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Summary Anatomy Item Literature (1738) Expression Attributions Wiki
XB-ANAT-15

Papers associated with midbrain (and nodal)

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Segregation of brain and organizer precursors is differentially regulated by Nodal signaling at blastula stage., Castro Colabianchi AM., Biol Open. February 25, 2021; 10 (2):                 


Pinhead signaling regulates mesoderm heterogeneity via the FGF receptor-dependent pathway., Ossipova O., Development. September 11, 2020; 147 (17):                 


Apcdd1 is a dual BMP/Wnt inhibitor in the developing nervous system and skin., Vonica A., Dev Biol. August 1, 2020; 464 (1): 71-87.      


Pinhead signaling regulates mesoderm heterogeneity via FGF receptor-dependent pathway., Ossipova O., Development. January 1, 2020;                                       


RAPGEF5 Regulates Nuclear Translocation of β-Catenin., Griffin JN., Dev Cell. January 22, 2018; 44 (2): 248-260.e4.                                                


Maternal Gdf3 is an obligatory cofactor in Nodal signaling for embryonic axis formation in zebrafish., Bisgrove BW., Elife. November 15, 2017; 6                 


Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates., Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.                                


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.                                    


Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.                                    


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


Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling., Bates TJ., Development. October 1, 2013; 140 (20): 4177-81.              


Regulation of early xenopus embryogenesis by Smad ubiquitination regulatory factor 2., Das S., Dev Dyn. August 1, 2012; 241 (8): 1260-73.                    


Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.                      


Serotonin signaling is required for Wnt-dependent GRP specification and leftward flow in Xenopus., Beyer T., Curr Biol. January 10, 2012; 22 (1): 33-9.                


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.                                                


PRDC regulates placode neurogenesis in chick by modulating BMP signalling., Kriebitz NN., Dev Biol. December 15, 2009; 336 (2): 280-92.  


Expression of Siamois and Twin in the blastula Chordin/Noggin signaling center is required for brain formation in Xenopus laevis embryos., Ishibashi H., Mech Dev. January 1, 2008; 125 (1-2): 58-66.              


The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.              


Cloning and expression of a zebrafish SCN1B ortholog and identification of a species-specific splice variant., Fein AJ., BMC Genomics. May 16, 2007; 8 226.                      


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.        


PP2A:B56epsilon is required for eye induction and eye field separation., Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.                  


SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C., Dev Dyn. December 1, 2005; 234 (4): 878-91.                    


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.                          


Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.                


Regulation of vertebrate eye development by Rx genes., Bailey TJ., Int J Dev Biol. January 1, 2004; 48 (8-9): 761-70.    


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.                            


Regulation of nodal and BMP signaling by tomoregulin-1 (X7365) through novel mechanisms., Chang C., Dev Biol. March 1, 2003; 255 (1): 1-11.                    


Wnt8 is required in lateral mesendodermal precursors for neural posteriorization in vivo., Erter CE., Development. September 1, 2001; 128 (18): 3571-83.


Mesendoderm induction and reversal of left-right pattern by mouse Gdf1, a Vg1-related gene., Wall NA., Dev Biol. November 15, 2000; 227 (2): 495-509.              


Zebrafish Dkk1, induced by the pre-MBT Wnt signaling, is secreted from the prechordal plate and patterns the anterior neural plate., Shinya M., Mech Dev. November 1, 2000; 98 (1-2): 3-17.


The HMG-box transcription factor XTcf-4 demarcates the forebrain-midbrain boundary., König A., Mech Dev. May 1, 2000; 93 (1-2): 211-4.    


Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.                


derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.                    

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