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Summary Anatomy Item Literature (3430) Expression Attributions Wiki
XB-ANAT-726

Papers associated with sensory system (and actc1)

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XIdx, a dominant negative regulator of bHLH function in early Xenopus embryos., Wilson R., Mech Dev. February 1, 1995; 49 (3): 211-22.          


The Xenopus homologue of Otx2 is a maternal homeobox gene that demarcates and specifies anterior body regions., Pannese M., Development. March 1, 1995; 121 (3): 707-20.                      


Localized BMP-4 mediates dorsal/ventral patterning in the early Xenopus embryo., Schmidt JE., Dev Biol. May 1, 1995; 169 (1): 37-50.              


Induction of dorsal mesoderm by soluble, mature Vg1 protein., Kessler DS., Development. July 1, 1995; 121 (7): 2155-64.            


Bone morphogenetic protein 2 in the early development of Xenopus laevis., Clement JH., Mech Dev. August 1, 1995; 52 (2-3): 357-70.            


Nodal-related signals induce axial mesoderm and dorsalize mesoderm during gastrulation., Jones CM., Development. November 1, 1995; 121 (11): 3651-62.                


Disruption of BMP signals in embryonic Xenopus ectoderm leads to direct neural induction., Hawley SH., Genes Dev. December 1, 1995; 9 (23): 2923-35.                


Xom: a Xenopus homeobox gene that mediates the early effects of BMP-4., Ladher R., Development. August 1, 1996; 122 (8): 2385-94.                          


The Xvent-2 homeobox gene is part of the BMP-4 signalling pathway controlling [correction of controling] dorsoventral patterning of Xenopus mesoderm., Onichtchouk D., Development. October 1, 1996; 122 (10): 3045-53.                  


A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation., Horb ME., Development. May 1, 1997; 124 (9): 1689-98.                    


Analysis of competence and of Brachyury autoinduction by use of hormone-inducible Xbra., Tada M., Development. June 1, 1997; 124 (11): 2225-34.                      


The ALK-2 and ALK-4 activin receptors transduce distinct mesoderm-inducing signals during early Xenopus development but do not co-operate to establish thresholds., Armes NA., Development. October 1, 1997; 124 (19): 3797-804.                


Epidermal induction and inhibition of neural fate by translation initiation factor 4AIII., Weinstein DC., Development. November 1, 1997; 124 (21): 4235-42.                  


Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.              


Xiro3 encodes a Xenopus homolog of the Drosophila Iroquois genes and functions in neural specification., Bellefroid EJ., EMBO J. January 2, 1998; 17 (1): 191-203.            


The Xenopus dorsalizing factor Gremlin identifies a novel family of secreted proteins that antagonize BMP activities., Hsu DR., Mol Cell. April 1, 1998; 1 (5): 673-83.                  


Xenopus Smad7 inhibits both the activin and BMP pathways and acts as a neural inducer., Casellas R., Dev Biol. June 1, 1998; 198 (1): 1-12.                


Geminin, a neuralizing molecule that demarcates the future neural plate at the onset of gastrulation., Kroll KL., Development. August 1, 1998; 125 (16): 3247-58.                


FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.                


Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.                


Subdivision of the cardiac Nkx2.5 expression domain into myogenic and nonmyogenic compartments., Raffin M., Dev Biol. February 15, 2000; 218 (2): 326-40.                  


Different activities of the frizzled-related proteins frzb2 and sizzled2 during Xenopus anteroposterior patterning., Bradley L., Dev Biol. November 1, 2000; 227 (1): 118-32.                    


Downregulation of Hedgehog signaling is required for organogenesis of the small intestine in Xenopus., Zhang J., Dev Biol. January 1, 2001; 229 (1): 188-202.                  


The FGFR pathway is required for the trunk-inducing functions of Spemann's organizer., Mitchell TS., Dev Biol. September 15, 2001; 237 (2): 295-305.        


Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.                    


Distinct enhancers regulate skeletal and cardiac muscle-specific expression programs of the cardiac alpha-actin gene in Xenopus embryos., Latinkić BV., Dev Biol. May 1, 2002; 245 (1): 57-70.          


The E3 ubiquitin ligase GREUL1 anteriorizes ectoderm during Xenopus development., Borchers AG., Dev Biol. November 15, 2002; 251 (2): 395-408.              


Xenopus, the next generation: X. tropicalis genetics and genomics., Hirsch N., Dev Dyn. December 1, 2002; 225 (4): 422-33.          


Isolation and growth factor inducibility of the Xenopus laevis Lmx1b gene., Haldin CE., Int J Dev Biol. May 1, 2003; 47 (4): 253-62.            


The fungicide benomyl inhibits differentiation of neural tissue in the Xenopus embryo and animal cap explants., Yoon CS., Environ Toxicol. October 1, 2003; 18 (5): 327-37.


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


XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis., Ataliotis P., Dev Dyn. April 1, 2005; 232 (4): 979-91.                  


Transgenic frogs expressing the highly fluorescent protein venus under the control of a strong mammalian promoter suitable for monitoring living cells., Sakamaki K., Dev Dyn. June 1, 2005; 233 (2): 562-9.            


BMP-3 is a novel inhibitor of both activin and BMP-4 signaling in Xenopus embryos., Gamer LW., Dev Biol. September 1, 2005; 285 (1): 156-68.              


Characteristics of initiation and early events for muscle development in the Xenopus limb bud., Satoh A., Dev Dyn. December 1, 2005; 234 (4): 846-57.            


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


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.          


FoxD3 regulation of Nodal in the Spemann organizer is essential for Xenopus dorsal mesoderm development., Steiner AB., Development. December 1, 2006; 133 (24): 4827-38.                    


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


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.            


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


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.                        


Involvement of Neptune in induction of the hatching gland and neural crest in the Xenopus embryo., Kurauchi T., Differentiation. January 1, 2010; 79 (4-5): 251-9.                


High-resolution whole-mount in situ hybridization using Quantum Dot nanocrystals., Ioannou A., J Biomed Biotechnol. January 1, 2012; 2012 627602.        


Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo., Martin LK., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.                


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


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.                


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


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


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.        

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