???pagination.result.count???
???pagination.result.page???
1
Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation. , Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning. , Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
Xenopus skip modulates Wnt/beta-catenin signaling and functions in neural crest induction. , Wang Y., J Biol Chem. April 2, 2010; 285 (14): 10890-901.
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.
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.
Axis induction by wnt signaling: Target promoter responsiveness regulates competence. , Darken RS ., Dev Biol. June 1, 2001; 234 (1): 42-54.
Expanded retina territory by midbrain transformation upon overexpression of Six6 ( Optx2) in Xenopus embryos. , Bernier G., Mech Dev. May 1, 2000; 93 (1-2): 59-69.
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.
The Xenopus homologue of the Drosophila gene tailless has a function in early eye development. , Hollemann T ., Development. July 1, 1998; 125 (13): 2425-32.