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Summary Anatomy Item Literature (1495) Expression Attributions Wiki
XB-ANAT-20

Papers associated with spinal cord (and tuba4b)

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Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components., Hantel F., J Cell Sci. May 1, 2022; 135 (9):                                     


The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos., Willsey HR., Development. June 22, 2020; 147 (21):                             


La-related protein 6 controls ciliated cell differentiation., Manojlovic Z., Cilia. January 1, 2017; 6 4.                


Identifying domains of EFHC1 involved in ciliary localization, ciliogenesis, and the regulation of Wnt signaling., Zhao Y., Dev Biol. March 15, 2016; 411 (2): 257-265.                      


ATP4a is required for development and function of the Xenopus mucociliary epidermis - a potential model to study proton pump inhibitor-associated pneumonia., Walentek P., Dev Biol. December 15, 2015; 408 (2): 292-304.                                


Astrocytes phagocytose focal dystrophies from shortening myelin segments in the optic nerve of Xenopus laevis at metamorphosis., Mills EA., Proc Natl Acad Sci U S A. August 18, 2015; 112 (33): 10509-14.                                          


TGF-β Signaling Regulates the Differentiation of Motile Cilia., Tözser J., Cell Rep. May 19, 2015; 11 (7): 1000-7.                


Microtubule-associated protein tau promotes neuronal class II β-tubulin microtubule formation and axon elongation in embryonic Xenopus laevis., Liu Y., Eur J Neurosci. May 1, 2015; 41 (10): 1263-75.            


ATP4 and ciliation in the neuroectoderm and endoderm of Xenopus embryos and tadpoles., Walentek P., Data Brief. April 20, 2015; 4 22-31.            


Regulation of ECM degradation and axon guidance by growth cone invadosomes., Santiago-Medina M., Development. February 1, 2015; 142 (3): 486-96.                        


The Rac1 regulator ELMO controls basal body migration and docking in multiciliated cells through interaction with Ezrin., Epting D., Development. January 1, 2015; 142 (1): 174-84.                                            


Transcriptional regulators in the Hippo signaling pathway control organ growth in Xenopus tadpole tail regeneration., Hayashi S., Dev Biol. December 1, 2014; 396 (1): 31-41.                      


Genome-wide expression profile of the response to spinal cord injury in Xenopus laevis reveals extensive differences between regenerative and non-regenerative stages., Lee-Liu D., Neural Dev. May 22, 2014; 9 12.              


RFX7 is required for the formation of cilia in the neural tube., Manojlovic Z., Mech Dev. May 1, 2014; 132 28-37.                  


A novel serotonin-secreting cell type regulates ciliary motility in the mucociliary epidermis of Xenopus tadpoles., Walentek P., Development. April 1, 2014; 141 (7): 1526-33.                        


Stabilization of speckle-type POZ protein (Spop) by Daz interacting protein 1 (Dzip1) is essential for Gli turnover and the proper output of Hedgehog signaling., Schwend T., J Biol Chem. November 8, 2013; 288 (45): 32809-32820.                


Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton., Ioannou A., Dev Biol. August 15, 2013; 380 (2): 243-58.                                  


Kidins220/ARMS is dynamically expressed during Xenopus laevis development., Marracci S., Int J Dev Biol. January 1, 2013; 57 (9-10): 787-92.            


Plakophilin-3 is required for late embryonic amphibian development, exhibiting roles in ectodermal and neural tissues., Munoz WA., PLoS One. January 1, 2012; 7 (4): e34342.              


IP3 signaling is required for cilia formation and left-right body axis determination in Xenopus embryos., Hatayama M., Biochem Biophys Res Commun. July 8, 2011; 410 (3): 520-4.      


MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.                                                      


Transplantation of Xenopus laevis ears reveals the ability to form afferent and efferent connections with the spinal cord., Elliott KL., Int J Dev Biol. January 1, 2010; 54 (10): 1443-51.          


Localization of Kv2.2 protein in Xenopus laevis embryos and tadpoles., Gravagna NG., J Comp Neurol. October 10, 2008; 510 (5): 508-24.                        


Development of the retinotectal system in the direct-developing frog Eleutherodactylus coqui in comparison with other anurans., Schlosser G., Front Zool. June 23, 2008; 5 9.              


Cilia-driven leftward flow determines laterality in Xenopus., Schweickert A., Curr Biol. January 9, 2007; 17 (1): 60-6.        


Neogenin interacts with RGMa and netrin-1 to guide axons within the embryonic vertebrate forebrain., Wilson NH., Dev Biol. August 15, 2006; 296 (2): 485-98.                      


Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.                                                            


Neurofilaments help maintain normal morphologies and support elongation of neurites in Xenopus laevis cultured embryonic spinal cord neurons., Lin W., J Neurosci. December 1, 1995; 15 (12): 8331-44.                


The appearance of acetylated alpha-tubulin during early development and cellular differentiation in Xenopus., Chu DT., Dev Biol. November 1, 1989; 136 (1): 104-17.                  

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