(Q54323943)

27 May 2018

title

DNA sequence analysis of mutations induced by N-2-acetylamino-7-iodofluorene in plasmid pBR322 in Escherichia coli. (English)

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27 May 2018

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Hoffmann GR

1

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27 May 2018

Fuchs RP

series ordinal

2

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27 May 2018

language of work or name

English

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publication date

1 May 1990

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27 May 2018

Journal of Molecular Biology

number of pages

8

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based on heuristic

inferred from page(s)

published in

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27 May 2018

volume

213

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27 May 2018

issue

2

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27 May 2018

page(s)

239-246

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27 May 2018

DNA binding and mutation spectra of the carcinogen N-2-aminofluorene in Escherichia coli. A correlation between the conformation of the premutagenic lesion and the mutation specificity.

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Construction and characterization of new cloning vehicle. II. A multipurpose cloning system

7 January 2021

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Construction of frameshift mutation hot spots within the tetracycline resistance gene of pBR322.

7 January 2021

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

7 January 2021

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In vitro recognition of carcinogen-induced local denaturation sites native DNA by S1 endonuclease from Aspergillus oryzae

7 January 2021

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DNA binding spectrum of the carcinogen N-acetoxy-N-2-acetylaminofluorene significantly differs from the mutation spectrum

7 January 2021

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Physical studies on deoxyribonucleic acid after covalent binding of a carcinogen

7 January 2021

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Physical basis of chemical carcinogenesis by N -2-fluorenylacetamide derivatives and analogs

7 January 2021

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Dynamic structure of DNA modified with the carcinogen N-acetoxy-N-2-acetylaminofluorene

7 January 2021

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Comparative orientation of the fluorene residue in native DNA modified by N-acetoxy-N-2-acetylaminofluorene and two 7-halogeno derivatives

7 January 2021

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Hot spots of frameshift mutations induced by the ultimate carcinogen N- acetoxy-N-2-acetylaminofluorene

7 January 2021

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A rapid boiling method for the preparation of bacterial plasmids

7 January 2021

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Strong structural effect of the position of a single acetylaminofluorene adduct within a mutation hot spot

7 January 2021

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Carcinogen-induced mutation spectrum in wild-type, uvrA and umuC strains of Escherichia coli. Strain specificity and mutation-prone sequences.

7 January 2021

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On the interaction of N-2-fluorenylhydroxylamine with nucleic acids in, vitro

7 January 2021

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8-(N-2-Fluorenylacetamido) guanosine, an Arylamidation Reaction Product of Guanosine and the Carcinogen N-Acetoxy-N-2-fluorenylacetamide in Neutral Solution*

7 January 2021

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Unwinding of supercoiled Col E1-DNA after covalent binding of the ultimate carcinogen N-acetoxy-N-2-acetylaminofluorene and its 7-iodo derivative

7 January 2021

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Comparative studies on the 7-iodo and 7-fluoro derivatives of N-acetoxy-N-2-acetylaminofluorene: binding sites on DNA and conformational change of modified deoxytrinucleotides

7 January 2021

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57 Sequencing end-labeled DNA with base-specific chemical cleavages

7 January 2021

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Spectrum of spontaneous frameshift mutations. Sequences of bacteriophage T4 rII gene frameshifts

7 January 2021

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Discrimination by antibodies between local defects in DNA induced by 2-aminofluorene derivatives

7 January 2021

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Mutagenicity of 7-iodo and 7-fluoro derivatives of N-hydroxy- and N-acetoxy-n-2-acetylaminoflourene in the Salmonella typbimurium assay

7 January 2021

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Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2805%2980187-1

Complete Nucleotide Sequence of the Escherichia coli Plasmid pBR322

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-2836%2805%2980187-1

Quantification of adducts formed in DNA treated with N-acetoxy-2-acetylaminofluorene or N-hydroxy-2-aminofluorene: comparison of trifluoroacetic acid and enzymatic degradation

7 January 2021

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Quantitative analysis of N-(guanin-8-yl)-N-acetyl-2-aminofluorene and N-(guanin-8-yl)-2-aminofluorene in modified DNA by hydrolysis in trifluoroacetic acid and high pressure liquid chromatography

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2805%2980187-1

10.1016/S0022-2836(05)80187-1

7 January 2021

Identifiers

DOI

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27 May 2018

PubMed ID

2187998

1 reference

27 May 2018