Papers associated with primary germ layer (and hpse)

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	Elevated pentose phosphate pathway flux supports appendage regeneration., Patel JH., Cell Rep. October 25, 2022; 41 (4): 111552.
	Xenopus laevis il11ra.L is an experimentally proven interleukin-11 receptor component that is required for tadpole tail regeneration., Suzuki S., Sci Rep. February 3, 2022; 12 (1): 1903.
	Mucociliary Epithelial Organoids from Xenopus Embryonic Cells: Generation, Culture and High-Resolution Live Imaging., Kang HJ., J Vis Exp. July 28, 2020; (161):
	The AP-1 transcription factor JunB functions in Xenopus tail regeneration by positively regulating cell proliferation., Nakamura M., Biochem Biophys Res Commun. February 19, 2020; 522 (4): 990-995.
	Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates., Kim HY, Kim HY., Nat Commun. January 31, 2020; 11 (1): 665.
	A transgenic reporter under control of an es1 promoter/enhancer marks wound epidermis and apical epithelial cap during tail regeneration in Xenopus laevis tadpole., Sato K., Dev Biol. January 15, 2018; 433 (2): 404-415.
	In vivo tracking of histone H3 lysine 9 acetylation in Xenopus laevis during tail regeneration., Suzuki M., Genes Cells. April 1, 2016; 21 (4): 358-69.
	Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus., Roberts NA., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.
	Expression analysis of XPhyH-like during development and tail regeneration in Xenopus tadpoles: possible role of XPhyH-like expressing immune cells in impaired tail regenerative ability., Naora Y., Biochem Biophys Res Commun. February 8, 2013; 431 (2): 152-7.
	Changes in the inflammatory response to injury and its resolution during the loss of regenerative capacity in developing Xenopus limbs., Mescher AL., PLoS One. January 1, 2013; 8 (11): e80477.
	In vivo electroporation of morpholinos into the regenerating adult zebrafish tail fin., Hyde DR., J Vis Exp. March 29, 2012; (61): .
	Two promoters with distinct activities in different tissues drive the expression of heparanase in Xenopus., Bertolesi GE., Dev Dyn. December 1, 2011; 240 (12): 2657-72.
	Patterned femtosecond-laser ablation of Xenopus laevis melanocytes for studies of cell migration, wound repair, and developmental processes., Mondia JP., Biomed Opt Express. August 1, 2011; 2 (8): 2383-91.
	HDAC activity is required during Xenopus tail regeneration., Tseng AS., PLoS One. January 1, 2011; 6 (10): e26382.
	Long-distance signals are required for morphogenesis of the regenerating Xenopus tadpole tail, as shown by femtosecond-laser ablation., Mondia JP., PLoS One. January 1, 2011; 6 (9): e24953.
	Induction of vertebrate regeneration by a transient sodium current., Tseng AS., J Neurosci. September 29, 2010; 30 (39): 13192-200.
	TGF-beta signaling is required for multiple processes during Xenopus tail regeneration., Ho DM., Dev Biol. March 1, 2008; 315 (1): 203-16.
	Apoptosis is required during early stages of tail regeneration in Xenopus laevis., Tseng AS., Dev Biol. January 1, 2007; 301 (1): 62-9.

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