Publikationen von P Haffter

Lopes, S.; Yang, X.; Müller, J.; Carney, T.; McAdow, A.; Rauch, G.-J.; Jacoby, A.; Hurst, L.; Delfino-Machín, M.; Haffter, P. et al.; Geisler, R.; Johnson, S.; Ward, A.; Kelsh, R.: Leukocyte tyrosine kinase functions in pigment cell development. PLoS Genetics 4 (3), e1000026 (2008)

Wolff, C.; Roy, S.; Lewis, K.; Schauerte, H.; Rauch, G.-J.; Kirn, A.; Weiler, C.; Geisler, R.; Haffter, P.; Ingham, P.: iguana encodes a novel zinc-finger protein with coiled-coil domains essential for Hedgehog signal transduction in the zebrafish embryo. Genes and Development 18 (13), S. 1565 - 1576 (2004)

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)

Yan, Y.-L.; Miller, C.; Nissen, R.; Singer, A.; Liu, D.; Kirn, A.; Draper, B.; Willoughby, J.; Morcos, P.; Amsterdam, A. et al.; Chung, B.-C.; Westerfield, M.; Haffter, P.; Hopkins, N.; Kimmel, C.; Postlethwait, J.: A zebrafish sox9 gene required for cartilage morphogenesis. Development 129 (21), S. 5065 - 5079 (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)

Chen, J.-N.; van Bebber, F.; Goldstein, A.; Serluca, F.; Jackson, D.; Childs, S.; Serbedzija, G.; Warren, K.; Mably, J.; Lindahl, P. et al.; Mayer, A.; Haffter, P.; Fishman, M.: Genetic Steps to Organ Laterality in Zebrafish. Comparative and Functional Genomics 2 (2), S. 60 - 68 (2001)

Boggetti, B.; Argenton, F.; Haffter, P.; Bianchi, M.; Cotelli, F.; Beltrame, M.: loning and expression pattern of a zebrafish homolog of forkhead activin signal transducer (FAST), a transcription factor mediating Nodal-related signals. Mechanisms of Development 99 (1-2), S. 187 - 190 (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)

Pöpperl, H.; Rikhof, H.; Chang, H.; Haffter, P.; Kimmel, C.; Moens, C.: lazarus is a novel pbx gene that globally mediates hox gene function in zebrafish. Molecular Cell 6 (2), S. 255 - 267 (2000)

Liu, A.; Majumdar, A.; Schauerte, H.; Haffter, P.; Drummond, I.: Zebrafish wnt4b expression in the floor plate is altered in sonic hedgehog and gli-2 mutants. Mechanisms of Development 91 (1-2), S. 409 - 413 (2000)

Odenthal, J.; van Eeden, F.; Haffter, P.; Ingham, P.; Nüsslein-Volhard, C.: Two distinct cell populations in the floor plate of the zebrafish are induced by different pathways. Developmental Biology 219 (2), S. 350 - 363 (2000)

Lewis, K.; Currie, P.; Roy, S.; Schauerte, H.; Haffter, P.; Ingham, P.: Control of muscle cell-type specification in the zebrafish embryo by Hedgehog signalling. Developmental Biology 216 (2), S. 469 - 480 (1999)

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)

Chandrasekhar, A.; Schauerte, H.; Haffter, P.; Kuwada, J.: The zebrafish detour gene is essential for cranial but not spinal motor neuron induction. Development 126 (12), S. 2727 - 2737 (1999)

Hild, M.; Dick, A.; Rauch, G.-J.; Meier, A.; Bouwmeester, T.; Haffter, P.; Hammerschmidt, M.: The smad5 mutation somitabun blocks Bmp2b signaling during early dorsoventral patterning of the zebrafish embryo. Development 126 (10), S. 2149 - 2159 (1999)

Campione, M.; Steinbeisser, H.; Schweickert, A.; Deissler, K.; van Bebber, F.; Lowe, L.; Nowotschin, S.; Viebahn, C.; Haffter, P.; Kuehn, M. et al.; Blum, M.: The homeobox gene Pitx2: mediator of asymmetric left-right signaling in vertebrate heart and gut looping. Development 126 (6), S. 1225 - 1234 (1999)

Schvarzstein, M.; Kirn, A.; Haffter, P.; Cordes, S.: Expression of Zkrml2, a homologue of the Krml1/val segmentation gene, during embryonic patterning of the zebrafish. Mechanisms of Development 80 (2), S. 223 - 226 (1999)

Chandrasekhar, A.; Warren Jr, J.; Takahashi, K.; Schauerte, H.; van Eeden, F.; Haffter, P.; Kuwada, J.: Role of sonic hedgehog in branchiomotor neuron induction in zebrafish. Mechanisms of Development 76 (1-2), S. 101 - 115 (1998)

Rebagliati, M.; Toyama, R.; Haffter, P.; Dawid, I.: cyclops encodes a nodal-related factor involved in midline signaling. Proceedings of the National Academy of Sciences of the United States of America 95 (17), S. 9932 - 9937 (1998)