Quantification of the 2-deoxyribonolactone and nucleoside 5'-aldehyde products of 2-deoxyribose oxidation in DNA and cells by isotope-dilution gas chromatography mass spectrometry: differential effects of gamma-radiation and Fe2+-EDTA (Q33816619)

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Language	Label	Description	Also known as
English	Quantification of the 2-deoxyribonolactone and nucleoside 5'-aldehyde products of 2-deoxyribose oxidation in DNA and cells by isotope-dilution gas chromatography mass spectrometry: differential effects of gamma-radiation and Fe2+-EDTA	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 July 2017

Quantification of the 2-deoxyribonolactone and nucleoside 5'-aldehyde products of 2-deoxyribose oxidation in DNA and cells by isotope-dilution gas chromatography mass spectrometry: differential effects of gamma-radiation and Fe2+-EDTA (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

author name string

Wan Chan

1

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Europe PubMed Central

PubMed publication ID

29 July 2017

Bingzi Chen

2

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29 July 2017

Lianrong Wang

3

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Europe PubMed Central

PubMed publication ID

29 July 2017

Koli Taghizadeh

4

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Europe PubMed Central

PubMed publication ID

29 July 2017

Michael S Demott

5

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Europe PubMed Central

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29 July 2017

Peter C Dedon

6

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29 July 2017

publication date

1 May 2010

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PubMed publication ID

29 July 2017

Journal of the American Chemical Society

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29 July 2017

132

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PubMed publication ID

29 July 2017

17

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Europe PubMed Central

PubMed publication ID

29 July 2017

6145-6153

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Europe PubMed Central

PubMed publication ID

29 July 2017

The chemical toxicology of 2-deoxyribose oxidation in DNA.

1 reference

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GC/MS methods to quantify the 2-deoxypentos-4-ulose and 3'-phosphoglycolate pathways of 4' oxidation of 2-deoxyribose in DNA: application to DNA damage produced by gamma radiation and bleomycin

1 reference

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Aerobic fate of the C-3'-thymidinyl radical in single-stranded DNA.

1 reference

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4 July 2018

Use of fluorescence sensors to determine that 2-deoxyribonolactone is the major alkali-labile deoxyribose lesion produced in oxidatively damaged DNA.

1 reference

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Preparation and analysis of oligonucleotides containing lesions resulting from C5'-oxidation

1 reference

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Selective detection of 2-deoxyribonolactone in DNA.

1 reference

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The variation in biological effectiveness of X-rays and gamma rays with energy

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The release of 5-methylene-2-furanone from irradiated DNA catalyzed by cationic polyamines and divalent metal cations

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Generation of a C-3'-thymidinyl radical in single-stranded oligonucleotides under anaerobic conditions

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Reactive nitrogen species in the chemical biology of inflammation

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Half-life and DNA strand scission products of 2-deoxyribonolactone oxidative DNA damage lesions

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The role of oxidative stress in carcinogenesis

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Response of base excision repair enzymes to complex DNA lesions

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Mechanisms of DNA cleavage by copper complexes of 3-clip-phen and of its conjugate with a distamycin analogue

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High-performance liquid chromatography--tandem mass spectrometry measurement of radiation-induced base damage to isolated and cellular DNA.

1 reference

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4 July 2018

The reactivity of the 2-deoxyribonolactone lesion in single-stranded DNA and its implication in reaction mechanisms of DNA damage and repair

1 reference

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DNA strand breaking by the hydroxyl radical is governed by the accessible surface areas of the hydrogen atoms of the DNA backbone

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The free radical theory of aging matures

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Supercoiling affects the accessibility of glutathione to DNA-bound molecules: positive supercoiling inhibits calicheamicin-induced DNA damage.

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Exclusive production of bistranded DNA damage by calicheamicin.

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Free-radical mechanisms involved in the formation of sequence-dependent bistranded DNA lesions by the antitumor antibiotics bleomycin, neocarzinostatin, and calicheamicin

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Efficient protection against oxidative DNA damage in chromatin

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γ-Radiolyses of DNA in Oxygenated Aqueous Solution. Structure of an Alkali-Labile Site

1 reference

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Identifiers

10.1021/JA910928N

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

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