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Summary Anatomy Item Literature (12667) Expression Attributions Wiki
XB-ANAT-175

Papers associated with nervous system (and gli1)

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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):                                     


Zic5 stabilizes Gli3 via a non-transcriptional mechanism during retinal development., Sun J., Cell Rep. February 1, 2022; 38 (5): 110312.                                          


Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease., Getwan M., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):                                                   


Non-canonical Hedgehog signaling regulates spinal cord and muscle regeneration in Xenopus laevis larvae., Hamilton AM., Elife. May 6, 2021; 10                               


TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9                                                                                           


Xenopus slc7a5 is essential for notochord function and eye development., Katada T., Mech Dev. February 1, 2019; 155 48-59.                


Evolutionarily conserved Tbx5-Wnt2/2b pathway orchestrates cardiopulmonary development., Steimle JD., Proc Natl Acad Sci U S A. November 6, 2018; 115 (45): E10615-E10624.                                  


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


High variability of expression profiles of homeologous genes for Wnt, Hh, Notch, and Hippo signaling pathways in Xenopus laevis., Michiue T., Dev Biol. June 15, 2017; 426 (2): 270-290.                  


Members of the Rusc protein family interact with Sufu and inhibit vertebrate Hedgehog signaling., Jin Z., Development. November 1, 2016; 143 (21): 3944-3955.                        


Inversion of Sonic hedgehog action on its canonical pathway by electrical activity., Belgacem YH., Proc Natl Acad Sci U S A. March 31, 2015; 112 (13): 4140-5.                              


Dorsoventral patterning of the Xenopus eye involves differential temporal changes in the response of optic stalk and retinal progenitors to Hh signalling., Wang X., Neural Dev. March 20, 2015; 10 7.              


Prepatterning and patterning of the thalamus along embryonic development of Xenopus laevis., Bandín S., Front Neuroanat. February 3, 2015; 9 107.                                                    


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.                    


Neural transcription factors: from embryos to neural stem cells., Lee HK., Mol Cells. October 31, 2014; 37 (10): 705-12.    


Transmembrane voltage potential of somatic cells controls oncogene-mediated tumorigenesis at long-range., Chernet BT., Oncotarget. May 30, 2014; 5 (10): 3287-306.              


Gli protein activity is controlled by multisite phosphorylation in vertebrate Hedgehog signaling., Niewiadomski P., Cell Rep. January 16, 2014; 6 (1): 168-81.


Stabilization of speckle-type POZ protein (Spop) by Daz interacting protein 1 (Dzip1) is essential for Gli turnover and the proper output of Hedgehog signaling., Schwend T., J Biol Chem. November 8, 2013; 288 (45): 32809-32820.                


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.                      


Transmembrane voltage potential is an essential cellular parameter for the detection and control of tumor development in a Xenopus model., Chernet BT., Dis Model Mech. May 1, 2013; 6 (3): 595-607.                  


Antagonistic cross-regulation between Wnt and Hedgehog signalling pathways controls post-embryonic retinal proliferation., Borday C., Development. October 1, 2012; 139 (19): 3499-509.                    


The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.                            


MIM regulates vertebrate neural tube closure., Liu W., Development. May 1, 2011; 138 (10): 2035-47.                            


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.                                                      


Sonic hedgehog is involved in formation of the ventral optic cup by limiting Bmp4 expression to the dorsal domain., Zhao L., Mech Dev. January 1, 2010; 127 (1-2): 62-72.                


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


Negative regulation of Hedgehog signaling by the cholesterogenic enzyme 7-dehydrocholesterol reductase., Koide T., Development. June 1, 2006; 133 (12): 2395-405.                


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.          


The amino-terminal region of Gli3 antagonizes the Shh response and acts in dorsoventral fate specification in the developing spinal cord., Meyer NP., Dev Biol. May 15, 2003; 257 (2): 343-55.


A novel function for Hedgehog signalling in retinal pigment epithelium differentiation., Perron M., Development. April 1, 2003; 130 (8): 1565-77.                                  


Conserved expression control and shared activity between cognate T-box genes Tbx2 and Tbx3 in connection with Sonic hedgehog signaling during Xenopus eye development., Takabatake Y., Dev Growth Differ. August 1, 2002; 44 (4): 257-71.              


Gli1 can rescue the in vivo function of Gli2., Bai CB., Development. December 1, 2001; 128 (24): 5161-72.


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


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


Mouse Gli1 mutants are viable but have defects in SHH signaling in combination with a Gli2 mutation., Park HL., Development. April 1, 2000; 127 (8): 1593-605.


Neuralization of the Xenopus embryo by inhibition of p300/ CREB-binding protein function., Kato Y., J Neurosci. November 1, 1999; 19 (21): 9364-73.          


Regulation of Gli2 and Gli3 activities by an amino-terminal repression domain: implication of Gli2 and Gli3 as primary mediators of Shh signaling., Sasaki H., Development. September 1, 1999; 126 (17): 3915-24.


Gli proteins encode context-dependent positive and negative functions: implications for development and disease., Ruiz i Altaba A., Development. June 1, 1999; 126 (14): 3205-16.                


Diminished Sonic hedgehog signaling and lack of floor plate differentiation in Gli2 mutant mice., Ding Q., Development. July 1, 1998; 125 (14): 2533-43.


Combinatorial Gli gene function in floor plate and neuronal inductions by Sonic hedgehog., Ruiz i Altaba A., Development. June 1, 1998; 125 (12): 2203-12.


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

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