Papers associated with whole organism (and eomes)

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	Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.
	Temporal and spatial transcriptomic dynamics across brain development in Xenopus laevis tadpoles., Ta AC., G3 (Bethesda). January 4, 2022; 12 (1):
	Huntingtin CAG expansion impairs germ layer patterning in synthetic human 2D gastruloids through polarity defects., Galgoczi S., Development. October 1, 2021; 148 (19):
	Tril dampens Nodal signaling through Pellino2- and Traf6-mediated activation of Nedd4l., Kim HS., Proc Natl Acad Sci U S A. September 7, 2021; 118 (36):
	Combinatorial transcription factor activities on open chromatin induce embryonic heterogeneity in vertebrates., Bright AR., EMBO J. May 3, 2021; 40 (9): e104913.
	Xenopus leads the way: Frogs as a pioneering model to understand the human brain., Exner CRT., Genesis. February 1, 2021; 59 (1-2): e23405.
	Hes5.9 Coordinate FGF and Notch Signaling to Modulate Gastrulation via Regulating Cell Fate Specification and Cell Migration in Xenopus tropicalis., Huang X., Genes (Basel). November 18, 2020; 11 (11):
	Sox17 and β-catenin co-occupy Wnt-responsive enhancers to govern the endoderm gene regulatory network., Mukherjee S., Elife. September 7, 2020; 9
	Skeletal muscle differentiation drives a dramatic downregulation of RNA polymerase III activity and differential expression of Polr3g isoforms., McQueen C., Dev Biol. October 1, 2019; 454 (1): 74-84.
	Maternal pluripotency factors initiate extensive chromatin remodelling to predefine first response to inductive signals., Gentsch GE., Nat Commun. September 19, 2019; 10 (1): 4269.
	The Spatiotemporal Control of Zygotic Genome Activation., Gentsch GE., iScience. June 28, 2019; 16 485-498.
	Mechanistic insights from the LHX1-driven molecular network in building the embryonic head., McMahon R., Dev Growth Differ. June 1, 2019; 61 (5): 327-336.
	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.
	Tbx2 is required for the suppression of mesendoderm during early Xenopus development., Teegala S., Dev Dyn. July 1, 2018; 247 (7): 903-913.
	EFhd2/Swiprosin-1 is a common genetic determinator for sensation-seeking/low anxiety and alcohol addiction., Mielenz D., Mol Psychiatry. May 1, 2018; 23 (5): 1303-1319.
	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.
	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.
	Pattern of Neurogenesis and Identification of Neuronal Progenitor Subtypes during Pallial Development in Xenopus laevis., Moreno N., Front Neuroanat. March 27, 2017; 11 24.
	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.
	A novel role for Ascl1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT., Gao L., Development. February 1, 2016; 143 (3): 492-503.
	The evolution of basal progenitors in the developing non-mammalian brain., Nomura T., Development. January 1, 2016; 143 (1): 66-74.
	E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation., Wills AE., Dev Cell. February 9, 2015; 32 (3): 345-57.
	Developmental enhancers are marked independently of zygotic Nodal signals in Xenopus., Gupta R., Dev Biol. November 1, 2014; 395 (1): 38-49.
	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.
	In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.
	TBX3 Directs Cell-Fate Decision toward Mesendoderm., Weidgang CE., Stem Cell Reports. August 29, 2013; 1 (3): 248-65.
	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.
	Dual origins of the mammalian accessory olfactory bulb revealed by an evolutionarily conserved migratory stream., Huilgol D., Nat Neurosci. February 1, 2013; 16 (2): 157-65.
	Conservation and evolutionary divergence in the activity of receptor-regulated smads., Sorrentino GM., Evodevo. October 1, 2012; 3 (1): 22.
	The Mix family of homeobox genes--key regulators of mesendoderm formation during vertebrate development., Pereira LA., Dev Biol. July 15, 2012; 367 (2): 163-77.
	A developmental requirement for HIRA-dependent H3.3 deposition revealed at gastrulation in Xenopus., Szenker E., Cell Rep. June 28, 2012; 1 (6): 730-40.
	fus/TLS orchestrates splicing of developmental regulators during gastrulation., Dichmann DS., Genes Dev. June 15, 2012; 26 (12): 1351-63.
	Snail2 controls mesodermal BMP/Wnt induction of neural crest., Shi J., Development. August 1, 2011; 138 (15): 3135-45.
	Negative autoregulation of Oct3/4 through Cdx1 promotes the onset of gastrulation., Rousso SZ., Dev Dyn. April 1, 2011; 240 (4): 796-807.
	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.
	Zygotic VegT is required for Xenopus paraxial mesoderm formation and is regulated by Nodal signaling and Eomesodermin., Fukuda M., Int J Dev Biol. January 1, 2010; 54 (1): 81-92.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
	Vegetally localized Xenopus trim36 regulates cortical rotation and dorsal axis formation., Cuykendall TN., Development. September 1, 2009; 136 (18): 3057-65.
	A microarray screen for direct targets of Zic1 identifies an aquaporin gene, aqp-3b, expressed in the neural folds., Cornish EJ., Dev Dyn. May 1, 2009; 238 (5): 1179-94.
	The role of FGF signaling in the establishment and maintenance of mesodermal gene expression in Xenopus., Fletcher RB., Dev Dyn. May 1, 2008; 237 (5): 1243-54.
	Anuran olfactory bulb organization: embryology, neurochemistry and hodology., Moreno N., Brain Res Bull. March 18, 2008; 75 (2-4): 241-5.
	PP2A:B56epsilon is required for eye induction and eye field separation., Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
	Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.
	Emilin1 links TGF-beta maturation to blood pressure homeostasis., Zacchigna L., Cell. March 10, 2006; 124 (5): 929-42.
	Genomic profiling of mixer and Sox17beta targets during Xenopus endoderm development., Dickinson K., Dev Dyn. February 1, 2006; 235 (2): 368-81.
	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.
	SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C., Dev Dyn. December 1, 2005; 234 (4): 878-91.
	Maternal Xenopus Zic2 negatively regulates Nodal-related gene expression during anteroposterior patterning., Houston DW., Development. November 1, 2005; 132 (21): 4845-55.
	Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.
	The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos., Callery EM., Dev Biol. February 15, 2005; 278 (2): 542-59.

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