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Combination of Phage Display and Molecular Grafting Generates Highly Specific Tumor-Targeting Miniproteins

Angewandte Chemie International Edition, 2012-12, Vol.51 (52), p.13136-13139

International ed. in English, 2012

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Miniproteins as phage display-scaffolds for clinical applications

Molecules, 2011-03, Vol.16 (3), p.2467-2485

2011

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Challenges in optimizing a prostate carcinoma binding peptide, identified through the phage display technology

Molecules (Basel, Switzerland), 2011-02, Vol.16 (2), p.1559-1578

2011

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Endoradiotherapy in cancer treatment — Basic concepts and future trends

European journal of pharmacology, 2009-12, Vol.625 (1), p.55-62

2009

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A Disulfide-Constrained Miniprotein with Striking Tumor-Binding Specificity Developed by Ribosome Display

Angewandte Chemie International Edition, 2013-11, Vol.52 (45), p.11760-11764

International ed. in English, 2013

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Engineering and Functionalization of the Disulfide-Constrained Miniprotein Min-23 as a Scaffold for Diagnostic Application

ChemMedChem, 2012-02, Vol.7 (2), p.237-247

2012

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A Disulfide‐Constrained Miniprotein with Striking Tumor‐Binding Specificity Developed by Ribosome Display

Angewandte Chemie, 2013-11, Vol.125 (45), p.11976-11980

2013

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Cover Picture: Engineering and Functionalization of the Disulfide-Constrained Miniprotein Min-23 as a Scaffold for Diagnostic Application (ChemMedChem 2/2012)

ChemMedChem, 2012-02, Vol.7 (2), p.177-177

2012

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Radiolabelling and preliminary evaluation of68 Ga-tetrapyrrole derivatives as potential tracers for PET

Nuclear medicine and biology, 2013, Vol.40 (2), p.280-288

2013

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Combination of Phage Display and Molecular Grafting Generates Highly Specific Tumor‐Targeting Miniproteins

Angewandte Chemie, 2012-12, Vol.124 (52), p.13313-13316

2012

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Endoradiotherapy in cancer treatment: Basic concepts and future trends: New Vistas in Anti-Cancer Therapy

European journal of pharmacology, 2009, Vol.625 (1-3), p.55-62

2009

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Radiolabelling and preliminary evaluation of 68Ga-tetrapyrrole derivatives as potential tracers for PET

Nuclear medicine and biology, 2013-02, Vol.40 (2), p.280-288

2013

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Efficient post-processing of aqueous generator eluates facilitates 68Ga-labelling under anhydrous conditions

Radiochimica acta, 2010-01, Vol.98 (3)

2010

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[ 68Ga]Ga-DO 2A-(OBu- l -tyr) 2: Synthesis, 68Ga-radiolabeling and in vitro studies of a novel 68Ga-DO 2A-tyrosine conjugate as potential tumor tracer for PET

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (13), p.3498-3501

2009

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[68Ga]Ga-DO2A-(OBu-L-tyr)2: Synthesis, 68Ga-radiolabeling and in vitro studies of a novel 68Ga-DO2A-tyrosine conjugate as potential tumor tracer for PET

Bioorganic & medicinal chemistry letters, 2009-07, Vol.19 (13), p.3498-3501

2009

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A Disulfide-Constrained Miniprotein with Striking Tumor-Binding Specificity Developed by Ribosome Display

Angewandte Chemie, 2013-11, Vol.125 (45), p.11976-11980

2013

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A dimerized urea-based inhibitor of the prostate-specific membrane antigen for 68Ga-PET imaging of prostate cancer

EJNMMI research, 2012-06, Vol.2 (1), p.23-23, Article 23

2012

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Combination of Phage Display and Molecular Grafting Generates Highly Specific Tumor-Targeting Miniproteins

Angewandte Chemie, 2012-12, Vol.124 (52), p.13313-13316

2012

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[(68)Ga]Ga-DO(2)A-(OBu-l-tyr)(2): synthesis, (68)Ga-radiolabeling and in vitro studies of a novel (68)Ga-DO(2)A-tyrosine conjugate as potential tumor tracer for PET

Bioorganic & medicinal chemistry letters, 2009-07, Vol.19 (13), p.3498-3501

2009

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Genomic vulnerability to rapid climate warming in a tree species with a long generation time

Global change biology, 2021-03, Vol.27 (6), p.1181-1195

2021

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Structure-Based Library Design and Fragment Screening for the Identification of Reversible Complement Factor D Protease Inhibitors

Journal of medicinal chemistry, 2017-03, Vol.60 (5), p.1946-1958

2017

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DCAF1-based PROTACs with activity against clinically validated targets overcoming intrinsic- and acquired-degrader resistance

Nature communications, 2024-01, Vol.15 (1), p.275-19, Article 275

2024

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Author Correction: DCAF1-based PROTACs with activity against clinically validated targets overcoming intrinsic- and acquired-degrader resistance

Nature communications, 2024-08, Vol.15 (1), p.7109-5

2024

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Discovery of Potent, Highly Selective, and In Vivo Efficacious, Allosteric MALT1 Inhibitors by Iterative Scaffold Morphing

Journal of medicinal chemistry, 2020-12, Vol.63 (23), p.14576-14593

2020

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N-aryl-piperidine-4-carboxamides as a novel class of potent inhibitors of MALT1 proteolytic activity

Bioorganic & medicinal chemistry letters, 2018-07, Vol.28 (12), p.2153-2158

2018

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Combination of Phage Display and Molecular Grafting Generates Highly Specific Tumor-Targeting Miniproteins

Miniproteins as phage display-scaffolds for clinical applications

Challenges in optimizing a prostate carcinoma binding peptide, identified through the phage display technology

Endoradiotherapy in cancer treatment — Basic concepts and future trends

A Disulfide-Constrained Miniprotein with Striking Tumor-Binding Specificity Developed by Ribosome Display

Engineering and Functionalization of the Disulfide-Constrained Miniprotein Min-23 as a Scaffold for Diagnostic Application

A Disulfide‐Constrained Miniprotein with Striking Tumor‐Binding Specificity Developed by Ribosome Display

Cover Picture: Engineering and Functionalization of the Disulfide-Constrained Miniprotein Min-23 as a Scaffold for Diagnostic Application (ChemMedChem 2/2012)

Radiolabelling and preliminary evaluation of68 Ga-tetrapyrrole derivatives as potential tracers for PET

Combination of Phage Display and Molecular Grafting Generates Highly Specific Tumor‐Targeting Miniproteins

Endoradiotherapy in cancer treatment: Basic concepts and future trends: New Vistas in Anti-Cancer Therapy

Radiolabelling and preliminary evaluation of 68Ga-tetrapyrrole derivatives as potential tracers for PET

Efficient post-processing of aqueous generator eluates facilitates 68Ga-labelling under anhydrous conditions

[ 68Ga]Ga-DO 2A-(OBu- l -tyr) 2: Synthesis, 68Ga-radiolabeling and in vitro studies of a novel 68Ga-DO 2A-tyrosine conjugate as potential tumor tracer for PET

[68Ga]Ga-DO2A-(OBu-L-tyr)2: Synthesis, 68Ga-radiolabeling and in vitro studies of a novel 68Ga-DO2A-tyrosine conjugate as potential tumor tracer for PET

A Disulfide-Constrained Miniprotein with Striking Tumor-Binding Specificity Developed by Ribosome Display

A dimerized urea-based inhibitor of the prostate-specific membrane antigen for 68Ga-PET imaging of prostate cancer

Combination of Phage Display and Molecular Grafting Generates Highly Specific Tumor-Targeting Miniproteins

[(68)Ga]Ga-DO(2)A-(OBu-l-tyr)(2): synthesis, (68)Ga-radiolabeling and in vitro studies of a novel (68)Ga-DO(2)A-tyrosine conjugate as potential tumor tracer for PET

Genomic vulnerability to rapid climate warming in a tree species with a long generation time

Structure-Based Library Design and Fragment Screening for the Identification of Reversible Complement Factor D Protease Inhibitors

DCAF1-based PROTACs with activity against clinically validated targets overcoming intrinsic- and acquired-degrader resistance

Author Correction: DCAF1-based PROTACs with activity against clinically validated targets overcoming intrinsic- and acquired-degrader resistance

Discovery of Potent, Highly Selective, and In Vivo Efficacious, Allosteric MALT1 Inhibitors by Iterative Scaffold Morphing

N-aryl-piperidine-4-carboxamides as a novel class of potent inhibitors of MALT1 proteolytic activity

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