"Extremities" 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 farthest or outermost projections of the body, such as the HAND and FOOT.
Descriptor ID |
D005121
|
MeSH Number(s) |
A01.378
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Extremities".
Below are MeSH descriptors whose meaning is more specific than "Extremities".
This graph shows the total number of publications written about "Extremities" by people in this website by year, and whether "Extremities" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2011 | 0 | 1 | 1 |
2012 | 2 | 0 | 2 |
2013 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2018 | 0 | 2 | 2 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Extremities" by people in Profiles.
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Convergent and lineage-specific genomic differences in limb regulatory elements in limbless reptile lineages. Cell Rep. 2022 01 18; 38(3):110280.
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Phenotype loss is associated with widespread divergence of the gene regulatory landscape in evolution. Nat Commun. 2018 11 09; 9(1):4737.
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Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort. Hum Mutat. 2018 09; 39(9):1246-1261.
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Are hemipenial spines related to limb reduction? A spiny discussion focused on gymnophthalmid lizards (Squamata: Gymnophthalmidae). Anat Rec (Hoboken). 2014 Mar; 297(3):482-95.
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A comparative analysis of the post-cranial skeleton of fossorial and non-fossorial gymnophthalmid lizards. J Morphol. 2013 Aug; 274(8):845-58.
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Skeletal development in the fossorial gymnophthalmids Calyptommatus sinebrachiatus and Nothobachia ablephara. Zoology (Jena). 2012 Oct; 115(5):289-301.
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Embryonic development of the fossorial gymnophthalmid lizards Nothobachia ablephara and Calyptommatus sinebrachiatus. Zoology (Jena). 2012 Oct; 115(5):302-18.
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Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice. PLoS Genet. 2011 Jul; 7(7):e1002114.