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Eva Kostenis (1966-)

Pharmakologin

Name	Eva Kostenis
Time	1966- (Date of birth and death)
Place	München (Geburtsort) Deutschland
Gender	weiblich
Academic degree	Prof. Dr.
Profession	Pharmakologin (characteristic profession) Hochschullehrerin
Variant	Evi Kostenis
Related	Rheinische Friedrich-Wilhelms-Universität Bonn. Institut für Pharmazeutische Biologie (Professorin)
Source	Internet: https://www.gleichstellung.uni-bonn.de/perspektive_wissenschaft/professorinnen/kostenis
Record type	Person
GND-Identifier	1111043671
Record ID	1111043671
Involved in show all A molecular mechanism to diversify Ca2+ signaling downstream of Gs protein-coupled receptors Development of a NanoBRET Assay Platform to Detect Intracellular Ligands for the Chemokine Receptors CCR6 and CXCR1 G protein-mediated signal transduction: a molecular choreography of G protein activation after GTP binding GRK specificity and Gβγ dependency determines the potential of a GPCR for arrestin-biased agonism Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice Front Cover: Development of a NanoBRET Assay Platform to Detect Intracellular Ligands for the Chemokine Receptors CCR6 and CXCR1 (ChemMedChem 20/2024) Development of a NanoBRET assay platform to detect intracellular ligands for the chemokine receptors CCR6 and CXCR1 Reply to: How carvedilol does not activate β2-adrenoceptors New insights into non-canonical desensitization of Gq signaling by GRK2/3 expression levels How Carvedilol activates β2-adrenoceptors Chemisch‐biologischer Werkzeugkasten für die intrazelluläre Bindungsstelle von CCR9: Fluoreszierende Liganden, neue Leitstrukturen und PROTACs A Chemical Biology Toolbox Targeting the Intracellular Binding Site of CCR9: Fluorescent Ligands, New Drug Leads and PROTACs How Carvedilol activates β 2 -adrenoceptors Thioesterase-mediated side chain transesterification generates potent Gq signaling inhibitor FR900359 Deciphering Specificity Determinants for FR900359‐Derived G q α Inhibitors Based on Computational and Structure–Activity Studies Front Cover: Deciphering Specificity Determinants for FR900359‐Derived G q α Inhibitors Based on Computational and Structure–Activity Studies (ChemMedChem 16/2018) Pseudomonas aeruginosaExoY, a cyclic GMP- and cyclic UMP-generating nucleotidyl cyclase Antagonism of the prostaglandin D2receptor CRTH2 attenuates asthma pathology in mouse eosinophilic airway inflammation Suche nach essentiellen Strukturelementen von allosterischen Modulatoren an muskarinischen Acetylcholinrezeptoren

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Katalog der Deutschen Nationalbibliothek

Eva Kostenis (1966-)

A molecular mechanism to diversify Ca2+ signaling downstream of Gs protein-coupled receptors

Development of a NanoBRET Assay Platform to Detect Intracellular Ligands for the Chemokine Receptors CCR6 and CXCR1

G protein-mediated signal transduction: a molecular choreography of G protein activation after GTP binding

GRK specificity and Gβγ dependency determines the potential of a GPCR for arrestin-biased agonism

Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice

Front Cover: Development of a NanoBRET Assay Platform to Detect Intracellular Ligands for the Chemokine Receptors CCR6 and CXCR1 (ChemMedChem 20/2024)

Development of a NanoBRET assay platform to detect intracellular ligands for the chemokine receptors CCR6 and CXCR1

Reply to: How carvedilol does not activate β2-adrenoceptors

New insights into non-canonical desensitization of Gq signaling by GRK2/3 expression levels

How Carvedilol activates β2-adrenoceptors

Chemisch‐biologischer Werkzeugkasten für die intrazelluläre Bindungsstelle von CCR9: Fluoreszierende Liganden, neue Leitstrukturen und PROTACs

A Chemical Biology Toolbox Targeting the Intracellular Binding Site of CCR9: Fluorescent Ligands, New Drug Leads and PROTACs

How Carvedilol activates β 2 -adrenoceptors

Thioesterase-mediated side chain transesterification generates potent Gq signaling inhibitor FR900359

Deciphering Specificity Determinants for FR900359‐Derived G q α Inhibitors Based on Computational and Structure–Activity Studies

Front Cover: Deciphering Specificity Determinants for FR900359‐Derived G q α Inhibitors Based on Computational and Structure–Activity Studies (ChemMedChem 16/2018)

Pseudomonas aeruginosaExoY, a cyclic GMP- and cyclic UMP-generating nucleotidyl cyclase

Antagonism of the prostaglandin D2receptor CRTH2 attenuates asthma pathology in mouse eosinophilic airway inflammation

Suche nach essentiellen Strukturelementen von allosterischen Modulatoren an muskarinischen Acetylcholinrezeptoren