Papers associated with anatomical space (and dkk1)

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	R-Spondin 2 governs Xenopus left-right body axis formation by establishing an FGF signaling gradient., Lee H, Lee H., Nat Commun. February 2, 2024; 15 (1): 1003.
	Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):
	Pinhead signaling regulates mesoderm heterogeneity via the FGF receptor-dependent pathway., Ossipova O., Development. September 11, 2020; 147 (17):
	Pinhead signaling regulates mesoderm heterogeneity via FGF receptor-dependent pathway., Ossipova O., Development. January 1, 2020;
	The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis., Guo Y., Dev Biol. May 1, 2019; 449 (1): 1-13.
	Leukemia inhibitory factor signaling in Xenopus embryo: Insights from gain of function analysis and dominant negative mutant of the receptor., Jalvy S., Dev Biol. March 15, 2019; 447 (2): 200-213.
	Nucleotide receptor P2RY4 is required for head formation via induction and maintenance of head organizer in Xenopus laevis., Harata A., Dev Growth Differ. February 1, 2019; 61 (2): 186-197.
	WDR5 regulates left-right patterning via chromatin-dependent and -independent functions., Kulkarni SS., Development. November 28, 2018; 145 (23):
	The phosphatase Pgam5 antagonizes Wnt/β-Catenin signaling in embryonic anterior-posterior axis patterning., Rauschenberger V., Development. June 15, 2017; 144 (12): 2234-2247.
	Apolipoprotein C-I mediates Wnt/Ctnnb1 signaling during neural border formation and is required for neural crest development., Yokota C., Int J Dev Biol. January 1, 2017; 61 (6-7): 415-425.
	Ventricular cell fate can be specified until the onset of myocardial differentiation., Caporilli S., Mech Dev. February 1, 2016; 139 31-41.
	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.
	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.
	Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.
	Insulin-like factor regulates neural induction through an IGF1 receptor-independent mechanism., Haramoto Y., Sci Rep. January 12, 2015; 5 11603.
	Chibby functions in Xenopus ciliary assembly, embryonic development, and the regulation of gene expression., Shi J., Dev Biol. November 15, 2014; 395 (2): 287-98.
	Self-regulation of the head-inducing properties of the Spemann organizer., Inui M., Proc Natl Acad Sci U S A. September 18, 2012; 109 (38): 15354-9.
	Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
	sizzled function and secreted factor network dynamics., Shi J., Biol Open. March 15, 2012; 1 (3): 286-94.
	Shox2 mediates Tbx5 activity by regulating Bmp4 in the pacemaker region of the developing heart., Puskaric S., Hum Mol Genet. December 1, 2010; 19 (23): 4625-33.
	Unc5B interacts with FLRT3 and Rnd1 to modulate cell adhesion in Xenopus embryos., Karaulanov E., PLoS One. May 29, 2009; 4 (5): e5742.
	The Wnt antagonists Frzb-1 and Crescent locally regulate basement membrane dissolution in the developing primary mouth., Dickinson AJ., Development. April 1, 2009; 136 (7): 1071-81.
	Sfrp5 coordinates foregut specification and morphogenesis by antagonizing both canonical and noncanonical Wnt11 signaling., Li Y., Genes Dev. November 1, 2008; 22 (21): 3050-63.
	The functions and possible significance of Kremen as the gatekeeper of Wnt signalling in development and pathology., Nakamura T., J Cell Mol Med. April 1, 2008; 12 (2): 391-408.
	Evolution of axis specification mechanisms in jawed vertebrates: insights from a chondrichthyan., Coolen M., PLoS One. April 18, 2007; 2 (4): e374.
	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.
	Xnr2 and Xnr5 unprocessed proteins inhibit Wnt signaling upstream of dishevelled., Onuma Y., Dev Dyn. December 1, 2005; 234 (4): 900-10.
	Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.
	Systematic screening and expression analysis of the head organizer genes in Xenopus embryos., Shibata M., Dev Biol. November 15, 2001; 239 (2): 241-56.
	The role of Xenopus dickkopf1 in prechordal plate specification and neural patterning., Kazanskaya O., Development. November 1, 2000; 127 (22): 4981-92.
	Xenopus crescent encoding a Frizzled-like domain is expressed in the Spemann organizer and pronephros., Shibata M., Mech Dev. September 1, 2000; 96 (2): 243-6.
	Dickkopf genes are co-ordinately expressed in mesodermal lineages., Monaghan AP., Mech Dev. September 1, 1999; 87 (1-2): 45-56.
	Characterization of a novel member of the FGF family, XFGF-20, in Xenopus laevis., Koga C., Biochem Biophys Res Commun. August 11, 1999; 261 (3): 756-65.
	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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