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Summary Anatomy Item Literature (2231) Expression Attributions Wiki
XB-ANAT-3282

Papers associated with posterior hypothalamus (and cat.2)

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Alterations in gene expression levels provide early indicators of chemical stress during Xenopus laevis embryo development: A case study with perfluorooctane sulfonate (PFOS)., San-Segundo L., Ecotoxicol Environ Saf. May 1, 2016; 127 51-60.


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.                                


Isoquercitrin suppresses colon cancer cell growth in vitro by targeting the Wnt/β-catenin signaling pathway., Amado NG., J Biol Chem. December 19, 2014; 289 (51): 35456-67.                  


The conserved barH-like homeobox-2 gene barhl2 acts downstream of orthodentricle-2 and together with iroquois-3 in establishment of the caudal forebrain signaling center induced by Sonic Hedgehog., Juraver-Geslin HA., Dev Biol. December 1, 2014; 396 (1): 107-20.                    


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.                  


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.                                          


Efficient modulation of γ-aminobutyric acid type A receptors by piperine derivatives., Schöffmann A., J Med Chem. July 10, 2014; 57 (13): 5602-19.                        


ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P., Cell Rep. May 31, 2012; 1 (5): 516-27.                              


Roles of ADAM13-regulated Wnt activity in early Xenopus eye development., Wei S., Dev Biol. March 1, 2012; 363 (1): 147-54.                          


Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.                          


Serotonin signaling is required for Wnt-dependent GRP specification and leftward flow in Xenopus., Beyer T., Curr Biol. January 10, 2012; 22 (1): 33-9.                


Overexpression of the wheat aquaporin gene, TaAQP7, enhances drought tolerance in transgenic tobacco., Zhou S., PLoS One. January 1, 2012; 7 (12): e52439.                    


Barhl2 limits growth of the diencephalic primordium through Caspase3 inhibition of beta-catenin activation., Juraver-Geslin HA., Proc Natl Acad Sci U S A. February 8, 2011; 108 (6): 2288-93.                    


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.                                                      


Syndecan-1 regulates BMP signaling and dorso-ventral patterning of the ectoderm during early Xenopus development., Olivares GH., Dev Biol. May 15, 2009; 329 (2): 338-49.    


Jade-1 inhibits Wnt signalling by ubiquitylating beta-catenin and mediates Wnt pathway inhibition by pVHL., Chitalia VC., Nat Cell Biol. October 1, 2008; 10 (10): 1208-16.        


Species-specific Differences among KCNMB3 BK beta3 auxiliary subunits: some beta3 N-terminal variants may be primate-specific subunits., Zeng X., J Gen Physiol. July 1, 2008; 132 (1): 115-29.                    


Peroxisome biogenesis occurs in late dorsal-anterior structures in the development of Xenopus laevis., Cooper CA., Dev Dyn. December 1, 2007; 236 (12): 3554-61.            


Xenopus galectin-VIa shows highly specific expression in cement glands and is regulated by canonical Wnt signaling., Michiue T., Gene Expr Patterns. October 1, 2007; 7 (8): 852-7.    


Wnt11/beta-catenin signaling in both oocytes and early embryos acts through LRP6-mediated regulation of axin., Kofron M., Development. February 1, 2007; 134 (3): 503-13.      


Identification of post-transcriptionally regulated Xenopus tropicalis maternal mRNAs by microarray., Graindorge A., Nucleic Acids Res. February 7, 2006; 34 (3): 986-95.        


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.                


Inhibition of nitric oxide synthase abrogates lipopolysaccharides-induced up-regulation of L-arginine uptake in rat alveolar macrophages., Hammermann R., Br J Pharmacol. June 1, 2001; 133 (3): 379-86.


Axis induction by wnt signaling: Target promoter responsiveness regulates competence., Darken RS., Dev Biol. June 1, 2001; 234 (1): 42-54.            


Differential expression of two skeletal muscle beta-tropomyosin mRNAs during Xenopus laevis development., Gaillard C., Int J Dev Biol. March 1, 1999; 43 (2): 175-8.      


Opl: a zinc finger protein that regulates neural determination and patterning in Xenopus., Kuo JS., Development. August 1, 1998; 125 (15): 2867-82.                  


The juxtamembrane region of the cadherin cytoplasmic tail supports lateral clustering, adhesive strengthening, and interaction with p120ctn., Yap AS., J Cell Biol. May 4, 1998; 141 (3): 779-89.                  


Loss of cell adhesion in Xenopus laevis embryos mediated by the cytoplasmic domain of XLerk, an erythropoietin-producing hepatocellular ligand., Jones TL., Proc Natl Acad Sci U S A. January 20, 1998; 95 (2): 576-81.            


Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor., Hata A., Genes Dev. January 15, 1998; 12 (2): 186-97.          

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