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Article

Requirement for ERCC-1 and ERCC-3 gene products in DNA excision repair in vitro. Complementation using rodent and human cell extracts.

The Journal of biological chemistry - 5 Apr 1992

Biggerstaff M, Wood R D

Abstract excerpt

Numerous rodent cell lines exist that have defects in nucleotide excision repair of DNA caused by alterations in genes that fall into 10 different complementation groups. The precise roles in the repair of these genes are unknown. We report here that extracts from Chinese hamster ovary cells of excision repair-defective complementation groups 1 and 3 are defective in DNA excision repair in a cell-free system. In...

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PMID: 1551896

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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Requirement for ERCC-1 and ERCC-3 gene products in DNA excision repair in vitro. Complementation using rodent and human cell extracts.PMID 1551896Read ↗

Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.Semantic proximity Read ↗

Molecular cloning and biological characterization of the human excision repair gene ERCC-3.Semantic proximity Read ↗

ERCC1 mutations in UV-sensitive Chinese hamster ovary (CHO) cell lines.Semantic proximity Read ↗

UV-sensitive rodent mutant cell lines of complementation groups 6 and 8 differ phenotypically from their human counterparts.Semantic proximity Read ↗

Activity of individual ERCC1 and XPF subunits in DNA nucleotide excision repair.Semantic proximity Read ↗

Reconstitution of mammalian excision repair activity with mutant cell-free extracts and XPAC and ERCC1 proteins expressed in Escherichia coli.Semantic proximity Read ↗

Phenotype of FAECB (Facility for Automated Experiments in Cell Biology) Chinese hamster ovary mutants with minimal UV-sensitivity.Semantic proximity Read ↗

Nucleotide excision repair proteins and their importance for radiation-enhanced transfection.Semantic proximity Read ↗

XR-C1, a new CHO cell mutant which is defective in DNA-PKcs, is impaired in both V(D)J coding and signal joint formation.Semantic proximity Read ↗

Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4.Semantic proximity Read ↗

Genetic complementation between UV-sensitive CHO mutants and xeroderma pigmentosum fibroblasts.Semantic proximity Read ↗

Molecular cloning of the human DNA excision repair gene ERCC-6.Semantic proximity Read ↗

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