Lista de obras - Linda M Haugaard-Kedström

Binding conformation and determinants of a single-chain peptide antagonist at the relaxin-3 receptor RXFP3

scientific article published on 21 August 2018

Chemically synthesized dicarba H2 relaxin analogues retain strong RXFP1 receptor activity but show an unexpected loss of in vitro serum stability

artículo científico publicado en 2015

Design, synthesis, and characterization of a single-chain peptide antagonist for the relaxin-3 receptor RXFP3.

artículo científico publicado en 2011

Design, synthesis, and characterization of fatty acid derivatives of a dimeric peptide-based postsynaptic density-95 (PSD-95) inhibitor

artículo científico publicado en 2015

Discovery of Human Signaling Systems: Pairing Peptides to G Protein-Coupled Receptors

scientific article published on 01 October 2019

Importance of a Conserved Lys/Arg Residue for Ligand/PDZ Domain Interactions as Examined by Protein Semisynthesis.

artículo científico publicado en 2016

Isolation and characterization of progenitor cells in uninjured, adult rat lacrimal gland.

artículo científico publicado en 2012

Molecular Details of a Coupled Binding and Folding Reaction between the Amyloid Precursor Protein and a Folded Domain

artículo científico publicado en 2021

Probing the Mint2 protein-protein interaction network with relevance for the pathophysiology of Alzheimer's disease.

artículo científico publicado en 2018

Solution structure, aggregation behavior, and flexibility of human relaxin-2

artículo científico publicado en 2015

Structural properties of relaxin chimeras.

artículo científico publicado en 2009

Structure–activity relationship and conformational studies of the natural product cyclic depsipeptides YM-254890 and FR900359

artículo científico publicado en 2018

Synthesis and pharmacological characterization of a europium-labelled single-chain antagonist for binding studies of the relaxin-3 receptor RXFP3.

artículo científico publicado en 2015

Synthesis, conformation, and activity of human insulin-like peptide 5 (INSL5).

artículo científico publicado en 2008

Targeting protein-protein interactions with trimeric ligands: high affinity inhibitors of the MAGUK protein family

artículo científico publicado en 2015

The α-defensin salt-bridge induces backbone stability to facilitate folding and confer proteolytic resistance

artículo científico publicado en 2012

Lista de obras de Linda M Haugaard-Kedström

Binding conformation and determinants of a single-chain peptide antagonist at the relaxin-3 receptor RXFP3

Chemically synthesized dicarba H2 relaxin analogues retain strong RXFP1 receptor activity but show an unexpected loss of in vitro serum stability

Design, synthesis, and characterization of a single-chain peptide antagonist for the relaxin-3 receptor RXFP3.

Design, synthesis, and characterization of fatty acid derivatives of a dimeric peptide-based postsynaptic density-95 (PSD-95) inhibitor

Discovery of Human Signaling Systems: Pairing Peptides to G Protein-Coupled Receptors

Importance of a Conserved Lys/Arg Residue for Ligand/PDZ Domain Interactions as Examined by Protein Semisynthesis.

Isolation and characterization of progenitor cells in uninjured, adult rat lacrimal gland.

Molecular Details of a Coupled Binding and Folding Reaction between the Amyloid Precursor Protein and a Folded Domain

Probing the Mint2 protein-protein interaction network with relevance for the pathophysiology of Alzheimer's disease.

Solution structure, aggregation behavior, and flexibility of human relaxin-2

Structural properties of relaxin chimeras.

Structure–activity relationship and conformational studies of the natural product cyclic depsipeptides YM-254890 and FR900359

Synthesis and pharmacological characterization of a europium-labelled single-chain antagonist for binding studies of the relaxin-3 receptor RXFP3.

Synthesis, conformation, and activity of human insulin-like peptide 5 (INSL5).

Targeting protein-protein interactions with trimeric ligands: high affinity inhibitors of the MAGUK protein family

The α-defensin salt-bridge induces backbone stability to facilitate folding and confer proteolytic resistance