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Summary Anatomy Item Literature (3035) Expression Attributions Wiki
XB-ANAT-12

Papers associated with forebrain∨derBy=4 (and fn1)

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TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B., JCI Insight. November 8, 2023; 8 (21):                                               


Impaired negative feedback and death following acute stress in glucocorticoid receptor knockout Xenopus tropicalis tadpoles., Paul B., Gen Comp Endocrinol. September 15, 2022; 326 114072.      


Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in Xenopus laevis., Mills A., Front Physiol. January 1, 2019; 10 431.                                          


Large, long range tensile forces drive convergence during Xenopus blastopore closure and body axis elongation., Shook DR., Elife. March 13, 2018; 7                           


Gene expression of the two developmentally regulated dermatan sulfate epimerases in the Xenopus embryo., Gouignard N., PLoS One. January 18, 2018; 13 (1): e0191751.                                                          


Identification of new regulators of embryonic patterning and morphogenesis in Xenopus gastrulae by RNA sequencing., Popov IK., Dev Biol. June 15, 2017; 426 (2): 429-441.                    


Mechanosensing is critical for axon growth in the developing brain., Koser DE., Nat Neurosci. December 1, 2016; 19 (12): 1592-1598.                  


EphA7 modulates apical constriction of hindbrain neuroepithelium during neurulation in Xenopus., Wang X., Biochem Biophys Res Commun. October 28, 2016; 479 (4): 759-765.        


Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.                              


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


Hedgehog activity controls opening of the primary mouth., Tabler JM., Dev Biol. December 1, 2014; 396 (1): 1-7.            


The need of MMP-2 on the sperm surface for Xenopus fertilization: its role in a fast electrical block to polyspermy., Iwao Y., Mech Dev. November 1, 2014; 134 80-95.                  


FAK is required for tension-dependent organization of collective cell movements in Xenopus mesendoderm., Bjerke MA., Dev Biol. October 15, 2014; 394 (2): 340-56.                        


In vivo collective cell migration requires an LPAR2-dependent increase in tissue fluidity., Kuriyama S., J Cell Biol. July 7, 2014; 206 (1): 113-27.                                


Enabling comparative gene expression studies of thyroid hormone action through the development of a flexible real-time quantitative PCR assay for use across multiple anuran indicator and sentinel species., Veldhoen N., Aquat Toxicol. March 1, 2014; 148 162-73.


Lamellipodin and the Scar/WAVE complex cooperate to promote cell migration in vivo., Law AL., J Cell Biol. November 25, 2013; 203 (4): 673-89.                    


Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos., Milet C., Proc Natl Acad Sci U S A. April 2, 2013; 110 (14): 5528-33.                      


Thyroid hormone-dependent development in Xenopus laevis: a sensitive screen of thyroid hormone signaling disruption by municipal wastewater treatment plant effluent., Searcy BT., Gen Comp Endocrinol. May 1, 2012; 176 (3): 481-92.


The involvement of Eph-Ephrin signaling in tissue separation and convergence during Xenopus gastrulation movements., Park EC., Dev Biol. February 15, 2011; 350 (2): 441-50.                          


Rapid differential transport of Nodal and Lefty on sulfated proteoglycan-rich extracellular matrix regulates left-right asymmetry in Xenopus., Marjoram L., Development. February 1, 2011; 138 (3): 475-85.            


A novel function for KIF13B in germ cell migration., Tarbashevich K., Dev Biol. January 15, 2011; 349 (2): 169-78.                    


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.                                                      


Tissue-Tissue Interaction-Triggered Calcium Elevation Is Required for Cell Polarization during Xenopus Gastrulation., Shindo A., PLoS One. February 2, 2010; 5 (2): e8897.              


Myosin-X is required for cranial neural crest cell migration in Xenopus laevis., Hwang YS., Dev Dyn. October 1, 2009; 238 (10): 2522-9.      


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.                      


FGF signal regulates gastrulation cell movements and morphology through its target NRH., Chung HA., Dev Biol. June 1, 2005; 282 (1): 95-110.                          


Xenopus ILK (integrin-linked kinase) is required for morphogenetic movements during gastrulation., Yasunaga T., Genes Cells. April 1, 2005; 10 (4): 369-79.          


Phosphorylation of DCC by Fyn mediates Netrin-1 signaling in growth cone guidance., Meriane M., J Cell Biol. November 22, 2004; 167 (4): 687-98.                  


Exposure to the herbicide acetochlor alters thyroid hormone-dependent gene expression and metamorphosis in Xenopus Laevis., Crump D., Environ Health Perspect. December 1, 2002; 110 (12): 1199-205.


Molecular cloning, expression and partial characterization of Xksy, Xenopus member of the Sky family of receptor tyrosine kinases., Kishi YA., Gene. April 17, 2002; 288 (1-2): 29-40.              


Mechanisms of mesendoderm internalization in the Xenopus gastrula: lessons from the ventral side., Ibrahim H., Dev Biol. December 1, 2001; 240 (1): 108-22.                      


Xoom is required for epibolic movement of animal ectodermal cells in Xenopus laevis gastrulation., Hasegawa K., Dev Growth Differ. August 1, 2000; 42 (4): 337-46.              


The HMG-box transcription factor XTcf-4 demarcates the forebrain-midbrain boundary., König A., Mech Dev. May 1, 2000; 93 (1-2): 211-4.    


Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.                


The expression pattern of thyroid hormone response genes in remodeling tadpole tissues defines distinct growth and resorption gene expression programs., Berry DL., Dev Biol. November 1, 1998; 203 (1): 24-35.                  


The expression pattern of thyroid hormone response genes in the tadpole tail identifies multiple resorption programs., Berry DL., Dev Biol. November 1, 1998; 203 (1): 12-23.                


Molecular cloning of XNLRR-1, a Xenopus homolog of mouse neuronal leucine-rich repeat protein expressed in the developing Xenopus nervous system., Hayata T., Gene. October 9, 1998; 221 (1): 159-66.          


Xwnt-2b is a novel axis-inducing Xenopus Wnt, which is expressed in embryonic brain., Landesman Y., Mech Dev. May 1, 1997; 63 (2): 199-209.            


Integrin alpha 6 expression is required for early nervous system development in Xenopus laevis., Lallier TE., Development. August 1, 1996; 122 (8): 2539-54.                                  


Expression of a homologue of the deleted in colorectal cancer (DCC) gene in the nervous system of developing Xenopus embryos., Pierceall WE., Dev Biol. December 1, 1994; 166 (2): 654-65.              


Follistatin, an antagonist of activin, is expressed in the Spemann organizer and displays direct neuralizing activity., Hemmati-Brivanlou A., Cell. April 22, 1994; 77 (2): 283-95.                    


Localized expression of a Xenopus POU gene depends on cell-autonomous transcriptional activation and induction-dependent inactivation., Frank D., Development. June 1, 1992; 115 (2): 439-48.            

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