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Results found for "Lauren T May"
- Community guidelines for GPCR ligand bias: IUPHAR review 32
Ligands eliciting biased signalling may constitute better drugs with higher efficacy and fewer adverse
- Adenosine receptor signalling in Alzheimer's disease
Despite a better understanding of the disease, the current mainstay of treatment cannot modify pathogenesis provide insights into some novel strategies, including allosterism and the targeting of oligomers, which may
- GPR110, a receptor for synaptamide, expressed in osteoclasts negatively regulates osteoclastogenesis
August 2022 "Bone remodeling is precisely regulated mainly by osteoblasts and osteoclasts. Considering that synaptamide is the endogenous metabolite of DHA, we hypothesized that DHA may inhibit
- 📰 GPCR Weekly News, January 30 to February 5, 2023
(May 22 - 26, 2023) 2nd LEAPS Meets Life Sciences Conference. (May 14 - 19, 2023) 8th and final ERNEST Meeting in Crete. (May 3 - 7, 2023).
- The complicated lives of GPCRs in cardiac fibroblasts
We discuss how such events may be distinct depending on where the GPCRs and their associated signaling
- Innovative Data-Driven Solutions: The pHSense Revolution
Behind Every Probe Is a Partnership While the final product may arrive neatly packaged, the journey behind
- 📰 GPCR Weekly News - January 9 to 15, 2023
(May 22 - 26, 2023) 2nd ERNEST Training School. (February 20 - March 3, 2023). GEM2023. (May 3-7, 2023). The Illuminating the Understudied Druggable Proteome Conference.
- Therapeutic validation of an orphan G protein-coupled receptor: The case of GPR84
Although blockade of GPR84 may potentially prove effective also in diseases associated with inflammation
- GPCR Therapeutics Expands Scientific Advisory Board
May 2022 "Seoul, South Korea, 28 April 2022 – GPCR therapeutics, Inc., a venture-backed clinical stage
- Nanobodies as Probes and Modulators of Cardiovascular G Protein-Coupled Receptors
We also discuss how advancing technologies to discover nanobodies with tailored specificities may expand
- Cholesterol occupies the lipid translocation pathway to block phospholipid scrambling by a GPCR
This mechanism may explain the inability of GPCRs to scramble lipids at the plasma membrane."
- A central alarm system that gates multi-sensory innate threat cues to the amygdala
The identification of unified innate threat pathways may provide insights into developing therapeutic
- Chemical Drug Matter : Rethinking the Molecules We Choose to Develop In Drug Discovery
This approach reveals: Hidden target overlap New therapeutic hypotheses “Off-target” effects that may They are mainstream pharmacology.
- Drug Discovery Picks Up the Pace, Stays on Target
A project to develop a perfect drug, or a drug that is as safe and effective as possible, may never begin
- GB83, an Agonist of PAR2 with a Unique Mechanism of Action Distinct from Trypsin and PAR2-AP
of the localization and function of PAR2 was significantly delayed after stimulation by GB83, which may
- The Five Traps of Ignoring Kinetics
Curves that “look fine” may hide non-equilibrated systems. The fix?
- Decoding Schild Analysis: The Pharmacologist’s Lens on Competitive Antagonism
Slopes <1 may reveal allosteric modulation , where the antagonist binds at a secondary site.
- Serotonin Receptor 5-HT2A Regulates TrkB Receptor Function in Heteroreceptor Complexes
cortex, hippocampus, and especially the striatum, demonstrating that the balance between TrkB and 5-HT2A may
- Successful prednisolone or calcimimetic treatment of acquired hypocalciuric hypercalcemia caused...
Our observations with these prominent commonalities may provide new insights into the phenotype and characteristics
- In vitro assays for the functional characterization of (psychedelic) substances at the serotonin...
perception, and thought, and have the activation of serotonin (5-HT) 2A receptors (5-HT2A Rs) as a main studies, both linked to the specific assay mechanism and linked to its specific execution, as these may
- Optimizing HTRF Assays with Fluorescent Ligands: Time-Resolved Fluorescence in GPCR Research
Curr Chem Genomics. 2009 May 28;3:22-32. doi: 10.2174/1875397300903010022.
- Pharmacological targeting of cGAS/STING-YAP axis suppresses pathological angiogenesis and...
Discovering new ways to ameliorate pathological angiogenesis may bypass organ fibrosis.
- Luciferase-based GloSensor™ cAMP assay: Temperature optimization and application to cell-based kinet
However, thermal instability of the biosensor may pose a problem for in vivo studies.
- Targeted Drug Design through GPCR Mutagenesis: Insights from β2AR
This suggests that conserved residues across species may be ideal drug targets, ensuring consistent efficacy
- Beyond Clearance: The Strategic Power of Irreversible Drug Binding
This PK/PD dissociation means: Drug exposure may end, but receptor occupancy remains.
- Increased Anxiety-like Behaviors in Adgra1-/- Male But Not Female Mice are Attributable to...
We found that Adgra1 is highly and exclusively expressed in the brain, suggesting that Adgra1 may be
- G protein-biased GPR3 signaling ameliorates amyloid pathology in a preclinical Alzheimer's disease..
accompanied by robust microglial and astrocytic hypertrophy, which suggest a protective glial response that may
- GASP1 enhances malignant phenotypes of breast cancer cells and decreases their response to...
their cellular response to paclitaxel by interacting with and stabilizing IGF1R, and suggests that it may
- High GPER expression in triple-negative breast cancer is linked to pro-metastatic pathways and...
These results may supply new insights into GPER-mediated estrogen carcinogenesis in TNBC, thus providing
- A new Kunitz-type snake toxin family associated with an original mode of interaction with the...
The number of MQ1 residues involved in V2R binding is large and may explain its absolute selectivity.







