"HEK293 Cells" 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 cell line generated from human embryonic kidney cells that were transformed with human adenovirus type 5.
| Descriptor ID |
D057809
|
| MeSH Number(s) |
A11.251.210.172.750 A11.436.334
|
| Concept/Terms |
HEK293 Cells- HEK293 Cells
- Cell, HEK293
- Cells, HEK293
- HEK293 Cell
- 293T Cells
- 293T Cell
- Cell, 293T
- Cells, 293T
- HEK 293 Cells
- 293 Cell, HEK
- 293 Cells, HEK
- Cell, HEK 293
- Cells, HEK 293
- HEK 293 Cell
- Human Kidney Cell Line 293
- Human Embryonic Kidney Cell Line 293
- HEK 293 Cell Line
|
Below are MeSH descriptors whose meaning is more general than "HEK293 Cells".
Below are MeSH descriptors whose meaning is more specific than "HEK293 Cells".
This graph shows the total number of publications written about "HEK293 Cells" by people in this website by year, and whether "HEK293 Cells" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 0 | 8 | 8 |
| 2011 | 0 | 24 | 24 |
| 2012 | 0 | 31 | 31 |
| 2013 | 0 | 38 | 38 |
| 2014 | 0 | 48 | 48 |
| 2015 | 0 | 36 | 36 |
| 2016 | 0 | 40 | 40 |
| 2017 | 0 | 52 | 52 |
| 2018 | 0 | 54 | 54 |
| 2019 | 0 | 42 | 42 |
| 2020 | 0 | 48 | 48 |
| 2021 | 0 | 46 | 46 |
| 2022 | 0 | 7 | 7 |
| 2023 | 1 | 5 | 6 |
| 2024 | 0 | 16 | 16 |
| 2025 | 0 | 34 | 34 |
| 2026 | 0 | 4 | 4 |
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Below are the most recent publications written about "HEK293 Cells" by people in Profiles.
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TFEB degradation is regulated by an IKK/?-TrCP2 phosphorylation-ubiquitination cascade. Nat Commun. 2026 04 01; 17(1).
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Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalities. Am J Hum Genet. 2026 03 05; 113(3):548-561.
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Structure-Activity Relationship Studies toward the Optimization of First-In-Class Selective Small Molecule Agonists of the GPCR Relaxin/Insulin-like Family Peptide Receptor 2. J Med Chem. 2026 Mar 12; 69(5):5956-5985.
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Unbalanced chromatin binding of Polycomb complexes drives neurodevelopmental disorders. Mol Cell. 2026 Feb 19; 86(4):604-624.e16.
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Mutational analysis of human norovirus VP2 elucidates critical molecular interactions for virus assembly. J Virol. 2026 02 17; 100(2):e0142025.
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Non-equilibrium snapshots of ligand efficacy at the ?-opioid receptor. Nature. 2026 04; 652(8110):794-802.
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Epigenome-wide association study of nuclear DNA methylation in relation to mitochondrial heteroplasmy. Nat Commun. 2025 Dec 02; 16(1):10962.
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Genetic variants in ESRRG are associated with a dominant non-progressive congenital movement disorder with ataxia. Am J Hum Genet. 2025 12 04; 112(12):2961-2972.
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MultiSite Assembly of Gateway Induced Clones (MAGIC): a flexible cloning toolbox for use in vertebrate model systems. Development. 2025 Nov 15; 152(22).
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ADNP Exhibits Methyltransferase Activity in Overexpression Systems and Modulates DNA and Histone Methylation. Autism Res. 2025 Nov; 18(11):2174-2191.