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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1990-6-27
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pubmed:abstractText |
Using a radiochromatographic assay, we have examined cis-syn cyclobutane-pyrimidine dimer removal after ultraviolet irradiation in cell lines representative of the first 6 complementation groups of Chinese hamster ovary DNA nucleotide excision repair mutants. AA8, the CHO cell line from which these mutants were derived, consistently showed normal dimer excision for a rodent cell. The mutants uniformly exhibited no significant dimer excision within the limits of determination. Additionally, V-H1, a mutant belonging to complementation group 2 and derived from V79 hamster cells, exhibited no dimer excision. Two UV5 derived transformants that carry the complementing human ERCC2 repair gene showed a capacity for dimer excision comparable to the AA8 wild-type cells.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0027-5107
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
235
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
157-63
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2342503-Animals,
pubmed-meshheading:2342503-Cell Line,
pubmed-meshheading:2342503-Cricetinae,
pubmed-meshheading:2342503-Cricetulus,
pubmed-meshheading:2342503-DNA, Bacterial,
pubmed-meshheading:2342503-DNA Repair,
pubmed-meshheading:2342503-Genes,
pubmed-meshheading:2342503-Humans,
pubmed-meshheading:2342503-Mutation,
pubmed-meshheading:2342503-Pyrimidine Dimers,
pubmed-meshheading:2342503-Transformation, Genetic,
pubmed-meshheading:2342503-Ultraviolet Rays
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pubmed:year |
1990
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pubmed:articleTitle |
Cyclobutane-pyrimidine dimer excision in UV-sensitive CHO mutants and the effect of the human ERCC2 repair gene.
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pubmed:affiliation |
Biology Division, Oak Ridge National Laboratory, TN 37831.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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