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Summary Anatomy Item Literature (1127) Expression Attributions Wiki
XB-ANAT-3329

Papers associated with pectoral appendage (and ctnnb1)

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Desmoplakin is required for epidermal integrity and morphogenesis in the Xenopus laevis embryo., Bharathan NK., Dev Biol. January 1, 2019; 450 (2): 115-131.                            


TMEM88 mediates inflammatory cytokines secretion by regulating JNK/P38 and canonical Wnt/β-catenin signaling pathway in LX-2 cells., Xu T., Inflammopharmacology. October 1, 2018; 26 (5): 1339-1348.


High variability of expression profiles of homeologous genes for Wnt, Hh, Notch, and Hippo signaling pathways in Xenopus laevis., Michiue T., Dev Biol. June 15, 2017; 426 (2): 270-290.                  


Identifying domains of EFHC1 involved in ciliary localization, ciliogenesis, and the regulation of Wnt signaling., Zhao Y., Dev Biol. March 15, 2016; 411 (2): 257-265.                      


JmjC Domain-containing Protein 6 (Jmjd6) Derepresses the Transcriptional Repressor Transcription Factor 7-like 1 (Tcf7l1) and Is Required for Body Axis Patterning during Xenopus Embryogenesis., Zhang X., J Biol Chem. August 14, 2015; 290 (33): 20273-83.                      


Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.                                  


Derricin and derricidin inhibit Wnt/β-catenin signaling and suppress colon cancer cell growth in vitro., Fonseca BF., PLoS One. January 1, 2015; 10 (3): e0120919.              


Loss of Xenopus cadherin-11 leads to increased Wnt/β-catenin signaling and up-regulation of target genes c-myc and cyclin D1 in neural crest., Koehler A., Dev Biol. November 1, 2013; 383 (1): 132-45.                        


Connective tissue cells, but not muscle cells, are involved in establishing the proximo-distal outcome of limb regeneration in the axolotl., Nacu E., Development. February 1, 2013; 140 (3): 513-8.


Imparting regenerative capacity to limbs by progenitor cell transplantation., Lin G., Dev Cell. January 14, 2013; 24 (1): 41-51.                          


A photoactivatable small-molecule inhibitor for light-controlled spatiotemporal regulation of Rho kinase in live embryos., Morckel AR., Development. January 1, 2012; 139 (2): 437-42.        


Different requirement for Wnt/β-catenin signaling in limb regeneration of larval and adult Xenopus., Yokoyama H., PLoS One. January 1, 2011; 6 (7): e21721.                


β-catenin is a molecular switch that regulates transition of cell-cell adhesion to fusion., Takezawa Y., Sci Rep. January 1, 2011; 1 68.          


Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.                        


N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements., Nandadasa S., Development. April 1, 2009; 136 (8): 1327-38.                      


The functions and possible significance of Kremen as the gatekeeper of Wnt signalling in development and pathology., Nakamura T., J Cell Mol Med. April 1, 2008; 12 (2): 391-408.          


Wise retained in the endoplasmic reticulum inhibits Wnt signaling by reducing cell surface LRP6., Guidato S., Dev Biol. October 15, 2007; 310 (2): 250-63.                


Domains of axin involved in protein-protein interactions, Wnt pathway inhibition, and intracellular localization., Fagotto F., J Cell Biol. May 17, 1999; 145 (4): 741-56.                  


The roles of maternal alpha-catenin and plakoglobin in the early Xenopus embryo., Kofron M., Development. April 1, 1997; 124 (8): 1553-60.        


Maternal beta-catenin establishes a ''dorsal signal'' in early Xenopus embryos., Wylie C., Development. October 1, 1996; 122 (10): 2987-96.              

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