about
Cysteine cathepsins: their role in tumor progression and recent trends in the development of imaging probesRational Structure-Based Rescaffolding Approach to De Novo Design of Interleukin 10 (IL-10) Receptor-1 MimeticsCyclopeptides containing the DEKS motif as conformationally restricted collagen telopeptide analogues: synthesis and conformational analysis.Antimalarial activity of azadipeptide nitrilesTargeting lysyl oxidase for molecular imaging in breast cancer.Tissue transglutaminase: an emerging target for therapy and imaging.Microplate assay for quantitative determination of cathepsin activities in viable cells using derivatives of 4-methoxy-beta-naphthylamide.Dipeptide-derived nitriles containing additional electrophilic sites: potentially irreversible inhibitors of cysteine proteases.Active Site Mapping of Human Cathepsin F with Dipeptide Nitrile Inhibitors.Tos-Nos-Mos: Synthesis of different aryl sulfonate precursors for the radiosynthesis of the alpha7 nicotinic acetylcholine receptor radioligand [(18)F]NS14490.A fluorescence anisotropy-based assay for determining the activity of tissue transglutaminase.Synthesis and Kinetic Characterisation of Water-Soluble Fluorogenic Acyl Donors for Transglutaminase 2.Evaluation of Fluorine-18-Labeled α1(I)-N-Telopeptide Analogs as Substrate-Based Radiotracers for PET Imaging of Melanoma-Associated Lysyl Oxidase.2-(diethylamino)thieno1,3ŏxazin-4-ones as stable inhibitors of human leukocyte elastaseCathepsin S inhibitors: WO2010070615Site-selective radiolabeling of peptides by (18)F-fluorobenzoylation with [(18F)]SFB in solution and on solid phase: a comparative studyCorrigendum: Synthesis and Kinetic Characterisation of Water-Soluble Fluorogenic Acyl Donors for Transglutaminase 2Nε-Acryloyllysine Piperazides as Irreversible Inhibitors of Transglutaminase 2: Synthesis, Structure-Activity Relationships, and Pharmacokinetic ProfilingSynthesis, 18F-labelling and radiopharmacological characterisation of the C-terminal 30mer of Clostridium perfringens enterotoxin as a potential claudin-targeting peptideSynthesis and preliminary radiopharmacological characterisation of an 11 C-labelled azadipeptide nitrile as potential PET tracer for imaging of cysteine cathepsinsCathepsin B: Active site mapping with peptidic substrates and inhibitors
P50
Q26827307-35997F4F-9C06-4E3C-A567-0EAB02DE1795Q28551658-04B60537-E059-4438-9BF9-0F0BF4E19F08Q30878012-0CE37C72-FFCB-46CE-A8CB-D83F78ACCACAQ33637348-590EDE62-93EB-4CD8-8682-27B8EEA8C088Q35945328-800DE078-80A1-411A-9DE2-607A92A36ABAQ38179010-5C7AF8A5-99CC-47F1-AF4C-C17440F8AFB0Q40214959-1D37A346-51DF-408D-A4B1-417ADC638068Q43242729-FB7DB854-608C-4DD0-950E-2E687E5499FFQ52934515-DE0C45B5-ED0F-4A3C-BF2E-2A0ACE77425AQ52982937-98647452-0804-4543-BF0E-F1DFBD9BEB07Q53174521-668494EC-035B-4192-BBD6-EAAD5AE34A89Q53764493-20AFF62A-6A56-468E-937B-9D1B214F30C1Q55276271-364DFA38-4E29-48FF-BC85-EE482AA67498Q73364987-2905D79B-04C1-40C2-B8DB-0FB23DB79A09Q83236621-72E4A62E-8F8D-4C8B-80B8-5192061A56D1Q83389072-FE87D20E-A639-4035-BC72-9AC49B02C73FQ88260992-4CE76CDA-D0E4-4B44-A2B0-4FBA89599CC7Q88385614-3B48FE01-B8FB-469B-941A-46C1EE3C1172Q91837209-BCDACFD2-E27C-4F84-941B-91AA8937B631Q92623695-90219202-C1AA-4184-9E3F-0BBF25693796Q93351534-2AF0041C-F3F6-4EA2-87D4-9E08CD308356
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Reik Löser
@ast
Reik Löser
@en
Reik Löser
@es
Reik Löser
@nl
Reik Löser
@sl
type
label
Reik Löser
@ast
Reik Löser
@en
Reik Löser
@es
Reik Löser
@nl
Reik Löser
@sl
prefLabel
Reik Löser
@ast
Reik Löser
@en
Reik Löser
@es
Reik Löser
@nl
Reik Löser
@sl
P214
P106
P214
P31
P496
0000-0003-1531-7601
P7859
viaf-55302483