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Summary Anatomy Item Literature (1369) Expression Attributions Wiki
XB-ANAT-247

Papers associated with neural plate (and wnt1)

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Xenopus leads the way: Frogs as a pioneering model to understand the human brain., Exner CRT., Genesis. February 1, 2021; 59 (1-2): e23405.          


MiR-9 and the Midbrain-Hindbrain Boundary: A Showcase for the Limited Functional Conservation and Regulatory Complexity of MicroRNAs., Alwin Prem Anand A., Front Cell Dev Biol. January 1, 2020; 8 586158.  


The neural border: Induction, specification and maturation of the territory that generates neural crest cells., Pla P., Dev Biol. December 1, 2018; 444 Suppl 1 S36-S46.    


An atlas of Wnt activity during embryogenesis in Xenopus tropicalis., Borday C., PLoS One. January 1, 2018; 13 (4): e0193606.                


Znf703, a novel target of Pax3 and Zic1, regulates hindbrain and neural crest development in Xenopus., Hong CS., Genesis. December 1, 2017; 55 (12):                               


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.                      


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.                        


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.                            


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.        


Pax3 and Zic1 trigger the early neural crest gene regulatory network by the direct activation of multiple key neural crest specifiers., Plouhinec JL., Dev Biol. February 15, 2014; 386 (2): 461-72.                                            


Xenopus Nkx6.1 and Nkx6.2 are required for mid-hindbrain boundary development., Ma P., Dev Genes Evol. July 1, 2013; 223 (4): 253-9.


Signaling and transcriptional regulation in neural crest specification and migration: lessons from xenopus embryos., Pegoraro C., Wiley Interdiscip Rev Dev Biol. January 1, 2013; 2 (2): 247-59.      


Current perspectives of the signaling pathways directing neural crest induction., Stuhlmiller TJ., Cell Mol Life Sci. November 1, 2012; 69 (22): 3715-37.          


Microarray-based identification of Pitx3 targets during Xenopus embryogenesis., Hooker L., Dev Dyn. September 1, 2012; 241 (9): 1487-505.                          


MicroRNA-9 reveals regional diversity of neural progenitors along the anterior-posterior axis., Bonev B., Dev Cell. January 18, 2011; 20 (1): 19-32.              


Anterior neural development requires Del1, a matrix-associated protein that attenuates canonical Wnt signaling via the Ror2 pathway., Takai A., Development. October 1, 2010; 137 (19): 3293-302.            


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.                                                


The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx., Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.                


Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal., Rhinn M., Neural Dev. April 2, 2009; 4 12.              


Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.                    


Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus., Park BY., Dev Biol. December 1, 2008; 324 (1): 108-21.      


Modulating the activity of neural crest regulatory factors., Taylor KM., Curr Opin Genet Dev. August 1, 2007; 17 (4): 326-31.  


The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border., Hong CS., Mol Biol Cell. June 1, 2007; 18 (6): 2192-202.                


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.      


The zic1 gene is an activator of Wnt signaling., Merzdorf CS., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.              


Early steps in neural crest specification., Barembaum M., Semin Cell Dev Biol. December 1, 2005; 16 (6): 642-6.      


An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation., Matsuo-Takasaki M., Development. September 1, 2005; 132 (17): 3885-94.                      


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.                          


Xenopus XsalF: anterior neuroectodermal specification by attenuating cellular responsiveness to Wnt signaling., Onai T., Dev Cell. July 1, 2004; 7 (1): 95-106.            


Expression analysis of chick Wnt and frizzled genes and selected inhibitors in early chick patterning., Chapman SC., Dev Dyn. March 1, 2004; 229 (3): 668-76.


PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J., Development. December 1, 2003; 130 (23): 5569-78.            


The homeoprotein Xiro1 is required for midbrain-hindbrain boundary formation., Glavic A., Development. April 1, 2002; 129 (7): 1609-21.                  


Gbx2 interacts with Otx2 and patterns the anterior-posterior axis during gastrulation in Xenopus., Tour E., Mech Dev. March 1, 2002; 112 (1-2): 141-51.      


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.                


The midbrain-hindbrain boundary genetic cascade is activated ectopically in the diencephalon in response to the widespread expression of one of its components, the medaka gene Ol-eng2., Ristoratore F., Development. September 1, 1999; 126 (17): 3769-79.


Neural crest induction by Xwnt7B in Xenopus., Chang C., Dev Biol. February 1, 1998; 194 (1): 129-34.      


Xwnt-2b is a novel axis-inducing Xenopus Wnt, which is expressed in embryonic brain., Landesman Y., Mech Dev. May 1, 1997; 63 (2): 199-209.            


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.                


Ectopic expression of the proto-oncogene int-1 in Xenopus embryos leads to duplication of the embryonic axis., McMahon AP., Cell. September 22, 1989; 58 (6): 1075-84.                

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