Papers associated with sensory 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.
	A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation., Hou K., Cells. May 15, 2019; 8 (5):
	Fam46a regulates BMP-dependent pre-placodal ectoderm differentiation in Xenopus., Watanabe T., Development. October 26, 2018; 145 (20):
	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.
	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.
	Cooperative and independent functions of FGF and Wnt signaling during early inner ear development., Wright KD., BMC Dev Biol. October 6, 2015; 15 33.
	Transcriptional regulator PRDM12 is essential for human pain perception., Chen YC, Chen YC., Nat Genet. July 1, 2015; 47 (7): 803-8.
	TRPP2-dependent Ca2+ signaling in dorso-lateral mesoderm is required for kidney field establishment in Xenopus., Futel M., J Cell Sci. March 1, 2015; 128 (5): 888-99.
	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.
	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.
	Xenopus as a model system for the study of GOLPH2/GP73 function: Xenopus GOLPH2 is required for pronephros development., Li L., PLoS One. January 1, 2012; 7 (6): e38939.
	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.
	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.
	Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus., Park BY., Dev Biol. December 1, 2008; 324 (1): 108-21.
	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.
	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.
	An ontology for Xenopus anatomy and development., Segerdell E., BMC Dev Biol. June 23, 2008; 8 92.
	Expression of marker genes during early ear development in medaka., Hochmann S., Gene Expr Patterns. January 1, 2007; 7 (3): 355-62.
	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.
	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.
	Synergism between Pax-8 and lim-1 in embryonic kidney development., Carroll TJ., Dev Biol. October 1, 1999; 214 (1): 46-59.
	Xenopus Pax-2/5/8 orthologues: novel insights into Pax gene evolution and identification of Pax-8 as the earliest marker for otic and pronephric cell lineages., Heller N., Dev Genet. January 1, 1999; 24 (3-4): 208-19.

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