Publikationen von David Meierhofer

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), S. 1965 - 1979 (2013)

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), S. 339 - 342 (2013)

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), S. 792 - 797 (2011)

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), S. 4566 - 4576 (2008)

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), S. 2270 - 2275 (2008)

Mayr, J. A.; Zimmermann, F.; Meierhofer, D.; Schmeller, N.; Sperl, W.; Kofler, B.: Biochemical consequences of a pathogenic A3243G mtDNA mutation. Mitochondrion 6 (5), S. 268 - 269 (2006)

Wiesbauer, M.; Meierhofer, D.; Mayr, J. A.; Sperl, W.; Paulweber, B.; Kofler, B.: Multiplex primer extension analysis for rapid detection of major European mitochondrial haplogroups. Electrophoresis 27 (19), S. 3864 - 2868 (2006)

Meierhofer, D.; Ebner, S.; Mayr, J. A.; Jones, N. D.; Kofler, B.; Sperl, W.: Platelet transfusion can mimic somatic mtDNA mutations. Leukemia: the Journal of Normal and Malignant Hemopoiese ; Official Journal of the Leukemia Research Fund U.K. 20 (2), S. 362 - 363 (2006)

Meierhofer, D.; Mayr, J. A.; Fink, K.; Schmeller, N.; Kofler, B.; Sperl, W.: Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolism. British Journal of Cancer 94 (2), S. 268 - 274 (2006)

Meierhofer, D.; Mayr, J. A.; Ebner, S.; Sperl, W.; Kofler, B.: Rapid screening of the entire mitochondrial DNA for low-level heteroplasmic mutations. Mitochondrion 5 (4), S. 282 - 296 (2005)

Meierhofer, D.; Mayr, J. A.; Foetschl, U.; Berger, A.; Fink, K.; Schmeller, N.; Hacker, G. W.; Hauser-Kronberger, C.; Kofler, B.; Sperl, W.: Decrease of mitochondrial DNA content and energy metabolism in renal cell carcinoma. Carcinogenesis 25 (6), S. 1005 - 1010 (2004)

Berger, A.; Mayr, J. A.; Meierhofer, D.; Fötschl, U.; Bittner, R.; Budka, H.; Grethen, C.; Huemer, M.; Kofler, B.; Sperl, W.: Severe depletion of mitochondrial DNA in spinal muscular atrophy. Acta Neuropathologica 105 (3), S. 245 - 251 (2003)

Meierhofer, D.; Kaiser, P.: Global Analysis of Ubiquitination. In: Neuroproteomics (Hg. Li, K. W.) (2011)

Kaiser, P.; Meierhofer, D.; Wang, X.; Huang, L.: Tandem affinity purification combined with mass spectrometry to identify components of protein complexes. In: Methods in molecular biology, Bd. 439, 2nd edition Aufl., S. 309 - 326 (Hg. Starkey, M.; Elaswarapu, R.). Humana Press (2008)

López-Anguita, N.; Gassaloglu, S. I.; Stötzel, M.; Typou, M.; Virta, I.; Hetzel, S.; Buschow, R.; Koksal, B.; Atilla, D.; Maitschke-Rajasekharan, R. et al.; Chen, R.; Mattei, A. L.; Bedzhov, I.; Meierhofer, D.; Meissner, A.; Veenvliet, J. V.; Bulut-Karslioglu, A.: Hypoxia induces a transcriptional early primitive streak signature in pluripotent cells enhancing spontaneous elongation and lineage representation in gastruloids. (2021)

Lammel, D. R.; Meierhofer, D.; Johnston, P.; Mbedi, S.; Rillig, M. C.: The effects of arbuscular mycorrhizal fungi (AMF) and Rhizophagus irregularis on soil microorganisms assessed by metatranscriptomics and metaproteomics. (2019)