Tumor Necrosis Factor Receptor Superfamily, Member 7
"Tumor Necrosis Factor Receptor Superfamily, Member 7" 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.
A member of the tumor necrosis factor receptor superfamily found on most T-LYMPHOCYTES. Activation of the receptor by CD70 ANTIGEN results in the increased proliferation of CD4-POSITIVE T-LYMPHOCYTES and CD8-POSITIVE T-LYMPHOCYTES. Signaling by the activated receptor occurs through its association with TNF RECEPTOR-ASSOCIATED FACTORS.
Descriptor ID |
D018127
|
MeSH Number(s) |
D12.776.543.750.705.852.760.048 D23.050.301.264.894.127 D23.101.100.894.127
|
Concept/Terms |
Tumor Necrosis Factor Receptor Superfamily, Member 7- Tumor Necrosis Factor Receptor Superfamily, Member 7
- CD27 Antigens
- TNFRSF7 Receptor
- Receptor, TNFRSF7
- T-Cell Activation Antigen
- Activation Antigen, T-Cell
- Antigen, T-Cell Activation
- T Cell Activation Antigen
- Antigen, CD27
- CD27 Antigen
- Antigens, CD27
|
Below are MeSH descriptors whose meaning is more general than "Tumor Necrosis Factor Receptor Superfamily, Member 7".
- 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, Immunologic [D12.776.543.750.705]
- Receptors, Cytokine [D12.776.543.750.705.852]
- Receptors, Tumor Necrosis Factor [D12.776.543.750.705.852.760]
- Tumor Necrosis Factor Receptor Superfamily, Member 7 [D12.776.543.750.705.852.760.048]
- Biological Factors [D23]
- Antigens [D23.050]
- Antigens, Surface [D23.050.301]
- Antigens, Differentiation [D23.050.301.264]
- Antigens, Differentiation, T-Lymphocyte [D23.050.301.264.894]
- Tumor Necrosis Factor Receptor Superfamily, Member 7 [D23.050.301.264.894.127]
- Biomarkers [D23.101]
- Antigens, Differentiation [D23.101.100]
- Antigens, Differentiation, T-Lymphocyte [D23.101.100.894]
- Tumor Necrosis Factor Receptor Superfamily, Member 7 [D23.101.100.894.127]
Below are MeSH descriptors whose meaning is more specific than "Tumor Necrosis Factor Receptor Superfamily, Member 7".
This graph shows the total number of publications written about "Tumor Necrosis Factor Receptor Superfamily, Member 7" by people in this website by year, and whether "Tumor Necrosis Factor Receptor Superfamily, Member 7" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2003 | 0 | 1 | 1 |
2008 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2016 | 0 | 2 | 2 |
2017 | 1 | 4 | 5 |
2018 | 1 | 3 | 4 |
2019 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Tumor Necrosis Factor Receptor Superfamily, Member 7" by people in Profiles.
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Optimization of antigen-specific CD8+ TÂ cell activation conditions for infectious diseases including COVID-19. STAR Protoc. 2021 09 17; 2(3):100789.
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Why does SARS-CoV-2 hit in different ways? Host genetic factors can influence the acquisition or the course of COVID-19. Eur J Med Genet. 2021 Jun; 64(6):104227.
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Interrogation of the cellular immunome of cancer patients with regard to the COVID-19 pandemic. J Immunother Cancer. 2021 03; 9(3).
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Storm of soluble immune checkpoints associated with disease severity of COVID-19. Signal Transduct Target Ther. 2020 09 07; 5(1):192.
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TLR9 signalling in HCV-associated atypical memory B cells triggers Th1 and rheumatoid factor autoantibody responses. J Hepatol. 2019 11; 71(5):908-919.
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Phenotypic Changes on Mycobacterium Tuberculosis-Specific CD4 T Cells as Surrogate Markers for Tuberculosis Treatment Efficacy. Front Immunol. 2018; 9:2247.
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Induction and Maintenance of CX3CR1-Intermediate Peripheral Memory CD8+ T Cells by Persistent Viruses and Vaccines. Cell Rep. 2018 Apr 17; 23(3):768-782.
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Activated Leukocyte Cell Adhesion Molecule Stimulates the T-Cell Response in Allergic Asthma. Am J Respir Crit Care Med. 2018 04 15; 197(8):994-1008.
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Enumeration, functional responses and cytotoxic capacity of MAIT cells in newly diagnosed and relapsed multiple myeloma. Sci Rep. 2018 03 07; 8(1):4159.
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Involvement of NK Cells in IL-28B-Mediated Immunity against Influenza Virus Infection. J Immunol. 2017 08 01; 199(3):1012-1020.