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Summary Anatomy Item Literature (1914) Expression Attributions Wiki
XB-ANAT-3755

Papers associated with rostral tuberal region (and fn1)

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E-cadherin is required for cranial neural crest migration in Xenopus laevis., Huang C., Dev Biol. March 15, 2016; 411 (2): 159-171.                        


The Lhx9-integrin pathway is essential for positioning of the proepicardial organ., Tandon P., Development. March 1, 2016; 143 (5): 831-40.                                    


Hmga2 is required for neural crest cell specification in Xenopus laevis., Macrì S., Dev Biol. March 1, 2016; 411 (1): 25-37.                                        


Snail2/Slug cooperates with Polycomb repressive complex 2 (PRC2) to regulate neural crest development., Tien CL., Development. February 15, 2015; 142 (4): 722-31.                


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.                  


Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.                                


NEDD4L regulates convergent extension movements in Xenopus embryos via Disheveled-mediated non-canonical Wnt signaling., Zhang Y., Dev Biol. August 1, 2014; 392 (1): 15-25.                              


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.                                


Migratory and adhesive properties of Xenopus laevis primordial germ cells in vitro., Dzementsei A., Biol Open. December 15, 2013; 2 (12): 1279-87.          


Calpain2 protease: A new member of the Wnt/Ca(2+) pathway modulating convergent extension movements in Xenopus., Zanardelli S., Dev Biol. December 1, 2013; 384 (1): 83-100.                        


Directional migration of leading-edge mesoderm generates physical forces: Implication in Xenopus notochord formation during gastrulation., Hara Y., Dev Biol. October 15, 2013; 382 (2): 482-95.                  


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.                      


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


Cell movements of the deep layer of non-neural ectoderm underlie complete neural tube closure in Xenopus., Morita H., Development. April 1, 2012; 139 (8): 1417-26.                        


High mobility group B proteins regulate mesoderm formation and dorsoventral patterning during zebrafish and Xenopus early development., Cao JM., Mech Dev. January 1, 2012; 129 (9-12): 263-74.    


Axial protocadherin (AXPC) regulates cell fate during notochordal morphogenesis., Yoder MD., Dev Dyn. November 1, 2011; 240 (11): 2495-504.          


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.                          


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.              


Distinct Xenopus Nodal ligands sequentially induce mesendoderm and control gastrulation movements in parallel to the Wnt/PCP pathway., Luxardi G., Development. February 1, 2010; 137 (3): 417-26.          


PDGF-A interactions with fibronectin reveal a critical role for heparan sulfate in directed cell migration during Xenopus gastrulation., Smith EM., Proc Natl Acad Sci U S A. December 22, 2009; 106 (51): 21683-8.    


Xenopus delta-catenin is essential in early embryogenesis and is functionally linked to cadherins and small GTPases., Gu D., J Cell Sci. November 15, 2009; 122 (Pt 22): 4049-61.            


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


Trim36/Haprin plays a critical role in the arrangement of somites during Xenopus embryogenesis., Yoshigai E., Biochem Biophys Res Commun. January 16, 2009; 378 (3): 428-32.          


TGF-beta signaling-mediated morphogenesis: modulation of cell adhesion via cadherin endocytosis., Ogata S., Genes Dev. July 15, 2007; 21 (14): 1817-31.                  


Neurotrophin receptor homolog (NRH1) proteins regulate mesoderm formation and apoptosis during early Xenopus development., Knapp D., Dev Biol. December 15, 2006; 300 (2): 554-69.                  


A role for GATA factors in Xenopus gastrulation movements., Fletcher G., Mech Dev. October 1, 2006; 123 (10): 730-45.    


Expression of Dickkopf genes is strongly reduced in malignant melanoma., Kuphal S., Oncogene. August 17, 2006; 25 (36): 5027-36.


Development of the primary mouth in Xenopus laevis., Dickinson AJ., Dev Biol. July 15, 2006; 295 (2): 700-13.                


TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.                


HIC-5 is a novel repressor of lymphoid enhancer factor/T-cell factor-driven transcription., Ghogomu SM., J Biol Chem. January 20, 2006; 281 (3): 1755-64.            


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


Notch signaling modulates the nuclear localization of carboxy-terminal-phosphorylated smad2 and controls the competence of ectodermal cells for activin A., Abe T., Mech Dev. May 1, 2005; 122 (5): 671-80.            


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


Identification and characterization of a second fibronectin gene in zebrafish., Sun L., Matrix Biol. February 1, 2005; 24 (1): 69-77.


Visualizing long-range movement of the morphogen Xnr2 in the Xenopus embryo., Williams PH., Curr Biol. November 9, 2004; 14 (21): 1916-23.      


A PTP-PEST-like protein affects alpha5beta1-integrin-dependent matrix assembly, cell adhesion, and migration in Xenopus gastrula., Cousin H., Dev Biol. January 15, 2004; 265 (2): 416-32.                  


The function of Xenopus germ cell nuclear factor (xGCNF) in morphogenetic movements during neurulation., Barreto G., Dev Biol. May 15, 2003; 257 (2): 329-42.            


Adenosine regulates the IL-1 beta-induced cellular functions of human gingival fibroblasts., Murakami S., Int Immunol. December 1, 2001; 13 (12): 1533-40.


Hyaluronan synthases, hyaluronan, and its CD44 receptor in tissue around loosened total hip prostheses., Konttinen YT., J Pathol. July 1, 2001; 194 (3): 384-90.


A novel POZ/zinc finger protein, champignon, interferes with gastrulation movements in Xenopus., Goto T., Dev Dyn. May 1, 2001; 221 (1): 14-25.                


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.                


Analysis of C-cadherin regulation during tissue morphogenesis with an activating antibody., Zhong Y., J Cell Biol. January 25, 1999; 144 (2): 351-9.            

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