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Summary Anatomy Item Literature (4219) Expression Attributions Wiki
XB-ANAT-1553

Papers associated with regenerating tissue (and myh6)

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A systemic cell cycle block impacts stage-specific histone modification profiles during Xenopus embryogenesis., Pokrovsky D., PLoS Biol. September 1, 2021; 19 (9): e3001377.                        


Analysis of Craniocardiac Malformations in Xenopus using Optical Coherence Tomography., Deniz E., Sci Rep. February 14, 2017; 7 42506.          


A developmentally regulated switch from stem cells to dedifferentiation for limb muscle regeneration in newts., Tanaka HV., Nat Commun. January 12, 2016; 7 11069.        


A thioredoxin fold protein Sh3bgr regulates Enah and is necessary for proper sarcomere formation., Jang DG., Dev Biol. September 1, 2015; 405 (1): 1-9.                                    


Ectopic blastema induction by nerve deviation and skin wounding: a new regeneration model in Xenopus laevis., Mitogawa K., Regeneration (Oxf). May 28, 2014; 1 (2): 26-36.            


Wiring the retinal circuits activated by light during early development., Bertolesi GE., Neural Dev. February 13, 2014; 9 3.              


The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.                            


Early development of the thymus in Xenopus laevis., Lee YH, Lee YH., Dev Dyn. February 1, 2013; 242 (2): 164-78.                            


Paralysis and delayed Z-disc formation in the Xenopus tropicalis unc45b mutant dicky ticker., Geach TJ., BMC Dev Biol. January 22, 2010; 10 75.                    


FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis., Schuff M., Dev Biol. January 15, 2010; 337 (2): 259-73.                  


Absence of heartbeat in the Xenopus tropicalis mutation muzak is caused by a nonsense mutation in cardiac myosin myh6., Abu-Daya A., Dev Biol. December 1, 2009; 336 (1): 20-9.            


Notch activates Wnt-4 signalling to control medio-lateral patterning of the pronephros., Naylor RW., Development. November 1, 2009; 136 (21): 3585-95.                                  


The keratin-related Ouroboros proteins function as immune antigens mediating tail regression in Xenopus metamorphosis., Mukaigasa K., Proc Natl Acad Sci U S A. October 27, 2009; 106 (43): 18309-14.      


Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size., Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.                                          


In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.                      


DM-GRASP/ALCAM/CD166 is required for cardiac morphogenesis and maintenance of cardiac identity in first heart field derived cells., Gessert S., Dev Biol. September 1, 2008; 321 (1): 150-61.            


Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline., Christine KS., Dev Cell. April 1, 2008; 14 (4): 616-23.                                


UNC-98 links an integrin-associated complex to thick filaments in Caenorhabditis elegans muscle., Miller RK., J Cell Biol. December 18, 2006; 175 (6): 853-9.          


Genetic screens for mutations affecting development of Xenopus tropicalis., Goda T., PLoS Genet. June 1, 2006; 2 (6): e91.                        


The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis., Huot ME., Mol Biol Cell. September 1, 2005; 16 (9): 4350-61.                  


Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.            


Inhibition of the cell cycle is required for convergent extension of the paraxial mesoderm during Xenopus neurulation., Leise WF., Development. April 1, 2004; 131 (8): 1703-15.              


Larval antigen molecules recognized by adult immune cells of inbred Xenopus laevis: partial characterization and implication in metamorphosis., Izutsu Y., Dev Growth Differ. December 1, 2002; 44 (6): 477-88.            


Xenopus bagpipe-related gene, koza, may play a role in regulation of cell proliferation., Newman CS., Dev Dyn. December 1, 2002; 225 (4): 571-80.    


Two myogenin-related genes are differentially expressed in Xenopus laevis myogenesis and differ in their ability to transactivate muscle structural genes., Charbonnier F., J Biol Chem. January 11, 2002; 277 (2): 1139-47.              


Larval antigen molecules recognized by adult immune cells of inbred Xenopus laevis: two pathways for recognition by adult splenic T cells., Izutsu Y., Dev Biol. May 15, 2000; 221 (2): 365-74.          


Expression of myogenic regulatory factors during muscle development of Xenopus: myogenin mRNA accumulation is limited strictly to secondary myogenesis., Nicolas N., Dev Dyn. November 1, 1998; 213 (3): 309-21.


Isoform transition of contractile proteins related to muscle remodeling with an axial gradient during metamorphosis in Xenopus laevis., Nishikawa A., Dev Biol. September 1, 1994; 165 (1): 86-94.                      


Cloning of the cDNA encoding a myosin heavy chain B isoform of Xenopus nonmuscle myosin with an insert in the head region., Bhatia-Dey N., Proc Natl Acad Sci U S A. April 1, 1993; 90 (7): 2856-9.


MHC class I antigens as surface markers of adult erythrocytes during the metamorphosis of Xenopus., Flajnik MF., Dev Biol. July 1, 1988; 128 (1): 198-206.


Suppression in Xenopus laevis: thymus inducer, spleen effector cells., Ruben LN., Immunology. January 1, 1985; 54 (1): 65-70.

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