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Furry is required for cell movements during gastrulation and functionally interacts with NDR1. , Cervino AS., Sci Rep. March 23, 2021; 11 (1): 6607.
Modeling endoderm development and disease in Xenopus. , Edwards NA ., Curr Top Dev Biol. January 1, 2021; 145 61-90.
CRISPRscan: designing highly efficient sgRNAs for CRISPR-Cas9 targeting in vivo. , Moreno-Mateos MA., Nat Methods. October 1, 2015; 12 (10): 982-8.
Global identification of Smad2 and Eomesodermin targets in zebrafish identifies a conserved transcriptional network in mesendoderm and a novel role for Eomesodermin in repression of ectodermal gene expression. , Nelson AC., BMC Biol. October 3, 2014; 12 81.
Retinoic acid-activated Ndrg1a represses Wnt/ β-catenin signaling to allow Xenopus pancreas, oesophagus, stomach, and duodenum specification. , Zhang T., PLoS One. May 15, 2013; 8 (5): e65058.
In vitro organogenesis from undifferentiated cells in Xenopus. , Asashima M ., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
Regulatory targets for transcription factor AP2 in Xenopus embryos. , Luo T., Dev Growth Differ. August 1, 2005; 47 (6): 403-13.
Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays. , Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.
Identification and characterization of Xenopus NDRG1. , Kyuno J ., Biochem Biophys Res Commun. September 12, 2003; 309 (1): 52-7.
Novel gene expression domains reveal early patterning of the Xenopus endoderm. , Costa RM ., Gene Expr Patterns. August 1, 2003; 3 (4): 509-19.