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Daniel Lars Ramsbeck (1981-)

Apotheker

Name	Daniel Lars Ramsbeck
Time	1981- (Date of birth and death)
Place	Aue-Bad Schlema- Bad Schlema (Geburtsort) Deutschland
Academic degree	Dr. rer. nat. habil. Dr. rer. nat. Dipl. Pharm.
Profession	Apotheker (characteristic profession)
Variant	Daniel Ramsbeck D. Ramsbeck
Record type	Person
GND-Identifier	1018722882
Record ID	1018722882
Involved in show all Dipeptidyl-Peptidase Activity of Meprin β Links N-truncation of Aβ with Glutaminyl Cyclase-Catalyzed pGlu-Aβ Formation Prefusion-specific antibody- derived peptides trivalently presented on DNA- nanoscaffolds as an innovative strategy against RSV entr Synthesis and structure–activity relationships of USP48 deubiquitinylase inhibitors Neuartige Inhibitoren humaner Astacinproteasen als Leitstrukturen für die Wirkstoffentwicklung und Targetvalidierung Helical ultrastructure of the metalloprotease meprin α in complex with a small molecule inhibitor A Diazirine‐Modified Membrane Lipid to Study Peptide/Lipid Interactions – Chances and Challenges Targeting isoaspartate-modified Aβ rescues behavioral deficits in transgenic mice with Alzheimer’s disease-like pathology Heteroaromatic Inhibitors of the Astacin Proteinases Meprin α, Meprin β and Ovastacin Discovered by a Scaffold‐Hopping Approach A Primary Evaluation of Potential Small‐Molecule Inhibitors of the Astacin Metalloproteinase Ovastacin, a Novel Drug Target in Female Infertility Treatment † Tertiary‐Amine‐Based Inhibitors of the Astacin Protease Meprin α Synthese und Struktur-Wirkungsbeziehungsuntersuchungen neuartiger Inhibitoren der humanen Glutaminyl Cyclase Selective Nucleophilic Substitution Reactions in 2,4,6‐Trisulfanyl‐Substituted Pyrimidine‐5‐carbonitriles by Secondary Amines.

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Daniel Lars Ramsbeck (1981-)

Dipeptidyl-Peptidase Activity of Meprin β Links N-truncation of Aβ with Glutaminyl Cyclase-Catalyzed pGlu-Aβ Formation

Prefusion-specific antibody- derived peptides trivalently presented on DNA- nanoscaffolds as an innovative strategy against RSV entr

Synthesis and structure–activity relationships of USP48 deubiquitinylase inhibitors

Neuartige Inhibitoren humaner Astacinproteasen als Leitstrukturen für die Wirkstoffentwicklung und Targetvalidierung

Helical ultrastructure of the metalloprotease meprin α in complex with a small molecule inhibitor

A Diazirine‐Modified Membrane Lipid to Study Peptide/Lipid Interactions – Chances and Challenges

Targeting isoaspartate-modified Aβ rescues behavioral deficits in transgenic mice with Alzheimer’s disease-like pathology

Heteroaromatic Inhibitors of the Astacin Proteinases Meprin α, Meprin β and Ovastacin Discovered by a Scaffold‐Hopping Approach

A Primary Evaluation of Potential Small‐Molecule Inhibitors of the Astacin Metalloproteinase Ovastacin, a Novel Drug Target in Female Infertility Treatment †

Tertiary‐Amine‐Based Inhibitors of the Astacin Protease Meprin α

Synthese und Struktur-Wirkungsbeziehungsuntersuchungen neuartiger Inhibitoren der humanen Glutaminyl Cyclase

Selective Nucleophilic Substitution Reactions in 2,4,6‐Trisulfanyl‐Substituted Pyrimidine‐5‐carbonitriles by Secondary Amines.