 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 |
|---|
| 2004 | 0 | 1 | 1 | | 2005 | 0 | 1 | 1 | | 2006 | 0 | 3 | 3 | | 2007 | 0 | 1 | 1 | | 2008 | 0 | 1 | 1 | | 2012 | 0 | 1 | 1 | | 2015 | 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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Adhikari AR, Geranpayeh T, Chu WK, Otteson DC. Improved cellular response of ion modified poly(lactic acid-co-glycolic acid) substrates for mouse fibroblast cells. Mater Sci Eng C Mater Biol Appl. 2016 Mar; 60:151-155.
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Xu R, Greening DW, Rai A, Ji H, Simpson RJ. Highly-purified exosomes and shed microvesicles isolated from the human colon cancer cell line LIM1863 by sequential centrifugal ultrafiltration are biochemically and functionally distinct. Methods. 2015 Oct 01; 87:11-25.
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Risebro CA, Petchey LK, Smart N, Gomes J, Clark J, Vieira JM, Yanni J, Dobrzynski H, Davidson S, Zuberi Z, Tinker A, Shui B, Tallini YI, Kotlikoff MI, Miquerol L, Schwartz RJ, Riley PR. Epistatic rescue of Nkx2.5 adult cardiac conduction disease phenotypes by prospero-related homeobox protein 1 and HDAC3. Circ Res. 2012 Jul 06; 111(2):e19-31.
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Ji H, Erfani N, Tauro BJ, Kapp EA, Zhu HJ, Moritz RL, Lim JW, Simpson RJ. Difference gel electrophoresis analysis of Ras-transformed fibroblast cell-derived exosomes. Electrophoresis. 2008 Jun; 29(12):2660-71.
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Sitharaman B, Tran LA, Pham QP, Bolskar RD, Muthupillai R, Flamm SD, Mikos AG, Wilson LJ. Gadofullerenes as nanoscale magnetic labels for cellular MRI. Contrast Media Mol Imaging. 2007 May-Jun; 2(3):139-46.
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Cariveaua MJ, Kalmus GW, Johnke RM, Allison RR, Evans M, Holbert D. Correlations between radiation-induced double strand breaks and cell cycle checkpoints in X-irradiated NIH/3T3 fibroblasts. Anticancer Res. 2006 Sep-Oct; 26(5A):3311-6.
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Lafontant PJ, Burns AR, Donnachie E, Haudek SB, Smith CW, Entman ML. Oncostatin M differentially regulates CXC chemokines in mouse cardiac fibroblasts. Am J Physiol Cell Physiol. 2006 Jul; 291(1):C18-26.
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Park JW, Kim S, Lim KJ, Simpson RJ, Kim YS, Bahk YY. A proteomic approach for unraveling the oncogenic H-Ras protein networks in NIH/3T3 mouse embryonic fibroblast cells. Proteomics. 2006 Feb; 6(4):1175-86.
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Cariveau MJ, Kovacs CJ, Allison RR, Johnke RM, Kalmus GW, Evans M. The expression of p21/WAF-1 and cyclin B1 mediate mitotic delay in x-irradiated fibroblasts. Anticancer Res. 2005 Mar-Apr; 25(2A):1123-9.
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Kalia SK, Lee S, Smith PD, Liu L, Crocker SJ, Thorarinsdottir TE, Glover JR, Fon EA, Park DS, Lozano AM. BAG5 inhibits parkin and enhances dopaminergic neuron degeneration. Neuron. 2004 Dec 16; 44(6):931-45.
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