Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
about
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 12p12Purification 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 cellsSequence of the mouse XPC cDNA and genomic structure of the human XPC geneSpecific association between the human DNA repair proteins XPA and ERCC1ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologsAn interaction between the DNA repair factor XPA and replication protein A appears essential for nucleotide excision repairClinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3Mechanisms of interstrand DNA crosslink repair and human disordersBinding 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 siteStructure of (5′ S )-8,5′-Cyclo-2′-deoxyguanosine in DNAYeast DNA-repair gene RAD14 encodes a zinc metalloprotein with affinity for ultraviolet-damaged DNA.Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3pPostnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G geneTwo-stage dynamic DNA quality check by xeroderma pigmentosum group C protein.Detection and determination of oligonucleotide triplex formation-mediated transcription-coupled DNA repair in HeLa nuclear extracts.Human nucleotide excision repair protein XPA: extended X-ray absorption fine-structure evidence for a metal-binding domain.An aromatic sensor with aversion to damaged strands confers versatility to DNA repairIn vivo destabilization and functional defects of the xeroderma pigmentosum C protein caused by a pathogenic missense mutationGene expression profiling of xeroderma pigmentosum.Cell cycle control, checkpoint mechanisms, and genotoxic stress.The initiative role of XPC protein in cisplatin DNA damaging treatment-mediated cell cycle regulation.Identification of HHR23A as a substrate for E6-associated protein-mediated ubiquitination.Episomal vectors for gene expression in mammalian cells.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.DNA repair genes: alternative transcription and gene expression at the exon level in response to the DNA damaging agent, ionizing radiationTranscription and DNA damage: a link to a kink.Mutations in XPA that prevent association with ERCC1 are defective in nucleotide excision repair.Cloning and characterization of the mouse XPAC geneA 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 proteinThe xeroderma pigmentosum group C gene leads to selective repair of cyclobutane pyrimidine dimers rather than 6-4 photoproducts.Molecular cloning of the human nucleotide-excision-repair gene ERCC4XPC inhibits NSCLC cell proliferation and migration by enhancing E-Cadherin expression.Preclinical corrective gene transfer in xeroderma pigmentosum human skin stem cells.Ubiquitylation-independent degradation of Xeroderma pigmentosum group C protein is required for efficient nucleotide excision repairProtective Effect of Diphlorethohydroxycarmalol against Ultraviolet B Radiation-Induced DNA Damage by Inducing the Nucleotide Excision Repair System in HaCaT Human KeratinocytesDNA Repair Gene Polymorphism and the Risk of Mitral Chordae Tendineae Rupture.Evidence for lack of DNA photoreactivating enzyme in humans.Modulation of DNA damage/DNA repair capacity by XPC polymorphisms
P2860
Q24306411-592196DE-C7BA-459C-86FF-7621DF03D4E4Q24311788-3FAA61E7-D82B-48D9-9100-69F80B3AE9A6Q24317605-28354FFF-B3F7-4B0D-9328-8B5564B63451Q24322863-EF90247A-1683-4E89-9105-59B947091E59Q24546146-2FB82757-B901-47A4-A4DA-1CCFABA34562Q24563058-EF29173E-886D-4FAF-A961-9812B3177DE8Q24647834-39AA84C8-0BB7-4180-87EA-97A646D7B035Q24651193-41B21BC3-D224-45DD-B2ED-A47B3273F40DQ24673129-9951C0A7-AAF9-4298-9B60-677B86D52256Q26746868-E6AF7D33-A4C5-415C-8FFA-CB1A36BC32CFQ27658074-12C7F2D7-1F2A-4FBA-B333-6BC4AEEE542BQ27675728-A3324CD0-92B5-45FB-A9C0-DB21585650B8Q27931297-47F023D2-23F3-43D1-B257-1F94EC985EBBQ28290801-339396B7-0173-4083-A8CE-8087B06A14E2Q28592787-2C5EC8FB-A25C-4F8B-BB55-6BD4D6AE242BQ30489886-21FD3DE0-F127-47ED-B3FC-EE824CDDF015Q30663313-95D91891-419F-464F-B857-6E9D34C91489Q32006420-1ACC51B5-C194-4C50-873D-6D15094B8AC4Q33278102-6F8BC67D-DA80-4721-B238-AC7B9E16867DQ33293339-C6B5F52F-FA19-40DE-8F4D-3D3CB158C0A4Q33540030-4E42A39F-5E43-4B6C-9287-10527E06E82BQ33608768-014D2F9A-4E9D-4359-BB15-C1AA6F849C4FQ33832707-0EC2A058-DAFD-4D93-A08B-B3C94C2E6181Q33865346-9238DAD0-1A9B-4D56-ACE6-FF05D073CBA4Q33916410-7A074645-43C5-4157-A0F2-2177C976538BQ34290755-06CEDB9F-BCFE-4E09-9E13-E8FF66AED120Q34535203-4CCE5561-0150-4872-BC9A-5712FB86D1FBQ34640431-671D819A-EA54-46EA-BEAE-22672DF3BC51Q34724045-C87948AF-0811-4E88-8A7D-A233E358DCF3Q34798167-26D192A5-3770-4F00-9077-1D131DCBE9DEQ34999430-E6E84D47-FA11-41CB-A6C9-F0A19F078E0AQ35050078-AE32B377-1E5A-4743-98C8-3733BE9F7DACQ35600010-F15E4AEE-4ED4-469C-9219-FAB4DE01703AQ35832914-D880E6FE-F075-492A-8362-522D299829F4Q35876180-0A0DFC53-830C-42DB-AC88-86929649D9E5Q36059498-B6BB52E7-411E-4A15-A4D1-77663988D2A4Q36096540-7C42451B-33FD-4B24-9F2F-BC1C70E8144BQ36269884-FA654982-F227-4FD0-AE03-35B047610F8AQ36296168-F1D965A3-FDEF-46FA-A670-3748072599BDQ36478743-7EB32FA1-E1EF-4366-A472-629B3AFCC7AA
P2860
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
description
1992 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Nature
@fr
scientific journal article
@en
vedecký článok (publikovaný 1992/09/03)
@sk
vědecký článek publikovaný v roce 1992
@cs
wetenschappelijk artikel (gepubliceerd op 1992/09/03)
@nl
наукова стаття, опублікована у вересні 1992
@uk
научни чланак (објављен 1992/09/03)
@sr
مقالة علمية (نشرت في 3-9-1992)
@ar
name
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
@ast
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
@en
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
@nl
type
label
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
@ast
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
@en
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
@nl
prefLabel
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
@ast
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
@en
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
@nl
P2860
P3181
P356
P1433
P1476
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
@en
P2093
C. Peterson
R. Legerski
P2860
P2888
P3181
P356
10.1038/359070A0
P407
P577
1992-09-03T00:00:00Z
P6179
1052632672