Papers associated with head region (and wnt5a)

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	Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration., Patel JH., Dev Biol. March 1, 2022; 483 157-168.
	FAM46B is a prokaryotic-like cytoplasmic poly(A) polymerase essential in human embryonic stem cells., Hu JL., Nucleic Acids Res. March 18, 2020; 48 (5): 2733-2748.
	Bioinformatics Screening of Genes Specific for Well-Regenerating Vertebrates Reveals c-answer, a Regulator of Brain Development and Regeneration., Korotkova DD., Cell Rep. October 22, 2019; 29 (4): 1027-1040.e6.
	Non-acylated Wnts Can Promote Signaling., Speer KF., Cell Rep. January 22, 2019; 26 (4): 875-883.e5.
	Vestigial-like 3 is a novel Ets1 interacting partner and regulates trigeminal nerve formation and cranial neural crest migration., Simon E., Biol Open. October 15, 2017; 6 (10): 1528-1540.
	Cholesterol-rich membrane microdomains modulate Wnt/β-catenin morphogen gradient during Xenopus development., Reis AH., Mech Dev. November 1, 2016; 142 30-39.
	Lens regeneration from the cornea requires suppression of Wnt/β-catenin signaling., Hamilton PW., Exp Eye Res. April 1, 2016; 145 206-215.
	Sebox regulates mesoderm formation in early amphibian embryos., Chen G., Dev Dyn. November 1, 2015; 244 (11): 1415-26.
	Xenopus Pkdcc1 and Pkdcc2 Are Two New Tyrosine Kinases Involved in the Regulation of JNK Dependent Wnt/PCP Signaling Pathway., Vitorino M., PLoS One. August 13, 2015; 10 (8): e0135504.
	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.
	Cholesterol selectively activates canonical Wnt signalling over non-canonical Wnt signalling., Sheng R., Nat Commun. July 15, 2014; 5 4393.
	Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus., Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
	Calpain2 protease: A new member of the Wnt/Ca(2+) pathway modulating convergent extension movements in Xenopus., Zanardelli S., Dev Biol. December 1, 2013; 384 (1): 83-100.
	Expression of pluripotency factors in larval epithelia of the frog Xenopus: evidence for the presence of cornea epithelial stem cells., Perry KJ., Dev Biol. February 15, 2013; 374 (2): 281-94.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Regulator of G-protein signaling 18 controls megakaryopoiesis and the cilia-mediated vertebrate mechanosensory system., Louwette S., FASEB J. May 1, 2012; 26 (5): 2125-36.
	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.
	Rspo3 binds syndecan 4 and induces Wnt/PCP signaling via clathrin-mediated endocytosis to promote morphogenesis., Ohkawara B., Dev Cell. March 15, 2011; 20 (3): 303-14.
	Wnt5a/Ror2-induced upregulation of xPAPC requires xShcA., Feike AC., Biochem Biophys Res Commun. October 1, 2010; 400 (4): 500-6.
	Oriented cell motility and division underlie early limb bud morphogenesis., Wyngaarden LA., Development. August 1, 2010; 137 (15): 2551-8.
	Overlapping functions of Cdx1, Cdx2, and Cdx4 in the development of the amphibian Xenopus tropicalis., Faas L., Dev Dyn. April 1, 2009; 238 (4): 835-52.
	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.
	Wnt5a and Wnt11 interact in a maternal Dkk1-regulated fashion to activate both canonical and non-canonical signaling in Xenopus axis formation., Cha SW., Development. November 1, 2008; 135 (22): 3719-29.
	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.
	The mother superior mutation ablates foxd3 activity in neural crest progenitor cells and depletes neural crest derivatives in zebrafish., Montero-Balaguer M., Dev Dyn. December 1, 2006; 235 (12): 3199-212.
	Role of crescent in convergent extension movements by modulating Wnt signaling in early Xenopus embryogenesis., Shibata M., Mech Dev. December 1, 2005; 122 (12): 1322-39.
	Xenopus frizzled-4S, a splicing variant of Xfz4 is a context-dependent activator and inhibitor of Wnt/beta-catenin signaling., Swain RK., Cell Commun Signal. October 19, 2005; 3 12.
	Reorganization of actin cytoskeleton by FRIED, a Frizzled-8 associated protein tyrosine phosphatase., Itoh K., Dev Dyn. September 1, 2005; 234 (1): 90-101.
	Mouse Wnt receptor gene Fzd5 is essential for yolk sac and placental angiogenesis., Ishikawa T., Development. January 1, 2001; 128 (1): 25-33.
	Mutual antagonism between dickkopf1 and dickkopf2 regulates Wnt/beta-catenin signalling., Wu W., Curr Biol. December 1, 2000; 10 (24): 1611-4.
	The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.
	The putative wnt receptor Xenopus frizzled-7 functions upstream of beta-catenin in vertebrate dorsoventral mesoderm patterning., Sumanas S., Development. May 1, 2000; 127 (9): 1981-90.
	Keeping a close eye on Wnt-1/wg signaling in Xenopus., Gradl D., Mech Dev. August 1, 1999; 86 (1-2): 3-15.
	Frizzled-8 is expressed in the Spemann organizer and plays a role in early morphogenesis., Deardorff MA., Development. July 1, 1998; 125 (14): 2687-700.
	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.
	In pursuit of the functions of the Wnt family of developmental regulators: insights from Xenopus laevis., Moon RT., Bioessays. February 1, 1993; 15 (2): 91-7.

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