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Nephron Patterning: Lessons from Xenopus, Zebrafish, and Mouse Studies. , Desgrange A., Cells. September 11, 2015; 4 (3): 483-99.
Activin ligands are required for the re-activation of Smad2 signalling after neurulation and vascular development in Xenopus tropicalis. , Nagamori Y., Int J Dev Biol. January 1, 2014; 58 (10-12): 783-91.
TMEPAI, a transmembrane TGF-beta-inducible protein, sequesters Smad proteins from active participation in TGF-beta signaling. , Watanabe Y., Mol Cell. January 15, 2010; 37 (1): 123-34.
Action range of BMP is defined by its N-terminal basic amino acid core. , Ohkawara B., Curr Biol. February 5, 2002; 12 (3): 205-9.
Multigenic control of the localization of the zone of polarizing activity in limb morphogenesis in the mouse. , Masuya H., Dev Biol. February 1, 1997; 182 (1): 42-51.
Trefoil peptides: a newly recognized family of epithelial mucin-associated molecules. , Poulsom R., Am J Physiol. August 1, 1993; 265 (2 Pt 1): G205-13.
xP1 and xP4. P-domain peptides expressed in Xenopus laevis stomach mucosa. , Hauser F., J Biol Chem. November 5, 1991; 266 (31): 21306-9.
Dermal glands of Xenopus laevis contain a polypeptide with a highly repetitive amino acid sequence. , Gmachl M., FEBS Lett. January 15, 1990; 260 (1): 145-8.
A new family of growth factor-like peptides. 'Trefoil' disulphide loop structures as a common feature in breast cancer associated peptide (pS2), pancreatic spasmolytic polypeptide (PSP), and frog skin peptides (spasmolysins). , Thim L., FEBS Lett. June 19, 1989; 250 (1): 85-90.