Effect of thymine glycol on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II
about
Pathogen DNA as target for host-generated oxidative stress: role for repair of bacterial DNA damage in Helicobacter pylori colonizationRepair of oxidized bases in DNA bubble structures by human DNA glycosylases NEIL1 and NEIL2UVSSA and USP7, a new couple in transcription-coupled DNA repairDifferent effects of CSA and CSB deficiency on sensitivity to oxidative DNA damageTranscription-coupled DNA repair: two decades of progress and surprisesFANCJ helicase uniquely senses oxidative base damage in either strand of duplex DNA and is stimulated by replication protein A to unwind the damaged DNA substrate in a strand-specific manner.Rotational dynamics of DNA on the nucleosome surface markedly impact accessibility to a DNA repair enzyme.Malondialdehyde adducts in DNA arrest transcription by T7 RNA polymerase and mammalian RNA polymerase II.Dynamic flexibility of DNA repair pathways in growth arrested Escherichia coliSingle-stranded breaks in DNA but not oxidative DNA base damages block transcriptional elongation by RNA polymerase II in HeLa cell nuclear extracts.Prereplicative repair of oxidized bases in the human genome is mediated by NEIL1 DNA glycosylase together with replication proteins.Synthesis of stable-isotope enriched 5-methylpyrimidines and their use as probes of base reactivity in DNA.Preferential repair of oxidized base damage in the transcribed genes of mammalian cellsTranscripts of damaged genes in the brain during cerebral oxidative stressIschemia-reperfusion-related repair deficit after oxidative stress: implications of faulty transcripts in neuronal sensitivity after brain injury.RNA polymerase II bypass of oxidative DNA damage is regulated by transcription elongation factorsNew paradigms in the repair of oxidative damage in human genome: mechanisms ensuring repair of mutagenic base lesions during replication and involvement of accessory proteins.Mfd is required for rapid recovery of transcription following UV-induced DNA damage but not oxidative DNA damage in Escherichia coli.Expression and the Peculiar Enzymatic Behavior of the Trypanosoma cruzi NTH1 DNA GlycosylaseTranscriptional mutagenesis: causes and involvement in tumour development.Transcription elongation past O6-methylguanine by human RNA polymerase II and bacteriophage T7 RNA polymerase8-Oxoguanine-mediated transcriptional mutagenesis causes Ras activation in mammalian cells.The RECQL4 protein, deficient in Rothmund-Thomson syndrome is active on telomeric D-loops containing DNA metabolism blocking lesionsA ubiquitylation site in Cockayne syndrome B required for repair of oxidative DNA damage, but not for transcription-coupled nucleotide excision repairListeria monocytogenes DNA Glycosylase AdlP Affects Flagellar Motility, Biofilm Formation, Virulence, and Stress Responses.DNA polymerase beta and PARP activities in base excision repair in living cells.Mechanisms of base substitution mutagenesis in cancer genomes.The Nonbulky DNA Lesions Spiroiminodihydantoin and 5-Guanidinohydantoin Significantly Block Human RNA Polymerase II Elongation in Vitro.Global genome removal of thymine glycol in Escherichia coli requires endonuclease III but the persistence of processed repair intermediates rather than thymine glycol correlates with cellular sensitivity to high doses of hydrogen peroxide.Construction and purification of site-specifically modified DNA templates for transcription assaysHuman RNA polymerase II is partially blocked by DNA adducts derived from tumorigenic benzo[c]phenanthrene diol epoxides: relating biological consequences to conformational preferences.A novel hydrogen peroxide-induced phosphorylation and ubiquitination pathway leading to RNA polymerase II proteolysis.Altered minor-groove hydrogen bonds in DNA block transcription elongation by T7 RNA polymerase.Transcription processing at 1,N2-ethenoguanine by human RNA polymerase II and bacteriophage T7 RNA polymeraseEffects of endogenous DNA base lesions on transcription elongation by mammalian RNA polymerase II. Implications for transcription-coupled DNA repair and transcriptional mutagenesis.Transcription arrest at a lesion in the transcribed DNA strand in vitro is not affected by a nearby lesion in the opposite strand.Multiple states of stalled T7 RNA polymerase at DNA lesions generated by platinum anticancer agents.Nucleotide excision repair activity varies among murine spermatogenic cell types.Behavior of T7 RNA polymerase and mammalian RNA polymerase II at site-specific cisplatin adducts in the template DNA.Archaeal RNA polymerase arrests transcription at DNA lesions.
P2860
Q24554222-75BE80FE-1A5C-4CA7-80D7-96B0B12C2924Q28206447-3020E40E-2F24-4EFC-94B9-62C07C568757Q28292625-93010BCC-2BB5-4D54-BB5F-3CE55BF86CF7Q28509765-E1424407-8607-414D-AF99-C5D81F454303Q29614662-39B4AAC1-14E1-4CC0-95ED-E46B82EA9B9EQ30863349-B2C6EE18-89C3-425C-A525-50E8D120B645Q33740808-4292F1AF-AB49-4D79-B5FC-B5A93436C90BQ33904473-73E856AC-6333-4AFA-B722-FA37BD1821BCQ33945554-DBE34067-77B9-4C1A-9EDD-63A9DF9E6B40Q34300281-ABB8354D-BDD7-4BA6-959A-C7591114954FQ34360665-281CEC12-81E4-4E59-A2C2-BAAFDFC833B9Q34367213-593256DE-0A76-40F4-A04E-93EED481A7CDQ34675663-41FE7DC6-87F1-41B5-887A-5823ED3E7540Q35005606-C00EE118-4313-40CD-B959-76AB23D25B56Q35059578-DBC08AC1-2D20-4D33-AE1C-75CB3BC5D6E7Q35191105-7691388F-0924-403B-80C7-846D30B5F5AEQ35395549-67E98709-3947-44AD-ADC8-369154D89DBAQ35943160-33E49E5D-9900-473A-958B-271D11D3FD56Q36048020-C2BDAB19-085F-458F-A506-DFECC11AA919Q36861991-C620F456-F90A-42C5-9D80-C1383C5BFB88Q36972108-12600D48-F920-444D-9713-560035746649Q36999922-8B347CEB-66EC-40F7-821B-A0EA1ADAE192Q37010194-1C3373D8-8347-426B-8BE1-71F7B8B25CDCQ37021545-BE0BE01D-90BD-4920-8CAB-0FC235EA7664Q37182769-D8B3D7C1-6086-414C-91D2-E6953DA02BE1Q37394688-7090A8D8-857C-4A23-BEB0-97C3ACC78FC0Q37689834-4FBAD915-0FD3-46C1-BA35-A920410572FEQ38780730-9F8FC47C-DD1E-4444-8FD9-3F9361A5627CQ39682097-5887E167-AE41-4939-A56E-DB571EDCDB43Q39744557-9CF86522-F76E-488E-9033-1D1B1029F4FFQ39982077-25992EF1-2FB0-48F9-B19C-4C6494ABF007Q40609421-8B95A2FC-F04D-4CC3-8866-BBAAEAB19CDBQ41061461-6EA8B4A4-4D9A-4D80-B9F7-D409D04582E9Q42054679-7171FB87-A605-43C3-9B87-EFEFDE7161C8Q44238573-498C8A3F-B5A0-4432-9496-E2691A09461CQ44368582-47B42CFC-9AB6-4DBE-A575-12A317233051Q44610986-9F4A3381-7F5B-4747-A404-F8D4862C4418Q46367896-3C713F67-F053-4ACF-8713-807DFB3A1467Q46504735-E8F2E1FB-4378-47A6-829B-A866CD36AA71Q50952368-A325F16E-6135-44EB-989C-5DB5C4D422F9
P2860
Effect of thymine glycol on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II
description
2001 nî lūn-bûn
@nan
2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Effect of thymine glycol on tr ...... nd mammalian RNA polymerase II
@ast
Effect of thymine glycol on tr ...... nd mammalian RNA polymerase II
@en
Effect of thymine glycol on tr ...... nd mammalian RNA polymerase II
@nl
type
label
Effect of thymine glycol on tr ...... nd mammalian RNA polymerase II
@ast
Effect of thymine glycol on tr ...... nd mammalian RNA polymerase II
@en
Effect of thymine glycol on tr ...... nd mammalian RNA polymerase II
@nl
prefLabel
Effect of thymine glycol on tr ...... nd mammalian RNA polymerase II
@ast
Effect of thymine glycol on tr ...... nd mammalian RNA polymerase II
@en
Effect of thymine glycol on tr ...... nd mammalian RNA polymerase II
@nl
P2093
P2860
P3181
P356
P1476
Effect of thymine glycol on tr ...... nd mammalian RNA polymerase II
@en
P2093
P C Hanawalt
S Tornaletti
P2860
P304
45367-45371
P3181
P356
10.1074/JBC.M105282200
P407
P577
2001-09-24T00:00:00Z