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Rab7 is required for mesoderm patterning and gastrulation in Xenopus. , Kreis J., Biol Open. July 15, 2021; 10 (7):
Xenopus gpx3 Mediates Posterior Development by Regulating Cell Death during Embryogenesis. , Lee H , Lee H ., Antioxidants (Basel). December 12, 2020; 9 (12):
Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos. , Lichtig H., Front Physiol. January 1, 2020; 11 75.
Shared evolutionary origin of vertebrate neural crest and cranial placodes. , Horie R., Nature. August 1, 2018; 560 (7717): 228-232.
RAPGEF5 Regulates Nuclear Translocation of β-Catenin. , Griffin JN., Dev Cell. January 22, 2018; 44 (2): 248-260.e4.
Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover. , Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.
RARβ2 is required for vertebrate somitogenesis. , Janesick A ., Development. June 1, 2017; 144 (11): 1997-2008.
FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue. , Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
Specification of anteroposterior axis by combinatorial signaling during Xenopus development. , Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation. , Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus. , Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.
Global identification of Smad2 and Eomesodermin targets in zebrafish identifies a conserved transcriptional network in mesendoderm and a novel role for Eomesodermin in repression of ectodermal gene expression. , Nelson AC., BMC Biol. October 3, 2014; 12 81.
Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification. , Yasuoka Y ., Nat Commun. July 9, 2014; 5 4322.
Active repression by RARγ signaling is required for vertebrate axial elongation. , Janesick A ., Development. June 1, 2014; 141 (11): 2260-70.
Left- right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions. , Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.
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.
The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling. , Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
β- Arrestin 1 mediates non-canonical Wnt pathway to regulate convergent extension movements. , Kim GH ., Biochem Biophys Res Commun. May 31, 2013; 435 (2): 182-7.
An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis. , Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
Gastrulation and pre-gastrulation morphogenesis, inductions, and gene expression: similarities and dissimilarities between urodelean and anuran embryos. , Kaneda T., Dev Biol. September 1, 2012; 369 (1): 1-18.
Comparison of Lim1 expression in embryos of frogs with different modes of reproduction. , Venegas-Ferrín M., Int J Dev Biol. January 1, 2010; 54 (1): 195-202.
Identification and gastrointestinal expression of Xenopus laevis FoxF2. , McLin VA ., Int J Dev Biol. January 1, 2010; 54 (5): 919-24.
Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus. , Thomas JT., J Biol Chem. July 10, 2009; 284 (28): 18994-9005.
The shroom family proteins play broad roles in the morphogenesis of thickened epithelial sheets. , Lee C , Lee C , Lee C ., Dev Dyn. June 1, 2009; 238 (6): 1480-91.
Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1. , Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction. , Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.
The mouse homeobox gene Noto regulates node morphogenesis, notochordal ciliogenesis, and left right patterning. , Beckers A., Proc Natl Acad Sci U S A. October 2, 2007; 104 (40): 15765-70.
ANR5, an FGF target gene product, regulates gastrulation in Xenopus. , Chung HA., Curr Biol. June 5, 2007; 17 (11): 932-9.
XGAP, an ArfGAP, is required for polarized localization of PAR proteins and cell polarity in Xenopus gastrulation. , Hyodo-Miura J., Dev Cell. July 1, 2006; 11 (1): 69-79.
Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning. , Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
Antagonistic interaction between IGF and Wnt/ JNK signaling in convergent extension in Xenopus embryo. , Carron C., Mech Dev. November 1, 2005; 122 (11): 1234-47.
XBtg2 is required for notochord differentiation during early Xenopus development. , Sugimoto K., Dev Growth Differ. September 1, 2005; 47 (7): 435-43.
Xenopus hairy2b specifies anterior prechordal mesoderm identity within Spemann's organizer. , Yamaguti M., Dev Dyn. September 1, 2005; 234 (1): 102-13.
Frzb modulates Wnt-9a-mediated beta-catenin signaling during avian atrioventricular cardiac cushion development. , Person AD., Dev Biol. February 1, 2005; 278 (1): 35-48.
R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis. , Kazanskaya O., Dev Cell. October 1, 2004; 7 (4): 525-34.
Xantivin suppresses the activity of EGF- CFC genes to regulate nodal signaling. , Tanegashima K ., Int J Dev Biol. June 1, 2004; 48 (4): 275-83.
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.
Chordin is required for the Spemann organizer transplantation phenomenon in Xenopus embryos. , Oelgeschläger M ., Dev Cell. February 1, 2003; 4 (2): 219-30.
Xolloid-related: a novel BMP1/Tolloid-related metalloprotease is expressed during early Xenopus development. , Dale L ., Mech Dev. December 1, 2002; 119 (2): 177-90.
Xenopus Cdc42 regulates convergent extension movements during gastrulation through Wnt/Ca2+ signaling pathway. , Choi SC., Dev Biol. April 15, 2002; 244 (2): 342-57.
Role of Goosecoid, Xnot and Wnt antagonists in the maintenance of the notochord genetic programme in Xenopus gastrulae. , Yasuo H., Development. October 1, 2001; 128 (19): 3783-93.
Siamois functions in the early blastula to induce Spemann's organiser. , Kodjabachian L ., Mech Dev. October 1, 2001; 108 (1-2): 71-9.
A direct screen for secreted proteins in Xenopus embryos identifies distinct activities for the Wnt antagonists Crescent and Frzb-1. , Pera EM ., Mech Dev. September 1, 2000; 96 (2): 183-95.
The fate of cells in the tailbud of Xenopus laevis. , Davis RL., Development. January 1, 2000; 127 (2): 255-67.
Identification of tissues and patterning events required for distinct steps in early migration of zebrafish primordial germ cells. , Weidinger G ., Development. December 1, 1999; 126 (23): 5295-307.
XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development. , Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
The role of paraxial protocadherin in selective adhesion and cell movements of the mesoderm during Xenopus gastrulation. , Kim SH., Development. December 1, 1998; 125 (23): 4681-90.
Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning. , Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
Vax1 is a novel homeobox-containing gene expressed in the developing anterior ventral forebrain. , Hallonet M., Development. July 1, 1998; 125 (14): 2599-610.
Analysis of the developing Xenopus tail bud reveals separate phases of gene expression during determination and outgrowth. , Beck CW ., Mech Dev. March 1, 1998; 72 (1-2): 41-52.