Modulation of Wnt signaling

References

• Peterson KJ, Lyons JB, Nowak KS, Takacs CM, Wargo MJ, McPeek MA. Estimating metazoan divergence times with a molecular clock. Proc Natl Acad Sci USA 2004; 101:6536 - 6541
   PubMed Web of Science ®Google Scholar
• Morris SC. The Cambrian “explosion”: Slow-fuse or megatonnage?. Proc Natl Acad Sci USA 2000; 97:4426 - 4429
   PubMed Web of Science ®Google Scholar
• Duffy DJ, Plickert G, Kuenzel T, Tilmann W, Frank U. Wnt signaling promotes oral but suppresses aboral structures in Hydractinia metamorphosis and regeneration. Development 2010; 137:3057 - 3066
   PubMed Web of Science ®Google Scholar
• Petersen CP, Reddien PW. Wnt signaling and the polarity of the primary body axis. Cell 2009; 139:1056 - 1068
   PubMed Web of Science ®Google Scholar
• Schneider S, Steinbeisser H, Warga RM, Hausen P. beta-catenin translocation into nuclei demarcates the dorsalizing centers in frog and fish embryos. Mech Dev 1996; 57:191 - 198
   PubMed Web of Science ®Google Scholar
• Niehrs C. Head in the WNT: the molecular nature of Spemann's head organizer. Trends Genet 1999; 15:314 - 319
   PubMed Web of Science ®Google Scholar
• Aulehla A, Wehrle C, Brand-Saberi B, Kemler R, Gossler A, Kanzler B, et al. Wnt3a plays a major role in the segmentation clock controlling somitogenesis. Dev Cell 2003; 4:395 - 406
   PubMed Web of Science ®Google Scholar
• Miyawaki K, Mito T, Sarashina I, Zhang H, Shinmyo Y, Ohuchi H, et al. Involvement of Wingless/Armadillo signaling in the posterior sequential segmentation in the cricket, Gryllus bimaculatus (Orthoptera), as revealed by RNAi analysis. Mech Dev 2004; 121:119 - 130
   PubMed Web of Science ®Google Scholar
• McGregor AP, Pechmann M, Schwager EE, Feitosa NM, Kruck S, Aranda M, et al. Wnt8 is required for growth-zone establishment and development of opisthosomal segments in a spider. Curr Biol 2008; 18:1619 - 1623
   PubMed Web of Science ®Google Scholar
• Niehrs C. On growth and form: a Cartesian coordinate system of Wnt and BMP signaling specifies bilaterian body axes. Development 2010; 137:845 - 857
   PubMed Web of Science ®Google Scholar
• Gurley KA, Rink JC, Alvarado AS. Beta-catenin defines head versus tail identity during planarian regeneration and homeostasis. Science 2008; 319:323 - 327
   PubMed Web of Science ®Google Scholar
• Iglesias M, Gomez-Skarmeta JL, Saló E, Adell T. Silencing of Smed-βcatenin1 generates radial-like hypercephalized planarians. Development 2008; 135:1215 - 1221
   PubMed Web of Science ®Google Scholar
• Petersen CP, Reddien PW. Smed-beta catenin-1 is required for anteroposterior blastema polarity in planarian regeneration. Science 2008; 319:327 - 330
   PubMed Web of Science ®Google Scholar
• Adamska M, Degnan SM, Green KM, Adamski M, Craigie A, Larroux C, et al. Wnt and TGFβ expression in the sponge Amphimedon queenslandica and the origin of metazoan embryonic patterning. PLoS ONE 2007; 2:1031
   PubMed Web of Science ®Google Scholar
• Hobmayer B, Rentzsch F, Kuhn K, Happel CM, von Laue CC, Snyder P, et al. WNT signaling molecules act in axis formation in the diploblastic metazoan Hydra. Nature 2000; 407:186 - 189
   PubMed Web of Science ®Google Scholar
• Müller WA, Teo R, Möhrlen F. Patterning a multi-headed mutant in Hydractinia: enhancement of head formation and its phenotypic normalization. Int J Dev Biol 2004; 48:9 - 15
   PubMed Web of Science ®Google Scholar
• Broun M, Gee L, Reinhardt B, Bode HR. Formation of the head organizer in hydra involves the canonical Wnt pathway. Development 2005; 132:2907 - 2916
   PubMed Web of Science ®Google Scholar
• Kusserow A, Pang K, Sturm C, Hrouda M, Lentfer J, Schmidt HA, et al. Unexpected complexity of the Wnt gene family in a sea anemone. Nature 2005; 433:156 - 160
   PubMed Web of Science ®Google Scholar
• Plickert G, Jacoby V, Frank U, Muller WA, Mokady O. Wnt signaling in hydroid development: Formation of the primary body axis in embryogenesis and its subsequent patterning. Dev Biol 2006; 298:368 - 378
   PubMed Web of Science ®Google Scholar
• Lee PN, Kumburegama S, Marlow HQ, Martindale MQ, Wikramanayake AH. Asymmetric developmental potential along the animal-vegetal axis in the anthozoan cnidarian, Nematostella vectensis, is mediated by Dishevelled. Dev Biol 2007; 310:169 - 186
   PubMed Web of Science ®Google Scholar
• Amiel A, Houliston E. Three distinct RNA localization mechanisms contribute to oocyte polarity establishment in the cnidarian Clytia hemispherica. Dev Biol 2009; 327:191 - 203
   PubMed Web of Science ®Google Scholar
• Momose T, Houliston E. Two oppositely localised Frizzled RNAs as axis determinants in a cnidarian embryo. PLoS Biol 2007; 5:70
   Web of Science ®Google Scholar
• Momose T, Derelle R, Houliston E. A maternally localised Wnt ligand required for axial patterning in the cnidarian Clytia hemisphaerica. Development 2008; 135:2105 - 2113
   PubMed Web of Science ®Google Scholar
• Chapman JA, Kirkness EF, Simakov O, Hampson SE, Mitros T, Weinmaier T, et al. The dynamic genome of Hydra. Nature 2010; 464:592 - 596
   PubMed Web of Science ®Google Scholar
• Hassel M, Albert K, Hofheinz S. Pattern formation in Hydra vulgaris is controlled by lithium-sensitive processes. Dev Biol 1993; 156:362 - 371
   PubMed Web of Science ®Google Scholar
• Wikramanayake AH, Hong M, Lee PN, Pang K, Byrum CA, Bince JM, et al. An ancient role for nuclear beta-catenin in the evolution of axial polarity and germ layer segregation. Nature 2003; 426:446 - 450
   PubMedGoogle Scholar
• Meinhardt H. Beta-catenin and axis formation in planarians. BioEssays 2009; 31:5 - 9
   PubMed Web of Science ®Google Scholar
• Lee PN, Pang K, Matus DQ, Martindale MQ. A WNT of things to come: evolution of Wnt signaling and polarity in cnidarians. Semin Cell Dev Biol 2006; 17:157 - 167
   PubMed Web of Science ®Google Scholar