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Valentin Wittmann

Chemiker

Name	Valentin Wittmann
Ort	Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Prof. Dr.
Beruf	Chemiker (charakteristischer Beruf)
Beziehung	Universität Konstanz. Fakultät für Chemie
Quelle	Homepage: http://www.uni-konstanz.de/FuF/chemie/wittmann/ (Stand: 08.04.2019)
Datensatztyp	Person
GND-Nummer	1182948766
Datensatz-ID	1182948766
Beteiligt an alle anzeigen Next‐Generation Metabolic Glycosylation Reporters Enable Detection of Protein O−GlcNAcylation in Living Cells without S ‐Glyco Modification Next‐Generation Metabolic Glycosylation Reporters Enable Detection of Protein O−GlcNAcylation in Living Cells without S ‐Glyco Modification Next‐Generation Metabolic Glycosylation Reporters Enable Detection of Protein O−GlcNAcylation in Living Cells without <i>S</i>‐Glyco Modification Carba-Sugar Analogs of Glucosamine-6-Phosphate : New Activators for the glmS Riboswitch Metabolic glycoengineering : exploring glycosylation with bioorthogonal chemistry Phosphonate and Thiasugar Analogues of Glucosamine-6-phosphate : Activation of the glmS Riboswitch and Antibiotic Activity Use of metabolic glycoengineering and pharmacological inhibitors to assess lipid and protein sialylation on cells Carba‐Sugar Analogs of Glucosamine‐6‐Phosphate: New Activators for the glmS Riboswitch Photoswitching Affinity and Mechanism of Multivalent Lectin Ligands Photoswitching Affinity and Mechanism of Multivalent Lectin Ligands An Advanced 'clickECM' that Can be Modified by the Inverse-Electron Demand Diels-Alder Reaction Molekulare Erkennung von Cellulose und Cellulose-Fragmenten durch Cellulose-Bindemodule & Interaktionsstudien zwischen den zytoplasmatischen Domänen von Integrin-β1/β3 und dem fokalen Adhäsionsprotein Paxillin Photoswitching Affinity and Mechanism of Multivalent Lectin Ligands An Advanced ‘clickECM’ That Can be Modified by the Inverse‐Electron‐Demand Diels‐Alder Reaction An Advanced ‘clickECM’ That Can be Modified by the Inverse‐Electron‐Demand Diels‐Alder Reaction An advanced ‘clickECM’ that can be modified by the inverse-electron demand Diels-Alder reaction Application of the Inverse-Electron-Demand Diels-Alder Reaction for Metabolic Glycoengineering In situ EPR spectroscopy of a bacterial membrane transporter using an expanded genetic code Ligand-Programmed Consecutive Symmetry Break(s) in Nanoparticle Based Materials Showing Emergent Phenomena: Transitioning from Sixfold to Threefold Symmetry in Anisotropic ZnO Colloids Ligand‐Programmed Consecutive Symmetry Break(s) in Nanoparticle Based Materials Showing Emergent Phenomena : Transitioning from Sixfold to Threefold Symmetry in Anisotropic ZnO Colloids Metabolic Glycoengineering with Azide- and Alkene-Modified Hexosamines : Quantification of Sialic Acid Levels Nucleophilic aromatic substitution reactions under aqueous, mild conditions using polymeric additive HPMC Rapid glycoconjugation with glycosyl amines Optimising broadband pulses for DEER depends on concentration and distance range of interest Optimising broadband pulses for DEER depends on concentration and distance range of interest Metabolic Glycoengineering with Azide‐ and Alkene‐Modified Hexosamines: Quantification of Sialic Acid Levels Machine learning prediction of cyanobacterial toxin (microcystin) toxicodynamics in humans Optimising broadband pulses for DEER depends on concentration and distance range of interest Precipitation-free high-affinity multivalent binding by inline lectin ligands Time and space-resolved quantification of plasma membrane sialylation for measurements of cell function and neurotoxicity Time and space-resolved quantification of plasma membrane sialylation for measurements of cell function and neurotoxicity Generation of an azide-modified extracellular matrix by adipose-derived stem cells using metabolic glycoengineering A Tripeptide Approach to the Solid‐Phase Synthesis of Peptide Thioacids and N‐Glycopeptides Triple Orthogonal Labeling of Glycans by Applying Photoclick Chemistry 3D Structure of the biomarker hepcidin-25 in its native state A Tripeptide Approach to the Solid-Phase Synthesis of Peptide Thioacids and N-Glycopeptides Cyclopropene derivatives of aminosugars for metabolic glycoengineering Generation of an azide-modified extracellular matrix by adipose-derived stem cells using metabolic glycoengineering Protein Spin Labeling with a Photocaged Nitroxide Using Diels-Alder Chemistry Simultaneous Detection of 14 Microcystin Congeners from Tissue Samples Using UPLC- ESI-MS/MS and Two Different Deuterated Synthetic Microcystins as Internal Standards Triple Orthogonal Labeling of Glycans by Applying Photoclick Chemistry Identification of d-amino acid oxidase and propiverine interaction partners and their potential role in the propiverine-mediated nephropathy Sweet surfactants : packing parameter-invariant amphiphiles as emulsifiers and capping agents for morphology control of inorganic particles Fluoro‐Carba‐Sugars are Glycomimetic Activators of the glmS Ribozyme Inside Back Cover: Dienophile‐Modified Mannosamine Derivatives for Metabolic Labeling of Sialic Acids: A Comparative Study (ChemBioChem 13/2017) Dienophile‐Modified Mannosamine Derivatives for Metabolic Labeling of Sialic Acids: A Comparative Study Activation of the glmS Ribozyme Confers Bacterial Growth Inhibition Exploring the Potential of Norbornene-Modified Mannosamine Derivatives for Metabolic Glycoengineering Total Synthesis of Microcystin-LF and Derivatives Thereof Real‐Time NMR Studies of Oxyamine Ligations of Reducing Carbohydrates under Equilibrium Conditions Regioselective Cleavage of Thioether Linkages in Microcystin Conjugates Exploring the Potential of Norbornene‐Modified Mannosamine Derivatives for Metabolic Glycoengineering Inside Cover: Exploring the Potential of Norbornene‐Modified Mannosamine Derivatives for Metabolic Glycoengineering (ChemBioChem 14/2016) Synthesis of Highly Selective Submicromolar Microcystin‐Based Inhibitors of Protein Phosphatase (PP) 2A over PP1 Visualisierung proteinspezifischer Glycosylierung in lebenden Zellen Synthesis of Highly Selective Submicromolar Microcystin‐Based Inhibitors of Protein Phosphatase (PP) 2A over PP1 Visualization of Protein‐Specific Glycosylation inside Living Cells Distinct CCR7 glycosylation pattern shapes receptor signaling and endocytosis to modulate chemotactic responses Real-Time NMR Studies of Oxyamine Ligations of Reducing Carbohydrates under Equilibrium Conditions Synthesis of highly selective submicromolar microcystin-based inhibitors of protein phosphatase (PP)2A over PP1

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Katalog der Deutschen Nationalbibliothek

Valentin Wittmann

Next‐Generation Metabolic Glycosylation Reporters Enable Detection of Protein O−GlcNAcylation in Living Cells without S ‐Glyco Modification

Next‐Generation Metabolic Glycosylation Reporters Enable Detection of Protein O−GlcNAcylation in Living Cells without S ‐Glyco Modification

Next‐Generation Metabolic Glycosylation Reporters Enable Detection of Protein O−GlcNAcylation in Living Cells without <i>S</i>‐Glyco Modification

Carba-Sugar Analogs of Glucosamine-6-Phosphate : New Activators for the glmS Riboswitch

Metabolic glycoengineering : exploring glycosylation with bioorthogonal chemistry

Phosphonate and Thiasugar Analogues of Glucosamine-6-phosphate : Activation of the glmS Riboswitch and Antibiotic Activity

Use of metabolic glycoengineering and pharmacological inhibitors to assess lipid and protein sialylation on cells

Carba‐Sugar Analogs of Glucosamine‐6‐Phosphate: New Activators for the glmS Riboswitch

Photoswitching Affinity and Mechanism of Multivalent Lectin Ligands

Photoswitching Affinity and Mechanism of Multivalent Lectin Ligands

An Advanced 'clickECM' that Can be Modified by the Inverse-Electron Demand Diels-Alder Reaction

Molekulare Erkennung von Cellulose und Cellulose-Fragmenten durch Cellulose-Bindemodule & Interaktionsstudien zwischen den zytoplasmatischen Domänen von Integrin-β1/β3 und dem fokalen Adhäsionsprotein Paxillin

Photoswitching Affinity and Mechanism of Multivalent Lectin Ligands

An Advanced ‘clickECM’ That Can be Modified by the Inverse‐Electron‐Demand Diels‐Alder Reaction

An Advanced ‘clickECM’ That Can be Modified by the Inverse‐Electron‐Demand Diels‐Alder Reaction

An advanced ‘clickECM’ that can be modified by the inverse-electron demand Diels-Alder reaction

Application of the Inverse-Electron-Demand Diels-Alder Reaction for Metabolic Glycoengineering

In situ EPR spectroscopy of a bacterial membrane transporter using an expanded genetic code

Ligand-Programmed Consecutive Symmetry Break(s) in Nanoparticle Based Materials Showing Emergent Phenomena: Transitioning from Sixfold to Threefold Symmetry in Anisotropic ZnO Colloids

Ligand‐Programmed Consecutive Symmetry Break(s) in Nanoparticle Based Materials Showing Emergent Phenomena : Transitioning from Sixfold to Threefold Symmetry in Anisotropic ZnO Colloids

Metabolic Glycoengineering with Azide- and Alkene-Modified Hexosamines : Quantification of Sialic Acid Levels

Nucleophilic aromatic substitution reactions under aqueous, mild conditions using polymeric additive HPMC

Rapid glycoconjugation with glycosyl amines

Optimising broadband pulses for DEER depends on concentration and distance range of interest

Optimising broadband pulses for DEER depends on concentration and distance range of interest

Metabolic Glycoengineering with Azide‐ and Alkene‐Modified Hexosamines: Quantification of Sialic Acid Levels

Machine learning prediction of cyanobacterial toxin (microcystin) toxicodynamics in humans

Optimising broadband pulses for DEER depends on concentration and distance range of interest

Precipitation-free high-affinity multivalent binding by inline lectin ligands

Time and space-resolved quantification of plasma membrane sialylation for measurements of cell function and neurotoxicity

Time and space-resolved quantification of plasma membrane sialylation for measurements of cell function and neurotoxicity

Generation of an azide-modified extracellular matrix by adipose-derived stem cells using metabolic glycoengineering

A Tripeptide Approach to the Solid‐Phase Synthesis of Peptide Thioacids and N‐Glycopeptides

Triple Orthogonal Labeling of Glycans by Applying Photoclick Chemistry

3D Structure of the biomarker hepcidin-25 in its native state

A Tripeptide Approach to the Solid-Phase Synthesis of Peptide Thioacids and N-Glycopeptides

Cyclopropene derivatives of aminosugars for metabolic glycoengineering

Generation of an azide-modified extracellular matrix by adipose-derived stem cells using metabolic glycoengineering

Protein Spin Labeling with a Photocaged Nitroxide Using Diels-Alder Chemistry

Simultaneous Detection of 14 Microcystin Congeners from Tissue Samples Using UPLC- ESI-MS/MS and Two Different Deuterated Synthetic Microcystins as Internal Standards

Triple Orthogonal Labeling of Glycans by Applying Photoclick Chemistry

Identification of d-amino acid oxidase and propiverine interaction partners and their potential role in the propiverine-mediated nephropathy

Sweet surfactants : packing parameter-invariant amphiphiles as emulsifiers and capping agents for morphology control of inorganic particles

Fluoro‐Carba‐Sugars are Glycomimetic Activators of the glmS Ribozyme

Inside Back Cover: Dienophile‐Modified Mannosamine Derivatives for Metabolic Labeling of Sialic Acids: A Comparative Study (ChemBioChem 13/2017)

Dienophile‐Modified Mannosamine Derivatives for Metabolic Labeling of Sialic Acids: A Comparative Study

Activation of the glmS Ribozyme Confers Bacterial Growth Inhibition

Exploring the Potential of Norbornene-Modified Mannosamine Derivatives for Metabolic Glycoengineering

Total Synthesis of Microcystin-LF and Derivatives Thereof

Real‐Time NMR Studies of Oxyamine Ligations of Reducing Carbohydrates under Equilibrium Conditions

Regioselective Cleavage of Thioether Linkages in Microcystin Conjugates

Exploring the Potential of Norbornene‐Modified Mannosamine Derivatives for Metabolic Glycoengineering

Inside Cover: Exploring the Potential of Norbornene‐Modified Mannosamine Derivatives for Metabolic Glycoengineering (ChemBioChem 14/2016)

Synthesis of Highly Selective Submicromolar Microcystin‐Based Inhibitors of Protein Phosphatase (PP) 2A over PP1

Visualisierung proteinspezifischer Glycosylierung in lebenden Zellen

Synthesis of Highly Selective Submicromolar Microcystin‐Based Inhibitors of Protein Phosphatase (PP) 2A over PP1

Visualization of Protein‐Specific Glycosylation inside Living Cells

Distinct CCR7 glycosylation pattern shapes receptor signaling and endocytosis to modulate chemotactic responses

Real-Time NMR Studies of Oxyamine Ligations of Reducing Carbohydrates under Equilibrium Conditions

Synthesis of highly selective submicromolar microcystin-based inhibitors of protein phosphatase (PP)2A over PP1