"Sequence Homology, Nucleic Acid" 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 sequential correspondence of nucleotides in one nucleic acid molecule with those of another nucleic acid molecule. Sequence homology is an indication of the genetic relatedness of different organisms and gene function.
Descriptor ID |
D012689
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MeSH Number(s) |
G02.111.810.550 G05.810.550
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Concept/Terms |
Sequence Homology, Nucleic Acid- Sequence Homology, Nucleic Acid
- Nucleic Acid Sequence Homology
- Sequence Homology, Base
- Homology, Base Sequence
- Base Sequence Homology
- Base Sequence Homologies
- Homologies, Base Sequence
- Sequence Homologies, Base
- Homology, Nucleic Acid Sequence
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Below are MeSH descriptors whose meaning is more general than "Sequence Homology, Nucleic Acid".
Below are MeSH descriptors whose meaning is more specific than "Sequence Homology, Nucleic Acid".
- Sequence Homology, Nucleic Acid
- Synteny
This graph shows the total number of publications written about "Sequence Homology, Nucleic Acid" by people in this website by year, and whether "Sequence Homology, Nucleic Acid" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1996 | 0 | 1 | 1 |
1999 | 0 | 1 | 1 |
2003 | 0 | 3 | 3 |
2004 | 0 | 1 | 1 |
2006 | 0 | 1 | 1 |
2007 | 0 | 3 | 3 |
2008 | 0 | 2 | 2 |
2009 | 0 | 2 | 2 |
2011 | 0 | 3 | 3 |
2012 | 0 | 1 | 1 |
2015 | 0 | 2 | 2 |
2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Sequence Homology, Nucleic Acid" by people in Profiles.
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A C. elegans homolog for the UV-hypersensitivity syndrome disease gene UVSSA. DNA Repair (Amst). 2016 05; 41:8-15.
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MINCR is a MYC-induced lncRNA able to modulate MYC's transcriptional network in Burkitt lymphoma cells. Proc Natl Acad Sci U S A. 2015 Sep 22; 112(38):E5261-70.
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Heterochrony underpins natural variation in Cardamine hirsuta leaf form. Proc Natl Acad Sci U S A. 2015 Aug 18; 112(33):10539-44.
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Identifying transcriptional miRNA biomarkers by integrating high-throughput sequencing and real-time PCR data. Methods. 2013 Jan; 59(1):154-63.
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Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. Am J Hum Genet. 2011 Nov 11; 89(5):668-74.
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The Arabidopsis lyrata genome sequence and the basis of rapid genome size change. Nat Genet. 2011 May; 43(5):476-81.
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Directed networks reveal genomic barriers and DNA repair bypasses to lateral gene transfer among prokaryotes. Genome Res. 2011 Apr; 21(4):599-609.
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Simultaneous alignment of short reads against multiple genomes. Genome Biol. 2009; 10(9):R98.
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Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis. Nat Genet. 2009 Feb; 41(2):228-33.
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Sequencing of natural strains of Arabidopsis thaliana with short reads. Genome Res. 2008 Dec; 18(12):2024-33.