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Summary Anatomy Item Literature (5836) Expression Attributions Wiki
XB-ANAT-2

Papers associated with ectoderm∨derBy=4 (and ddx59)

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Characterization of convergent thickening, a major convergence force producing morphogenic movement in amphibians., Shook DR., Elife. April 11, 2022; 11                                     


HCN2 Channel-Induced Rescue of Brain Teratogenesis via Local and Long-Range Bioelectric Repair., Pai VP., Front Cell Neurosci. January 1, 2020; 14 136.                      


Ingression-type cell migration drives vegetal endoderm internalisation in the Xenopus gastrula., Wen JW., Elife. August 10, 2017; 6                           


Mechanical roles of apical constriction, cell elongation, and cell migration during neural tube formation in Xenopus., Inoue Y., Biomech Model Mechanobiol. December 1, 2016; 15 (6): 1733-1746.              


Ca2+/H+ exchange by acidic organelles regulates cell migration in vivo., Melchionda M., J Cell Biol. March 28, 2016; 212 (7): 803-13.            


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.                  


Normalized shape and location of perturbed craniofacial structures in the Xenopus tadpole reveal an innate ability to achieve correct morphology., Vandenberg LN., Dev Dyn. May 1, 2012; 241 (5): 863-78.                    


DAAM1 is a formin required for centrosome re-orientation during cell migration., Ang SF., PLoS One. September 7, 2010; 5 (9): .              


Identification of germ plasm-associated transcripts by microarray analysis of Xenopus vegetal cortex RNA., Cuykendall TN., Dev Dyn. June 1, 2010; 239 (6): 1838-48.                              


Directional migration of neural crest cells in vivo is regulated by Syndecan-4/Rac1 and non-canonical Wnt signaling/RhoA., Matthews HK., Development. May 1, 2008; 135 (10): 1771-80.                    


"Optical patch-clamping": single-channel recording by imaging Ca2+ flux through individual muscle acetylcholine receptor channels., Demuro A., J Gen Physiol. September 1, 2005; 126 (3): 179-92.                    

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