Imidazopurinones are markers of physiological genomic damage linked to DNA instability and glyoxalase 1-associated tumour multidrug resistance (Q39708396)

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English	Imidazopurinones are markers of physiological genomic damage linked to DNA instability and glyoxalase 1-associated tumour multidrug resistance	scientific article

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scholarly article

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Europe PubMed Central

14 September 2017

Imidazopurinones are markers of physiological genomic damage linked to DNA instability and glyoxalase 1-associated tumour multidrug resistance (English)

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Europe PubMed Central

14 September 2017

multiple drug resistance

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based on heuristic

inferred from title

Sarah Jane Larkin

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Sarah J Larkin

5

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Paul J Thornalley

object named as

Paul J Thornalley

1

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Michael Stratton

7

object named as

Michael R Stratton

1 reference

Europe PubMed Central

14 September 2017

8

object named as

Naila Rabbani

1 reference

Europe PubMed Central

14 September 2017

2

object named as

Sahar Waris

1 reference

Europe PubMed Central

14 September 2017

Thomas Santarius

4

object named as

Thomas Santarius

1 reference

Europe PubMed Central

14 September 2017

author name string

Thomas Fleming

3

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Europe PubMed Central

14 September 2017

Brigitte M Winklhofer-Roob

6

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Europe PubMed Central

14 September 2017

language of work or name

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publication date

30 April 2010

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Europe PubMed Central

14 September 2017

Nucleic Acids Research

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Europe PubMed Central

14 September 2017

38

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Europe PubMed Central

14 September 2017

5432-5442

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Europe PubMed Central

14 September 2017

16

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Europe PubMed Central

14 September 2017

copyright license

Creative Commons Attribution-NonCommercial 2.5 Generic

5 October 2016

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April 2022 Public Data File from Crossref

copyright status

0 references

Quantification of N2-carboxymethyl-2'-deoxyguanosine in calf thymus DNA and cultured human kidney epithelial cells by capillary high-performance liquid chromatography-tandem mass spectrometry coupled with stable isotope dilution method

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Advanced glycation end products of DNA: quantification of N2-(1-Carboxyethyl)-2'-deoxyguanosine in biological samples by liquid chromatography electrospray ionization tandem mass spectrometry

1 reference

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Efficient and accurate bypass of N2-(1-carboxyethyl)-2'-deoxyguanosine by DinB DNA polymerase in vitro and in vivo.

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Measurement and meaning of oxidatively modified DNA lesions in urine

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Stereospecific synthesis and characterization of oligodeoxyribonucleotides containing an N2-(1-carboxyethyl)-2'-deoxyguanosine

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Selective activation of apoptosis program by S-p-bromobenzylglutathione cyclopentyl diester in glyoxalase I-overexpressing human lung cancer cells

1 reference

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1 reference

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N(2)-(1-Carboxyethyl)deoxyguanosine, a nonenzymatic glycation adduct of DNA, induces single-strand breaks and increases mutation frequencies

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The glyoxalase system in health and disease

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Preparation of nucleotide advanced glycation endproducts--imidazopurinone adducts formed by glycation of deoxyguanosine with glyoxal and methylglyoxal

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Identifiers

10.1093/NAR/GKQ306

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

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