Site-specific mutagenicity of stereochemically defined 1,N2-deoxyguanosine adducts of trans-4-hydroxynonenal in mammalian cells.
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Trans-4-hydroxy-2-nonenal inhibits nucleotide excision repair in human cells: a possible mechanism for lipid peroxidation-induced carcinogenesisThe Stereochemistry of trans -4-Hydroxynonenal-Derived Exocyclic 1, N 2 -2′-Deoxyguanosine Adducts Modulates Formation of Interstrand Cross-Links in the 5′-CpG-3′ Sequence †Conformational Interconversion of the trans -4-Hydroxynonenal-Derived (6 S ,8 R ,11 S ) 1, N 2 -Deoxyguanosine Adduct When Mismatched with Deoxyadenosine in DNAReplication Bypass of the trans -4-Hydroxynonenal-Derived (6 S ,8 R ,11 S )-1, N 2 -Deoxyguanosine DNA Adduct by the Sulfolobus solfataricus DNA Polymerase IVRepair kinetics of trans-4-hydroxynonenal-induced cyclic 1,N2-propanodeoxyguanine DNA adducts by human cell nuclear extractsBiological properties of single chemical-DNA adducts: a twenty year perspectiveReplication past a trans-4-hydroxynonenal minor-groove adduct by the sequential action of human DNA polymerases iota and kappa.Synthesis and mutagenesis of the butadiene-derived N3 2'-deoxyuridine adducts.Synthesis of the four stereoisomers of 2,3-epoxy-4-hydroxynonanal and their reactivity with deoxyguanosine.Chemistry and biology of DNA containing 1,N(2)-deoxyguanosine adducts of the alpha,beta-unsaturated aldehydes acrolein, crotonaldehyde, and 4-hydroxynonenal.DNA cross-link induced by trans-4-hydroxynonenal.Damage of DNA and proteins by major lipid peroxidation products in genome stability.Covalent modification of DNA by α, β-unsaturated aldehydes derived from lipid peroxidation: Recent progress and challenges.Mutagenic spectra arising from replication bypass of the 2,6-diamino-4-hydroxy-N(5)-methyl formamidopyrimidine adduct in primate cells.Rearrangement of the (6S,8R,11S) and (6R,8S,11R) exocyclic 1,N2-deoxyguanosine adducts of trans-4-hydroxynonenal to N2-deoxyguanosine cyclic hemiacetal adducts when placed complementary to cytosine in duplex DNA.Mutagenic potential of DNA glycation: miscoding by (R)- and (S)-N2-(1-carboxyethyl)-2'-deoxyguanosine.Interstrand DNA cross-links induced by alpha,beta-unsaturated aldehydes derived from lipid peroxidation and environmental sources.
P2860
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P2860
Site-specific mutagenicity of stereochemically defined 1,N2-deoxyguanosine adducts of trans-4-hydroxynonenal in mammalian cells.
description
2003 nî lūn-bûn
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2003年の論文
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name
Site-specific mutagenicity of ...... oxynonenal in mammalian cells.
@en
Site-specific mutagenicity of ...... oxynonenal in mammalian cells.
@nl
type
label
Site-specific mutagenicity of ...... oxynonenal in mammalian cells.
@en
Site-specific mutagenicity of ...... oxynonenal in mammalian cells.
@nl
prefLabel
Site-specific mutagenicity of ...... oxynonenal in mammalian cells.
@en
Site-specific mutagenicity of ...... oxynonenal in mammalian cells.
@nl
P2093
P356
P1476
Site-specific mutagenicity of ...... roxynonenal in mammalian cells
@en
P2093
Priscilla H Fernandes
R Stephen Lloyd
P356
10.1002/EM.10174
P577
2003-01-01T00:00:00Z