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The role of Xenopus developmental biology in unraveling Wnt signalling and antero- posterior axis formation. , Niehrs C ., Dev Biol. February 1, 2022; 482 1-6.
The RNF146 E3 ubiquitin ligase is required for the control of Wnt signaling and body pattern formation in Xenopus. , Zhu X., Mech Dev. October 1, 2017; 147 28-36.
Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells. , Zhang Z ., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula. , Ding Y ., Dev Biol. June 15, 2017; 426 (2): 176-187.
The phosphatase Pgam5 antagonizes Wnt/ β-Catenin signaling in embryonic anterior- posterior axis patterning. , Rauschenberger V., Development. June 15, 2017; 144 (12): 2234-2247.
Folate receptor 1 is necessary for neural plate cell apical constriction during Xenopus neural tube formation. , Balashova OA., Development. April 15, 2017; 144 (8): 1518-1530.
Xenopus Pkdcc1 and Pkdcc2 Are Two New Tyrosine Kinases Involved in the Regulation of JNK Dependent Wnt/PCP Signaling Pathway. , Vitorino M., PLoS One. August 13, 2015; 10 (8): e0135504.
Klhl31 attenuates β-catenin dependent Wnt signaling and regulates embryo myogenesis. , Abou-Elhamd A., Dev Biol. June 1, 2015; 402 (1): 61-71.
Spatial and temporal aspects of Wnt signaling and planar cell polarity during vertebrate embryonic development. , Sokol SY ., Semin Cell Dev Biol. June 1, 2015; 42 78-85.
Planar polarization of Vangl2 in the vertebrate neural plate is controlled by Wnt and Myosin II signaling. , Ossipova O., Biol Open. April 24, 2015; 4 (6): 722-30.
ATP4 and ciliation in the neuroectoderm and endoderm of Xenopus embryos and tadpoles. , Walentek P ., Data Brief. April 20, 2015; 4 22-31.
Early development of the neural plate: new roles for apoptosis and for one of its main effectors caspase-3. , Juraver-Geslin HA ., Genesis. February 1, 2015; 53 (2): 203-24.
Fezf2 promotes neuronal differentiation through localised activation of Wnt/ β-catenin signalling during forebrain development. , Zhang S ., Development. December 1, 2014; 141 (24): 4794-805.
The conserved barH-like homeobox-2 gene barhl2 acts downstream of orthodentricle-2 and together with iroquois-3 in establishment of the caudal forebrain signaling center induced by Sonic Hedgehog. , Juraver-Geslin HA ., Dev Biol. December 1, 2014; 396 (1): 107-20.
FAK is required for tension-dependent organization of collective cell movements in Xenopus mesendoderm. , Bjerke MA., Dev Biol. October 15, 2014; 394 (2): 340-56.
The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish. , Young T., Development. September 1, 2014; 141 (18): 3505-16.
Maternal syntabulin is required for dorsal axis formation and is a germ plasm component in Xenopus. , Colozza G ., Differentiation. July 1, 2014; 88 (1): 17-26.
Role of Rab11 in planar cell polarity and apical constriction during vertebrate neural tube closure. , Ossipova O., Nat Commun. May 13, 2014; 5 3734.
PTK7 modulates Wnt signaling activity via LRP6. , Bin-Nun N., Development. January 1, 2014; 141 (2): 410-21.
A secreted splice variant of the Xenopus frizzled-4 receptor is a biphasic modulator of Wnt signalling. , Gorny AK., Cell Commun Signal. November 19, 2013; 11 89.
Neurulation and neurite extension require the zinc transporter ZIP12 ( slc39a12). , Chowanadisai W., Proc Natl Acad Sci U S A. June 11, 2013; 110 (24): 9903-8.
Retinoic acid-activated Ndrg1a represses Wnt/ β-catenin signaling to allow Xenopus pancreas, oesophagus, stomach, and duodenum specification. , Zhang T., PLoS One. May 15, 2013; 8 (5): e65058.
Ptk7 promotes non-canonical Wnt/PCP-mediated morphogenesis and inhibits Wnt/ β-catenin-dependent cell fate decisions during vertebrate development. , Hayes M., Development. April 1, 2013; 140 (8): 1807-18.
Current perspectives of the signaling pathways directing neural crest induction. , Stuhlmiller TJ., Cell Mol Life Sci. November 1, 2012; 69 (22): 3715-37.
ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left- right development. , Walentek P ., Cell Rep. May 31, 2012; 1 (5): 516-27.
Serotonin signaling is required for Wnt-dependent GRP specification and leftward flow in Xenopus. , Beyer T., Curr Biol. January 10, 2012; 22 (1): 33-9.
CRIM1 complexes with ß-catenin and cadherins, stabilizes cell-cell junctions and is critical for neural morphogenesis. , Ponferrada VG ., PLoS One. January 1, 2012; 7 (3): e32635.
Effects of natural compounds on Xenopus embryogenesis: a potential read out for functional drug discovery targeting Wnt/ β-catenin signaling. , Amado NG., Curr Top Med Chem. January 1, 2012; 12 (19): 2103-13.
The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo. , Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.
Expression analysis of epb41l4a during Xenopus laevis embryogenesis. , Guo Y., Dev Genes Evol. June 1, 2011; 221 (2): 113-9.
Barhl2 limits growth of the diencephalic primordium through Caspase3 inhibition of beta-catenin activation. , Juraver-Geslin HA ., Proc Natl Acad Sci U S A. February 8, 2011; 108 (6): 2288-93.
Strange as it may seem: the many links between Wnt signaling, planar cell polarity, and cilia. , Wallingford JB ., Genes Dev. February 1, 2011; 25 (3): 201-13.
Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo. , Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
Collective chemotaxis requires contact-dependent cell polarity. , Theveneau E ., Dev Cell. July 20, 2010; 19 (1): 39-53.
MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization. , Suzuki M ., Development. July 1, 2010; 137 (14): 2329-39.
Nectin-2 and N-cadherin interact through extracellular domains and induce apical accumulation of F-actin in apical constriction of Xenopus neural tube morphogenesis. , Morita H., Development. April 1, 2010; 137 (8): 1315-25.
Bone morphogenetic protein 15 ( BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis. , Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
Retinoid signaling can repress blastula Wnt signaling and impair dorsal development in Xenopus embryo. , Li S., Differentiation. October 1, 2008; 76 (8): 897-907.
TBX5 is required for embryonic cardiac cell cycle progression. , Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
A requirement for NF-protocadherin and TAF1/Set in cell adhesion and neural tube formation. , Rashid D., Dev Biol. March 1, 2006; 291 (1): 170-81.
HIC-5 is a novel repressor of lymphoid enhancer factor/T-cell factor-driven transcription. , Ghogomu SM., J Biol Chem. January 20, 2006; 281 (3): 1755-64.
PR72, a novel regulator of Wnt signaling required for Naked cuticle function. , Creyghton MP., Genes Dev. February 1, 2005; 19 (3): 376-86.
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.
Beta-catenin, MAPK and Smad signaling during early Xenopus development. , Schohl A ., Development. January 1, 2002; 129 (1): 37-52.
The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling. , Domingos PM ., Dev Biol. November 1, 2001; 239 (1): 148-60.
XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development. , Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
Sizzled: a secreted Xwnt8 antagonist expressed in the ventral marginal zone of Xenopus embryos. , Salic AN., Development. December 1, 1997; 124 (23): 4739-48.
A role for Siamois in Spemann organizer formation. , Fan MJ., Development. July 1, 1997; 124 (13): 2581-9.
Analysis of Dishevelled signalling pathways during Xenopus development. , Sokol SY ., Curr Biol. November 1, 1996; 6 (11): 1456-67.
Beta-catenin localization during Xenopus embryogenesis: accumulation at tissue and somite boundaries. , Fagotto F ., Development. December 1, 1994; 120 (12): 3667-79.