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Summary Anatomy Item Literature (979) Expression Attributions Wiki
XB-ANAT-95

Papers associated with pharyngeal arch (and lhx1)

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Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.                      


Comparative expression analysis of cysteine-rich intestinal protein family members crip1, 2 and 3 during Xenopus laevis embryogenesis., Hempel A., Int J Dev Biol. January 1, 2014; 58 (10-12): 841-9.                                              


Microarray-based identification of Pitx3 targets during Xenopus embryogenesis., Hooker L., Dev Dyn. September 1, 2012; 241 (9): 1487-505.                          


Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.                      


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


Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.                              


Comparison of Lim1 expression in embryos of frogs with different modes of reproduction., Venegas-Ferrin M., Int J Dev Biol. January 1, 2010; 54 (1): 195-202.            


Two Hoxc6 transcripts are differentially expressed and regulate primary neurogenesis in Xenopus laevis., Bardine N., Dev Dyn. March 1, 2009; 238 (3): 755-65.              


A functional screen for genes involved in Xenopus pronephros development., Kyuno J., Mech Dev. July 1, 2008; 125 (7): 571-86.                                                                                      


Expression cloning in Xenopus identifies RNA-binding proteins as regulators of embryogenesis and Rbmx as necessary for neural and muscle development., Dichmann DS., Dev Dyn. July 1, 2008; 237 (7): 1755-66.                                


Upstream stimulatory factors, USF1 and USF2 are differentially expressed during Xenopus embryonic development., Fujimi TJ., Gene Expr Patterns. July 1, 2008; 8 (6): 376-81.                          


FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.                    


Isolation and characterization of Xenopus Hey-1: a downstream mediator of Notch signaling., Rones MS., Dev Dyn. December 1, 2002; 225 (4): 554-60.                      


The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.                  


Synthesis and release of activin and noggin by cultured human amniotic epithelial cells., Koyano S., Dev Growth Differ. April 1, 2002; 44 (2): 103-12.            


Identification of NKL, a novel Gli-Kruppel zinc-finger protein that promotes neuronal differentiation., Lamar E., Development. April 1, 2001; 128 (8): 1335-46.              


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


derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.                    


Differential expression of non-muscle myosin heavy chain genes during Xenopus embryogenesis., Bhatia-Dey N., Mech Dev. November 1, 1998; 78 (1-2): 33-6.


XIPOU 2 is a potential regulator of Spemann''s Organizer., Witta SE., Development. March 1, 1997; 124 (6): 1179-89.                


v-erbA and citral reduce the teratogenic effects of all-trans retinoic acid and retinol, respectively, in Xenopus embryogenesis., Schuh TJ., Development. November 1, 1993; 119 (3): 785-98.                  

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