Papers associated with tail bud (and tp53)

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	Functions of block of proliferation 1 during anterior development in Xenopus laevis., Gärtner C., PLoS One. August 2, 2022; 17 (8): e0273507.
	Systematic mapping of rRNA 2'-O methylation during frog development and involvement of the methyltransferase Fibrillarin in eye and craniofacial development in Xenopus laevis., Delhermite J., PLoS Genet. January 18, 2022; 18 (1): e1010012.
	The Ribosomal Protein L5 Functions During Xenopus Anterior Development Through Apoptotic Pathways., Schreiner C., Front Cell Dev Biol. January 1, 2022; 10 777121.
	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.
	Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
	Lineage commitment of embryonic cells involves MEK1-dependent clearance of pluripotency regulator Ventx2., Scerbo P., Elife. June 27, 2017; 6
	Loss of Xenopus tropicalis EMSY causes impairment of gastrulation and upregulation of p53., Rana AA., N Biotechnol. July 1, 2011; 28 (4): 334-41.
	VentX trans-activates p53 and p16ink4a to regulate cellular senescence., Wu X., J Biol Chem. April 8, 2011; 286 (14): 12693-701.
	SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
	B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo., Okuda Y., PLoS Genet. May 6, 2010; 6 (5): e1000936.
	Claudin-like protein 24 interacts with the VEGFR-2 and VEGFR-3 pathways and regulates lymphatic vessel development., Saharinen P., Genes Dev. May 1, 2010; 24 (9): 875-80.
	DeltaNp63 antagonizes p53 to regulate mesoderm induction in Xenopus laevis., Barton CE., Dev Biol. May 1, 2009; 329 (1): 130-9.
	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.
	Maternal Interferon Regulatory Factor 6 is required for the differentiation of primary superficial epithelia in Danio and Xenopus embryos., Sabel JL., Dev Biol. January 1, 2009; 325 (1): 249-62.
	A functional screen for genes involved in Xenopus pronephros development., Kyuno J., Mech Dev. July 1, 2008; 125 (7): 571-86.
	Gene expression in Pre-MBT embryos and activation of maternally-inherited program of apoptosis to be executed at around MBT as a fail-safe mechanism in Xenopus early embryogenesis., Shiokawa K., Gene Regul Syst Bio. May 29, 2008; 2 213-31.
	Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination., Hilton EN., Hum Mol Genet. July 15, 2007; 16 (14): 1773-82.
	Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.
	Metazoan Scc4 homologs link sister chromatid cohesion to cell and axon migration guidance., Seitan VC., PLoS Biol. July 1, 2006; 4 (8): e242.
	Links between tumor suppressors: p53 is required for TGF-beta gene responses by cooperating with Smads., Cordenonsi M., Cell. May 2, 2003; 113 (3): 301-14.
	A Xenopus homolog of a human p53-activated gene, PA26, is specifically expressed in the notochord., Hikasa H., Mech Dev. February 1, 2001; 100 (2): 309-12.
	p53 activity is essential for normal development in Xenopus., Wallingford JB., Curr Biol. October 1, 1997; 7 (10): 747-57.

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