Papers associated with tail (and gdf3)

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	Endodermal Maternal Transcription Factors Establish Super-Enhancers during Zygotic Genome Activation., Paraiso KD., Cell Rep. June 4, 2019; 27 (10): 2962-2977.e5.
	Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus., Gentsch GE., Dev Cell. March 12, 2018; 44 (5): 597-610.e10.
	Maternal Gdf3 is an obligatory cofactor in Nodal signaling for embryonic axis formation in zebrafish., Bisgrove BW., Elife. November 15, 2017; 6
	Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A., Development. June 1, 2014; 141 (11): 2260-70.
	High-resolution analysis of gene activity during the Xenopus mid-blastula transition., Collart C., Development. May 1, 2014; 141 (9): 1927-39.
	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.
	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.
	Toward an unbiased evolutionary platform for unraveling Xenopus developmental gene networks., Beer R., Genesis. March 1, 2012; 50 (3): 186-91.
	Bone morphogenetic protein-3 family members and their biological functions., Hino J., Front Biosci. May 1, 2004; 9 1520-9.
	ALK4 functions as a receptor for multiple TGF beta-related ligands to regulate left-right axis determination and mesoderm induction in Xenopus., Chen Y., Dev Biol. April 15, 2004; 268 (2): 280-94.
	Coordination of BMP-3b and cerberus is required for head formation of Xenopus embryos., Hino J., Dev Biol. August 1, 2003; 260 (1): 138-57.

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