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Cited by 451

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Detection of viral sequences of low reiteration frequency by in situ hybridization.

Open access
Brahic, M, Haase, A T·1978·Proceedings of the National Academy of Sciences

Abstract

The sensitivity of in situ hybridization has been increased at least 10-fold by hybridizing in cDNA excess, by increasing the diffusion of the cDNA through the cells, by hybridizing at optimum temperature, and by stabilizing hybrids during autoradiography. Saturation of intracellular RNA with [3H]cDNA has been achieved. The assay is quantitative. In situ hybridization has been used to detect and quantitate visna virus RNA in infected cells. By using [3H]cDNA with specific activity of 2 X 10(8) dpm/micrograms and conditions that reduce background to negligible levels, 10--20 copies of viral RNA per cell can be detected and quantitated after 2 days of autoradiographic exposure.

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Crossref · 10.1073/pnas.75.12.6125

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Metadata

Authors
Brahic, M., & Haase, A. T.
Venue
Proceedings of the National Academy of Sciences
Published
1978-12
Volume
75
Issue
12
Pages
6125-6129
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W1980292565
Cited by
451
References
9
FWCI
3.58
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Detection of viral sequences of low reiteration frequency by in situ hybridization. https://app.cochat.ai/papers/10.1073/pnas.75.12.6125
The paper
Brahic, M., & Haase, A. T. (1978). Detection of viral sequences of low reiteration frequency by in situ hybridization. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.75.12.6125

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

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.