Papers associated with ectoderm (and actc1)

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	A systemic cell cycle block impacts stage-specific histone modification profiles during Xenopus embryogenesis., Pokrovsky D., PLoS Biol. September 1, 2021; 19 (9): e3001377.
	Temporal transcriptomic profiling reveals dynamic changes in gene expression of Xenopus animal cap upon activin treatment., Satou-Kobayashi Y., Sci Rep. July 15, 2021; 11 (1): 14537.
	Defective heart chamber growth and myofibrillogenesis after knockout of adprhl1 gene function by targeted disruption of the ancestral catalytic active site., Smith SJ., PLoS One. July 29, 2020; 15 (7): e0235433.
	The Xenopus animal cap transcriptome: building a mucociliary epithelium., Angerilli A., Nucleic Acids Res. September 28, 2018; 46 (17): 8772-8787.
	Dkk2 promotes neural crest specification by activating Wnt/β-catenin signaling in a GSK3β independent manner., Devotta A., Elife. July 23, 2018; 7
	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.
	Tbx3 represses bmp4 expression and, with Pax6, is required and sufficient for retina formation., Motahari Z., Development. October 1, 2016; 143 (19): 3560-3572.
	Cell-fate determination by ubiquitin-dependent regulation of translation., Werner A., Nature. September 24, 2015; 525 (7570): 523-7.
	PV.1 induced by FGF-Xbra functions as a repressor of neurogenesis in Xenopus embryos., Yoon J., BMB Rep. December 1, 2014; 47 (12): 673-8.
	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.
	Expression cloning of camelid nanobodies specific for Xenopus embryonic antigens., Itoh K., PLoS One. January 1, 2014; 9 (10): e107521.
	Maturin is a novel protein required for differentiation during primary neurogenesis., Martinez-De Luna RI., Dev Biol. December 1, 2013; 384 (1): 26-40.
	Germline Transgenic Methods for Tracking Cells and Testing Gene Function during Regeneration in the Axolotl., Khattak S., Stem Cell Reports. June 4, 2013; 1 (1): 90-103.
	Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural development., Xu Y, Xu Y., Cell. December 7, 2012; 151 (6): 1200-13.
	Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B., Dev Dyn. May 1, 2012; 241 (5): 995-1007.
	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.
	High-resolution whole-mount in situ hybridization using Quantum Dot nanocrystals., Ioannou A., J Biomed Biotechnol. January 1, 2012; 2012 627602.
	Skin regeneration in adult axolotls: a blueprint for scar-free healing in vertebrates., Seifert AW., PLoS One. January 1, 2012; 7 (4): e32875.
	Mef2d acts upstream of muscle identity genes and couples lateral myogenesis to dermomyotome formation in Xenopus laevis., Della Gaspera B., PLoS One. January 1, 2012; 7 (12): e52359.
	Involvement of Neptune in induction of the hatching gland and neural crest in the Xenopus embryo., Kurauchi T., Differentiation. January 1, 2010; 79 (4-5): 251-9.
	Comparative gene expression analysis and fate mapping studies suggest an early segregation of cardiogenic lineages in Xenopus laevis., Gessert S., Dev Biol. October 15, 2009; 334 (2): 395-408.
	Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
	Xmc mediates Xctr1-independent morphogenesis in Xenopus laevis., Haremaki T., Dev Dyn. September 1, 2009; 238 (9): 2382-7.
	Embryonic lethality of fortilin-null mutant mice by BMP-pathway overactivation., Koide Y., Biochim Biophys Acta. May 1, 2009; 1790 (5): 326-38.
	Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.
	DM-GRASP/ALCAM/CD166 is required for cardiac morphogenesis and maintenance of cardiac identity in first heart field derived cells., Gessert S., Dev Biol. September 1, 2008; 321 (1): 150-61.
	The postsynaptic density 95/disc-large/zona occludens protein syntenin directly interacts with frizzled 7 and supports noncanonical Wnt signaling., Luyten A., Mol Biol Cell. April 1, 2008; 19 (4): 1594-604.
	The myocardin-related transcription factor, MASTR, cooperates with MyoD to activate skeletal muscle gene expression., Meadows SM., Proc Natl Acad Sci U S A. February 5, 2008; 105 (5): 1545-50.
	FoxD3 regulation of Nodal in the Spemann organizer is essential for Xenopus dorsal mesoderm development., Steiner AB., Development. December 1, 2006; 133 (24): 4827-38.
	Xtn3 is a developmentally expressed cardiac and skeletal muscle-specific novex-3 titin isoform., Brown DD., Gene Expr Patterns. October 1, 2006; 6 (8): 913-8.
	XHas2 activity is required during somitogenesis and precursor cell migration in Xenopus development., Ori M., Development. February 1, 2006; 133 (4): 631-40.
	Characteristics of initiation and early events for muscle development in the Xenopus limb bud., Satoh A., Dev Dyn. December 1, 2005; 234 (4): 846-57.
	BMP-3 is a novel inhibitor of both activin and BMP-4 signaling in Xenopus embryos., Gamer LW., Dev Biol. September 1, 2005; 285 (1): 156-68.
	Transgenic frogs expressing the highly fluorescent protein venus under the control of a strong mammalian promoter suitable for monitoring living cells., Sakamaki K., Dev Dyn. June 1, 2005; 233 (2): 562-9.
	Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.
	The fungicide benomyl inhibits differentiation of neural tissue in the Xenopus embryo and animal cap explants., Yoon CS., Environ Toxicol. October 1, 2003; 18 (5): 327-37.
	Isolation and growth factor inducibility of the Xenopus laevis Lmx1b gene., Haldin CE., Int J Dev Biol. May 1, 2003; 47 (4): 253-62.
	Xenopus Nbx, a novel NK-1 related gene essential for neural crest formation., Kurata T., Dev Biol. May 1, 2003; 257 (1): 30-40.
	Xenopus, the next generation: X. tropicalis genetics and genomics., Hirsch N., Dev Dyn. December 1, 2002; 225 (4): 422-33.
	The E3 ubiquitin ligase GREUL1 anteriorizes ectoderm during Xenopus development., Borchers AG., Dev Biol. November 15, 2002; 251 (2): 395-408.
	Distinct enhancers regulate skeletal and cardiac muscle-specific expression programs of the cardiac alpha-actin gene in Xenopus embryos., Latinkić BV., Dev Biol. May 1, 2002; 245 (1): 57-70.
	Cloning and characterization of the T-box gene Tbx6 in Xenopus laevis., Uchiyama H., Dev Growth Differ. December 1, 2001; 43 (6): 657-69.
	The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling., Domingos PM., Dev Biol. November 1, 2001; 239 (1): 148-60.
	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 FGFR pathway is required for the trunk-inducing functions of Spemann's organizer., Mitchell TS., Dev Biol. September 15, 2001; 237 (2): 295-305.
	Endoderm specification and differentiation in Xenopus embryos., Horb ME., Dev Biol. August 15, 2001; 236 (2): 330-43.
	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.
	A role for BMP signalling in heart looping morphogenesis in Xenopus., Breckenridge RA., Dev Biol. April 1, 2001; 232 (1): 191-203.
	Downregulation of Hedgehog signaling is required for organogenesis of the small intestine in Xenopus., Zhang J., Dev Biol. January 1, 2001; 229 (1): 188-202.
	FGF signaling restricts the primary blood islands to ventral mesoderm., Kumano G., Dev Biol. December 15, 2000; 228 (2): 304-14.

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