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Claudia Birkemeyer

Researcher at Leipzig University

Publications -  76
Citations -  3432

Claudia Birkemeyer is an academic researcher from Leipzig University. The author has contributed to research in topics: Mass spectrometry & Glycation. The author has an hindex of 23, co-authored 67 publications receiving 2933 citations. Previous affiliations of Claudia Birkemeyer include RWTH Aachen University & Rothamsted Research.

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GMD@CSB.DB: the Golm Metabolome Database

TL;DR: GD, The Golm Metabolome Database is presented, an open access metabolome database, which provides public access to custom mass spectral libraries, metabolite profiling experiments as well as additional information and tools, e.g. with regard to methods, spectral information or compounds.
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DOF transcription factor AtDof1.1 (OBP2) is part of a regulatory network controlling glucosinolate biosynthesis in Arabidopsis

TL;DR: Evidence is provided that OBP2 is part of a regulatory network that regulates glucosinolate biosynthesis in Arabidopsis and that plant size is diminished due to a reduction in cell size.
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Identification of Volatile Compounds Used in Host Location by the Black Bean Aphid, Aphis Fabae

TL;DR: Olfactometer response was observed to a 15-component synthetic blend that comprised all identified compounds at the same concentration and ratio as in the natural sample, with the aphids spending significantly more time in the treated regions of the olfactometers where volatiles were present than in the control regions.
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Comprehensive chemical derivatization for gas chromatography–mass spectrometry-based multi-targeted profiling of the major phytohormones

TL;DR: Analysis of gibberellic acid A3, trans-zeatin riboside and (+/-)-abscisic acid-beta-D-glucopyranosyl ester was best when coupled by splitting extracts and trimethysilylation, and the MTBSTFA derivatization protocol was optimised, and validated.
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Metabolome analysis: the potential of in vivo labeling with stable isotopes for metabolite profiling

TL;DR: Saturation in vivo labeling with stable isotopes enables the biosynthesis of differentially mass-labeled metabolite mixtures, which can be exploited for highly standardized metabolite profiling by mass isotopomer ratios.