These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 11123965)

  • 1. 4-Hydroxy-2-nonenal and ethyl linoleate form N(2),3-ethenoguanine under peroxidizing conditions.
    Ham AJ; Ranasinghe A; Koc H; Swenberg JA
    Chem Res Toxicol; 2000 Dec; 13(12):1243-50. PubMed ID: 11123965
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Simultaneous quantitation of N(2),3-ethenoguanine and 1,N(2)-ethenoguanine with an immunoaffinity/gas chromatography/high-resolution mass spectrometry assay.
    Morinello EJ; Ham AJ; Ranasinghe A; Sangaiah R; Swenberg JA
    Chem Res Toxicol; 2001 Mar; 14(3):327-34. PubMed ID: 11258983
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Immunoaffinity/gas chromatography/high-resolution mass spectrometry method for the detection of N(2),3-ethenoguanine.
    Ham AJ; Ranasinghe A; Morinello EJ; Nakamura J; Upton PB; Johnson F; Swenberg JA
    Chem Res Toxicol; 1999 Dec; 12(12):1240-6. PubMed ID: 10604874
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Covalent modifications to 2'-deoxyguanosine by 4-oxo-2-nonenal, a novel product of lipid peroxidation.
    Rindgen D; Nakajima M; Wehrli S; Xu K; Blair IA
    Chem Res Toxicol; 1999 Dec; 12(12):1195-204. PubMed ID: 10604869
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of 4-oxo-2-hexenal and other direct mutagens formed in model lipid peroxidation reactions as dGuo adducts.
    Maekawa M; Kawai K; Takahashi Y; Nakamura H; Watanabe T; Sawa R; Hachisuka K; Kasai H
    Chem Res Toxicol; 2006 Jan; 19(1):130-8. PubMed ID: 16411666
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Predominance of the 1,N2-propano 2'-deoxyguanosine adduct among 4-hydroxy-2-nonenal-induced DNA lesions.
    Douki T; Odin F; Caillat S; Favier A; Cadet J
    Free Radic Biol Med; 2004 Jul; 37(1):62-70. PubMed ID: 15183195
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 4-Hydroperoxy-2-nonenal-induced formation of 1,N2-etheno-2'-deoxyguanosine adducts.
    Lee SH; Arora JA; Oe T; Blair IA
    Chem Res Toxicol; 2005 Apr; 18(4):780-6. PubMed ID: 15833039
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Formation of a substituted 1,N(6)-etheno-2'-deoxyadenosine adduct by lipid hydroperoxide-mediated generation of 4-oxo-2-nonenal.
    Rindgen D; Lee SH; Nakajima M; Blair IA
    Chem Res Toxicol; 2000 Sep; 13(9):846-52. PubMed ID: 10995257
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Long-chain adducts of trans-4-hydroxy-2-nonenal to DNA bases cause recombination, base substitutions and frameshift mutations in M13 phage.
    Kowalczyk P; Cieśla JM; Komisarski M; Kuśmierek JT; Tudek B
    Mutat Res; 2004 Jun; 550(1-2):33-48. PubMed ID: 15135639
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Liquid chromatography/mass spectrometry analysis of bifunctional electrophiles and DNA adducts from vitamin C mediated decomposition of 15-hydroperoxyeicosatetraenoic acid.
    Williams MV; Lee SH; Blair IA
    Rapid Commun Mass Spectrom; 2005; 19(6):849-58. PubMed ID: 15723435
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthesis and 32P-postlabeling/high-performance liquid chromatography separation of diastereomeric 1,N2-(1,3-propano)-2'-deoxyguanosine 3'-phosphate adducts formed from 4-hydroxy-2-nonenal.
    Yi P; Zhan D; Samokyszyn VM; Doerge DR; Fu PP
    Chem Res Toxicol; 1997 Nov; 10(11):1259-65. PubMed ID: 9403180
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Formation of etheno adducts in reactions of enals via autoxidation.
    Chen HJ; Chung FL
    Chem Res Toxicol; 1994; 7(6):857-60. PubMed ID: 7696543
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structural characterization of diastereoisomeric ethano adducts derived from the reaction of 2'-deoxyguanosine with trans,trans-2,4-decadienal.
    Loureiro AP; de Arruda Campos IP; Gomes OF; di Mascio P; Medeiros MH
    Chem Res Toxicol; 2004 May; 17(5):641-9. PubMed ID: 15144221
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mass spectrometric characterization of modifications to angiotensin II by lipid peroxidation products, 4-oxo-2(E)-nonenal and 4-hydroxy-2(E)-nonenal.
    Lee SH; Takahashi R; Goto T; Oe T
    Chem Res Toxicol; 2010 Nov; 23(11):1771-85. PubMed ID: 20977208
    [TBL] [Abstract][Full Text] [Related]  

  • 15. trans,trans-2,4-decadienal-induced 1,N(2)-etheno-2'-deoxyguanosine adduct formation.
    Loureiro AP; Di Mascio P; Gomes OF; Medeiros MH
    Chem Res Toxicol; 2000 Jul; 13(7):601-9. PubMed ID: 10898592
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of 1,N2-propanodeoxyguanosine adducts of trans-4-hydroxy-2-nonenal after gavage of trans-4-hydroxy-2-nonenal or induction of lipid peroxidation with carbon tetrachloride in F344 rats.
    Wacker M; Wanek P; Eder E
    Chem Biol Interact; 2001 Sep; 137(3):269-83. PubMed ID: 11566294
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Low glutathione level favors formation of DNA adducts to 4-hydroxy-2(E)-nonenal, a major lipid peroxidation product.
    Falletti O; Douki T
    Chem Res Toxicol; 2008 Nov; 21(11):2097-105. PubMed ID: 18847228
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Detoxification of cytotoxic alpha,beta-unsaturated aldehydes by carnosine: characterization of conjugated adducts by electrospray ionization tandem mass spectrometry and detection by liquid chromatography/mass spectrometry in rat skeletal muscle.
    Aldini G; Granata P; Carini M
    J Mass Spectrom; 2002 Dec; 37(12):1219-28. PubMed ID: 12489081
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Direct characterization of protein adducts of the lipid peroxidation product 4-hydroxy-2-nonenal using electrospray mass spectrometry.
    Bruenner BA; Jones AD; German JB
    Chem Res Toxicol; 1995 Jun; 8(4):552-9. PubMed ID: 7548735
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of an ethenoformyl adduct formed in the reaction of the potent bacterial mutagen 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone with guanosine.
    Munter T; Le Curieux F; Sjöholm R; Kronberg L
    Chem Res Toxicol; 1999 Jan; 12(1):46-52. PubMed ID: 9894017
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.