scholarly article | Q13442814 |
P356 | DOI | 10.1007/BF02369437 |
P698 | PubMed publication ID | 9131015 |
P2093 | author name string | Weber CA | |
Salazar EP | |||
Lamerdin JE | |||
Kadkhodayan S | |||
P2860 | cites work | Molecular cloning and biological characterization of a human gene, ERCC2, that corrects the nucleotide excision repair defect in CHO UV5 cells | Q24339649 |
Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A. | Q34374647 | ||
Repair of (6-4)photoproducts correlates with split-dose recovery in UV-irradiated normal and hypersensitive rodent cells | Q38348045 | ||
Validation of conditions for efficient detection of HPRT and APRT mutations in suspension-cultured Chinese hamster ovary cells | Q42802074 | ||
Mutagenicity testing in mammalian cells. I. Derivation of a Chinese hamster ovary cell line heterozygous for the adenine phosphoribosyltransferase and thymidine kinase loci | Q42822811 | ||
P433 | issue | 6 | |
P304 | page(s) | 453-460 | |
P577 | publication date | 1996-11-01 | |
P1433 | published in | Somatic Cell and Molecular Genetics | Q7559232 |
P1476 | title | Construction of a functional cDNA clone of the hamster ERCC2 DNA repair and transcription gene | |
P478 | volume | 22 |
Q24554333 | A cell cycle-specific requirement for the XRCC1 BRCT II domain during mammalian DNA strand break repair |
Q36119231 | A requirement for PARP-1 for the assembly or stability of XRCC1 nuclear foci at sites of oxidative DNA damage |
Q24299831 | APLF (C2orf13) is a novel human protein involved in the cellular response to chromosomal DNA strand breaks |
Q40826799 | Codominance associated with overexpression of certain XPD mutations |
Q40674599 | Development and characterization of CHO repair-proficient cell lines for comparative mutagenicity and metabolism of heterocyclic amines from cooked food |
Q41075490 | Molecular analysis of ERCC2 mutations in the repair deficient hamster mutants UVL-1 and V-H1. |
Q34012637 | Restoration of nucleotide excision repair in a helicase-deficient XPD mutant from intragenic suppression by a trichothiodystrophy mutation |
Q28254858 | The protein kinase CK2 facilitates repair of chromosomal DNA single-strand breaks |