| scholarly article | Q13442814 |
| P2093 | author name string | Schmid K | |
| Lengeler JW | |||
| Hochhut B | |||
| Jahreis K | |||
| P2860 | cites work | Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase | Q26778389 |
| Genomic organization and physical mapping of the transfer RNA genes in Escherichia coli K12. | Q33993095 | ||
| Cosmid vectors for rapid genomic walking, restriction mapping, and gene transfer | Q34611719 | ||
| Analysis of the Escherichia coli genome VI: DNA sequence of the region from 92.8 through 100 minutes. | Q34756531 | ||
| SfiI genomic cleavage map of Escherichia coli K-12 strain MG1655. | Q35062141 | ||
| Chromosomal insertion sites for phages and plasmids | Q35536155 | ||
| A new type of conjugative transposon encodes resistance to sulfamethoxazole, trimethoprim, and streptomycin in Vibrio cholerae O139. | Q35609627 | ||
| Characterization of the novel nisin-sucrose conjugative transposon Tn5276 and its insertion in Lactococcus lactis | Q36118343 | ||
| Excision, transfer, and integration of NBU1, a mobilizable site-selective insertion element | Q36123078 | ||
| Selection for loss of tetracycline resistance by Escherichia coli. | Q36322268 | ||
| Conjugative transposons: an unusual and diverse set of integrated gene transfer elements. | Q36670389 | ||
| Characterization of transmissible genetic elements from sucrose-fermenting Salmonella strains | Q36763055 | ||
| Analysis of Melibiose Mutants Deficient in α-Galactosidase and Thiomethylgalactoside Permease II in Escherichia coli K-12 | Q36849640 | ||
| Molecular analysis of two ScrR repressors and of a ScrR-FruR hybrid repressor for sucrose and D-fructose specific regulons from enteric bacteria | Q38317773 | ||
| Molecular analysis of the scrA and scrB genes from Klebsiella pneumoniae and plasmid pUR400, which encode the sucrose transport protein Enzyme II Scr of the phosphotransferase system and a sucrose-6-phosphate invertase | Q38361864 | ||
| Plasmid-mediated uptake and metabolism of sucrose by Escherichia coli K-12 | Q39984134 | ||
| Construction of an Hfr strain useful for transferring recA mutations between Escherichia coli strains | Q40336158 | ||
| Conjugative transposition | Q40945171 | ||
| pACYC184-derived cloning vectors containing the multiple cloning site and lacZ alpha reporter gene of pUC8/9 and pUC18/19 plasmids | Q48317530 | ||
| Transmissible Substrate-utilizing Ability in Enterobacteria | Q50229430 | ||
| Transfer of the IncJ plasmid R391 to recombination deficient Escherichia coli K12: evidence that R391 behaves as a conjugal transposon. | Q54598301 | ||
| XbaI and BlnI genomic cleavage maps of Escherichia coli K-12 strain MG1655 and comparative analysis of other strains. | Q54654325 | ||
| Plasmid-mediated sucrose metabolism in Escherichia coli K12: mapping of the scr genes of pUR400. | Q54757263 | ||
| Mapping of the sor genes for L-sorbose degradation in the chromosome of Klebsiella pneumoniae | Q68197391 | ||
| Transposon-encoded sucrose metabolism in Lactococcus lactis. Purification of sucrose-6-phosphate hydrolase and genetic linkage to N5-(L-1-carboxyethyl)-L-ornithine synthase in strain K1 | Q68246970 | ||
| Properties of a commercial non-precious casting alloy | Q69060054 | ||
| Analysis of sucrose catabolism in Klebsiella pneumoniae and in Scr+ derivatives of Escherichia coli K12 | Q70244529 | ||
| Identification of a Sex-factor-affinity Site in E. coli as | Q72911552 | ||
| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 2097-2102 | |
| P577 | publication date | 1997-04-01 | |
| P1433 | published in | Journal of Bacteriology | Q478419 |
| P1476 | title | CTnscr94, a conjugative transposon found in enterobacteria | |
| P478 | volume | 179 |
| Q46786460 | A quantitative approach to catabolite repression in Escherichia coli |
| Q34318797 | Adaptation of sucrose metabolism in the Escherichia coli wild-type strain EC3132. |
| Q39654695 | Afa, a diffuse adherence fibrillar adhesin associated with enteropathogenic Escherichia coli. |
| Q37356533 | Antimicrobial resistance: its emergence and transmission |
| Q41928754 | Characterization of MtfA, a novel regulatory output signal protein of the glucose-phosphotransferase system in Escherichia coli K-12. |
| Q33987062 | Characterization of a novel integrative element, ICESt1, in the lactic acid bacterium Streptococcus thermophilus |
| Q33990026 | Characterization of the 13-kilobase ermF region of the Bacteroides conjugative transposon CTnDOT. |
| Q39853025 | Composition, acquisition, and distribution of the Vi exopolysaccharide-encoding Salmonella enterica pathogenicity island SPI-7. |
| Q38174149 | Conjugative and mobilizable genomic islands in bacteria: evolution and diversity. |
| Q34985996 | Conjugative transposons: the tip of the iceberg. |
| Q43453420 | Control of genes for conjugative transfer of plasmids and other mobile elements |
| Q34263261 | Ecological fitness, genomic islands and bacterial pathogenicity. A Darwinian view of the evolution of microbes |
| Q33988772 | Evidence for extensive resistance gene transfer among Bacteroides spp. and among Bacteroides and other genera in the human colon |
| Q30599966 | Evolution of microbial pathogens. |
| Q34465580 | Evolution of rhizobia by acquisition of a 500-kb symbiosis island that integrates into a phe-tRNA gene |
| Q34068595 | Genome plasticity in Enterobacteriaceae |
| Q39679833 | Genomic and functional analyses of SXT, an integrating antibiotic resistance gene transfer element derived from Vibrio cholerae |
| Q35752419 | Genomic islands in pathogenic and environmental microorganisms |
| Q33551386 | Instability of pathogenicity islands in uropathogenic Escherichia coli 536. |
| Q34528191 | Integration sites for genetic elements in prokaryotic tRNA and tmRNA genes: sublocation preference of integrase subfamilies |
| Q37529766 | Integrative and Conjugative Elements (ICEs): What They Do and How They Work |
| Q35692026 | Integrative conjugative elements of the ICEPan family play a potential role in Pantoea ananatis ecological diversification and antibiosis |
| Q36289677 | Mobile catabolic genes in bacteria |
| Q39538924 | Mobilization of plasmids and chromosomal DNA mediated by the SXT element, a constin found in Vibrio cholerae O139 |
| Q38609060 | Mobilization of the incQ plasmid R300B with a chromosomal conjugation system in Salmonella enterica serovar typhi |
| Q28709546 | Molecular control of sucrose utilization in Escherichia coli W, an efficient sucrose-utilizing strain |
| Q34321205 | Molecular genetic analysis of ICEF, an integrative conjugal element that is present as a repetitive sequence in the chromosome of Mycoplasma fermentans PG18. |
| Q34288954 | Pathogenicity islands: the tip of the iceberg |
| Q40559072 | Precise excision of the large pathogenicity island, SPI7, in Salmonella enterica serovar Typhi |
| Q33551329 | Salmonella enterica serovar Typhi strains from which SPI7, a 134-kilobase island with genes for Vi exopolysaccharide and other functions, has been deleted |
| Q39515860 | Salmonella enterica serovar typhi uses type IVB pili to enter human intestinal epithelial cells |
| Q42685814 | The ICESt1 element of Streptococcus thermophilus belongs to a large family of integrative and conjugative elements that exchange modules and change their specificity of integration |
| Q44981604 | The genes and enzymes for the catabolism of galactitol, D-tagatose, and related carbohydrates in Klebsiella oxytoca M5a1 and other enteric bacteria display convergent evolution |
| Q39558171 | Tn916 family conjugative transposons and dissemination of antimicrobial resistance determinants |
| Q35013459 | When phage, plasmids, and transposons collide: genomic islands, and conjugative- and mobilizable-transposons as a mosaic continuum |
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