Papers associated with neural tube (and wnt1)

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	The role of Xenopus developmental biology in unraveling Wnt signalling and antero-posterior axis formation., Niehrs C., Dev Biol. February 1, 2022; 482 1-6.
	Folate-dependent methylation of septins governs ciliogenesis during neural tube closure., Toriyama M., FASEB J. August 1, 2017; 31 (8): 3622-3635.
	Identifying domains of EFHC1 involved in ciliary localization, ciliogenesis, and the regulation of Wnt signaling., Zhao Y., Dev Biol. March 15, 2016; 411 (2): 257-265.
	Mechanotransduction During Vertebrate Neurulation., Sokol SY., Curr Top Dev Biol. January 1, 2016; 117 359-76.
	The PTK7 and ROR2 Protein Receptors Interact in the Vertebrate WNT/Planar Cell Polarity (PCP) Pathway., Martinez S., J Biol Chem. December 18, 2015; 290 (51): 30562-72.
	Klhl31 attenuates β-catenin dependent Wnt signaling and regulates embryo myogenesis., Abou-Elhamd A., Dev Biol. June 1, 2015; 402 (1): 61-71.
	Spatial and temporal aspects of Wnt signaling and planar cell polarity during vertebrate embryonic development., Sokol SY., Semin Cell Dev Biol. June 1, 2015; 42 78-85.
	Mef2c-F10N enhancer driven β-galactosidase (LacZ) and Cre recombinase mice facilitate analyses of gene function and lineage fate in neural crest cells., Aoto K., Dev Biol. June 1, 2015; 402 (1): 3-16.
	Fezf2 promotes neuronal differentiation through localised activation of Wnt/β-catenin signalling during forebrain development., Zhang S., Development. December 1, 2014; 141 (24): 4794-805.
	DIPA-family coiled-coils bind conserved isoform-specific head domain of p120-catenin family: potential roles in hydrocephalus and heterotopia., Markham NO., Mol Biol Cell. September 1, 2014; 25 (17): 2592-603.
	Vangl-dependent planar cell polarity signalling is not required for neural crest migration in mammals., Pryor SE., Development. August 1, 2014; 141 (16): 3153-8.
	Current perspectives of the signaling pathways directing neural crest induction., Stuhlmiller TJ., Cell Mol Life Sci. November 1, 2012; 69 (22): 3715-37.
	MicroRNA-9 reveals regional diversity of neural progenitors along the anterior-posterior axis., Bonev B., Dev Cell. January 18, 2011; 20 (1): 19-32.
	Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
	Frizzled-10 promotes sensory neuron development in Xenopus embryos., Garcia-Morales C., Dev Biol. November 1, 2009; 335 (1): 143-55.
	Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
	Modulating the activity of neural crest regulatory factors., Taylor KM., Curr Opin Genet Dev. August 1, 2007; 17 (4): 326-31.
	Frizzled7 mediates canonical Wnt signaling in neural crest induction., Abu-Elmagd M., Dev Biol. October 1, 2006; 298 (1): 285-98.
	The Xfeb gene is directly upregulated by Zic1 during early neural development., Li S., Dev Dyn. October 1, 2006; 235 (10): 2817-27.
	HIC-5 is a novel repressor of lymphoid enhancer factor/T-cell factor-driven transcription., Ghogomu SM., J Biol Chem. January 20, 2006; 281 (3): 1755-64.
	R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis., Kazanskaya O., Dev Cell. October 1, 2004; 7 (4): 525-34.
	Regulation of vertebrate eye development by Rx genes., Bailey TJ., Int J Dev Biol. January 1, 2004; 48 (8-9): 761-70.
	PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J., Development. December 1, 2003; 130 (23): 5569-78.
	Early head specification in Xenopus laevis., Lake BB., ScientificWorldJournal. August 2, 2003; 3 655-76.
	Essential function of Wnt-4 for tubulogenesis in the Xenopus pronephric kidney., Saulnier DM., Dev Biol. August 1, 2002; 248 (1): 13-28.
	The homeoprotein Xiro1 is required for midbrain-hindbrain boundary formation., Glavic A., Development. April 1, 2002; 129 (7): 1609-21.
	Otx2 can activate the isthmic organizer genetic network in the Xenopus embryo., Tour E., Mech Dev. January 1, 2002; 110 (1-2): 3-13.
	Kermit, a frizzled interacting protein, regulates frizzled 3 signaling in neural crest development., Tan C., Development. October 1, 2001; 128 (19): 3665-74.
	Neural crest induction by Xwnt7B in Xenopus., Chang C., Dev Biol. February 1, 1998; 194 (1): 129-34.
	Control of dorsoventral somite patterning by Wnt-1 and beta-catenin., Capdevila J., Dev Biol. January 15, 1998; 193 (2): 182-94.
	Regulation of dorsal fate in the neuraxis by Wnt-1 and Wnt-3a., Saint-Jeannet JP., Proc Natl Acad Sci U S A. December 9, 1997; 94 (25): 13713-8.
	Noggin acts downstream of Wnt and Sonic Hedgehog to antagonize BMP4 in avian somite patterning., Hirsinger E., Development. November 1, 1997; 124 (22): 4605-14.
	Frzb-1 is a secreted antagonist of Wnt signaling expressed in the Spemann organizer., Leyns L., Cell. March 21, 1997; 88 (6): 747-56.
	Expression of a dominant-negative Wnt blocks induction of MyoD in Xenopus embryos., Hoppler S., Genes Dev. November 1, 1996; 10 (21): 2805-17.
	Dorsalizing and neuralizing properties of Xdsh, a maternally expressed Xenopus homolog of dishevelled., Sokol SY., Development. June 1, 1995; 121 (6): 1637-47.
	Comparative analysis of Engrailed-1 and Wnt-1 expression in the developing central nervous system of Xenopus laevis., Eizema K., Int J Dev Biol. December 1, 1994; 38 (4): 623-32.
	Xwnt-11: a maternally expressed Xenopus wnt gene., Ku M., Development. December 1, 1993; 119 (4): 1161-73.
	Xwnt-5A: a maternal Wnt that affects morphogenetic movements after overexpression in embryos of Xenopus laevis., Moon RT., Development. September 1, 1993; 119 (1): 97-111.
	Induction of the Xenopus organizer: expression and regulation of Xnot, a novel FGF and activin-regulated homeo box gene., von Dassow G., Genes Dev. March 1, 1993; 7 (3): 355-66.
	Overlapping expression of Xwnt-3A and Xwnt-1 in neural tissue of Xenopus laevis embryos., Wolda SL., Dev Biol. January 1, 1993; 155 (1): 46-57.
	Expression of four zebrafish wnt-related genes during embryogenesis., Krauss S., Development. September 1, 1992; 116 (1): 249-59.

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