about
Modification of different IgG1 antibodies via glutamine and lysine using bacterial and human tissue transglutaminase.Convergent Synthesis of 2H-Chromenes - a Formal [3+3] Cycloaddition by a One-pot, Three-Step Cascade.1,2,3-Triazole Stabilized Neurotensin-Based Radiopeptidomimetics for Improved Tumor Targeting.TESOTf-induced rearrangement of quinols. Efficient construction of the fully functionalized carbon skeleton of the griseusins by a divergent-reconvergent approachComparison of the octadentate bifunctional chelator DFO*-pPhe-NCS and the clinically used hexadentate bifunctional chelator DFO-pPhe-NCS for 89Zr-immuno-PETMetal chelating systems synthesized using the copper(I) catalyzed azide-alkyne cycloaddition.Click-to-Chelate: development of technetium and rhenium-tricarbonyl labeled radiopharmaceuticals.1,2,3-Triazoles as amide-bond surrogates in peptidomimetics.Methoxinine - an alternative stable amino acid substitute for oxidation-sensitive methionine in radiolabelled peptide conjugates.Toward the Optimization of Bombesin-Based Radiotracers for Tumor Targeting.Probing the Backbone Function of Tumor Targeting Peptides by an Amide-to-Triazole Substitution Strategy.An octadentate bifunctional chelating agent for the development of stable zirconium-89 based molecular imaging probes.Expression of different neurokinin-1 receptor (NK1R) isoforms in glioblastoma multiforme: potential implications for targeted therapy.Radiolabeled antagonistic bombesin peptidomimetics for tumor targeting.Fluorescent gallium and indium bis(thiosemicarbazonates) and their radiolabelled analogues: synthesis, structures and cellular confocal fluorescence imaging investigations.Molecular assembly of multifunctional ⁹⁹(m)Tc radiopharmaceuticals using "clickable" amino acid derivatives.A click approach to structurally diverse conjugates containing a central di-1,2,3-triazole metal chelate.Evaluation of a novel radiofolate in tumour-bearing mice: promising prospects for folate-based radionuclide therapy.A "click chemistry" approach to the efficient synthesis of multiple imaging probes derived from a single precursor."Click-to-chelate": in vitro and in vivo comparison of a 99mTc(CO)3-labeled N(tau)-histidine folate derivative with its isostructural, clicked 1,2,3-triazole analogue.A bombesin-shepherdin radioconjugate designed for combined extra- and intracellular targeting.1,2,3-Triazoles as amide bond mimics: triazole scan yields protease-resistant peptidomimetics for tumor targeting.Fluorine-18 click radiosynthesis and preclinical evaluation of a new 18F-labeled folic acid derivative."Click-to-chelate": design and incorporation of triazole-containing metal-chelating systems into biomolecules of diagnostic and therapeutic interest.Cu(I)-catalyzed intramolecular cyclization of alkynoic acids in aqueous media: a "click side reaction".A solid phase-assisted approach for the facile synthesis of a highly water-soluble zirconium-89 chelator for radiopharmaceutical development.Glycated 99m Tc-Tricarbonyl-Labeled Peptide Conjugates for Tumor Targeting by "Click-to-Chelate".Structure-Activity Relationship Studies of Amino Acid Substitutions in Radiolabeled Neurotensin Conjugates.Novel chemoselective (18)F-radiolabeling of thiol-containing biomolecules under mild aqueous conditions.Dual-targeting conjugates designed to improve the efficacy of radiolabeled peptides.EANM guideline for the preparation of an Investigational Medicinal Product Dossier (IMPD)Guidance on current good radiopharmacy practice for the small-scale preparation of radiopharmaceuticals using automated modules: a European perspectivePosition paper on requirements for toxicological studies in the specific case of radiopharmaceuticalsDevelopment of 68Ga- and 89Zr-Labeled Exendin-4 as Potential Radiotracers for the Imaging of Insulinomas by PETEffect of amino acid infusion on potassium serum levels in neuroendocrine tumour patients treated with targeted radiopeptide therapyImaging of activated macrophages in experimental osteoarthritis using folate-targeted animal single-photon-emission computed tomography/computed tomography“Click to Chelate”: Synthesis and Installation of Metal Chelates into Biomolecules in a Single StepHeterocycle Annulation of Enolizable Vinyl Quinone Imides. Dihydroquinolines and Quinolines from Thermal 6π-Electrocyclizations and Indoles from Photochemical CyclizationsElectrocyclic Ring Closure of the Enols of Vinyl Quinones. A2H-Chromene SynthesisManganese in PET imaging: Opportunities and challenges
P50
Q33305264-4C06A7B7-E9BF-46CE-86B8-181D997271DEQ35673329-697D8ED1-3C4D-482A-BEC4-62DD2F8DCED6Q35766559-022F2486-FFA8-4BDC-89BB-C8EFBEC402FFQ37157372-3AF3C05C-BC97-466C-8533-E0F92A153FB5Q37560052-0E9D415D-C119-411F-AF84-3C78B5C9088FQ37672349-9CA838A5-11F7-4964-87B5-C049C25EA229Q38088564-4767FF24-D062-4620-90A4-47AA5670B1CAQ38130703-936ACA57-0FE7-4E23-8344-541D215BA4BAQ38722877-5EADEC0E-D669-4AD3-AFDB-91341F41FE68Q38780032-C3BE2C4F-CDC3-4236-BB38-C575377C6C62Q38840655-82C8E82E-AA2D-4E12-974E-F34C71E49065Q38965023-19E28186-6239-4090-A40F-C6B93B318E08Q39022536-65B45C54-194E-43CC-A6A7-6E57AE4FD7DAQ39044587-B932EE2B-AA49-4DC1-9062-F75A01C176C4Q39540051-5733C2AB-07A6-4973-B8AD-B6387363D72CQ39648059-B0CDEFFF-8905-4F4E-B0A6-247A5642D7D9Q39880737-FD4B4678-B20B-4EFA-9772-9D58C67BF49AQ39888892-0875AED3-59FF-409A-9A76-325F2C7C8A07Q39941758-28E482A7-A296-48C7-8EAA-4A59B8194169Q39958385-F93B06DD-BADD-41FF-9E69-683704625B5AQ41811649-6E8ACC22-29FE-475E-8CC5-EF3081D4DF0DQ44277672-1DD995F7-7EBC-4013-BCF3-57E5A7AEC843Q46216608-BAE42EE1-D2FE-4ACF-A274-3FFEF9F33D62Q46584205-303BE8BE-1AFE-40F6-B71C-1887E261933BQ46877390-485ED18D-F1A7-46BF-89F3-9427E640DC0CQ47800160-E0C61D7F-AF91-40AF-8894-40FC03F65390Q48918816-04F1BBD8-D756-411B-8F9A-A18A3A4AD0AFQ52901225-465B811F-80C3-4F23-9394-654B12858542Q52983939-2ACEF8B8-3DF7-4EFF-8726-416151932A7FQ53150916-5D03D364-4434-4EC0-B0D1-96D8F78E8998Q57757547-582C8945-90DD-4E38-B985-AC5ED9CEA007Q57757557-E3506C43-1E07-4744-88D4-F8041C56468BQ59469661-F6ABCEA6-088D-45E4-B138-4A567D534536Q60146343-1D45AEDD-0A63-47C8-8258-25E34F658C13Q60146347-A3A3FFDC-0BA8-4276-9E25-A1FE22B77472Q60146348-A57D2C10-1F3D-45F9-B316-9B3A1FD0BFE8Q60146351-E551178F-A223-4924-B0CE-A38DA46E48A9Q60146353-4544AA66-BA04-42FD-8829-459EF3098F50Q60146354-F069165A-BADA-4A82-ADEB-91A40CAE7019Q92204176-729EF32F-D85D-4815-84BA-7A7BBF7FE1C3
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Thomas L Mindt
@nl
Thomas L Mindt
@sl
Thomas L. Mindt
@en
Thomas L. Mindt
@es
type
label
Thomas L Mindt
@nl
Thomas L Mindt
@sl
Thomas L. Mindt
@en
Thomas L. Mindt
@es
prefLabel
Thomas L Mindt
@nl
Thomas L Mindt
@sl
Thomas L. Mindt
@en
Thomas L. Mindt
@es
P1053
S-7805-2017
P106
P1153
6508321397
P21
P31
P3829
P496
0000-0002-2090-1725