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282 items found for "cAMP signaling"
- Ep 140 with Dr Alix A J Rouault
I then undertook my first project where I demonstrated that MRAP2 regulates the signaling of multiple Concurrently, I described the mechanisms by which MRAP2 regulates GHSR1a signaling; this project brought Using this novel technique, I showed that MRAP2 biased GHSR1a signaling and shut down its constitutive activity; this work resulted in a first author publication in Science Signaling. to create a scientific session at the American Physiology Summit (APS) 2024 dedicated to GPCR biased signaling
- GPCR Retreat Schedule 2023
of Saskatchewan Read More Friday, November 3rd / 11:55 AM Unveiling Non-Canonical Functions for Gαq Signaling Friday, November 3rd / 1:30 PM Interaction with the cell adhesion molecule NEGR1 affects mGluR5 cell signalling Silvio Gutkind UC San Diego Read More Friday, November 3rd / 3:55 PM Inhibition of Relaxin Autocrine Signaling November 4th / 7:30 AM Breakfast 2 Read More Saturday, November 4th / 8:15 AM Distinct sub-cellular signal Read More Saturday, November 4th / 8:40 AM Biochemical Mechanisms Underlying Location Bias in GPCR Signaling
- Developing a PROTAC to Degrade the Constitutively Active Onco-GPCR in Uveal Melanoma
Thomas Sakmar’s laboratory at Rockefeller University, where she studies the signaling and degradation She is currently working to understand the signaling and degradation of GPCRs in disease states to help
- Ep 64 with Dylan Eiger
Dylan's graduate research focuses on the mechanisms underlying biased signaling at GPCRs, specifically , the role of differential receptor phosphorylation (phosphorylation barcodes) and subcellular GPCR signaling
- Opposite Effects of Src Family Kinases on YAP and ERK Activation in Pancreatic Cancer Cells: Implications for Targeted Therapy
we identified potent positive crosstalk between insulin/IGF-1 receptors and G protein-coupled (GPCR) signaling systems leading to mitogenic signaling in PDAC cells. in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Deciphering a GPCR-lncRNA-miRNA Nexus: Identification of an Aberrant Therapeutic Target in Ovarian Cancer
Previous studies have identified the pivotal role of Lysophosphatidic acid (LPA)-signaling in ovarian In this study, we elucidate the tripartite interaction between LPA-signaling, UCA1, and let-7 miRNAs in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Ultrasensitive dose-response for asbestos cancer risk implied by new inflammation-mutation model
Such switches exhibit nonlinear signal-activation relationships. is here hypothesized to block or impede inflammation resolution (e.g., by doing so for GPCR-mediated signal in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Lactate receptor GPR81 drives breast cancer growth and invasiveness through regulation of ECM properties and Notch ligand DLL4
altered expression of genes related to GO/KEGG terms extracellular matrix, cell adhesion, and Notch signaling Notch signaling, particularly the Notch ligand Delta-like-4 (DLL4), was strikingly downregulated upon in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Exploiting frequent and specific expression of PRL3 in pediatric solid tumors for first-in-child use of PRL3-zumab humanized antibody
angiogenesis markers, and G-protein-coupled receptor (GPCR)-mitogen-activated protein kinase (MAPK) signaling Microarray profiling of PRL3-positive tumors showed elevation of angiogenin, TIMP1 and TIMP2, and GPCR-MAPK signaling in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Interrogating Multiscale Receptors Functions in Space
Beaulieu has pioneered work establishing a role for Beta-arrestin signaling in the brain in vivo and has demonstrated that mood stabilizer drugs (e.g. lithium) used for bipolar disorder therapy target signaling is presently investigating how cell surface express proteins can act as allosteric modulators of D2R signaling
- Comparative Analysis of the GNAI Family Genes in Glioblastoma through Transcriptomics and Single-Cell Technologies
ontology (GO) analyses were conducted to explore the role of GNAI3 in co-expressed genes and associated signaling G-protein-coupled receptor (GPCR) , genome , glioblastoma , malignancy , molecular biomarker , prognosis , signaling in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Ep 36 with Dr. Michel Bouvier
Since 2001, he holds the Canada Research Chair in Signal Transduction and Molecular Pharmacology. He is a world-renowned expert in the field of cell signaling and GPCRs and made seminal contributions In addition to paradigm shifts including inverse agonism, biased signaling, and pharmacological chaperones
- Emerging GPCR targets for AUD: Insights from preclinical studies
the largest group of membrane receptors in the central nervous system and one of the key proteins for signal in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Ep 85 with Nicholas Holliday
regulating appetite, metabolism, and the immune system, and the molecular mechanisms underlying the signaling where he is now Associate Professor, establishing a lab focused on G protein-coupled receptor kinetics, signaling
- Ep 73 with Dr. Aylin Hanyaloglu
she identified novel core cellular machinery critical for G protein-coupled receptor trafficking and signaling fundamental cell biological mechanisms regulating GPCR activity, including spatial control of GPCR signaling
- Activation of PI3K/Akt pathway by G protein-coupled receptor 37 promotes resistance to cisplatin-induced apoptosis in non-small cell lung cancer
Alterations in GPCR gene expression and dysregulation of signal transduction have been recognized as sensitivity to cisplatin, and affects tumor formation and growth. (3) GPR37 activates PI3K/Akt/mTOR signal in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Stimulation of ectopically expressed muscarinic receptors induces IFN-γ but suppresses IL-2 production by inhibiting activation of pAKT pathways in primary T cells
, 2023 Abstract "T cell antigen receptor stimulation induces tyrosine phosphorylation of downstream signaling Tags GPCR; T cells; muscarinic receptor; signaling. in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Ep 82 with Dr. Lauren M. Slosky
These ligands stimulate receptor β-arrestin recruitment without activating canonical G protein signaling Because BAMs engage less well-conserved allosteric sites and exert pathway-specific effects on receptor signaling , they are exciting tools for linking distinct signaling pathways with their physiological effects and
- Olfactory Receptors and Tumorigenesis: Implications for Diagnosis and Targeted Therapy
This review highlights the specific molecular actions and signaling pathways of olfactory receptors in in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Dopamine-Mediated Motor Recovery after Ischemic Stroke
The Tiberi Lab pursues the study of the molecular, structural, pharmacological and signaling features More specifically, we investigate the druggability potential of new signaling partners we identified
- Ep 151 with Dr GPCR Board
research program is to gain a thorough and mechanistic understanding of processes that control cell signaling The precise control of PAR signaling is critical for proper temporal and spatial dynamics of signaling Discovering new aspects of PAR signaling is important for increasing the fundamental knowledge of GPCR She has made numerous important discoveries related to the mechanisms that control PAR1 signaling and
- Ep 33 with Dr. David E. Gloriam
He is one of the coordinators of recommendations to describe ligand bias towards signaling probes and group recently developed an online resource of biased ligands and pathway effects to advance the biased signaling
- GPR37 promotes colorectal cancer against ferroptosis by reprogramming lipid metabolism via p38-SCD1 axis
that GPR37 modulates lipid metabolism in tumor cells by promoting SCD1 transcription via the MAPK-p38 signaling in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Ep 109 with Dr. Katarina Nemec
pharmacology while performing various cell-based experiments to understand the binding, activation, and signaling Babu lab to progress in the understanding of spatiotemporal regulation of biased GPCR activation and signaling
- Chemokine Cxcl1-Cxcl2 heterodimer is a potent neutrophil chemoattractant
Chemokine-mediated neutrophil recruitment is determined by Cxcr2 receptor signaling, Cxcr2 endocytosis in Oncology and Immunology Structural and molecular insights into GPCR function GPCR Activation and Signaling
- Illuminating Functional Selectivity and Allosterism at GPCRs.
innovative methods for in-cellulo measurement of protein-protein interactions, receptor trafficking and signalling His research program also studies the allosteric, biased signalling regulation of GPCR and has contributed
- Session V | Adhesion GPCR Workshop 2024 | Dr. GPCR Ecosystem
October 23-25 Download PDF Program HERE < Back to Full Agenda Session V Structural mechanisms of AGPCR signaling CELSR1 extracellular region reveal a compact multidomain module of fourteen domains which regulates signaling CELSR1 extracellular region reveal a compact multidomain module of fourteen domains which regulates signaling employ cellular assays with full-length CELSR1 and truncation constructs to assess the adhesive and signaling CADH1-8 module as necessary for cell adhesion and we show the C-terminal CAHD9-GAIN module regulates signaling
- GPCR Retreat 2023 - Part II
He has been also studying what aspects of GPCR signaling are regulated in a sex-selective manner and Thomas Sakmar’s laboratory at The Rockefeller University, where she study’s the signaling and degradation She is currently working to understand the signaling and degradation of GPCRs in disease states to help