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Activation of a T-box- Otx2- Gsc gene network independent of TBP and TBP-related factors. , Gazdag E., Development. April 15, 2016; 143 (8): 1340-50.
Hspa9 is required for pronephros specification and formation in Xenopus laevis. , Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning. , Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
TRPP2-dependent Ca2+ signaling in dorso- lateral mesoderm is required for kidney field establishment in Xenopus. , Futel M., J Cell Sci. March 1, 2015; 128 (5): 888-99.
Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development. , Buisson I ., Dev Biol. January 15, 2015; 397 (2): 175-90.
Heat shock 70-kDa protein 5 ( Hspa5) is essential for pronephros formation by mediating retinoic acid signaling. , Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.
Comparative expression analysis of cysteine-rich intestinal protein family members crip1, 2 and 3 during Xenopus laevis embryogenesis. , Hempel A., Int J Dev Biol. January 1, 2014; 58 (10-12): 841-9.
Regulation of primitive hematopoiesis by class I histone deacetylases. , Shah RR., Dev Dyn. February 1, 2013; 242 (2): 108-21.
Comparative Functional Analysis of ZFP36 Genes during Xenopus Development. , Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.
Microarray-based identification of Pitx3 targets during Xenopus embryogenesis. , Hooker L., Dev Dyn. September 1, 2012; 241 (9): 1487-505.
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 as a model system for the study of GOLPH2/ GP73 function: Xenopus GOLPH2 is required for pronephros development. , Li L., PLoS One. January 1, 2012; 7 (6): e38939.
mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/ nodal signaling in Xenopus ectodermal cells. , Miyazaki A., PLoS One. January 1, 2012; 7 (10): e46630.
The nephrogenic potential of the transcription factors osr1, osr2, hnf1b, lhx1 and pax8 assessed in Xenopus animal caps. , Drews C., BMC Dev Biol. January 31, 2011; 11 5.
Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2. , Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis. , Lee SJ., Mech Dev. January 1, 2010; 127 (1-2): 49-61.
The miR-30 miRNA family regulates Xenopus pronephros development and targets the transcription factor Xlim1/ Lhx1. , Agrawal R ., Development. December 1, 2009; 136 (23): 3927-36.
Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system. , Strate I., Development. February 1, 2009; 136 (3): 461-72.
Hex acts with beta-catenin to regulate anteroposterior patterning via a Groucho-related co-repressor and Nodal. , Zamparini AL., Development. September 1, 2006; 133 (18): 3709-22.
The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo. , Collart C ., Development. October 1, 2005; 132 (20): 4575-86.
New roles for FoxH1 in patterning the early embryo. , Kofron M ., Development. October 1, 2004; 131 (20): 5065-78.
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.
The germ cell nuclear factor is required for retinoic acid signaling during Xenopus development. , Barreto G., Mech Dev. April 1, 2003; 120 (4): 415-28.
The roles of three signaling pathways in the formation and function of the Spemann Organizer. , Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.
Antisense inhibition of Xbrachyury impairs mesoderm formation in Xenopus embryos. , Giovannini N., Dev Growth Differ. April 1, 2002; 44 (2): 147-59.
Synthesis and release of activin and noggin by cultured human amniotic epithelial cells. , Koyano S., Dev Growth Differ. April 1, 2002; 44 (2): 103-12.
Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis. , Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.
A study of Xlim1 function in the Spemann-Mangold organizer. , Kodjabachian L ., Int J Dev Biol. January 1, 2001; 45 (1): 209-18.
A role for Xlim-1 in pronephros development in Xenopus laevis. , Chan TC ., Dev Biol. December 15, 2000; 228 (2): 256-69.
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.
XIPOU 2 is a potential regulator of Spemann's Organizer. , Witta SE., Development. March 1, 1997; 124 (6): 1179-89.
XIPOU 2, a noggin-inducible gene, has direct neuralizing activity. , Witta SE., Development. March 1, 1995; 121 (3): 721-30.