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Summary Anatomy Item Literature (2127) Expression Attributions Wiki
XB-ANAT-3747

Papers associated with cytoplasm (and gsc)

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Phosphorylation-dependent ubiquitination of paraxial protocadherin (PAPC) controls gastrulation cell movements., Kai M., PLoS One. January 12, 2015; 10 (1): e0115111.              


NEDD4L regulates convergent extension movements in Xenopus embryos via Disheveled-mediated non-canonical Wnt signaling., Zhang Y., Dev Biol. August 1, 2014; 392 (1): 15-25.                              


Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins., Callery EM., Open Biol. April 1, 2012; 2 (4): 120060.                      


Rab5-mediated endocytosis of activin is not required for gene activation or long-range signalling in Xenopus., Hagemann AI., Development. August 1, 2009; 136 (16): 2803-13.                


Identification of a novel negative regulator of activin/nodal signaling in mesendodermal formation of Xenopus embryos., Cheong SM., J Biol Chem. June 19, 2009; 284 (25): 17052-60.                        


Ryk cooperates with Frizzled 7 to promote Wnt11-mediated endocytosis and is essential for Xenopus laevis convergent extension movements., Kim GH., J Cell Biol. September 22, 2008; 182 (6): 1073-82.          


Mechanism of activation of the Formin protein Daam1., Liu W., Proc Natl Acad Sci U S A. January 8, 2008; 105 (1): 210-5.                


Interpretation of BMP signaling in early Xenopus development., Simeoni I., Dev Biol. August 1, 2007; 308 (1): 82-92.                  


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


Kinesin-mediated transport of Smad2 is required for signaling in response to TGF-beta ligands., Batut J., Dev Cell. February 1, 2007; 12 (2): 261-74.  


A cell cycle arrest is necessary for bottle cell formation in the early Xenopus gastrula: integrating cell shape change, local mitotic control and mesodermal patterning., Kurth T., Mech Dev. December 1, 2005; 122 (12): 1251-65.                  


A role for biliverdin IXalpha in dorsal axis development of Xenopus laevis embryos., Falchuk KH., Proc Natl Acad Sci U S A. January 8, 2002; 99 (1): 251-6.                


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.                    


Two-step induction of primitive erythrocytes in Xenopus laevis embryos: signals from the vegetal endoderm and the overlying ectoderm., Kikkawa M., Int J Dev Biol. April 1, 2001; 45 (2): 387-96.                


A role for GATA5 in Xenopus endoderm specification., Weber H., Development. October 1, 2000; 127 (20): 4345-60.                  


The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.              


Distribution of dorsal-forming activity in precleavage embryos of the Japanese newt, Cynops pyrrhogaster: effects of deletion of vegetal cytoplasm, UV irradiation, and lithium treatment., Doi JY., Dev Biol. July 1, 2000; 223 (1): 154-68.


Analysis of HIV-1 Tat effects in Xenopus laevis embryos., Venanzi S., J Biomed Sci. January 1, 1998; 5 (3): 211-20.


The KH domain protein encoded by quaking functions as a dimer and is essential for notochord development in Xenopus embryos., Zorn AM., Genes Dev. September 1, 1997; 11 (17): 2176-90.                  


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.                    


Expression cloning of a Xenopus T-related gene (Xombi) involved in mesodermal patterning and blastopore lip formation., Lustig KD., Development. December 1, 1996; 122 (12): 4001-12.                  

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