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73 items found for "Marie Sklodowska Curie"
- Lack of Oestrogen Receptor Expression in Breast Cancer Cells Does Not Correlate with Kisspeptin...
Not Correlate with Kisspeptin Signalling and Migration "Kisspeptin is an anti-metastatic mediator in many is related to the observed differences in β-arrestin complements warrants further investigation and may
- Role of G Protein-Coupled Receptors in Hepatic Stellate Cells and Approaches to Anti-Fibrotic ...
Like many other organs, various GPCRs play a role in regulating liver function. the role of GPCRs in hepatic stellate cells (HSCs), the primary cells that regulate liver fibrosis, may
- Rescue of Cell Surface Expression and Signaling of Mutant Follicle-Stimulating Hormone Receptors
Many cause receptor misfolding and failure to reach the cell surface.
- G protein-coupled receptor interactions and modification of signalling involving the ghrelin ...
receptors (MCR3), as well as the MCR3 accessory protein, MRAP2, providing possible mechanisms for its many
- A role for BET proteins in regulating basal, dopamine-induced and cAMP/PKA-dependent ...
Finally, we report that JQ1 treatment downregulated expression of many GPCRs and also impaired ERK1/2
- 📰 GPCR Weekly News, October 23 to 29, 2023
Find speaker details on the Live Talks page and mark your calendar HERE. extracellular calcium pathways Versatile lactate signaling via HCAR1: a multifaceted GPCR involved in many 2024 | Ligand Recognition and Molecular Gating Conference April 5 - 10, 2024 | AACR Annual Meeting May 13 - 17, 2024 | 20th Annual PEGS Boston Summit May 16 - 19, 2024 | ASPET 2024 May 27 - 29, 2024 | SLAS
- Decoding β-Arrestins: from Structure to function
The hypothesis arises that GPCR and β-arrestin-centered effector complexes vary based on subcellular For example, the binding sites for many β-arrestin interaction partners remain elusive, and certain effector proteins with overlapping sites may experience mutually exclusive binding due to steric hindrance (Crépieux Profiling Interactive Analysis (GEPIA) tool, it is evident that β-arrestin expression is dysregulated in many In certain cancer types, only one β-arrestin isoform's expression may be altered, while the other remains
- 📰 GPCR Weekly News, March 20 to 26, 2023
The delisting dilemma: Why do so many biotechs face being kicked off the Nasdaq?. (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).
- 📰 GPCR Weekly News, November 13 to 19, 2023
GPCR Newsletter and stay ahead of the curve with news on the Dr. agonists of FFAR4 for type 2 diabetes mellitus therapy Industry News OMass Therapeutics Welcomes Melissa Faris Physiology Summit April 5 - 10, 2024 | AACR Annual Meeting April 22 - 23, 2024 | Endocrine Metabolic GPCRs May 13 - 17, 2024 | 20th Annual PEGS Boston Summit May 16 - 19, 2024 | ASPET 2024 May 27 - 29, 2024 | SLAS
- Harnessing Deep Mutational Scanning for Enhanced Drug Discovery
combines high-throughput DNA sequencing with systematic mutagenesis to create and assess the impact of many
- 📰 GPCR Weekly News, May 29 to June 4, 2023
Below is your Classified GPCR News at a glance for May 29th to June 4th, 2023. Activity Models of Key GPCR Families in the Central Nervous System: A Tool for Many Purposes.
- Unlocking the Therapeutic Potential of Previously Undruggable GPCRs
However, the receptors that these medicines target have been described as the ‘low-hanging’ fruit, and many While these small protein GPCRs are valuable drug targets linked to serious diseases, many remain undrugged Since many inflammatory diseases are driven by inappropriate recruitment of monocytes into tissues, CCR2
- Transformative GPCR Insights: Unleash New Horizons in Science | Sep 9 - 15, 2024
by a single G protein-coupled receptor type (5-HT2A) GPCRs in Oncology and Immunology The power of many
- Unlocking Cell's Secrets: Spontaneous β-Arrestin-Membrane Preassociation Drives Receptor-Activation
physical barrier this lipid bilayer creates is dynamic and interactive, becoming the foundation for many
- Overview of adhesion GPCRs self-activation
its structure were not already complex enough, during their synthesis in the endoplasmic reticulum, many
- Glyco-sulfo hotspots in the chemokine receptor system
GalNAc-Ts, GalNAc-T1 was shown to be the most likely candidate for directly glycosylating CCR5 although T11 may are important PTMs in chemokine receptor biology and pharmacology however the reported effects can vary although direct effects of O-glycosylation removal are ruled out it is possible that indirect effects may also contribute to the observed phenotype since many glycosyltransferases and the two TPSTs also carry understanding on the dynamics and biological relevance of these PTMs in the chemokine receptor system which may
- An overview of the compartmentalized GPCR Signaling: Relevance and Implications
For example, the lipid composition of intracellular membranes may influence GPCR dynamics and signaling cellular compartments such as the nucleus or endosomes presents several pharmaceutical challenges for many These compartments have distinct biochemical environments, which may affect the stability and functionality This may involve the development of specialized delivery vehicles, such as nanoparticles or liposomes Tagging molecules may alter the conformation or activity of GPCRs, leading to unintended effects on downstream