A novel triplex-forming oligonucleotide targeted to human cyclin D1 (bcl-1, proto-oncogene) promoter inhibits transcription in HeLa cells

Biochemistry

Volumn 37, Issue 8, 1998, Pages 2666-2672

  Kim, Hyung Gyoon ^a,c   Miller, Donald M ^a,b  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^b Department of Pharmacology and Toxicology and Mass Spectrometry Core Facility   (United States)

^c UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN D1; DEOXYRIBONUCLEASE I; OLIGONUCLEOTIDE; PHOSPHOROTHIOIC ACID DERIVATIVE; PURINE; PYRIMIDINE; TRANSCRIPTION FACTOR SP1;

ARTICLE; BINDING AFFINITY; BINDING SITE; CELL CULTURE; ELECTROPHORETIC MOBILITY; GENE TRANSLOCATION; GENETIC TRANSCRIPTION; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTO ONCOGENE;

BASE SEQUENCE; BINDING SITES; CYCLIN D1; GENES, BCL-1; HELA CELLS; HUMANS; NUCLEIC ACID CONFORMATION; OLIGODEOXYRIBONUCLEOTIDES; PROMOTER REGIONS (GENETICS); PROTEIN BINDING; RECOMBINANT PROTEINS; SP1 TRANSCRIPTION FACTOR; TRANSCRIPTION, GENETIC; TRANSFECTION;

EID: 0032562127     PISSN: 00062960     EISSN: None     Source Type: Journal    
DOI: 10.1021/bi972399i     Document Type: Article

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