Papers associated with sensory system (and sox17a)

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	Cell landscape of larval and adult Xenopus laevis at single-cell resolution., Liao Y., Nat Commun. July 25, 2022; 13 (1): 4306.
	Hes5.9 Coordinate FGF and Notch Signaling to Modulate Gastrulation via Regulating Cell Fate Specification and Cell Migration in Xenopus tropicalis., Huang X., Genes (Basel). November 18, 2020; 11 (11):
	Serine Threonine Kinase Receptor-Associated Protein Deficiency Impairs Mouse Embryonic Stem Cells Lineage Commitment Through CYP26A1-Mediated Retinoic Acid Homeostasis., Jin L., Stem Cells. September 1, 2018; 36 (9): 1368-1379.
	Expression pattern of bcar3, a downstream target of Gata2, and its binding partner, bcar1, during Xenopus development., Green YS., Gene Expr Patterns. January 1, 2016; 20 (1): 55-62.
	Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
	The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.
	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
	Sirtuin inhibitor Ex-527 causes neural tube defects, ventral edema formations, and gastrointestinal malformations in Xenopus laevis embryos., Ohata Y., Dev Growth Differ. August 1, 2014; 56 (6): 460-8.
	Suv4-20h histone methyltransferases promote neuroectodermal differentiation by silencing the pluripotency-associated Oct-25 gene., Nicetto D., PLoS Genet. January 1, 2013; 9 (1): e1003188.
	Loss of Xenopus tropicalis EMSY causes impairment of gastrulation and upregulation of p53., Rana AA., N Biotechnol. July 1, 2011; 28 (4): 334-41.
	Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.
	FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis., Schuff M., Dev Biol. January 15, 2010; 337 (2): 259-73.
	FGF signalling during embryo development regulates cilia length in diverse epithelia., Neugebauer JM., Nature. April 2, 2009; 458 (7238): 651-4.
	XHAPLN3 plays a key role in cardiogenesis by maintaining the hyaluronan matrix around heart anlage., Ito Y., Dev Biol. July 1, 2008; 319 (1): 34-45.
	IRE1beta is required for mesoderm formation in Xenopus embryos., Yuan L., Mech Dev. January 1, 2008; 125 (3-4): 207-22.
	The competence of Xenopus blastomeres to produce neural and retinal progeny is repressed by two endo-mesoderm promoting pathways., Yan B., Dev Biol. May 1, 2007; 305 (1): 103-19.
	Bisphenol A causes malformation of the head region in embryos of Xenopus laevis and decreases the expression of the ESR-1 gene mediated by Notch signaling., Imaoka S., Biol Pharm Bull. February 1, 2007; 30 (2): 371-4.
	Expression of Sox1 during Xenopus early embryogenesis., Nitta KR., Biochem Biophys Res Commun. December 8, 2006; 351 (1): 287-93.
	FGF8, Wnt8 and Myf5 are target genes of Tbx6 during anteroposterior specification in Xenopus embryo., Li HY., Dev Biol. February 15, 2006; 290 (2): 470-81.
	Genomic profiling of mixer and Sox17beta targets during Xenopus endoderm development., Dickinson K., Dev Dyn. February 1, 2006; 235 (2): 368-81.
	Maternal Xenopus Zic2 negatively regulates Nodal-related gene expression during anteroposterior patterning., Houston DW., Development. November 1, 2005; 132 (21): 4845-55.
	An atlas of differential gene expression during early Xenopus embryogenesis., Pollet N., Mech Dev. March 1, 2005; 122 (3): 365-439.
	XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B., Development. February 1, 2005; 132 (3): 591-602.
	Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition., Delaune E., Development. January 1, 2005; 132 (2): 299-310.
	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.
	The latent-TGFbeta-binding-protein-1 (LTBP-1) is expressed in the organizer and regulates nodal and activin signaling., Altmann CR., Dev Biol. August 1, 2002; 248 (1): 118-27.
	Overexpression of the secreted factor Mig30 expressed in the Spemann organizer impairs morphogenetic movements during Xenopus gastrulation., Hayata T., Mech Dev. March 1, 2002; 112 (1-2): 37-51.
	Gene expression in the embryonic Xenopus liver., Zorn AM., Mech Dev. May 1, 2001; 103 (1-2): 153-7.
	A role for GATA5 in Xenopus endoderm specification., Weber H., Development. October 1, 2000; 127 (20): 4345-60.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	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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