Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:2818863rdf:typepubmed:Citationlld:pubmed
pubmed-article:2818863lifeskim:mentionsumls-concept:C0028948lld:lifeskim
pubmed-article:2818863lifeskim:mentionsumls-concept:C0043442lld:lifeskim
pubmed-article:2818863lifeskim:mentionsumls-concept:C0600436lld:lifeskim
pubmed-article:2818863lifeskim:mentionsumls-concept:C0026377lld:lifeskim
pubmed-article:2818863lifeskim:mentionsumls-concept:C0008813lld:lifeskim
pubmed-article:2818863lifeskim:mentionsumls-concept:C0332256lld:lifeskim
pubmed-article:2818863lifeskim:mentionsumls-concept:C2603343lld:lifeskim
pubmed-article:2818863pubmed:issue6lld:pubmed
pubmed-article:2818863pubmed:dateCreated1989-12-26lld:pubmed
pubmed-article:2818863pubmed:abstractTextA number of fully self-complementary oligodeoxynucleotides have been synthesized and examined for their ability to assume the left-handed Z-DNA conformation in high salt solutions. The B- and Z-forms are identified by circular dichroism spectra, covering both the long- (220-300 nm) and short-wavelength (185-220 nm) regions, the latter showing CD bands very useful for identifying the sense of the helix winding. The main results of the study can be summarized as follows: a) sequences composed by AT and CG blocks do support the B to Z transition, even when the AT contents amounts to 50%; b) the occurrence of consecutive purine-purine or pyrimidine-pyrimidine dyads does not inhibit the B to Z transition, although a stronger reduction of water activity is required; c) (AC)n and (GT)n containing oligonucleotides do undergo the B to Z transition in solution; d) a millimolar quantity of Ni2+ concomitant with 5 M NaClO4 is found to be very effective in bringing about the B to Z transition in most of the sequences considered in this study.lld:pubmed
pubmed-article:2818863pubmed:languageenglld:pubmed
pubmed-article:2818863pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2818863pubmed:citationSubsetIMlld:pubmed
pubmed-article:2818863pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2818863pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2818863pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2818863pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2818863pubmed:statusMEDLINElld:pubmed
pubmed-article:2818863pubmed:monthJunlld:pubmed
pubmed-article:2818863pubmed:issn0739-1102lld:pubmed
pubmed-article:2818863pubmed:authorpubmed-author:van BoomJ HJHlld:pubmed
pubmed-article:2818863pubmed:authorpubmed-author:YathindraNNlld:pubmed
pubmed-article:2818863pubmed:authorpubmed-author:ManziniGGlld:pubmed
pubmed-article:2818863pubmed:authorpubmed-author:QuadrifoglioF...lld:pubmed
pubmed-article:2818863pubmed:authorpubmed-author:van der...lld:pubmed
pubmed-article:2818863pubmed:authorpubmed-author:XodoL ELElld:pubmed
pubmed-article:2818863pubmed:issnTypePrintlld:pubmed
pubmed-article:2818863pubmed:volume6lld:pubmed
pubmed-article:2818863pubmed:ownerNLMlld:pubmed
pubmed-article:2818863pubmed:authorsCompleteYlld:pubmed
pubmed-article:2818863pubmed:pagination1217-31lld:pubmed
pubmed-article:2818863pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:2818863pubmed:meshHeadingpubmed-meshheading:2818863-...lld:pubmed
pubmed-article:2818863pubmed:meshHeadingpubmed-meshheading:2818863-...lld:pubmed
pubmed-article:2818863pubmed:meshHeadingpubmed-meshheading:2818863-...lld:pubmed
pubmed-article:2818863pubmed:meshHeadingpubmed-meshheading:2818863-...lld:pubmed
pubmed-article:2818863pubmed:meshHeadingpubmed-meshheading:2818863-...lld:pubmed
pubmed-article:2818863pubmed:meshHeadingpubmed-meshheading:2818863-...lld:pubmed
pubmed-article:2818863pubmed:meshHeadingpubmed-meshheading:2818863-...lld:pubmed
pubmed-article:2818863pubmed:meshHeadingpubmed-meshheading:2818863-...lld:pubmed
pubmed-article:2818863pubmed:meshHeadingpubmed-meshheading:2818863-...lld:pubmed
pubmed-article:2818863pubmed:meshHeadingpubmed-meshheading:2818863-...lld:pubmed
pubmed-article:2818863pubmed:year1989lld:pubmed
pubmed-article:2818863pubmed:articleTitleThe left-handed Z-DNA conformation in oligodeoxynucleotides containing different amounts of AT base pairs: a far UV circular dichroism study.lld:pubmed
pubmed-article:2818863pubmed:affiliationDepartment of Biochemistry, Biophysics and Macromolecular Chemistry, University of Trieste, Italy.lld:pubmed
pubmed-article:2818863pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2818863pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:2818863lld:pubmed