Papers associated with early embryonic cell (and gsc)

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	Cdx1 and Gsc distinctly regulate the transcription of BMP4 target gene ventx3.2 by directly binding to the proximal promoter region in Xenopus gastrulae., Goutam RS., Mol Cells. March 23, 2024; 47 (4): 100058.
	ZSWIM4 regulates embryonic patterning and BMP signaling by promoting nuclear Smad1 degradation., Wang C., EMBO Rep. February 1, 2024; 25 (2): 646-671.
	Two Homeobox Transcription Factors, Goosecoid and Ventx1.1, Oppositely Regulate Chordin Transcription in Xenopus Gastrula Embryos., Kumar V., Cells. March 11, 2023; 12 (6):
	Recognition of H2AK119ub plays an important role in RSF1-regulated early Xenopus development., Parast SM., Front Cell Dev Biol. January 1, 2023; 11 1168643.
	Retinoic Acid is Required for Normal Morphogenetic Movements During Gastrulation., Gur M., Front Cell Dev Biol. January 1, 2022; 10 857230.
	Chromatin accessibility and histone acetylation in the regulation of competence in early development., Esmaeili M., Dev Biol. June 1, 2020; 462 (1): 20-35.
	Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos., Lichtig H., Front Physiol. January 1, 2020; 11 75.
	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.
	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):
	Role of dipeptidyl peptidase-4 as a potentiator of activin/nodal signaling pathway., Park DS., BMB Rep. December 1, 2018; 51 (12): 636-641.
	Head formation requires Dishevelled degradation that is mediated by March2 in concert with Dapper1., Lee H, Lee H., Development. April 10, 2018; 145 (7):
	Phosphorylation states change Otx2 activity for cell proliferation and patterning in the Xenopus embryo., Satou Y., Development. March 12, 2018; 145 (5):
	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.
	Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling., Vacca B., Sci Rep. January 19, 2018; 8 (1): 1204.
	Sorting at embryonic boundaries requires high heterotypic interfacial tension., Canty L., Nat Commun. July 31, 2017; 8 (1): 157.
	Lineage commitment of embryonic cells involves MEK1-dependent clearance of pluripotency regulator Ventx2., Scerbo P., Elife. June 27, 2017; 6
	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.
	Ubiquitin C-terminal hydrolase37 regulates Tcf7 DNA binding for the activation of Wnt signalling., Han W., Sci Rep. February 15, 2017; 7 42590.
	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.
	FoxH1 mediates a Grg4 and Smad2 dependent transcriptional switch in Nodal signaling during Xenopus mesoderm development., Reid CD., Dev Biol. June 1, 2016; 414 (1): 34-44.
	Differential requirement of bone morphogenetic protein receptors Ia (ALK3) and Ib (ALK6) in early embryonic patterning and neural crest development., Schille C., BMC Dev Biol. January 19, 2016; 16 1.
	Early neural ectodermal genes are activated by Siamois and Twin during blastula stages., Klein SL., Genesis. May 1, 2015; 53 (5): 308-20.
	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.
	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.
	Insulin-like factor regulates neural induction through an IGF1 receptor-independent mechanism., Haramoto Y., Sci Rep. January 12, 2015; 5 11603.
	Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.
	Fezf2 promotes neuronal differentiation through localised activation of Wnt/β-catenin signalling during forebrain development., Zhang S., Development. December 1, 2014; 141 (24): 4794-805.
	EphA4-dependent Brachyury expression is required for dorsal mesoderm involution in the Xenopus gastrula., Evren S., Development. October 1, 2014; 141 (19): 3649-61.
	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.
	NEDD4L regulates convergent extension movements in Xenopus embryos via Disheveled-mediated non-canonical Wnt signaling., Zhang Y., Dev Biol. August 1, 2014; 392 (1): 15-25.
	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.
	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.
	The Xenopus homologue of Down syndrome critical region protein 6 drives dorsoanterior gene expression and embryonic axis formation by antagonising polycomb group proteins., Li HY., Development. December 1, 2013; 140 (24): 4903-13.
	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.
	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.
	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.
	The Wnt signaling mediator tcf1 is required for expression of foxd3 during Xenopus gastrulation., Janssens S., Int J Dev Biol. January 1, 2013; 57 (1): 49-54.
	Transcriptional regulation of mesoderm genes by MEF2D during early Xenopus development., Kolpakova A., PLoS One. January 1, 2013; 8 (7): e69693.
	Klf4 is required for germ-layer differentiation and body axis patterning during Xenopus embryogenesis., Cao Q., Development. November 1, 2012; 139 (21): 3950-61.
	Conservation and evolutionary divergence in the activity of receptor-regulated smads., Sorrentino GM., Evodevo. October 1, 2012; 3 (1): 22.
	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.
	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.
	Ventx factors function as Nanog-like guardians of developmental potential in Xenopus., Scerbo P., PLoS One. January 1, 2012; 7 (5): e36855.
	HEB and E2A function as SMAD/FOXH1 cofactors., Yoon SJ., Genes Dev. August 1, 2011; 25 (15): 1654-61.
	Siamois and Twin are redundant and essential in formation of the Spemann organizer., Bae S., Dev Biol. April 15, 2011; 352 (2): 367-81.
	SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.

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