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Summary Anatomy Item Literature (7382) Expression Attributions Wiki
XB-ANAT-11

Papers associated with brain (and actc1)

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Predation threats for a 24-h period activated the extension of axons in the brains of Xenopus tadpoles., Mori T., Sci Rep. January 1, 2020; 10 (1): 11737.                    


Defective heart chamber growth and myofibrillogenesis after knockout of adprhl1 gene function by targeted disruption of the ancestral catalytic active site., Smith SJ., PLoS One. January 1, 2020; 15 (7): e0235433.                                            


Role of the visual experience-dependent nascent proteome in neuronal plasticity., Liu HH., Elife. January 1, 2018; 7                     


Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus., Gentsch GE., Dev Cell. January 1, 2018; 44 (5): 597-610.e10.                                            


Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G., PLoS Genet. May 1, 2017; 13 (5): e1006757.                                    


The CapZ interacting protein Rcsd1 is required for cardiogenesis downstream of Wnt11a in Xenopus laevis., Hempel A., Dev Biol. January 1, 2017; 424 (1): 28-39.                                  


FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue., Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.              


The cardiac-restricted protein ADP-ribosylhydrolase-like 1 is essential for heart chamber outgrowth and acts on muscle actin filament assembly., Smith SJ., Dev Biol. August 15, 2016; 416 (2): 373-88.                                                      


Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development., Owens ND., Cell Rep. January 26, 2016; 14 (3): 632-47.                                                  


Cell-fate determination by ubiquitin-dependent regulation of translation., Werner A., Nature. September 24, 2015; 525 (7570): 523-7.                            


A method for using direct injection of plasmid DNA to study cis-regulatory element activity in F0 Xenopus embryos and tadpoles., Wang C., Dev Biol. February 1, 2015; 398 (1): 11-23.              


Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.                                          


PV.1 induced by FGF-Xbra functions as a repressor of neurogenesis in Xenopus embryos., Yoon J., BMB Rep. December 1, 2014; 47 (12): 673-8.        


Congenital heart disease protein 5 associates with CASZ1 to maintain myocardial tissue integrity., Sojka S., Development. August 1, 2014; 141 (15): 3040-9.                


Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification., Yasuoka Y., Nat Commun. July 9, 2014; 5 4322.      


Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus., Young JJ., Development. April 1, 2014; 141 (8): 1683-93.                                                                


Comparative analysis reveals distinct and overlapping functions of Mef2c and Mef2d during cardiogenesis in Xenopus laevis., Guo Y., PLoS One. January 1, 2014; 9 (1): e87294.                


Circadian genes, xBmal1 and xNocturnin, modulate the timing and differentiation of somites in Xenopus laevis., Curran KL., PLoS One. January 1, 2014; 9 (9): e108266.                            


Expression cloning of camelid nanobodies specific for Xenopus embryonic antigens., Itoh K., PLoS One. January 1, 2014; 9 (10): e107521.            


Maturin is a novel protein required for differentiation during primary neurogenesis., Martinez-De Luna RI., Dev Biol. December 1, 2013; 384 (1): 26-40.                        


Tcf21 regulates the specification and maturation of proepicardial cells., Tandon P., Development. June 1, 2013; 140 (11): 2409-21.                                


Germline Transgenic Methods for Tracking Cells and Testing Gene Function during Regeneration in the Axolotl., Khattak S., Stem Cell Reports. January 1, 2013; 1 (1): 90-103.            


Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural development., Xu Y, Xu Y., Cell. December 7, 2012; 151 (6): 1200-13.                


Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B., Dev Dyn. May 1, 2012; 241 (5): 995-1007.                                    


SHP-2 acts via ROCK to regulate the cardiac actin cytoskeleton., Langdon Y., Development. March 1, 2012; 139 (5): 948-57.                


A homolog of Subtilisin-like Proprotein Convertase 7 is essential to anterior neural development in Xenopus., Senturker S., PLoS One. January 1, 2012; 7 (6): e39380.                


Mef2d acts upstream of muscle identity genes and couples lateral myogenesis to dermomyotome formation in Xenopus laevis., Della Gaspera B., PLoS One. January 1, 2012; 7 (12): e52359.                  


The forkhead transcription factor FoxB1 regulates the dorsal-ventral and anterior-posterior patterning of the ectoderm during early Xenopus embryogenesis., Takebayashi-Suzuki K., Dev Biol. December 1, 2011; 360 (1): 11-29.              


Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.                              


The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos., Maczkowiak F., Dev Biol. April 15, 2010; 340 (2): 381-96.                                                  


Lymph heart musculature is under distinct developmental control from lymphatic endothelium., Peyrot SM., Dev Biol. March 15, 2010; 339 (2): 429-38.        


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.                        


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


Embryonic lethality of fortilin-null mutant mice by BMP-pathway overactivation., Koide Y., Biochim Biophys Acta. May 1, 2009; 1790 (5): 326-38.      


Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.              


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.                                


The myocardin-related transcription factor, MASTR, cooperates with MyoD to activate skeletal muscle gene expression., Meadows SM., Proc Natl Acad Sci U S A. February 5, 2008; 105 (5): 1545-50.        


The amphibian second heart field: Xenopus islet-1 is required for cardiovascular development., Brade T., Dev Biol. November 15, 2007; 311 (2): 297-310.          


Vertebrate Ctr1 coordinates morphogenesis and progenitor cell fate and regulates embryonic stem cell differentiation., Haremaki T., Proc Natl Acad Sci U S A. July 17, 2007; 104 (29): 12029-34.                    


The homeodomain factor Xanf represses expression of genes in the presumptive rostral forebrain that specify more caudal brain regions., Ermakova GV., Dev Biol. July 15, 2007; 307 (2): 483-97.        


Cell cycling and differentiation do not require the retinoblastoma protein during early Xenopus development., Cosgrove RA., Dev Biol. March 1, 2007; 303 (1): 311-24.                      


Xtn3 is a developmentally expressed cardiac and skeletal muscle-specific novex-3 titin isoform., Brown DD., Gene Expr Patterns. October 1, 2006; 6 (8): 913-8.          


The Xfeb gene is directly upregulated by Zic1 during early neural development., Li S., Dev Dyn. October 1, 2006; 235 (10): 2817-27.      


TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.                


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


FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.            


XHas2 activity is required during somitogenesis and precursor cell migration in Xenopus development., Ori M., Development. February 1, 2006; 133 (4): 631-40.                        


The zic1 gene is an activator of Wnt signaling., Merzdorf CS., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.              


Temporal analysis of the early BMP functions identifies distinct anti-organizer and mesoderm patterning phases., Marom K., Dev Biol. June 15, 2005; 282 (2): 442-54.              

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