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48 items found for "Leigh C Walker"
- Emerging GPCR targets for AUD: Insights from preclinical studies
Authors Roberta Goncalves Anversa, Maiya L Barron, Leigh C Walker, Andrew J Lawrence Source Contribute
- Phase 1/2 study of sorafenib added to cladribine, high-dose cytarabine, G-CSF, and mitoxantrone in untreated AML
Authors Anna B Halpern , Eduardo Rodríguez-Arbolí , Megan Othus , Kelsey-Leigh A Garcia , Mary-Elizabeth , Pamela S Becker , Jacob S Appelbaum , Janis L Abkowitz , Johnnie J Orozco , Siobán B Keel , Paul C Hendrie , Bart L Scott , M Cristina Ghiuzeli , Elihu H Estey , Roland B Walter Source Contribute to the
- [1,2,4]Triazolo[1,5-c]pyrimidines as Tools to Investigate A3 Adenosine Receptors in Cancer Cell Lines
< GPCR News < GPCRs in Oncology and Immunology [1,2,4]Triazolo[1,5-c]pyrimidines as Tools to Investigate In this work, a structural investigation on the two position of the [1,2,4]triazolo[1,5-c]pyrimidines adenosine receptor antagonists like the ethyl 2-(4-methoxyphenyl)-5-(methylamino)-[1,2,4]triazolo[1,5-c]
- [Inhibitory effect of downregulating G protein-coupled receptor class C group 5 member A expression on lipopolysaccharide-induced inflammatory response in human gingival fibroblasts]
GPCRs in Oncology and Immunology [Inhibitory effect of downregulating G protein-coupled receptor class C 2024 Abstract "Objective: To clarify the effect and the mechanism of G protein-coupled receptor class C
- G Protein-coupled Receptor-mediated Membrane Targeting of PLCγ2 is Essential for Neutrophil Chemotaxis
current dogma is that chemoattractants G protein-coupled receptors (GPCRs) activate β phospholipase C (PLCβ) while receptor tyrosine kinases (RTKs) activate γ phospholipase C (PLCγ). chemoattractant/GPCR-mediated membrane recruitment of PLCγ2 constitutes GPCR-mediated phospholipase C receptor (GPCR) , calcium-promoted Ras inactivator (CAPRI) , chemotaxis , neutrophils , phospholipase C (PLC) , g2 phospholipase C (PLCγ2) .
- Ep 74 with Dr. Daniel Wacker
Daniel Wacker About Dr. Daniel Wacker I obtained my B.Sc. degree from the University of Munich performing work in the lab of Daniel Wacker on the web Website LinkedIn Twitter PubMed Dr.
- The binding mechanism of an anti-multiple myeloma antibody to the human GPRC5D homodimer
antibody to the human GPRC5D homodimer Published date June 19, 2024 Abstract "GPRC5D is an atypical Class C Our structural analysis reveals that the GPRC5D presents a close resemblance to the typical Class C GPCRs head-to-head homodimer arrangement and interface mainly involving TM4, setting it apart from other Class C These insights not only unveil the distinctive dimer organization of this unconventional Class C GPCR
- Ep 140 with Dr Alix A J Rouault
described the molecular mechanisms of MRAP2 regulation of the GHSR1a, and where I notably developed the C-terminal This theory states that the post-translational modification of GHSR1a’ C-terminal tail is not a docking creating connections with biomedical industry, assessing professional opportunities, and seriously weighing
- GprC of the nematode-trapping fungus Arthrobotrys flagrans activates mitochondria and reprograms fungal cells for nematode hunting
The C. elegans ascaroside-sensing GPCR, SRBC66 and GPCRs of many fungi are also predicted for dual localization An SRBC64/66-GprC chimaeric protein was functional in A. flagrans, and C. elegans SRBC64/66 and DAF38 Authors Xiaodi Hu, David S Hoffmann, Mai Wang, Lars Schuhmacher, Maria C Stroe, Birgit Schreckenberger
- Natural carboxyterminal truncation of human CXCL10 attenuates glycosaminoglycan binding, CXCR3A signaling and lymphocyte chemotaxis, while retaining angiostatic activity
However, the biological effect of natural posttranslational processing of CXCL10 at the carboxy (C)-terminus We studied CXCL10(1-73), lacking the four endmost C-terminal amino acids, which was previously identified In contrast, loss of the four endmost C-terminal residues did not affect the inhibitory properties of Conclusion: Our study shows that the C-terminal residues Lys74-Pro77 of CXCL10 are important for GAG
- The β2-adrenergic receptor associates with CXCR4 multimers in human cancer cells
cancer cells Published date April 2, 2024 Abstract "While the existence and functional role of class C The C-X-C motif chemokine receptor 4 (CXCR4) is a class A GPCR that is a promising target of anticancer
- Expanding role of CXCR2 and therapeutic potential of CXCR2 antagonists in inflammatory diseases and cancers
of CXCR2 antagonists in inflammatory diseases and cancers Published date March 15, 2023 Abstract " C-X-C
- Structural Basis for the Recognition of GPRC5D by Talquetamab, a Bispecific Antibody for Multiple Myeloma
G-protein-coupled receptor class C group 5 member D (GPRC5D), an orphan GPCR predominantly expressed Jeong, Junhyeon Park, Geun Young Mo, Jinwoo Shin, Yunje Cho Tags GPRC5D , Multiple myeloma , class C
- Identification of Small-Molecule Antagonists Targeting the Growth Hormone Releasing Hormone Receptor (GHRHR)
growth hormone-releasing hormone (GHRH), have been proposed to bind in a two-step model, where first the C-terminal Panagiotopoulos, Robin du Preez, Michail Papadourakis, Konstantinos Tsianakas, Robert P Millar, Ross C
- Simultaneous activation of CXC chemokine receptor 4 and histamine receptor H1 enhances calcium signaling and cancer cell migration
receptor H1 enhances calcium signaling and cancer cell migration Published date February 1, 2023 Abstract "C-X-C
- Mechanistic exploration of bioactive constituents in Gnetum gnemon for GPCR-related cancer treatment through network pharmacology and molecular docking
Additionally, molecular docking experiments demonstrated the strong binding affinity of gnetin A, gnetin C, Authors Moragot Chatatikun, Nawanwat C Pattaranggoon, Imran Sama-Ae, Onggan Ranteh, Manlika Poolpirom
- G protein-coupled estrogen receptor (GPER)/GPR30 forms a complex with the β1-adrenergic receptor, a membrane-associated guanylate kinase (MAGUK) scaffold protein, and protein kinase A anchoring protein (AKAP) 5 in MCF7 breast cancer cells
Both receptors contain PSD-95/Discs-large/ZO-1 homology (PDZ) motifs in their C-terminal tails through Deleting the GPR30 C-terminal PDZ motif (-SSAV) does not interfere with the receptor complex, indicating
- Ep 23 with Dr. Qing Fan
Qing is a structural biologist interested in the molecular mechanisms controlling how class C GPCRs transmit
- Classified News | Dr. GPCR Ecosystem
receptors Read More October 29, 2024 Receptor determinants for ß-arrestin functional specificity at C-X-C
- Coronavirus Porcine Epidemic Diarrhea Virus Utilizes Chemokine Interleukin-8 to Facilitate Viral Replication by Regulating Ca2+ Flux
Finally, we identified that G protein-coupled receptor (GPCR)-phospholipase C (PLC)-inositol trisphosphate G protein-coupled receptor (GPCR)-phospholipase C (PLC)-inositol trisphosphate receptor (IP3R)-SOC signaling
- Exploration of prognostic and treatment markers in hepatocellular carcinoma via GPCR-related genes analysis
GPCR-related risk score containing eight GPCR-related genes (atypical chemokine receptor 3 (ACKR3), C-C
- Chemoattractant receptor signaling in humoral immunity
binding, GPCRs are phosphorylated by different GPCR kinases (GRKs) at distinct sites on the receptor C
- Ep 102 with Dr Caron Tribute Part 3
Josh C Snyder (2012) Dr.
- Neuroimmune interplay during type 2 inflammation: symptoms, mechanisms and therapeutic targets in atopic diseases
dermatitis , BAM8-22 , BP , Beta chain , Bovine adrenal medulla peptide 8-22 , Bullous pemphigoid , C-C
- CCL5-producing migratory dendritic cells guide CCR5+ monocytes into the draining lymph nodes
identified LN mononuclear phagocytes as monocytes, resident, or migratory type 1 and type 2 conventional (c)
- Ep 87 with Dr. Bianca Plouffe
molecular mechanisms involved in the opposite regulation of dopamine D1 and D5 receptors by protein kinase C.
- The GPCR adaptor protein Norbin controls the trafficking of C5aR1 and CXCR4 in mouse neutrophils
Authors Stephen A Chetwynd, Richard J Ward, Graeme Milligan, Heidi C E Welch Tags C5aR1 , CXCR4 , G protein-coupled
- Blockade of vasoactive intestinal peptide receptor 2 (VIPR2) signaling suppresses cyclin D1-dependent cell-cycle progression in MCF-7 cells
molecules, such as protein kinase A (PKA), phosphatidylinositol 3-kinase (PI3K), and phospholipase C.