Werner Syndrome
"Werner Syndrome" 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.
An autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcification, muscular atrophy, a tendency to diabetes mellitus, aged appearance of the face, baldness, and a high incidence of neoplastic disease.
Descriptor ID |
D014898
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MeSH Number(s) |
C16.320.925 C18.452.284.960
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Concept/Terms |
Werner Syndrome- Werner Syndrome
- Syndrome, Werner
- Werner's Syndrome
- Syndrome, Werner's
- Werners Syndrome
- Progeria, Adult
- Adult Progeria
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Below are MeSH descriptors whose meaning is more general than "Werner Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Werner Syndrome".
This graph shows the total number of publications written about "Werner Syndrome" by people in UAMS Profiles by year, and whether "Werner Syndrome" 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 |
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2017 | 1 | 0 | 1 | 2008 | 1 | 0 | 1 | 2007 | 1 | 0 | 1 | 2006 | 0 | 1 | 1 | 1995 | 0 | 1 | 1 | 1994 | 1 | 1 | 2 | 1993 | 1 | 0 | 1 | 1991 | 1 | 0 | 1 | 1990 | 2 | 0 | 2 | 1989 | 1 | 0 | 1 |
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Below are the most recent publications written about "Werner Syndrome" by people in Profiles over the past ten years.
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Ketkar A, Voehler M, Mukiza T, Eoff RL. Residues in the RecQ C-terminal Domain of the Human Werner Syndrome Helicase Are Involved in Unwinding G-quadruplex DNA. J Biol Chem. 2017 02 24; 292(8):3154-3163.
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People People who have written about this concept. _
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