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

Papers associated with spinal cord (and chrd.1)

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Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates., Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.                                


Spemann organizer transcriptome induction by early beta-catenin, Wnt, Nodal, and Siamois signals in Xenopus laevis., Ding Y., Proc Natl Acad Sci U S A. April 11, 2017; 114 (15): E3081-E3090.                        


Members of the Rusc protein family interact with Sufu and inhibit vertebrate Hedgehog signaling., Jin Z., Development. November 1, 2016; 143 (21): 3944-3955.                        


NF2/Merlin is required for the axial pattern formation in the Xenopus laevis embryo., Zhu X., Mech Dev. November 1, 2015; 138 Pt 3 305-12.                


Early development of the neural plate: new roles for apoptosis and for one of its main effectors caspase-3., Juraver-Geslin HA., Genesis. February 1, 2015; 53 (2): 203-24.          


The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.                                          


40LoVe and Samba are involved in Xenopus neural development and functionally distinct from hnRNP AB., Andreou M., PLoS One. January 1, 2014; 9 (1): e85026.                


FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos., Murgan S., PLoS One. January 1, 2014; 9 (10): e110559.                              


Developmental mechanisms directing early anterior forebrain specification in vertebrates., Andoniadou CL., Cell Mol Life Sci. October 1, 2013; 70 (20): 3739-52.        


Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling., Bates TJ., Development. October 1, 2013; 140 (20): 4177-81.              


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.                                  


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


Transcriptional regulation of mesoderm genes by MEF2D during early Xenopus development., Kolpakova A., PLoS One. January 1, 2013; 8 (7): e69693.                  


Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.                    


Dynamic in vivo binding of transcription factors to cis-regulatory modules of cer and gsc in the stepwise formation of the Spemann-Mangold organizer., Sudou N., Development. May 1, 2012; 139 (9): 1651-61.                  


The cytoplasmic tyrosine kinase Arg regulates gastrulation via control of actin organization., Bonacci G., Dev Biol. April 1, 2012; 364 (1): 42-55.                                        


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


Xenopus staufen2 is required for anterior endodermal organ formation., Bilogan CK., Genesis. March 1, 2012; 50 (3): 251-9.                      


The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.                            


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


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.                              


Expression of Transposable Elements in Neural Tissues during Xenopus Development., Faunes F., PLoS One. January 1, 2011; 6 (7): e22569.                    


Neuronatin promotes neural lineage in ESCs via Ca(2+) signaling., Lin HH., Stem Cells. November 1, 2010; 28 (11): 1950-60.              


BMP antagonists and FGF signaling contribute to different domains of the neural plate in Xenopus., Wills AE., Dev Biol. January 15, 2010; 337 (2): 335-50.                  


The RNA-binding protein Seb4/RBM24 is a direct target of MyoD and is required for myogenesis during Xenopus early development., Li HY., Mech Dev. January 1, 2010; 127 (5-6): 281-91.        


Tumor necrosis factor-receptor-associated factor-4 is a positive regulator of transforming growth factor-beta signaling that affects neural crest formation., Kalkan T., Mol Biol Cell. July 1, 2009; 20 (14): 3436-50.                          


Xenopus Wntless and the retromer complex cooperate to regulate XWnt4 secretion., Kim H., Mol Cell Biol. April 1, 2009; 29 (8): 2118-28.  


Extracellular regulation of developmental cell signaling by XtSulf1., Freeman SD., Dev Biol. August 15, 2008; 320 (2): 436-45.            


Crossveinless-2 Is a BMP feedback inhibitor that binds Chordin/BMP to regulate Xenopus embryonic patterning., Ambrosio AL., Dev Cell. August 1, 2008; 15 (2): 248-60.                            


Regulation of TGF-(beta) signalling by N-acetylgalactosaminyltransferase-like 1., Herr P., Development. May 1, 2008; 135 (10): 1813-22.                    


Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation., Chang C., Development. November 1, 2007; 134 (21): 3861-72.                


The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.              


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


Expression analysis of IGFBP-rP10, IGFBP-like and Mig30 in early Xenopus development., Kuerner KM., Dev Dyn. October 1, 2006; 235 (10): 2861-7.                                          


Differential role of 14-3-3 family members in Xenopus development., Lau JM., Dev Dyn. July 1, 2006; 235 (7): 1761-76.                                                    


Negative regulation of Hedgehog signaling by the cholesterogenic enzyme 7-dehydrocholesterol reductase., Koide T., Development. June 1, 2006; 133 (12): 2395-405.                


Cooperative non-cell and cell autonomous regulation of Nodal gene expression and signaling by Lefty/Antivin and Brachyury in Xenopus., Cha YR., Dev Biol. February 15, 2006; 290 (2): 246-64.                        


Twisted gastrulation is required for forebrain specification and cooperates with Chordin to inhibit BMP signaling during X. tropicalis gastrulation., Wills A., Dev Biol. January 1, 2006; 289 (1): 166-78.                                  


Tsukushi controls ectodermal patterning and neural crest specification in Xenopus by direct regulation of BMP4 and X-delta-1 activity., Kuriyama S., Development. January 1, 2006; 133 (1): 75-88.            


Regulation of ADMP and BMP2/4/7 at opposite embryonic poles generates a self-regulating morphogenetic field., Reversade B., Cell. December 16, 2005; 123 (6): 1147-60.                      


Role of crescent in convergent extension movements by modulating Wnt signaling in early Xenopus embryogenesis., Shibata M., Mech Dev. December 1, 2005; 122 (12): 1322-39.                    


Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.            


The pro-apoptotic activity of a vertebrate Bar-like homeobox gene plays a key role in patterning the Xenopus neural plate by limiting the number of chordin- and shh-expressing cells., Offner N., Development. April 1, 2005; 132 (8): 1807-18.          


The Notch-target gene hairy2a impedes the involution of notochordal cells by promoting floor plate fates in Xenopus embryos., López SL., Development. March 1, 2005; 132 (5): 1035-46.              


Olfactory and lens placode formation is controlled by the hedgehog-interacting protein (Xhip) in Xenopus., Cornesse Y., Dev Biol. January 15, 2005; 277 (2): 296-315.                          


Sequences downstream of the bHLH domain of the Xenopus hairy-related transcription factor-1 act as an extended dimerization domain that contributes to the selection of the partners., Taelman V., Dev Biol. December 1, 2004; 276 (1): 47-63.                          


Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.                


Differential gene expression between the embryonic tail bud and regenerating larval tail in Xenopus laevis., Sugiura T., Dev Growth Differ. February 1, 2004; 46 (1): 97-105.        


Identification of a second Xenopus twisted gastrulation gene., Oelgeschläger M., Int J Dev Biol. February 1, 2004; 48 (1): 57-61.            


Inhibition of mesodermal fate by Xenopus HNF3beta/FoxA2., Suri C., Dev Biol. January 1, 2004; 265 (1): 90-104.              

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