N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

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Minor-groove binding models for acetylaminofluorene modified DNA.

P2860

Q44304845-C69CB340-8837-42DC-957A-DCC054528052

P2860

N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

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http://www.wikidata.org/entity/Q35559045

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1985 nî lūn-bûn

@nan

1985年の論文

@ja

1985年論文

@yue

1985年論文

@zh-hant

1985年論文

@zh-hk

1985年論文

@zh-mo

1985年論文

@zh-tw

1985年论文

@wuu

1985年论文

@zh

1985年论文

@zh-cn

name

N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

@ast

N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

@en

type

Item

label

N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

@ast

N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

@en

prefLabel

N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

@ast

N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

@en

P1476

N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

@en

P2093

D G Sanford

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

T R Krugh

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

P2860

Molecular structure of a left-handed double helical DNA fragment at atomic resolution

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

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

Conformation of oligonucleotides and nucleic acids modified with 2-aminofluorene or 2-acetylaminofluorene.

Induction of the Z conformation in poly(dG-dC).poly(dG-dC) by binding of N-2-acetylaminofluorene to guanine residues.

Conformation of poly(dG-dC) . poly(dG-dC) modified by the carcinogens N-acetoxy-N-acetyl-2-aminofluorene and N-hydroxy-N-2-aminofluorene.

Ethidium bromide as a cooperative effector of a DNA structure.

Modification of ribonucleic acid by chemical carcinogens. IV. Circular dichroism and proton magnetic resonance studies of oligonucleotides modified with N-2-acetylaminofluorene.

Some current perspectives on chemical carcinogenesis in humans and experimental animals: Presidential Address.

Conformation of the deoxydinucleoside monophosphate dCpdG modified at carbon 8 of guanine with 2-(acetylamino)fluorene.

P304

5907-5917

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

P31

scholarly article

P356

10.1093/NAR/13.16.5907

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

P407

English

P433

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

P478

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

P577

1985-08-01T00:00:00Z

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

P5875

19128342

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

P698

4034398

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

P932

321921

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

N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

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P2860

P2860

N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P932