|1.||O'Neill, Peter: 1 article (05/2013)|
|2.||Folkes, Lisa K: 1 article (05/2013)|
|3.||Masutani, Chikahide: 1 article (04/2008)|
|4.||Hanaoka, Fumio: 1 article (04/2008)|
|5.||Shibutani, Shinya: 1 article (04/2008)|
|6.||Gruz, Petr: 1 article (04/2008)|
|7.||Yasui, Manabu: 1 article (04/2008)|
|8.||Honma, Masamitsu: 1 article (04/2008)|
|9.||Koyama, Naoki: 1 article (04/2008)|
|10.||Suenaga, Emi: 1 article (04/2008)|
04/04/2008 - "At the site of inflammation, nitrosatively deaminated DNA adducts such as 2'-deoxyinosine (dI) and 2'-deoxyxanthosine are primarily formed by *NO and may be associated with the development of cancer. "
01/01/2008 - "To overcome these problems, we developed a general and sensitive liquid chromatographic tandem mass spectrometry (LC/MS-MS) method to quantify, in a single DNA sample, the nucleoside forms of seven DNA lesions reflecting the range of chemistries associated with inflammation: 2'-deoxyuridine, 2'-deoxyxanthosine and 2'-deoxyinosine from nitrosative deamination; 8-oxo-2'-deoxyguanosine from oxidation; and 1,N(2)-etheno-2'-deoxyguanosine, 1,N(6)-etheno-2'-deoxyadenosine and 3,N(4)-etheno-2'-deoxycytidine arising from reaction of DNA with lipid peroxidation products. "
|3.||DNA (Deoxyribonucleic Acid)
|8.||2'-deoxyguanosine 5'-phosphate (dGMP)