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Summary Anatomy Item Literature (14955) Expression Attributions Wiki
XB-ANAT-468

Papers associated with whole organism (and mhc2-dab)

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Proteomic screen reveals diverse protein transport between connected neurons in the visual system., Schiapparelli LM., Cell Rep. January 25, 2022; 38 (4): 110287.                                  


The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus., Beckers A., Sci Rep. June 25, 2021; 11 (1): 13333.                    


Zebrafish transgenic constructs label specific neurons in Xenopus laevis spinal cord and identify frog V0v spinal neurons., Juárez-Morales JL., Dev Neurobiol. September 1, 2017; 77 (8): 1007-1020.    


Mesodermal origin of median fin mesenchyme and tail muscle in amphibian larvae., Taniguchi Y., Sci Rep. June 18, 2015; 5 11428.                


Sterol carrier protein 2 regulates proximal tubule size in the Xenopus pronephric kidney by modulating lipid rafts., Cerqueira DM., Dev Biol. October 1, 2014; 394 (1): 54-64.                                          


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


Xenopus as a model system for the study of GOLPH2/GP73 function: Xenopus GOLPH2 is required for pronephros development., Li L., PLoS One. January 1, 2012; 7 (6): e38939.                                              


Notch destabilises maternal beta-catenin and restricts dorsal-anterior development in Xenopus., Acosta H., Development. June 1, 2011; 138 (12): 2567-79.                          


Identification and characterization of alternative promoters of zebrafish Rtn-4/Nogo genes in cultured cells and zebrafish embryos., Chen YC., Nucleic Acids Res. August 1, 2010; 38 (14): 4635-50.              


Membrane targeted horseradish peroxidase as a marker for correlative fluorescence and electron microscopy studies., Li J., Front Neural Circuits. February 26, 2010; 4 6.              


TMEPAI, a transmembrane TGF-beta-inducible protein, sequesters Smad proteins from active participation in TGF-beta signaling., Watanabe Y., Mol Cell. January 15, 2010; 37 (1): 123-34.                                      


Dynamic expression of axon guidance cues required for optic tract development is controlled by fibroblast growth factor signaling., Atkinson-Leadbeater K., J Neurosci. January 13, 2010; 30 (2): 685-93.            


FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy., Wuebbles RD., Dis Model Mech. January 1, 2009; 2 (5-6): 267-74.                  


Overexpression of 5-HT2B receptor results in retinal dysplasia and defective ocular morphogenesis in Xenopus embryos., Reisoli E., Dev Biol. December 9, 2008; 1244 32-9.          


HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.                        


Ectopic germline cells in embryos of Xenopus laevis., Ikenishi K., Dev Growth Differ. September 1, 2007; 49 (7): 561-70.      


Developmental and regional expression of NADPH-diaphorase/nitric oxide synthase in spinal cord neurons correlates with the emergence of limb motor networks in metamorphosing Xenopus laevis., Ramanathan S., Eur J Neurosci. October 1, 2006; 24 (7): 1907-22.                  


Control of muscle regeneration in the Xenopus tadpole tail by Pax7., Chen Y, Chen Y., Development. June 1, 2006; 133 (12): 2303-13.    


Limb regeneration in Xenopus laevis froglet., Suzuki M, Suzuki M., ScientificWorldJournal. May 12, 2006; 6 Suppl 1 26-37.        


XCR2, one of three Xenopus EGF-CFC genes, has a distinct role in the regulation of left-right patterning., Onuma Y., Development. January 1, 2006; 133 (2): 237-50.                                      


Connexin 43 expression in glial cells of developing rhombomeres of Xenopus laevis., Katbamna B., Int J Dev Neurosci. February 1, 2004; 22 (1): 47-55.            


A trial for induction of supernumerary primordial germ cells in Xenopus tadpoles by injecting RNA of Xenopus vasa homologue into germline cells of 32-cell embryos., Ikenishi K., Dev Growth Differ. January 1, 2003; 45 (5-6): 417-26.                  


Meiotic maturation induces animal-vegetal asymmetric distribution of aPKC and ASIP/PAR-3 in Xenopus oocytes., Nakaya M., Development. December 1, 2000; 127 (23): 5021-31.                


XCS-1, a maternally expressed gene product involved in regulating mitosis in Xenopus., Nakamura H., J Cell Sci. July 1, 2000; 113 ( Pt 13) 2497-505.                


Nitric oxide in the retinotectal system: a signal but not a retrograde messenger during map refinement and segregation., Rentería RC., J Neurosci. August 15, 1999; 19 (16): 7066-76.          


Specific modulation of ectodermal cell fates in Xenopus embryos by glycogen synthase kinase., Itoh K., Development. December 1, 1995; 121 (12): 3979-88.              


Distribution of galanin-like immunoreactivity in the brain of Rana esculenta and Xenopus laevis., Lázár GY., J Comp Neurol. August 1, 1991; 310 (1): 45-67.                                                              


The midblastula cell cycle transition and the character of mesoderm in u.v.-induced nonaxial Xenopus development., Cooke J., Development. February 1, 1987; 99 (2): 197-210.              


Early development of descending pathways from the brain stem to the spinal cord in Xenopus laevis., van Mier P., Anat Embryol (Berl). January 1, 1984; 170 (3): 295-306.

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