| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1992PNAS...89..261F |
| P356 | DOI | 10.1073/PNAS.89.1.261 |
| P932 | PMC publication ID | 48216 |
| P698 | PubMed publication ID | 1729695 |
| P5875 | ResearchGate publication ID | 21425482 |
| P2093 | author name string | E C Friedberg | |
| R A Schultz | |||
| D Johns | |||
| W L Flejter | |||
| L D McDaniel | |||
| P2860 | cites work | Functional complementation of ataxia-telangiectasia group D (AT-D) cells by microcell-mediated chromosome transfer and mapping of the AT-D locus to the region 11q22-23. | Q37543742 |
| Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids | Q39536397 | ||
| Gene complementing xeroderma pigmentosum group A cells maps to distal human chromosome 9q. | Q41728943 | ||
| Human chromosome 15 confers partial complementation of phenotypes to xeroderma pigmentosum group F cells | Q41885493 | ||
| Purification and characterization of Rad3 ATPase/DNA helicase from Saccharomyces cerevisiae | Q43871631 | ||
| Human chromosome 9 can complement UV sensitivity of xeroderma pigmentosum group A cells | Q54324693 | ||
| Lack of complementation between xeroderma pigmentosum complementation groups D and H. | Q54360151 | ||
| An eighth complementation group of rodent cells hypersensitive to ultraviolet radiation | Q54373861 | ||
| Correction of a nucleotide-excision-repair mutation by human chromosome 19 in hamster-human hybrid cells | Q54458509 | ||
| DNA excision-repair processes in human cells can eliminate the cytotoxic and mutagenic consequences of ultraviolet irradiation | Q54567450 | ||
| Use of tritium-labeled precursors to select mutants | Q68221617 | ||
| Transient correction of excision repair defects in fibroblasts of 9 xeroderma pigmentosum complementation groups by microinjection of crude human cell extracts | Q68874149 | ||
| Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19 | Q69362984 | ||
| The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I | Q69949766 | ||
| A ninth complementation group in xeroderma pigmentosum, XP I | Q70077184 | ||
| A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome | Q24306514 | ||
| ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3 | Q24321908 | ||
| Molecular cloning and biological characterization of a human gene, ERCC2, that corrects the nucleotide excision repair defect in CHO UV5 cells | Q24339649 | ||
| Molecular cloning of the human DNA excision repair gene ERCC-6 | Q24596936 | ||
| A rapid alkaline extraction procedure for screening recombinant plasmid DNA | Q24614998 | ||
| Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 | ||
| Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain | Q28260027 | ||
| Molecular cloning of a human DNA repair gene | Q28268869 | ||
| Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization | Q29616823 | ||
| Expression of the cDNA for the beta subunit of human casein kinase II confers partial UV resistance on xeroderma pigmentosum cells | Q33256194 | ||
| Assignment of the human casein kinase II beta-subunit gene to 6p12----p21. | Q34286354 | ||
| Molecular cloning of a mouse DNA repair gene that complements the defect of group-A xeroderma pigmentosum | Q34291583 | ||
| Complementation of a DNA repair defect in xeroderma pigmentosum cells by transfer of human chromosome 9. | Q34319427 | ||
| Complementation of the UV-sensitive phenotype of a xeroderma pigmentosum human cell line by transfection with a cDNA clone library | Q34375550 | ||
| Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10. | Q34383546 | ||
| Microcell-mediated transfer of a single human chromosome complements xeroderma pigmentosum group A fibroblasts | Q34631750 | ||
| Cloning of the functional human excision repair gene ERCC-5: potential gene regulatory features conserved with other human repair genes. | Q34867667 | ||
| Mutation of lysine-48 to arginine in the yeast RAD3 protein abolishes its ATPase and DNA helicase activities but not the ability to bind ATP. | Q35990517 | ||
| Ultraviolet light induction of diphtheria toxin-resistant mutants of normal and xeroderma pigmentosum human fibroblasts | Q37340364 | ||
| A DNA repair gene required for the incision of damaged DNA is essential for viability in Saccharomyces cerevisiae | Q37344904 | ||
| Isolation and characterization of the RAD3 gene of Saccharomyces cerevisiae and inviability of rad3 deletion mutants | Q37349371 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | xeroderma pigmentosum | Q612693 |
| P304 | page(s) | 261-265 | |
| P577 | publication date | 1992-01-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene | |
| P478 | volume | 89 |
| Q98502743 | A Japanese girl with mild xeroderma pigmentosum group D neurological disease diagnosed using whole-exome sequencing |
| Q40540731 | A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy. |
| Q38358848 | ATPase activity of UvrB protein form Thermus thermophilus HB8 and its interaction with DNA. |
| Q34387466 | Analysis of Mutations in the XPD Gene in Italian Patients with Trichothiodystrophy: Site of Mutation Correlates with Repair Deficiency, but Gene Dosage Appears to Determine Clinical Severity |
| Q49761534 | Association Between the Asp312Asn, Lys751Gln, and Arg156Arg Polymorphisms in XPD and the Risk of Prostate Cancer |
| Q35535254 | Association between XPD Lys751Gln and Asp312Asn polymorphisms and hepatocellular carcinoma risk: a systematic review and meta-analysis |
| Q40021383 | Characterization of DNA synthesis and DNA-dependent ATPase activity at a restrictive temperature in temperature-sensitive tsFT848 cells with thermolabile DNA helicase B. |
| Q41597647 | Characterization of a complex chromosomal rearrangement maps the locus for in vitro complementation of xeroderma pigmentosum group D to human chromosome band 19q13 |
| Q24673129 | Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3 |
| Q36757154 | Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro |
| Q24532391 | Cockayne syndrome: defective repair of transcription? |
| Q28268594 | Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2 |
| Q48392528 | DNA Repair Gene ERCC1 and XPD Polymorphisms Predict Glioma Susceptibility and Prognosis |
| Q39583788 | DNA adduct levels and DNA repair polymorphisms in traffic-exposed workers and a general population sample |
| Q35961508 | DNA helicases involved in DNA repair and their roles in cancer |
| Q37586665 | DNA repair gene polymorphisms and risk of cutaneous melanoma: a systematic review and meta-analysis |
| Q57417728 | DNA repair gene polymorphisms, bulky DNA adducts in white blood cells and bladder cancer in a case-control study |
| Q36718103 | DNA repair protein XPA binds replication protein A (RPA). |
| Q67482181 | DNA repair: two pieces of the puzzle |
| Q59034732 | Damage-limitation exercises |
| Q35881437 | Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy |
| Q35955386 | Diagnosis of eight groups of xeroderma pigmentosum by genetic complementation using recombinant adenovirus vectors |
| Q26851006 | Do mutator mutations fuel tumorigenesis? |
| Q24647834 | ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs |
| Q46002619 | Electron crystal structure of the transcription factor and DNA repair complex, core TFIIH. |
| Q24564202 | Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15 |
| Q41581872 | Elevation of sister chromatid exchange frequency in transformed human fibroblasts following exposure to widely used aminoglycosides |
| Q73833651 | Evidence for Nucleotide Excision Repair as a Modifying Factor ofO6-Methylguanine-DNA Methyltransferase-Mediated Innate Chloroethylnitrosourea Resistance in Human Tumor Cell Lines |
| Q40873926 | Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F. |
| Q48469185 | Excision Repair Cross-complementing Rodent Repair Deficiency Gene 2 Expression and Chloroethylnitrosourea Resistance in Human Glioma Cell Lines |
| Q36694414 | Expression and Functional Analyses of the Dxpa Gene, the Drosophila Homolog of the Human Excision Repair Gene XPA |
| Q28115748 | Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C |
| Q48784329 | From xeroderma pigmentosum to the biological clock contributions of Dirk Bootsma to human genetics |
| Q35847090 | Functional interactions between p53 and the TFIIH complex are affected by tumour-associated mutations |
| Q36793490 | Genomic copy number changes of DNA repair genes ERCC1 and ERCC2 in human gliomas |
| Q40019757 | HHR23B, a human Rad23 homolog, stimulates XPC protein in nucleotide excision repair in vitro |
| Q24629606 | Human ERCC5 cDNA-cosmid complementation for excision repair and bipartite amino acid domains conserved with RAD proteins of Saccharomyces cerevisiae and Schizosaccharomyces pombe |
| Q70497043 | Human chromosome 11 complements ataxia-telangiectasia cells but does not complement the defect in AT-like Chinese hamster cell mutants |
| Q32006420 | Human nucleotide excision repair protein XPA: Extended X‐ray absorption fine‐structure evidence for a metal‐binding domain |
| Q28268603 | Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5 |
| Q24321650 | Implication of mammalian ribosomal protein S3 in the processing of DNA damage |
| Q28587990 | Mice with DNA repair gene (ERCC-1) deficiency have elevated levels of p53, liver nuclear abnormalities and die before weaning |
| Q43978101 | Molecular Diagnosis of Genodermatoses |
| Q49734875 | Molecular and Clinical Insights into the Role and Significance of Mutated DNA Repair Genes in Bladder Cancer |
| Q24672295 | Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome |
| Q24306411 | Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli Rec Q helicase and localization of the gene at chromosome 12p12 |
| Q35600010 | Molecular cloning of the human nucleotide-excision-repair gene ERCC4 |
| Q38708551 | Monochromosomal Hybrids and Chromosome Transfer: A Functional Approach for Gene Identification |
| Q38307435 | Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function |
| Q32014449 | Mutational analysis of a function of xeroderma pigmentosum group A (XPA) protein in strand-specific DNA repair |
| Q35238400 | Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group |
| Q41465447 | Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy |
| Q44241769 | Parental 5-methylcytosine methylation patterns are stable upon inter-species hybridization of Xiphophorus (Teleostei: Poeciliidae) fish |
| Q36685713 | Partial characterization of the DNA repair protein complex, containing the ERCC1, ERCC4, ERCC11 and XPF correcting activities |
| Q34671366 | Persistent DNA damage inhibits S-phase and G2 progression, and results in apoptosis |
| Q33643996 | Polymorphisms of DNA repair genes OGG1 and XPD and the risk of age-related cataract in Egyptians |
| Q54318714 | Polymorphisms of DNA repair genes and risk of squamous cell carcinoma of the head and neck in young adults |
| Q33236760 | Polymorphisms of the XRCC1, XRCC3 and XPD genes and risk of colorectal adenoma and carcinoma, in a Norwegian cohort: a case control study |
| Q36658207 | Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome |
| Q24311788 | Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23 |
| Q58794947 | Relevance of polymorphisms to neuroblastoma risk in Chinese children: a four-center case-control study |
| Q24678938 | Retracted: A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function |
| Q33959543 | SNP-SNP interactions between DNA repair genes were associated with breast cancer risk in a Korean population |
| Q35757364 | Shining a light on xeroderma pigmentosum |
| Q36818976 | Stable and specific association between the yeast recombination and DNA repair proteins RAD1 and RAD10 in vitro |
| Q24596325 | Structure and expression of the excision repair gene ERCC6, involved in the human disorder Cockayne's syndrome group B |
| Q41836999 | Studies on phenotypic complementation of ataxia-telangiectasia cells by chromosome transfer. |
| Q40707413 | Studying nucleotide excision repair of mammalian DNA in a cell-free system |
| Q24595611 | The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor |
| Q40853477 | The Rad3 protein from Saccharomyces cerevisiae: a DNA and DNA:RNA helicase with putative RNA helicase activity |
| Q58318854 | Transcription factor b (TFIIH) is required during nucleotide-excision repair in yeast |
| Q33594900 | Transcription-coupled repair of DNA damage: unanticipated players, unexpected complexities |
| Q41342786 | UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I. |
| Q37666472 | XPD Asp312Asn and Lys751Gln polymorphisms and breast cancer susceptibility: a meta-analysis |
| Q35758935 | XPD Lys(751)Gln and Asp(312)Asn polymorphisms and hepatocellular carcinoma susceptibility: A meta-analysis of 11 case-control studies in an Asian population |
| Q36481400 | XRCC3 and XPD/ERCC2 single nucleotide polymorphisms and the risk of cancer: a HuGE review |
| Q72146618 | Xeroderma pigmentosum |
| Q35194613 | Xeroderma pigmentosum complementation group G associated with Cockayne syndrome |
| Q34013081 | Xeroderma pigmentosum group D 751 polymorphism as a predictive factor in resected gastric cancer treated with chemo-radiotherapy |
| Q35205692 | Yeast RAD3 protein binds directly to both SSL2 and SSL1 proteins: implications for the structure and function of transcription/repair factor b. |
| Q73866479 | [Genetically induced hair diseases] |
| Q24336880 | p53 modulation of TFIIH–associated nucleotide excision repair activity |
| Q41640484 | p53 tumor-suppressor gene: Clues to molecular carcinogenesis |
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