"Receptors, CCR" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Chemokine receptors that are specific for CC CHEMOKINES.
| Descriptor ID |
D054388
|
| MeSH Number(s) |
D12.776.543.750.695.160.150 D12.776.543.750.705.852.125.150
|
| Concept/Terms |
Receptors, CCR- Receptors, CCR
- CC Chemokine Receptor
- Chemokine Receptor, CC
- CC Chemokine Receptors
- Chemokine Receptors, CC
- Chemokine (C-C Motif) Receptors
- CCR Receptors
|
Below are MeSH descriptors whose meaning is more general than "Receptors, CCR".
- Chemicals and Drugs [D]
- Amino Acids, Peptides, and Proteins [D12]
- Proteins [D12.776]
- Membrane Proteins [D12.776.543]
- Receptors, Cell Surface [D12.776.543.750]
- Receptors, G-Protein-Coupled [D12.776.543.750.695]
- Receptors, Chemokine [D12.776.543.750.695.160]
- Receptors, CCR [D12.776.543.750.695.160.150]
- Receptors, Immunologic [D12.776.543.750.705]
- Receptors, Cytokine [D12.776.543.750.705.852]
- Receptors, Chemokine [D12.776.543.750.705.852.125]
- Receptors, CCR [D12.776.543.750.705.852.125.150]
Below are MeSH descriptors whose meaning is more specific than "Receptors, CCR".
- Receptors, CCR
- Receptors, CCR1
- Receptors, CCR10
- Receptors, CCR2
- Receptors, CCR3
- Receptors, CCR4
- Receptors, CCR5
- Receptors, CCR6
- Receptors, CCR7
- Receptors, CCR8
This graph shows the total number of publications written about "Receptors, CCR" by people in this website by year, and whether "Receptors, CCR" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2017 | 0 | 3 | 3 |
| 2018 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Receptors, CCR" by people in Profiles.
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Association of CXCR6 with COVID-19 severity: delineating the host genetic factors in transcriptomic regulation. Hum Genet. 2021 Sep; 140(9):1313-1328.
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Genome and epigenome editing identify CCR9 and SLC6A20 as target genes at the 3p21.31 locus associated with severe COVID-19. Signal Transduct Target Ther. 2021 02 22; 6(1):85.
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[A poisoned gift]. Med Sci (Paris). 2020 Dec; 36(12):1233-1236.
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The Atypical Receptor CCRL2 Is Essential for Lung Cancer Immune Surveillance. Cancer Immunol Res. 2019 Nov; 7(11):1775-1788.
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A new method to cluster genomes based on cumulative Fourier power spectrum. Gene. 2018 Oct 05; 673:239-250.
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Gut microbiome influences efficacy of PD-1-based immunotherapy against epithelial tumors. Science. 2018 Jan 05; 359(6371):91-97.
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Gut-homing ?42PD1+Vd2 T cells promote innate mucosal damage via TLR4 during acute HIV type 1 infection. Nat Microbiol. 2017 Oct; 2(10):1389-1402.
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The atypical receptor CCRL2 is required for CXCR2-dependent neutrophil recruitment and tissue damage. Blood. 2017 09 07; 130(10):1223-1234.
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CCRL2, a fringe member of the atypical chemoattractant receptor family. Eur J Immunol. 2013 Jun; 43(6):1418-22.
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MyD88 is required for protection from lethal infection with a mouse-adapted SARS-CoV. PLoS Pathog. 2008 Dec; 4(12):e1000240.