The origin of hybrid variants derived from subtype strains of foot-and-mouth disease virus.
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Antigens↗
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Results for “Genetics, Microbial”
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Virus RNA synthesis by ultraviolet-irradiated Newcastle disease virus and interferon production.
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Animals↗
Hybridization studies with the RNA of the WS strain of influenza virus and its neurotropic variant NWS.
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Animals↗
Streptomycin resistance and morphological variation in Phytophthora cactorum.
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Drug Resistance, Microbial↗
Genetic heterology between Escherichia coli K12 and a smooth strain of E. coli.
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Amino Acids↗
Transformation of Micrococcus lysodeikticus by various members of the family micrococcaceae.
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Adenine↗
Transmissible plasmid factors and fertility inhibition in Vibrio cholerae.
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Antigens, Bacterial↗
Cytoplasmic inheritance of a cold-sensitive mutant in Aspergillus nidulans.
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Aspergillus nidulans↗
Chromosomal integration of Klebsiella nitrogen fixation genes in Escherichia coli.
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Carbon Radioisotopes↗
Death of nystatin-resistant mutants of Saccharomyces cerevisiae during refrigeration.
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Cell Count↗
Nucleic acid homologies between the A and T types of Pasteurella haemolytica.
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DNA, Bacterial↗
The regulation and mechanism of DNA synthesis in bacteriophage lambda.
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Chloramphenicol↗
Prophage P1, and extrachromosomal replication unit.
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Centrifugation, Density Gradient↗
On the regulation of the initiation of DNA replication in bacteria.
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Bacillus subtilis↗
The chemical and genetic structure of bacterial ribosomes.
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Bacterial Proteins↗
Formation of polysomes in T2-infected Escherichia coli during inhibition of protein synthesis.
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Bacterial Proteins↗
Separation of spores from diploid cells of yeast by stable-flow free-boundary electrophoresis.
By the use of stable-flow free-boundary (Staflo) electrophoresis and the electrophoretic mobility difference between ascospores and diploid cells of Saccharomyces cerevisiae, a mixture of the two can be separated into spore and diploid cell fractions. The spore fraction that is obtained can then be used for genetic analysis.
Diploidy↗
Selective stimulation of one of the mechanisms for genetic recombination of bacteriophage S13.
In certain recombination-deficient (Rec(-)) bacterial strains genetic recombination of bacteriophage S13 is reduced, but the existence of some residual recombination has suggested that there is a secondary mechanism of phage recombination that is still functioning. In these Rec(-)strains it is found that there is no stimulation of recombination by irradiation of the parental phage with ultraviolet light, in contrast to the large increase found when irradiated phage particles infect a Rec(+) host. This selective stimulation of phage recombination in the Rec(+) but not in the Rec(-) strains supports the view that the phage uses at least two mechanisms of genetic recombination.
Coliphages↗