| pubmed-article:18802636 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18802636 | lifeskim:mentions | umls-concept:C0018321 | lld:lifeskim |
| pubmed-article:18802636 | lifeskim:mentions | umls-concept:C0040087 | lld:lifeskim |
| pubmed-article:18802636 | lifeskim:mentions | umls-concept:C0063146 | lld:lifeskim |
| pubmed-article:18802636 | lifeskim:mentions | umls-concept:C0596040 | lld:lifeskim |
| pubmed-article:18802636 | lifeskim:mentions | umls-concept:C0030011 | lld:lifeskim |
| pubmed-article:18802636 | lifeskim:mentions | umls-concept:C0039778 | lld:lifeskim |
| pubmed-article:18802636 | lifeskim:mentions | umls-concept:C1522492 | lld:lifeskim |
| pubmed-article:18802636 | lifeskim:mentions | umls-concept:C0127400 | lld:lifeskim |
| pubmed-article:18802636 | pubmed:issue | 18 | lld:pubmed |
| pubmed-article:18802636 | pubmed:dateCreated | 2008-9-19 | lld:pubmed |
| pubmed-article:18802636 | pubmed:abstractText | The role of local geometric and stereo-electronic effects in tuning the preference for different cross-linked adducts between thymine and purinic bases has been analyzed by a computational approach rooted in density functional theory. Our study points out that G--T and T--G tandem lesions are produced according to the same mechanism as A--T and T--A intrastrand adducts, and in both cases purine--T adducts are preferred rather than the opposite sequences. Moreover, use of conceptual DFT tools allows the rationalization of the preferential occurrence of G--T and T--G tandem lesions in place of their A--T and T--A counterparts. | lld:pubmed |
| pubmed-article:18802636 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18802636 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18802636 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18802636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18802636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18802636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18802636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18802636 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18802636 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:18802636 | pubmed:issn | 1477-0539 | lld:pubmed |
| pubmed-article:18802636 | pubmed:author | pubmed-author:EngleG CGC | lld:pubmed |
| pubmed-article:18802636 | pubmed:author | pubmed-author:BaroneVincenz... | lld:pubmed |
| pubmed-article:18802636 | pubmed:author | pubmed-author:CiminoPaolaP | lld:pubmed |
| pubmed-article:18802636 | pubmed:author | pubmed-author:GrandAndréA | lld:pubmed |
| pubmed-article:18802636 | pubmed:author | pubmed-author:MorellChristo... | lld:pubmed |
| pubmed-article:18802636 | pubmed:author | pubmed-author:LabetVanessaV | lld:pubmed |
| pubmed-article:18802636 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18802636 | pubmed:day | 21 | lld:pubmed |
| pubmed-article:18802636 | pubmed:volume | 6 | lld:pubmed |
| pubmed-article:18802636 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18802636 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18802636 | pubmed:pagination | 3300-5 | lld:pubmed |
| pubmed-article:18802636 | pubmed:meshHeading | pubmed-meshheading:18802636... | lld:pubmed |
| pubmed-article:18802636 | pubmed:meshHeading | pubmed-meshheading:18802636... | lld:pubmed |
| pubmed-article:18802636 | pubmed:meshHeading | pubmed-meshheading:18802636... | lld:pubmed |
| pubmed-article:18802636 | pubmed:meshHeading | pubmed-meshheading:18802636... | lld:pubmed |
| pubmed-article:18802636 | pubmed:meshHeading | pubmed-meshheading:18802636... | lld:pubmed |
| pubmed-article:18802636 | pubmed:meshHeading | pubmed-meshheading:18802636... | lld:pubmed |
| pubmed-article:18802636 | pubmed:meshHeading | pubmed-meshheading:18802636... | lld:pubmed |
| pubmed-article:18802636 | pubmed:meshHeading | pubmed-meshheading:18802636... | lld:pubmed |
| pubmed-article:18802636 | pubmed:meshHeading | pubmed-meshheading:18802636... | lld:pubmed |
| pubmed-article:18802636 | pubmed:meshHeading | pubmed-meshheading:18802636... | lld:pubmed |
| pubmed-article:18802636 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18802636 | pubmed:articleTitle | Formation of cross-linked adducts between guanine and thymine mediated by hydroxyl radical and one-electron oxidation: a theoretical study. | lld:pubmed |
| pubmed-article:18802636 | pubmed:affiliation | Laboratoire Lésions des Acides Nucléiques, INAC/SCIB, UMR-E 3 (CEA/UJF), CEA-Grenoble, 17 rue des Martyrs, 38054, Grenoble cedex 9, France. | lld:pubmed |
| pubmed-article:18802636 | pubmed:publicationType | Journal Article | lld:pubmed |
