Publikationen von David Meierhofer
Alle Typen
Zeitschriftenartikel (86)
61.
Zeitschriftenartikel
15 (5), S. 1728 - 1739 (2016)
Atxn2-Knock-Out mice show branched chain amino acids and fatty acids pathway alterations. Molecular and Cellular Proteomics 62.
Zeitschriftenartikel
17 (5), pii: E632 (2016)
Advantages and Pitfalls of Mass Spectrometry Based Metabolome Profiling in Systems Biology. International Journal of Molecular Sciences 63.
Zeitschriftenartikel
46 (6), S. 2538 - 2553 (2016)
Phosphorylation of the chromatin remodeling factor DPF3a induces cardiac hypertrophy through releasing HEY repressors from DNA. Nucleic Acids Research (London) 64.
Zeitschriftenartikel
7, 7:11212 (2016)
Serial interactome capture of the human cell nucleus. Nature Communications 65.
Zeitschriftenartikel
98, S. 1 - 17 (2016)
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 66.
Zeitschriftenartikel
135 (10), S. 2368 - 2376 (2015)
GORAB Missense Mutations Disrupt RAB6 and ARF5 Binding and Golgi Targeting. The Journal of Investigative Dermatology: an International Journal for Research in Cutaneous Biology 67.
Zeitschriftenartikel
4 (12), S. 891 - 901 (2015)
Bioenergetic cues shift FXR splicing towards FXRα2 to modulate hepatic lipolysis and fatty acid metabolism. Molecular Metabolism 68.
Zeitschriftenartikel
97 (3), S. 483 - 492 (2015)
Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa. The American Journal of Human Genetics 69.
Zeitschriftenartikel
14 (3), S. 1643 - 1644 (2015)
Correction to "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 70.
Zeitschriftenartikel
14 (12), S. 224 - 235 (2015)
Metabolome and Proteome Profiling of Complex I Deficiency Induced by Rotenone. Journal of Proteome Research 71.
Zeitschriftenartikel
13 (12), S. 5592 - 5602 (2014)
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 72.
Zeitschriftenartikel
14 (16), S. 1882 - 1889 (2014)
Transcriptomics assisted proteomic analysis of Nicotiana occidentalis infected by Candidatus Phytoplasma mali strain AT. Proteomics 73.
Zeitschriftenartikel
103 (Suppl 1), S 1 (2014)
5Regulation of myogenesis via kinase driven activation of DPF3a, a BAF complex member and its interaction with transcription repressor HEY1. Cardiovascular Research 74.
Zeitschriftenartikel
13 (23-24), S. 3424 - 3428 (2013)
Comprehensive proteomic data sets for studying adipocyte-macrophage cell-cell communication. Proteomics 75.
Zeitschriftenartikel
12 (7), S. 1965 - 1979 (2013)
Protein sets define disease states and predict in vivo effects of drug treatment. Molecular and Cellular Proteomics 76.
Zeitschriftenartikel
10 (4), S. 339 - 342 (2013)
A Y2H-seq approach defines the human protein methyltransferase interactome. Nature methods 77.
Zeitschriftenartikel
89 (6), S. 792 - 797 (2011)
Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation. The American Journal of Human Genetics 78.
Zeitschriftenartikel
7 (10), S. 4566 - 4576 (2008)
Quantitative analysis of global ubiquitination in HeLa cells by mass spectrometry. Journal of Proteome Research 79.
Zeitschriftenartikel
14 (8), S. 2270 - 2275 (2008)
Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma. Clinical Cancer Research 80.
Zeitschriftenartikel
6 (5), S. 268 - 269 (2006)
Biochemical consequences of a pathogenic A3243G mtDNA mutation. Mitochondrion