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Results found for "FRET BRET"
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GPCR Binders, Drugs, and more Development of Macrocyclic Neurotensin Receptor Type 2 (NTS2) Opioid-Free Get your 5-day free trial TODAY!
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Structure-based drug discovery of a corticotropin-releasing hormone receptor 1 antagonist using an X-ray free-electron in GPCRs as Drug Targets: Allosteric Function and Biased Signaling" at the DOT NEW October 3, 2023 | FREE
- Structural basis for receptor selectivity and inverse agonism in S1P5 receptors
agonist determined by serial femtosecond crystallography (SFX) at the Pohang Accelerator Laboratory X-Ray Free
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- Structures of β 1-adrenergic receptor in complex with Gs and ligands of different efficacies
Biochemical investigations uncover that the intermediate state complex comprising β1-AR and nucleotide-free
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- GPR84 signaling promotes intestinal mucosal inflammation via enhancing NLRP3 inflammasome activation
inflammation via enhancing NLRP3 inflammasome activation in macrophages "The putative medium-chain free
- Identification and functional characterization of the sulfakinin and sulfakinin receptor in the...
in mortality of D. armandi and also led to an increase in trehalose and a decrease in glycogen and free
- C5aR2 receptor: The genomic twin of the flamboyant C5aR1
attempted to close the gap by generating highly refined model structures of C5aR2, respectively in free
- GPCR Weekly Whirlwind: Top Receptor Highlights from Sep 30 - Oct 6, 2024!
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- 📰 GPCR Weekly News, March 13 to 19, 2023
GPCR Binders, Drugs, and more Design of Drug Efficacy Guided by Free Energy Simulations of the β2-Adrenoceptor Monitoring the Reversibility of GPCR Signaling by Combining Photochromic Ligands with Label-free Impedance
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- From GPCR Data Chaos to Decisive Action
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Oncogenic signaling of the free-fatty acid receptors FFA1 and FFA4 in human breast carcinoma cells. Oligomerization of the heteromeric γ-aminobutyric acid receptor GABAB in a eukaryotic cell-free system
- High GPER expression in triple-negative breast cancer is linked to pro-metastatic pathways and...
a median follow-up interval of 67.1 months, a significant trend towards reduced distant metastasis-free
- The Imprecision Problem: Why Your GPCR Drug Discovery Program Is Off-Track Before It Even Starts
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- Conjugation Strategies for Probe Development
coupling is the most suited for bioconjugation with proteins, DNA, etc, thanks to its reaction with the free
- 📰 GPCR Weekly News, March 27 to April 4, 2023
FREE Symposium - IPI Surfacing (June 15, 2023) Training School on “Cell-based assays to study Adhesion (June 28 - 30, 2023) FREE 11th Adrenoceptor Symposium: Adrenoceptors and GPCR Signalling (June 30 - July
- Fluorescence based HTS compatible ligand binding assays for dopamine D3 receptors in baculovirus preparations and live cells
fluorescent label upon receptor binding, thus does not require the physical separation of the bound and free due to the ratiometric nature of the assay, the FA signal depends on the concentration of both the free Therefore, FA requires sufficient receptor concentration to achieve free achieve depletion of free fluorescent
- Molecular creativity in drug discovery
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- Radioligands vs. Fluorescent Ligands: Binding Assays
If you are curious about fluorescent probes, fluorescent probe design or GPCR tools, feel free to contact
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- How Schild Analysis Protects Your Conclusions in GPCR Research
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- Irreversible Drugs, Real Control: Design for Durable Target Engagement
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- How to Design GPCR Drugs That Work in Vivo: Strategy, Tools, and Insights
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- How to Use Statistical Methods to Strengthen Every GPCR Drug Discovery Decision
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- 📰 GPCR Weekly News, October 9 to 15, 2023
investigating the functional impact of other components of the Gαi3 heterotrimers Activation/Deactivation Free-Energy


















