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Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos. , Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling. , Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
Klf4 is required for germ-layer differentiation and body axis patterning during Xenopus embryogenesis. , Cao Q., Development. November 1, 2012; 139 (21): 3950-61.
Conservation and evolutionary divergence in the activity of receptor-regulated smads. , Sorrentino GM ., Evodevo. October 1, 2012; 3 (1): 22.
Self-regulation of the head-inducing properties of the Spemann organizer. , Inui M., Proc Natl Acad Sci U S A. September 18, 2012; 109 (38): 15354-9.
Dynamic in vivo binding of transcription factors to cis-regulatory modules of cer and gsc in the stepwise formation of the Spemann-Mangold organizer. , Sudou N ., Development. May 1, 2012; 139 (9): 1651-61.
A gene regulatory network controlling hhex transcription in the anterior endoderm of the organizer. , Rankin SA , Rankin SA ., Dev Biol. March 15, 2011; 351 (2): 297-310.
Mix.1/2-dependent control of FGF availability during gastrulation is essential for pronephros development in Xenopus. , Colas A., Dev Biol. August 15, 2008; 320 (2): 351-65.
Sumoylation differentially regulates Goosecoid-mediated transcriptional repression. , Izzi L., Exp Cell Res. April 15, 2008; 314 (7): 1585-94.
Expression of Siamois and Twin in the blastula Chordin/ Noggin signaling center is required for brain formation in Xenopus laevis embryos. , Ishibashi H., Mech Dev. January 1, 2008; 125 (1-2): 58-66.
Xenopus glucose transporter 1 (xGLUT1) is required for gastrulation movement in Xenopus laevis. , Suzawa K ., Int J Dev Biol. January 1, 2007; 51 (3): 183-90.
The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos. , Callery EM ., Dev Biol. February 15, 2005; 278 (2): 542-59.
Shisa promotes head formation through the inhibition of receptor protein maturation for the caudalizing factors, Wnt and FGF. , Yamamoto A., Cell. January 28, 2005; 120 (2): 223-35.
Selective degradation of excess Ldb1 by Rnf12/ RLIM confers proper Ldb1 expression levels and Xlim-1/ Ldb1 stoichiometry in Xenopus organizer functions. , Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.
Molecular link in the sequential induction of the Spemann organizer: direct activation of the cerberus gene by Xlim-1, Xotx2, Mix.1, and Siamois, immediately downstream from Nodal and Wnt signaling. , Yamamoto S., Dev Biol. May 1, 2003; 257 (1): 190-204.
Molecular regulation of vertebrate early endoderm development. , Shivdasani RA ., Dev Biol. September 15, 2002; 249 (2): 191-203.
Effects of heterodimerization and proteolytic processing on Derrière and Nodal activity: implications for mesoderm induction in Xenopus. , Eimon PM., Development. July 1, 2002; 129 (13): 3089-103.
FGF signaling restricts the primary blood islands to ventral mesoderm. , Kumano G ., Dev Biol. December 15, 2000; 228 (2): 304-14.
Cngsc, a homologue of goosecoid, participates in the patterning of the head, and is expressed in the organizer region of Hydra. , Broun M., Development. December 1, 1999; 126 (23): 5245-54.
Characterization of CMIX, a chicken homeobox gene related to the Xenopus gene mix.1. , Peale FV., Mech Dev. July 1, 1998; 75 (1-2): 167-70.
Competition between noggin and bone morphogenetic protein 4 activities may regulate dorsalization during Xenopus development. , Re'em-Kalma Y., Proc Natl Acad Sci U S A. December 19, 1995; 92 (26): 12141-5.