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Summary Anatomy Item Literature (79) Expression Attributions Wiki
XB-ANAT-3411

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Development of the ectoderm in Xenopus: tissue specification and the role of cell association and division., Jones EA., Cell. January 31, 1986; 44 (2): 345-55.                


Regulation of embryonic cell adhesion by the cadherin cytoplasmic domain., Kintner C., Cell. April 17, 1992; 69 (2): 225-36.          


Spatial, temporal, and hormonal regulation of epidermal keratin expression during development of the frog, Xenopus laevis., Nishikawa A., Dev Biol. May 1, 1992; 151 (1): 145-53.                


Sequence and specificity of a soluble lactose-binding lectin from Xenopus laevis skin., Marschal P., J Biol Chem. June 25, 1992; 267 (18): 12942-9.                


Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos., Smith WC., Cell. September 4, 1992; 70 (5): 829-40.              


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.              


XIdx, a dominant negative regulator of bHLH function in early Xenopus embryos., Wilson R., Mech Dev. February 1, 1995; 49 (3): 211-22.          


Integrin alpha 5 during early development of Xenopus laevis., Joos TO., Mech Dev. April 1, 1995; 50 (2-3): 187-99.                    


The mRNA encoding a beta subunit of heterotrimeric GTP-binding proteins is localized to the animal pole of Xenopus laevis oocyte and embryos., Devic E., Mech Dev. October 1, 1996; 59 (2): 141-51.              


Expression of a new G protein-coupled receptor X-msr is associated with an endothelial lineage in Xenopus laevis., Devic E., Mech Dev. October 1, 1996; 59 (2): 129-40.        


Differential effects on Xenopus development of interference with type IIA and type IIB activin receptors., New HV., Mech Dev. January 1, 1997; 61 (1-2): 175-86.          


Xbap, a vertebrate gene related to bagpipe, is expressed in developing craniofacial structures and in anterior gut muscle., Newman CS., Dev Biol. January 15, 1997; 181 (2): 223-33.            


Altered ionic selectivity of the sodium channel revealed by cysteine mutations within the pore., Tsushima RG., J Gen Physiol. April 1, 1997; 109 (4): 463-75.                


Functional interactions between the estrogen receptor and the transcription activator Sp1 regulate the estrogen-dependent transcriptional activity of the vitellogenin A1 io promoter., Batistuzzo de Medeiros SR., J Biol Chem. July 18, 1997; 272 (29): 18250-60.


A conserved arginine residue in the pore region of an inward rectifier K channel (IRK1) as an external barrier for cationic blockers., Sabirov RZ., J Gen Physiol. December 1, 1997; 110 (6): 665-77.                  


Coupled ion movement underlies rectification in an inward-rectifier K+ channel., Spassova M., J Gen Physiol. August 1, 1998; 112 (2): 211-21.            


The Xenopus bagpipe-related homeobox gene zampogna is expressed in the pharyngeal endoderm and the visceral musculature of the midgut., Newman CS., Dev Genes Evol. February 1, 1999; 209 (2): 132-4.


Ca2+-dependent gating mechanisms for dSlo, a large-conductance Ca2+-activated K+ (BK) channel., Moss BL., Biophys J. June 1, 1999; 76 (6): 3099-117.


Tuning the voltage dependence of tetraethylammonium block with permeant ions in an inward-rectifier K+ channel., Spassova M., J Gen Physiol. September 1, 1999; 114 (3): 415-26.                


Regulation of melanosome movement in the cell cycle by reversible association with myosin V., Rogers SL., J Cell Biol. September 20, 1999; 146 (6): 1265-76.              


A mutation linked with Bartter's syndrome locks Kir 1.1a (ROMK1) channels in a closed state., Flagg TP., J Gen Physiol. November 1, 1999; 114 (5): 685-700.                      


The cytoskeletal effector xPAK1 is expressed during both ear and lateral line development in Xenopus., Islam N., Int J Dev Biol. February 1, 2000; 44 (2): 245-8.          


Mechanism of IRK1 channel block by intracellular polyamines., Guo D., J Gen Physiol. June 1, 2000; 115 (6): 799-814.                          


Mechanism of cGMP-gated channel block by intracellular polyamines., Guo D., J Gen Physiol. June 1, 2000; 115 (6): 783-98.                      


Pore block versus intrinsic gating in the mechanism of inward rectification in strongly rectifying IRK1 channels., Guo D., J Gen Physiol. October 1, 2000; 116 (4): 561-8.              


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.          


A conducting state with properties of a slow inactivated state in a shaker K(+) channel mutant., Olcese R., J Gen Physiol. February 1, 2001; 117 (2): 149-63.                            


Kinetics of inward-rectifier K+ channel block by quaternary alkylammonium ions. dimension and properties of the inner pore., Guo D., J Gen Physiol. May 1, 2001; 117 (5): 395-406.                          


IRK1 inward rectifier K(+) channels exhibit no intrinsic rectification., Guo D., J Gen Physiol. October 1, 2002; 120 (4): 539-51.                            


Activin A induces craniofacial cartilage from undifferentiated Xenopus ectoderm in vitro., Furue M., Proc Natl Acad Sci U S A. November 26, 2002; 99 (24): 15474-9.    


All-trans-retinal is a closed-state inhibitor of rod cyclic nucleotide-gated ion channels., McCabe SL., J Gen Physiol. May 1, 2004; 123 (5): 521-31.                


Effect of dissociating cytosolic calcium and metabolic rate on intracellular PO2 kinetics in single frog myocytes., Kindig CA., J Physiol. January 15, 2005; 562 (Pt 2): 527-34.


Mechanism of the voltage sensitivity of IRK1 inward-rectifier K+ channel block by the polyamine spermine., Shin HG., J Gen Physiol. April 1, 2005; 125 (4): 413-26.                      


Evolutionary innovation in the vertebrate jaw: A derived morphology in anuran tadpoles and its possible developmental origin., Svensson ME., Bioessays. May 1, 2005; 27 (5): 526-32.


Evidence for sequential ion-binding loci along the inner pore of the IRK1 inward-rectifier K+ channel., Shin HG., J Gen Physiol. August 1, 2005; 126 (2): 123-35.                            


State-dependent block of BK channels by synthesized shaker ball peptides., Li W., J Gen Physiol. October 1, 2006; 128 (4): 423-41.                        


Measurement of conformational changes accompanying desensitization in an ionotropic glutamate receptor., Armstrong N., Cell. October 6, 2006; 127 (1): 85-97.            


FoxN3 is required for craniofacial and eye development of Xenopus laevis., Schuff M., Dev Dyn. January 1, 2007; 236 (1): 226-39.                            


Runx2 is essential for larval hyobranchial cartilage formation in Xenopus laevis., Kerney R., Dev Dyn. June 1, 2007; 236 (6): 1650-62.                  


Pescadillo is required for Xenopus laevis eye development and neural crest migration., Gessert S., Dev Biol. October 1, 2007; 310 (1): 99-112.                  


MEC-2 and MEC-6 in the Caenorhabditis elegans sensory mechanotransduction complex: auxiliary subunits that enable channel activity., Brown AL., J Gen Physiol. June 1, 2008; 131 (6): 605-16.            


Expression study of cadherin7 and cadherin20 in the embryonic and adult rat central nervous system., Takahashi M., BMC Dev Biol. June 23, 2008; 8 87.                


Mutations reveal voltage gating of CNGA1 channels in saturating cGMP., Martínez-François JR., J Gen Physiol. August 1, 2009; 134 (2): 151-64.                      


Xenopus development from late gastrulation to feeding tadpole in simulated microgravity., Olson WM., Int J Dev Biol. January 1, 2010; 54 (1): 167-74.  


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.              


Activation of Slo2.1 channels by niflumic acid., Dai L., J Gen Physiol. March 1, 2010; 135 (3): 275-95.                                


FMR1/FXR1 and the miRNA pathway are required for eye and neural crest development., Gessert S., Dev Biol. May 1, 2010; 341 (1): 222-35.                                                              


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.                            


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.                                


A role for FoxN3 in the development of cranial cartilages and muscles in Xenopus laevis (Amphibia: Anura: Pipidae) with special emphasis on the novel rostral cartilages., Schmidt J., J Anat. February 1, 2011; 218 (2): 226-42.

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