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Proteomics
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EFO:0001352
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pride
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Metabolic dysfunction-associated steatotic liver disease
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Bottom-up proteomics
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Mass Spectrometry
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Publication Date
2025
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2020
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2025
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Lab affiliation
1. Singapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), 8A Biomedical Grove, Immunos, Singapore 138648, Republic of Singapore 2. Department of Pharmacy, National University of Singapore 3. Biomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University, 3584 CH Utrecht, the Netherlands
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xref:PubMed:37690681
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Structural insights into CXCR4 modulation and oligomerization.
Not available
S-EPMC11832422
|
biostudies-literature
Cite
Chemokine receptor CXCR4 oligomerization is disrupted selectively by the antagonist ligand IT1t.
Not available
S-EPMC7949023
|
biostudies-literature
Cite
CCR5/CD4/CXCR4 oligomerization prevents HIV-1 gp120IIIB binding to the cell surface.
Not available
S-EPMC4024905
|
biostudies-literature
Cite
Single-molecule imaging reveals dimerization/oligomerization of CXCR4 on plasma membrane closely related to its function.
Not available
S-EPMC5715067
|
biostudies-literature
Cite
CXCR7/CXCR4 heterodimer constitutively recruits beta-arrestin to enhance cell migration.
Not available
S-EPMC3173186
|
biostudies-literature
Cite
Heparin oligosaccharides inhibit chemokine (CXC motif) ligand 12 (CXCL12) cardioprotection by binding orthogonal to the dimerization interface, promoting oligomerization, and competing with the chemokine (CXC motif) receptor 4 (CXCR4) N terminus.
Not available
S-EPMC3537072
|
biostudies-literature
Cite
The CXCL12/CXCR4/ACKR3 Signaling Axis Regulates PKM2 and Glycolysis
Not available
S-EPMC9179862
|
biostudies-literature
Cite
Disruption of constitutive CXCR4 oligomers impairs oncogenic properties in lymphoid neoplasms.
Not available
S-EPMC12184429
|
biostudies-literature
Cite
Regulation of CXCR4 function by S1P<sub>1</sub> through heteromerization.
Not available
S-EPMC11863771
|
biostudies-literature
Cite
Advanced fluorescence microscopy reveals disruption of dynamic CXCR4 dimerization by subpocket-specific inverse agonists.
Not available
S-EPMC7682396
|
biostudies-literature
Cite
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