Papers associated with inhba (and morpholino)

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	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A, Gillis WQ, Zhu H, Thomsen GH., Dev Biol. August 15, 2014; 392 (2): 358-67.
	Activin ligands are required for the re-activation of Smad2 signalling after neurulation and vascular development in Xenopus tropicalis., Nagamori Y, Roberts S, Maciej M, Dorey K., Int J Dev Biol. January 1, 2014; 58 (10-12): 783-91.
	Activin ligands are required for the re-activation of Smad2 signalling after neurulation and vascular development in Xenopus tropicalis., Nagamori Y, Roberts S, Maciej M, Dorey K., Int J Dev Biol. January 1, 2014; 58 (10-12): 783-91.
	Optimal histone H3 to linker histone H1 chromatin ratio is vital for mesodermal competence in Xenopus., Lim CY, Reversade B, Knowles BB, Solter D., Development. February 1, 2013; 140 (4): 853-60.
	ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P, Beyer T, Thumberger T, Schweickert A, Blum M., Cell Rep. May 31, 2012; 1 (5): 516-27.
	Geminin is required for zygotic gene expression at the Xenopus mid-blastula transition., Kerns SL, Schultz KM, Barry KA, Thorne TM, McGarry TJ., PLoS One. January 1, 2012; 7 (5): e38009.
	Vertebrate development requires ARVCF and p120 catenins and their interplay with RhoA and Rac., Fang X, Ji H, Kim SW, Park JI, Vaught TG, Anastasiadis PZ, Ciesiolka M, McCrea PD., J Cell Biol. April 1, 2004; 165 (1): 87-98.

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