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Rab7 is required for mesoderm patterning and gastrulation in Xenopus. , Kreis J., Biol Open. July 15, 2021; 10 (7):
Furry is required for cell movements during gastrulation and functionally interacts with NDR1. , Cervino AS., Sci Rep. March 23, 2021; 11 (1): 6607.
TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis. , Chen M., Elife. September 14, 2020; 9
Natural size variation among embryos leads to the corresponding scaling in gene expression. , Leibovich A., Dev Biol. June 15, 2020; 462 (2): 165-179.
The tumor suppressor PTPRK promotes ZNRF3 internalization and is required for Wnt inhibition in the Spemann organizer. , Chang LS., Elife. January 14, 2020; 9
RAPGEF5 Regulates Nuclear Translocation of β-Catenin. , Griffin JN., Dev Cell. January 22, 2018; 44 (2): 248-260.e4.
A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates. , Plouhinec JL., PLoS Biol. October 19, 2017; 15 (10): e2004045.
Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates. , Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.
sall1 and sall4 repress pou5f3 family expression to allow neural patterning, differentiation, and morphogenesis in Xenopus laevis. , Exner CRT., Dev Biol. May 1, 2017; 425 (1): 33-43.
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.
Specification of anteroposterior axis by combinatorial signaling during Xenopus development. , Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
Identification of microRNAs and microRNA targets in Xenopus gastrulae: The role of miR-26 in the regulation of Smad1. , Liu C., Dev Biol. January 1, 2016; 409 (1): 26-38.
Early neural ectodermal genes are activated by Siamois and Twin during blastula stages. , Klein SL., Genesis. May 1, 2015; 53 (5): 308-20.
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.
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.
Zygotic expression of Exostosin1 ( Ext1) is required for BMP signaling and establishment of dorsal- ventral pattern in Xenopus. , Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
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.
A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance. , Livigni A., Curr Biol. November 18, 2013; 23 (22): 2233-2244.
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.
Directional migration of leading-edge mesoderm generates physical forces: Implication in Xenopus notochord formation during gastrulation. , Hara Y., Dev Biol. October 15, 2013; 382 (2): 482-95.
The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling. , Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis. , Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
Essential role of AWP1 in neural crest specification in Xenopus. , Seo JH., Int J Dev Biol. January 1, 2013; 57 (11-12): 829-36.
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.
Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation. , Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
TAK1 promotes BMP4/ Smad1 signaling via inhibition of erk MAPK: a new link in the FGF/BMP regulatory network. , Liu C., Differentiation. April 1, 2012; 83 (4): 210-9.
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.
Yes-associated protein 65 ( YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone. , Gee ST ., PLoS One. January 1, 2011; 6 (6): e20309.
Xenopus furry contributes to release of microRNA gene silencing. , Goto T ., Proc Natl Acad Sci U S A. November 9, 2010; 107 (45): 19344-9.
Distinct Xenopus Nodal ligands sequentially induce mesendoderm and control gastrulation movements in parallel to the Wnt/PCP pathway. , Luxardi G ., Development. February 1, 2010; 137 (3): 417-26.
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.
Bestrophin genes are expressed in Xenopus development. , Onuma Y ., Biochem Biophys Res Commun. July 3, 2009; 384 (3): 290-5.
Unc5B interacts with FLRT3 and Rnd1 to modulate cell adhesion in Xenopus embryos. , Karaulanov E., PLoS One. May 29, 2009; 4 (5): e5742.
Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1. , Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
VegT, eFGF and Xbra cause overall posteriorization while Xwnt8 causes eye-level restricted posteriorization in synergy with chordin in early Xenopus development. , Fujii H., Dev Growth Differ. March 1, 2008; 50 (3): 169-80.
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.
TGF-beta signaling-mediated morphogenesis: modulation of cell adhesion via cadherin endocytosis. , Ogata S., Genes Dev. July 15, 2007; 21 (14): 1817-31.
ANR5, an FGF target gene product, regulates gastrulation in Xenopus. , Chung HA., Curr Biol. June 5, 2007; 17 (11): 932-9.
Early molecular effects of ethanol during vertebrate embryogenesis. , Yelin R ., Differentiation. June 1, 2007; 75 (5): 393-403.
Evolution of axis specification mechanisms in jawed vertebrates: insights from a chondrichthyan. , Coolen M., PLoS One. April 18, 2007; 2 (4): e374.
Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning. , Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
New tools for visualization and analysis of morphogenesis in spherical embryos. , Tyszka JM., Dev Dyn. December 1, 2005; 234 (4): 974-83.
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.
Temporal analysis of the early BMP functions identifies distinct anti- organizer and mesoderm patterning phases. , Marom K., Dev Biol. June 15, 2005; 282 (2): 442-54.
XIC is required for Siamois activity and dorsoanterior development. , Snider L ., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.
JNK and ROKalpha function in the noncanonical Wnt/ RhoA signaling pathway to regulate Xenopus convergent extension movements. , Kim GH ., Dev Dyn. April 1, 2005; 232 (4): 958-68.
Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures. , Khokha MK ., Dev Cell. March 1, 2005; 8 (3): 401-11.