox and meis3., Durant-Vesga J., Dev Biol. January 1, 2023; 493 17-28.
	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.
	Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components., Hantel F., J Cell Sci. May 1, 2022; 135 (9):
	TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9
	Heparan sulfate proteoglycans regulate BMP signalling during neural crest induction., Pegge J., Dev Biol. April 15, 2020; 460 (2): 108-114.
	no privacy, a Xenopus tropicalis mutant, is a model of human Hermansky-Pudlak Syndrome and allows visualization of internal organogenesis during tadpole development., Nakayama T., Dev Biol. June 15, 2017; 426 (2): 472-486.
	Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development., Neilson KM., Dev Biol. January 15, 2017; 421 (2): 171-182.
	The E3 ubiquitin ligase Hace1 is required for early embryonic development in Xenopus laevis., Iimura A., BMC Dev Biol. September 21, 2016; 16 (1): 31.
	Mesodermal origin of median fin mesenchyme and tail muscle in amphibian larvae., Taniguchi Y., Sci Rep. June 18, 2015; 5 11428.
	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 alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform., Dichmann DS., Cell Rep. February 3, 2015; 10 (4): 527-36.
	Methylmercury exposure during early Xenopus laevis development affects cell proliferation and death but not neural progenitor specification., Huyck RW., Neurotoxicol Teratol. January 1, 2015; 47 102-13.
	Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton., Ioannou A., Dev Biol. August 15, 2013; 380 (2): 243-58.
	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.
	Homeoprotein hhex-induced conversion of intestinal to ventral pancreatic precursors results in the formation of giant pancreata in Xenopus embryos., Zhao H., Proc Natl Acad Sci U S A. May 29, 2012; 109 (22): 8594-9.
	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.
	Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis., Barnett C., Mech Dev. January 1, 2012; 129 (9-12): 324-38.
	A homolog of Subtilisin-like Proprotein Convertase 7 is essential to anterior neural development in Xenopus., Senturker S., PLoS One. January 1, 2012; 7 (6): e39380.
	Transdifferentiation from cornea to lens in Xenopus laevis depends on BMP signalling and involves upregulation of Wnt signalling., Day RC., BMC Dev Biol. January 26, 2011; 11 54.
	Expression patterns of genes encoding small GTPases Ras-dva-1 and Ras-dva-2 in the Xenopus laevis tadpoles., Tereshina MB., Gene Expr Patterns. January 1, 2011; 11 (1-2): 156-61.
	Characterization of new otic enhancers of the pou3f4 gene reveal distinct signaling pathway regulation and spatio-temporal patterns., Robert-Moreno À., PLoS One. December 31, 2010; 5 (12): e15907.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	Dazap2 is required for FGF-mediated posterior neural patterning, independent of Wnt and Cdx function., Roche DD., Dev Biol. September 1, 2009; 333 (1): 26-36.
	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.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx., Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.
	XsFRP5 modulates endodermal organogenesis in Xenopus laevis., Damianitsch K., Dev Biol. May 15, 2009; 329 (2): 327-37.
	Xenopus ADAM19 is involved in neural, neural crest and muscle development., Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
	A dual requirement for Iroquois genes during Xenopus kidney development., Alarcón P., Development. October 1, 2008; 135 (19): 3197-207.
	Cold-inducible RNA binding protein (CIRP), a novel XTcf-3 specific target gene regulates neural development in Xenopus., van Venrooy S., BMC Dev Biol. August 7, 2008; 8 77.
	Eya1 and Six1 promote neurogenesis in the cranial placodes in a SoxB1-dependent fashion., Schlosser G., Dev Biol. August 1, 2008; 320 (1): 199-214.
	Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline., Christine KS., Dev Cell. April 1, 2008; 14 (4): 616-23.
	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.
	Xenopus cDNA microarray identification of genes with endodermal organ expression., Park EC., Dev Dyn. June 1, 2007; 236 (6): 1633-49.
	Odd-skipped genes encode repressors that control kidney development., Tena JJ., Dev Biol. January 15, 2007; 301 (2): 518-31.
	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.
	Cold-inducible RNA binding protein is required for the expression of adhesion molecules and embryonic cell movement in Xenopus laevis., Peng Y., Biochem Biophys Res Commun. May 26, 2006; 344 (1): 416-24.
	xBtg-x regulates Wnt/beta-Catenin signaling during early Xenopus development., Wessely O., Dev Biol. July 1, 2005; 283 (1): 17-28.
	The transcription factor Sox9 is required for cranial neural crest development in Xenopus., Spokony RF., Development. January 1, 2002; 129 (2): 421-32.
	Xenopus Eya1 demarcates all neurogenic placodes as well as migrating hypaxial muscle precursors., David R., Mech Dev. May 1, 2001; 103 (1-2): 189-92.
	Use of large-scale expression cloning screens in the Xenopus laevis tadpole to identify gene function., Grammer TC., Dev Biol. December 15, 2000; 228 (2): 197-210.
	Regional gene expression in the epithelia of the Xenopus tadpole gut., Chalmers AD., Mech Dev. August 1, 2000; 96 (1): 125-8.
	Xenopus brain factor-2 controls mesoderm, forebrain and neural crest development., Gómez-Skarmeta JL., Mech Dev. January 1, 1999; 80 (1): 15-27.
	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.

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