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Retinoic acid control of pax8 during renal specification of Xenopus pronephros involves hox and meis3. , Durant-Vesga J., Dev Biol. January 1, 2023; 493 17-28.
Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome. , Adams DS ., J Physiol. June 15, 2016; 594 (12): 3245-70.
Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites. , Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.
Chibby functions in Xenopus ciliary assembly, embryonic development, and the regulation of gene expression. , Shi J., Dev Biol. November 15, 2014; 395 (2): 287-98.
The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling. , Iwasaki Y ., Development. October 1, 2014; 141 (19): 3740-51.
Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning. , Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.
In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency. , Gentsch GE ., Cell Rep. September 26, 2013; 4 (6): 1185-96.
Retinoic acid-dependent control of MAP kinase phosphatase-3 is necessary for early kidney development in Xenopus. , Le Bouffant R ., Biol Cell. September 1, 2012; 104 (9): 516-32.
RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm. , Janesick A ., Development. March 1, 2012; 139 (6): 1213-24.
Transdifferentiation from cornea to lens in Xenopus laevis depends on BMP signalling and involves upregulation of Wnt signalling. , Day RC., BMC Dev Biol. January 26, 2011; 11 54.
Different requirement for Wnt/ β-catenin signaling in limb regeneration of larval and adult Xenopus. , Yokoyama H., PLoS One. January 1, 2011; 6 (7): e21721.
Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus. , Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.
Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2. , Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
Dazap2 is required for FGF-mediated posterior neural patterning, independent of Wnt and Cdx function. , Roche DD., Dev Biol. September 1, 2009; 333 (1): 26-36.
Temporal and spatial expression of FGF ligands and receptors during Xenopus development. , Lea R., Dev Dyn. June 1, 2009; 238 (6): 1467-79.
FGF signalling during embryo development regulates cilia length in diverse epithelia. , Neugebauer JM., Nature. April 2, 2009; 458 (7238): 651-4.
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.
Binding of sFRP-3 to EGF in the extra-cellular space affects proliferation, differentiation and morphogenetic events regulated by the two molecules. , Scardigli R., PLoS One. June 18, 2008; 3 (6): e2471.
A ubiquitin-conjugating enzyme, ube2d3.2, regulates xMLK2 and pronephros formation in Xenopus. , Jean S., Differentiation. April 1, 2008; 76 (4): 431-41.
Enhanced sensitivity and stability in two-color in situ hybridization by means of a novel chromagenic substrate combination. , Hurtado R., Dev Dyn. October 1, 2006; 235 (10): 2811-6.
FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development. , Urban AE ., Dev Biol. September 1, 2006; 297 (1): 103-17.
Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity. , Suga A., Dev Biol. July 1, 2006; 295 (1): 26-39.
Expression patterns of Xenopus FGF receptor-like 1/ nou-darake in early Xenopus development resemble those of planarian nou-darake and Xenopus FGF8. , Hayashi S., Dev Dyn. August 1, 2004; 230 (4): 700-7.
FGF-8 is associated with anteroposterior patterning and limb regeneration in Xenopus. , Christen B ., Dev Biol. December 15, 1997; 192 (2): 455-66.