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Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula. , Ding Y ., Dev Biol. June 15, 2017; 426 (2): 176-187.
A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo. , Blitz IL ., Dev Biol. June 15, 2017; 426 (2): 409-417.
Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos. , Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
Regulation of nodal and BMP signaling by tomoregulin-1 ( X7365) through novel mechanisms. , Chang C ., Dev Biol. March 1, 2003; 255 (1): 1-11.
Antimorphic PV.1 causes secondary axis by inducing ectopic organizer. , Hwang YS., Biochem Biophys Res Commun. April 12, 2002; 292 (4): 1081-6.
The role of BMP signaling in outgrowth and patterning of the Xenopus tail bud. , Beck CW ., Dev Biol. October 15, 2001; 238 (2): 303-14.
Xenopus embryonic E2F is required for the formation of ventral and posterior cell fates during early embryogenesis. , Suzuki A ., Mol Cell. February 1, 2000; 5 (2): 217-29.
Requirement for Xvent-1 and Xvent-2 gene function in dorsoventral patterning of Xenopus mesoderm. , Onichtchouk D., Development. April 1, 1998; 125 (8): 1447-56.
XBMPRII, a novel Xenopus type II receptor mediating BMP signaling in embryonic tissues. , Frisch A., Development. February 1, 1998; 125 (3): 431-42.
The Xvent-2 homeobox gene is part of the BMP-4 signalling pathway controlling [correction of controling] dorsoventral patterning of Xenopus mesoderm. , Onichtchouk D., Development. October 1, 1996; 122 (10): 3045-53.
Xenopus mothers against decapentaplegic is an embryonic ventralizing agent that acts downstream of the BMP-2/4 receptor. , Thomsen GH ., Development. August 1, 1996; 122 (8): 2359-66.
A novel homeobox gene PV.1 mediates induction of ventral mesoderm in Xenopus embryos. , Ault KT., Proc Natl Acad Sci U S A. June 25, 1996; 93 (13): 6415-20.
Localized BMP-4 mediates dorsal/ ventral patterning in the early Xenopus embryo. , Schmidt JE., Dev Biol. May 1, 1995; 169 (1): 37-50.