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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.
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.
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.
Transcriptional dynamics of tail regeneration in Xenopus tropicalis. , Chang J., Genesis. January 1, 2017; 55 (1-2):
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.
In vivo electroporation of morpholinos into the regenerating adult zebrafish tail fin. , Hyde DR., J Vis Exp. March 29, 2012; (61): .
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.