Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro. - Wikidata - awgldk - TriplyDB

Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro.

Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro.

http://www.wikidata.org/entity/Q36757154

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Deficient expression of DNA repair enzymes in early progression to sporadic colon cancer The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells High mobility group A2 protein and its derivatives bind a specific region of the promoter of DNA repair gene ERCC1 and modulate its activity Mapping of interaction domains between human repair proteins ERCC1 and XPF Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23 Crystal structure and DNA binding functions of ERCC1, a subunit of the DNA structure-specific endonuclease XPF-ERCC1 Characterization of the XRCC1-DNA ligase III complex in vitro and its absence from mutant hamster cells Mutational analysis of the human nucleotide excision repair gene ERCC1 XPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexes Specific association between the human DNA repair proteins XPA and ERCC1 Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH)ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs An interaction between the DNA repair factor XPA and replication protein A appears essential for nucleotide excision repair First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure RAD1 and RAD10, but not other excision repair genes, are required for double-strand break-induced recombination in Saccharomyces cerevisiae.Activity of individual ERCC1 and XPF subunits in DNA nucleotide excision repair The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif.The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells ERCC1-XPF endonuclease facilitates DNA double-strand break repair Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia Oligo/polynucleotide-based gene modification: strategies and therapeutic potential Reduced hematopoietic reserves in DNA interstrand crosslink repair-deficient Ercc1-/- mice The structure-specific endonuclease Ercc1-Xpf is required to resolve DNA interstrand cross-link-induced double-strand breaks The XPA-binding domain of ERCC1 is required for nucleotide excision repair but not other DNA repair pathways.DNA repair gets physical: mapping an XPA-binding site on ERCC1 Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patients Prognostic significance of ERCC1 expression in postoperative patients with gastric cancer.The Drosophila meiotic recombination gene mei-9 encodes a homologue of the yeast excision repair protein Rad1.Processing of joint molecule intermediates by structure-selective endonucleases during homologous recombination in eukaryotes.Recruitment of damaged DNA to the nuclear matrix in hamster cells following ultraviolet irradiation.Mutations in XPA that prevent association with ERCC1 are defective in nucleotide excision repair.Polymorphisms in DNA-repair genes in a cohort of prostate cancer patients from different areas in Spain: heterogeneity between populations as a confounding factor in association studies.Role of the human ERCC-1 gene in gene-specific repair of cisplatin-induced DNA damage.DNA repair biomarkers XPF and phospho-MAPKAP kinase 2 correlate with clinical outcome in advanced head and neck cancer Oxaliplatin: pre-clinical perspectives on the mechanisms of action, response and resistance.Molecular cloning of the human nucleotide-excision-repair gene ERCC4 The ERCC1 and ERCC4 (XPF) genes and gene products Comparison of ERCC1/XPF genetic variation, mRNA and protein levels in women with advanced stage ovarian cancer treated with intraperitoneal platinum.An XPG DNA repair defect causing mutagen hypersensitivity in mouse leukemia L1210 cells.FANCM and FAAP24 maintain genome stability via cooperative as well as unique functions

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Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro.

http://www.wikidata.org/entity/Q36757154

description

1993 nî lūn-bûn

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Co-correction of the ERCC1, ER ...... F DNA repair defects in vitro.

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Co-correction of the ERCC1, ER ...... F DNA repair defects in vitro.

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Co-correction of the ERCC1, ER ...... F DNA repair defects in vitro.

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Co-correction of the ERCC1, ER ...... F DNA repair defects in vitro.

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Co-correction of the ERCC1, ER ...... F DNA repair defects in vitro.

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The EMBO Journal

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Co-correction of the ERCC1, ER ...... F DNA repair defects in vitro.

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Biggerstaff M

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Szymkowski DE

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Wood RD

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P2860

Oxidative stress and heat shock induce a human gene encoding a protein-tyrosine phosphatase

Evolution and mutagenesis of the mammalian excision repair gene ERCC-1

A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome

ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3

Rapid and efficient site-specific mutagenesis without phenotypic selection

RAD1, an excision repair gene of Saccharomyces cerevisiae, is also involved in recombination

Removal of nonhomologous DNA ends in double-strand break recombination: the role of the yeast ultraviolet repair gene RAD1.

RAD10, an excision repair gene of Saccharomyces cerevisiae, is involved in the RAD1 pathway of mitotic recombination.

Proliferating cell nuclear antigen is required for DNA excision repair

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

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