 Plasmids
"Plasmids" 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.
Extrachromosomal, usually CIRCULAR DNA molecules that are self-replicating and transferable from one organism to another. They are found in a variety of bacterial, archaeal, fungal, algal, and plant species. They are used in GENETIC ENGINEERING as CLONING VECTORS.
| Descriptor ID |
D010957
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| MeSH Number(s) |
G05.360.600
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Plasmids".
Below are MeSH descriptors whose meaning is more specific than "Plasmids".
This graph shows the total number of publications written about "Plasmids" by people in this website by year, and whether "Plasmids" 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 |
|---|
| 1996 | 0 | 1 | 1 | | 1999 | 0 | 1 | 1 | | 2004 | 0 | 1 | 1 | | 2012 | 0 | 2 | 2 |
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Below are the most recent publications written about "Plasmids" by people in Profiles.
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Cottell JL, Kanwar N, Castillo-Courtade L, Chalmers G, Scott HM, Norby B, Loneragan GH, Boerlin P. blaCTX-M-32 on an IncN plasmid in Escherichia coli from beef cattle in the United States. Antimicrob Agents Chemother. 2013 Feb; 57(2):1096-7.
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Ramamoorthy A, Li L, Gaedigk A, Bradford LD, Benson EA, Flockhart DA, Skaar TC. In silico and in vitro identification of microRNAs that regulate hepatic nuclear factor 4a expression. Drug Metab Dispos. 2012 Apr; 40(4):726-33.
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Vyhlidal CA, Rogan PK, Leeder JS. Development and refinement of pregnane X receptor (PXR) DNA binding site model using information theory: insights into PXR-mediated gene regulation. J Biol Chem. 2004 Nov 05; 279(45):46779-86.
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McArthur CP, Wang Y, Heruth D, Gustafson S. Amplification of extracellular matrix and oncogenes in tat-transfected human salivary gland cell lines with expression of laminin, fibronectin, collagens I, III, IV, c-myc and p53. Arch Oral Biol. 2001 Jun; 46(6):545-55.
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Iwakuma T, Cui Y, Chang LJ. Self-inactivating lentiviral vectors with U3 and U5 modifications. Virology. 1999 Aug 15; 261(1):120-32.
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Martin ML, Lieberman PM, Curran T. Fos-Jun dimerization promotes interaction of the basic region with TFIIE-34 and TFIIF. Mol Cell Biol. 1996 May; 16(5):2110-8.
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Milch H, Czir?k E, Gad? I, Herpay M, Jakab M, Szalai G, Lantos J, Kiss L, Sztroj T, Csisz?r K, et al. Clonal distribution of K1 and K5 antigen possessing Escherichia coli isolates. Acta Microbiol Hung. 1991; 38(1):61-73.
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Gius D, Cao XM, Rauscher FJ, Cohen DR, Curran T, Sukhatme VP. Transcriptional activation and repression by Fos are independent functions: the C terminus represses immediate-early gene expression via CArG elements. Mol Cell Biol. 1990 Aug; 10(8):4243-55.
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Cohen DR, Ferreira PC, Gentz R, Franza BR, Curran T. The product of a fos-related gene, fra-1, binds cooperatively to the AP-1 site with Jun: transcription factor AP-1 is comprised of multiple protein complexes. Genes Dev. 1989 Feb; 3(2):173-84.
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Lee WM, Lin C, Curran T. Activation of the transforming potential of the human fos proto-oncogene requires message stabilization and results in increased amounts of partially modified fos protein. Mol Cell Biol. 1988 Dec; 8(12):5521-7.
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