Distamycins inhibit the binding of OTF-1 and NFE-1 transfactors to their conserved DNA elements.
about
Distamycin A affects the stability of NF-kappaB p50-DNA complexes in a sequence-dependent manner.New agents in cancer clinical trials.Development of distamycin-related DNA binding anticancer drugs.Preclinical and clinical results with the natural marine product ET-743.Specific inhibition of formation of transcription complexes by a calicheamicin oligosaccharide: a paradigm for the development of transcriptional antagonists.O6-methylguanine inhibits the binding of transcription factors to DNA.Interference of transcriptional activation by the antineoplastic drug ecteinascidin-743.Distamycin inhibition of topoisomerase I-DNA interaction: a mechanistic analysis.Characterisation of a LoVo subline resistant to a benzoyl mustard derivative of distamycin A (FCE 24517).CCAAT-box binding protein NF-Y (CBF, CP1) recognizes the minor groove and distorts DNA.Distamycin-induced inhibition of formation of a nucleoprotein complex between the terminase small subunit G1P and the non-encapsidated end (pacL site) of Bacillus subtilis bacteriophage SPP1.Characterization of a protein recognizing minor groove binders-damaged DNA.Cancer chemotherapy: identifying novel anticancer drugsDifferential effects of distamycin analogues on amplification of human gene sequences by polymerase-chain reaction.Distamycin A and tallimustine inhibit TBP binding and basal in vitro transcription.Intra- and intermolecular triplex DNA formation in the murine c-myb proto-oncogene promoter are inhibited by mithramycin.Targeting of the HIV-1 long terminal repeat with chromomycin potentiates the inhibitory effects of a triplex-forming oligonucleotide on Sp1-DNA interactions and in vitro transcription.Intragenomic heterogeneity of DNA damage formation and repair: a review of cellular responses to covalent drug DNA interaction.Sequence-specific recognition of the HIV-1 long terminal repeat by distamycin: a DNAase I footprinting study.Distamycin-induced inhibition of homeodomain-DNA complexes.Biological profile of FCE 24517, a novel benzoyl mustard analogue of distamycin A.Sequence-selective binding to DNA of bis(amidinophenoxy)alkanes related to propamidine and pentamidine.Effect of DNA-binding drugs on early growth response factor-1 and TATA box-binding protein complex formation with the herpes simplex virus latency promoter.Iron(II) supramolecular helicates condense plasmid DNA and inhibit vital DNA-related enzymatic activities.An overview of recent advances in duplex DNA recognition by small molecules.
P2860
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P2860
Distamycins inhibit the binding of OTF-1 and NFE-1 transfactors to their conserved DNA elements.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
Distamycins inhibit the bindin ...... their conserved DNA elements.
@en
type
label
Distamycins inhibit the bindin ...... their conserved DNA elements.
@en
prefLabel
Distamycins inhibit the bindin ...... their conserved DNA elements.
@en
P2093
P2860
P356
P1476
Distamycins inhibit the bindin ...... their conserved DNA elements.
@en
P2093
Broggini M
D'Incalci M
Mantovani R
Mongelli N
Ottolenghi S
P2860
P304
P356
10.1093/NAR/17.3.1051
P407
P577
1989-02-01T00:00:00Z