 Transfection
"Transfection" 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.
The uptake of naked or purified DNA by CELLS, usually meaning the process as it occurs in eukaryotic cells. It is analogous to bacterial transformation (TRANSFORMATION, BACTERIAL) and both are routinely employed in GENE TRANSFER TECHNIQUES.
| Descriptor ID |
D014162
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| MeSH Number(s) |
E05.393.350.810 G05.355.760.860
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Transfection".
Below are MeSH descriptors whose meaning is more specific than "Transfection".
This graph shows the total number of publications written about "Transfection" by people in this website by year, and whether "Transfection" 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 |
|---|
| 1981 | 0 | 2 | 2 | | 1982 | 1 | 0 | 1 | | 1983 | 0 | 1 | 1 | | 1987 | 2 | 1 | 3 | | 1988 | 1 | 6 | 7 | | 1989 | 2 | 9 | 11 | | 1990 | 2 | 11 | 13 | | 1991 | 0 | 16 | 16 | | 1992 | 0 | 11 | 11 | | 1993 | 1 | 28 | 29 | | 1994 | 1 | 29 | 30 | | 1995 | 1 | 23 | 24 | | 1996 | 3 | 26 | 29 | | 1997 | 1 | 28 | 29 | | 1998 | 1 | 21 | 22 | | 1999 | 1 | 28 | 29 | | 2000 | 2 | 30 | 32 | | 2001 | 3 | 47 | 50 | | 2002 | 0 | 42 | 42 | | 2003 | 1 | 36 | 37 | | 2004 | 0 | 37 | 37 | | 2005 | 1 | 52 | 53 | | 2006 | 2 | 38 | 40 | | 2007 | 1 | 41 | 42 | | 2008 | 0 | 28 | 28 | | 2009 | 2 | 29 | 31 | | 2010 | 1 | 28 | 29 | | 2011 | 0 | 20 | 20 | | 2012 | 0 | 23 | 23 | | 2013 | 0 | 9 | 9 | | 2014 | 1 | 6 | 7 | | 2015 | 0 | 13 | 13 | | 2016 | 0 | 12 | 12 | | 2017 | 1 | 4 | 5 | | 2018 | 0 | 6 | 6 | | 2019 | 0 | 2 | 2 | | 2020 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Transfection" by people in Profiles.
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Du X, Carvalho-de-Souza JL, Wei C, Carrasquel-Ursulaez W, Lorenzo Y, Gonzalez N, Kubota T, Staisch J, Hain T, Petrossian N, Xu M, Latorre R, Bezanilla F, Gomez CM. Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia. Proc Natl Acad Sci U S A. 2020 03 17; 117(11):6023-6034.
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Zhang Z, Liu J, Zeng Z, Fan J, Huang S, Zhang L, Zhang B, Wang X, Feng Y, Ye Z, Zhao L, Cao D, Yang L, Pakvasa M, Liu B, Wagstaff W, Wu X, Luo H, Zhang J, Zhang M, He F, Mao Y, Ding H, Zhang Y, Niu C, Haydon RC, Luu HH, Lee MJ, Wolf JM, Shao Z, He TC. lncRNA Rmst acts as an important mediator of BMP9-induced osteogenic differentiation of mesenchymal stem cells (MSCs) by antagonizing Notch-targeting microRNAs. Aging (Albany NY). 2019 12 11; 11(24):12476-12496.
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Rauch S, He E, Srienc M, Zhou H, Zhang Z, Dickinson BC. Programmable RNA-Guided RNA Effector Proteins Built from Human Parts. Cell. 2019 06 27; 178(1):122-134.e12.
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Kim JW, Kane JR, Panek WK, Young JS, Rashidi A, Yu D, Kanojia D, Hasan T, Miska J, Gómez-Lim MA, Ulasov IV, Balyasnikova IV, Ahmed AU, Wainwright DA, Lesniak MS. A Dendritic Cell-Targeted Adenoviral Vector Facilitates Adaptive Immune Response Against Human Glioma Antigen (CMV-IE) and Prolongs Survival in a Human Glioma Tumor Model. Neurotherapeutics. 2018 10; 15(4):1127-1138.
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Luo C, Yang X, Li M, Huang H, Kang Q, Zhang X, Hui H, Zhang X, Cen C, Luo Y, Xie L, Wang C, He T, Jiang D, Li T, An H. A novel strategy for in vivo angiogenesis and osteogenesis: magnetic micro-movement in a bone scaffold. Artif Cells Nanomed Biotechnol. 2018; 46(sup2):636-645.
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Liu M, Gou L, Xia J, Wan Q, Jiang Y, Sun S, Tang M, He T, Zhang Y. LncRNA ITGB2-AS1 Could Promote the Migration and Invasion of Breast Cancer Cells through Up-Regulating ITGB2. Int J Mol Sci. 2018 Jun 25; 19(7).
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Jara O, Minogue PJ, Berthoud VM, Beyer EC. Chemical chaperone treatment improves levels and distributions of connexins in Cx50D47A mouse lenses. Exp Eye Res. 2018 10; 175:192-198.
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Fry AE, Fawcett KA, Zelnik N, Yuan H, Thompson BAN, Shemer-Meiri L, Cushion TD, Mugalaasi H, Sims D, Stoodley N, Chung SK, Rees MI, Patel CV, Brueton LA, Layet V, Giuliano F, Kerr MP, Banne E, Meiner V, Lerman-Sagie T, Helbig KL, Kofman LH, Knight KM, Chen W, Kannan V, Hu C, Kusumoto H, Zhang J, Swanger SA, Shaulsky GH, Mirzaa GM, Muir AM, Mefford HC, Dobyns WB, Mackenzie AB, Mullins JGL, Lemke JR, Bahi-Buisson N, Traynelis SF, Iago HF, Pilz DT. De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain. 2018 03 01; 141(3):698-712.
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Pastor PDH, Du X, Fazal S, Davies AN, Gomez CM. Targeting the CACNA1A IRES as a Treatment for Spinocerebellar Ataxia Type 6. Cerebellum. 2018 02; 17(1):72-77.
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Alcantara D, Timms AE, Gripp K, Baker L, Park K, Collins S, Cheng C, Stewart F, Mehta SG, Saggar A, Sztriha L, Zombor M, Caluseriu O, Mesterman R, Van Allen MI, Jacquinet A, Ygberg S, Bernstein JA, Wenger AM, Guturu H, Bejerano G, Gomez-Ospina N, Lehman A, Alfei E, Pantaleoni C, Conti V, Guerrini R, Moog U, Graham JM, Hevner R, Dobyns WB, O'Driscoll M, Mirzaa GM. Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly. Brain. 2017 Oct 01; 140(10):2610-2622.
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