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Binding Selectivity of Abaloparatide for PTH-Type-1-Receptor Conformations and Effects on Downstream Signaling

Endocrinology (Philadelphia), 2016-01, Vol.157 (1), p.141-149

2016

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High constitutive activity is an intrinsic feature of ghrelin receptor protein: a study with a functional monomeric GHS-R1a receptor reconstituted in lipid discs

The Journal of biological chemistry, 2012-02, Vol.287 (6), p.3630-3641

2012

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A G protein signaling-biased agonist at the μ-opioid receptor reverses morphine tolerance while preventing morphine withdrawal

Neuropsychopharmacology (New York, N.Y.), 2020-01, Vol.45 (2), p.416-425

2020

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Convergent cross-species pro-cognitive effects of RGH-235, a new potent and selective histamine H 3 receptor antagonist/inverse agonist

European journal of pharmacology, 2022-02, Vol.916, p.174621

2022

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Structures of the Noncanonical RNA Ligase RtcB Reveal the Mechanism of Histidine Guanylylation

Biochemistry (Easton), 2013-04, Vol.52 (15), p.2518-2525

2013

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Neuroanatomical characterization of the G protein-coupled receptor activity evoked by galanin-related ligands

Journal of chemical neuroanatomy, 2023-03, Vol.128, p.102226-102226, Article 102226

2023

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[ 35 S]GTPγS (Guanosine-5'-O-(γ-thio)triphosphate-[ 35 S]) Binding Scintillation Proximity Assay Experiments in Postmortem Brain Tissue

Methods in molecular biology (Clifton, N.J.), 2023, Vol.2687, p.31

2023

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Nucleotide-dependent farnesyl switch orchestrates polymerization and membrane binding of human guanylate-binding protein 1

Proceedings of the National Academy of Sciences - PNAS, 2017-07, Vol.114 (28), p.E5559-E5568

2017

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GPR37 and GPR37L1 are receptors for the neuroprotective and glioprotective factors prosaptide and prosaposin

Proceedings of the National Academy of Sciences - PNAS, 2013-06, Vol.110 (23), p.9529-9534

2013

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Tolerance to high‐internalizing δ opioid receptor agonist is critically mediated by arrestin 2

British journal of pharmacology, 2018-07, Vol.175 (14), p.3050-3059

2018

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The δ‐opioid receptor positive allosteric modulator BMS 986187 is a G‐protein‐biased allosteric agonist

British journal of pharmacology, 2019-06, Vol.176 (11), p.1649-1663

2019

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GTPγS-Autoradiography for Studies of Opioid Receptor Functionality

Methods in molecular biology (Clifton, N.J.), 2021, Vol.2201, p.109

2021

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Mu Opioids Induce Biased Signaling at the Full-Length Seven Transmembrane C-Terminal Splice Variants of the mu Opioid Receptor Gene, Oprm1

Cellular and molecular neurobiology, 2021-07, Vol.41 (5), p.1059-1074

2021

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Stratification of Cannabinoid 1 Receptor (CB1R) Agonist Efficacy: Manipulation of CB1R Density through Use of Transgenic Mice Reveals Congruence between In Vivo and In Vitro Assays

The Journal of pharmacology and experimental therapeutics, 2016-11, Vol.359 (2), p.329

2016

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Structural insight into the rearrangement of the switch I region in GTP‐bound G12A K‐Ras

Acta crystallographica. Section D, Biological crystallography., 2017-12, Vol.73 (12), p.970-984

2017

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Effect of N‑Terminal Myristoylation on the Active Conformation of Gα i1–GTP

Biochemistry (Easton), 2017-01, Vol.56 (1), p.271-280

2017

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Alternatively spliced mu opioid receptor C termini impact the diverse actions of morphine

The Journal of clinical investigation, 2017-04, Vol.127 (4), p.1561-1573

2017

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Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6

The Journal of biological chemistry, 2009-06, Vol.284 (26), p.17731-17741

2009

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Small Molecule CXCR3 Antagonists

Journal of medicinal chemistry, 2016-04, Vol.59 (7), p.2894-2917

2016

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Cannabidiol displays unexpectedly high potency as an antagonist of CB1 and CB2 receptor agonists in vitro

British journal of pharmacology, 2007-03, Vol.150 (5), p.613-623

2007

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Directional transition from initiation to elongation in bacterial translation

Nucleic acids research, 2015-12, Vol.43 (22), p.10700

2015

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Allosteric Modulation of the Cannabinoid CB1 Receptor

Molecular pharmacology, 2005-11, Vol.68 (5), p.1484-1495

2005

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Defining the Molecular Basis for the First Potent and Selective Orthosteric Agonists of the FFA2 Free Fatty Acid Receptor

The Journal of biological chemistry, 2013-06, Vol.288 (24), p.17296-17312

2013

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Functional Characterization of Human Receptors for Short Chain Fatty Acids and Their Role in Polymorphonuclear Cell Activation

The Journal of biological chemistry, 2003-07, Vol.278 (28), p.25481-25489

2003

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Novel Electrophilic and Photoaffinity Covalent Probes for Mapping the Cannabinoid 1 Receptor Allosteric Site(s)

Journal of medicinal chemistry, 2016-01, Vol.59 (1), p.44-60

2016

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Binding Selectivity of Abaloparatide for PTH-Type-1-Receptor Conformations and Effects on Downstream Signaling

High constitutive activity is an intrinsic feature of ghrelin receptor protein: a study with a functional monomeric GHS-R1a receptor reconstituted in lipid discs

A G protein signaling-biased agonist at the μ-opioid receptor reverses morphine tolerance while preventing morphine withdrawal

Convergent cross-species pro-cognitive effects of RGH-235, a new potent and selective histamine H 3 receptor antagonist/inverse agonist

Structures of the Noncanonical RNA Ligase RtcB Reveal the Mechanism of Histidine Guanylylation

Neuroanatomical characterization of the G protein-coupled receptor activity evoked by galanin-related ligands

[ 35 S]GTPγS (Guanosine-5'-O-(γ-thio)triphosphate-[ 35 S]) Binding Scintillation Proximity Assay Experiments in Postmortem Brain Tissue

Nucleotide-dependent farnesyl switch orchestrates polymerization and membrane binding of human guanylate-binding protein 1

GPR37 and GPR37L1 are receptors for the neuroprotective and glioprotective factors prosaptide and prosaposin

Tolerance to high‐internalizing δ opioid receptor agonist is critically mediated by arrestin 2

The δ‐opioid receptor positive allosteric modulator BMS 986187 is a G‐protein‐biased allosteric agonist

GTPγS-Autoradiography for Studies of Opioid Receptor Functionality

Mu Opioids Induce Biased Signaling at the Full-Length Seven Transmembrane C-Terminal Splice Variants of the mu Opioid Receptor Gene, Oprm1

Stratification of Cannabinoid 1 Receptor (CB1R) Agonist Efficacy: Manipulation of CB1R Density through Use of Transgenic Mice Reveals Congruence between In Vivo and In Vitro Assays

Structural insight into the rearrangement of the switch I region in GTP‐bound G12A K‐Ras

Effect of N‑Terminal Myristoylation on the Active Conformation of Gα i1–GTP

Alternatively spliced mu opioid receptor C termini impact the diverse actions of morphine

Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6

Small Molecule CXCR3 Antagonists

Cannabidiol displays unexpectedly high potency as an antagonist of CB1 and CB2 receptor agonists in vitro

Directional transition from initiation to elongation in bacterial translation

Allosteric Modulation of the Cannabinoid CB1 Receptor

Defining the Molecular Basis for the First Potent and Selective Orthosteric Agonists of the FFA2 Free Fatty Acid Receptor

Functional Characterization of Human Receptors for Short Chain Fatty Acids and Their Role in Polymorphonuclear Cell Activation

Novel Electrophilic and Photoaffinity Covalent Probes for Mapping the Cannabinoid 1 Receptor Allosteric Site(s)

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