
| Administration | Basic Sciences | Clinical Sciences | Centers of Excellence |
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| Degrees |
Diploma Molecular Genetics - 1992 PhD Natural Sciences - 1997 |
| Bio |
Dr. Wessely's laboratory is studying kidney development and its perturbation during diseases. The focus is on understanding the molecular nature of this regulation at the level of signal transduction and transcription using the amphibian Xenopus laevis. In contrast to slow developing mouse, Xenopus forms a functional pronephros (primitive kidney) within 31 hours. It thereby facilitates the fast identification and characterization of novel genes and regulatory pathways involved in kidney development and how those are perturbed during diseases such as Polycystic Kidney Disease. The results from these studies are then directly applied to subsequent studies in our lab using transgenic mice.
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| Research Interests |
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| Selected Publications |
Wessely O, Kim JI, Tran U, Fuentaelba L and De Robertis EM, xBtg-x-Regulates Wnt/-Catenin Signaling During Early Xenopus Development, Dev. Biol. (in press), 2005. Wessely O, Kim JI, Geissert D, Tran U and De Robertis EM, Analysis of Spemann Organizer Formation in Xenopus Embryos by cDNA Macroarrays, Dev. Biol. 269, 552-566, 2004. Kuroda H, Wessley O and De Robertis EM, The Preorganizer Center Mediates Neural Induction in Ectoderm via -Catenin, Chordin and Noggin signals, PLOS Biology 2, 0623-0634, 2004. De Robertis EM, Larrain J, Oelgeschlager M and Wessely O, The Establishment of Spemann Organizer and Patterning of the Vertebrate Embryo, Nature Reviews Genetics 1; 171-181, 2000. Wessely O and De Robertis EM, The Xenopus homologue of Bicaudal-C is a localized maternal RNA that functions in endoderm differentiation, Development 127(10); 2053-2062, 2000. |
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