Lista de obras - Markus Muttenthaler - Dominio Público Uruguay

Advancing the Frontiers of Chemical Protein Synthesis-The 7th CPS Meeting, Haifa, Israel.

artículo científico publicado en 2018

Alpha-conotoxin AuIB isomers exhibit distinct inhibitory mechanisms and differential sensitivity to stoichiometry of alpha3beta4 nicotinic acetylcholine receptors.

artículo científico publicado en 2010

Chemical synthesis of human trefoil factor 1 (TFF1) and its homodimer provides novel insights into their mechanisms of action

scientific article published on 11 May 2020

Conopressin-T from Conus tulipa reveals an antagonist switch in vasopressin-like peptides

artículo científico publicado en 2008

Conotoxins: Chemistry and Biology

scientific article published on 21 October 2019

Contractility Measurements of Human Uterine Smooth Muscle to Aid Drug Development.

artículo científico publicado en 2018

Correction: Chemical synthesis of human trefoil factor 1 (TFF1) and its homodimer provides novel insights into their mechanisms of action

scientific article published on 17 June 2020

Design and Characterization of Superpotent Bivalent Ligands Targeting Oxytocin Receptor Dimers via a Channel-Like Structure

artículo científico publicado en 2016

Development of a human vasopressin V1a-receptor antagonist from an evolutionary-related insect neuropeptide.

artículo científico publicado en 2017

Discovery of defense- and neuropeptides in social ants by genome-mining

artículo científico publicado en 2012

Discovery, synthesis, and structure-activity relationships of conotoxins.

artículo científico publicado en 2014

Evaluation of Chemical Strategies for Improving the Stability and Oral Toxicity of Insecticidal Peptides

article

Evaluation of diverse peptidyl motifs for cellular delivery of semiconductor quantum dots

artículo científico publicado en 2013

Insights into the molecular evolution of oxytocin receptor ligand binding

artículo científico publicado en 2013

Ligand-based peptide design and combinatorial peptide libraries to target G protein-coupled receptors

artículo científico publicado en 2010

Lipid bilayer crossing--the gate of symmetry. Water-soluble phenylproline-based blood-brain barrier shuttles

artículo científico publicado en 2015

Methods, setup and safe handling for anhydrous hydrogen fluoride cleavage in Boc solid-phase peptide synthesis

artículo científico publicado en 2015

Modulating oxytocin activity and plasma stability by disulfide bond engineering

artículo científico publicado en 2010

Mucosal Biofilms Are an Endoscopic Feature of Irritable Bowel Syndrome and Ulcerative Colitis

artículo científico publicado en 2021

Nanoparticle cellular uptake by dendritic wedge peptides: achieving single peptide facilitated delivery.

artículo científico publicado en 2017

Oxytocic plant cyclotides as templates for peptide G protein-coupled receptor ligand design

artículo científico publicado en 2013

Oxytocin-like signaling in ants influences metabolic gene expression and locomotor activity

article

Pharmacological applications of natural peptide libraries.

artículo científico publicado en 2012

Selenoether oxytocin analogues have analgesic properties in a mouse model of chronic abdominal pain

scientific article published in Nature Communications

Selenopeptide chemistry.

artículo científico publicado en 2008

Site-Specific pKa Determination of Selenocysteine Residues in Selenovasopressin by Using 77Se NMR Spectroscopy

artículo científico publicado en 2011

Solving the alpha-conotoxin folding problem: efficient selenium-directed on-resin generation of more potent and stable nicotinic acetylcholine receptor antagonists.

artículo científico publicado en 2010

Structure-Activity Studies on Alpha-Conotoxins ⬇️

artículo científico publicado el 1 de diciembre de 2011

Subtle modifications to oxytocin produce ligands that retain potency and improved selectivity across species

artículo científico publicado en 2017

The Tumor Suppressor TFF1 Occurs in Different Forms and Interacts with Multiple Partners in the Human Gastric Mucus Barrier: Indications for Diverse Protective Functions

scientific article published on 04 April 2020

The oxytocin receptor signalling system and breast cancer: a critical review

artículo científico publicado en 2020

Trefoil Factor Family: Unresolved Questions and Clinical Perspectives.

artículo científico publicado en 2019

Two for the Price of One: Heterobivalent Ligand Design Targeting Two Binding Sites on Voltage-Gated Sodium Channels Slows Ligand Dissociation and Enhances Potency

artículo científico publicado en 2020

p-Nitrobenzyl protection for cysteine and selenocysteine: a more stable alternative to the acetamidomethyl group

artículo científico publicado en 2010

Lista de obras de Markus Muttenthaler

Advancing the Frontiers of Chemical Protein Synthesis-The 7th CPS Meeting, Haifa, Israel.

Alpha-conotoxin AuIB isomers exhibit distinct inhibitory mechanisms and differential sensitivity to stoichiometry of alpha3beta4 nicotinic acetylcholine receptors.

Chemical synthesis of human trefoil factor 1 (TFF1) and its homodimer provides novel insights into their mechanisms of action

Conopressin-T from Conus tulipa reveals an antagonist switch in vasopressin-like peptides

Conotoxins: Chemistry and Biology

Contractility Measurements of Human Uterine Smooth Muscle to Aid Drug Development.

Correction: Chemical synthesis of human trefoil factor 1 (TFF1) and its homodimer provides novel insights into their mechanisms of action

Design and Characterization of Superpotent Bivalent Ligands Targeting Oxytocin Receptor Dimers via a Channel-Like Structure

Development of a human vasopressin V1a-receptor antagonist from an evolutionary-related insect neuropeptide.

Discovery of defense- and neuropeptides in social ants by genome-mining

Discovery, synthesis, and structure-activity relationships of conotoxins.

Evaluation of Chemical Strategies for Improving the Stability and Oral Toxicity of Insecticidal Peptides

Evaluation of diverse peptidyl motifs for cellular delivery of semiconductor quantum dots

Insights into the molecular evolution of oxytocin receptor ligand binding

Ligand-based peptide design and combinatorial peptide libraries to target G protein-coupled receptors

Lipid bilayer crossing--the gate of symmetry. Water-soluble phenylproline-based blood-brain barrier shuttles

Methods, setup and safe handling for anhydrous hydrogen fluoride cleavage in Boc solid-phase peptide synthesis

Modulating oxytocin activity and plasma stability by disulfide bond engineering

Mucosal Biofilms Are an Endoscopic Feature of Irritable Bowel Syndrome and Ulcerative Colitis

Nanoparticle cellular uptake by dendritic wedge peptides: achieving single peptide facilitated delivery.

Oxytocic plant cyclotides as templates for peptide G protein-coupled receptor ligand design

Oxytocin-like signaling in ants influences metabolic gene expression and locomotor activity

Pharmacological applications of natural peptide libraries.

Selenoether oxytocin analogues have analgesic properties in a mouse model of chronic abdominal pain

Selenopeptide chemistry.

Site-Specific pKa Determination of Selenocysteine Residues in Selenovasopressin by Using 77Se NMR Spectroscopy

Solving the alpha-conotoxin folding problem: efficient selenium-directed on-resin generation of more potent and stable nicotinic acetylcholine receptor antagonists.

Structure-Activity Studies on Alpha-Conotoxins ⬇️

Subtle modifications to oxytocin produce ligands that retain potency and improved selectivity across species

The Tumor Suppressor TFF1 Occurs in Different Forms and Interacts with Multiple Partners in the Human Gastric Mucus Barrier: Indications for Diverse Protective Functions

The oxytocin receptor signalling system and breast cancer: a critical review

Trefoil Factor Family: Unresolved Questions and Clinical Perspectives.

Two for the Price of One: Heterobivalent Ligand Design Targeting Two Binding Sites on Voltage-Gated Sodium Channels Slows Ligand Dissociation and Enhances Potency

p-Nitrobenzyl protection for cysteine and selenocysteine: a more stable alternative to the acetamidomethyl group