Publikationen von R Geisler

Piotrowski, T.; Ahn, D.-G.; Schilling, T.; Nair, S.; Ruvinsky, I.; Geisler, R.; Rauch, G.-J.; Haffter, P.; Zon, L.; Zhou, Y. et al.; Foott, H.; Dawid, I.; Ho, R.: The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans. Development 130 (20), S. 5043 - 5052 (2003)

Bahadori, R.; Huber, M.; Rinner, O.; Seeliger, M.; Geiger-Rudolph, S.; Geisler, R.; Neuhauss, S.: Retinal function and morphology in two zebrafish models of oculo-renal syndromes. European Journal of Neuroscience 18 (6), S. 1377 - 1386 (2003)

Bink, R.; Habuchi, H.; Lele, Z.; Dolk, E.; Joore, J.; Rauch, G.-J.; Geisler, R.; Wilson, S.; den Hertog, J.; Kimata, K. et al.; Zivkovic, D.: Heparan sulfate 6-o-sulfotransferase is essential for muscle development in zebrafish. The Journal of Biological Chemistry 278 (33), S. 31118 - 31127 (2003)

Knaut, H.; Werz, C.; Geisler, R.; The Tübingen 2000 Screen Consortium; Nüsslein-Volhard, C.: A zebrafish homologue of the chemokine receptor Cxcr4 is a germ-cell guidance receptor. Nature 421 (6920), S. 279 - 282 (2003)

Lele, Z.; Folchert, A.; Concha, M.; Rauch, G.-J.; Geisler, R.; Rosa, F.; Wilson, S.; Hammerschmidt, M.; Bally-Cuif, L.: parachute/n-cadherin is required for morphogenesis and maintained integrity of the zebrafish neural tube. Development 129 (14), S. 3281 - 3294 (2002)

Grandel, H.; Lun, K.; Rauch, G.-J.; Rhimm, M.; Piotrowski, T.; Houart, C.; Sordino, P.; Küchler, A.; Schulte-Merker, S.; Geisler, R. et al.; Holder, N.; Wilson, S.; Brand, M.: Retinoic acid signalling in the zebrafish embryo is necessary during pre-segmentation stages to pattern the anterior- posterior axis of the CNS and to induce a pectoral fin bud. Development 129 (12), S. 2851 - 2865 (2002)

Holley, S.; Jülich, D.; Rauch, G.-J.; Geisler, R.; Nüsslein-Volhard, C.: her1 and the notch pathway function within the oscillator mechanism that regulates zebrafish somitogenesis. Development 129 (5), S. 1175 - 1183 (2002)

Dutton, K.; Pauliny, A.; Lopes, S.; Elworthy, S.; Carney, T.; Rauch, J.; Geisler, R.; Haffter, P.; Kelsh, R.: Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates. Development 128 (21), S. 4113 - 4125 (2001)

Begemann, G.; Schilling, T.; Rauch, G.-J.; Geisler, R.; Ingham, P.: The zebrafish neckless mutation reveals a requirement for raldh2 in mesodermal signals that pattern the hindbrain. Development 128 (16), S. 3081 - 3094 (2001)

Heisenberg, C.-P.; Houart, C.; Take-uchi , M.; Rauch, G.-J.; Young, N.; Coutinho, P.; Masai, I.; Caneparo , L.; Concha, M.; Geisler, R. et al.; Dale, C.; Wilson, S.; Stemple, D.: A mutation in the Gsk3-binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon. Genes and Development 15 (11), S. 1427 - 1434 (2001)

Bauer, H.; Lele, Z.; Rauch, G.-J.; Geisler, R.; Hammerschmidt, M.: The type I serine/threonine kinase receptor Alk8/Lost-a-fin is required for Bmp2b/7 signal transduction during dorsoventral patterning of the zebrafish embryo. Development 128 (6), S. 849 - 858 (2001)

Sültmann, H.; Sato, A.; Murray, B.; Takezaki, N.; Geisler, R.; Rauch, G.-J.; Klein, J.: Conservation of Mhc class III region synteny between zebrafish and human as determined by radiation hybrid mapping. The Journal of Immunology 165 (12), S. 6984 - 6993 (2000)

Ernest, S.; Rauch, G.-J.; Haffter, P.; Geisler, R.; Petit, C.; Nicolson, T.: Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness. Human Molecular Genetics 9 (14), S. 2189 - 2196 (2000)

Holley, S.; Geisler, R.; Nüsslein-Volhard, C.: Control of her1 expression during zebrafish somitogenesis by a delta-dependent oscillator and an independent wave-front activity. Genes and Development 14 (13), S. 1678 - 1690 (2000)

Heisenberg, C.-P.; Tada, M.; Rauch, G.-J.; Saúde, L.; Concha, M.; Geisler, R.; Stemple, D.; Smith, J.; Wilson, S.: Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation. Nature 405 (6782), S. 76 - 81 (2000)

Geisler, R.; Rauch, G.-J.; Baier, H.; van Bebber, F.; Broß, L.; Dekens, M.; Finger, K.; Fricke, C.; Gates, M.; Geiger, H. et al.; Geiger-Rudolph, S.; Gilmour, D.; Glaser, S.; Gnügge, L.; Habeck, H.; Hingst, K.; Holley, S.; Keenan, J.; Kirn, A.; Knaut, H.; Lashkari, D.; Maderspacher, F.; Martyn, U.; Neuhauss, S.; Neumann, C.; Nicolson, T.; Pelegri, F.; Ray, R.; Rick, J.; Roehl, H.; Roeser, T.; Schauerte, H.; Schier, A.; Schönberger, U.; Schönthaler, H.-B.; Schulte-Merker, S.; Seydler, C.; Talbot, W.; Weiler, C.; Nüsslein-Volhard, C.; Haffter, P.: A radiation hybrid map of the zebrafish genome. Nature Genetics 23 (1), S. 86 - 89 (1999)

Dorsky, R.; Snyder, A.; Cretekos, C.; Grunewald, D.; Geisler, R.; Haffter, P.; Moon, R.; Raible, D.: Maternal and embryonic expression of zebrafish lef1. Mechanisms of Development 86 (1-2), S. 147 - 150 (1999)

Bergmann, A.; Stein, D.; Geisler, R.; Hagenmaier, S.; Schmid, B.; Fernandez, L.; Schnell, B.; Nüsslein-Volhard, C.: A gradient of cytoplasmic Cactus degradation establishes the nuclear localization gradient of the dorsal morphogen in Drosophila. Mechanisms of Development 60 (1), S. 109 - 123 (1996)

Geisler, R.; Bergmann, A.; Hiromi, Y.; Nüsslein-Volhard, C.: cactus, a gene involved in dorsoventral pattern formation of Drosophila, is related to the I kappa B gene family of vertebrates. Cell 71 (4), S. 613 - 621 (1992)

Koch, R.; Rauch, G.-J.; Humphray, S.; Geisler, R.; Plasterk, R.: Bacterial Artificial Chromosome (BAC) Clones and the Current Clone Map of the Zebrafish Genome. In: The Zebrafish: Genetics, Genomics, and Informatics, S. 295 - 304 (Hg. Dietrich, H.; Westerfield, M.; Zon, L.). Elsevier, Amsterdam, The Netherlands (2004)