Publication for ICOS and BTLA
| Species | Symbol | Function* | Entrez Gene ID* | Other ID | Gene coexpression |
CoexViewer |
|---|---|---|---|---|---|---|
| hsa | ICOS | inducible T cell costimulator | 29851 | [link] | ||
| hsa | BTLA | B and T lymphocyte associated | 151888 |
| Pubmed ID | Priority | Text |
|---|---|---|
| 27577071 | 0.97 | B-and T-lymphocyte attenuator (BTLA), CD28, CD27, TIGIT and CD278, in circulating CD4+ and CD8+ T cells that were derived from normal donors (n = 10) or esophageal cancer patients (n = 10, Figure 1). |
| 0.97 | CD278, CD200, PD-1, BTLA, CD137L, CD273 and CD274) in CD4+ and CD8+ T cells of normal donors' peripheral blood mononuclear cells (PBMC) and esophageal cancer patients' PBMC. | |
| 0.54 | CD278, CD273 and CD274 on patient CD8+ T cells) showing expression and mean fluorescence intensity (MFI) of CD158, CTLA-4, CD28, CD27, CD160, TIM-3, CD137, TIGIT, CD278, CD200, PD-1, BTLA, CD137L, CD273 and CD274 in CD4+ and CD8+ T cells. | |
| 27911271 | 0.97 | BTLA, ITGAL, CTLA4, ICOS, PDCD1, and VTCN1 were reported as breast cancer risk mutations in previous studies (Supplementary Table S6). |
| 19247441 | 0.96 | BTLA and ICOS expressions by percentage and MFI in total CD8 T cells from blood and in liver-derived CD8 T cell subsets (PD-1-CTLA-4-, PD-1+CTLA-4-, PD-1+CTLA-4+) ex vivo from 5 chronic HCV patients. |
| 0.96 | BTLA and ICOS expression in PD-1+CTLA-4+ (Red), PD-1+CTLA-4- (Green) and PD-1-CTLA-4- (Blue) CD8 T cell subsets relative to isotype control (gray shade) in the histograms on the right. | |
| 0.93 | ICOS and BTLA expression levels were generally low, although a slight increase in ICOS expression was observed in PD-1+CTLA-4+ subset compared to others (median 2.4% vs 0.5% vs 0.1%, p = 0.049). | |
| 0.92 | ICOS or BTLA. | |
| 0.91 | ICOS or BTLA. | |
| 0.78 | BTLA+ (intrahepatic CD8 subsets: 0.1% vs. 0.4% vs. 0.3%, p = 0.364); %ICOS+ (intrahepatic CD8 subsets: 0.1% vs. 0.5% vs. 2.4%, p = 0.049); ICOS MFI (intrahepatic CD8 subsets: 43 vs. 50 vs. 78, p = 0.021). | |
| 28428203 | 0.96 | ICOS, PD1, BCL6, BTLA, and SAP, among other Tfh markers. |
| 0.69 | ICOS, BTLA, SAP, CD200, CXCL13, IL-21, C-MAF, BCL6, and BLIMP1) by TSLP-DC-induced CXCR5hiPD1hi cells was similar to tonsillar Tfh and GC Tfh cells. | |
| 24030473 | 0.95 | ICOS, BTLA, and Fas were higher in the TFH cell subset (Figure 5D). |
| 22753927 | 0.91 | ICOS, CD40 ligand (CD40L), OX40, PD-1, BTLA and CD84, the cytokine IL-21, the cytoplasmic adaptor protein SLAM-associated protein (SAP), and the transcription factors Bcl-6 and c-Maf. |
| 30984188 | 0.91 | ICOS), programmed death-1 (PD-1), and B and T-lymphocyte attenuator (BTLA); and the second is the tumor necrosis factor receptor (TNFR) superfamily (TNFRSF), which includes CD27, CD30, 4-1BB, herpesvirus entry mediator (HVEM), CD40, and OX40 (Table 1). |
| 27314219 | 0.87 | ICOS and BTLA receptors. |
| 30319637 | 0.75 | BTLA and VISTA, and of the latter 4-1BB (CD137), OX40 (CD134), ICOS, and CD40. |
| 24198743 | 0.72 | ICOS, and BTLA that transmit co-signals into T cells (Fig. 1). |
| 21074063 | 0.69 | ICOS, and BTLA. |
| 22548114 | 0.66 | ICOS; CD278), and B- and T-lymphocyte attenuator (BTLA; CD272); (2) CD2/signaling lymphocyte activation molecule (SLAM) family including SLAM (CD150), 2B4 (CD244), and CD48; (3) Ig family including T-cell immunoglobulin mucin-3 (TIM-3), CD160, and Lymphocyte-activation gene 3 (Lag-3); and (4) TNF-receptor superfamily including CD27. |
| 29995563 | 0.62 | BTLA, TIGIT, OX40, 4-1BB, CD27 and ICOS. |
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