Papers associated with pronephric kidney (and ctnnb1)

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	TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B., JCI Insight. November 8, 2023; 8 (21):
	Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):
	Modeling congenital kidney diseases in Xenopus laevis., Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4):
	Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
	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.
	Phosphorylation-dependent ubiquitination of paraxial protocadherin (PAPC) controls gastrulation cell movements., Kai M., PLoS One. January 12, 2015; 10 (1): e0115111.
	The Wnt/JNK signaling target gene alcam is required for embryonic kidney development., Cizelsky W., Development. May 1, 2014; 141 (10): 2064-74.
	FAK transduces extracellular forces that orient the mitotic spindle and control tissue morphogenesis., Petridou NI., Nat Commun. January 1, 2014; 5 5240.
	Vertebrate kidney tubules elongate using a planar cell polarity-dependent, rosette-based mechanism of convergent extension., Lienkamp SS., Nat Genet. December 1, 2012; 44 (12): 1382-7.
	ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P., Cell Rep. May 31, 2012; 1 (5): 516-27.
	Expression analysis of epb41l4a during Xenopus laevis embryogenesis., Guo Y., Dev Genes Evol. June 1, 2011; 221 (2): 113-9.
	Different requirement for Wnt/β-catenin signaling in limb regeneration of larval and adult Xenopus., Yokoyama H., PLoS One. January 1, 2011; 6 (7): e21721.
	Expression of Wnt signaling components during Xenopus pronephros development., Zhang B., PLoS One. January 1, 2011; 6 (10): e26533.
	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.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	Beta-catenin, MAPK and Smad signaling during early Xenopus development., Schohl A., Development. January 1, 2002; 129 (1): 37-52.
	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.
	A cell-free assay system for beta-catenin signaling that recapitulates direct inductive events in the early xenopus laevis embryo., Nelson RW., J Cell Biol. October 18, 1999; 147 (2): 367-74.
	XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development., Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
	The juxtamembrane region of the cadherin cytoplasmic tail supports lateral clustering, adhesive strengthening, and interaction with p120ctn., Yap AS., J Cell Biol. May 4, 1998; 141 (3): 779-89.
	Catenins in Xenopus embryogenesis and their relation to the cadherin-mediated cell-cell adhesion system., Schneider S., Development. June 1, 1993; 118 (2): 629-40.

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