Journal Article (116)

61.
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)
62.
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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)
63.
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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)
64.
Journal Article
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)
65.
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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)
66.
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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)
67.
Journal Article
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)
68.
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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)
69.
Journal Article
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)
70.
Journal Article
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)
71.
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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)
72.
Journal Article
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)
73.
Journal Article
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)
74.
Journal Article
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)
75.
Journal Article
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)
76.
Journal Article
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)
77.
Journal Article
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)
78.
Journal Article
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)
79.
Journal Article
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)
80.
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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