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Summary Anatomy Item Literature (6278) Expression Attributions Wiki
XB-ANAT-475

Papers associated with primary germ layer (and gli3)

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Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components., Hantel F., J Cell Sci. May 1, 2022; 135 (9):                                     


Uncovering the mesendoderm gene regulatory network through multi-omic data integration., Jansen C., Cell Rep. February 15, 2022; 38 (7): 110364.                            


Modeling endoderm development and disease in Xenopus., Edwards NA., Curr Top Dev Biol. January 1, 2021; 145 61-90.


Endosome-Mediated Epithelial Remodeling Downstream of Hedgehog-Gli Is Required for Tracheoesophageal Separation., Nasr T., Dev Cell. December 16, 2019; 51 (6): 665-674.e6.                  


Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.                      


Generation of iPSC-derived limb progenitor-like cells for stimulating phalange regeneration in the adult mouse., Chen Y., Cell Discov. December 19, 2017; 3 17046.          


Sonic hedgehog antagonists reduce size and alter patterning of the frog inner ear., Zarei S., Dev Neurobiol. December 1, 2017; 77 (12): 1385-1400.                


A Retinoic Acid-Hedgehog Cascade Coordinates Mesoderm-Inducing Signals and Endoderm Competence during Lung Specification., Rankin SA, Rankin SA., Cell Rep. June 28, 2016; 16 (1): 66-78.                                              


Hedgehog activity controls opening of the primary mouth., Tabler JM., Dev Biol. December 1, 2014; 396 (1): 1-7.            


Chibby functions in Xenopus ciliary assembly, embryonic development, and the regulation of gene expression., Shi J., Dev Biol. November 15, 2014; 395 (2): 287-98.                    


Gene regulatory networks governing lung specification., Rankin SA, Rankin SA., J Cell Biochem. August 1, 2014; 115 (8): 1343-50.


Developmental expression and role of Kinesin Eg5 during Xenopus laevis embryogenesis., Fernández JP., Dev Dyn. April 1, 2014; 243 (4): 527-40.              


The cytoskeletal protein Zyxin inhibits Shh signaling during the CNS patterning in Xenopus laevis through interaction with the transcription factor Gli1., Martynova NY., Dev Biol. August 1, 2013; 380 (1): 37-48.                      


Indian hedgehog signaling is required for proper formation, maintenance and migration of Xenopus neural crest., Agüero TH., Dev Biol. April 15, 2012; 364 (2): 99-113.                    


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.                                                      


PP2A:B56epsilon is required for eye induction and eye field separation., Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.                  


Cooperative requirement of the Gli proteins in neurogenesis., Nguyen V., Development. July 1, 2005; 132 (14): 3267-79.                      


The pro-apoptotic activity of a vertebrate Bar-like homeobox gene plays a key role in patterning the Xenopus neural plate by limiting the number of chordin- and shh-expressing cells., Offner N., Development. April 1, 2005; 132 (8): 1807-18.          


Notch activates sonic hedgehog and both are involved in the specification of dorsal midline cell-fates in Xenopus., López SL., Development. May 1, 2003; 130 (10): 2225-38.        


A direct requirement for Hedgehog signaling for normal specification of all ventral progenitor domains in the presumptive mammalian spinal cord., Wijgerde M., Genes Dev. November 15, 2002; 16 (22): 2849-64.


Anorectal malformations caused by defects in sonic hedgehog signaling., Mo R., Am J Pathol. August 1, 2001; 159 (2): 765-74.


Distinct expression of two types of Xenopus Patched genes during early embryogenesis and hindlimb development., Takabatake T., Mech Dev. November 1, 2000; 98 (1-2): 99-104.            


Gli2 functions in FGF signaling during antero-posterior patterning., Brewster R., Development. October 1, 2000; 127 (20): 4395-405.            


Shh and Wnt signaling pathways converge to control Gli gene activation in avian somites., Borycki A., Development. May 1, 2000; 127 (10): 2075-87.


Functional association of retinoic acid and hedgehog signaling in Xenopus primary neurogenesis., Franco PG., Development. October 1, 1999; 126 (19): 4257-65.          


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


Activation of the transcription factor Gli1 and the Sonic hedgehog signalling pathway in skin tumours., Dahmane N., Nature. October 23, 1997; 389 (6653): 876-81.


Evidence for the involvement of the Gli gene family in embryonic mouse lung development., Grindley JC., Dev Biol. August 15, 1997; 188 (2): 337-48.


Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4., Dunn NR., Dev Biol. August 15, 1997; 188 (2): 235-47.


Gli1 is a target of Sonic hedgehog that induces ventral neural tube development., Lee J., Development. July 1, 1997; 124 (13): 2537-52.                  


A role for Xenopus Gli-type zinc finger proteins in the early embryonic patterning of mesoderm and neuroectoderm., Marine JC., Mech Dev. May 1, 1997; 63 (2): 211-25.              


Multigenic control of the localization of the zone of polarizing activity in limb morphogenesis in the mouse., Masuya H., Dev Biol. February 1, 1997; 182 (1): 42-51.


Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development., Mo R., Development. January 1, 1997; 124 (1): 113-23.

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