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Summary Anatomy Item Literature (1447) Expression Attributions Wiki
XB-ANAT-10

Papers associated with retina (and tbxt)

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The complete dorsal structure is formed from only the blastocoel roof of Xenopus blastula: insight into the gastrulation movement evolutionarily conserved among chordates., Sato Y., Dev Genes Evol. June 1, 2023; 233 (1): 1-12.                

BAP1 regulates epigenetic switch from pluripotency to differentiation in developmental lineages giving rise to BAP1-mutant cancers., Kuznetsov JN., Sci Adv. September 18, 2019; 5 (9): eaax1738.        

Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G., PLoS Genet. May 12, 2017; 13 (5): e1006757.                                    

Efficient retina formation requires suppression of both Activin and BMP signaling pathways in pluripotent cells., Wong KA., Biol Open. March 6, 2015; 4 (4): 573-83.                

Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.                                          

The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.                                          

Histology of plastic embedded amphibian embryos and larvae., Kurth T., Genesis. March 1, 2012; 50 (3): 235-50.                                

Comparative expression analysis of the H3K27 demethylases, JMJD3 and UTX, with the H3K27 methylase, EZH2, in Xenopus., Kawaguchi A., Int J Dev Biol. January 1, 2012; 56 (4): 295-300.                                          

The RNA-binding protein Xp54nrb isolated from a Ca²+-dependent screen is expressed in neural structures during Xenopus laevis development., Neant I., Int J Dev Biol. January 1, 2011; 55 (10-12): 923-31.        

FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis., Schuff M., Dev Biol. January 15, 2010; 337 (2): 259-73.                  

Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size., Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.                                          

Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis., Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.          

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

Extracellular regulation of developmental cell signaling by XtSulf1., Freeman SD., Dev Biol. August 15, 2008; 320 (2): 436-45.            

The competence of Xenopus blastomeres to produce neural and retinal progeny is repressed by two endo-mesoderm promoting pathways., Yan B., Dev Biol. May 1, 2007; 305 (1): 103-19.        

CHD4/Mi-2beta activity is required for the positioning of the mesoderm/neuroectoderm boundary in Xenopus., Linder B., Genes Dev. April 15, 2007; 21 (8): 973-83.            

Regulation of Xenopus gastrulation by ErbB signaling., Nie S., Dev Biol. March 1, 2007; 303 (1): 93-107.                    

Xnr2 and Xnr5 unprocessed proteins inhibit Wnt signaling upstream of dishevelled., Onuma Y., Dev Dyn. December 1, 2005; 234 (4): 900-10.          

Identification of shared transcriptional targets for the proneural bHLH factors Xath5 and XNeuroD., Logan MA., Dev Biol. September 15, 2005; 285 (2): 570-83.          

Olfactory and lens placode formation is controlled by the hedgehog-interacting protein (Xhip) in Xenopus., Cornesse Y., Dev Biol. January 15, 2005; 277 (2): 296-315.                          

Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways., Moore KB., Dev Cell. January 1, 2004; 6 (1): 55-67.                

Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.              

Coordination of BMP-3b and cerberus is required for head formation of Xenopus embryos., Hino J., Dev Biol. August 1, 2003; 260 (1): 138-57.                            

Integrin-ECM interactions regulate cadherin-dependent cell adhesion and are required for convergent extension in Xenopus., Marsden M., Curr Biol. July 15, 2003; 13 (14): 1182-91.                  

Overexpression of the secreted factor Mig30 expressed in the Spemann organizer impairs morphogenetic movements during Xenopus gastrulation., Hayata T., Mech Dev. March 1, 2002; 112 (1-2): 37-51.                

RGS proteins inhibit Xwnt-8 signaling in Xenopus embryonic development., Wu C., Development. July 1, 2000; 127 (13): 2773-84.    

Xenopus GDF6, a new antagonist of noggin and a partner of BMPs., Chang C., Development. August 1, 1999; 126 (15): 3347-57.              

Tbx5 is essential for heart development., Horb ME., Development. April 1, 1999; 126 (8): 1739-51.              

A single morphogenetic field gives rise to two retina primordia under the influence of the prechordal plate., Li H., Development. February 1, 1997; 124 (3): 603-15.                  

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