Results 1 to 10 of about 369,183 (362)

Spatio-temporal regulation of concurrent developmental processes by generic signaling downstream of chemokine receptors [PDF]

open access: yeseLife, 2018
Chemokines are secreted proteins that regulate a range of processes in eukaryotic organisms. Interestingly, different chemokine receptors control distinct biological processes, and the same receptor can direct different cellular responses, but the basis ...
Divyanshu Malhotra   +3 more
doaj   +3 more sources

Endosomal chemokine receptor signalosomes regulate central mechanisms underlying cell migration [PDF]

open access: yeseLife
Chemokine receptors are GPCRs that regulate the chemotactic migration of a wide variety of cells including immune and cancer cells. Most chemokine receptors contain features associated with the ability to stimulate G protein signaling during β-arrestin ...
Hyunggu Hahn   +7 more
doaj   +2 more sources

Structural basis for chemokine recognition and receptor activation of chemokine receptor CCR5

open access: yesNature Communications, 2021
The chemokine receptor CCR5 plays multiple roles in the immune system. Here, structures of Gi1 protein-coupled CCR5 with or without a chemokine bound and of the CCR5- chemokine MIP-1 α complex offer insight into the distinct binding modes of the ligands ...
Hui Zhang   +11 more
doaj   +1 more source

Prospects for targeting ACKR1 in cancer and other diseases

open access: yesFrontiers in Immunology, 2023
The chemokine network is comprised of a family of signal proteins that encode messages for cells displaying chemokine G-protein coupled receptors (GPCRs).
Kyler S. Crawford, Brian F. Volkman
doaj   +1 more source

A Scintillation Proximity Assay for Real-Time Kinetic Analysis of Chemokine–Chemokine Receptor Interactions

open access: yesCells, 2022
Chemokine receptors are extensively involved in a broad range of physiological and pathological processes, making them attractive drug targets. However, despite considerable efforts, there are very few approved drugs targeting this class of seven ...
Stefanie Alexandra Eberle   +1 more
doaj   +1 more source

Development of tolerance to chemokine receptor antagonists: current paradigms and the need for further investigation

open access: yesFrontiers in Immunology, 2023
Chemokine G-protein coupled receptors are validated drug targets for many diseases, including cancer, neurological, and inflammatory disorders. Despite much time and effort spent on therapeutic development, very few chemokine receptor antagonists are ...
Patrick Grudzien   +3 more
doaj   +1 more source

Differential expression of chemokine receptors and their role in cancer imaging

open access: yesFrontiers in Oncology, 2012
Chemokine/chemokine receptor interactions play diverse roles in cell migration and homeostasis. Emerging evidence suggests that cancer cells co-opt chemokine networks for survival, proliferation, immune evasion and metastasis.
Sridhar eNimmagadda
doaj   +1 more source

Complex interplay of kinetic factors governs the synergistic properties of HIV-1 entry inhibitors. [PDF]

open access: yes, 2017
The homotrimeric HIV-1 envelope glycoprotein (Env) undergoes receptor-triggered structural changes that mediate viral entry through membrane fusion. This process is inhibited by chemokine receptor antagonists (CoRAs) that block Env-receptor interactions ...
Ahn, Koree W., Root, Michael J.
core   +2 more sources

The bovine chemokine receptors and their mRNA abundance in mononuclear phagocytes

open access: yesBMC Genomics, 2010
Background The chemokine and chemokine receptor families play critical roles in both the healthy and diseased organism mediating the migration of cells.
Ashley George   +7 more
doaj   +1 more source

Elevated ACKR2 expression is a common feature of inflammatory arthropathies [PDF]

open access: yes, 2017
Objectives. Chemokines are essential contributors to leucocyte accumulation at sites of inflammatory pathology. Interfering with chemokine or chemokine receptor function therefore represents a plausible therapeutic option.
Baldwin, Helen M.   +6 more
core   +1 more source

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