Multiple roles for neurofibromin in skeletal development and growth von Kolanczyk, Mateusz, Kossler, Nadine, Kühnisch, Jirko, Lavitas, Liron, Stricker, Sigmar, Wilkening, Ulrich, Manjubala, Inderchand, Fratzl, Peter, Spörle, Ralf, Herrmann, Bernhard G., Parada, Luis F., Kornak, Uwe, Mundlos, Stefan

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An RNA interference phenotypic screen identifies a role for FGF signals in colon cancer progression von Leushacke, Marc, Spörle, Ralf, Bernemann, Christof, Brouwer-Lehmitz, Antje, Fritzmann, Johannes, Theis, Mirko, Buchholz, Frank, Herrmann, Bernhard G, Morkel, Markus

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Epaxial-adaxial-hypaxial regionalisation of the vertebrate somite: evidence for a somitic organiser and a mirror-image duplication von Sporle, Ralf

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Computer-based three-dimensional visualization of developmental gene expression von Streicher, Johannes, Donat, Markus A, Strauss, Bernhard, Spörle, Ralf, Schughart, Klaus, Müller, Gerd B

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Cloning of mouse ojoplano, a reticular cytoplasmic protein expressed during embryonic development von Mertes, Florian, Martinez-Morales, Juan-Ramon, Nolden, Tobias, Spörle, Ralf, Wittbrodt, Joachim, Lehrach, Hans, Himmelbauer, Heinz

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The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formation von Nagai, T, Aruga, J, Takada, S, Günther, T, Spörle, R, Schughart, K, Mikoshiba, K

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The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney von Favor, J, Sandulache, R, Neuhäuser-Klaus, A, Pretsch, W, Chatterjee, B, Senft, E, Wurst, W, Blanquet, V, Grimes, P, Spörle, R, Schughart, K

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Characterization and Expression Pattern of thefrizzledGeneFzd9,the Mouse Homolog ofFZD9Which Is Deleted in Williams–Beuren Syndrome von Wang, Yu-Ker, Spörle, Ralf, Paperna, Tamar, Schughart, Klaus, Francke, Uta

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The Expression of the MouseZic1, Zic2,andZic3Gene Suggests an Essential Role forZicGenes in Body Pattern Formation von Nagai, Takeharu, Aruga, Jun, Takada, Shinji, Günther, Thomas, Spörle, Ralf, Schughart, Klaus, Mikoshiba, Katsuhiko

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Isolation and Embryonic Expression of the Novel Mouse Gene Hic1, the Homologue of HIC1, a Candidate Gene for the Miller-Dieker Syndrome von Grimm, Christina, Spörle, Ralf, Schmid, Thomas E., Adler, Ilse-Dore, Adamski, Jerzy, Schughart, Klaus, Graw, Jochen

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Somite Development: Constructing the Vertebrate Body von Tajbakhsh, Shahragim, Spörle, Ralf

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Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome von WANG, Y.-K, SPÖRLE, R, PAPERNA, T, SCHUGHART, K, FRANCKE, U

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The mouse Pax21Neu mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney... von Favor, Jack, Sandulache, Rodica, Neuhäuser-Klaus, Angelika, Pretsch, Walter, Chatterjee, Bimal, Senft, Elfriede, Wurst, Wolfgang, Blanquet, Véronique, Grimes, Patricia, Spörle, Ralf, Schughart, Klaus

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Expression of Ndufb11 encoding the neuronal protein 15.6 during neurite outgrowth and development von Gurok, Ulf, Bork, Kaya, Nuber, Ulrike, Spörle, Ralf, Nöhring, Sabine, Horstkorte, Rüdiger

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A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C von Jensen, Lars R, Bartenschlager, Heinz, Rujirabanjerd, Sinitdhorn, Tzschach, Andreas, Nümann, Astrid, Janecke, Andreas R, Spörle, Ralf, Stricker, Sigmar, Raynaud, Martine, Nelson, John, Hackett, Anna, Fryns, Jean-Pierre, Chelly, Jamel, de Brouwer, Arjan Pm, Hamel, Ben, Gecz, Jozef, Ropers, Hans-Hilger, Kuss, Andreas W

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System to identify individual somites and their derivatives in the developing mouse embryo von Spörle, Ralf, Schughart, Klaus

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Paradox segmentation along inter- and intrasomitic borderlines is followed by dysmorphology of the axial skeleton in theopen brain (opb) mouse mutant von Spörle, Ralf, Schughart, Klaus

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Neural tube morphogenesis von Spörle, Ralf, Schughart, Klaus

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Severe defects in the formation of epaxial musculature in open brain (opb) mutant mouse embryos von Spörle, Ralf, Günther, Thomas, Struwe, Marina, Schughart, Klaus

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The open brain (opb) mutation maps to mouse chromosome 1 von Günther, T, Spörle, R, Schughart, K

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