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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1979-12-18
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pubmed:abstractText |
Cells from a xeroderma pigmentosum patient XP2BI who has reached 17 years of age with no keratoses or skin tumours constitute a new, 7th complementation group G. These cells exhibit a low residual level of excision repair, 2% of normal after a UV dose of 5 J/m2 and an impairment of post-replication repair characteristic of excision-defective XPs. They are also sensitive to the lethal effects of UV and defective in host-cell reactivation of UV-irradiated SV40 DNA.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
|
pubmed:issn |
0027-5107
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
62
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
183-90
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:492197-Adolescent,
pubmed-meshheading:492197-Cells, Cultured,
pubmed-meshheading:492197-DNA,
pubmed-meshheading:492197-DNA Repair,
pubmed-meshheading:492197-Female,
pubmed-meshheading:492197-Genetic Complementation Test,
pubmed-meshheading:492197-Humans,
pubmed-meshheading:492197-Skin,
pubmed-meshheading:492197-Ultraviolet Rays,
pubmed-meshheading:492197-Xeroderma Pigmentosum
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pubmed:year |
1979
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pubmed:articleTitle |
A seventh complementation group in excision-deficient xeroderma pigmentosum.
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pubmed:publicationType |
Journal Article,
Case Reports
|