Papers associated with ectoderm∨derBy=4 (and pou5f3)

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	A single-cell, time-resolved profiling of Xenopus mucociliary epithelium reveals nonhierarchical model of development., Lee J., Sci Adv. April 7, 2023; 9 (14): eadd5745.
	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.
	Engagement of Foxh1 in chromatin regulation revealed by protein interactome analyses., Zhou JJ., Dev Growth Differ. August 1, 2022; 64 (6): 297-305.
	The functional diversity of the POUV-class proteins across vertebrates., Bakhmet EI., Open Biol. June 1, 2022; 12 (6): 220065.
	Combinatorial transcription factor activities on open chromatin induce embryonic heterogeneity in vertebrates., Bright AR., EMBO J. May 3, 2021; 40 (9): e104913.
	A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation., Hou K., Cells. May 15, 2019; 8 (5):
	The Xenopus animal cap transcriptome: building a mucociliary epithelium., Angerilli A., Nucleic Acids Res. September 28, 2018; 46 (17): 8772-8787.
	Serine Threonine Kinase Receptor-Associated Protein Deficiency Impairs Mouse Embryonic Stem Cells Lineage Commitment Through CYP26A1-Mediated Retinoic Acid Homeostasis., Jin L., Stem Cells. September 1, 2018; 36 (9): 1368-1379.
	Histone deacetylase activity has an essential role in establishing and maintaining the vertebrate neural crest., Rao A., Development. August 8, 2018; 145 (15):
	microRNAs associated with early neural crest development in Xenopus laevis., Ward NJ., BMC Genomics. January 18, 2018; 19 (1): 59.
	Lineage commitment of embryonic cells involves MEK1-dependent clearance of pluripotency regulator Ventx2., Scerbo P., Elife. June 27, 2017; 6
	MicroRNAs and ectodermal specification I. Identification of miRs and miR-targeted mRNAs in early anterior neural and epidermal ectoderm., Shah VV., Dev Biol. June 15, 2017; 426 (2): 200-210.
	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.
	Inhibition of FGF signaling accelerates neural crest cell differentiation of human pluripotent stem cells., Jaroonwitchawan T., Biochem Biophys Res Commun. December 2, 2016; 481 (1-2): 176-181.
	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.
	Pou5f3.2-induced proliferative state of embryonic cells during gastrulation of Xenopus laevis embryo., Nishitani E., Dev Growth Differ. December 1, 2015; 57 (9): 591-600.
	NEURODEVELOPMENT. Shared regulatory programs suggest retention of blastula-stage potential in neural crest cells., Buitrago-Delgado E., Science. June 19, 2015; 348 (6241): 1332-5.
	Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus., Young JJ., Development. April 1, 2014; 141 (8): 1683-93.
	A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance., Livigni A., Curr Biol. November 18, 2013; 23 (22): 2233-2244.
	TBX3 Directs Cell-Fate Decision toward Mesendoderm., Weidgang CE., Stem Cell Reports. August 29, 2013; 1 (3): 248-65.
	MRAS GTPase is a novel stemness marker that impacts mouse embryonic stem cell plasticity and Xenopus embryonic cell fate., Mathieu ME., Development. August 1, 2013; 140 (16): 3311-22.
	Expression of pluripotency factors in larval epithelia of the frog Xenopus: evidence for the presence of cornea epithelial stem cells., Perry KJ., Dev Biol. February 15, 2013; 374 (2): 281-94.
	Suv4-20h histone methyltransferases promote neuroectodermal differentiation by silencing the pluripotency-associated Oct-25 gene., Nicetto D., PLoS Genet. January 1, 2013; 9 (1): e1003188.
	Pou-V factor Oct25 regulates early morphogenesis in Xenopus laevis., Julier A., Dev Growth Differ. September 1, 2012; 54 (7): 702-16.
	Ventx factors function as Nanog-like guardians of developmental potential in Xenopus., Scerbo P., PLoS One. January 1, 2012; 7 (5): e36855.
	Dual roles of Oct4 in the maintenance of mouse P19 embryonal carcinoma cells: as negative regulator of Wnt/β-catenin signaling and competence provider for Brachyury induction., Marikawa Y., Stem Cells Dev. April 1, 2011; 20 (4): 621-33.
	Interaction of Sox1, Sox2, Sox3 and Oct4 during primary neurogenesis., Archer TC., Dev Biol. February 15, 2011; 350 (2): 429-40.
	Transdifferentiation from cornea to lens in Xenopus laevis depends on BMP signalling and involves upregulation of Wnt signalling., Day RC., BMC Dev Biol. January 26, 2011; 11 54.
	Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus., Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.
	Neuronatin promotes neural lineage in ESCs via Ca(2+) signaling., Lin HH., Stem Cells. November 1, 2010; 28 (11): 1950-60.
	The Oct4 homologue PouV and Nanog regulate pluripotency in chicken embryonic stem cells., Lavial F., Development. October 1, 2007; 134 (19): 3549-63.
	The Xenopus POU class V transcription factor XOct-25 inhibits ectodermal competence to respond to bone morphogenetic protein-mediated embryonic induction., Takebayashi-Suzuki K., Mech Dev. January 1, 2007; 124 (11-12): 840-55.
	Xenopus laevis POU91 protein, an Oct3/4 homologue, regulates competence transitions from mesoderm to neural cell fates., Snir M., EMBO J. August 9, 2006; 25 (15): 3664-74.
	Xenopus POU factors of subclass V inhibit activin/nodal signaling during gastrulation., Cao Y., Mech Dev. August 1, 2006; 123 (8): 614-25.
	Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development., Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.
	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.
	A POU protein regulates mesodermal competence to FGF in Xenopus., Henig C., Mech Dev. February 1, 1998; 71 (1-2): 131-42.
	Localized expression of a Xenopus POU gene depends on cell-autonomous transcriptional activation and induction-dependent inactivation., Frank D., Development. June 1, 1992; 115 (2): 439-48.

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