Journal Article (89)

71.
Journal Article
Gielisch, I.; Meierhofer, D.: Metabolome and Proteome Profiling of Complex I Deficiency Induced by Rotenone. Journal of Proteome Research 14 (12), pp. 224 - 235 (2015)
72.
Journal Article
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), pp. 5592 - 5602 (2014)
73.
Journal Article
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), pp. 1882 - 1889 (2014)
74.
Journal Article
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)
75.
Journal Article
Freiwald, A.; Weidner, C.; Witzke, A.; Huang, S.-Y.; Meierhofer, D.; Sauer, S.: Comprehensive proteomic data sets for studying adipocyte-macrophage cell-cell communication. Proteomics 13 (23-24), pp. 3424 - 3428 (2013)
76.
Journal Article
Meierhofer, D.; Weidner, C.; Hartmann, L.; Mayr, J. A.; Han, C.-T.; Schroeder, F. C.; Sauer, S.: Protein sets define disease states and predict in vivo effects of drug treatment. Molecular and Cellular Proteomics 12 (7), pp. 1965 - 1979 (2013)
77.
Journal Article
Weimann, M.; Grossmann, A.; Woodsmith, J.; Özkan, Z.; Birth, P.; Meierhofer, D.; Benlasfer, N.; Valovka, T.; Timmermann, B.; Wanker, E. E. et al.; Sauer, S.; Stelzl, U.: A Y2H-seq approach defines the human protein methyltransferase interactome. Nature methods 10 (4), pp. 339 - 342 (2013)
78.
Journal Article
Mayr, J. A.; Zimmermann, F. A.; Fauth, C.; Bergheim, C.; Meierhofer, D.; Radmayr, D.; Zschocke, J.; Koch, J.; Sperl, W.: Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation. The American Journal of Human Genetics 89 (6), pp. 792 - 797 (2011)
79.
Journal Article
Meierhofer, D.; Wang, X.; Huang, L.; Kaiser, P.: Quantitative analysis of global ubiquitination in HeLa cells by mass spectrometry. Journal of Proteome Research 7 (10), pp. 4566 - 4576 (2008)
80.
Journal Article
Mayr, J. A.; Meierhofer, D.; Zimmermann, F.; Feichtinger, R.; Kögler, C.; Ratschek, M.; Schmeller, N.; Sperl, W.; Kofler, B.: Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma. Clinical Cancer Research 14 (8), pp. 2270 - 2275 (2008)
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