"NIH 3T3 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 continuous cell line of high contact-inhibition established from NIH Swiss mouse embryo cultures. The cells are useful for DNA transfection and transformation studies. (From ATCC [Internet]. Virginia: American Type Culture Collection; c2002 [cited 2002 Sept 26]. Available from http://www.atcc.org/)
| Descriptor ID |
D041681
|
| MeSH Number(s) |
A11.251.210.100.550 A11.329.228.100.550
|
| Concept/Terms |
NIH 3T3 Cells- NIH 3T3 Cells
- 3T3 Cell, NIH
- Cell, NIH 3T3
- Cells, NIH 3T3
- NIH 3T3 Cell
- NIH-3T3 Cells
- Cell, NIH-3T3
- Cells, NIH-3T3
- NIH-3T3 Cell
- 3T3 Cells, NIH
|
Below are MeSH descriptors whose meaning is more general than "NIH 3T3 Cells".
Below are MeSH descriptors whose meaning is more specific than "NIH 3T3 Cells".
This graph shows the total number of publications written about "NIH 3T3 Cells" by people in this website by year, and whether "NIH 3T3 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 |
|---|
| 2003 | 0 | 8 | 8 |
| 2004 | 0 | 15 | 15 |
| 2005 | 0 | 13 | 13 |
| 2006 | 0 | 16 | 16 |
| 2007 | 1 | 19 | 20 |
| 2008 | 0 | 15 | 15 |
| 2009 | 0 | 9 | 9 |
| 2010 | 0 | 12 | 12 |
| 2011 | 0 | 9 | 9 |
| 2012 | 0 | 6 | 6 |
| 2013 | 0 | 4 | 4 |
| 2014 | 0 | 3 | 3 |
| 2015 | 0 | 9 | 9 |
| 2016 | 0 | 3 | 3 |
| 2017 | 0 | 3 | 3 |
| 2018 | 0 | 6 | 6 |
| 2019 | 0 | 5 | 5 |
| 2020 | 0 | 1 | 1 |
| 2021 | 0 | 3 | 3 |
| 2022 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
| 2024 | 0 | 2 | 2 |
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Below are the most recent publications written about "NIH 3T3 Cells" by people in Profiles.
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Genipin crosslinked quaternary ammonium chitosan hydrogels for wound dressings. Biomed Mater. 2024 Jun 26; 19(4).
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Gallic acid-loaded chitosan nanoparticles enhance the DNA damage and apoptotic features through inhibiting flap endonuclease-1 in triple-negative breast cancer cells. Environ Toxicol. 2024 Aug; 39(8):4171-4183.
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Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling. PLoS Genet. 2023 Nov; 19(11):e1011005.
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CIC missense variants contribute to susceptibility for spina bifida. Hum Mutat. 2022 12; 43(12):2021-2032.
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DNA polymerase zeta contributes to heterochromatin replication to prevent genome instability. EMBO J. 2021 11 02; 40(21):e104543.
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Quantitative proteomics identifies the core proteome of exosomes with syntenin-1 as the highest abundant protein and a putative universal biomarker. Nat Cell Biol. 2021 06; 23(6):631-641.
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PAF remodels the DREAM complex to bypass cell quiescence and promote lung tumorigenesis. Mol Cell. 2021 04 15; 81(8):1698-1714.e6.
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Adiponectin promotes myogenic differentiation via a Mef2C-AdipoR1 positive feedback loop. Gene. 2021 Mar 01; 771:145380.
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The synergy of germline C634Y and V292M RET mutations in a northern Chinese family with multiple endocrine neoplasia type 2A. J Cell Mol Med. 2020 11; 24(22):13163-13170.
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Enhancement of cell proliferation and motility of mammalian cells grown in co-culture with Pichia pastoris expressing recombinant human FGF-2. Protein Expr Purif. 2020 12; 176:105724.