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Summary Anatomy Item Literature (423) Expression Attributions Wiki
XB-ANAT-543

Papers associated with skeletal system (and otx2)

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Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development., Shah AM., Dis Model Mech. March 3, 2020; 13 (3):                                               


What are the roles of retinoids, other morphogens, and Hox genes in setting up the vertebrate body axis?, Durston AJ., Genesis. July 1, 2019; 57 (7-8): e23296.            


Mouth development., Chen J., Wiley Interdiscip Rev Dev Biol. September 1, 2017; 6 (5):               


Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula., Ding Y., Dev Biol. June 15, 2017; 426 (2): 176-187.                                  


SMOC can act as both an antagonist and an expander of BMP signaling., Thomas JT., Elife. March 21, 2017; 6                         


The positive transcriptional elongation factor (P-TEFb) is required for neural crest specification., Hatch VL., Dev Biol. August 15, 2016; 416 (2): 361-72.                                    


Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.                              


Sp8 regulates inner ear development., Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.                                                    


Role of Sp5 as an essential early regulator of neural crest specification in xenopus., Park DS., Dev Dyn. December 1, 2013; 242 (12): 1382-94.                


Expression and functional characterization of Xhmg-at-hook genes in Xenopus laevis., Macrì S., PLoS One. July 1, 2013; 8 (7): e69866.              


Signaling and transcriptional regulation in neural crest specification and migration: lessons from xenopus embryos., Pegoraro C., Wiley Interdiscip Rev Dev Biol. January 1, 2013; 2 (2): 247-59.      


Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning., Steventon B., Dev Biol. July 1, 2012; 367 (1): 55-65.                


V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.                        


The zic1 gene is an activator of Wnt signaling., Merzdorf CS., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.              


Coordination of BMP-3b and cerberus is required for head formation of Xenopus embryos., Hino J., Dev Biol. August 1, 2003; 260 (1): 138-57.                            


Characterizing gene expression during lens formation in Xenopus laevis: evaluating the model for embryonic lens induction., Henry JJ., Dev Dyn. June 1, 2002; 224 (2): 168-85.        


The mouse Cer1 (Cerberus related or homologue) gene is not required for anterior pattern formation., Simpson EH., Dev Biol. September 1, 1999; 213 (1): 202-6.


Xenopus eomesodermin is expressed in neural differentiation., Ryan K., Mech Dev. July 1, 1998; 75 (1-2): 155-8.    


The Xenopus Emx genes identify presumptive dorsal telencephalon and are induced by head organizer signals., Pannese M., Mech Dev. April 1, 1998; 73 (1): 73-83.                

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