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9708364
Source:
http://linkedlifedata.com/resource/pubmed/id/9708364
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rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0032550
,
umls-concept:C0242246
,
umls-concept:C1704241
pubmed:issue
1-3
pubmed:dateCreated
1998-9-16
pubmed:abstractText
3',5'-Di-O-benzoyldeoxyadenosine forms stable dT:dA:dT type complexes with poly(dT) and an oligo(dT)-cholesteryl conjugate in dilute aqueous solution. The benzoyl groups play an essential role in stabilizing these "triple stranded" complexes.
pubmed:grant
http://linkedlifedata.com/resource/pubmed/grant/GM 10265
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/8215930
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine
,
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol
,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxyadenosines
,
http://linkedlifedata.com/resource/pubmed/chemical/Oligodeoxyribonucleotides
,
http://linkedlifedata.com/resource/pubmed/chemical/Poly A
,
http://linkedlifedata.com/resource/pubmed/chemical/Poly T
,
http://linkedlifedata.com/resource/pubmed/chemical/poly(dA)
pubmed:status
MEDLINE
pubmed:issn
0732-8311
pubmed:author
pubmed-author:ChaturvediS KSK
,
pubmed-author:LetsingerR LRL
pubmed:issnType
Print
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
585-92
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:9708364-Adenosine
,
pubmed-meshheading:9708364-Cholesterol
,
pubmed-meshheading:9708364-Circular Dichroism
,
pubmed-meshheading:9708364-Deoxyadenosines
,
pubmed-meshheading:9708364-Nucleic Acid Conformation
,
pubmed-meshheading:9708364-Nucleic Acid Denaturation
,
pubmed-meshheading:9708364-Oligodeoxyribonucleotides
,
pubmed-meshheading:9708364-Poly A
,
pubmed-meshheading:9708364-Poly T
,
pubmed-meshheading:9708364-Spectrometry, Fluorescence
,
pubmed-meshheading:9708364-Spectrophotometry
,
pubmed-meshheading:9708364-Temperature
pubmed:articleTitle
Stabilization of deoxyadenosine/polynucleotide complexes by 3',5'-di-O-benzoyl substituents.
pubmed:affiliation
Department of Chemistry, Northwestern University, Evanston, IL 60208, USA.
pubmed:publicationType
Journal Article
,
Research Support, U.S. Gov't, P.H.S.