Quantitation of transcribing native simian virus 40 minichromosomes extracted from CV1 cells late in infection.
about
Transcription of Simian Virus 40 chromosomes in an extract of HeLa cells.Thermal unwinding of simian virus 40 transcription complex DNATopoisomerase I is preferentially associated with normal SV40 replicative intermediates, but is associated with both replicating and nonreplicating SV40 DNAs which are deficient in histones.Two deletions within genes for simian virus 40 structural proteins VP2 and VP3 lead to formation of abnormal transcriptional complexes.Enhancer-activated plasmid transcription complexes contain constrained supercoiling.Association of nucleosome-free regions and basal transcription factors with in vivo-assembled chromatin templates active in vitro.Mapping in vivo topoisomerase I sites on simian virus 40 DNA: asymmetric distribution of sites on replicating moleculesCapturing nuclear sequence-specific DNA-binding proteins by using simian virus 40-derived minichromosomesFactor interactions at simian virus 40 GC-box promoter elements in intact nuclei.Stable transcription complex on a class III gene in a minichromosome.Separation and properties of two kinds of simian virus 40 late transcription complexes.Barriers to nuclease Bal31 digestion across specific sites in simian virus 40 chromatin.Simian virus 40 minichromosomes contain torsionally strained DNA molecules.In vitro initiation of transcription by RNA polymerase II on in vivo-assembled chromatin templates.Chromatin structure of simian virus 40-pBR322 recombinant plasmids in COS-1 cellsChromatin structure and factor site occupancies in an in vivo-assembled transcription elongation complex.RNA footprint mapping of RNA polymerase II molecules stalled in the intergenic region of polyomavirus DNA.Immunoprecipitation of SV40 replicating minichromosomes complexed with bacteriophage T4 gene 32 protein.Transcriptionally active SV40 minichromosomes are restriction enzyme sensitive and contain a nucleosome-free origin region.Assembly of transfected DNA into chromatin: structural changes in the origin-promoter-enhancer region upon replication.A direct analysis of transcribed minichromosomes: all transcribed SV40 minichromosomes have a nuclease-hypersensitive region within a nucleosome-free domain.
P2860
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P2860
Quantitation of transcribing native simian virus 40 minichromosomes extracted from CV1 cells late in infection.
description
1981 nî lūn-bûn
@nan
1981 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1981 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1981年の論文
@ja
1981年論文
@yue
1981年論文
@zh-hant
1981年論文
@zh-hk
1981年論文
@zh-mo
1981年論文
@zh-tw
1981年论文
@wuu
name
Quantitation of transcribing n ...... m CV1 cells late in infection.
@ast
Quantitation of transcribing n ...... m CV1 cells late in infection.
@en
type
label
Quantitation of transcribing n ...... m CV1 cells late in infection.
@ast
Quantitation of transcribing n ...... m CV1 cells late in infection.
@en
prefLabel
Quantitation of transcribing n ...... m CV1 cells late in infection.
@ast
Quantitation of transcribing n ...... m CV1 cells late in infection.
@en
P2093
P2860
P1433
P1476
Quantitation of transcribing n ...... om CV1 cells late in infection
@en
P2093
P2860
P407
P577
1981-04-01T00:00:00Z