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Segregation of brain and organizer precursors is differentially regulated by Nodal signaling at blastula stage. , Castro Colabianchi AM., Biol Open. February 25, 2021; 10 (2):
Apcdd1 is a dual BMP/Wnt inhibitor in the developing nervous system and skin. , Vonica A ., Dev Biol. August 1, 2020; 464 (1): 71-87.
The tumor suppressor PTPRK promotes ZNRF3 internalization and is required for Wnt inhibition in the Spemann organizer. , Chang LS., Elife. January 14, 2020; 9
Nucleotide receptor P2RY4 is required for head formation via induction and maintenance of head organizer in Xenopus laevis. , Harata A., Dev Growth Differ. February 1, 2019; 61 (2): 186-197.
Maternal Gdf3 is an obligatory cofactor in Nodal signaling for embryonic axis formation in zebrafish. , Bisgrove BW., Elife. November 15, 2017; 6
Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates. , Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.
Identification of new regulators of embryonic patterning and morphogenesis in Xenopus gastrulae by RNA sequencing. , Popov IK., Dev Biol. June 15, 2017; 426 (2): 429-441.
Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition. , Wagner G., PLoS Genet. May 12, 2017; 13 (5): e1006757.
Functional differences between Tcf1 isoforms in early Xenopus development. , Roël G., Int J Dev Biol. January 1, 2017; 61 (1-2): 29-34.
Sebox regulates mesoderm formation in early amphibian embryos. , Chen G., Dev Dyn. November 1, 2015; 244 (11): 1415-26.
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.
JmjC Domain-containing Protein 6 ( Jmjd6) Derepresses the Transcriptional Repressor Transcription Factor 7-like 1 ( Tcf7l1) and Is Required for Body Axis Patterning during Xenopus Embryogenesis. , Zhang X., J Biol Chem. August 14, 2015; 290 (33): 20273-83.
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 serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation. , Acosta H., Development. March 15, 2015; 142 (6): 1146-58.
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.
The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling. , Iwasaki Y ., Development. October 1, 2014; 141 (19): 3740-51.
Custos controls β-catenin to regulate head development during vertebrate embryogenesis. , Komiya Y., Proc Natl Acad Sci U S A. September 9, 2014; 111 (36): 13099-104.
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.
FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos. , Murgan S., PLoS One. January 1, 2014; 9 (10): e110559.
Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling. , Bates TJ., Development. October 1, 2013; 140 (20): 4177-81.
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.
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 Zic3 controls notochord and organizer development through suppression of the Wnt/ β-catenin signaling pathway. , Fujimi TJ ., Dev Biol. January 15, 2012; 361 (2): 220-31.
Waif1/5T4 inhibits Wnt/ β-catenin signaling and activates noncanonical Wnt pathways by modifying LRP6 subcellular localization. , Kagermeier-Schenk B., Dev Cell. December 13, 2011; 21 (6): 1129-43.
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.
BMP antagonists and FGF signaling contribute to different domains of the neural plate in Xenopus. , Wills AE ., Dev Biol. January 15, 2010; 337 (2): 335-50.
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.
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.
Ethanol induces embryonic malformations by competing for retinaldehyde dehydrogenase activity during vertebrate gastrulation. , Kot-Leibovich H., Dis Model Mech. January 1, 2009; 2 (5-6): 295-305.
Robust stability of the embryonic axial pattern requires a secreted scaffold for chordin degradation. , Inomata H ., Cell. September 5, 2008; 134 (5): 854-65.
Crossveinless-2 Is a BMP feedback inhibitor that binds Chordin/BMP to regulate Xenopus embryonic patterning. , Ambrosio AL., Dev Cell. August 1, 2008; 15 (2): 248-60.
The mych gene is required for neural crest survival during zebrafish development. , Hong SK., PLoS One. April 9, 2008; 3 (4): e2029.
Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways. , Zhao H ., Development. April 1, 2008; 135 (7): 1283-93.
The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning. , Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
ANR5, an FGF target gene product, regulates gastrulation in Xenopus. , Chung HA., Curr Biol. June 5, 2007; 17 (11): 932-9.
PP2A:B56epsilon is required for eye induction and eye field separation. , Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
Xenopus Xotx2 and Drosophila otd share similar activities in anterior patterning of the frog embryo. , Lunardi A ., Dev Genes Evol. September 1, 2006; 216 (9): 511-21.
Metastasis-associated kinase modulates Wnt signaling to regulate brain patterning and morphogenesis. , Kibardin A., Development. August 1, 2006; 133 (15): 2845-54.
Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning. , Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development. , Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.
Twisted gastrulation is required for forebrain specification and cooperates with Chordin to inhibit BMP signaling during X. tropicalis gastrulation. , Wills A ., Dev Biol. January 1, 2006; 289 (1): 166-78.
Novel Daple-like protein positively regulates both the Wnt/beta-catenin pathway and the Wnt/ JNK pathway in Xenopus. , Kobayashi H., Mech Dev. October 1, 2005; 122 (10): 1138-53.
PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development. , Yang J ., Development. December 1, 2003; 130 (23): 5569-78.
Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos. , Galli A., Development. October 1, 2003; 130 (20): 4919-29.
Xenopus Nbx, a novel NK-1 related gene essential for neural crest formation. , Kurata T ., Dev Biol. May 1, 2003; 257 (1): 30-40.
Cell fate specification and competence by Coco, a maternal BMP, TGFbeta and Wnt inhibitor. , Bell E ., Development. April 1, 2003; 130 (7): 1381-9.
Xhex-expressing endodermal tissues are essential for anterior patterning in Xenopus. , Smithers LE ., Mech Dev. December 1, 2002; 119 (2): 191-200.