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Volumn 6, Issue 22, 2008, Pages 4212-4217
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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-propynyluridine
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINATION;
AMINES;
COLLOIDS;
GELATION;
NEGATIVE IONS;
NUCLEIC ACIDS;
NUCLEOTIDES;
OLIGONUCLEOTIDES;
ORGANIC ACIDS;
SUGAR (SUCROSE);
SUGARS;
ASSOCIATION RATES;
ENHANCED STABILITIES;
NUCLEOSIDE ANALOGUES;
OPTIMIZED DISTRIBUTIONS;
PHYSIOLOGICAL CONDITIONS;
TRIPLEX FORMATIONS;
TRIPLEXES;
FORMING;
2' O METHYL 5 (3 AMINO 1 PROPYNYL)URIDINE;
2' O METHYL 5 PROPYNYLURIDINE;
2'-O-METHYL-5-(3-AMINO-1-PROPYNYL)URIDINE;
2'-O-METHYL-5-PROPYNYLURIDINE;
DNA;
DRUG DERIVATIVE;
OLIGONUCLEOTIDE;
TRIPLEX DNA;
URIDINE;
ANIMAL;
ARTICLE;
CHEMISTRY;
DNA DENATURATION;
ENZYME SPECIFICITY;
GENETICS;
HAMSTER;
METABOLISM;
NUCLEOTIDE SEQUENCE;
POLYACRYLAMIDE GEL ELECTROPHORESIS;
TRANSITION TEMPERATURE;
ANIMALS;
BASE SEQUENCE;
CRICETINAE;
DNA;
ELECTROPHORESIS, POLYACRYLAMIDE GEL;
NUCLEIC ACID DENATURATION;
OLIGONUCLEOTIDES;
SUBSTRATE SPECIFICITY;
TRANSITION TEMPERATURE;
URIDINE;
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EID: 55549089296
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/b810709b Document Type: Article |
Times cited : (8)
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References (30)
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