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Cited by 176

The DOI matches its Crossref record.

Cloning and analysis of strong promoters is made possible by the downstream placement of a RNA termination signal.

Open access
Gentz, R, Langner, A, Chang, A C, Cohen, S N, Bujard, H·1981·Proceedings of the National Academy of Sciences
DOI 10.1073/pnas.78.8.4936
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Abstract

Downstream placement of a strong transcriptional termination signal has made possible the cloning of bacteriophage T5 promoters known to exhibit high signal strength. The cloning system constructed contains two easily assayable indicator functions whose expression is controlled by the integration of promoters and terminators, respectively. By assessing transcription within the indicator regions, the efficiency of promoters as well as termination signals can be determined in vitro and in vivo.

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Metadata

Authors
Gentz, R., Langner, A., Chang, A. C., Cohen, S. N., & Bujard, H.
Venue
Proceedings of the National Academy of Sciences
Publisher
Proceedings of the National Academy of Sciences
Published
1981-08
Volume
78
Issue
8
Pages
4936-4940
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
DOI
10.1073/pnas.78.8.4936
OpenAlex
W2013189569
Cited by
176
References
0
FWCI
10.51
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Cloning and analysis of strong promoters is made possible by the downstream placement of a RNA termination signal. https://app.cochat.ai/papers/10.1073/pnas.78.8.4936
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Gentz, R., Langner, A., Chang, A. C., Cohen, S. N., & Bujard, H. (1981). Cloning and analysis of strong promoters is made possible by the downstream placement of a RNA termination signal. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.78.8.4936

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.