 Base Pair Mismatch
"Base Pair Mismatch" 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 presence of an uncomplimentary base in double-stranded DNA caused by spontaneous deamination of cytosine or adenine, mismatching during homologous recombination, or errors in DNA replication. Multiple, sequential base pair mismatches lead to formation of heteroduplex DNA; (NUCLEIC ACID HETERODUPLEXES).
| Descriptor ID |
D020137
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| MeSH Number(s) |
G05.365.590.060
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| Concept/Terms |
Base Pair Mismatch- Base Pair Mismatch
- Mismatch, Base Pair
- Base Pair Mismatches
- Mismatches, Base Pair
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Below are MeSH descriptors whose meaning is more general than "Base Pair Mismatch".
Below are MeSH descriptors whose meaning is more specific than "Base Pair Mismatch".
This graph shows the total number of publications written about "Base Pair Mismatch" by people in this website by year, and whether "Base Pair Mismatch" 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 |
|---|
| 2001 | 0 | 1 | 1 | | 2002 | 0 | 2 | 2 | | 2004 | 1 | 0 | 1 | | 2006 | 0 | 2 | 2 | | 2009 | 0 | 1 | 1 | | 2010 | 0 | 1 | 1 | | 2015 | 0 | 1 | 1 | | 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Base Pair Mismatch" by people in Profiles.
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Potapov V, Ong JL, Langhorst BW, Bilotti K, Cahoon D, Canton B, Knight TF, Evans TC, Lohman GJS. A single-molecule sequencing assay for the comprehensive profiling of T4 DNA ligase fidelity and bias during DNA end-joining. Nucleic Acids Res. 2018 07 27; 46(13):e79.
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Lohman GJ, Bauer RJ, Nichols NM, Mazzola L, Bybee J, Rivizzigno D, Cantin E, Evans TC. A high-throughput assay for the comprehensive profiling of DNA ligase fidelity. Nucleic Acids Res. 2016 Jan 29; 44(2):e14.
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Mauris J, Evans TC. A human PMS2 homologue from Aquifex aeolicus stimulates an ATP-dependent DNA helicase. J Biol Chem. 2010 Apr 09; 285(15):11087-92.
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Huber DE, Markel ML, Pennathur S, Patel KD. Oligonucleotide hybridization and free-solution electrokinetic separation in a nanofluidic device. Lab Chip. 2009 Oct 21; 9(20):2933-40.
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Campbell CJ, Mountford CP, Stoquert HC, Buck AH, Dickinson P, Ferapontova E, Terry JG, Beattie JS, Walton AJ, Crain J, Ghazal P, Mount AR. A DNA nanoswitch incorporating the fluorescent base analogue 2-aminopurine detects single nucleotide mismatches in unlabelled targets. Analyst. 2009 Sep; 134(9):1873-9.
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Hardin JW, Batey RT. The bipartite architecture of the sRNA in an archaeal box C/D complex is a primary determinant of specificity. Nucleic Acids Res. 2006; 34(18):5039-51.
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Seinfeld J, Kleinschmidt-Demasters BK, Tayal S, Lillehei KO. Desmoid-type fibromatoses involving the brachial plexus: treatment options and assessment of c-KIT mutational status. J Neurosurg. 2006 May; 104(5):749-56.
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Ramirez-Aguilar KA, Kuchta RD. Herpes simplex virus-1 primase: a polymerase with extraordinarily low fidelity. Biochemistry. 2004 Jul 20; 43(28):9084-91.
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Yeager ME, Golpon HA, Voelkel NF, Tuder RM. Microsatellite mutational analysis of endothelial cells within plexiform lesions from patients with familial, pediatric, and sporadic pulmonary hypertension. Chest. 2002 Mar; 121(3 Suppl):61S.
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Kvaratskhelia M, Budihas SR, Le Grice SF. Pre-existing distortions in nucleic acid structure aid polypurine tract selection by HIV-1 reverse transcriptase. J Biol Chem. 2002 May 10; 277(19):16689-96.
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