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Person

Stephan Hann

Chemiker

Name	Stephan Hann
Zeit	2001- (Wirkungsdaten)
Ort	Wien (Wirkungsort) Sonstiges Ausland / Unbekanntes Land
Geschlecht	männlich
Akademischer Grad bzw. Titel	Univ. Prof. Dr.
Beruf	Chemiker (charakteristischer Beruf) Hochschullehrer
Sprache	Deutsch Englisch
Variante	S. Hann Stefan Hann
Beziehung	Universität für Bodenkultur Wien (2001-)
Weitere Angaben	2001: PhD in Technical Chemistry from Vienna University of Technology: "Novel applications of HPIC-ICP-SFMS" 2005: Habilitation in the field of "Analytical Chemistry" at the University of Natural Resources and Applied Life Sciences: "Analysis of platinum group elements in environmental and biological matrices by inductively coupled plasma mass spectrometry"
Quelle	https://forschung.boku.ac.at/de/researcher/Stephan-Hann-21EB7DD55F3AE04A (Stand: 05.02.2025)
Datensatztyp	Person
GND-Nummer	1180419154
Datensatz-ID	1180419154
Beteiligt an alle anzeigen Neighbour-induced changes in root exudation patterns of buckwheat results in altered root architecture of redroot pigweed Fine-tuning root exudation sampling procedures– evaluating the effect of sampling solution volume and the suitability of Micropur as microbial activity inhibitor Protein production dynamics and physiological adaptation of recombinant Komagataella phaffii at near-zero growth rates The oxygen-tolerant reductive glycine pathway assimilates methanol, formate and CO2 in the yeast Komagataella phaffii Tailored extraction and ion mobility-mass spectrometry enables isotopologue analysis of tetrahydrofolate vitamers The effect of root hairs on exudate composition: a comparative non-targeted metabolomics approach Critical evaluation of the role of external calibration strategies for IM-MS Non-targeted analysis with high-resolution mass spectrometry for investigation of riverbank filtration processes Yeast-based reference materials for quantitative metabolomics Correction to: LC–MS based metabolic fingerprinting of apricot pistils after self-compatible and self-incompatible pollinations Comparison of preconcentration methods for nontargeted analysis of natural waters using HPLC‐HRMS: Large volume injection versus solid‐phase extraction LC–MS based metabolic fingerprinting of apricot pistils after self-compatible and self-incompatible pollinations Identity confirmation of anthocyanins in berries by LC–DAD–IM‐QTOFMS Fundamental study of ion trapping and multiplexing using drift tube-ion mobility time-of-flight mass spectrometry for non-targeted metabolomics A single Gal4-like transcription factor activates the Crabtree effect in Komagataella phaffii In situ observation of localized, sub-mm scale changes of phosphorus biogeochemistry in the rhizosphere Comparison of fully wettable RPLC stationary phases for LC‐MS‐based cellular metabolomics Determination of size‐dependent metal distribution in dissolved organic matter by SEC‐UV/VIS‐ICP‐MS with special focus on changes in seawater Systems-level organization of yeast methylotrophic lifestyle Accurate LC‐ESI‐MS/MS quantification of 2′‐deoxymugineic acid in soil and root related samples employing porous graphitic carbon as stationary phase and a 13 C 4 ‐labeled internal standard Analysis of iron‐phytosiderophore complexes in soil related samples: LC‐ESI‐MS/MS versus CE‐MS Hydrophilic interaction LC combined with electrospray MS for highly sensitive analysis of underivatized amino acids in rhizosphere research Complexation of metals by phytosiderophores revealed by CE‐ESI‐MS and CE‐ICP‐MS

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Katalog der Deutschen Nationalbibliothek

Stephan Hann

Neighbour-induced changes in root exudation patterns of buckwheat results in altered root architecture of redroot pigweed

Fine-tuning root exudation sampling procedures– evaluating the effect of sampling solution volume and the suitability of Micropur as microbial activity inhibitor

Protein production dynamics and physiological adaptation of recombinant Komagataella phaffii at near-zero growth rates

The oxygen-tolerant reductive glycine pathway assimilates methanol, formate and CO2 in the yeast Komagataella phaffii

Tailored extraction and ion mobility-mass spectrometry enables isotopologue analysis of tetrahydrofolate vitamers

The effect of root hairs on exudate composition: a comparative non-targeted metabolomics approach

Critical evaluation of the role of external calibration strategies for IM-MS

Non-targeted analysis with high-resolution mass spectrometry for investigation of riverbank filtration processes

Yeast-based reference materials for quantitative metabolomics

Correction to: LC–MS based metabolic fingerprinting of apricot pistils after self-compatible and self-incompatible pollinations

Comparison of preconcentration methods for nontargeted analysis of natural waters using HPLC‐HRMS: Large volume injection versus solid‐phase extraction

LC–MS based metabolic fingerprinting of apricot pistils after self-compatible and self-incompatible pollinations

Identity confirmation of anthocyanins in berries by LC–DAD–IM‐QTOFMS

Fundamental study of ion trapping and multiplexing using drift tube-ion mobility time-of-flight mass spectrometry for non-targeted metabolomics

A single Gal4-like transcription factor activates the Crabtree effect in Komagataella phaffii

In situ observation of localized, sub-mm scale changes of phosphorus biogeochemistry in the rhizosphere

Comparison of fully wettable RPLC stationary phases for LC‐MS‐based cellular metabolomics

Determination of size‐dependent metal distribution in dissolved organic matter by SEC‐UV/VIS‐ICP‐MS with special focus on changes in seawater

Systems-level organization of yeast methylotrophic lifestyle

Accurate LC‐ESI‐MS/MS quantification of 2′‐deoxymugineic acid in soil and root related samples employing porous graphitic carbon as stationary phase and a 13 C 4 ‐labeled internal standard

Analysis of iron‐phytosiderophore complexes in soil related samples: LC‐ESI‐MS/MS versus CE‐MS

Hydrophilic interaction LC combined with electrospray MS for highly sensitive analysis of underivatized amino acids in rhizosphere research

Complexation of metals by phytosiderophores revealed by CE‐ESI‐MS and CE‐ICP‐MS