Papers associated with tail bud (and tbx6)

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	Mechanical Tensions Regulate Gene Expression in the Xenopus laevis Axial Tissues., Eroshkin FM., Int J Mol Sci. January 10, 2024; 25 (2):
	Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):
	Evolution of Somite Compartmentalization: A View From Xenopus., Della Gaspera B., Front Cell Dev Biol. January 1, 2021; 9 790847.
	Xenopus gpx3 Mediates Posterior Development by Regulating Cell Death during Embryogenesis., Lee H, Lee H., Antioxidants (Basel). December 12, 2020; 9 (12):
	Pinhead signaling regulates mesoderm heterogeneity via FGF receptor-dependent pathway., Ossipova O., Development. January 1, 2020;
	Gon4l regulates notochord boundary formation and cell polarity underlying axis extension by repressing adhesion genes., Williams MLK., Nat Commun. April 3, 2018; 9 (1): 1319.
	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.
	Conservatism and variability of gene expression profiles among homeologous transcription factors in Xenopus laevis., Watanabe M., Dev Biol. June 15, 2017; 426 (2): 301-324.
	RARβ2 is required for vertebrate somitogenesis., Janesick A., Development. June 1, 2017; 144 (11): 1997-2008.
	Development of the vertebrate tailbud., Beck CW., Wiley Interdiscip Rev Dev Biol. January 1, 2015; 4 (1): 33-44.
	Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A., Development. June 1, 2014; 141 (11): 2260-70.
	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.
	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.
	Early transcriptional targets of MyoD link myogenesis and somitogenesis., Maguire RJ., Dev Biol. November 15, 2012; 371 (2): 256-68.
	A divergent Tbx6-related gene and Tbx6 are both required for neural crest and intermediate mesoderm development in Xenopus., Callery EM., Dev Biol. April 1, 2010; 340 (1): 75-87.
	The RNA-binding protein Seb4/RBM24 is a direct target of MyoD and is required for myogenesis during Xenopus early development., Li HY., Mech Dev. January 1, 2010; 127 (5-6): 281-91.
	The Xenopus Bowline/Ripply family proteins negatively regulate the transcriptional activity of T-box transcription factors., Hitachi K., Int J Dev Biol. January 1, 2009; 53 (4): 631-9.
	Tbx6, Thylacine1, and E47 synergistically activate bowline expression in Xenopus somitogenesis., Hitachi K., Dev Biol. January 15, 2008; 313 (2): 816-28.
	Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.
	Identification of novel genes affecting mesoderm formation and morphogenesis through an enhanced large scale functional screen in Xenopus., Chen JA., Mech Dev. March 1, 2005; 122 (3): 307-31.
	Cloning and characterization of the T-box gene Tbx6 in Xenopus laevis., Uchiyama H., Dev Growth Differ. December 1, 2001; 43 (6): 657-69.
	The bHLH class protein pMesogenin1 can specify paraxial mesoderm phenotypes., Yoon JK., Dev Biol. June 15, 2000; 222 (2): 376-91.
	Characterization of the zebrafish tbx16 gene and evolution of the vertebrate T-box family., Ruvinsky I., Dev Genes Evol. April 1, 1998; 208 (2): 94-9.

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