| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1052632672 |
| P356 | DOI | 10.1038/359070A0 |
| P3181 | OpenCitations bibliographic resource ID | 1925736 |
| P698 | PubMed publication ID | 1522891 |
| P2093 | author name string | C. Peterson | |
| R. Legerski | |||
| P2860 | cites work | Selective repair of specific chromatin domains in UV-irradiated cells from xeroderma pigmentosum complementation group C. | Q54324697 |
| Cloning and nucleotide sequence analysis of the Saccharomyces cerevisiae RAD4 gene required for excision repair of UV-damaged DNA | Q70261278 | ||
| Role of the Conserved AAUAAA Sequence: Four AAUAAA Point Mutants Prevent Messenger RNA 3′ End Formation | Q72749074 | ||
| A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome | Q24306514 | ||
| Molecular cloning and biological characterization of a human gene, ERCC2, that corrects the nucleotide excision repair defect in CHO UV5 cells | Q24339649 | ||
| High-efficiency transformation of mammalian cells by plasmid DNA | Q27860469 | ||
| A conserved AU sequence from the 3' untranslated region of GM-CSF mRNA mediates selective mRNA degradation | Q27860824 | ||
| Selective extraction of polyoma DNA from infected mouse cell cultures | Q29547500 | ||
| Molecular cloning of a CD28 cDNA by a high-efficiency COS cell expression system | Q29614579 | ||
| High efficiency transformation of E. coli by high voltage electroporation | Q29615278 | ||
| Unidirectional digestion with exonuclease III in DNA sequence analysis | Q29620554 | ||
| High-frequency transformation of human repair-deficient cell lines by an Epstein-Barr virus-based cDNA expression vector | Q33239612 | ||
| Defective Repair Replication of DNA in Xeroderma Pigmentosum | Q34054000 | ||
| Molecular cloning of a mouse DNA repair gene that complements the defect of group-A xeroderma pigmentosum | Q34291583 | ||
| Genetic diversity of UV-sensitive DNA repair mutants of Chinese hamster ovary cells | Q35383320 | ||
| Nucleotide sequence of the wild-type RAD4 gene of Saccharomyces cerevisiae and characterization of mutant rad4 alleles | Q36175532 | ||
| Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes | Q36728551 | ||
| Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene | Q36767352 | ||
| Transient complementation of xeroderma pigmentosum cells by microinjection of poly(A)+ RNA | Q37567662 | ||
| Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation | Q37584671 | ||
| An immortalized xeroderma pigmentosum, group C, cell line which replicates SV40 shuttle vectors | Q43417251 | ||
| P433 | issue | 6390 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA repair | Q210538 |
| xeroderma pigmentosum | Q612693 | ||
| XPC complex subunit, DNA damage recognition and repair factor | Q21114096 | ||
| xeroderma pigmentosum group C | Q32143719 | ||
| P304 | page(s) | 70–73 | |
| P577 | publication date | 1992-09-03 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C | |
| P478 | volume | 359 |
| Q34999430 | A 127 kDa component of a UV-damaged DNA-binding complex, which is defective in some xeroderma pigmentosum group E patients, is homologous to a slime mold protein |
| Q30777037 | A Transmembrane Trap Method for Efficient Cloning of Genes Encoding Proteins Possessing Transmembrane Domain |
| Q38301768 | A novel role for DNA photolyase: binding to DNA damaged by drugs is associated with enhanced cytotoxicity in Saccharomyces cerevisiae |
| Q55035903 | A novel specific role for I kappa B kinase complex-associated protein in cytosolic stress signaling. |
| Q36685083 | A system utilizing Epstein-Barr virus-based expression vectors for the functional cloning of human fibroblast growth regulators |
| Q33278102 | An aromatic sensor with aversion to damaged strands confers versatility to DNA repair |
| Q24651193 | An interaction between the DNA repair factor XPA and replication protein A appears essential for nucleotide excision repair |
| Q33702814 | Applications of oriP plasmids and their mode of replication |
| Q90572486 | Astaxanthin enhances erlotinib-induced cytotoxicity by p38 MAPK mediated xeroderma pigmentosum complementation group C (XPC) down-regulation in human lung cancer cells |
| Q27658074 | Binding of the human nucleotide excision repair proteins XPA and XPC/HR23B to the 5R-thymine glycol lesion and structure of the cis-(5R,6S) thymine glycol epimer in the 5'-GTgG-3' sequence: destabilization of two base pairs at the lesion site |
| Q33608768 | Cell cycle control, checkpoint mechanisms, and genotoxic stress |
| Q28259157 | Characterization of molecular defects in xeroderma pigmentosum group C |
| Q37633368 | Characterization of two protein kinases from Schizosaccharomyces pombe involved in the regulation of DNA repair |
| Q40277237 | Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosum |
| Q24673129 | Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3 |
| Q34798167 | Cloning and characterization of the mouse XPAC gene |
| Q40224782 | Cloning the Drosophila homolog of the xeroderma pigmentosum complementation group C gene reveals homology between the predicted human and Drosophila polypeptides and that encoded by the yeast RAD4 gene |
| Q28268594 | Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2 |
| Q24317605 | Correction of chromosomal instability and sensitivity to diverse mutagens by a cloned cDNA of the XRCC3 DNA repair gene |
| Q36269884 | DNA Repair Gene Polymorphism and the Risk of Mitral Chordae Tendineae Rupture |
| Q72883771 | DNA repair |
| Q34535203 | DNA repair genes: alternative transcription and gene expression at the exon level in response to the DNA damaging agent, ionizing radiation |
| Q36718103 | DNA repair protein XPA binds replication protein A (RPA). |
| Q59034732 | Damage-limitation exercises |
| Q32068354 | Defective Global Genome Repair in XPC Mice Is Associated with Skin Cancer Susceptibility But Not with Sensitivity to UVB Induced Erythema and Edema |
| Q54525290 | Deficient Regulation of DNA Double-strand Break Repair in Fanconi Anemia Fibroblasts |
| Q30663313 | Detection and determination of oligonucleotide triplex formation-mediated transcription-coupled DNA repair in HeLa nuclear extracts |
| Q38678701 | Different dynamics in nuclear entry of subunits of the repair/transcription factor TFIIH |
| Q28251866 | Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II |
| Q24647834 | ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs |
| Q36656161 | Elevated frequency of microsatellite mutations in TK6 human lymphoblast clones selected for mutations at the thymidine kinase locus |
| Q33916410 | Episomal vectors for gene expression in mammalian cells |
| Q36296168 | Evidence for lack of DNA photoreactivating enzyme in humans |
| Q36694414 | Expression and Functional Analyses of the Dxpa Gene, the Drosophila Homolog of the Human Excision Repair Gene XPA |
| Q40543709 | Expression cloning of multiple human cDNAs that complement the phenotypic defects of ataxia-telangiectasia group D fibroblasts |
| Q48784329 | From xeroderma pigmentosum to the biological clock contributions of Dirk Bootsma to human genetics |
| Q36908627 | Functional heterogeneity of vaccine-induced CD8(+) T cells |
| Q33540030 | Gene expression profiling of xeroderma pigmentosum |
| Q40580193 | Genetic and physical mapping of the ataxia-telangiectasia locus on chromosome 11q22-q23. |
| Q41225009 | Genetic complementation of radiation response by 3' untranslated regions (UTR) of RNA. |
| Q46501421 | Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile |
| Q39639979 | Hepatitis C Virus Inhibits DNA Damage Repair through Reactive Oxygen and Nitrogen Species and by Interfering with the ATM-NBS1/Mre11/Rad50 DNA Repair Pathway in Monocytes and Hepatocytes |
| Q38291559 | High susceptibility to ultraviolet-induced carcinogenesis in mice lacking XPC |
| Q32006420 | Human nucleotide excision repair protein XPA: Extended X‐ray absorption fine‐structure evidence for a metal‐binding domain |
| Q38341326 | Identification and Characterization of XPC-Binding Domain of hHR23B |
| Q33865346 | Identification of HHR23A as a substrate for E6-associated protein-mediated ubiquitination. |
| Q44548417 | Improved EBV-based shuttle vector system: dicistronic mRNA couples the synthesis of the Epstein-Barr nuclear antigen-1 protein to neomycin resistance |
| Q33293339 | In vivo destabilization and functional defects of the xeroderma pigmentosum C protein caused by a pathogenic missense mutation |
| Q41146056 | Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD gene |
| Q26746868 | Mechanisms of interstrand DNA crosslink repair and human disorders |
| Q28290801 | Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p |
| Q30765879 | Microsatellite-Containing Genes from the Channel Catfish Brain: Evidence of Trinucleotide Repeat Expansion in the Coding Region of Nucleotide Excision Repair Gene RAD23B |
| Q36478743 | Modulation of DNA damage/DNA repair capacity by XPC polymorphisms |
| Q41689624 | Molecular biology of Fanconi anemia |
| Q24328767 | Molecular cloning of a novel human gene encoding a 63-kDa protein and its sublocalization within the 11q13 locus |
| 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 |
| Q37875117 | Multiple DNA damage recognition factors involved in mammalian nucleotide excision repair |
| 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 |
| Q34724045 | Mutations in XPA that prevent association with ERCC1 are defective in nucleotide excision repair |
| Q36678686 | Nucleotide Excision Repair Factor XPC Enhances DNA Damage–Induced Apoptosis by Downregulating the Antiapoptotic Short Isoform of Caspase-2 |
| Q36226849 | Nucleotide excision repair |
| Q72236445 | Nucleotide excision repair in yeast |
| Q36947492 | Nucleotide excision repair pathway review I: implications in ovarian cancer and platinum sensitivity |
| Q41175756 | Overproduction, purification, and characterization of the XPC subunit of the human DNA repair excision nuclease |
| Q28592787 | Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene |
| Q35876180 | Preclinical corrective gene transfer in xeroderma pigmentosum human skin stem cells. |
| Q36096540 | Protective Effect of Diphlorethohydroxycarmalol against Ultraviolet B Radiation-Induced DNA Damage by Inducing the Nucleotide Excision Repair System in HaCaT Human Keratinocytes |
| Q24311788 | Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23 |
| Q36847628 | Quantification of XPA gene expression levels in human and mouse cell lines by competitive RT-PCR. |
| Q36559434 | Rad23 is required for transcription-coupled repair and efficient overrall repair in Saccharomyces cerevisiae |
| Q38359257 | Reaction mechanism of human DNA repair excision nuclease |
| Q27648368 | Recognition of DNA damage by the Rad4 nucleotide excision repair protein |
| Q38322541 | Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients |
| Q40598246 | Repair and transcription. Collision or collusion? |
| Q38360489 | Repair of rDNA in Saccharomyces cerevisiae: RAD4-independent strand-specific nucleotide excision repair of RNA polymerase I transcribed genes |
| Q24546146 | Sequence of the mouse XPC cDNA and genomic structure of the human XPC gene |
| Q42363341 | Single-Molecule Imaging Reveals that Rad4 Employs a Dynamic DNA Damage Recognition Process |
| Q24563058 | Specific association between the human DNA repair proteins XPA and ERCC1 |
| Q27675728 | Structure of (5′S)-8,5′-Cyclo-2′-deoxyguanosine in DNA |
| 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 |
| Q24336968 | The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH |
| Q24313355 | The Fanconi anaemia proteins, FAA and FAC interact to form a nuclear complex |
| Q41526534 | The Molecular Basis of Xeroderma Pigmentosum |
| Q38304692 | The RAD7 and RAD16 genes, which are essential for pyrimidine dimer removal from the silent mating type loci, are also required for repair of the nontranscribed strand of an active gene in Saccharomyces cerevisiae |
| Q38359094 | The carboxy-terminal domain of the XPC protein plays a crucial role in nucleotide excision repair through interactions with transcription factor IIH. |
| Q34290755 | The human XPC DNA repair gene: arrangement, splice site information content and influence of a single nucleotide polymorphism in a splice acceptor site on alternative splicing and function |
| Q24322863 | The human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells |
| Q33832707 | The initiative role of XPC protein in cisplatin DNA damaging treatment-mediated cell cycle regulation. |
| Q38336958 | The involvement of XPC protein in the cisplatin DNA damaging treatment-mediated cellular response. |
| Q36648506 | The rad16 gene of Schizosaccharomyces pombe: a homolog of the RAD1 gene of Saccharomyces cerevisiae |
| Q41193565 | The role of DNA repair in the prevention of cancer |
| Q35050078 | The xeroderma pigmentosum group C gene leads to selective repair of cyclobutane pyrimidine dimers rather than 6-4 photoproducts |
| Q34640431 | Transcription and DNA damage: a link to a kink |
| Q38358612 | Two budding yeast RAD4 homologs in fission yeast play different roles in the repair of UV-induced DNA damage. |
| Q30489886 | Two-stage dynamic DNA quality check by xeroderma pigmentosum group C protein |
| Q24321848 | Two-step recognition of DNA damage for mammalian nucleotide excision repair: Directional binding of the XPC complex and DNA strand scanning |
| Q41356307 | UV-induced signal transduction |
| Q28253282 | UV-induced ubiquitylation of XPC complex, the UV-DDB-ubiquitin ligase complex, and DNA repair |
| Q36059498 | Ubiquitylation-independent degradation of Xeroderma pigmentosum group C protein is required for efficient nucleotide excision repair |
| Q84927632 | XPC gene variants: a risk factor for recurrence of urothelial bladder carcinoma in patients on BCG immunotherapy |
| Q35832914 | XPC inhibits NSCLC cell proliferation and migration by enhancing E-Cadherin expression |
| Q37198847 | XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptoms |
| Q28239093 | XPC interacts with both HHR23B and HHR23A in vivo |
| Q24312736 | Xeroderma Pigmentosum Group C Protein Complex Is the Initiator of Global Genome Nucleotide Excision Repair |
| Q72146618 | Xeroderma pigmentosum |
| Q27931297 | Yeast DNA-repair gene RAD14 encodes a zinc metalloprotein with affinity for ultraviolet-damaged DNA. |
| Q38307487 | Yeast nucleotide excision repair proteins Rad2 and Rad4 interact with RNA polymerase II basal transcription factor b (TFIIH) |
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