Papers associated with mesoderm (and h3-3a)

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	The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis., Guo Y., Dev Biol. May 1, 2019; 449 (1): 1-13.
	The left-right asymmetry of liver lobation is generated by Pitx2c-mediated asymmetries in the hepatic diverticulum., Womble M., Dev Biol. July 15, 2018; 439 (2): 80-91.
	Noggin is required for first pharyngeal arch differentiation in the frog Xenopus tropicalis., Young JJ., Dev Biol. June 15, 2017; 426 (2): 245-254.
	Role of JNK during buccopharyngeal membrane perforation, the last step of embryonic mouth formation., Houssin NS., Dev Dyn. February 1, 2017; 246 (2): 100-115.
	Activation of a T-box-Otx2-Gsc gene network independent of TBP and TBP-related factors., Gazdag E., Development. April 15, 2016; 143 (8): 1340-50.
	Pou5f3.2-induced proliferative state of embryonic cells during gastrulation of Xenopus laevis embryo., Nishitani E., Dev Growth Differ. December 1, 2015; 57 (9): 591-600.
	Klhl31 attenuates β-catenin dependent Wnt signaling and regulates embryo myogenesis., Abou-Elhamd A., Dev Biol. June 1, 2015; 402 (1): 61-71.
	Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm., Nordin K., Dev Cell. November 10, 2014; 31 (3): 374-382.
	PPARβ interprets a chromatin signature of pluripotency to promote embryonic differentiation at gastrulation., Rotman N., PLoS One. December 9, 2013; 8 (12): e83300.
	On becoming neural: what the embryo can tell us about differentiating neural stem cells., Moody SA., Am J Stem Cells. June 30, 2013; 2 (2): 74-94.
	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.
	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.
	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.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	Repression of zygotic gene expression in the Xenopus germline., Venkatarama T., Development. February 1, 2010; 137 (4): 651-60.
	The F-box protein Cdc4/Fbxw7 is a novel regulator of neural crest development in Xenopus laevis., Almeida AD., Neural Dev. January 4, 2010; 5 1.
	The shroom family proteins play broad roles in the morphogenesis of thickened epithelial sheets., Lee C, Lee C, Lee C., Dev Dyn. June 1, 2009; 238 (6): 1480-91.
	Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline., Christine KS., Dev Cell. April 1, 2008; 14 (4): 616-23.
	The protein encoded by the germ plasm RNA Germes associates with dynein light chains and functions in Xenopus germline development., Berekelya LA., Differentiation. July 1, 2007; 75 (6): 546-58.
	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.
	Role of TSC-22 during early embryogenesis in Xenopus laevis., Hashiguchi A., Dev Growth Differ. December 1, 2004; 46 (6): 535-44.
	Neurotrophin-independent attraction of growing sensory and motor axons towards developing Xenopus limb buds in vitro., Tonge DA., Dev Biol. January 1, 2004; 265 (1): 169-80.

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