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Summary Anatomy Item Literature (2282) Expression Attributions Wiki
XB-ANAT-1506

Papers associated with skeletal element (and gal.2)

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PV.1 suppresses the expression of FoxD5b during neural induction in Xenopus embryos., Yoon J., Mol Cells. March 1, 2014; 37 (3): 220-5.        

RAB8B is required for activity and caveolar endocytosis of LRP6., Demir K., Cell Rep. September 26, 2013; 4 (6): 1224-34.                    

The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.                            

Syndecan 4 interacts genetically with Vangl2 to regulate neural tube closure and planar cell polarity., Escobedo N., Development. July 1, 2013; 140 (14): 3008-17.            

Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos., Milet C., Proc Natl Acad Sci U S A. April 2, 2013; 110 (14): 5528-33.                      

Prolonged FGF signaling is necessary for lung and liver induction in Xenopus., Shifley ET., BMC Dev Biol. September 18, 2012; 12 27.                      

Hyaluronan is required for cranial neural crest cells migration and craniofacial development., Casini P., Dev Dyn. February 1, 2012; 241 (2): 294-302.              

mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/nodal signaling in Xenopus ectodermal cells., Miyazaki A., PLoS One. January 1, 2012; 7 (10): e46630.        

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

Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice., Rainger J., PLoS Genet. July 1, 2011; 7 (7): e1002114.      

Gsx transcription factors repress Iroquois gene expression., Winterbottom EF., Dev Dyn. June 1, 2011; 240 (6): 1422-9.        

Activity of the RhoU/Wrch1 GTPase is critical for cranial neural crest cell migration., Fort P., Dev Biol. February 15, 2011; 350 (2): 451-63.                      

Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis., Tazumi S., Dev Biol. October 15, 2010; 346 (2): 170-80.                                

Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.                                                

Serotonin 2B receptor signaling is required for craniofacial morphogenesis and jaw joint formation in Xenopus., Reisoli E., Development. September 1, 2010; 137 (17): 2927-37.                            

ADAM13 induces cranial neural crest by cleaving class B Ephrins and regulating Wnt signaling., Wei S., Dev Cell. August 17, 2010; 19 (2): 345-52.        

The Syk kinase SmTK4 of Schistosoma mansoni is involved in the regulation of spermatogenesis and oogenesis., Beckmann S., PLoS Pathog. February 12, 2010; 6 (2): e1000769.              

Myosin-X is critical for migratory ability of Xenopus cranial neural crest cells., Nie S., Dev Biol. November 1, 2009; 335 (1): 132-42.                        

Myosin-X is required for cranial neural crest cell migration in Xenopus laevis., Hwang YS., Dev Dyn. October 1, 2009; 238 (10): 2522-9.      

Involvement of an inner nuclear membrane protein, Nemp1, in Xenopus neural development through an interaction with the chromatin protein BAF., Mamada H., Dev Biol. March 15, 2009; 327 (2): 497-507.            

Pleiotropic effects in Eya3 knockout mice., Söker T., BMC Dev Biol. June 23, 2008; 8 118.                    

Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation., Chang C., Development. November 1, 2007; 134 (21): 3861-72.                

Vertebrate Ctr1 coordinates morphogenesis and progenitor cell fate and regulates embryonic stem cell differentiation., Haremaki T., Proc Natl Acad Sci U S A. July 17, 2007; 104 (29): 12029-34.                    

Xenopus hairy2 functions in neural crest formation by maintaining cells in a mitotic and undifferentiated state., Nagatomo K., Dev Dyn. June 1, 2007; 236 (6): 1475-83.          

The competence of Xenopus blastomeres to produce neural and retinal progeny is repressed by two endo-mesoderm promoting pathways., Yan B., Dev Biol. May 1, 2007; 305 (1): 103-19.        

The Xenopus POU class V transcription factor XOct-25 inhibits ectodermal competence to respond to bone morphogenetic protein-mediated embryonic induction., Takebayashi-Suzuki K., Mech Dev. January 1, 2007; 124 (11-12): 840-55.    

Novel insights regarding the operational characteristics and teleological purpose of the renal Na+-K+-Cl2 cotransporter (NKCC2s) splice variants., Brunet GM., J Gen Physiol. October 1, 2005; 126 (4): 325-37.              

Geminin regulates neuronal differentiation by antagonizing Brg1 activity., Seo S., Genes Dev. July 15, 2005; 19 (14): 1723-34.      

To proliferate or to die: role of Id3 in cell cycle progression and survival of neural crest progenitors., Kee Y., Genes Dev. March 15, 2005; 19 (6): 744-55.            

XMAN1, an inner nuclear membrane protein, antagonizes BMP signaling by interacting with Smad1 in Xenopus embryos., Osada S., Development. May 1, 2003; 130 (9): 1783-94.            

The cdk inhibitor p27Xic1 is required for differentiation of primary neurones in Xenopus., Vernon AE., Development. January 1, 2003; 130 (1): 85-92.          

A single cdk inhibitor, p27Xic1, functions beyond cell cycle regulation to promote muscle differentiation in Xenopus., Vernon AE., Development. January 1, 2003; 130 (1): 71-83.            

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.                  

Effects of heterodimerization and proteolytic processing on Derrière and Nodal activity: implications for mesoderm induction in Xenopus., Eimon PM., Development. July 1, 2002; 129 (13): 3089-103.          

Smad10 is required for formation of the frog nervous system., LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.            

Embryonic expression of an Nkx2-5/Cre gene using ROSA26 reporter mice., Moses KA., Genesis. December 1, 2001; 31 (4): 176-80.

Isolation and characterization of a Xenopus gene (XMLP) encoding a MARCKS-like protein., Zhao H., Int J Dev Biol. October 1, 2001; 45 (7): 817-26.                        

Suppression of head formation by Xmsx-1 through the inhibition of intracellular nodal signaling., Yamamoto TS., Development. July 1, 2001; 128 (14): 2769-79.      

Ectopic Hoxa2 induction after neural crest migration results in homeosis of jaw elements in Xenopus., Pasqualetti M., Development. December 1, 2000; 127 (24): 5367-78.          

Zebrafish nma is involved in TGFbeta family signaling., Tsang M., Genesis. October 1, 2000; 28 (2): 47-57.  

Opposite effects of FGF and BMP-4 on embryonic blood formation: roles of PV.1 and GATA-2., Xu RH., Dev Biol. April 15, 1999; 208 (2): 352-61.    

Immunohistochemical analysis of the relation between 5-hydroxytryptamine- and neuropeptide-immunoreactive elements in the spinal cord of an amphibian (Xenopus laevis)., Pieribone VA., J Comp Neurol. March 22, 1994; 341 (4): 492-506.

Distinct elements of the xsna promoter are required for mesodermal and ectodermal expression., Mayor R., Development. November 1, 1993; 119 (3): 661-71.                  

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