"Cellular Senescence" 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.
Process by which cells irreversibly stop dividing and enter a state of permanent growth arrest without undergoing CELL DEATH. Senescence can be induced by DNA DAMAGE or other cellular stresses, such as OXIDATIVE STRESS.
Descriptor ID |
D016922
|
MeSH Number(s) |
G04.043
|
Concept/Terms |
Cell Aging- Cell Aging
- Cellular Ageing
- Ageing, Cellular
- Aging, Cell
- Senescence, Replicative
- Cellular Aging
- Aging, Cellular
- Replicative Senescence
- Cell Ageing
- Ageing, Cell
Senescence-Associated Secretory Phenotype- Senescence-Associated Secretory Phenotype
- Phenotype, Senescence-Associated Secretory
- Secretory Phenotype, Senescence-Associated
- Senescence Associated Secretory Phenotype
|
Below are MeSH descriptors whose meaning is more general than "Cellular Senescence".
Below are MeSH descriptors whose meaning is more specific than "Cellular Senescence".
This graph shows the total number of publications written about "Cellular Senescence" by people in this website by year, and whether "Cellular Senescence" 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 |
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1994 | 1 | 1 | 2 |
1995 | 0 | 4 | 4 |
1996 | 0 | 1 | 1 |
1997 | 0 | 1 | 1 |
1998 | 1 | 0 | 1 |
2000 | 0 | 2 | 2 |
2001 | 0 | 3 | 3 |
2004 | 0 | 1 | 1 |
2006 | 0 | 2 | 2 |
2007 | 1 | 2 | 3 |
2008 | 2 | 0 | 2 |
2009 | 2 | 2 | 4 |
2010 | 0 | 3 | 3 |
2011 | 3 | 2 | 5 |
2012 | 1 | 1 | 2 |
2013 | 1 | 2 | 3 |
2014 | 1 | 5 | 6 |
2015 | 0 | 4 | 4 |
2016 | 3 | 0 | 3 |
2017 | 3 | 2 | 5 |
2018 | 1 | 2 | 3 |
2019 | 4 | 0 | 4 |
2020 | 2 | 2 | 4 |
2021 | 3 | 0 | 3 |
2022 | 0 | 3 | 3 |
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Below are the most recent publications written about "Cellular Senescence" by people in Profiles.
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Targeting telomerase reverse transcriptase with the covalent inhibitor NU-1 confers immunogenic radiation sensitization. Cell Chem Biol. 2022 10 20; 29(10):1517-1531.e7.
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Far-red Fluorescent Senescence-associated ?-Galactosidase Probe for Identification and Enrichment of Senescent Tumor Cells by Flow Cytometry. J Vis Exp. 2022 09 13; (187).
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Long-term male-specific chronic pain via telomere- and p53-mediated spinal cord cellular senescence. J Clin Invest. 2022 04 15; 132(8).
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Therapy-Induced Senescence: Opportunities to Improve Anticancer Therapy. J Natl Cancer Inst. 2021 10 01; 113(10):1285-1298.
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Elimination of Radiation-Induced Senescence in the Brain Tumor Microenvironment Attenuates Glioblastoma Recurrence. Cancer Res. 2021 12 01; 81(23):5935-5947.
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Autophagy and senescence in cancer therapy. Adv Cancer Res. 2021; 150:1-74.
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The Roles of Autophagy and Senescence in the Tumor Cell Response to Radiation. Radiat Res. 2020 08 01; 194(2):103-115.
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Advanced Age Increases Immunosuppression in the Brain and Decreases Immunotherapeutic Efficacy in Subjects with Glioblastoma. Clin Cancer Res. 2020 10 01; 26(19):5232-5245.
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Studies of Non-Protective Autophagy Provide Evidence that Recovery from Therapy-Induced Senescence is Independent of Early Autophagy. Int J Mol Sci. 2020 02 20; 21(4).
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Pan-cancer analysis of whole genomes. Nature. 2020 02; 578(7793):82-93.