"Genetic Vectors" 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.
DNA molecules capable of autonomous replication within a host cell and into which other DNA sequences can be inserted and thus amplified. Many are derived from PLASMIDS; BACTERIOPHAGES; or VIRUSES. They are used for transporting foreign genes into recipient cells. Genetic vectors possess a functional replicator site and contain GENETIC MARKERS to facilitate their selective recognition.
Descriptor ID |
D005822
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MeSH Number(s) |
G05.360.337
|
Concept/Terms |
Genetic Vectors- Genetic Vectors
- Genetic Vector
- Vector, Genetic
- Vectors, Genetic
Shuttle Vectors- Shuttle Vectors
- Shuttle Vector
- Vector, Shuttle
- Vectors, Shuttle
Cloning Vectors- Cloning Vectors
- Cloning Vector
- Vector, Cloning
- Vectors, Cloning
|
Below are MeSH descriptors whose meaning is more general than "Genetic Vectors".
Below are MeSH descriptors whose meaning is more specific than "Genetic Vectors".
This graph shows the total number of publications written about "Genetic Vectors" by people in this website by year, and whether "Genetic Vectors" 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 |
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1994 | 0 | 1 | 1 |
1996 | 0 | 1 | 1 |
2000 | 0 | 2 | 2 |
2001 | 0 | 3 | 3 |
2002 | 2 | 5 | 7 |
2003 | 0 | 3 | 3 |
2004 | 1 | 4 | 5 |
2005 | 1 | 7 | 8 |
2006 | 1 | 3 | 4 |
2007 | 0 | 2 | 2 |
2008 | 2 | 3 | 5 |
2009 | 1 | 2 | 3 |
2010 | 0 | 1 | 1 |
2011 | 1 | 3 | 4 |
2012 | 1 | 1 | 2 |
2013 | 0 | 2 | 2 |
2014 | 0 | 2 | 2 |
2015 | 0 | 2 | 2 |
2016 | 1 | 3 | 4 |
2017 | 0 | 2 | 2 |
2018 | 2 | 1 | 3 |
2019 | 1 | 1 | 2 |
2020 | 1 | 0 | 1 |
2021 | 0 | 2 | 2 |
2022 | 1 | 0 | 1 |
2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genetic Vectors" by people in Profiles.
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Analyzing efficiency of a lentiviral shRNA knockdown system in human enteroids using western blot and flow cytometry. STAR Protoc. 2024 Jun 21; 5(2):103082.
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Cloning BRD4 long isoform into overexpression vectors for stable overexpression of BRD4-L in mammalian cells. STAR Protoc. 2022 12 16; 3(4):101785.
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Combined ASBT Inhibitor and FGF15 Treatment Improves Therapeutic Efficacy in Experimental Nonalcoholic Steatohepatitis. Cell Mol Gastroenterol Hepatol. 2021; 12(3):1001-1019.
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Comparison of E. coli based self-inducible expression systems containing different human heat shock proteins. Sci Rep. 2021 02 25; 11(1):4576.
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Development of a Rat Sandwich-Cultured Hepatocytes Model Expressing Functional Human Organic Anion Transporting Polypeptide (OATP) 1B3: A Potential Screening Tool for Liver-Targeting Compounds. J Pharm Pharm Sci. 2021; 24:475-483.
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Intravesical nadofaragene firadenovec gene therapy for BCG-unresponsive non-muscle-invasive bladder cancer: a single-arm, open-label, repeat-dose clinical trial. Lancet Oncol. 2021 01; 22(1):107-117.
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Intravitreal AAV2.COMP-Ang1 Attenuates Deep Capillary Plexus Expansion in the Aged Diabetic Mouse Retina. Invest Ophthalmol Vis Sci. 2019 06 03; 60(7):2494-2502.
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Targeted Gene Replacement in Acinetobacter baumannii. Methods Mol Biol. 2019; 1946:95-106.
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Switchable genome editing via genetic code expansion. Sci Rep. 2018 07 03; 8(1):10051.
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Nanoparticles as Delivery Vehicles for the Treatment of Retinal Degenerative Diseases. Adv Exp Med Biol. 2018; 1074:117-123.