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A Comprehensive Evaluation of the Activity and Selectivity Profile of Ligands for RGD-binding Integrins

Scientific reports, 2017-01, Vol.7 (1), p.39805-39805, Article 39805

2017

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Identification of phenothiazine derivatives as UHM-binding inhibitors of early spliceosome assembly

Nature communications, 2020-11, Vol.11 (1), p.5621-11, Article 5621

2020

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Validation of [125I]CPCR4.3 as an investigative tool for the sensitive and specific detection of hCXCR4 and mCXCR4 expression in vitro and in vivo

EJNMMI research, 2019-08, Vol.9 (1), p.75-9, Article 75

2019

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αvβ3- or α5β1-Integrin-Selective Peptidomimetics for Surface Coating

Angewandte Chemie (International ed.), 2016-06, Vol.55 (25), p.7048-7067

2016

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Cloning, expression and purification of the human Islet Amyloid Polypeptide (hIAPP) from Escherichia coli

Protein expression and purification, 2015-02, Vol.106, p.49-56

2015

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Small Cause, Great Impact: Modification of the Guanidine Group in the RGD Motif Controls Integrin Subtype Selectivity

Angewandte Chemie (International ed.), 2016-01, Vol.55 (4), p.1540-1543

International ed. in English, 2016

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Stable Peptides Instead of Stapled Peptides: Highly Potent αvβ6-Selective Integrin Ligands

Angewandte Chemie (International ed.), 2016-01, Vol.55 (4), p.1535-1539

2016

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Benefits of NOPO as chelator in gallium-68 peptides, exemplified by preclinical characterization of (68)Ga-NOPO-c(RGDfK)

Molecular pharmaceutics, 2014-05, Vol.11 (5), p.1687-1695

2014

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Integrin modulators: a patent review

Expert opinion on therapeutic patents, 2013-10, Vol.23 (10), p.1273-1295

2013

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Selective Targeting of Integrin αvβ8 by a Highly Active Cyclic Peptide

Journal of medicinal chemistry, 2019-02, Vol.62 (4), p.2024-2037

2019

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Rational Design of Cyclic Peptide Inhibitors of U2AF Homology Motif (UHM) Domains To Modulate Pre-mRNA Splicing

Journal of medicinal chemistry, 2016-11, Vol.59 (22), p.10190-10197

2016

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Overcoming the Lack of Oral Availability of Cyclic Hexapeptides: Design of a Selective and Orally Available Ligand for the Integrin αvβ3

Angewandte Chemie International Edition, 2017-12, Vol.56 (51), p.16405-16409

2017

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Modification and Functionalization of the Guanidine Group by Tailor-made Precursors

Journal of visualized experiments, 2017-04 (122)

2017

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Kleine Ursache, große Wirkung: Modifikation der Guanidiniumgruppe im RGD-Motiv reguliert die Integrinsubtypselektivität

Angewandte Chemie, 2016-01, Vol.128 (4), p.1564-1568

2016

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A Cyclen-Based Tetraphosphinate Chelator for the Preparation of Radiolabeled Tetrameric Bioconjugates

Chemistry : a European journal, 2013-06, Vol.19 (24), p.7748-7757

2013

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Functionalization of Ruthenium(II) Terpyridine Complexes with Cyclic RGD Peptides To Target Integrin Receptors in Cancer Cells

European journal of inorganic chemistry, 2017-03, Vol.2017 (12), p.1667-1672

2017

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In Vivo PET Imaging of the Cancer Integrin αvβ6 Using 68 Ga-Labeled Cyclic RGD Nonapeptides

Journal of Nuclear Medicine, 2017-04, Vol.58 (4), p.671-677

2017

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The Integrin Ligand c(RGDf(NMe)Nal) Reduces Neointimal Hyperplasia in a Polymer-Free Drug-Eluting Stent System

ChemMedChem, 2014-07, Vol.9 (7), p.1413-1418

2014

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Back Cover: The Integrin Ligand c(RGDf(NMe)Nal) Reduces Neointimal Hyperplasia in a Polymer-Free Drug-Eluting Stent System (ChemMedChem 7/2014)

ChemMedChem, 2014-07, Vol.9 (7), p.1620-1620

2014

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Modification and Functionalization of the Guanidine Group by Tailor-made Precursors

Journal of visualized experiments, 2017-04 (122)

2017

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N -Methylation of iso DGR Peptides: Discovery of a Selective α5β1-Integrin Ligand as a Potent Tumor Imaging Agent

Journal of medicinal chemistry, 2018-03, Vol.61 (6), p.2490-2499

2018

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[alpha]v[beta]3- or [alpha]5[beta]1-Integrin-Selective Peptidomimetics for Surface Coating

Angewandte Chemie International Edition, 2016-06, Vol.55 (25), p.7048

International ed. in English, 2016

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[alpha]v[beta]3- oder [alpha]5[beta]1-Integrin-selektive Peptidmimetika fur die Oberflächenbeschichtung

Angewandte Chemie, 2016-06, Vol.128 (25), p.7162

2016

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Complementary, Selective PET Imaging of Integrin Subtypes [alpha]^sub 5^[Beta]^sub 1^ and [alpha]^sub v^[Beta]^sub 3^ Using ^sup 68^Ga-Aquibeprin and 68Ga-Avebetrin

The Journal of nuclear medicine (1978), 2016-03, Vol.57 (3), p.460

2016

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Complementary, Selective PET Imaging of Integrin Subtypes [alpha] sub( 5)[Beta] sub( 1) and [alpha] sub( v)[Beta] sub( 3) Using super( 68)Ga-Aquibeprin and 68Ga-Avebetrin

The Journal of nuclear medicine (1978), 2016-03, Vol.57 (3), p.460-460

2016

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A Comprehensive Evaluation of the Activity and Selectivity Profile of Ligands for RGD-binding Integrins

Identification of phenothiazine derivatives as UHM-binding inhibitors of early spliceosome assembly

Validation of [125I]CPCR4.3 as an investigative tool for the sensitive and specific detection of hCXCR4 and mCXCR4 expression in vitro and in vivo

αvβ3- or α5β1-Integrin-Selective Peptidomimetics for Surface Coating

Cloning, expression and purification of the human Islet Amyloid Polypeptide (hIAPP) from Escherichia coli

Small Cause, Great Impact: Modification of the Guanidine Group in the RGD Motif Controls Integrin Subtype Selectivity

Stable Peptides Instead of Stapled Peptides: Highly Potent αvβ6-Selective Integrin Ligands

Benefits of NOPO as chelator in gallium-68 peptides, exemplified by preclinical characterization of (68)Ga-NOPO-c(RGDfK)

Integrin modulators: a patent review

Selective Targeting of Integrin αvβ8 by a Highly Active Cyclic Peptide

Rational Design of Cyclic Peptide Inhibitors of U2AF Homology Motif (UHM) Domains To Modulate Pre-mRNA Splicing

Overcoming the Lack of Oral Availability of Cyclic Hexapeptides: Design of a Selective and Orally Available Ligand for the Integrin αvβ3

Modification and Functionalization of the Guanidine Group by Tailor-made Precursors

Kleine Ursache, große Wirkung: Modifikation der Guanidiniumgruppe im RGD-Motiv reguliert die Integrinsubtypselektivität

A Cyclen-Based Tetraphosphinate Chelator for the Preparation of Radiolabeled Tetrameric Bioconjugates

Functionalization of Ruthenium(II) Terpyridine Complexes with Cyclic RGD Peptides To Target Integrin Receptors in Cancer Cells

In Vivo PET Imaging of the Cancer Integrin αvβ6 Using 68 Ga-Labeled Cyclic RGD Nonapeptides

The Integrin Ligand c(RGDf(NMe)Nal) Reduces Neointimal Hyperplasia in a Polymer-Free Drug-Eluting Stent System

Back Cover: The Integrin Ligand c(RGDf(NMe)Nal) Reduces Neointimal Hyperplasia in a Polymer-Free Drug-Eluting Stent System (ChemMedChem 7/2014)

Modification and Functionalization of the Guanidine Group by Tailor-made Precursors

N -Methylation of iso DGR Peptides: Discovery of a Selective α5β1-Integrin Ligand as a Potent Tumor Imaging Agent

[alpha]v[beta]3- or [alpha]5[beta]1-Integrin-Selective Peptidomimetics for Surface Coating

[alpha]v[beta]3- oder [alpha]5[beta]1-Integrin-selektive Peptidmimetika fur die Oberflächenbeschichtung

Complementary, Selective PET Imaging of Integrin Subtypes [alpha]^sub 5^[Beta]^sub 1^ and [alpha]^sub v^[Beta]^sub 3^ Using ^sup 68^Ga-Aquibeprin and 68Ga-Avebetrin

Complementary, Selective PET Imaging of Integrin Subtypes [alpha] sub( 5)[Beta] sub( 1) and [alpha] sub( v)[Beta] sub( 3) Using super( 68)Ga-Aquibeprin and 68Ga-Avebetrin

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