Zeitschriftenartikel (1124)

761.
Zeitschriftenartikel
Meierhofer, D.; Weidner, C.; Sauer, S.: Integrative analysis of transcriptomics, proteomics and metabolomics data of white adipose and liver tissue of high-fat diet and rosiglitazone-treated insulin-resistant mice identified pathway alterations and molecular hubs. Journal of Proteome Research 13 (12), S. 5592 - 5602 (2014)
762.
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Herwig, R.: Computational modelling of drug response with applications to neuroscience. Dialogues in Clinical Neuroscience 16 (4), S. 465 - 477 (2014)
763.
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Willems, T.; Gymrek, M.; Highnam, G.; The 1000 Genomes Project, C.; Herwig, R.; Lehrach, H.; Sudbrak, R.; Timmermann, B.; Mittelman, D.; Erlich, Y.: The landscape of human STR variation. Genome Research 24 (11), S. 1894 - 1904 (2014)
764.
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Röthlein, C.; Miettinen, M. S.; Borwankar, .; Bürger, J.; Mielke, T.; Kumke, M. U.; Ignatova, Z.: Architecture of polyglutamine-containing fibrils from time-resolved fluorescence decay. The Journal of Biological Chemistry 289 (39), S. 26817 - 26828 (2014)
765.
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Luge, T.; Kube, M.; Freiwald, A.; Meierhofer, D.; Seemüller, E.; Sauer, S.: Transcriptomics assisted proteomic analysis of Nicotiana occidentalis infected by Candidatus Phytoplasma mali strain AT. Proteomics 14 (16), S. 1882 - 1889 (2014)
766.
Zeitschriftenartikel
Huang, X.; Zi, Z.: Inferring cellular regulatory networks with Bayesian model averaging for linear regression (BMALR). Molecular BioSystems 10 (8), S. 2023 - 2030 (2014)
767.
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Seumois, G.; Chavez, L.; Gerasimova, A.; Lienhard, M.; Omran, N.; Kalinke, L.; Vedanayagam, M.; Ganesan, A. P. V.; Chawla, A.; Djukanović, R. et al.; Ansel, K. M.; Peters, B.; Rao, A.; Vijayanand, P.: Epigenomic analysis of primary human T cells reveals enhancers associated with TH2 memory cell differentiation and asthma susceptibility. Nature Immunology 15 (8), S. 777 - 788 (2014)
768.
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Yamamoto, H.; Unbehaun, A.; Loerke, J.; Behrmann, E.; Collier, M.; Bürger, J.; Mielke, T.; Spahn, C. M. T.: Structure of the mammalian 80S initiation complex with initiation factor 5B on HCV-IRES RNA. Nature Structural and Molecular Biology 21 (8), S. 721 - 727 (2014)
769.
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Donczew, R.; Mielke, T.; Jaworski, P.; Zakrzewska-Czerwińska, J.; Zawilak-Pawlik, A.: Assembly of Helicobacter pylori initiation complex is determined by sequence-specific and topology-sensitive DnaA-oriC interactions. Journal of Molecular Biology (London) 426 (15), S. 2769 - 2782 (2014)
770.
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Barucker, C.; Harmeier, A.; Weiske, J.; Fauler, B.; Albring, K. F.; Prokop, S.; Hildebrand, P.; Lurz, R.; Heppner, F. L.; Huber, O. et al.; Multhaup, G.: Nuclear translocation uncovers the amyloid peptide Aβ42 as a regulator of gene transcription. The Journal of Biological Chemistry 289 (29), S. 20182 - 20191 (2014)
771.
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Budkevich, T. V.; Giesebrecht, J.; Behrmann, E.; Loerke, J.; Ramrath, D. J.; Mielke, T.; Ismer, J.; Hildebrand, P. W.; Tung, C. S.; Nierhaus, K. H. et al.; Sanbonmatsu, K. Y.; Spahn, C. M.: Regulation of the mammalian elongation cycle by subunit rolling: a eukaryotic-specific ribosome rearrangement. Cell 158 (1), S. 121 - 131 (2014)
772.
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Cui, H.; Schlesinger, J.; Bansal, V.; Dunkel, I.; Meierhofer, D.; Rickert-Sperling, S.: 5Regulation of myogenesis via kinase driven activation of DPF3a, a BAF complex member and its interaction with transcription repressor HEY1. Cardiovascular Research 103 (Suppl 1), S 1 (2014)
773.
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Grunert, M.; Dorn, C.; Schueler, M.; Dunkel, I.; Schlesinger, J.; Mebus, S.; Alexi-Meskishvili, V.; Perrot, A.; Wassilew, K.; Timmermann, B. et al.; Hetzer, R.; Berger, F.; Sperling, S. R.: Rare and Private Variations in Neural Crest, Apoptosis and Sarcomere Genes Define the Polygenic Background of Isolated Tetralogy of Fallot. Human Molecular Genetics 23 (12), S. 3115 - 3128 (2014)
774.
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Bertram, L.; Böckenhoff, A.; Demuth, I.; Düzel, S.; Eckardt, R.; Li, S.-C.; Lindenberger, U.; Pawelec, G.; Siedler, T.; Wagner, G. G. et al.; Steinhagen-Thiessen, E.: Cohort Profile: The Berlin Aging Study II (BASE-II). International Journal of Epidemiology 43 (3), S. 703 - 712 (2014)
775.
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Hooli, B. V.; Kovacs-Vajna, Z. M.; Mullin, K.; Blumenthal, M. A.; Mattheisen, M.; Zhang, C.; Lange, C.; Mohapatra, G.; Bertram, L.; Tanzi, R. E.: Rare autosomal copy number variations in early-onset familial Alzheimer's disease. Molecular Psychiatry 19 (6), S. 676 - 681 (2014)
776.
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Papenberg, G.; Bäckman, L.; Nagel, I. E.; Nietfeld, W.; Schröder, J.; Bertram, L.; Heekeren, H. R.; Lindenberger, U.; Li, S.-C.: COMT Polymorphism and Memory Dedifferentiation in Old Age. Psychology and Aging 29 (2), S. 374 - 383 (2014)
777.
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Saisawat, P.; Kohl, S.; Hilger, A. C.; Hwang, D.-Y.; Gee, H. Y.; Dworschak, G. C.; Tasic, V.; Pennimpede, T.; Natarajan, S.; Sperry, E. et al.; Matassa, D. S.; Stajic, N.; Bogdanovic, R.; de Blaauw, I.; Marcelis, C. L. M.; Wijers, C. H. W.; Bartels, E.; Schmiedeke, E.; Schmidt, D.; Märzheuser, S.; Grasshoff-Derr, S.; Holland-Cunz, S.; Ludwig, M.; Nöthen, M. M.; Draaken, M.; Brosens, E.; Heij, H.; Tibboel, D.; Hermann, B. G.; Solomon, B. D.; de Klein, A.; van Rooij, I. A. L. M.; Esposito, F.; Reutter, H. M.; Hildebrandt, F.: Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association. Kidney International 85 (6), S. 1310 - 1317 (2014)
778.
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Shen, L.; Thompson, P.M.; Potkin, S.G.; Bertram, L.; Farrer, L.A.; Foroud, T.M.; Green, R.C.; Hu, X.; Huentelman, M.J.; Kim, S. et al.; Kauwe, J.S.K.; Li, Q.; Liu, E.; Macciardi, F.; Moore, J.H.; Munsie, L.: Genetic Analysis of Quantitative Phenotypes in AD and MCI: Imaging, Cognition and Biomarkers. Brain Imaging and Behavior 8 (2), S. 183 - 207 (2014)
779.
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Doktorova, T. Y.; Yildirimman, R.; Ceelen, L.; Vilardell, M.; Vanhaecke, T.; Vinken, M.; Ates, G.; Heymans, A.; Gmuender, H.; Bort, R. et al.; Corvi, R.; Phrakonkham, P.; Li, R.; Mouchet, N.; Chesne, C.; van Delft, J.; Kleinjans, J.; Castell, J.; Herwig, R.; Rogiers, V.: Testing chemical carcinogenicity by using a transcriptomics HepaRG-based model. Experimental and Clinical Sciences Journal (EXCLI Journal) 13, S. 623 - 637 (2014)
780.
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Møller, R. S.; Jensen, L. R.; Maas, S. M.; Filmus, J.; Capurro, M.; Hansen, C.; Marcelis, C. L.; Ravn, K.; Andrieux, J.; Mathieu, M. et al.; Kirchhoff, M.; Rodningen, O. K.; de Leeuw, N.; Yntema, H. G.; Froyen, G.; Vandewalle, J.; Ballon, K.; Klopocki, E.; Joss, S.; Tolmie, J.; Knegt, A. C.; Lund, A. M.; Hjalgrim, H.; Kuss, A. W.; Tommerup, N.; Ullmann, R.; de Brouwer, A. P.; Stromme, P.; Kjaergaard, S.; Tumer, Z.; Kleefstra, T.: X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome. Human Genetics 133 (5), S. 625 - 638 (2014)
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