Combining nucleoside analogues to achieve recognition of oligopurine tracts by triplex-forming oligonucleotides at physiological pH.
about
The triple helix: 50 years later, the outcome.Selectivity and affinity of DNA triplex forming oligonucleotides containing the nucleoside analogues 2'-O-methyl-5-(3-amino-1-propynyl)uridine and 2'-O-methyl-5-propynyluridineUnnatural nucleosides with unusual base pairing properties.Formation of stable DNA triplexes.Secondary binding sites for heavily modified triplex forming oligonucleotides.LNA effects on DNA binding and conformation: from single strand to duplex and triplex structuresDNA triplex formation with 5-dimethylaminopropargyl deoxyuridineKinetic studies on the formation of DNA triplexes containing the nucleoside analogue 2'-O-(2-aminoethyl)-5-(3-amino-1-propynyl)uridine.Optomagnetic detection of DNA triplex nanoswitches.
P2860
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P2860
Combining nucleoside analogues to achieve recognition of oligopurine tracts by triplex-forming oligonucleotides at physiological pH.
description
2005 nî lūn-bûn
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2005年の論文
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2005年学术文章
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2005年学术文章
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2005年学术文章
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2005年学术文章
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name
Combining nucleoside analogues ...... cleotides at physiological pH.
@en
Combining nucleoside analogues ...... cleotides at physiological pH.
@nl
type
label
Combining nucleoside analogues ...... cleotides at physiological pH.
@en
Combining nucleoside analogues ...... cleotides at physiological pH.
@nl
prefLabel
Combining nucleoside analogues ...... cleotides at physiological pH.
@en
Combining nucleoside analogues ...... cleotides at physiological pH.
@nl
P2093
P2860
P1433
P1476
Combining nucleoside analogues ...... cleotides at physiological pH.
@en
P2093
David A Rusling
James Booth
Keith R Fox
Loic Le Strat
Oliver Lack
Vicki E C Powers
Victoria J Broughton-Head
P2860
P304
P356
10.1016/J.FEBSLET.2005.10.056
P407
P577
2005-11-09T00:00:00Z