Xeroderma Pigmentosum
"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 |
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1984 | 0 | 2 | 2 | 1997 | 1 | 0 | 1 | 2011 | 0 | 1 | 1 | 2015 | 1 | 0 | 1 | 2019 | 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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Godley LA. FouNdER mutations confer risk for leukemias. Blood. 2019 06 20; 133(25):2636-2638.
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Shah P, He YY. Molecular regulation of UV-induced DNA repair. Photochem Photobiol. 2015 Mar-Apr; 91(2):254-64.
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Liu D, Wu HZ, Zhang YN, Kang H, Sun MJ, Wang EH, Yang XL, Lian MQ, Yu ZJ, Zhao L, Olopade OI, Wei MJ. DNA repair genes XPC, XPG polymorphisms: relation to the risk of colorectal carcinoma and therapeutic outcome with Oxaliplatin-based adjuvant chemotherapy. Mol Carcinog. 2012 Oct; 51 Suppl 1:E83-93.
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Sam L, Liu Y, Li J, Friedman C, Lussier YA. Discovery of protein interaction networks shared by diseases. Pac Symp Biocomput. 2007; 76-87.
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Kim N, Kage K, Matsuda F, Lefranc MP, Storb U. B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes. J Exp Med. 1997 Aug 04; 186(3):413-9.
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Dritschilo A, Brennan T, Weichselbaum RR, Mossman KL. Response of human fibroblasts to low dose rate gamma irradiation. Radiat Res. 1984 Nov; 100(2):387-95.
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Weichselbaum RR. The role of DNA repair processes in the response of human tumors to fractionated radiotherapy. Int J Radiat Oncol Biol Phys. 1984 Jul; 10(7):1127-34.
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Selsky CA, Henson P, Weichselbaum RR, Little JB. Defective reactivation of ultraviolet light-irradiated herpesvirus by a Bloom's syndrome fibroblast strain. Cancer Res. 1979 Sep; 39(9):3392-6.
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Weichselbaum RR, Nove J, Little JB. Deficient recovery from potentially lethal radiation damage in ataxia telengiectasia and xeroderma pigmentosum. Nature. 1978 Jan 19; 271(5642):261-2.
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