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Journal of Fluorescence|February 12, 2013
The pH probe CypHer™5E is effectively quenched by FM dyesOliver Welzel, Kristina Loy, Carsten H Tischbirek, et al.Scientific Reports|November 10, 2019
Differential allosteric modulation within dopamine D<sub>2</sub>R - neurotensin NTS1R and D<sub>2</sub>R - serotonin 5-HT<sub>2A</sub>R receptor complexes gives bias to intracellular calcium signallingMichael Plach, Thorsten Schäfer, Dasiel Oscar Borroto-Escuela, et al.ACS Pharmacology & Translational Science|May 16, 2024
Development of a Fluorescent Ligand for the Intracellular Allosteric Binding Site of the Neurotensin Receptor 1Hannah Vogt, Patrick Shinkwin, Max E Huber, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|January 11, 2024
"Photo-Adrenalines": Photoswitchable β<sub>2</sub> -Adrenergic Receptor Agonists as Molecular Probes for the Study of Spatiotemporal Adrenergic SignalingAlexandra Sink, Hubert Gerwe, Harald Hübner, et al.Pharmaceuticals (Basel, Switzerland)|March 14, 2017
Theranostic Value of Multimers: Lessons Learned from Trimerization of Neurotensin Receptor Ligands and Other Targeting VectorsSimone Maschauer, Jürgen Einsiedel, Dominik Reich, et al.Bioanalysis|November 19, 2010
Tetracycline sensing using novel doxycycline derivatives immobilized on different surface plasmon resonance biosensor surfacesUlrike Andree, Erika Mueller-Seitz, Igor Usai, et al.Steroids|February 6, 2008
A simple chemical method for synthesizing malonyl hemiesters of 21-hydroxypregnanes, potential intermediates in cardenolide biosynthesisRodrigo M Pádua, Reiner Waibel, Serge Philibert Kuate, et al.Journal of Medicinal Chemistry|May 11, 2019
Conjugation of Short Peptides to Dibenzodiazepinone-Type Muscarinic Acetylcholine Receptor Ligands Determines M<sub>2</sub>R SelectivityAndrea Pegoli, David Wifling, Corinna G Gruber, et al.Scientific Reports|December 15, 2020
Fluorescent ligands for dopamine D<sub>2</sub>/D<sub>3</sub> receptorsAnni Allikalt, Nirupam Purkayastha, Khajidmaa Flad, et al.Psychopharmacology|March 10, 2004
FAUC 213, a highly selective dopamine D4 receptor full antagonist, exhibits atypical antipsychotic properties in behavioural and neurochemical models of schizophreniaFrank Boeckler, Holger Russig, Weining Zhang, et al.Pageof 25