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 (116)

Journal Article
Oh, S.; Flynn, R. A.; Floor, S. N.; Purzner, J.; Martin, L.; Do, B. T.; Schubert, S.; Vaka, D.; Morrissy, S.; Li, Y. et al.; Kool, M.; Hovestadt, V.; Jones, D. T.; Northcott, P. A.; Risch, T.; Warnatz, H. J.; Yaspo, M. L.; Adams, C. M.; Leib, R. D.; Breese, M.; Marra, M. A.; Malkin, D.; Lichter, P.; Doudna, J. A.; Pfister, S. M.; Taylor, M. D.; Chang, H. Y.; Cho, Y. J.: Medulloblastoma-associated DDX3 variant selectively alters the translational response to stress. Oncotarget 7 (19), pp. 28169 - 28182 (2016)
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Aretz, I.; Hardt, C.; Wittig, I.; Meierhofer, D.: An impaired respiratory electron chain triggers down-regulation of the energy metabolism and de-ubiquitination of solute carrier amino acid transporters. Molecular and Cellular Proteomics 15 (5), pp. 1526 - 1538 (2016)
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Broecker, F.; Hardt, C.; Herwig, R.; Timmermann, B.; Kerick, M.; Wunderlich, A.; Schweiger, M. R.; Borsig, L.; Heikenwalder, M.; Lehrach, H. et al.; Moelling, K.: Transcriptional signature induced by a metastasis-promoting c-Src mutant in a human breast cell line. The FEBS Journal 283 (9), pp. 1669 - 1688 (2016)
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Meierhofer, D.; Halbach, M.; Şen, N. E.; Gispert, S.; Auburger, G.: Atxn2-Knock-Out mice show branched chain amino acids and fatty acids pathway alterations. Molecular and Cellular Proteomics 15 (5), pp. 1728 - 1739 (2016)
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Spielmann, M.; Marx, S.; Barbi, G.; Flottmann, R.; Kehrer-Sawatzki, H.; Konig, R.; Horn, D.; Mundlos, S.; Nader, S.; Borck, G.: Femoral facial syndrome associated with a de novo complex chromosome 2q37 rearrangement. American Journal of Medical Genetics Part A 170A (5), pp. 1202 - 1207 (2016)
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Aretz, I.; Meierhofer, D.: Advantages and Pitfalls of Mass Spectrometry Based Metabolome Profiling in Systems Biology. International Journal of Molecular Sciences 17 (5), pii: E632 (2016)
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Tusche, A.; Böckler, A.; Kanske, P.; Trautwein, F.-M.; Singer, T.: Decoding the charitable brain: Empathy, perspective taking and attention shifts differentially predict altruistic giving. The Journal of Neuroscience 36 (17), pp. 4719 - 4732 (2016)
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Vij, S.; Kuhl, H.; Kuznetsova, I. S.; Komissarov, A.; Yurchenko, A. A.; Van Heusden, P.; Singh, S.; et al: Chromosomal-Level Assembly of the Asian Seabass Genome Using Long Sequence Reads and Multi-layered Scaffolding. PLoS Genetics 12 (4), e1005954 (2016)
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Hardt, C.; Beber, M. E.; Rasche, A.; Kamburov, A.; Hebels, D. G.; Kleinjans, J. C.; Herwig, R.: ToxDB: pathway-level interpretation of drug-treatment data. Database (Oxford) 2016, baw052 (2016)
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Cui, H.; Schlesinger, J.; Schoenhals, S.; Tönjes, M.; Dunkel, I.; Meierhofer, D.; Cano, E.; Schulz, K.; Berger, M. F.; Haack, T. et al.; Abdelilah-Seyfried, S.; Bulyk, M. L.; Sauer, S.; Sperling, S. R.: Phosphorylation of the chromatin remodeling factor DPF3a induces cardiac hypertrophy through releasing HEY repressors from DNA. Nucleic Acids Research (London) 46 (6), pp. 2538 - 2553 (2016)
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Conrad, T.; Albrecht, A.-S.; Rodrigues de Melo Costa, V.; Sauer, S.; Meierhofer, D.; Ørom, U. A.: Serial interactome capture of the human cell nucleus. Nature Communications 7, 7:11212 (2016)
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Baez, S.; Kanske, P.; Matallana, D.; Montanes, P.; Reyes, P.; Slachevsky, A.; Matus, C.; Vigliecca, N. S.; Torralva, T.; Manes, F. et al.; Ibanez, A.: Integration of intention and outcome for moral judgment in frontotemporal dementia: Brain structural signatures. Neurodegenerative Diseases 16 (3-4), pp. 206 - 217 (2016)
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Lupiáñez, D. G.; Spielmann, M.; Mundlos, S.: Breaking TADs: How Alterations of Chromatin Domains Result in Disease. Trends in Genetics 32 (4), pp. 225 - 237 (2016)
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Mackenroth, L.; Fischer-Zirnsak, B.; Egerer, J.; Hecht, J.; Kallinich, T.; Stenzel, W.; Spors, B.; von Moers, A.; Mundlos, S.; Kornak, U. et al.; Gerhold, K.; Horn, D.: An overlapping phenotype of Osteogenesis imperfecta and Ehlers-Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing. American Journal of Medical Genetics Part A 170A (4), pp. 1080 - 1085 (2016)
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Mayer, A.; Churchman, L. S.: Genome-wide profiling of RNA polymerase transcription at nucleotide resolution in human cells with native elongating transcript sequencing. Nature Protocols 11 (4), pp. 813 - 433 (2016)
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Zaki, J.; Wager, T. D.; Singer, T.; Keysers, C.; Gazzola, V.: The anatomy of suffering: Understanding the relationship between nociceptive and empathic pain. Trends in Cognitive Sciences 20 (4), pp. 249 - 259 (2016)
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Louro, B.; Kuhl, H.; Tine, M.; de Koning, D.-J.; Batargias, C.; Volckaert, F. A. M.; Reinhardt, R.; Canario, A. V. M.; Power, D. M.: Characterization and refinement of growth related quantitative trait loci in European sea bass (Dicentrarchus labrax) using a comparative approach. Aquaculture 455, pp. 8 - 21 (2016)
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Corradi-Dell’Acqua, C.; Tusche, A.; Vuilleumier, P.; Singer, T.: Cross-modal representations of first-hand and vicarious pain, disgust and fairness in insular and cingulate cortex. Nature Communications 7, 10904 (2016)
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Sprink, T.; Ramrath, D. J. F.; Yamamoto, H.; Yamamoto, K.; Loerke, J.; Ismer, J.; Hildebrand, P. W.; Scheerer, P.; Bürger, J.; Mielke, T. et al.; Spahn, C. M. T.: Structures of ribosome-bound initiation factor 2 reveal mechanism of subunit association. Science Advances 2 (3), e1501502 (2016)
Journal Article
Knierim, E.; Hirata, H.; Wolf, N. I.; Morales-Gonzalez, S.; Schottmann, G.; Tanaka, Y.; Rudnik-Schöneborn, S.; Orgeur, M.; Zerres, K.; Vogt, S. et al.; van Riesen, A.; Gill, E.; Seifert, F.; Zwirner, A.; Kirschner, J.; Goebel, H. H.; Hübner, C.; Stricker, S.; Meierhofer, D.; Stenzel, W.; Schuelke, M.: Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures. The American Journal of Human Genetics 98, pp. 1 - 17 (2016)
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