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Brain enlargement with rostral bias in larvae from a spontaneously occurring female variant line of Xenopus; role of aberrant embryonic Wnt/β-catenin signaling. , Hongo I., Cells Dev. April 3, 2024; 203918.
Transmembrane protein 150b attenuates BMP signaling in the Xenopus organizer. , Keum BR., J Cell Physiol. August 1, 2023; 238 (8): 1850-1866.
Lysosomes are required for early dorsal signaling in the Xenopus embryo. , Tejeda-Muñoz N., Proc Natl Acad Sci U S A. April 26, 2022; 119 (17): e2201008119.
Smad2 and Smad3 differentially modulate chordin transcription via direct binding on the distal elements in gastrula Xenopus embryos. , Kumar V ., Biochem Biophys Res Commun. June 25, 2021; 559 168-175.
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):
Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endoderm gene regulatory network. , Mukherjee S ., Elife. September 7, 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.
Chromatin accessibility and histone acetylation in the regulation of competence in early development. , Esmaeili M., Dev Biol. June 1, 2020; 462 (1): 20-35.
Evolution of cis-regulatory modules for the head organizer gene goosecoid in chordates: comparisons between Branchiostoma and Xenopus. , Yasuoka Y ., Zoological Lett. August 2, 2019; 5 27.
Barhl2 maintains T cell factors as repressors and thereby switches off the Wnt/ β-Catenin response driving Spemann organizer formation. , Sena E., Development. May 22, 2019; 146 (10):
Non-acylated Wnts Can Promote Signaling. , Speer KF., Cell Rep. January 22, 2019; 26 (4): 875-883.e5.
Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis. , Ding Y ., Proc Natl Acad Sci U S A. September 25, 2018; 115 (39): E9135-E9144.
Embryonic regeneration by relocalization of the Spemann organizer during twinning in Xenopus. , Moriyama Y ., Proc Natl Acad Sci U S A. May 22, 2018; 115 (21): E4815-E4822.
ADMP controls the size of Spemann's organizer through a network of self-regulating expansion-restriction signals. , Leibovich A., BMC Biol. January 22, 2018; 16 (1): 13.
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.
Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula. , Ding Y ., Dev Biol. June 15, 2017; 426 (2): 176-187.
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.
A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo. , Blitz IL ., Dev Biol. June 15, 2017; 426 (2): 409-417.
Identification and comparative analyses of Siamois cluster genes in Xenopus laevis and tropicalis. , Haramoto Y ., Dev Biol. June 15, 2017; 426 (2): 374-383.
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.
Spemann organizer transcriptome induction by early beta-catenin, Wnt, Nodal, and Siamois signals in Xenopus laevis. , Ding Y ., Proc Natl Acad Sci U S A. April 11, 2017; 114 (15): E3081-E3090.
Leftward Flow Determines Laterality in Conjoined Twins. , Tisler M., Curr Biol. February 20, 2017; 27 (4): 543-548.
Ubiquitin C-terminal hydrolase37 regulates Tcf7 DNA binding for the activation of Wnt signalling. , Han W., Sci Rep. February 15, 2017; 7 42590.
The MLL/Setd1b methyltransferase is required for the Spemann's organizer gene activation in Xenopus. , Lin H., Mech Dev. November 1, 2016; 142 1-9.
Capsaicin inhibits the Wnt/ β-catenin signaling pathway by down-regulating PP2A. , Park DS., Biochem Biophys Res Commun. September 9, 2016; 478 (1): 455-461.
Gtpbp2 is a positive regulator of Wnt signaling and maintains low levels of the Wnt negative regulator Axin. , Gillis WQ., Cell Commun Signal. August 2, 2016; 14 (1): 15.
Neural transcription factors bias cleavage stage blastomeres to give rise to neural ectoderm. , Gaur S., Genesis. June 1, 2016; 54 (6): 334-49.
A gradient of maternal Bicaudal-C controls vertebrate embryogenesis via translational repression of mRNAs encoding cell fate regulators. , Park S., Development. March 1, 2016; 143 (5): 864-71.
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.
NF2/ Merlin is required for the axial pattern formation in the Xenopus laevis embryo. , Zhu X., Mech Dev. November 1, 2015; 138 Pt 3 305-12.
Early neural ectodermal genes are activated by Siamois and Twin during blastula stages. , Klein SL., Genesis. May 1, 2015; 53 (5): 308-20.
Direct regulation of siamois by VegT is required for axis formation in Xenopus embryo. , Li HY., Int J Dev Biol. January 1, 2015; 59 (10-12): 443-51.
The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling. , Iwasaki Y ., Development. October 1, 2014; 141 (19): 3740-51.
Symmetry breakage in the vertebrate embryo: when does it happen and how does it work? , Blum M ., Dev Biol. September 1, 2014; 393 (1): 109-23.
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.
Maternal Dead-End1 is required for vegetal cortical microtubule assembly during Xenopus axis specification. , Mei W., Development. June 1, 2013; 140 (11): 2334-44.
Optimal histone H3 to linker histone H1 chromatin ratio is vital for mesodermal competence in Xenopus. , Lim CY., Development. February 1, 2013; 140 (4): 853-60.
Klf4 is required for germ-layer differentiation and body axis patterning during Xenopus embryogenesis. , Cao Q., Development. November 1, 2012; 139 (21): 3950-61.
Maternal Mga is required for Wnt signaling and organizer formation in the early Xenopus embryo. , Gu F., Acta Biochim Biophys Sin (Shanghai). November 1, 2012; 44 (11): 939-47.
Transcriptional integration of Wnt and Nodal pathways in establishment of the Spemann organizer. , Reid CD., Dev Biol. August 15, 2012; 368 (2): 231-41.
Subfunctionalization and neofunctionalization of vertebrate Lef/Tcf transcription factors. , Klingel S., Dev Biol. August 1, 2012; 368 (1): 44-53.
Dynamic in vivo binding of transcription factors to cis-regulatory modules of cer and gsc in the stepwise formation of the Spemann-Mangold organizer. , Sudou N ., Development. May 1, 2012; 139 (9): 1651-61.
Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo. , Martin LK., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.
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.
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.
Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus. , Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.
mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/ nodal signaling in Xenopus ectodermal cells. , Miyazaki A., PLoS One. January 1, 2012; 7 (10): e46630.
Cortical rotation and messenger RNA localization in Xenopus axis formation. , Houston DW ., Wiley Interdiscip Rev Dev Biol. January 1, 2012; 1 (3): 371-88.
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.