Termination of RNA transcription on the replicative form DNA of bacteriophage fd
Journal of Molecular Biology, ISSN: 0022-2836, Vol: 62, Issue: 1, Page: 81-88
1971
- 29Citations
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations29
- Citation Indexes29
- CrossRef29
- 26
Article Description
In an RNA synthesizing system consisting of the doubly closed replicative form DNA of bacteriophage fd as template and purified Escherichia coli RNA polymerase holoenzyme, synthesis of RNA chains starting with pppA— proceeded to a size corresponding to about one turn of the template and terminated at either low or high salt. Transcription of the (pppA—) RNA chains was restricted to at least five different sites by adding the rho factor. Rho-induced termination at two of these sites was active even at high salt (0.2 m -KCl), whereas the termination at the other sites functioned only at low salt (less than 0.1 m -KCl).
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/002228367190132X; http://dx.doi.org/10.1016/0022-2836(71)90132-x; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0015243814&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/4945537; http://linkinghub.elsevier.com/retrieve/pii/002228367190132X; http://api.elsevier.com/content/article/PII:002228367190132X?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:002228367190132X?httpAccept=text/plain; https://linkinghub.elsevier.com/retrieve/pii/002228367190132X; http://dx.doi.org/10.1016/0022-2836%2871%2990132-x; https://dx.doi.org/10.1016/0022-2836%2871%2990132-x
Elsevier BV
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