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Cdc2-like kinase 2 (Clk2) promotes early neural development in Xenopus embryos. , Virgirinia RP., Dev Growth Differ. August 1, 2019; 61 (6): 365-377.
Lineage commitment of embryonic cells involves MEK1-dependent clearance of pluripotency regulator Ventx2. , Scerbo P ., Elife. June 27, 2017; 6
sall1 and sall4 repress pou5f3 family expression to allow neural patterning, differentiation, and morphogenesis in Xenopus laevis. , Exner CRT., Dev Biol. May 1, 2017; 425 (1): 33-43.
NEURODEVELOPMENT. Shared regulatory programs suggest retention of blastula-stage potential in neural crest cells. , Buitrago-Delgado E., Science. June 19, 2015; 348 (6241): 1332-5.
Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus. , Young JJ ., Development. April 1, 2014; 141 (8): 1683-93.
A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance. , Livigni A., Curr Biol. November 18, 2013; 23 (22): 2233-2244.
Suv4-20h histone methyltransferases promote neuroectodermal differentiation by silencing the pluripotency-associated Oct-25 gene. , Nicetto D., PLoS Genet. January 1, 2013; 9 (1): e1003188.
Transdifferentiation from cornea to lens in Xenopus laevis depends on BMP signalling and involves upregulation of Wnt signalling. , Day RC., BMC Dev Biol. January 26, 2011; 11 54.
Geminin cooperates with Polycomb to restrain multi-lineage commitment in the early embryo. , Lim JW., Development. January 1, 2011; 138 (1): 33-44.
The Xenopus POU class V transcription factor XOct-25 inhibits ectodermal competence to respond to bone morphogenetic protein-mediated embryonic induction. , Takebayashi-Suzuki K., Mech Dev. January 1, 2007; 124 (11-12): 840-55.
Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development. , Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.
The POU factor Oct-25 regulates the Xvent-2B gene and counteracts terminal differentiation in Xenopus embryos. , Cao Y , Cao Y ., J Biol Chem. October 15, 2004; 279 (42): 43735-43.