Targeting of the Sp1 binding sites of HIV-1 long terminal repeat with chromomycin. Disruption of nuclear factor.DNA complexes and inhibition of in vitro transcription

Sequence selectivity of DNA-binding drugs has recently been reported in a number of studies employing footprinting and gel retardation approaches. In this paper, we studied the biochemical effects of the sequence-selective binding of chromomycin to the long terminal repeat of the human immunodeficie...

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Veröffentlicht in:Biochemical pharmacology 1996-11, Vol.52 (10), p.1489-1498
Hauptverfasser: Bianchi, N, Passadore, M, Rutigliano, C, Feriotto, G, Mischiati, C, Gambari, R
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Sprache:eng
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