Papers associated with epidermis (and gsc)

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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.
	Quantitative analysis of transcriptome dynamics provides novel insights into developmental state transitions., Johnson K., BMC Genomics. October 23, 2022; 23 (1): 723.
	Evo-Devo of Urbilateria and its larval forms., De Robertis EM., Dev Biol. July 1, 2022; 487 10-20.
	Retinoic Acid is Required for Normal Morphogenetic Movements During Gastrulation., Gur M., Front Cell Dev Biol. January 1, 2022; 10 857230.
	Establishing embryonic territories in the context of Wnt signaling., Velloso I., Int J Dev Biol. January 1, 2021; 65 (4-5-6): 227-233.
	TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9
	Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling., Vacca B., Sci Rep. January 19, 2018; 8 (1): 1204.
	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.
	Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover., Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.
	Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates., Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.
	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.
	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.
	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.
	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.
	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.
	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.
	The function of heterodimeric AP-1 comprised of c-Jun and c-Fos in activin mediated Spemann organizer gene expression., Lee SY., PLoS One. January 1, 2011; 6 (7): e21796.
	DeltaNp63 antagonizes p53 to regulate mesoderm induction in Xenopus laevis., Barton CE., Dev Biol. May 1, 2009; 329 (1): 130-9.
	Maternal Interferon Regulatory Factor 6 is required for the differentiation of primary superficial epithelia in Danio and Xenopus embryos., Sabel JL., Dev Biol. January 1, 2009; 325 (1): 249-62.
	A new triple staining method for double in situ hybridization in combination with cell lineage tracing in whole-mount Xenopus embryos., Koga M., Dev Growth Differ. October 1, 2007; 49 (8): 635-45.
	The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
	ANR5, an FGF target gene product, regulates gastrulation in Xenopus., Chung HA., Curr Biol. June 5, 2007; 17 (11): 932-9.
	A novel gene, BENI is required for the convergent extension during Xenopus laevis gastrulation., Homma M., Dev Biol. March 1, 2007; 303 (1): 270-80.
	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.
	Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition., Delaune E., Development. January 1, 2005; 132 (2): 299-310.
	Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.
	Xhex-expressing endodermal tissues are essential for anterior patterning in Xenopus., Smithers LE., Mech Dev. December 1, 2002; 119 (2): 191-200.
	From intestine to muscle: nuclear reprogramming through defective cloned embryos., Byrne JA., Proc Natl Acad Sci U S A. April 30, 2002; 99 (9): 6059-63.
	Synthesis and release of activin and noggin by cultured human amniotic epithelial cells., Koyano S., Dev Growth Differ. April 1, 2002; 44 (2): 103-12.
	Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.
	The orphan receptor ALK7 and the Activin receptor ALK4 mediate signaling by Nodal proteins during vertebrate development., Reissmann E., Genes Dev. August 1, 2001; 15 (15): 2010-22.
	Neural induction in the absence of mesoderm: beta-catenin-dependent expression of secreted BMP antagonists at the blastula stage in Xenopus., Wessely O., Dev Biol. June 1, 2001; 234 (1): 161-73.
	Two-step induction of primitive erythrocytes in Xenopus laevis embryos: signals from the vegetal endoderm and the overlying ectoderm., Kikkawa M., Int J Dev Biol. April 1, 2001; 45 (2): 387-96.
	Gli2 functions in FGF signaling during antero-posterior patterning., Brewster R., Development. October 1, 2000; 127 (20): 4395-405.
	Endodermal Nodal-related signals and mesoderm induction in Xenopus., Agius E., Development. March 1, 2000; 127 (6): 1173-83.
	Neuralization of the Xenopus embryo by inhibition of p300/ CREB-binding protein function., Kato Y., J Neurosci. November 1, 1999; 19 (21): 9364-73.
	Antagonist activity of DWnt-4 and wingless in the Drosophila embryonic ventral ectoderm and in heterologous Xenopus assays., Gieseler K., Mech Dev. July 1, 1999; 85 (1-2): 123-31.
	GATA-1 inhibits the formation of notochord and neural tissue in Xenopus embryo., Shibata K., Biochem Biophys Res Commun. November 9, 1998; 252 (1): 241-8.
	The role of maternal VegT in establishing the primary germ layers in Xenopus embryos., Zhang J., Cell. August 21, 1998; 94 (4): 515-24.
	Smad7 inhibits mesoderm formation and promotes neural cell fate in Xenopus embryos., Bhushan A., Dev Biol. August 15, 1998; 200 (2): 260-8.
	Direct binding of follistatin to a complex of bone-morphogenetic protein and its receptor inhibits ventral and epidermal cell fates in early Xenopus embryo., Iemura S., Proc Natl Acad Sci U S A. August 4, 1998; 95 (16): 9337-42.
	Frizzled-8 is expressed in the Spemann organizer and plays a role in early morphogenesis., Deardorff MA., Development. July 1, 1998; 125 (14): 2687-700.
	Expression of Xfz3, a Xenopus frizzled family member, is restricted to the early nervous system., Shi DL., Mech Dev. January 1, 1998; 70 (1-2): 35-47.
	Misexpression of chick Vg1 in the marginal zone induces primitive streak formation., Shah SB., Development. December 1, 1997; 124 (24): 5127-38.
	p53 activity is essential for normal development in Xenopus., Wallingford JB., Curr Biol. October 1, 1997; 7 (10): 747-57.
	The ALK-2 and ALK-4 activin receptors transduce distinct mesoderm-inducing signals during early Xenopus development but do not co-operate to establish thresholds., Armes NA., Development. October 1, 1997; 124 (19): 3797-804.
	Analysis of competence and of Brachyury autoinduction by use of hormone-inducible Xbra., Tada M., Development. June 1, 1997; 124 (11): 2225-34.
	A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation., Horb ME., Development. May 1, 1997; 124 (9): 1689-98.
	The Xenopus T-box gene, Antipodean, encodes a vegetally localised maternal mRNA and can trigger mesoderm formation., Stennard F., Development. December 1, 1996; 122 (12): 4179-88.

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