 NIH 3T3 Cells
"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
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| MeSH Number(s) |
A11.251.210.100.550 A11.329.228.100.550
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| 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
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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, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 0 | 3 | 3 | | 2004 | 0 | 7 | 7 | | 2005 | 0 | 3 | 3 | | 2006 | 0 | 5 | 5 | | 2007 | 0 | 8 | 8 | | 2008 | 0 | 9 | 9 | | 2009 | 0 | 12 | 12 | | 2010 | 0 | 4 | 4 | | 2011 | 0 | 5 | 5 | | 2012 | 0 | 3 | 3 | | 2013 | 0 | 11 | 11 | | 2014 | 0 | 5 | 5 | | 2015 | 0 | 5 | 5 | | 2016 | 0 | 8 | 8 | | 2017 | 0 | 3 | 3 | | 2018 | 0 | 6 | 6 | | 2019 | 0 | 4 | 4 | | 2020 | 0 | 4 | 4 | | 2021 | 0 | 3 | 3 | | 2022 | 0 | 1 | 1 | | 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "NIH 3T3 Cells" by people in Profiles.
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Ni Q, Ge Z, Li Y, Shatkin G, Fu J, Sen A, Bera K, Yang Y, Wang Y, Wu Y, Nogueira Vasconcelos AC, Yan Y, Lin D, Feinberg AP, Konstantopoulos K, Sun SX. Cytoskeletal activation of NHE1 regulates mechanosensitive cell volume adaptation and proliferation. Cell Rep. 2024 12 24; 43(12):114992.
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Yitzhak Y, Gaikwad H, Weiss-Sadan T, Merquiol E, Turk B, Blum G. Improved Cathepsin Probes for Sensitive Molecular Imaging. Molecules. 2022 Jan 27; 27(3).
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Nick HJ, Zeitlin PL, Yadav S, Bratcher PE. Measurements of spontaneous CFTR-mediated ion transport without acute channel activation in airway epithelial cultures after modulator exposure. Sci Rep. 2021 11 19; 11(1):22616.
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Gupta A, Sasse SK, Gruca MA, Sanford L, Dowell RD, Gerber AN. Deconvolution of multiplexed transcriptional responses to wood smoke particles defines rapid aryl hydrocarbon receptor signaling dynamics. J Biol Chem. 2021 10; 297(4):101147.
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Yilmaz E, Kuehn HS, Odakir E, Niemela JE, Ozcan A, Eken A, Rohlfs M, Cansever M, Gok V, Aydin F, Karakukcu M, Hauck F, Klein C, Unal E, Rosenzweig SD, Patiroglu T. Common Variable Immunodeficiency, Autoimmune Hemolytic Anemia, and Pancytopenia Associated With a Defect in IKAROS. J Pediatr Hematol Oncol. 2021 04 01; 43(3):e351-e357.
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Li J, Agarwal E, Bertolini I, Seo JH, Caino MC, Ghosh JC, Kossenkov AV, Liu Q, Tang HY, Goldman AR, Languino LR, Speicher DW, Altieri DC. The mitophagy effector FUNDC1 controls mitochondrial reprogramming and cellular plasticity in cancer cells. Sci Signal. 2020 07 28; 13(642).
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Goldfarbmuren KC, Jackson ND, Sajuthi SP, Dyjack N, Li KS, Rios CL, Plender EG, Montgomery MT, Everman JL, Bratcher PE, Vladar EK, Seibold MA. Dissecting the cellular specificity of smoking effects and reconstructing lineages in the human airway epithelium. Nat Commun. 2020 05 19; 11(1):2485.
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Masuda M, Yamamoto H, Takei Y, Nakahashi O, Adachi Y, Ohnishi K, Ohminami H, Yamanaka-Okumura H, Sakaue H, Miyazaki M, Takeda E, Taketani Y. All-trans retinoic acid reduces the transcriptional regulation of intestinal sodium-dependent phosphate co-transporter gene (Npt2b). Biochem J. 2020 02 28; 477(4):817-831.
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Carberry BJ, Rao VV, Anseth KS. Phototunable Viscoelasticity in Hydrogels Through Thioester Exchange. Ann Biomed Eng. 2020 Jul; 48(7):2053-2063.
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Broeckel RM, Haese N, Ando T, Dmitriev I, Kreklywich CN, Powers J, Denton M, Smith P, Morrison TE, Heise M, DeFilippis V, Messaoudi I, Curiel DT, Streblow DN. Vaccine-Induced Skewing of T Cell Responses Protects Against Chikungunya Virus Disease. Front Immunol. 2019; 10:2563.
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