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Summary Expression Phenotypes Gene Literature (37) GO Terms (3) Nucleotides (116) Proteins (58) Interactants (277) Wiki
XB--490755

Papers associated with rbpj (and morpholino)



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The Prdm13 histone methyltransferase encoding gene is a Ptf1a-Rbpj downstream target that suppresses glutamatergic and promotes GABAergic neuronal fate in the dorsal neural tube., Hanotel J, Bessodes N, Thélie A, Hedderich M, Parain K, Van Driessche B, Brandão Kde O, Kricha S, Jorgensen MC, Grapin-Botton A, Serup P, Van Lint C, Perron M, Pieler T, Henningfeld KA, Bellefroid EJ., Dev Biol. February 15, 2014; 386 (2): 340-57.                                                                    

A gene regulation network controlled by Celf1 protein-rbpj mRNA interaction in Xenopus somite segmentation., Cibois M, Gautier-Courteille C, Kodjabachian L, Paillard L., Biol Open. August 21, 2013; 2 (10): 1078-83.          

Dishevelled limits Notch signalling through inhibition of CSL., Collu GM, Hidalgo-Sastre A, Acar A, Bayston L, Gildea C, Leverentz MK, Mills CG, Owens TW, Meurette O, Dorey K, Brennan K., Development. December 1, 2012; 139 (23): 4405-15.      

Notch destabilises maternal beta-catenin and restricts dorsal-anterior development in Xenopus., Acosta H, López SL, Revinski DR, Carrasco AE., Development. June 1, 2011; 138 (12): 2567-79.                          

Perturbation of Notch/Suppressor of Hairless pathway disturbs migration of primordial germ cells in Xenopus embryo., Morichika K, Kataoka K, Terayama K, Tazaki A, Kinoshita T, Watanabe K, Mochii M., Dev Growth Differ. February 1, 2010; 52 (2): 235-44.

XSu(H)2 is an essential factor for gene expression and morphogenesis of the Xenopus gastrula embryo., Ito M, Katada T, Miyatani S, Kinoshita T., Int J Dev Biol. January 1, 2007; 51 (1): 27-36.            

EDEN-BP-dependent post-transcriptional regulation of gene expression in Xenopus somitic segmentation., Gautier-Courteille C, Gautier-Courteille C, Le Clainche C, Barreau C, Audic Y, Graindorge A, Maniey D, Osborne HB, Paillard L., Development. December 1, 2004; 131 (24): 6107-17.                  

A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos., Stancheva I, Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR., Mol Cell. August 1, 2003; 12 (2): 425-35.                          

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