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Summary Anatomy Item Literature (4087) Expression Attributions Wiki
XB-ANAT-3714

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Integrin alpha5beta1 and fibronectin regulate polarized cell protrusions required for Xenopus convergence and extension., Davidson LA, Davidson LA., Curr Biol. May 9, 2006; 16 (9): 833-44.                


Limb regeneration in Xenopus laevis froglet., Suzuki M, Suzuki M., ScientificWorldJournal. May 12, 2006; 6 Suppl 1 26-37.        


The effect of VEGF on blood vessels and blood cells during Xenopus development., Koibuchi N., Biochem Biophys Res Commun. May 26, 2006; 344 (1): 339-45.        


Genetic screens for mutations affecting development of Xenopus tropicalis., Goda T., PLoS Genet. June 1, 2006; 2 (6): e91.                        


Combined ectopic expression of Pdx1 and Ptf1a/p48 results in the stable conversion of posterior endoderm into endocrine and exocrine pancreatic tissue., Afelik S., Genes Dev. June 1, 2006; 20 (11): 1441-6.                        


Membrane stretch slows the concerted step prior to opening in a Kv channel., Laitko U., J Gen Physiol. June 1, 2006; 127 (6): 687-701.                  


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


Control of muscle regeneration in the Xenopus tadpole tail by Pax7., Chen Y, Chen Y., Development. June 1, 2006; 133 (12): 2303-13.    


Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation., Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.                


deltaEF1 and SIP1 are differentially expressed and have overlapping activities during Xenopus embryogenesis., van Grunsven LA., Dev Dyn. June 1, 2006; 235 (6): 1491-500.  


Heart defects in X-linked heterotaxy: evidence for a genetic interaction of Zic3 with the nodal signaling pathway., Ware SM., Dev Dyn. June 1, 2006; 235 (6): 1631-7.


Developmental expression of FoxJ1.2, FoxJ2, and FoxQ1 in Xenopus tropicalis., Choi VM., Gene Expr Patterns. June 1, 2006; 6 (5): 443-7.      


Excess Mcm2-7 license dormant origins of replication that can be used under conditions of replicative stress., Woodward AM., J Cell Biol. June 5, 2006; 173 (5): 673-83.              


Genomic analysis of Xenopus organizer function., Hufton AL., BMC Dev Biol. June 6, 2006; 6 27.                  


Induction and specification of cranial placodes., Schlosser G., Dev Biol. June 15, 2006; 294 (2): 303-51.                


The role of Paraxial Protocadherin in Xenopus otic placode development., Hu RY., Biochem Biophys Res Commun. June 23, 2006; 345 (1): 239-47.            


Neofunctionalization in vertebrates: the example of retinoic acid receptors., Escriva H., PLoS Genet. July 1, 2006; 2 (7): e102.                  


XGAP, an ArfGAP, is required for polarized localization of PAR proteins and cell polarity in Xenopus gastrulation., Hyodo-Miura J., Dev Cell. July 1, 2006; 11 (1): 69-79.                                


Nodal-related gene Xnr5 is amplified in the Xenopus genome., Takahashi S., Genesis. July 1, 2006; 44 (7): 309-21.          


The Wnt-dependent signaling pathways as target in oncology drug discovery., Janssens N., Invest New Drugs. July 1, 2006; 24 (4): 263-80.        


Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.                            


PCNS: a novel protocadherin required for cranial neural crest migration and somite morphogenesis in Xenopus., Rangarajan J., Dev Biol. July 1, 2006; 295 (1): 206-18.              


Differential role of 14-3-3 family members in Xenopus development., Lau JM., Dev Dyn. July 1, 2006; 235 (7): 1761-76.                                                    


Isolation and characterization of a novel gene, xMADML, involved in Xenopus laevis eye development., Elkins MB., Dev Dyn. July 1, 2006; 235 (7): 1845-57.                  


Xenopus fibrillin is expressed in the organizer and is the earliest component of matrix at the developing notochord-somite boundary., Skoglund P., Dev Dyn. July 1, 2006; 235 (7): 1974-83.            


Analysis of mouse EphA knockins and knockouts suggests that retinal axons programme target cells to form ordered retinotopic maps., Willshaw D., Development. July 1, 2006; 133 (14): 2705-17.  


Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity., Suga A., Dev Biol. July 1, 2006; 295 (1): 26-39.    


IgD, like IgM, is a primordial immunoglobulin class perpetuated in most jawed vertebrates., Ohta Y., Proc Natl Acad Sci U S A. July 11, 2006; 103 (28): 10723-8.              


Inhibitor-resistant type I receptors reveal specific requirements for TGF-beta signaling in vivo., Ho DM., Dev Biol. July 15, 2006; 295 (2): 730-42.            


Development of the primary mouth in Xenopus laevis., Dickinson AJ., Dev Biol. July 15, 2006; 295 (2): 700-13.                


Molecular evidence for deep evolutionary roots of bilaterality in animal development., Matus DQ., Proc Natl Acad Sci U S A. July 25, 2006; 103 (30): 11195-200.            


Systematic analysis of the role of target site accessibility in the activity of DNA enzymes., Doran G., J RNAi Gene Silencing. July 28, 2006; 2 (2): 205-14.          


The Notch-effector HRT1 gene plays a role in glomerular development and patterning of the Xenopus pronephros anlagen., Taelman V., Development. August 1, 2006; 133 (15): 2961-71.                  


Transgenic Xenopus laevis strain expressing cre recombinase in muscle cells., Waldner C., Dev Dyn. August 1, 2006; 235 (8): 2220-8.          


Metastasis-associated kinase modulates Wnt signaling to regulate brain patterning and morphogenesis., Kibardin A., Development. August 1, 2006; 133 (15): 2845-54.                    


Mathematical model of morphogen electrophoresis through gap junctions., Esser AT., Dev Dyn. August 1, 2006; 235 (8): 2144-59.                  


Developmental cell death during Xenopus metamorphosis involves BID cleavage and caspase 2 and 8 activation., Du Pasquier D., Dev Dyn. August 1, 2006; 235 (8): 2083-94.                  


Role for retinoid signaling in left-right asymmetric digestive organ morphogenesis., Lipscomb K., Dev Dyn. August 1, 2006; 235 (8): 2266-75.    


ACE2 orthologues in non-mammalian vertebrates (Danio, Gallus, Fugu, Tetraodon and Xenopus)., Chou CF., Gene. August 1, 2006; 377 46-55.          


Cholesterol homeostasis in development: the role of Xenopus 7-dehydrocholesterol reductase (Xdhcr7) in neural development., Tadjuidje E., Dev Dyn. August 1, 2006; 235 (8): 2095-110.                          


Heading in a new direction: implications of the revised fate map for understanding Xenopus laevis development., Lane MC., Dev Biol. August 1, 2006; 296 (1): 12-28.                


A novel gene, Ami is expressed in vascular tissue in Xenopus laevis., Inui M., Gene Expr Patterns. August 1, 2006; 6 (6): 613-9.        


Ring of negative charge in BK channels facilitates block by intracellular Mg2+ and polyamines through electrostatics., Zhang Y., J Gen Physiol. August 1, 2006; 128 (2): 185-202.                


Temporal requirement for bone morphogenetic proteins in regeneration of the tail and limb of Xenopus tadpoles., Beck CW., Mech Dev. September 1, 2006; 123 (9): 674-88.              


Hex acts with beta-catenin to regulate anteroposterior patterning via a Groucho-related co-repressor and Nodal., Zamparini AL., Development. September 1, 2006; 133 (18): 3709-22.                                    


PTEN is required for the normal progression of gastrulation by repressing cell proliferation after MBT in Xenopus embryos., Ueno S., Dev Biol. September 1, 2006; 297 (1): 274-83.            


Grainyhead-like 3, a transcription factor identified in a microarray screen, promotes the specification of the superficial layer of the embryonic epidermis., Chalmers AD., Mech Dev. September 1, 2006; 123 (9): 702-18.                                                  


Kermit 2/XGIPC, an IGF1 receptor interacting protein, is required for IGF signaling in Xenopus eye development., Wu J., Development. September 1, 2006; 133 (18): 3651-60.          


FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.                    


The Xdsg protein in presumptive primordial germ cells (pPGCs) is essential to their differentiation into PGCs in Xenopus., Ikenishi K., Dev Biol. September 15, 2006; 297 (2): 483-92.      

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