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Summary Anatomy Item Literature (1230) Expression Attributions Wiki
XB-ANAT-736

Papers associated with neural tube (and lhx1)

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Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.                                          

Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.                            

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.                                              

Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.                    

Variation in the schedules of somite and neural development in frogs., Sáenz-Ponce N., Proc Natl Acad Sci U S A. December 11, 2012; 109 (50): 20503-7.    

Contexts for dopamine specification by calcium spike activity in the CNS., Velázquez-Ulloa NA., J Neurosci. January 5, 2011; 31 (1): 78-88.                    

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

Embryogenesis and laboratory maintenance of the foam-nesting túngara frogs, genus Engystomops (= Physalaemus)., Romero-Carvajal A., Dev Dyn. June 1, 2009; 238 (6): 1444-54.      

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): 376-381.                          

Odd-skipped genes encode repressors that control kidney development., Tena JJ., Dev Biol. January 15, 2007; 301 (2): 518-31.          

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.                    

Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.                  

Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.                    

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.                  

Essential function of Wnt-4 for tubulogenesis in the Xenopus pronephric kidney., Saulnier DM., Dev Biol. August 1, 2002; 248 (1): 13-28.                    

Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.                    

Xiro-1 controls mesoderm patterning by repressing bmp-4 expression in the Spemann organizer., Glavic A., Dev Dyn. November 1, 2001; 222 (3): 368-76.      

Role of Goosecoid, Xnot and Wnt antagonists in the maintenance of the notochord genetic programme in Xenopus gastrulae., Yasuo H., Development. October 1, 2001; 128 (19): 3783-93.      

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

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

Analysis of the developing Xenopus tail bud reveals separate phases of gene expression during determination and outgrowth., Beck CW., Mech Dev. March 1, 1998; 72 (1-2): 41-52.                                                                

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

Ectodermal patterning in vertebrate embryos., Sasai Y., Dev Biol. February 1, 1997; 182 (1): 5-20.              

Expression of murine Lhx5 suggests a role in specifying the forebrain., Sheng HZ., Dev Dyn. February 1, 1997; 208 (2): 266-77.

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

Molecular cloning, structure, and chromosomal localization of the mouse LIM/homeobox gene Lhx5., Bertuzzi S., Genomics. September 1, 1996; 36 (2): 234-9.

XIPOU 2, a noggin-inducible gene, has direct neuralizing activity., Witta SE., Development. March 1, 1995; 121 (3): 721-30.                

Expression of the LIM class homeobox gene Xlim-1 in pronephros and CNS cell lineages of Xenopus embryos is affected by retinoic acid and exogastrulation., Taira M., Development. June 1, 1994; 120 (6): 1525-36.        

Expression of LIM class homeobox gene Xlim-3 in Xenopus development is limited to neural and neuroendocrine tissues., Taira M., Dev Biol. September 1, 1993; 159 (1): 245-56.              

The LIM domain-containing homeo box gene Xlim-1 is expressed specifically in the organizer region of Xenopus gastrula embryos., Taira M., Genes Dev. March 1, 1992; 6 (3): 356-66.              

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