"Xeroderma Pigmentosum" 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.
A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA.
| Descriptor ID |
D014983
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| MeSH Number(s) |
C04.834.867 C16.131.831.936 C16.320.850.970 C17.800.600.925 C17.800.621.936 C17.800.804.936 C17.800.827.970 C18.452.284.975
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Xeroderma Pigmentosum".
Below are MeSH descriptors whose meaning is more specific than "Xeroderma Pigmentosum".
This graph shows the total number of publications written about "Xeroderma Pigmentosum" by people in this website by year, and whether "Xeroderma Pigmentosum" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 1 | 0 | 1 |
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Below are the most recent publications written about "Xeroderma Pigmentosum" by people in Profiles.
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Evans MD, Mistry V, Singh R, Gackowski D, R?zalski R, Siomek-Gorecka A, Phillips DH, Zuo J, Mullenders L, Pines A, Nakabeppu Y, Sakumi K, Sekiguchi M, Tsuzuki T, Bignami M, Olinski R, Cooke MS. Nucleotide excision repair of oxidised genomic DNA is not a source of urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine. Free Radic Biol Med. 2016 10; 99:385-391.
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Zeng X, Negrete GA, Kasmer C, Yang WW, Gearhart PJ. Absence of DNA polymerase eta reveals targeting of C mutations on the nontranscribed strand in immunoglobulin switch regions. J Exp Med. 2004 Apr 05; 199(7):917-24.