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Codon recognition by glycine transfer RNAs of Escherichia coli in vivo.
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Genetic mapping and dominance of the amber suppressor, Su1 (supD), in Escherichia coli K-12.
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Anticodon shift in tRNA: a novel mechanism in missense and nonsense suppression.
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Suppression in vitro: Identification of a Serine-sRNA as a "Nonsense" Suppressor.
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Mutations determining generalized resistance to aminoglycoside antibiotics in Escherichia coli.
Mol Gen Genet. 1978 Apr 25;161(1):89-98
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Glutamic acid codon suppressors derived from a unique species of glycine transfer ribonucleic acid.
J Bacteriol. 1980 Apr;142(1):131-7
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AMINO ACID SUBSTITUTIONS RESULTING FROM SUPPRESSION OF NONSENSE MUTATIONS. I. SERINE INSERTION BY THE SU-1 SUPPRESSOR GENE.
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Packaging recombinant DNA molecules into bacteriophage particles in vitro.
Proc Natl Acad Sci U S A. 1977 Aug;74(8):3259-63
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SUPPRESSION OF A COAT PROTEIN MUTANT OF THE BACTERIOPHAGE F2.
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Temperature-inducible amber suppressor: construction of plasmids containing the Escherichia coli serU- (supD-) gene under control of the bacteriophage lambda pL promoter.
J Bacteriol. 1983 Sep;155(3):1417-25
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Primary structure of an unusual glycine tRNA UGA suppressor.
Nucleic Acids Res. 1981 Dec 11;9(23):6421-8
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Fractionation of a suppressor sRNA.
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The construction in vitro of transducing derivatives of phage lambda.
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A system for shotgun DNA sequencing.
Nucleic Acids Res. 1981 Jan 24;9(2):309-21
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Linkage map of Escherichia coli K-12, edition 7.
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Nucleotide insertion in the anticodon loop of a glycine transfer RNA causes missense suppression.
Proc Natl Acad Sci U S A. 1981 Dec;78(12):7408-11
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A new pair of M13 vectors for selecting either DNA strand of double-digest restriction fragments.
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Suppressors of a UGG missense mutation in Escherichia coli.
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Deletions and insertions in the immunity region of coliphage lambda: revised measurement of the promoter-startpoint distance.
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Correlation between the abundance of Escherichia coli transfer RNAs and the occurrence of the respective codons in its protein genes.
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The conversion of amber suppressors to ochre suppressors.
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DNA sequencing with chain-terminating inhibitors.
Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7
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Suppressor genes for nonsense mutations. I. The Su-1, Su-2 and Su-3 genes of Escherichia coli.
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Molecular cloning and sequencing of pheU, a gene for Escherichia coli tRNAPhe.
Nucleic Acids Res. 1983 Jul 11;11(13):4379-89
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PREPARATION OF TRANSFORMING DEOXYRIBONUCLEIC ACID BY PHENOL TREATMENT.
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Gross map location of Escherichia coli transfer RNA genes.
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Lambdoid phages that simplify the recovery of in vitro recombinants.
Mol Gen Genet. 1977 Jan 7;150(1):53-61
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The filamentous phage (Ff) as vectors for recombinant DNA--a review.
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Variations among glyV-derived glycine tRNA suppressors of glutamic acid codons.
J Bacteriol. 1978 Jun;134(3):801-7
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Compilation and analysis of Escherichia coli promoter DNA sequences.
Nucleic Acids Res. 1983 Apr 25;11(8):2237-55
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The biochemistry of mutagenesis.
Annu Rev Biochem. 1976;45:11-37
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Studies of the complex between transfer RNAs with complementary anticodons. I. Origins of enhanced affinity between complementary triplets.
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Map positions and specificities of suppressor mutations in Escherichia coli K-12.
Genetics. 1965 Aug;52(2):319-40
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Missense and nonsense suppressors derived from a glycine tRNA by nucleotide insertion and deletion in vivo.
Mol Gen Genet. 1984;193(1):76-81
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Primary structure of Escherichia coli tRNA UUR Leu. Presence of an unknown adenosine derivative in the first position of the anticodon which recognizes the UU codon series.
J Biol Chem. 1980 Mar 10;255(5):2220-5
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A nucleotide change in the anticodon of an Escherichia coli serine transfer RNA results in supD-amber suppression.
Nucleic Acids Res. 1983 Jun 11;11(11):3823-32
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Isolation and characterization of lambda transducing bacteriophages for the su1+ (supD minus) amber suppressor of Escherichia coli.
J Bacteriol. 1975 Apr;122(1):120-8
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Suppressors causing temperature sensitivity of growth in Escherichia coli.
Genetics. 1968 Oct;60(2):269-80
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Purification of five leucine transfer ribonucleic acid species from Escherichia coli and their acylation by heterologous leucyl-transfer ribonucleic acid synthetase.
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In vitro studies on the mechanism of suppression of a nonsense mutation.
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