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Murder or not? Cold temperature makes criminals appear to be cold-blooded and warm temperature to be hot-headed

PloS one, 2014-04, Vol.9 (4), p.e96231-e96231

2014

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Community guidelines for GPCR ligand bias: IUPHAR review 32

British journal of pharmacology, 2022-07, Vol.179 (14), p.3651-3674

2022

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NMR-Based Metabolite Profiling and the Application of STOCSY toward the Quality and Authentication Assessment of European EVOOs

Molecules (Basel, Switzerland), 2023-02, Vol.28 (4), p.1738

2023

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Docking screens: right for the right reasons?

Current topics in medicinal chemistry, 2009-06, Vol.9 (9), p.755

2009

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Docking and chemoinformatic screens for new ligands and targets

Current opinion in biotechnology, 2009-08, Vol.20 (4), p.429-436

2009

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Guava (Psidium guajava) Fruit Extract Prepared by Supercritical CO2 Extraction Inhibits Intestinal Glucose Resorption in a Double-Blind, Randomized Clinical Study

Nutrients, 2019-07, Vol.11 (7), p.1512

2019

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Analyzing Kinase Similarity in Small Molecule and Protein Structural Space to Explore the Limits of Multi-Target Screening

Molecules (Basel, Switzerland), 2021-01, Vol.26 (3), p.629

2021

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An open source pharma roadmap

PLoS medicine, 2017-04, Vol.14 (4), p.e1002276-e1002276

2017

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Limits of ligand selectivity from docking to models: in silico screening for A(1) adenosine receptor antagonists

PloS one, 2012, Vol.7 (11), p.e49910-e49910

2012

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In Vitro Measurements of Cellular Forces and their Importance in the Lung—From the Sub- to the Multicellular Scale

Life (Basel, Switzerland), 2021-07, Vol.11 (7), p.691

2021

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Impact of Global Climate Change on the European Barley Market Requires Novel Multi-Method Approaches to Preserve Crop Quality and Authenticity

Foods, 2021-07, Vol.10 (7), p.1592

2021

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Preparation and High-Throughput Testing of TiO2-Supported Co Catalysts for Fischer‒Tropsch Synthesis

Catalysts, 2021-03, Vol.11 (3), p.352

2021

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Pseudorapidity dependence of anisotropic flows in relativistic heavy-ion collisions

Physics letters. B, 2005-01, Vol.605 (1-2), p.95-100

2005

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Allosteric modulation of GPCRs: From structural insights to in silico drug discovery

Pharmacology & therapeutics (Oxford), 2022-09, Vol.237, p.108242-108242, Article 108242

2022

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Stimulus-dependent deliberation process leading to a specific motor action demonstrated via a multi-channel EEG analysis

Frontiers in human neuroscience, 2015-07, Vol.9, p.355-355

2015

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Early thermalization at RHIC

Nuclear physics. A, 2002-05, Vol.702 (1), p.269-280

2002

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Structure-based discovery of novel cruzain inhibitors with distinct trypanocidal activity profiles

European journal of medicinal chemistry, 2023-09, Vol.257, p.115498-115498, Article 115498

2023

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Radial and elliptic flow at RHIC: further predictions

Physics letters. B, 2001-03, Vol.503 (1), p.58-64

2001

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Sicherheit in Europa – Hindernisse und Möglichkeiten einer europäischen Sicherheitspolitik

Zeitschrift für Aussen- und sicherheitspolitik, 2018, Vol.11 (2), p.181-201

2018

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Drugging specific conformational states of GPCRs: challenges and opportunities for computational chemistry

Drug discovery today, 2016-04, Vol.21 (4), p.625-631

2016

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Fragment evolution for GPCRs: the role of secondary binding sites in optimization

Chemical communications (Cambridge, England), 2021-10, Vol.57 (81), p.1516-1519

2021

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Pose, duplicate, then elaborate: Steps towards increased affinity for inhibitors targeting the specificity surface of the Pim-1 kinase

European journal of medicinal chemistry, 2023-01, Vol.245, p.114914-114914, Article 114914

2023

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Three stories on Eph kinase inhibitors: From in silico discovery to in vivo validation

European journal of medicinal chemistry, 2016-04, Vol.112, p.347-366

2016

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The allosteric site regulates the voltage sensitivity of muscarinic receptors

Cellular signalling, 2018-01, Vol.42, p.114-126

2018

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De novo design of selective compounds: a fragment-based pipeline applied to the β2 adrenergic receptor

Journal of cheminformatics, 2014-03, Vol.6 (Suppl 1), p.P25-P25, Article P25

2014

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Murder or not? Cold temperature makes criminals appear to be cold-blooded and warm temperature to be hot-headed

Community guidelines for GPCR ligand bias: IUPHAR review 32

NMR-Based Metabolite Profiling and the Application of STOCSY toward the Quality and Authentication Assessment of European EVOOs

Docking screens: right for the right reasons?

Docking and chemoinformatic screens for new ligands and targets

Guava (Psidium guajava) Fruit Extract Prepared by Supercritical CO2 Extraction Inhibits Intestinal Glucose Resorption in a Double-Blind, Randomized Clinical Study

Analyzing Kinase Similarity in Small Molecule and Protein Structural Space to Explore the Limits of Multi-Target Screening

An open source pharma roadmap

Limits of ligand selectivity from docking to models: in silico screening for A(1) adenosine receptor antagonists

In Vitro Measurements of Cellular Forces and their Importance in the Lung—From the Sub- to the Multicellular Scale

Impact of Global Climate Change on the European Barley Market Requires Novel Multi-Method Approaches to Preserve Crop Quality and Authenticity

Preparation and High-Throughput Testing of TiO2-Supported Co Catalysts for Fischer‒Tropsch Synthesis

Pseudorapidity dependence of anisotropic flows in relativistic heavy-ion collisions

Allosteric modulation of GPCRs: From structural insights to in silico drug discovery

Stimulus-dependent deliberation process leading to a specific motor action demonstrated via a multi-channel EEG analysis

Early thermalization at RHIC

Structure-based discovery of novel cruzain inhibitors with distinct trypanocidal activity profiles

Radial and elliptic flow at RHIC: further predictions

Sicherheit in Europa – Hindernisse und Möglichkeiten einer europäischen Sicherheitspolitik

Drugging specific conformational states of GPCRs: challenges and opportunities for computational chemistry

Fragment evolution for GPCRs: the role of secondary binding sites in optimization

Pose, duplicate, then elaborate: Steps towards increased affinity for inhibitors targeting the specificity surface of the Pim-1 kinase

Three stories on Eph kinase inhibitors: From in silico discovery to in vivo validation

The allosteric site regulates the voltage sensitivity of muscarinic receptors

De novo design of selective compounds: a fragment-based pipeline applied to the β2 adrenergic receptor

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