Accumulation of (5'S)-8,5'-cyclo-2'-deoxyadenosine in organs of Cockayne syndrome complementation group B gene knockout mice. - Wikidata - awgldk - TriplyDB

Accumulation of (5'S)-8,5'-cyclo-2'-deoxyadenosine in organs of Cockayne syndrome complementation group B gene knockout mice.

Accumulation of (5'S)-8,5'-cyclo-2'-deoxyadenosine in organs of Cockayne syndrome complementation group B gene knockout mice.

http://www.wikidata.org/entity/Q37219471

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Structure and Stability of Duplex DNA Containing (5′ S )-5′,8-Cyclo-2′-deoxyadenosine: An Oxidatively Generated Lesion Repaired by NER Structure of (5′ S )-8,5′-Cyclo-2′-deoxyguanosine in DNA Structures of (5′ S )-8,5′-Cyclo-2′-deoxyguanosine Mismatched with dA or dT Insight into mechanisms of 3'-5' exonuclease activity and removal of bulky 8,5'-cyclopurine adducts by apurinic/apyrimidinic endonucleases DNA repair diseases: What do they tell us about cancer and aging?High-throughput analysis of the mutagenic and cytotoxic properties of DNA lesions by next-generation sequencing.Structural basis for the recognition of diastereomeric 5',8-cyclo-2'-deoxypurine lesions by the human nucleotide excision repair system Evidence for the involvement of DNA repair enzyme NEIL1 in nucleotide excision repair of (5'R)- and (5'S)-8,5'-cyclo-2'-deoxyadenosines.Mechanisms of free radical-induced damage to DNA.DNA repair deficiency in neurodegeneration.Elements That Regulate the DNA Damage Response of Proteins Defective in Cockayne Syndrome Impact of age-associated cyclopurine lesions on DNA repair helicases.Quantification of oxidative DNA lesions in tissues of Long-Evans Cinnamon rats by capillary high-performance liquid chromatography-tandem mass spectrometry coupled with stable isotope-dilution method.A 5', 8-cyclo-2'-deoxypurine lesion induces trinucleotide repeat deletion via a unique lesion bypass by DNA polymerase β (5'S)-8,5'-cyclo-2'-deoxyguanosine is a strong block to replication, a potent pol V-dependent mutagenic lesion, and is inefficiently repaired in Escherichia coli Cockayne syndrome B protects against methamphetamine-enhanced oxidative DNA damage in murine fetal brain and postnatal neurodevelopmental deficits Dysmyelination not demyelination causes neurological symptoms in preweaned mice in a murine model of Cockayne syndrome.Bypass of a 5',8-cyclopurine-2'-deoxynucleoside by DNA polymerase β during DNA replication and base excision repair leads to nucleotide misinsertions and DNA strand breaks.Stability of N-glycosidic bond of (5'S)-8,5'-cyclo-2'-deoxyguanosine.Nucleotide excision repair-initiating proteins bind to oxidative DNA lesions in vivo.The CSB chromatin remodeler and CTCF architectural protein cooperate in response to oxidative stress.Induction of 8,5'-cyclo-2'-deoxyadenosine and 8,5'-cyclo-2'-deoxyguanosine in isolated DNA by Fenton-type reagents Mutagenicity and genotoxicity of (5'S)-8,5'-cyclo-2'-deoxyadenosine in Escherichia coli and replication of (5'S)-8,5'-cyclopurine-2'-deoxynucleosides in vitro by DNA polymerase IV, exo-free Klenow fragment, and Dpo4.Synthesis of [1,3, NH2-(15)N3] (5'S)-8,5'-cyclo-2'-deoxyguanosine Purine 5',8-cyclonucleoside lesions: chemistry and biology.Quantitative and in situ detection of oxidatively generated DNA damage 8,5'-cyclo-2'-deoxyadenosine using an immunoassay with a novel monoclonal antibody.Repair efficiency of (5'S)-8,5'-cyclo-2'-deoxyguanosine and (5'S)-8,5'-cyclo-2'-deoxyadenosine depends on the complementary base.Measurement of oxidatively induced DNA damage and its repair, by mass spectrometric techniques.Occurrence, Biological Consequences, and Human Health Relevance of Oxidative Stress-Induced DNA Damage.Transcription-coupled repair: an update.Formation and repair of oxidatively generated damage in cellular DNA.Divergent effects of oxidatively induced modification to the C8 of 2'-deoxyadenosine on transcription factor binding: 8,5'(S)-cyclo-2'-deoxyadenosine inhibits the binding of multiple sequence specific transcription factors, while 8-oxo-2'-deoxyadeno

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Accumulation of (5'S)-8,5'-cyclo-2'-deoxyadenosine in organs of Cockayne syndrome complementation group B gene knockout mice.

http://www.wikidata.org/entity/Q37219471

description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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2008年學術文章

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2008年學術文章

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Accumulation of (5'S)-8,5'-cyc ...... on group B gene knockout mice.

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Accumulation of (5'S)-8,5'-cyc ...... on group B gene knockout mice.

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Accumulation of (5'S)-8,5'-cyc ...... on group B gene knockout mice.

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Accumulation of (5'S)-8,5'-cyc ...... on group B gene knockout mice.

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J.DNAREP.2008.09.009

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Accumulation of (5'S)-8,5'-cyc ...... on group B gene knockout mice.

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Güldal Kirkali

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Miral Dizdaroglu

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Nadja C de Souza-Pinto

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Pawel Jaruga

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Vilhelm A Bohr

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P2860

The role of CSA in the response to oxidative DNA damage in human cells

Molecular cloning of the human DNA excision repair gene ERCC-6

Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship

A simple salting out procedure for extracting DNA from human nucleated cells

Oxidative damage to DNA in mammalian chromatin

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

Different effects of CSA and CSB deficiency on sensitivity to oxidative DNA damage

Regulation of reactive oxygen species, DNA damage, and c-Myc function by peroxiredoxin 1

A global DNA repair mechanism involving the Cockayne syndrome B (CSB) gene product can prevent the in vivo accumulation of endogenous oxidative DNA base damage

Premature aging in mice deficient in DNA repair and transcription

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