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Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development. , Buisson I ., Dev Biol. January 15, 2015; 397 (2): 175-90.
The Xenopus homologue of Down syndrome critical region protein 6 drives dorsoanterior gene expression and embryonic axis formation by antagonising polycomb group proteins. , Li HY., Development. December 1, 2013; 140 (24): 4903-13.
Vertebrate kidney tubules elongate using a planar cell polarity-dependent, rosette-based mechanism of convergent extension. , Lienkamp SS ., Nat Genet. December 1, 2012; 44 (12): 1382-7.
The involvement of lethal giant larvae and Wnt signaling in bottle cell formation in Xenopus embryos. , Choi SC., Dev Biol. December 1, 2009; 336 (1): 68-75.
Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling. , Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
Mad is required for wingless signaling in wing development and segment patterning in Drosophila. , Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
N- and E-cadherins in Xenopus are specifically required in the neural and non- neural ectoderm, respectively, for F-actin assembly and morphogenetic movements. , Nandadasa S., Development. April 1, 2009; 136 (8): 1327-38.
TBX5 is required for embryonic cardiac cell cycle progression. , Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development. , Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.
Connective- tissue growth factor modulates WNT signalling and interacts with the WNT receptor complex. , Mercurio S., Development. May 1, 2004; 131 (9): 2137-47.