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Paper · 321802

Shutoff of host RNA synthesis in bacteriophage T4-infected Escherichia coli in the absence of host DNA degradation and nuclear disruption.

Snustad DP and 1 other. J Virol, 1977. Cited by 6 papers, by iCite.

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ConductScience Library. Shutoff of host RNA synthesis in bacteriophage T4-infected Escherichia coli in the absence of host DNA degradation and nuclear disruption. Papers, record 321802. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/321802

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Shutoff of host RNA synthesis in bacteriophage T4-infected Escherichia coli in the absence of host DNA degradation and nuclear disruption.
PubMed
Journal
J Virol
PubMed
Year
1977
PubMed
Publication types
Journal Article, Research Support, U.S. Gov't, P.H.S.
PubMed
Citations, by iCite
6
iCite
Relative citation ratio, by iCite
0.17
iCite
Revised in PubMed
2020-07-24
PubMed

Authors2

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Snustad DPD P
2Bursch CJC J

Source PubMed

Topics7

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
ColiphagesMajor topic
DNA, BacterialMajor topic
Escherichia coliMajor topic
MutationMajor topic
RNA, BacterialMajor topic
Cell Nucleus
RNA, Viral

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References13

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
34,615,166Mutants of bacteriophage T4 deficient in the ability to induce nuclear disruption. II. Physiological state of the host nucleoid in infected cells.J Mol Biol1974https://conductscience.org/library/papers/4615166PubMed
44,615,165Mutants of bacteriophage T4 deficient in the ability to induce nuclear disruption. I. Isolation and genetic characterization.J Mol Biol1974https://conductscience.org/library/papers/4615165PubMed
54,579,886Control of T4 endonuclease IV by the D2a region of bacteriophage T4.Virology1973https://conductscience.org/library/papers/4579886PubMed
64,918,524Biological activity of bacteriophage ghosts and "take-over" of host functions by bacteriophage.Bacteriol Rev1970https://conductscience.org/library/papers/4918524PubMed
74,914,096Isolation of bacteriophage T4 mutants defective in the ability to degrade host deoxyribonucleic acid.J Virol1970https://conductscience.org/library/papers/4914096PubMed
84,930,062Mutants of bacteriophage T4 defective in the induction of T4 endonuclease II.J Biol Chem1971https://conductscience.org/library/papers/4930062PubMed
94,863,170Incorporation of uracil-14C into nucleic acids in Escherichia coli infected with bacteriophage T4 and T4 amber mutants.Virology1967https://conductscience.org/library/papers/4863170PubMed
105,323,019Early intracellular events in the replication of T4 phage DNA. I. Complex formation of replicative DNA.Proc Natl Acad Sci U S A1965https://conductscience.org/library/papers/5323019PubMed
111,089,802
Host DNA degradation after infection of Escherichia coli with bacteriophage T4: dependence of the alternate pathway of degradation which occurs in the absence of both T4 endonuclease II and nuclear disruption on T4 endonuclease IV.
J Virol1975https://conductscience.org/library/papers/1089802PubMed
12768,523
Mutants of bacteriophage T4 deficient in the ability to induce nuclear disruption: shutoff of host DNA and protein synthesis gene dosage experiments, identification of a restrictive host, and possible biological significance.
J Virol1976https://conductscience.org/library/papers/768523PubMed

Cited by6

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 6 citations.

PMIDTitleJournalYearIn PapersSource
29,876,748The plasmid vectors, pBS2ndd and pBS3ndd, for versatile cloning with low background in Escherichia coli.World J Microbiol Biotechnol2018https://conductscience.org/library/papers/29876748PubMed
6,456,362Genetic complementation by cloned bacteriophage T4 late genes.J Virol1981https://conductscience.org/library/papers/6456362PubMed
390,354Shutoff of host macromolecular synthesis after T-even bacteriophage infection.Microbiol Rev1979https://conductscience.org/library/papers/390354PubMed
390,166Host transcription in bacteriophage P22-infected Salmonella typhimurium.J Virol1979https://conductscience.org/library/papers/390166PubMed
384,022Protein induced by bacteriophage T4 which is absent in Escherichia coli infected with nuclear disruption-deficient phage mutants.J Virol1979https://conductscience.org/library/papers/384022PubMed
201,776Slow switchover from host RNA synthesis to bacteriophage RNA synthesis after infection of Escherichia coli with a T4 mutant defective in the bacteriophage T4-induced unfolding of the host nucleoid.J Virol1977https://conductscience.org/library/papers/201776PubMed

Genes0

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

None in this release.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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