 DNA Primers
"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
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| MeSH Number(s) |
D13.695.578.424.450.275 D27.720.470.530.600.223.600
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| Concept/Terms |
DNA Primers- DNA Primers
- Primers, DNA
- Oligodeoxyribonucleotide Primers
- Primers, Oligodeoxyribonucleotide
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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 | 15 | 15 | | 1995 | 0 | 19 | 19 | | 1996 | 0 | 21 | 21 | | 1997 | 0 | 12 | 12 | | 1998 | 0 | 9 | 9 | | 1999 | 0 | 7 | 7 | | 2000 | 0 | 5 | 5 | | 2001 | 0 | 6 | 6 | | 2002 | 0 | 5 | 5 | | 2003 | 0 | 9 | 9 | | 2004 | 0 | 11 | 11 | | 2005 | 0 | 13 | 13 | | 2006 | 0 | 9 | 9 | | 2007 | 0 | 8 | 8 | | 2008 | 0 | 7 | 7 | | 2009 | 0 | 3 | 3 | | 2010 | 0 | 7 | 7 | | 2011 | 1 | 5 | 6 | | 2012 | 0 | 6 | 6 | | 2013 | 0 | 4 | 4 | | 2014 | 0 | 3 | 3 | | 2015 | 0 | 2 | 2 |
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Below are the most recent publications written about "DNA Primers" by people in Profiles.
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Strong E, Butcher DT, Singhania R, Mervis CB, Morris CA, De Carvalho D, Weksberg R, Osborne LR. Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23. Am J Hum Genet. 2015 Aug 06; 97(2):216-27.
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Tong Y, Merino D, Nimmervoll B, Gupta K, Wang YD, Finkelstein D, Dalton J, Ellison DW, Ma X, Zhang J, Malkin D, Gilbertson RJ. Cross-Species Genomics Identifies TAF12, NFYC, and RAD54L as Choroid Plexus Carcinoma Oncogenes. Cancer Cell. 2015 May 11; 27(5):712-27.
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Reddy S, Fung A, Manlhiot C, Tierney ES, Chung WK, Blume E, Kaufman BD, Goldmuntz E, Colan S, Mital S. Adrenergic receptor genotype influences heart failure severity and ß-blocker response in children with dilated cardiomyopathy. Pediatr Res. 2015 Feb; 77(2):363-9.
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Caolo V, Swennen G, Chalaris A, Wagenaar A, Verbruggen S, Rose-John S, Molin DG, Vooijs M, Post MJ. ADAM10 and ADAM17 have opposite roles during sprouting angiogenesis. Angiogenesis. 2015 Jan; 18(1):13-22.
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Lin C, Chen MH, Yao E, Song H, Gacayan R, Hui CC, Chuang PT. Differential regulation of Gli proteins by Sufu in the lung affects PDGF signaling and myofibroblast development. Dev Biol. 2014 Aug 15; 392(2):324-33.
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Genovesi LA, Ng CG, Davis MJ, Remke M, Taylor MD, Adams DJ, Rust AG, Ward JM, Ban KH, Jenkins NA, Copeland NG, Wainwright BJ. Sleeping Beauty mutagenesis in a mouse medulloblastoma model defines networks that discriminate between human molecular subgroups. Proc Natl Acad Sci U S A. 2013 Nov 12; 110(46):E4325-34.
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Muñoz DM, Singh S, Tung T, Agnihotri S, Nagy A, Guha A, Zadeh G, Hawkins C. Differential transformation capacity of neuro-glial progenitors during development. Proc Natl Acad Sci U S A. 2013 Aug 27; 110(35):14378-83.
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Hayes M, Naito M, Daulat A, Angers S, Ciruna B. Ptk7 promotes non-canonical Wnt/PCP-mediated morphogenesis and inhibits Wnt/ß-catenin-dependent cell fate decisions during vertebrate development. Development. 2013 Apr; 140(8):1807-18.
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van de Hoef DL, Bonner JM, Boulianne GL. FKBP14 is an essential gene that regulates Presenilin protein levels and Notch signaling in Drosophila. Development. 2013 Feb; 140(4):810-9.
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Siriwardena K, Mackay N, Levandovskiy V, Blaser S, Raiman J, Kantor PF, Ackerley C, Robinson BH, Schulze A, Cameron JM. Mitochondrial citrate synthase crystals: novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations. Mol Genet Metab. 2013 Jan; 108(1):40-50.
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