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The Human Host‐Defense Peptide Cathelicidin LL‐37 is a Nanomolar Inhibitor of Amyloid Self‐Assembly of Islet Amyloid Polypeptide (IAPP)

Angewandte Chemie (International ed.), 2020-07, Vol.59 (31), p.12837-12841

International ed. in English, 2020

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Designed Macrocyclic Peptides as Nanomolar Amyloid Inhibitors Based on Minimal Recognition Elements

Angewandte Chemie International Edition, 2018-10, Vol.57 (44), p.14503-14508

International ed. in English, 2018

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Key aromatic/hydrophobic amino acids controlling a cross-amyloid peptide interaction versus amyloid self-assembly

The Journal of biological chemistry, 2017-09, Vol.292 (35), p.14587-14602

2017

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Designed peptides as nanomolar cross-amyloid inhibitors acting via supramolecular nanofiber co-assembly

Nature communications, 2022-08, Vol.13 (1), p.5004-5004, Article 5004

2022

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Identification of an Arg-Leu-Arg tripeptide that contributes to the binding interface between the cytokine MIF and the chemokine receptor CXCR4

Scientific reports, 2018-03, Vol.8 (1), p.5171-17, Article 5171

2018

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Designed CXCR4 mimic acts as a soluble chemokine receptor that blocks atherogenic inflammation by agonist-specific targeting

Nature communications, 2020-11, Vol.11 (1), p.5981-18, Article 5981

2020

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Heterocomplexes between the atypical chemokine MIF and the CXC-motif chemokine CXCL4L1 regulate inflammation and thrombus formation

Cellular and molecular life sciences : CMLS, 2022-10, Vol.79 (10), p.512-512, Article 512

2022

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Structural Insight into IAPP‐Derived Amyloid Inhibitors and Their Mechanism of Action

Angewandte Chemie (International ed.), 2020-03, Vol.59 (14), p.5771-5781

International ed. in English, 2020

Volltextzugriff (PDF)

A MIF‐Derived Cyclopeptide that Inhibits MIF Binding and Atherogenic Signaling via the Chemokine Receptor CXCR2

Chembiochem : a European journal of chemical biology, 2021-03, Vol.22 (6), p.1012-1019

2021

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Das humane Wirtsabwehrpeptid Cathelicidin LL‐37 ist ein nanomolarer Inhibitor der amyloiden Selbstassoziation von Inselamyloid‐Polypeptid (IAPP)

Angewandte Chemie, 2020-07, Vol.132 (31), p.12937-12941

2020

Volltextzugriff (PDF)

Designed Macrocyclic Peptides as Nanomolar Amyloid Inhibitors Based on Minimal Recognition Elements

Angewandte Chemie, 2018-10, Vol.130 (44), p.14711-14716

2018

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Structural Insight into IAPP‐Derived Amyloid Inhibitors and Their Mechanism of Action

Angewandte Chemie, 2020-03, Vol.132 (14), p.5820-5830

2020

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Phosphorylation of serine residues S252, S268/S269, and S879 in p120 catenin activates migration of presomitic mesoderm in gastrulating zebrafish embryos

Developmental dynamics, 2022-12, Vol.251 (12), p.1952-1967

2022

Volltextzugriff (PDF)

Tuberculosis transmission in the Indigenous peoples of the Canadian prairies

PloS one, 2017-11, Vol.12 (11), p.e0188189-e0188189

2017

Volltextzugriff (PDF)

Optimizing Conservation Strategies for a Threatened Tree Species: In Situ Conservation of White Ash (Fraxinus americana L.) Genetic Diversity through Insecticide Treatment

Forests, 2018-04, Vol.9 (4), p.202

2018

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Analyses of health outcomes from the 5 sites participating in the Africa and Asia clinical efficacy trials of the oral pentavalent rotavirus vaccine

Vaccine, 2012-04, Vol.30, p.A24-A29

2012

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Families at high and low risk for depression: A three-generation startle study

Biological psychiatry (1969), 2005-05, Vol.57 (9), p.953-960

2005

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Startle reactivity in children at risk for migraine

Clinical neurophysiology, 2008-12, Vol.119 (12), p.2733-2737

2008

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Intracellular responses to gonadotropin-releasing hormone in a clonal cell line of the gonadotrope lineage

Molecular endocrinology (Baltimore, Md.), 1991-03, Vol.5 (3), p.347-355

1991

Volltextzugriff (PDF)

Identifying clinical scholarship guidelines for faculty practice

Journal of professional nursing, 2004-05, Vol.20 (3), p.147-155

2004

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The Human Host‐Defense Peptide Cathelicidin LL‐37 is a Nanomolar Inhibitor of Amyloid Self‐Assembly of Islet Amyloid Polypeptide (IAPP)

Designed Macrocyclic Peptides as Nanomolar Amyloid Inhibitors Based on Minimal Recognition Elements

Key aromatic/hydrophobic amino acids controlling a cross-amyloid peptide interaction versus amyloid self-assembly

Designed peptides as nanomolar cross-amyloid inhibitors acting via supramolecular nanofiber co-assembly

Identification of an Arg-Leu-Arg tripeptide that contributes to the binding interface between the cytokine MIF and the chemokine receptor CXCR4

Designed CXCR4 mimic acts as a soluble chemokine receptor that blocks atherogenic inflammation by agonist-specific targeting

Heterocomplexes between the atypical chemokine MIF and the CXC-motif chemokine CXCL4L1 regulate inflammation and thrombus formation

Structural Insight into IAPP‐Derived Amyloid Inhibitors and Their Mechanism of Action

A MIF‐Derived Cyclopeptide that Inhibits MIF Binding and Atherogenic Signaling via the Chemokine Receptor CXCR2

Das humane Wirtsabwehrpeptid Cathelicidin LL‐37 ist ein nanomolarer Inhibitor der amyloiden Selbstassoziation von Inselamyloid‐Polypeptid (IAPP)

Designed Macrocyclic Peptides as Nanomolar Amyloid Inhibitors Based on Minimal Recognition Elements

Structural Insight into IAPP‐Derived Amyloid Inhibitors and Their Mechanism of Action

Phosphorylation of serine residues S252, S268/S269, and S879 in p120 catenin activates migration of presomitic mesoderm in gastrulating zebrafish embryos

Tuberculosis transmission in the Indigenous peoples of the Canadian prairies

Optimizing Conservation Strategies for a Threatened Tree Species: In Situ Conservation of White Ash (Fraxinus americana L.) Genetic Diversity through Insecticide Treatment

Analyses of health outcomes from the 5 sites participating in the Africa and Asia clinical efficacy trials of the oral pentavalent rotavirus vaccine

Families at high and low risk for depression: A three-generation startle study

Startle reactivity in children at risk for migraine

Intracellular responses to gonadotropin-releasing hormone in a clonal cell line of the gonadotrope lineage

Identifying clinical scholarship guidelines for faculty practice

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