The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (195)

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Goswami, C.; Hucho, T.: Novel aspects of the submembraneous microtubule cytoskeleton. FEBS Journal 275 (19), p. 4653 - 4653 (2008)
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Tsend-Ayush, E.; Dodge, N.; Mohr, J.; Casey, A.; Himmelbauer, H.; Kremitzki, C. L.; Schatzkamer, K.; Graves, T.; Warren, W. C.; Grützner, F.: Higher-order genome organization in platypus and chicken sperm and repositioning of sex chromosomes during mammalian evolution. Chromosoma 118 (1), pp. 53 - 69 (2008)
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Groth, D.; Hartmann, S.; Panopoulou, G.; Poustka, A. J.; Hennig, S.: GOblet: annotation of anonymous sequence data with Gene Ontology and pathway terms. Journal of Integrative Bioinformatics 5 (2), p. 104 - 104 (2008)
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Van Maldergem, L.; Yuksel-Apak, M.; Kayserili, H.; Seemanova, E.; Giurgea, S.; Basel-Vanagaite, L.; Leao-Teles, E.; Vigneron, J.; Foulon, M.; Greally, M. et al.; Jaeken, J.; Mundlos, S.; Dobyns, W. B.: Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre type. Neurology, pp. 1602 - 1608 (2008)
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Erdogan, F.; Larsen, L. A.; Zhang, L.; Tümer, Z.; Tommerup, N.; Chen, W.; Jacobsen, J. R.; Schubert, M.; Jurkatis, J.; Tzschach, A. et al.; Ropers, H. H.; Ullmann, R.: High frequency of submicroscopic genomic aberrations detected by tiling path array CGH in patients with isolated congenital heart disease. Journal of Medical Genetics 11, pp. 705 - 709 (2008)
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Winkel, A.; Stricker, S.; Tylzanowski, P.; Seiffart, V.; Mundlos, S.; Gross, G.; Hoffmann, A.: Wnt-ligand-dependent interaction of TAK1 (TGF-beta-activated kinase-1) with the receptor tyrosine kinase Ror2 modulates canonical Wnt-signalling. Cellular Signalling 20 (11), pp. 2134 - 2144 (2008)
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Sultan, M.; Schulz, M. H.; Hugues, R.; Magen, A.; Klingenhoff, A.; Scherf, M.; Seifert, M.; Borodina, T.; Soldatov, A.; i Parkhomchuk, D. et al.; Schmidt, D.; O'Keeffe, S.; Haas, S.; Vingron, M.; Lehrach, H.; Yaspo, M.-L.: A Global View of Gene Activity and Alternative Splicing by Deep Sequencing of the Human Transcriptome. Science 321 (5891), pp. 956 - 960 (2008)
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Zi, Z.; Zheng, Y.; Rundell, A. E.; Klipp, E.: A systems biology markup language (SBML) based sensitivity analysis tool. BMC Bioinformatics 15 (9), p. 342 - 342 (2008)
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Mann, K.; Poustka, A. J.; Mann, M.: The sea urchin (Strongylocentrotus purpuratus) test and spine proteomes. Proteome Science 2008 (6), p. 6:22 - 6:22 (2008)
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Klopocki, E.; Graul-Neumann, L. M.; Grieben, U.; Tönnies, H.; Ropers, H.-H.; Horn, D.; Mundlos, S.; Ullmann, R.: A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH. European Journal of Pediatrics 167 (8), pp. 903 - 908 (2008)
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Niesner, U.; Albrecht, I.; Janke, M.; Doebis, C.; Loddenkemper, C.; Lexberg, M. H.; Eulenburg, K.; Kreher, S.; Koeck, J.; Baumgrass, R. et al.; Bonhagen, K.; Kamradt, T.; Enghard, P.; Humrich, J. Y.; Rutz, S.; Schulze-Topphoff, U.; Aktas, O.; Bartfeld, S.; Radbruch, H.; Hegazy, A. N.; Löhning, M.; Baumgart, D. C.; Duchmann, R.; Rudwaleit, M.; Häupl, T.; Gitelman, I.; Krenn, V.; Gruen, J.; Sieper, J.; Zeitz, M.; Wiedenmann, B.; Zipp, F.; Hamann, A.; Janitz, M.; Scheffold, A.; Burmester, G. R.; Chang, H. D.; Radbruch, A.: Autoregulation of Th1-mediated inflammation by twist1. Journal of Experimental Medicine 205 (8), pp. 1889 - 1901 (2008)
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Parsons, M. J.; Grimm, C. H.; Paya-Cano, J. L.; Sugden, K.; Nietfeld, W.; Lehrach, H.; Schalkwyk, L. C.: Using hippocampal microRNA expression differences between mouse inbred strains to characterise miRNA function. Mammalian Genome 19 (7-8), pp. 552 - 560 (2008)
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Kolanczyk, M.; Kühnisch, J.; Kossler, N.; Osswald, M.; Stumpp, S.; Thurisch, B.; Kornak, U.; Mundlos, S.: Modelling neurofibromatosis type 1 tibial dysplasia and its treatment with lovastatin. BMC Medicine 31 (6), p. 21 - 21 (2008)
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Sauer, S.; Freiwald, A.; Maier, T.; Kube, M.; Reinhardt, R.; Kostrzewa, M.; Geider, K.: Classification and identification of bacteria by mass spectrometry and computational analysis. PLoS One (7), p. e2843 - e2843 (2008)
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Costa, I. G.; Roepcke, S.; Hafemeister, C.; Schliep, A.: Inferring differentiation pathways from gene expression. Bioinformatics 24 (13), pp. i56 - 164 (2008)
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Winter, J.; Roepcke, S.; Krause, S.; Müller, E.-C.; Otto, A.; Vingron, M.; Schweiger, S.: Comparative 3’UTR analysis allows identification of regulatory clusters that drive Eph/ephrin expression in cancer cell lines. PLoS One 3 (7), p. e2780 - e2780 (2008)
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Burmeister, T.; Meyer, C.; Thiel, G.; Reinhardt, R.; Thiel, E.; Marschalek, R.: A MLL-KIAA0284 fusion gene in a patient with secondary acute myeloid leukemia and t(11;14)(q23;q32). Blood Cells, Molecules, and Diseases 41 (2), pp. 210 - 214 (2008)
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Jeong, J.-H.; Jin, J.-S.; Kim, H.-N.; Kang, S.-M.; Liu, J. C.; Lengner, C. J.; Otto, F.; Mundlos, S.; Stein, J. L.; van Wijnen, A. J. et al.; Lian, J. B.; Stein, G. S.; Choi, J.-Y.: Expression of Runx2 transcription factor in non-skeletal tissues, sperm and brain. Journal of Cellular Physiology 217 (2), pp. 511 - 517 (2008)
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Budkevich, T. V.; El'skaya, A. V.; Nierhaus, K. H.: Features of 80S mammalian ribosome and its subunits. Nucleic Acids Research 36( (14), pp. 4736 - 4744 (2008)
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Douzgou, S.; Lehmann, K.; Mingarelli, R.; Mundlos, S.; Dallapiccola, B.: Compound heterozygosity for GDF5 in Du Pan type chondrodysplasia. American Journal of Medical Genetics Part A 146A (16), pp. 2116 - 2121 (2008)
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