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Summary Anatomy Item Literature (1562) Expression Attributions Wiki
XB-ANAT-55

Papers associated with notochord (and not)

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Tissue-specific expression of carbohydrate sulfotransferases drives keratan sulfate biosynthesis in the notochord and otic vesicles of Xenopus embryos., Yasuoka Y., Front Cell Dev Biol. January 1, 2023; 11 957805.                                          


ARVCF catenin controls force production during vertebrate convergent extension., Huebner RJ., Dev Cell. May 9, 2022; 57 (9): 1119-1131.e5.                      


Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):                                           


Pinhead antagonizes Admp to promote notochord formation., Itoh K., iScience. May 7, 2021; 24 (6): 102520.                            


Furry is required for cell movements during gastrulation and functionally interacts with NDR1., Cervino AS., Sci Rep. March 23, 2021; 11 (1): 6607.                                  


Tissue segregation in the early vertebrate embryo., Fagotto F., Semin Cell Dev Biol. November 1, 2020; 107 130-146.


Comprehensive RNA-Seq analysis of notochord-enriched genes induced during Xenopus tropicalis tail resorption., Nakajima K., Gen Comp Endocrinol. February 1, 2020; 287 113349.              


The tumor suppressor PTPRK promotes ZNRF3 internalization and is required for Wnt inhibition in the Spemann organizer., Chang LS., Elife. January 14, 2020; 9                                                                                               


A unique role of thyroid hormone receptor β in regulating notochord resorption during Xenopus metamorphosis., Nakajima K., Gen Comp Endocrinol. June 1, 2019; 277 66-72.            


Shared evolutionary origin of vertebrate neural crest and cranial placodes., Horie R., Nature. August 1, 2018; 560 (7717): 228-232.      


Intracellular calcium signal at the leading edge regulates mesodermal sheet migration during Xenopus gastrulation., Hayashi K., Sci Rep. February 5, 2018; 8 (1): 2433.              


Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover., Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.                                


interleukin-11 induces and maintains progenitors of different cell lineages during Xenopus tadpole tail regeneration., Tsujioka H., Nat Commun. September 8, 2017; 8 (1): 495.                                


sall1 and sall4 repress pou5f3 family expression to allow neural patterning, differentiation, and morphogenesis in Xenopus laevis., Exner CRT., Dev Biol. May 1, 2017; 425 (1): 33-43.                                    


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.              


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.        


Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A., Development. June 1, 2014; 141 (11): 2260-70.                    


A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance., Livigni A., Curr Biol. November 18, 2013; 23 (22): 2233-2244.                                    


Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.                    


Directional migration of leading-edge mesoderm generates physical forces: Implication in Xenopus notochord formation during gastrulation., Hara Y., Dev Biol. October 15, 2013; 382 (2): 482-95.                  


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


An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.                                      


Essential role of AWP1 in neural crest specification in Xenopus., Seo JH., Int J Dev Biol. January 1, 2013; 57 (11-12): 829-36.                  


Gastrulation and pre-gastrulation morphogenesis, inductions, and gene expression: similarities and dissimilarities between urodelean and anuran embryos., Kaneda T., Dev Biol. September 1, 2012; 369 (1): 1-18.          


Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.                          


A revised model of Xenopus dorsal midline development: differential and separable requirements for Notch and Shh signaling., Peyrot SM., Dev Biol. April 15, 2011; 352 (2): 254-66.                              


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.            


Xenopus furry contributes to release of microRNA gene silencing., Goto T., Proc Natl Acad Sci U S A. November 9, 2010; 107 (45): 19344-9.                        


Distinct Xenopus Nodal ligands sequentially induce mesendoderm and control gastrulation movements in parallel to the Wnt/PCP pathway., Luxardi G., Development. February 1, 2010; 137 (3): 417-26.          


Comparison of Lim1 expression in embryos of frogs with different modes of reproduction., Venegas-Ferrín M., Int J Dev Biol. January 1, 2010; 54 (1): 195-202.            


Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus., Thomas JT., J Biol Chem. July 10, 2009; 284 (28): 18994-9005.                    


The shroom family proteins play broad roles in the morphogenesis of thickened epithelial sheets., Lee C, Lee C, Lee C., Dev Dyn. June 1, 2009; 238 (6): 1480-91.                            


VegT, eFGF and Xbra cause overall posteriorization while Xwnt8 causes eye-level restricted posteriorization in synergy with chordin in early Xenopus development., Fujii H., Dev Growth Differ. March 1, 2008; 50 (3): 169-80.                  


Coordination of cell polarity during Xenopus gastrulation., Shindo A., PLoS One. February 6, 2008; 3 (2): e1600.              


Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction., Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.            


The mouse homeobox gene Noto regulates node morphogenesis, notochordal ciliogenesis, and left right patterning., Beckers A., Proc Natl Acad Sci U S A. October 2, 2007; 104 (40): 15765-70.


TGF-beta signaling-mediated morphogenesis: modulation of cell adhesion via cadherin endocytosis., Ogata S., Genes Dev. July 15, 2007; 21 (14): 1817-31.                  


Early molecular effects of ethanol during vertebrate embryogenesis., Yelin R., Differentiation. June 1, 2007; 75 (5): 393-403.                    


Inca: a novel p21-activated kinase-associated protein required for cranial neural crest development., Luo T., Development. April 1, 2007; 134 (7): 1279-89.      


XGAP, an ArfGAP, is required for polarized localization of PAR proteins and cell polarity in Xenopus gastrulation., Hyodo-Miura J., Dev Cell. July 1, 2006; 11 (1): 69-79.                                


Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.                            


Msx1 and Msx2 have shared essential functions in neural crest but may be dispensable in epidermis and axis formation in Xenopus., Khadka D., Int J Dev Biol. January 1, 2006; 50 (5): 499-502.          


New tools for visualization and analysis of morphogenesis in spherical embryos., Tyszka JM., Dev Dyn. December 1, 2005; 234 (4): 974-83.              


Antagonistic interaction between IGF and Wnt/JNK signaling in convergent extension in Xenopus embryo., Carron C., Mech Dev. November 1, 2005; 122 (11): 1234-47.                


XBtg2 is required for notochord differentiation during early Xenopus development., Sugimoto K., Dev Growth Differ. September 1, 2005; 47 (7): 435-43.        


Xenopus hairy2b specifies anterior prechordal mesoderm identity within Spemann's organizer., Yamaguti M., Dev Dyn. September 1, 2005; 234 (1): 102-13.          


Subcellular localization and signaling properties of dishevelled in developing vertebrate embryos., Park TJ., Curr Biol. June 7, 2005; 15 (11): 1039-44.                


XIC is required for Siamois activity and dorsoanterior development., Snider L., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.


Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures., Khokha MK., Dev Cell. March 1, 2005; 8 (3): 401-11.                          


Xenopus p21-activated kinase 5 regulates blastomeres' adhesive properties during convergent extension movements., Faure S., Dev Biol. January 15, 2005; 277 (2): 472-92.    

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