Papers associated with nervous system (and pax8)

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	In vitro modeling of cranial placode differentiation: Recent advances, challenges, and perspectives., Griffin C., Dev Biol. February 1, 2024; 506 20-30.
	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;
	Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.
	Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism., Vick P., Genes (Basel). November 24, 2021; 12 (12):
	Molecular mechanisms of hearing loss in Nager syndrome., Maharana SK., Dev Biol. August 1, 2021; 476 200-208.
	Betel quid dependence mechanism and potential cessation therapy., Ko AM., Prog Neuropsychopharmacol Biol Psychiatry. December 20, 2020; 103 109982.
	Arid3a regulates nephric tubule regeneration via evolutionarily conserved regeneration signal-response enhancers., Suzuki N., Elife. January 8, 2019; 8
	The voltage sensing phosphatase (VSP) localizes to the apical membrane of kidney tubule epithelial cells., Ratzan W., PLoS One. January 1, 2019; 14 (4): e0209056.
	Fam46a regulates BMP-dependent pre-placodal ectoderm differentiation in Xenopus., Watanabe T., Development. October 26, 2018; 145 (20):
	Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome., Braun DA., J Clin Invest. October 1, 2018; 128 (10): 4313-4328.
	Pou3f transcription factor expression during embryonic development highlights distinct pou3f3 and pou3f4 localization in the Xenopus laevis kidney., Cosse-Etchepare C., Int J Dev Biol. January 1, 2018; 62 (4-5): 325-333.
	Peroxiredoxin1, a novel regulator of pronephros development, influences retinoic acid and Wnt signaling by controlling ROS levels., Chae S., Sci Rep. August 21, 2017; 7 (1): 8874.
	Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.
	pdzrn3 is required for pronephros morphogenesis in Xenopus laevis., Marracci S., Int J Dev Biol. January 1, 2016; 60 (1-3): 57-63.
	Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
	Transcriptional regulator PRDM12 is essential for human pain perception., Chen YC, Chen YC., Nat Genet. July 1, 2015; 47 (7): 803-8.
	Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.
	Understanding early organogenesis using a simplified in situ hybridization protocol in Xenopus., Deimling SJ., J Vis Exp. January 12, 2015; (95): e51526.
	Specific induction of cranial placode cells from Xenopus ectoderm by modulating the levels of BMP, Wnt and FGF signaling., Watanabe T., Genesis. October 1, 2014; .
	The evolutionary history of vertebrate cranial placodes--I: cell type evolution., Patthey C., Dev Biol. May 1, 2014; 389 (1): 82-97.
	The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning., Schlosser G., Dev Biol. May 1, 2014; 389 (1): 98-119.
	Sp8 regulates inner ear development., Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.
	Comparative Functional Analysis of ZFP36 Genes during Xenopus Development., Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.
	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.
	Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning., Steventon B., Dev Biol. July 1, 2012; 367 (1): 55-65.
	Evolution of a tissue-specific silencer underlies divergence in the expression of pax2 and pax8 paralogues., Ochi H., Nat Commun. May 22, 2012; 3 848.
	Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B., Dev Dyn. May 1, 2012; 241 (5): 995-1007.
	Origin and segregation of cranial placodes in Xenopus laevis., Pieper M., Dev Biol. December 15, 2011; 360 (2): 257-75.
	V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.
	PAPC and the Wnt5a/Ror2 pathway control the invagination of the otic placode in Xenopus., Jung B., BMC Dev Biol. June 10, 2011; 11 36.
	The secreted integrin ligand nephronectin is necessary for forelimb formation in Xenopus tropicalis., Abu-Daya A., Dev Biol. January 15, 2011; 349 (2): 204-12.
	XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis., Lee SJ., Mech Dev. January 1, 2010; 127 (1-2): 49-61.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	An increase in intracellular Ca2+ is involved in pronephric tubule differentiation in the amphibian Xenopus laevis., Leclerc C., Dev Biol. September 15, 2008; 321 (2): 357-67.
	Fli1 acts at the top of the transcriptional network driving blood and endothelial development., Liu F., Curr Biol. August 26, 2008; 18 (16): 1234-40.
	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.
	A functional screen for genes involved in Xenopus pronephros development., Kyuno J., Mech Dev. July 1, 2008; 125 (7): 571-86.
	Odd-skipped genes encode repressors that control kidney development., Tena JJ., Dev Biol. January 15, 2007; 301 (2): 518-31.
	FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.
	Induction and specification of cranial placodes., Schlosser G., Dev Biol. June 15, 2006; 294 (2): 303-51.
	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.
	A novel role for lbx1 in Xenopus hypaxial myogenesis., Martin BL., Development. January 1, 2006; 133 (2): 195-208.
	SoxE factors function equivalently during neural crest and inner ear development and their activity is regulated by SUMOylation., Taylor KM., Dev Cell. November 1, 2005; 9 (5): 593-603.
	Evi-1 expression in Xenopus., Mead PE., Gene Expr Patterns. June 1, 2005; 5 (5): 601-8.
	Molecular anatomy of placode development in Xenopus laevis., Schlosser G., Dev Biol. July 15, 2004; 271 (2): 439-66.
	Specification of the otic placode depends on Sox9 function in Xenopus., Saint-Germain N., Development. April 1, 2004; 131 (8): 1755-63.
	Wnt-6 is expressed in the ureter bud and induces kidney tubule development in vitro., Itäranta P., Genesis. April 1, 2002; 32 (4): 259-68.
	Synergism between Pax-8 and lim-1 in embryonic kidney development., Carroll TJ., Dev Biol. October 1, 1999; 214 (1): 46-59.
	Towards a molecular anatomy of the Xenopus pronephric kidney., Brändli AW., Int J Dev Biol. January 1, 1999; 43 (5): 381-95.

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