Papers associated with embryonic structure (and id2)

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	ZSWIM4 regulates embryonic patterning and BMP signaling by promoting nuclear Smad1 degradation., Wang C., EMBO Rep. February 1, 2024; 25 (2): 646-671.
	Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;
	HMCES modulates the transcriptional regulation of nodal/activin and BMP signaling in mESCs., Liang T., Cell Rep. July 12, 2022; 40 (2): 111038.
	Xenopus SOX5 enhances myogenic transcription indirectly through transrepression., Della Gaspera B., Dev Biol. October 15, 2018; 442 (2): 262-275.
	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.
	ZC4H2 stabilizes Smads to enhance BMP signalling, which is involved in neural development in Xenopus., Ma P., Open Biol. August 1, 2017; 7 (8):
	Genomic integration of Wnt/β-catenin and BMP/Smad1 signaling coordinates foregut and hindgut transcriptional programs., Stevens ML., Development. April 1, 2017; 144 (7): 1283-1295.
	Signaling crosstalk between TGFβ and Dishevelled/Par1b., Mamidi A., Cell Death Differ. October 1, 2012; 19 (10): 1689-97.
	Analyzing the function of a hox gene: an evolutionary approach., Michaut L., Dev Growth Differ. December 1, 2011; 53 (9): 982-93.
	The non-methylated DNA-binding function of Kaiso is not required in early Xenopus laevis development., Ruzov A., Development. March 1, 2009; 136 (5): 729-38.
	Identification of novel transcripts with differential dorso-ventral expression in Xenopus gastrula using serial analysis of gene expression., Faunes F., Genome Biol. February 11, 2009; 10 (2): R15.
	Xenopus Id3 is required downstream of Myc for the formation of multipotent neural crest progenitor cells., Light W., Development. April 1, 2005; 132 (8): 1831-41.
	To proliferate or to die: role of Id3 in cell cycle progression and survival of neural crest progenitors., Kee Y., Genes Dev. March 15, 2005; 19 (6): 744-55.
	Cardiac neural crest ablation alters Id2 gene expression in the developing heart., Martinsen BJ., Dev Biol. August 1, 2004; 272 (1): 176-90.
	A slug, a fox, a pair of sox: transcriptional responses to neural crest inducing signals., Heeg-Truesdell E., Birth Defects Res C Embryo Today. June 1, 2004; 72 (2): 124-39.
	Cloning and characterization of Xenopus Id4 reveals differing roles for Id genes., Liu KJ, Liu KJ., Dev Biol. December 15, 2003; 264 (2): 339-51.
	Localized XId3 mRNA activation in Xenopus embryos by cytoplasmic polyadenylation., Afouda AB., Mech Dev. October 1, 1999; 88 (1): 15-31.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
	Electrophysiological characteristics of cloned skeletal and cardiac muscle sodium channels., Chahine M., Am J Physiol. August 1, 1996; 271 (2 Pt 2): H498-506.
	Multiple domains contribute to the distinct inactivation properties of human heart and skeletal muscle Na+ channels., Makita N., Circ Res. February 1, 1996; 78 (2): 244-52.
	Id gene activity during Xenopus embryogenesis., Zhang H., Mech Dev. April 1, 1995; 50 (2-3): 119-30.
	XIdx, a dominant negative regulator of bHLH function in early Xenopus embryos., Wilson R., Mech Dev. February 1, 1995; 49 (3): 211-22.

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