"DNA Primers" 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.
Short sequences (generally about 10 base pairs) of DNA that are complementary to sequences of messenger RNA and allow reverse transcriptases to start copying the adjacent sequences of mRNA. Primers are used extensively in genetic and molecular biology techniques.
| Descriptor ID |
D017931
|
| MeSH Number(s) |
D13.695.578.424.450.275 D27.720.470.530.600.223.600
|
| Concept/Terms |
DNA Primers- DNA Primers
- Primers, DNA
- Oligodeoxyribonucleotide Primers
- Primers, Oligodeoxyribonucleotide
|
Below are MeSH descriptors whose meaning is more general than "DNA Primers".
Below are MeSH descriptors whose meaning is more specific than "DNA Primers".
This graph shows the total number of publications written about "DNA Primers" by people in this website by year, and whether "DNA Primers" 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 |
|---|
| 1994 | 0 | 3 | 3 |
| 1995 | 0 | 7 | 7 |
| 1996 | 0 | 1 | 1 |
| 1997 | 0 | 2 | 2 |
| 1998 | 0 | 4 | 4 |
| 1999 | 0 | 2 | 2 |
| 2000 | 0 | 2 | 2 |
| 2001 | 0 | 4 | 4 |
| 2002 | 0 | 3 | 3 |
| 2003 | 0 | 9 | 9 |
| 2004 | 0 | 11 | 11 |
| 2005 | 0 | 15 | 15 |
| 2006 | 0 | 2 | 2 |
| 2007 | 0 | 9 | 9 |
| 2008 | 0 | 3 | 3 |
| 2009 | 0 | 5 | 5 |
| 2010 | 1 | 0 | 1 |
| 2011 | 0 | 11 | 11 |
| 2012 | 0 | 9 | 9 |
| 2013 | 0 | 14 | 14 |
| 2014 | 0 | 6 | 6 |
| 2015 | 0 | 6 | 6 |
| 2016 | 0 | 4 | 4 |
| 2017 | 1 | 18 | 19 |
| 2018 | 1 | 14 | 15 |
| 2019 | 2 | 3 | 5 |
| 2020 | 4 | 15 | 19 |
| 2021 | 2 | 4 | 6 |
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Below are the most recent publications written about "DNA Primers" by people in Profiles.
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CoVrimer: A tool for aligning SARS-CoV-2 primer sequences and selection of conserved/degenerate primers. Genomics. 2021 09; 113(5):3174-3184.
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Isothermal recombinase polymerase amplification-lateral flow detection of SARS-CoV-2, the etiological agent of COVID-19. J Virol Methods. 2021 10; 296:114227.
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Highly Selective Multiplex Quantitative Polymerase Chain Reaction with a Nanomaterial Composite Hydrogel for Precise Diagnosis of Viral Infection. ACS Appl Mater Interfaces. 2021 Jul 07; 13(26):30295-30305.
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Comparison of SARS-CoV-2 N gene real-time RT-PCR targets and commercially available mastermixes. J Virol Methods. 2021 09; 295:114215.
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In-silico analysis of Covid-19 genome sequences of Indian origin: Impact of mutations in identification of SARS-Co-V2. Mol Cell Probes. 2021 08; 58:101748.
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Design and in silico validation of polymerase chain reaction primers to detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Sci Rep. 2021 06 15; 11(1):12565.
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Optimization of reaction condition of recombinase polymerase amplification to detect SARS-CoV-2 DNA and RNA using a statistical method. Biochem Biophys Res Commun. 2021 08 27; 567:195-200.
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Assessment of Successful qRT-PCR of SARS-CoV-2 Assay in Pool Screening Using Isopropyl Alcohol Purification Step in RNA Extraction. Biomed Res Int. 2021; 2021:6653950.
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Development and validation of a new triplex real-time quantitative reverse Transcriptase-PCR assay for the clinical detection of SARS-CoV-2. Mol Cell Probes. 2021 08; 58:101744.
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A DNA intercalating dye-based RT-qPCR alternative to diagnose SARS-CoV-2. RNA Biol. 2021 12; 18(12):2218-2225.