Publications
| Title | Abstract | Year(sorted ascending) Filter | PMID Filter |
|---|
| nucleotide accumulations in escherichia coli infected with some bacteriophage t4 amber mutants. | 1968 | 4302002 | |
| transcription during bacteriophage t4 development: requirements for late messenger synthesis. | 1968 | 4302631 | |
| comparison of a t4 resin sponge uptake method with a protein-bound iodine procedure. | 1968 | 4175133 | |
| enzymatic synthesis of deoxyribonucleic acid. xxv. purification and properties of deoxyribonucleic acid polymerase induced by infection with phage t4. | 1968 | 4866523 | |
| host-controlled restriction of t-even bacteriophages: relation of endonuclease i and t-even-induced nucleases to restriction. | restriction of nonglucosylated t2 phage (t(*)2) as a function of bacterial growth state was the same for endonuclease i-containing and endonuclease i-deficient strains of escherichia coli b. furthermore, e. coli strains with various levels of restriction for t2 had comparable endonuclease i activities. it was also found that a t4 mutant temperature-sensitive for gene 46 and 47 functions was fully restricted at 42 c. it therefore appears that neither endonuclease i nor the phage-induced nucleases ... | 1968 | 4911845 |
| bacteriophage-induced inhibition of host functions. i. degradation of escherichia coli deoxyribonucleic acid after t4 infection. | the kinetics of degradation of bacterial deoxyribonucleic acid (dna) after infection of escherichia coli with t4d, ultraviolet-irradiated t4d, and two amber mutants, n122 and n94, was studied by zone sedimentation through linear glycerol gradients. within 5 min after infection with any of the bacteriophages, breakdown of host genome was evident. the first product was a high-molecular-weight material (50s to 70s) and further degradation appeared to occur in discrete steps. rapid and extensive bre ... | 1968 | 4911847 |
| reversible repression of early enzyme synthesis in bacteriophage t4-infected escherichia coli. | a mutant of escherichia coli b, defective in its accumulation of k(+), was found to synthesize protein at a rate proportional to the level of this cation in the growth medium. when bacteriophage t4-infected cells were incubated in growth medium containing 1 mm k(+), phage deoxyribonucleic acid (dna) was synthesized at a rate 25% that of normal, and phage protein was synthesized at a rate of 50% of normal. deoxycytidine pyrophosphatase, a phage-directed early enzyme, shut off at a level of 55% th ... | 1968 | 4911851 |
| control of lysis of t4-infected escherichia coli. | the lysis of escherichia coli b/5 infected with t4dr48 could be delayed by addition of 9-aminoacridine (9aa). infected cells showed an early period of maximal response followed by a decline in sensitivity. the ultimate rate of lysis was also affected by the dye. deoxyribonucleic acid (dna), protein, and lysozyme synthesis began at the normal time in complexes inhibited by 9aa addition. the rates of synthesis of these macromolecules were lower in the presence of the dye, with dna and lysozyme syn ... | 1968 | 4911852 |
| molecular recombination in the ligase negative t4 amber mutant. | 1968 | 4894254 | |
| intermediates in t4 dna replication in a t4 ligase deficient strain. | 1968 | 4891959 | |
| studies on the joining of dna by polynucleotide ligase of phage t4. | 1968 | 4891960 | |
| repair and recombination in phage t4. i. genes affecting recombination. | 1968 | 4891972 | |
| repair and recombination in phage t4. ii. genes affecting uv sensitivity. | 1968 | 4891973 | |
| the function of t4 dna polymerase. | 1968 | 4891974 | |
| evidence for a possible direct role of dcmp hydroxymethylase in t4 phage dna synthesis. | 1968 | 4891975 | |
| replication and recombination of dna fragments in bacteriophage t4. | 1968 | 4891976 | |
| phage dna synthesis in bacteria infected with t4 light particles. | 1968 | 4891977 | |
| dna polymerase and the cell membrane after t4 infection. | 1968 | 4891988 | |
| initiation and propagation of growing points in the dna of phage t4. | 1968 | 4891989 | |
| purification of bacteriophage t4 lysozyme. | 1968 | 4865643 | |
| non-repeating nucleotide sequences in the genome of bacteriophage t4. | 1968 | 4866115 | |
| polyriboadenylate polymerase and its inhibition in t4-infected escherichia coli and shigella dysenteriae. | 1968 | 4866301 | |
| transcription during bacteriophage t4 development: synthesis and relative stability of early and late rna. | 1968 | 4866329 | |
| bacterial genetic factors controlling the suppression of t4 phage amber mutants. i. suppression patterns of a collection of e. coli strains. | 1968 | 4890344 | |
| bacterial genetic factors controlling the suppression of t4 phage amber mutants. ii. suppression patterns among the segregants of bacterial crosses. | 1968 | 4890345 | |
| acridine binding by escherichia coli: ph dependency and strain differences. | acridine dye binding by cells of escherichia coli has been characterized in terms of a number of parameters. there is a temperature-dependent, readily reversible binding of acriflavine which occurs to a greater extent with acridine-sensitive mutants of e. coli k-12 than with wild-type e. coli b or k-12. there is an essentially irreversible internal binding of acriflavine which occurs when the cellular permeability barriers are destroyed or altered by heat-treatment, elevated ph, treatment with t ... | 1968 | 4867737 |
| location of glucosyl transferase genes on the genetic map of phage t4. | 1968 | 4867911 | |
| assembly of the tail of bacteriophage t4. | 1968 | 4868421 | |
| some steps in the assembly of bacteriophage t4. | 1968 | 4868422 | |
| exhaustive hybridization and its application to an analysis of the ribonucleic acid synthesized in t4-infected cells. | 1968 | 4868543 | |
| modified dna-dependent rna polymerase from e. coli infected with bacteriophage t4. | 1968 | 4869542 | |
| specificity of polyribosomes in the synthesis of t4 bacteriophage head protein. | 1968 | 4870334 | |
| fractionation of the complementary strands of coliphage t4 dna based on the asymmetric distribution of the poly u and poly u,g binding sites. | 1968 | 4870391 | |
| studies on the morphopoiesis of the head of phage t-even. v. the components of the t4 capsid and of other, capsid-related structures. | 1968 | 4870477 | |
| lysis of t4-infected bacteria in the absence of lysozyme. | 1968 | 4871001 | |
| failure of incomplete t4 genomes to replicate under conditions of single infection. | 1968 | 4871002 | |
| inhibition of gamma-ray-induced degradation of e. coli bs-1 dna by infection with t1, t2 and t4 bacteriophage. | 1968 | 4871998 | |
| evidence for long dna strands in the replicating pool after t4 infection. | 1968 | 4873341 | |
| genetic transformation of the bacteriophage t4. ii. biological activity of dna fragments. | 1968 | 4873555 | |
| genetic transformation of the bacteriophage t4. i. an outline and some properties of the phage transformation system. | 1968 | 4873560 | |
| nonsense suppression in a multiauxotrophic derivative of escherichia coli 15t-: identification and consequences of an amber triplet in the deoxyribomutase gene. | previously, arginine revertants of escherichia coli wwu, a derivative of e. coli 15t(-), have been subdivided by two independent methods: (i) the streak morphology on nutrient agar, and (ii) the pattern of phage growth using amber and ochre mutants of bacteriophage t4. in the first assay, revertants were subdivided into two classes according to the appearance of streaks after incubation on nutrient agar, a thick, even line of growth defining normal revertants and a thin, irregular line defining ... | 1968 | 4874302 |
| metabolism of deoxythymidine 3'-mono- and diphosphate in normal and t4 bacteriophage-infected escherichia coli. | 1968 | 4875414 | |
| studies of dna replication in vivo. 3. accumulation of a single-stranded isolation product of dna replication by conditional mutant strains of t4. | 1968 | 4875804 | |
| influence of t4 on the formation of rna phage-specific polyribosomes and polymerase. | 1968 | 4877003 | |
| role of polynucleotide ligase in t4 dna replication. | 1968 | 4877007 | |
| coding by t4 phage dna of soluble rna containing pseudouridylic acid. | 1968 | 4877271 | |
| [t4 phage-induced lysozyme dependent e. coli treated with mytomycin c]. | 1968 | 4878093 | |
| [correlation between filament formation of e. coli and plaque-type changes of bacteriophage t4]. | 1968 | 4878095 | |
| enzymatic breakage and joining of deoxyribonucleic acid. vi. further purification and properties of polynucleotide ligase from escherichia coli infected with bacteriophage t4. | 1968 | 4879167 | |
| control of phage and host ribonucleic acid synthesis in phage t4 infected escherichia coli. | 1968 | 4879187 | |
| phospholipid synthesis in escherichia coli infected with t4 bacteriophages. | after infection of escherichia coli with t4 phage, phospholipid synthesis continued but at a reduced rate. the same phospholipid components were synthesized as in uninfected cells; however, the relative rates of (32)p(i) incorporation into phosphatidylglycerol (pg) and phosphatidylethanolamine (pe) were altered. this alteration was most pronounced during the first 10 min after infection. under these conditions, the isotope incorporated into pg equaled or exceeded that found in pg from uninfected ... | 1968 | 4880428 |
| effect of t4 infection on messenger rna synthesis in escherichia coli. | 1968 | 4880561 | |
| transfer rna coded by the t4 bacteriophage genome. | 1968 | 4880604 | |
| biochemistry of deoxyribonucleic acid-defective amber mutant of bacteriophage t4. i. ribonucleic acid metabolism. | 1968 | 4880757 | |
| the role of phage lysozyme in the life cycle of phage t4. | 1968 | 4881032 | |
| a structural gene for bacteriophage t4-induced deoxycytidine triphosphate-deoxyuridine triphosphage nucleotidohydrolase. | 1968 | 4881036 | |
| mode of action of colicins of types e1, e2, e3, and k. | the effect of colicins on deoxyribonucleic acid and protein synthesis, and also their effect on the ability of t4 phage to replicate in escherichia coli k-12, were studied. colicins of type k inhibited deoxyribonucleic acid synthesis, protein synthesis, and phage growth. among colicins of type e, there was an absolute correlation between mode of action and subdivision into types e(1), e(2), and e(3). | 1968 | 4882019 |
| [polarity mutation of t4 phage]. | 1968 | 4882392 | |
| distribution of growing points in dna of bacteriophage t4. | 1968 | 4882615 | |
| inhibition of host protein synthesis during infection of escherichia coli by bacteriophage t4. i. continued synthesis of host ribonucleic acid. | the ribonucleic acid (rna) synthesized at specified intervals during infection of escherichia coli k-12 by bacteriophage t4 was hybridized to denatured e. coli or t4 deoxyribonucleic acids (dna). the reactions were performed under conditions that maximized the yield and at rna/dna inputs such that excess dna sites were available for all rna species. most of the rna synthesized at any time during the first 3 min of infection was host-specific. the fraction declined rapidly as infection progressed ... | 1968 | 4883015 |
| further studies on the requirement for formyl residues in the synthesis of bacteriophage t4 proteins. | 1968 | 4883326 | |
| studies on the lysozyme from the bacteriophage t4 ejd7ejd4, carrying two frame shift mutations. | 1968 | 4883531 | |
| amino acid control of rna synthesis in t4-infected escherichia coli. | 1968 | 4884582 | |
| recovery of uv-inactivated e. coli cells by the v-gene action of phage t4. | 1968 | 4884675 | |
| enzymatic breakage and joining of deoxyribonucleic acid. iv. dna synthesis in e. coli infected with ligase-negative mutants of phage t4. | 1968 | 4884682 | |
| evidence for a magnesium pump induced by bacteriophage t4. | 1968 | 4972798 | |
| an in vitro transversion by a mutationally altered t4-induced dna polymerase. | 1968 | 4939629 | |
| chain growth rate of messenger rna in escherichia coli infected with bacteriophage t4. | 1968 | 4938556 | |
| identification of the transcribing dna strand for the rii and endolysin genes of coliphage t4. | 1968 | 4938565 | |
| complete primary structure of phage lysozyme from escherichia coli t4. | 1968 | 4939036 | |
| direction of translation of the lysozyme gene of bacteriophage t4 relative to the linkage map. | 1968 | 5637201 | |
| indices during administration of t4 and t3 to euthyroid adults. | 1968 | 5641753 | |
| genotypic reversion by methylene blue: the orientation of guanine-hydroxymethylcytosine at mutated sites in rii mutants of phage t4. | 1968 | 5646389 | |
| the extent of rii deletions in phage t4. | 1968 | 5647634 | |
| genetic transformation of the bacteriophage t4. 3. | 1968 | 5661361 | |
| mutagenic treatment of double- and single-stranded dna phages t4 ans s13 with hydroxylamine. | 1968 | 5663335 | |
| viscosity study of dna. ii. the effect of simple salt concentration on the viscosity of high molecular weight dna and application of viscometry to the study of dna isolated from t4 and t5 bacteriophage mutants. | 1968 | 5663405 | |
| the mutagenic effect of hydroxyaminopurine derivatives on phage t4. | 1968 | 5672975 | |
| the mechanism of inactivation of t4 bacteriophage by tritium decay. | coliphage t4 was used as a model system to study the mechanism of biological inactivation produced by tritium decay. experimentally, tritiated precursors were incorporated into phage dna (thymidine-(3)h) or into phage protein ((3)h-amino acids). the ratio of killing efficiencies for decays originating in phage dna to those originating in phage protein was 2.6. inactivation by decays from labeled amino acids was assumed to occur exclusively from beta-particle irradiation of phage dna. if decays o ... | 1968 | 5678320 |
| induction of mutation in phage t4 by extracellular treatment with methylene blue and visible light. | 1968 | 5683001 | |
| the effect of ultraviolet light on the intracellular stability of the dna of bacteriophages t2 and t4. | 1968 | 5683009 | |
| frame shift mutations near the beginning of the lysozyme gene of bacteriophage t4. | a pair of frame shift mutations in the lysozyme gene of bacteriophage t4 results in the substitution of a glutamyl-tyrosyl sequence for the asparagine residue that is the penultimate amino-terminal amino acid in the lysozyme of the wild-type strain. one of the mutations has been identified as the insertion of two bases, the other as the insertion of a single base. | 1968 | 5686221 |
| transfer of ultraviolet light induced thymine dimer from parental to progeny dna in bacteriophage t1 and t4. | 1968 | 5696504 | |
| autonomous replication of short dna fragments in the ligase negative t4 am h39x. | 1968 | 5697273 | |
| change of tryptophan residue at the 158th position of t4 bacteriophage lysozyme into a tyrosine residue by suppression and spontaneous reversion of an amber mutatnt. | 1968 | 5700428 | |
| effect of prophage w on the propagation of bacteriophages t2 and t4. | studies have been undertaken to determine whether the temperate phage omega present in escherichia coli strain w is responsible for the inability of this strain to act as a host for t2 and t4. e. coli ws, cured of phage omega, was sensitive to t2 and t4. lysogenation of e. coli c and ws with phage omega resulted in loss of ability to plate t2 and t4. however, e. coli k-12 lysogens still served as hosts for the t -even phage. two of three ws lysogens studied resembled strain w at the biochemical ... | 1968 | 5701827 |
| a map of distances along the dna molecule of phage t4. | 1968 | 5702346 | |
| the effect of helper phages and--or multiplicity of infection on the repair of ultraviolet damages in t4. | 1968 | 5722186 | |
| inactivation of phage t4 by ethylmethane sulfonate. | 1968 | 5722213 | |
| inactivating and mutagenic effects of 1-methyl-3-nitro-1-nitrosoguanidine on intracellular bacteriophage. | 1-methyl-3-nitro-1-nitrosoguanidine (ng) was able to inactivate and mutate adsorbed but not free coliphage t2. coliphage t4 was as sensitive to ng as t2. when treatment was delayed for 5 min or longer after adsorption of t2, the phage became increasingly refractory to ng inactivation. | 1968 | 5725321 |
| t4 bacteriophage mutants suppressible by a missense suppressor which inserts glycine in place of arginine for the codon aga. | phage mutants of t4 have been isolated which can multiply only on escherichia coli strains which contain a missense suppressor which is known to cause the substitution of glycine for arginine in response to the aga codon. mutations producing the suppressible phenotype were mapped and shown to occur in six different phage cistrons. two of the cistrons were concerned with deoxyribonucleic acid synthesis, two were concerned with phage structural components, and two were concerned with functions req ... | 1968 | 5725322 |
| in vitro synthesis of t4 late messenger rna. | 1968 | 5238977 | |
| dna replication in vivo by a temperature-sensitive polynucleotide ligase mutant of t4. | 1968 | 5246564 | |
| antimutagenic dna polymerases of bacteriophage t4. | 1968 | 5254574 | |
| dna replication after t4 infection. | 1968 | 5254576 | |
| a biological assay for in vitro repair of phage t4 dna. | 1968 | 5254577 | |
| amino acid acceptor activity of bacteriophage t4 transfer rna. | 1968 | 11946263 | |
| the luria-latarjet effect studied by t4-lysozyme production. | the replication of bacteriophage t4 in escherichia coli is sensitive to ultraviolet light (uv). the classical plaque assay shows a considerable increase in uv resistance starting at about 5 minutes after the bacteria are infected. production of phage lysozyme starts about 10 minutes after infection and is sensitive to irradiation. its uv resistance increases at about 4 minutes. the appearance of resistance, measured by both the plaque assay and lysozyme production, is inhibited by p-fluorophenyl ... | 1968 | 18614109 |
| mechanism of bacteriophage t4 neutralization by rabbit immunoglobulin and its proteolytic digestion fragments. | 1969 | 4185044 | |
| a semiautomated method which does not require digestion for the determination of serum thyroxine iodine (t4). | 1969 | 4304015 |