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 (247)

Journal Article
Steininger, A.; Mobs, M.; Ullmann, R.; Kochert, K.; Kreher, S.; Lamprecht, B.; Anagnostopoulos, I.; Hummel, M.; Richter, J.; Beyer, M. et al.; Janz, M.; Klemke, C. D.; Stein, H.; Dorken, B.; Sterry, W.; Schrock, E.; Mathas, S.; Assaf, C.: Genomic loss of the putative tumor suppressor gene E2A in human lymphoma. J Exp Med 208 (8), pp. 1585 - 93 (2011)
Journal Article
Stricker, S.; Mathia, S.; Haupt, J.; Seemann, P.; Meier, J.; Mundlos, S.: Odd-Skipped Related Genes Regulate Differentiation of Embryonic Limb Mesenchyme and Bone Marrow Mesenchymal Stromal Cells. Stem Cells Dev (2011)
Journal Article
Stricker, S.; Mundlos, S.: FGF and ROR2 receptor tyrosine kinase signaling in human skeletal development. Curr Top Dev Biol 97, pp. 179 - 206 (2011)
Journal Article
Stricker, S.; Mundlos, S.: Mechanisms of digit formation: Human malformation syndromes tell the story. Dev Dyn 240 (5), pp. 990 - 1004 (2011)
Journal Article
Strobl-Wildemann, G.; Kalscheuer, V. M.; Hu, H.; Wrogemann, K.; Ropers, H. H.; Tzschach, A.: Novel GDI1 mutation in a large family with nonsyndromic X-linked intellectual disability. Am J Med Genet A 155A (12), pp. 3067 - 70 (2011)
Journal Article
Suk, E. K.; McEwen, G. K.; Duitama, J.; Nowick, K.; Schulz, S.; Palczewski, S.; Schreiber, S.; Holloway, D. T.; McLaughlin, S.; Peckham, H. et al.; Lee, C.; Huebsch, T.; Hoehe, M. R.: A comprehensively molecular haplotype-resolved genome of a European individual. Genome Research 21 (10), pp. 1672 - 85 (2011)
Journal Article
Szczurek, E.; Markowetz, F.; Gat-Viks, I.; Biecek, P.; Tiuryn, J.; Vingron, M.: Deregulation upon DNA damage revealed by joint analysis of context-specific perturbation data. BMC Bioinformatics 12, p. 249 (2011)
Journal Article
Thomas-Chollier, M.; Defrance, M.; Medina-Rivera, A.; Sand, O.; Herrmann, C.; Thieffry, D.; van Helden, J.: RSAT 2011: regulatory sequence analysis tools. Nucleic Acids Res 39 (Web Server issue), pp. W86 - 91 (2011)
Journal Article
Thomas-Chollier, M.; Herrmann, C.; Defrance, M.; Sand, O.; Thieffry, D.; van Helden, J.: RSAT peak-motifs: motif analysis in full-size ChIP-seq datasets. Nucleic Acids Res (2011)
Journal Article
Thomas-Chollier, M.; Hufton, A.; Heinig, M.; O'Keeffe, S.; Masri, N. E.; Roider, H. G.; Manke, T.; Vingron, M.: Transcription factor binding predictions using TRAP for the analysis of ChIP-seq data and regulatory SNPs. Nat Protoc 6 (12), pp. 1860 - 9 (2011)
Journal Article
Thormann, A.; Rasche, A.: Functional Context Network of T2DM, Medical Complications of Type 2 Diabetes. Intech Publishing (2011)
Journal Article
Turkmen, S.; Riehn, M.; Klopocki, E.; Molkentin, M.; Reinhardt, R.; Burmeister, T.: A BACH2-BCL2L1 fusion gene resulting from a t(6;20)(q15;q11.2) chromosomal translocation in the lymphoma cell line BLUE-1. Genes Chromosomes Cancer 50 (6), pp. 389 - 96 (2011)
Journal Article
Tzschach, A.; Ullmann, R.; Ahmed, A.; Martin, T.; Weber, G.; Decker-Schwering, O.; Pauly, F.; Shamdeen, M. G.; Reith, W.; Oehl-Jaschkowitz, B.: Christianson syndrome in a patient with an interstitial Xq26.3 deletion. Am J Med Genet A 155A (11), pp. 2771 - 4 (2011)
Journal Article
Vilardell, M.; Rasche, A.; Thormann, A.; Maschke-Dutz, E.; Perez-Jurado, L. A.; Lehrach, H.; Herwig, R.: Meta-analysis of heterogeneous Down Syndrome data reveals consistent genome-wide dosage effects related to neurological processes. BMC Genomics 12, p. 229 (2011)
Journal Article
Vinayagam, A.; Stelzl, U.; Foulle, R.; Plassmann, S.; Zenkner, M.; Timm, J.; Assmus, H. E.; Andrade-Navarro, M. A.; Wanker, E. E.: A directed protein interaction network for investigating intracellular signal transduction. Sci Signal 4 (189), p. rs8 (2011)
Journal Article
Viswanathan, J.; Haapasalo, A.; Bottcher, C.; Miettinen, R.; Kurkinen, K. M.; Lu, A.; Thomas, A.; Maynard, C. J.; Romano, D.; Hyman, B. T. et al.; Berezovska, O.; Bertram, L.; Soininen, H.; Dantuma, N. P.; Tanzi, R. E.; Hiltunen, M.: Alzheimer's disease-associated ubiquilin-1 regulates presenilin-1 accumulation and aggresome formation. Traffic 12 (3), pp. 330 - 48 (2011)
Journal Article
von Keyserling, H.; Bergmann, T.; Schuetz, M.; Schiller, U.; Stanke, J.; Hoffmann, C.; Schneider, A.; Lehrach, H.; Dahl, A.; Kaufmann, A. M.: Analysis of 4 single-nucleotide polymorphisms in relation to cervical dysplasia and cancer development using a high-throughput ligation-detection reaction procedure. International Journal of Gynecological Cancer: Official Journal of the International Gynecological Cancer Society 21 (9), pp. 1664 - 71 (2011)
Journal Article
Walther, D. J.; Stahlberg, S.; Vowinckel, J.: Novel roles for biogenic monoamines: from monoamines in transglutaminase-mediated post-translational protein modification to monoaminylation deregulation diseases. FEBS J 278 (24), pp. 4740 - 55 (2011)
Journal Article
Wang, Y.; Adjaye, J.: A cyclic AMP analog, 8-Br-cAMP, enhances the induction of pluripotency in human fibroblast cells. Stem Cell Reviews 7 (2), pp. 331 - 41 (2011)
Journal Article
Warman, M. L.; Cormier-Daire, V.; Hall, C.; Krakow, D.; Lachman, R.; LeMerrer, M.; Mortier, G.; Mundlos, S.; Nishimura, G.; Rimoin, D. L. et al.; Robertson, S.; Savarirayan, R.; Sillence, D.; Spranger, J.; Unger, S.; Zabel, B.; Superti-Furga, A.: Nosology and classification of genetic skeletal disorders: 2010 revision. Am J Med Genet A 155A (5), pp. 943 - 68 (2011)
Go to Editor View