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New connections in the prokaryotic toxin-antitoxin network: relationship with the eukaryotic nonsense-mediated RNA decay system.
Anantharaman V, Aravind L
Genome Biol
2003,
4
:R81
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PubMed Central articles that cite the above article:
1.
Toxin-antitoxin loci are highly abundant in free-living but lost from host-associated prokaryotes.
Pandey DP, Gerdes K
Nucleic Acids Res
2005,
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RNase/anti-RNase activities of the bacterial parD toxin-antitoxin system.
Muñoz-Gómez AJ, Lemonnier M, Santos-Sierra S, Berzal-Herranz A, Díaz-Orejas R
J Bacteriol
2005 May,
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Comparative genomics of Thermus thermophilus and Deinococcus radiodurans: divergent routes of adaptation to thermophily and radiation resistance.
Omelchenko MV, Wolf YI, Gaidamakova EK, Matrosova VY, Vasilenko A, Zhai M, Daly MJ, Koonin EV, Makarova KS
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2005,
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Structures of the PIN domains of SMG6 and SMG5 reveal a nuclease within the mRNA surveillance complex.
Glavan F, Behm-Ansmant I, Izaurralde E, Conti E
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Toxin-antitoxin systems are ubiquitous and plasmid-encoded in vancomycin-resistant enterococci.
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Characterization of a higBA toxin-antitoxin locus in Vibrio cholerae.
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An antisense RNA controls synthesis of an SOS-induced toxin evolved from an antitoxin.
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The solution structure of ParD, the antidote of the ParDE toxin antitoxin module, provides the structural basis for DNA and toxin binding.
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The bacterial toxin RelE induces specific mRNA cleavage in the A site of the eukaryote ribosome.
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Translation affects YoeB and MazF messenger RNA interferase activities by different mechanisms.
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Crystallization of the C-terminal domain of the addiction antidote CcdA in complex with its toxin CcdB.
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What is the benefit to Escherichia coli of having multiple toxin-antitoxin systems in its genome?
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