"Base Sequence" 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 sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
| Descriptor ID |
D001483
|
| MeSH Number(s) |
G02.111.570.080 G05.360.080 L01.453.245.667.080
|
| Concept/Terms |
Base Sequence- Base Sequence
- Base Sequences
- Sequence, Base
- Sequences, Base
- Nucleotide Sequence
- Nucleotide Sequences
- Sequence, Nucleotide
- Sequences, Nucleotide
RNA Sequence- RNA Sequence
- RNA Sequences
- Sequence, RNA
- Sequences, RNA
DNA Sequence- DNA Sequence
- Sequence, DNA
- Sequences, DNA
- DNA Sequences
|
Below are MeSH descriptors whose meaning is more general than "Base Sequence".
Below are MeSH descriptors whose meaning is more specific than "Base Sequence".
This graph shows the total number of publications written about "Base Sequence" by people in this website by year, and whether "Base Sequence" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 |
| 1996 | 0 | 1 | 1 |
| 1999 | 0 | 1 | 1 |
| 2000 | 0 | 1 | 1 |
| 2005 | 0 | 2 | 2 |
| 2006 | 0 | 3 | 3 |
| 2007 | 0 | 2 | 2 |
| 2009 | 0 | 1 | 1 |
| 2013 | 0 | 1 | 1 |
| 2015 | 0 | 2 | 2 |
| 2019 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Base Sequence" by people in Profiles.
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Assessment and validation of enrichment and target capture approaches to improve Mycobacterium tuberculosis WGS from direct patient samples. J Clin Microbiol. 2023 10 24; 61(10):e0038223.
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Deep-intronic variants in CNGB3 cause achromatopsia by pseudoexon activation. Hum Mutat. 2020 01; 41(1):255-264.
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A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred. Clin Genet. 2016 07; 90(1):90-5.
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Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia. Am J Hum Genet. 2015 Apr 02; 96(4):519-31.
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Association between blood pressure and DNA methylation of retrotransposons and pro-inflammatory genes. Int J Epidemiol. 2013 Feb; 42(1):270-80.
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Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testing. Genet Med. 2011 Mar; 13(3):218-29.
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Human genetic variation recognizes functional elements in noncoding sequence. Genome Res. 2010 Mar; 20(3):311-9.
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Combinational polymorphisms of seven CXCL12-related genes are protective against breast cancer in Taiwan. OMICS. 2009 Apr; 13(2):165-72.
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Single nucleotide polymorphisms (SNPs) are highly conserved in rhesus (Macaca mulatta) and cynomolgus (Macaca fascicularis) macaques. BMC Genomics. 2007 Dec 31; 8:480.
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Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Nat Genet. 2007 May; 39(5):645-9.