"United Kingdom" 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.
Country in northwestern Europe including Great Britain and the northern one-sixth of Ireland, located between the North Sea and north Atlantic Ocean. The capital is London.
| Descriptor ID |
D006113
|
| MeSH Number(s) |
Z01.542.363
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "United Kingdom".
Below are MeSH descriptors whose meaning is more specific than "United Kingdom".
This graph shows the total number of publications written about "United Kingdom" by people in this website by year, and whether "United Kingdom" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 2 | 2 |
| 2014 | 0 | 1 | 1 |
| 2015 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
| 2021 | 0 | 3 | 3 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "United Kingdom" by people in Profiles.
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Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank. BMC Med Genomics. 2022 05 21; 15(1):119.
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Impact of maternal antibodies and microbiota development on the immunogenicity of oral rotavirus vaccine in African, Indian, and European infants. Nat Commun. 2021 12 15; 12(1):7288.
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Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity. Hum Genet. 2022 Jan; 141(1):147-173.
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Early IFN-a signatures and persistent dysfunction are distinguishing features of NK cells in severe COVID-19. Immunity. 2021 11 09; 54(11):2650-2669.e14.
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Increasing prevalence of a fluoroquinolone resistance mutation amongst Campylobacter jejuni isolates from four human infectious intestinal disease studies in the United Kingdom. PLoS One. 2020; 15(1):e0227535.
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Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2. PLoS One. 2019; 14(12):e0225943.
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The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A. Sci Rep. 2015 Oct 14; 5:15065.
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The oestrogen receptor 2 (ESR2) gene in female-pattern hair loss: replication of association with rs10137185 in German patients. Br J Dermatol. 2014 Apr; 170(4):982-5.
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Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss. J Dermatol Sci. 2013 Nov; 72(2):186-8.
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Genome-wide comparison of medieval and modern Mycobacterium leprae. Science. 2013 Jul 12; 341(6142):179-83.
MeSH information
