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1
Bactericidal action of sulfhydryl binding compounds.
Antimicrob Agents Chemother. 1973 Feb;3(2):157-61. doi: 10.1128/AAC.3.2.157.
2
Some biological effects of carbamoyloxyurea, an oxidation product of hydroxyurea.
J Bacteriol. 1970 Apr;102(1):20-3. doi: 10.1128/jb.102.1.20-23.1970.
3
Mechanism of action of nalidixic acid on Escherichia coli. 3. Conditions required for lethality.
J Bacteriol. 1966 Feb;91(2):768-73. doi: 10.1128/jb.91.2.768-773.1966.
4
Effects of mitomycin C on macromolecular synthesis in Escherichia coli.
J Bacteriol. 1967 Feb;93(2):675-82. doi: 10.1128/jb.93.2.675-682.1967.
5
Bactericidal effect against Escherichia coli of nalidixic acid and four structurally related compounds.
J Antimicrob Chemother. 1980 Jul;6(4):535-42. doi: 10.1093/jac/6.4.535.
6
Selective inhibition of f2 RNA translation by sulfhydryl reagents.
Arch Biochem Biophys. 1973 Sep;158(1):257-65. doi: 10.1016/0003-9861(73)90620-6.
7
Action of phyenethyl alcohol on the synthesis of macromolecules in Escherichia coli.
J Bacteriol. 1966 Apr;91(4):1446-52. doi: 10.1128/jb.91.4.1446-1452.1966.
9
Inhibition of Escherichia coli by thioglycerol.
Antimicrob Agents Chemother. 1981 Apr;19(4):556-61. doi: 10.1128/AAC.19.4.556.

引用本文的文献

1
Antiviral activity of 3-methyleneoxindole.
Antimicrob Agents Chemother. 1974 May;5(5):479-84. doi: 10.1128/AAC.5.5.479.
2
Mechanism of the antiviral action of 3-methyleneoxindole.
Antimicrob Agents Chemother. 1974 May;5(5):485-91. doi: 10.1128/AAC.5.5.485.

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2
Nucleic acid metabolism in relation to the lysogenic phenomenon.
J Bacteriol. 1955 Apr;69(4):460-7. doi: 10.1128/jb.69.4.460-467.1955.
7
The role of 3-methyleneoxindole in auxin action.
J Biol Chem. 1969 Sep 25;244(18):4916-20.
10
Physiology and genetics of the "ribonucleic acid control" locus in escherichia coli.
Bacteriol Rev. 1968 Sep;32(3):206-26. doi: 10.1128/br.32.3.206-226.1968.

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