| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0733-8635(18)30120-7 |
| P698 | PubMed publication ID | 7712643 |
| P2093 | author name string | Lambert WC | |
| Lambert MW | |||
| Kuo HR | |||
| P2860 | cites work | Evolution and mutagenesis of the mammalian excision repair gene ERCC-1 | Q24297867 |
| A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome | Q24306514 | ||
| Localization of two human homologs, HHR6A and HHR6B, of the yeast DNA repair gene RAD6 to chromosomes Xq24-q25 and 5q23-q31 | Q24321697 | ||
| ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3 | Q24321908 | ||
| A role for the human single-stranded DNA binding protein HSSB/RPA in an early stage of nucleotide excision repair | Q24337036 | ||
| Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6 | Q24337556 | ||
| Molecular cloning and biological characterization of a human gene, ERCC2, that corrects the nucleotide excision repair defect in CHO UV5 cells | Q24339649 | ||
| Characterization of a splicing mutation in group A xeroderma pigmentosum | Q24556519 | ||
| Structure and expression of the excision repair gene ERCC6, involved in the human disorder Cockayne's syndrome group B | Q24596325 | ||
| Molecular cloning of the human DNA excision repair gene ERCC-6 | Q24596936 | ||
| Molecular cloning and biological characterization of the human excision repair gene ERCC-3 | Q24599958 | ||
| Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome | Q24628413 | ||
| Molecular and functional analysis of theXPBC/ERCC-3promoter: transcription activity is dependent on the integrity of an Sp1-binding site | Q24630383 | ||
| A new technique for the assay of infectivity of human adenovirus 5 DNA | Q27860797 | ||
| RAD3 protein of Saccharomyces cerevisiae is a DNA helicase | Q27929894 | ||
| Defective DNA endonuclease activity on anthramycin treated DNA in xeroderma pigmentosum and mouse melanoma cells | Q72766600 | ||
| Nuclear deoxyribonuclease activities in normal and xeroderma pigmentosum lymphoblastoid cells | Q72771354 | ||
| Nuclear DNA endonuclease activities on partially apurinic/apyrimidinic DNA in normal human and xeroderma pigmentosum lymphoblastoid and mouse melanoma cells | Q72794484 | ||
| Purification of human and monkey endonucleases acting on ultraviolet-irradiated DNA | Q72857976 | ||
| RAD1, an excision repair gene of Saccharomyces cerevisiae, is also involved in recombination | Q27931055 | ||
| Yeast excision repair gene RAD2 encodes a single-stranded DNA endonuclease | Q27934231 | ||
| RAD10, an excision repair gene of Saccharomyces cerevisiae, is involved in the RAD1 pathway of mitotic recombination | Q27939437 | ||
| Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C | Q28115748 | ||
| Identification of splicing mutations of the last nucleotides of exons, a nonsense mutation, and a missense mutation of the XPAC gene as causes of group A xeroderma pigmentosum | Q28186181 | ||
| Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9 | Q28208042 | ||
| ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes | Q28213725 | ||
| Molecular basis of group A xeroderma pigmentosum: a missense mutation and two deletions located in a zinc finger consensus sequence of the XPAC gene | Q28213758 | ||
| The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
| Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer | Q28257360 | ||
| Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain | Q28260027 | ||
| Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2 | Q28268594 | ||
| Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5 | Q28268603 | ||
| Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening | Q28273305 | ||
| Xeroderma pigmentosum group E cells lack a nuclear factor that binds to damaged DNA | Q28292106 | ||
| Prevention of skin cancer in xeroderma pigmentosum with the use of oral isotretinoin | Q28294912 | ||
| Localization of the xeroderma pigmentosum group B-correcting gene ERCC3 to human chromosome 2q21 | Q28307621 | ||
| DNA strand-specific repair of (+-)-3 alpha,4 beta-dihydroxy-1 alpha,2 alpha-epoxy-1,2,3,4-tetrahydrobenzo[c]phenanthrene adducts in the hamster dihydrofolate reductase gene | Q28317807 | ||
| Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's syndrome | Q28512437 | ||
| Mice with DNA repair gene (ERCC-1) deficiency have elevated levels of p53, liver nuclear abnormalities and die before weaning | Q28587990 | ||
| DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor | Q29619833 | ||
| Xeroderma pigmentosum-Cockayne syndrome complex in two patients: Absence of slun tumors despite severe deficiency of DNA excision repair | Q29999250 | ||
| Xeroderma pigmentosum endonuclease complexes show reduced activity on and affinity for psoralen cross-linked nucleosomal DNA | Q30736548 | ||
| Repair of damaged DNA by extracts from a xeroderma pigmentosum complementation group A revertant and expression of a protein absent in its parental cell line | Q31122071 | ||
| High-frequency transformation of human repair-deficient cell lines by an Epstein-Barr virus-based cDNA expression vector | Q33239612 | ||
| Molecular cloning of human XPAC gene homologs from chicken, Xenopus laevis and Drosophila melanogaster | Q33291290 | ||
| The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA. | Q33640104 | ||
| Increased UV resistance in xeroderma pigmentosum group A cells after transformation with a human genomic DNA clone | Q33774544 | ||
| Defective Repair Replication of DNA in Xeroderma Pigmentosum | Q34054000 | ||
| 8-oxoguanine (8-hydroxyguanine) DNA glycosylase and its substrate specificity | Q34119141 | ||
| Cockayne syndrome: Review of 140 cases | Q34232807 | ||
| Cleavage of pyrimidine dimers in specific DNA sequences by a pyrimidine dimer DNA-glycosylase of M. luteus | Q34251730 | ||
| Molecular cloning of a mouse DNA repair gene that complements the defect of group-A xeroderma pigmentosum | Q34291583 | ||
| Molecular cloning and characterization of a mammalian excision repair gene that partially restores UV resistance to xeroderma pigmentosum complementation group D cells | Q34303550 | ||
| Unique DNA repair properties of a xeroderma pigmentosum revertant | Q36921671 | ||
| Human nucleotide excision nuclease removes thymine dimers from DNA by incising the 22nd phosphodiester bond 5' and the 6th phosphodiester bond 3' to the photodimer | Q36968114 | ||
| Mechanisms and biological effects of mismatch repair | Q37041860 | ||
| Specific complex formation between proteins encoded by the yeast DNA repair and recombination genes RAD1 and RAD10 | Q37186939 | ||
| DNA repair and the role of chromatin structure | Q37300437 | ||
| RAD25 (SSL2), the yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential for viability | Q37323177 | ||
| UV-endonuclease from calf thymus with specificity toward pyrimidine dimers in DNA | Q37339161 | ||
| Restricted ultraviolet mutational spectrum in a shuttle vector propagated in xeroderma pigmentosum cells | Q37405923 | ||
| Gene specific DNA repair | Q37431201 | ||
| Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation | Q37584671 | ||
| Molecular mechanisms of ultraviolet radiation carcinogenesis | Q37793351 | ||
| Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias | Q37928644 | ||
| Structure and function of the (A)BC excinuclease of Escherichia coli | Q37952080 | ||
| Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repair | Q38313225 | ||
| A damage-recognition protein which binds to DNA containing interstrand cross-links is absent or defective in Fanconi anemia, complementation group A, cells | Q38316130 | ||
| Long-term survival and preservation of natural killer cell activity in a xeroderma pigmentosum patient with spontaneous regression and multiple deposits of malignant melanoma | Q63407780 | ||
| Impairment of Natural-Killer-Cell Activity in Xeroderma Pigmentosum | Q63407816 | ||
| Repair of UV-endonuclease-susceptible sites in the 7 complementation groups of xeroderma pigmentosum a through G | Q66965940 | ||
| 5,6-Dihydroxyindole is a melanin precursor showing potent cytotoxicity | Q67421310 | ||
| A case of xeroderma pigmentosum group A diagnosed with a polymerase chain reaction (PCR) technique. Usefulness of PCR in the detection of point mutation in a patient with a hereditary disease | Q67518528 | ||
| Restoration of proliferating cell nuclear antigen (PCNA) complex formation in xeroderma pigmentosum group A cells following cis-diamminedichloroplatinum (II)-treatment by cell fusion with normal cells | Q67520102 | ||
| UV-C sensitivity of unstimulated and stimulated human lymphocytes from normal and xeroderma pigmentosum donors in the comet assay: a potential diagnostic technique | Q67532815 | ||
| Xeroderma pigmentosum group A correcting protein from calf thymus | Q67541630 | ||
| Infrequent mutation of the ras genes in skin tumors of xeroderma pigmentosum patients in Japan | Q67743635 | ||
| Yeast RAD14 and human xeroderma pigmentosum group A DNA-repair genes encode homologous proteins | Q67756410 | ||
| Xeroderma pigmentosum complementation group H is withdrawn and reassigned to group D | Q67792102 | ||
| Xeroderma pigmentosum complementation group H falls into complementation group D | Q68016717 | ||
| The relative cytotoxicity of (6-4) photoproducts and cyclobutane dimers in mammalian cells | Q68016811 | ||
| Assignment of a Chinese xeroderma pigmentosum patient from Taiwan to complementation group C | Q68044769 | ||
| Limitations of the in vitro repair synthesis assay for probing the role of DNA repair in platinum resistance | Q68064660 | ||
| Striking differences in cellular catalase activity between two DNA repair-deficient diseases: xeroderma pigmentosum and trichothiodystrophy | Q68074017 | ||
| Xeroderma pigmentosum complementation group F in a non-Japanese patient | Q68370005 | ||
| Defective DNA repair in cultured melanocytes from xeroderma pigmentosum patients | Q68586545 | ||
| DNA repair mechanisms and their biologic implications in mammalian cells. Report of a NATO advanced research workshop, Fontevraud, France, Oct. 2-7, 1988 | Q68727130 | ||
| Etiological differences between subtypes of cutaneous malignant melanoma: Western Canada Melanoma Study | Q68746930 | ||
| Unusual features in the inheritance of ataxia telangiectasia | Q68781657 | ||
| Xeroderma pigmentosum complementation group G--report of two cases | Q69200444 | ||
| Prenatal diagnosis of Cockayne's syndrome | Q69381336 | ||
| CHO mutant UV61 removes (6-4) photoproducts but not cyclobutane dimers | Q69507165 | ||
| Intermediate (6-4) photoproduct repair in Chinese hamster V79 mutant V-H1 correlates with intermediate levels of DNA incision and repair replication | Q69602833 | ||
| Xeroderma pigmentosum complementation group XP-I withdrawn | Q69706199 | ||
| Reduced superoxide dismutase activity in xeroderma pigmentosum fibroblasts | Q69724624 | ||
| The Cockayne syndrome--an inherited multisystem disorder with cutaneous photosensitivity and defective repair of DNA. Comparison with xeroderma pigmentosum | Q69809110 | ||
| The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I | Q69949766 | ||
| Prenatal diagnosis of xeroderma pigmentosum. Report of the first successful case | Q70026701 | ||
| The erythropoietic porphyrias | Q70027905 | ||
| Porphyria cutanea tarda. Diagnosis, management, and differentiation from other hepatic porphyrias | Q70027907 | ||
| Facial resurfacing in xeroderma pigmentosum with monoblock full-thickness skin graft | Q70158795 | ||
| DNA repair. Engagement with transcription | Q70683866 | ||
| Repair of ultraviolet radiation damage in xeroderma pigmentosum cells belonging to complementation group F | Q70701617 | ||
| Age-dependent Changes in Fibroblast Cultures from a Xeroderma Pigmentosum Variant | Q70799146 | ||
| Instrumentation and action spectra in light-associated diseases | Q70831280 | ||
| Genetic complementation groups in Cockayne syndrome | Q70925603 | ||
| Defect in DNA Synthesis in Skin of Patients with Xeroderma Pigmentosum Demonstrated in vivo | Q71509246 | ||
| Complementation of xeroderma pigmentosum cells by microinjection of mRNA fractionated under denaturing conditions: an estimation of sizes of XP-E and XP-G mRNA | Q71600125 | ||
| Involvement of proliferating cell nuclear antigen in DNA repair after damage induced by genotoxic agents in human fibroblasts | Q71604081 | ||
| Increased sensitivity of a xeroderma pigmentosum lymphoblastoid cell line to serum deprivation in vitro | Q71827139 | ||
| Clonal cytogenetic evolution in a squamous cell carcinoma of the skin from a xeroderma pigmentosum patient | Q72088885 | ||
| The Saccharomyces cerevisiae DNA repair gene RAD25 is required for transcription by RNA polymerase II | Q72102254 | ||
| Transcription-coupled DNA repair | Q72536012 | ||
| Prevention of skin cancer in xeroderma pigmentosum: the physician as advocate | Q72619971 | ||
| Three complementation groups in Cockayne syndrome | Q72687806 | ||
| UV damage-specific DNA-binding protein in xeroderma pigmentosum complementation group E. | Q38336006 | ||
| Substrate overlap and functional competition between human nucleotide excision repair and Escherichia coli photolyase and (a)BC excision nuclease | Q38340400 | ||
| The biology of the (6-4) photoproduct | Q38684048 | ||
| Somatic cell genetics approach to dissecting mammalian DNA repair | Q38723368 | ||
| Clinical and photobiological characteristics of xeroderma pigmentosum complementation group F: a review of cases from Japan | Q38769279 | ||
| Xeroderma pigmentosum. A clinical study of 24 Libyan cases | Q39133214 | ||
| Immunology and photocarcinogenesis. New light on an old problem | Q39477739 | ||
| A mechanism for relief of replication blocks by activation of unused origins and age-dependent change in the caffeine susceptibility in xeroderma pigmentosum variant | Q39512053 | ||
| Ataxia-telangiectasia: an inherited disorder of ionizing-radiation sensitivity in man. Progress in the elucidation of the underlying biochemical defect | Q39761489 | ||
| Yearly review: new forms of diseases with DNA repair defects | Q39852055 | ||
| Human nucleotide excision repair in vitro: repair of pyrimidine dimers, psoralen and cisplatin adducts by HeLa cell-free extract. | Q40450557 | ||
| Mutant rodent cell lines sensitive to ultraviolet light, ionizing radiation and cross-linking agents: a comprehensive survey of genetic and biochemical characteristics | Q40484333 | ||
| Complementation of the xeroderma pigmentosum DNA repair synthesis defect with Escherichia coli UvrABC proteins in a cell-free system | Q40513521 | ||
| Cloning and characterization of the Drosophila homolog of the xeroderma pigmentosum complementation-group B correcting gene, ERCC3. | Q40535083 | ||
| Effect of DNA damage on the expression of the chloramphenicol acetyltransferase gene after transfection into diploid human fibroblasts | Q40568488 | ||
| DNA strand specificity for UV-induced mutations in mammalian cells | Q40646667 | ||
| DNA repair genes and proteins of Saccharomyces cerevisiae | Q40722184 | ||
| It was a very good year for DNA repair | Q40804105 | ||
| Nucleotide excision repair. II: From yeast to mammals | Q40828389 | ||
| Properties and biological functions of the NTH and FPG proteins of Escherichia coli: two DNA glycosylases that repair oxidative damage in DNA. | Q40848841 | ||
| The genetic defect in DNA repair deficiency syndromes. EACR--Mühlbock Memorial Lecture, 1993. | Q40858769 | ||
| Mechanism of action of the Escherichia coli UvrABC nuclease: clues to the damage recognition problem | Q40893801 | ||
| Low Catalase Levels in the Epidermis of Patients with Vitiligo | Q41144137 | ||
| The genetic defect in the Chinese hamster ovary cell mutant UV61 permits moderate selective repair of cyclobutane pyrimidine dimers in an expressed gene | Q41167103 | ||
| Hypermutability and mismatch repair deficiency in RER+ tumor cells | Q41508298 | ||
| Aphidicolin and 1-beta-D-arabinofuranosylcytosine strongly inhibit transcriptionally active DNA repair in normal human fibroblasts | Q41510617 | ||
| A sixth complementation group in xeroderma pigmentosum | Q41514219 | ||
| Ultraviolet hypermutability of a shuttle vector propagated in xeroderma pigmentosum variant cells | Q41517133 | ||
| Cytogenetic evidence for differences in DNA incision activity in xeroderma pigmentosum group A, C and D cells after X-irradiation during G2 phase | Q41540645 | ||
| UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum | Q41543664 | ||
| Deficient gene specific repair of cisplatin-induced lesions in Xeroderma pigmentosum and Fanconi's anemia cell lines | Q41554880 | ||
| Repair of N-methylpurines in the mitochondrial DNA of xeroderma pigmentosum complementation group D cells | Q41554888 | ||
| A single-site mutation in the XPAC gene alters photoproduct recognition | Q41569022 | ||
| Complementation of DNA repair defect in xeroderma pigmentosum cells of group C by the transfer of human chromosome 5. | Q41580176 | ||
| Isolation of a DNA endonuclease complex in XPD cells which is defective in ability to incise nucleosomal DNA containing pyrimidine dimers | Q41589370 | ||
| Characterization of a complex chromosomal rearrangement maps the locus for in vitro complementation of xeroderma pigmentosum group D to human chromosome band 19q13 | Q41597647 | ||
| A possible involvement of DNA topoisomerase I in "caffeine effect" after ultraviolet irradiation | Q41601625 | ||
| Repair of thymine dimers and (6-4) photoproducts in group A xeroderma pigmentosum cell lines harboring a transferred normal chromosome 9 | Q41605037 | ||
| Ultraviolet mutagenesis in human lymphocytes: the effect of cellular transformation | Q41612323 | ||
| Skin cancer and chromosomal aberrations induced by ultraviolet radiation. Evidence for lack of correlation in xeroderma pigmentosum variant and group E patients | Q41620718 | ||
| Defective DNA endonuclease activities in Fanconi's anemia cells, complementation groups A and B | Q41648932 | ||
| Evidence for detective repair of cyclobutane pyrimidine dimers with normal repair of other DNA photoproducts in a transcriptionally active gene transfected into Cockayne syndrome cells | Q41658772 | ||
| Identification of a Specific Protein Factor Defective in Group A Xeroderma Pigmentosum Cells1 | Q41663099 | ||
| Effect of UV light on DNA chain growth and replicon initiation in xeroderma pigmentosum variant cells | Q41676262 | ||
| DNA repair characteristics and mutability of the UV-sensitive V79 Chinese hamster cell mutant V-B11 (complementation group 7). | Q41686824 | ||
| Molecular analysis of ultraviolet-induced mutations in a xeroderma pigmentosum cell line | Q41699264 | ||
| Gene complementing xeroderma pigmentosum group A cells maps to distal human chromosome 9q. | Q41728943 | ||
| Immune function, mutant frequency, and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum, Cockayne's syndrome, and trichothiodystrophy | Q41750551 | ||
| Immune defects in families and patients with xeroderma pigmentosum and trichothiodystrophy | Q41914628 | ||
| A seventh complementation group in excision-deficient xeroderma pigmentosum | Q42019517 | ||
| Biochemical heterogeneity in xeroderma pigmentosum complementation group E | Q42026787 | ||
| Two types of proliferating cell nuclear antigen (PCNA) complex formation in quiescent normal and xeroderma pigmentosum group A fibroblasts following ultraviolet light (uv) irradiation | Q42087151 | ||
| Dna Repair in Tumor Cells from the Variant form of Xeroderma Pigmentosum | Q42447514 | ||
| Chemoprevention of Skin Cancer in Xeroderma Pigmentosum | Q42450262 | ||
| Malignant melanoma in xeroderma pigmentosum: search for a precursor lesion | Q42510867 | ||
| Xeroderma pigmentosum. Defective DNA repair causes skin cancer and neurodegeneration | Q42518877 | ||
| Clues to the pathogenesis of familial colorectal cancer | Q42622043 | ||
| Three nonsense mutations responsible for group A xeroderma pigmentosum | Q42805018 | ||
| Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: studies using cells from patients with trichothiodystrophy | Q43411720 | ||
| Defects in antioxidant defense and calcium transport in the epidermis of xeroderma pigmentosum patients | Q43558507 | ||
| A gene that partially complements xeroderma pigmentosum group A cells maps to human chromosome 8 | Q43889819 | ||
| Yeast DNA repair and recombination proteins Rad1 and Rad10 constitute a single-stranded-DNA endonuclease | Q43986392 | ||
| In vivo excision of pyrimidine dimers is mediated by a DNA N-glycosylase in Micrococcus luteus but not in human fibroblasts | Q44096837 | ||
| Enhanced repair of pyrimidine dimers in coding and non-coding genomic sequences in CHO cells expressing a prokaryotic DNA repair gene | Q44209809 | ||
| Xeroderma pigmentosum variants have decreased repair of ultraviolet-damaged DNA | Q44409928 | ||
| Transcription-dependent and independent DNA excision repair pathways in human cells | Q44670059 | ||
| Five complementation groups in xeroderma pigmentosum | Q44971679 | ||
| Induction of proliferating cell nuclear antigen (PCNA) complex formation in quiescent fibroblasts from a xeroderma pigmentosum patient | Q45220902 | ||
| Host-cell reactivation in mammalian cells. II. Survival of herpes simplex virus and vaccinia virus in normal human and xeroderma pigmentosum cells | Q45820433 | ||
| Stranded in an active gene | Q46181255 | ||
| A shuttle vector plasmid for studying carcinogen-induced point mutations in mammalian cells | Q46397982 | ||
| A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3, a human excision repair gene | Q47071558 | ||
| SSL2, a suppressor of a stem-loop mutation in the HIS4 leader encodes the yeast homolog of human ERCC-3 | Q48169666 | ||
| A case of xeroderma pigmentosum complementation group F with neurological abnormalities | Q48361356 | ||
| Neurological disease in xeroderma pigmentosum. Documentation of a late onset type of the juvenile onset form | Q48709124 | ||
| Clinically asymptomatic xeroderma pigmentosum neurological disease in an adult: evidence for a neurodegeneration in later life caused by defective DNA repair. | Q50532282 | ||
| Substrate specificity of the Escherichia coli Fpg protein (formamidopyrimidine-DNA glycosylase): excision of purine lesions in DNA produced by ionizing radiation or photosensitization. | Q50796195 | ||
| Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity. | Q52077519 | ||
| Co-recessive inheritance: a model for DNA repair and other surveillance genes in higher eukaryotes | Q52425345 | ||
| Elevated hprt mutant frequency in circulating T-lymphocytes of xeroderma pigmentosum patients | Q53438310 | ||
| Visible light generates oxidative DNA base modifications in high excess of strand breaks in mammalian cells. | Q53474237 | ||
| Visualization of chromatin events during DNA excision repair in XP cells: deficiency in localized but not generalized chromatin events. | Q53533482 | ||
| Defective thymine dimer excision from xeroderma pigmentosum chromatin and its characteristic catalysis by cell-free extracts. | Q53557258 | ||
| A comparison of the response of unstimulated and stimulated T-lymphocytes and fibroblasts from normal, xeroderma pigmentosum and trichothiodystrophy donors to the lethal action of UV-C | Q54275103 | ||
| Selective repair of specific chromatin domains in UV-irradiated cells from xeroderma pigmentosum complementation group C. | Q54324697 | ||
| Lack of complementation between xeroderma pigmentosum complementation groups D and H. | Q54360151 | ||
| An eighth complementation group of rodent cells hypersensitive to ultraviolet radiation. | Q54373861 | ||
| Genetic complementation between UV-sensitive CHO mutants and xeroderma pigmentosum fibroblasts. | Q54449044 | ||
| DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall. | Q54455838 | ||
| DNA repair and transcription: the helicase connection. | Q54659177 | ||
| UV mutagenic photoproducts in Escherichia coli and human cells: a molecular genetics perspective on human skin cancer. | Q54746195 | ||
| Domainal evolution of a prokaryotic DNA repair protein and its relationship to active-transport proteins. | Q54774466 | ||
| Complementation of the xeroderma pigmentosum DNA repair defect in cell-free extracts. | Q55060652 | ||
| Workshop on DNA repair | Q56944716 | ||
| Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair | Q57971900 | ||
| A pyrimidine dimer–DNA glycosylase activity associated with the v gene product of bacteriophage T4 | Q59091026 | ||
| DNA repair gene RAD3 of S. cerevisiae is essential for transcription by RNA polymerase II | Q59097138 | ||
| Molecular analysis of mutations in the hprt gene in circulating lymphocytes from normal and DNA-repair-deficient donors | Q60035827 | ||
| Effect of exogenous DNA fragments on human cell extract-mediated DNA repair synthesis | Q60311339 | ||
| Requirement for the replication protein SSB in human DMA excision repair | Q60311342 | ||
| Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells | Q34348395 | ||
| Human xeroderma pigmentosum group D gene encodes a DNA helicase | Q34358690 | ||
| Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10. | Q34383546 | ||
| Chromatin-associated DNA endonucleases from xeroderma pigmentosum cells are defective in interaction with damaged nucleosomal DNA. | Q34453541 | ||
| Electroporation of normal human DNA endonucleases into xeroderma pigmentosum cells corrects their DNA repair defect | Q34461921 | ||
| A novel repair enzyme: UVRABC excision nuclease of Escherichia coli cuts a DNA strand on both sides of the damaged region | Q34708982 | ||
| Correction of the ultraviolet light induced DNA-repair defect in xeroderma pigmentosum cells by electroporation of a normal human endonuclease | Q34718850 | ||
| A role for sunlight in skin cancer: UV-induced p53 mutations in squamous cell carcinoma | Q34982679 | ||
| Defective thymine dimer excision by cell-free extracts of xeroderma pigmentosum cells | Q35016572 | ||
| Genetic heterogeneity in xeroderma pigmentosum: complementation groups and their relationship to DNA repair rates | Q35065881 | ||
| Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation | Q35067081 | ||
| DNA repair investigations in nine Italian patients affected by trichothiodystrophy. | Q35311688 | ||
| The XPD complementation group. Insights into xeroderma pigmentosum, Cockayne's syndrome and trichothiodystrophy | Q35311705 | ||
| Xeroderma pigmentosum variant associated with multiple skin cancers and a lung cancer | Q35363676 | ||
| Xeroderma pigmentosum, Cockayne's syndrome, helicases, and DNA repair: what's the relationship? | Q35571383 | ||
| Strand specificity for UV-induced DNA repair and mutations in the Chinese hamster HPRT gene | Q35804859 | ||
| The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA | Q35907237 | ||
| Methylene blue plus light mediates 8-hydroxy 2'-deoxyguanosine formation in DNA preferentially over strand breakage | Q35907978 | ||
| An ultraviolet light-damaged DNA recognition protein absent in xeroderma pigmentosum group E cells binds selectively to pyrimidine (6-4) pyrimidone photoproducts | Q35933800 | ||
| DNA excision-repair defect of xeroderma pigmentosum prevents removal of a class of oxygen free radical-induced base lesions | Q36407505 | ||
| Evidence that xeroderma pigmentosum cells do not perform the first step in the repair of ultraviolet damage to their DNA. | Q36444039 | ||
| Comparison of histones in normal and xeroderma pigmentosum lymphoblastoid cells | Q36481308 | ||
| Repair by human cell extracts of single (6-4) and cyclobutane thymine-thymine photoproducts in DNA | Q36615580 | ||
| Specific UV-induced mutation spectrum in the p53 gene of skin tumors from DNA-repair-deficient xeroderma pigmentosum patients | Q36659736 | ||
| Defective replication of psoralen adducts detected at the gene-specific level in xeroderma pigmentosum variant cells | Q36661116 | ||
| Cell cycle-dependent strand bias for UV-induced mutations in the transcribed strand of excision repair-proficient human fibroblasts but not in repair-deficient cells | Q36688064 | ||
| Evidence from mutation spectra that the UV hypermutability of xeroderma pigmentosum variant cells reflects abnormal, error-prone replication on a template containing photoproducts | Q36690666 | ||
| Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes | Q36728551 | ||
| Absence of DNA repair deficiency in the confirmed heterozygotes of xeroderma pigmentosum group A. | Q36741612 | ||
| Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene | Q36767352 | ||
| Evidence that xeroderma pigmentosum cells from complementation group E are deficient in a homolog of yeast photolyase | Q36796011 | ||
| Stable and specific association between the yeast recombination and DNA repair proteins RAD1 and RAD10 in vitro | Q36818976 | ||
| Quantification of expression of linked cloned genes in a simian virus 40-transformed xeroderma pigmentosum cell line | Q36903583 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 169-209 | |
| P577 | publication date | 1995-01-01 | |
| P1433 | published in | Dermatologic Clinics | Q15758379 |
| P1476 | title | Xeroderma pigmentosum | |
| P478 | volume | 13 |
| Q41674118 | Atypical fibroxanthoma: an unusual skin neoplasm in xeroderma pigmentosum |
| Q36380439 | B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes |
| Q30783237 | DNA repair and chromatin structure in genetic diseases |
| Q35146743 | DNA repair phenotype and cancer susceptibility--a mini review |
| Q34638737 | Epidemiology of ultraviolet-DNA repair capacity and human cancer |
| Q41617058 | Foulds' dangerous idea revisited: the multistep development of tumors 40 years later. |
| Q37584949 | Multiple cutaneous malignancies in a child with xeroderma pigmentosum: A case report |
| Q34003490 | Pediatric skin tumors |
| Q41033568 | Premalignant keratinocytic neoplasms |
| Q54983880 | Roles of UVA radiation and DNA damage responses in melanoma pathogenesis. |
| Q33890709 | Smoking and the molecular epidemiology of lung cancer |
| Q41526534 | The Molecular Basis of Xeroderma Pigmentosum |
| Q36400909 | The role of DNA repair in somatic hypermutation of immunoglobulin genes |
| Q82543600 | [De Sanctis-Cacchione syndrome] |
| Q53450210 | p53 mutations in solar keratoses. |
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