Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues. - Wikidata - awgldk - TriplyDB

Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.

Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.

http://www.wikidata.org/entity/Q37327779

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C8-linked bulky guanosine DNA adducts: experimental and computational insights into adduct conformational preferences and resulting mutagenicity.

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Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.

http://www.wikidata.org/entity/Q37327779

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on June 2011

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.

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Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.

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type

label

Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.

@en

Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.

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prefLabel

Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.

@en

Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.

@nl

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European Journal of Organic Chemistry

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Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.

@en

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Heidi A Dahlmann

http://www.w3.org/2001/XMLSchema#string

Shana J Sturla

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P2860

Site-specific incorporation of N-(deoxyguanosin-8-yl)-2-acetylaminofluorene (dG-AAF) into oligonucleotides using modified 'ultra-mild' DNA synthesis

DNA Sequence Modulates the Conformation of the Food Mutagen 2-Amino-3-methylimidazo[4,5- f ]quinoline in the Recognition Sequence of the Nar I Restriction Enzyme † , ‡

Mechanism of replication blocking and bypass of Y-family polymerase by bulky acetylaminofluorene DNA adducts

8-Alkylaminoadenyl nucleotides as probes of dehydrogenase interactions with nucleotide analogs of different glycosyl conformation

Molecular orbital studies on the conformations of 8-amino- and 8-dimethylaminoadenosine 5'-monophosphate

Sensitivity of the conformation of deoxyguanosine to binding at the C-8 position by N-acetylated and unacetylated 2-aminofluorene.

Base-displaced intercalated structure of the food mutagen 2-amino-3-methylimidazo[4,5-f]quinoline in the recognition sequence of the NarI restriction enzyme, a hotspot for -2 bp deletions.

Conformational differences of the C8-deoxyguanosine adduct of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) within the NarI recognition sequence.

Biological properties of single chemical-DNA adducts: a twenty year perspective

Coding and conformational properties of oligonucleotides modified with the carcinogen N-2-acetylaminofluorene.

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scholarly article

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10.1002/EJOC.201100013

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16

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2011

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2011-06-01T00:00:00Z

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24273446

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3834893

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