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Summary Anatomy Item Literature (553) Expression Attributions Wiki
XB-ANAT-33

Papers associated with cement gland (and lhx1)

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Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.                        

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.                                              

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.                    

Xenopus as a model system for the study of GOLPH2/GP73 function: Xenopus GOLPH2 is required for pronephros development., Li L., PLoS One. January 1, 2012; 7 (6): e38939.                                              

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

In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.                      

Evolution of axis specification mechanisms in jawed vertebrates: insights from a chondrichthyan., Coolen M., PLoS One. April 18, 2007; 2 (4): e374.              

The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos., Callery EM., Dev Biol. February 15, 2005; 278 (2): 542-59.                              

Adult and embryonic blood and endothelium derive from distinct precursor populations which are differentially programmed by BMP in Xenopus., Walmsley M., Development. December 1, 2002; 129 (24): 5683-95.          

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.                  

A study of Xlim1 function in the Spemann-Mangold organizer., Kodjabachian L., Int J Dev Biol. January 1, 2001; 45 (1): 209-18.            

A role for Xlim-1 in pronephros development in Xenopus laevis., Chan TC., Dev Biol. December 15, 2000; 228 (2): 256-69.      

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.                    

Xenopus brain factor-2 controls mesoderm, forebrain and neural crest development., Gómez-Skarmeta JL., Mech Dev. January 1, 1999; 80 (1): 15-27.              

Frzb-1 is a secreted antagonist of Wnt signaling expressed in the Spemann organizer., Leyns L., Cell. March 21, 1997; 88 (6): 747-56.              

Analysis of Dishevelled signalling pathways during Xenopus development., Sokol SY., Curr Biol. November 1, 1996; 6 (11): 1456-67.                  

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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