Papers associated with left (and hpse)

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	Chromatin accessibility analysis reveals distinct functions for HDAC and EZH2 activities in early appendage regeneration., Arbach HE., Wound Repair Regen. November 1, 2022; 30 (6): 707-725.
	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.
	Bacterial lipopolysaccharides can initiate regeneration of the Xenopus tadpole tail., Bishop TF., iScience. November 19, 2021; 24 (11): 103281.
	The Expression of Key Guidance Genes at a Forebrain Axon Turning Point Is Maintained by Distinct Fgfr Isoforms but a Common Downstream Signal Transduction Mechanism., Yang JJ., eNeuro. April 9, 2019; 6 (2):
	Early redox activities modulate Xenopus tail regeneration., Ferreira F., Nat Commun. October 16, 2018; 9 (1): 4296.
	Cross-limb communication during Xenopus hindlimb regenerative response: non-local bioelectric injury signals., Busse SM., Development. October 8, 2018; 145 (19):
	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.
	interleukin-11 induces and maintains progenitors of different cell lineages during Xenopus tadpole tail regeneration., Tsujioka H., Nat Commun. September 8, 2017; 8 (1): 495.
	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.
	A lectin-based glycomic approach to identify characteristic features of Xenopus embryogenesis., Onuma Y., PLoS One. January 1, 2013; 8 (2): e56581.
	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.
	About a snail, a toad, and rodents: animal models for adaptation research., Roubos EW., Front Endocrinol (Lausanne). January 1, 2010; 1 4.
	H+ pump-dependent changes in membrane voltage are an early mechanism necessary and sufficient to induce Xenopus tail regeneration., Adams DS., Development. April 1, 2007; 134 (7): 1323-35.
	Apoptosis is required during early stages of tail regeneration in Xenopus laevis., Tseng AS., Dev Biol. January 1, 2007; 301 (1): 62-9.
	Expression of a cloned adenovirus gene is inhibited by in vitro methylation., Vardimon L., Proc Natl Acad Sci U S A. February 1, 1982; 79 (4): 1073-7.

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