Mutant rodent cell lines sensitive to ultraviolet light, ionizing radiation and cross-linking agents: a comprehensive survey of genetic and biochemical characteristics.
about
Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23Correction of chromosomal instability and sensitivity to diverse mutagens by a cloned cDNA of the XRCC3 DNA repair geneThe human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cellsThe XRCC2 DNA repair gene from human and mouse encodes a novel member of the recA/RAD51 familyXPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexesDisruption of mouse SNM1 causes increased sensitivity to the DNA interstrand cross-linking agent mitomycin CNucleotide excision repair- and polymerase eta-mediated error-prone removal of mitomycin C interstrand cross-linksSpecific association between the human DNA repair proteins XPA and ERCC1Gene for the catalytic subunit of the human DNA-activated protein kinase maps to the site of the XRCC7 gene on chromosome 8DNA interstrand cross-links induce futile repair synthesis in mammalian cell extracts.Regulation of double-strand break-induced mammalian homologous recombination by UBL1, a RAD51-interacting proteinDNA interstrand crosslink repair in mammalian cells: step by step.Severe intrauterine growth retardation with increased mitomycin C sensitivity: a further chromosome breakage syndrome.Interstrand cross-links induce DNA synthesis in damaged and undamaged plasmids in mammalian cell extracts.Mutations in XPA that prevent association with ERCC1 are defective in nucleotide excision repair.Role of ERCC1 in removal of long non-homologous tails during targeted homologous recombination.Involvement of the Ku autoantigen in the cellular response to DNA double-strand breaks.Fork-like DNA templates support bypass replication of lesions that block DNA synthesis on single-stranded templates.DNA double-strand-break sensitivity, DNA replication, and cell cycle arrest phenotypes of Ku-deficient Saccharomyces cerevisiaeDeficient DNA repair capacity, a predisposing factor in breast cancer.Ku86 defines the genetic defect and restores X-ray resistance and V(D)J recombination to complementation group 5 hamster cell mutants.Functional nucleotide excision repair is required for the preferential removal of N-ethylpurines from the transcribed strand of the dihydrofolate reductase gene of Chinese hamster ovary cells.An XPG DNA repair defect causing mutagen hypersensitivity in mouse leukemia L1210 cells.DNA interstrand crosslink repair and cancer.Characterization of CHO XPF mutant UV41: influence of XPF heterozygosity on double-strand break-induced intrachromosomal recombination.ERCC1 is required for FANCD2 focus formation.Contributions of DNA interstrand cross-links to aging of cells and organisms.Ionizing radiation induces microhomology-mediated end joining in trans in yeast and mammalian cells.Immunodetection of DNA repair endonuclease ERCC1-XPF in human tissue.Ubiquitylation and the Fanconi anemia pathway.DNA interstrand crosslink repair in mammalian cells.Translesion DNA synthesis polymerases in DNA interstrand crosslink repair.EGFR-activating mutations correlate with a Fanconi anemia-like cellular phenotype that includes PARP inhibitor sensitivity.Defining the roles of nucleotide excision repair and recombination in the repair of DNA interstrand cross-links in mammalian cells.Role of the nucleotide excision repair gene ERCC1 in formation of recombination-dependent rearrangements in mammalian cells.XPF-ERCC1 participates in the Fanconi anemia pathway of cross-link repair.HHR23B, a human Rad23 homolog, stimulates XPC protein in nucleotide excision repair in vitro.Properties of damage-dependent DNA incision by nucleotide excision repair in human cell-free extracts.Repair kinetics of genomic interstrand DNA cross-links: evidence for DNA double-strand break-dependent activation of the Fanconi anemia/BRCA pathway.Branched oligonucleotides induce in vivo gene conversion of a mutated EGFP reporter.
P2860
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P2860
Mutant rodent cell lines sensitive to ultraviolet light, ionizing radiation and cross-linking agents: a comprehensive survey of genetic and biochemical characteristics.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh
1993年學術文章
@zh-hant
name
Mutant rodent cell lines sensi ...... d biochemical characteristics.
@en
type
label
Mutant rodent cell lines sensi ...... d biochemical characteristics.
@en
prefLabel
Mutant rodent cell lines sensi ...... d biochemical characteristics.
@en
P1433
P1476
Mutant rodent cell lines sensi ...... d biochemical characteristics.
@en
P2093
Collins AR
P304
P356
10.1016/0921-8777(93)90062-L
P407
P577
1993-01-01T00:00:00Z