| scholarly article | Q13442814 |
| P50 | author | Gérard Guédon | Q41783072 |
| Sophie Payot | Q42890040 | ||
| Nathalie Leblond-Bourget | Q47161642 | ||
| Xavier Bellanger | Q59439961 | ||
| P2093 | author name string | Sophie Payot | |
| Nathalie Leblond-Bourget | |||
| Gérard Guédon | |||
| Xavier Bellanger | |||
| P2860 | cites work | ICESp2905, the erm(TR)-tet(O) element of Streptococcus pyogenes, is formed by two independent integrative and conjugative elements | Q40327655 |
| Sequence analysis of the mobile genome island pKLC102 of Pseudomonas aeruginosa C | Q40387879 | ||
| Unconstrained bacterial promiscuity: the Tn916–Tn1545 family of conjugative transposons | Q40466981 | ||
| Conjugative transfer of the Lactococcus lactis chromosomal sex factor promotes dissemination of the Ll.LtrB group II intron | Q40946449 | ||
| Integrative gene cloning and expression system for Streptomyces sp. US 24 and Streptomyces sp. TN 58 bioactive molecule producing strains. | Q41306035 | ||
| Identification of the origin of transfer (oriT) and a new gene required for mobilization of the SXT/R391 family of integrating conjugative elements | Q41340424 | ||
| Structure, diversity, and mobility of the Salmonella pathogenicity island 7 family of integrative and conjugative elements within Enterobacteriaceae | Q41420271 | ||
| ICEEc2, a new integrative and conjugative element belonging to the pKLC102/PAGI-2 family, identified in Escherichia coli strain BEN374. | Q41432926 | ||
| Independent acquisition of site-specific recombination factors by asn tRNA gene-targeting genomic islands | Q41453705 | ||
| A novel integrative and conjugative element (ICE) of Escherichia coli: the putative progenitor of the Yersinia high-pathogenicity island | Q41464046 | ||
| Dynamics of the SetCD-regulated integration and excision of genomic islands mobilized by integrating conjugative elements of the SXT/R391 family | Q41584437 | ||
| The conjugative transposon Tn5397 has a strong preference for integration into its Clostridium difficile target site | Q41668794 | ||
| Roles of two large serine recombinases in mobilizing the methicillin-resistance cassette SCCmec | Q41816424 | ||
| Integrative conjugative elements and related elements are major contributors to the genome diversity of Streptococcus agalactiae. | Q41868819 | ||
| Autonomous plasmid-like replication of a conjugative transposon | Q41899135 | ||
| Heterologous expression of novobiocin and clorobiocin biosynthetic gene clusters | Q41932715 | ||
| Evolution of conjugation and type IV secretion systems | Q41992246 | ||
| Determinants of entry exclusion within Eex and TraG are cytoplasmic | Q42057223 | ||
| Identification of a novel transposon (Tn6072) and a truncated staphylococcal cassette chromosome mec element in methicillin-resistant Staphylococcus aureus ST239. | Q42111323 | ||
| Identification of a novel variant of staphylococcal cassette chromosome mec, type II.5, and Its truncated form by insertion of putative conjugative transposon Tn6012. | Q42111652 | ||
| Novel mobile variants of staphylococcal cassette chromosome mec in Staphylococcus aureus | Q42112430 | ||
| Conjugative transfer of the integrative conjugative elements ICESt1 and ICESt3 from Streptococcus thermophilus | Q42144435 | ||
| XerCD-Mediated Site-Specific Recombination Leads to Loss of the 57-Kilobase Gonococcal Genetic Island | Q42165046 | ||
| Identification and characterization of the immunity repressor (ImmR) that controls the mobile genetic element ICEBs1 of Bacillus subtilis | Q42284018 | ||
| Insertion sequence evolutionary patterns highlight convergent genetic inactivations and recent genomic island acquisitions among epidemic Burkholderia cenocepacia | Q42619236 | ||
| Characterization of transposon Tn1549, conferring VanB-type resistance in Enterococcus spp. | Q42627595 | ||
| IS1294, a DNA element that transposes by RC transposition | Q42628926 | ||
| Complete genome sequence of enterohemorrhagic Escherichia coli O157:H7 and genomic comparison with a laboratory strain K-12. | Q42645426 | ||
| Circularization of Tn916 is required for expression of the transposon-encoded transfer functions: characterization of long tetracycline-inducible transcripts reading through the attachment site | Q42677860 | ||
| Modulation of virulence within a pathogenicity island in vancomycin-resistant Enterococcus faecalis | Q42678341 | ||
| 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 | Q42685814 | ||
| Genetic profile of pNOB8 from Sulfolobus: the first conjugative plasmid from an archaeon | Q42686824 | ||
| Two novel conjugative plasmids from a single strain of Sulfolobus | Q42689642 | ||
| Conjugal plasmid transfer in Streptomyces resembles bacterial chromosome segregation by FtsK/SpoIIIE | Q42762762 | ||
| ZouA, a putative relaxase, is essential for dna amplification in Streptomyces kanamyceticus | Q42792762 | ||
| The SXT/R391 family of integrative conjugative elements is composed of two exclusion groups | Q42845397 | ||
| A probabilistic model of local sequence alignment that simplifies statistical significance estimation | Q21092573 | ||
| The genome of the versatile nitrogen fixer Azorhizobium caulinodans ORS571 | Q21093358 | ||
| Characterization of a new SCCmec element in Staphylococcus cohnii | Q21136049 | ||
| Horizontal transfer, not duplication, drives the expansion of protein families in prokaryotes | Q22065251 | ||
| Whole-Genome Sequencing of Staphylococcus haemolyticus Uncovers the Extreme Plasticity of Its Genome and the Evolution of Human-Colonizing Staphylococcal Species | Q22065446 | ||
| Role of Mobile DNA in the Evolution of Vancomycin-Resistant Enterococcus faecalis | Q22065825 | ||
| A Genomic View of the Human-Bacteroides thetaiotaomicron Symbiosis | Q22065827 | ||
| Determination of the genome sequence of Porphyromonas gingivalis strain ATCC 33277 and genomic comparison with strain W83 revealed extensive genome rearrangements in P. gingivalis | Q22066058 | ||
| Complete Genomic Sequence of Nitrogen-fixing Symbiotic Bacterium Bradyrhizobium japonicum USDA110 | Q22066066 | ||
| Lateral gene transfer and the nature of bacterial innovation | Q22122396 | ||
| Gapped BLAST and PSI-BLAST: a new generation of protein database search programs | Q24545170 | ||
| Behavior of restriction-modification systems as selfish mobile elements and their impact on genome evolution | Q24555229 | ||
| Ecological genomics of marine picocyanobacteria | Q24644523 | ||
| Dynamics of Pseudomonas aeruginosa genome evolution | Q24652525 | ||
| A multicopy plasmid of the extremely thermophilic archaeon Sulfolobus effects its transfer to recipients by mating | Q24671302 | ||
| A genomic island present along the bacterial chromosome of the Parachlamydiaceae UWE25, an obligate amoebal endosymbiont, encodes a potentially functional F-like conjugative DNA transfer system | Q24799946 | ||
| Pirates of the Caudovirales | Q26862538 | ||
| Characterization of the Staphylococcus aureus rRNA Methyltransferase Encoded by orfX, the Gene Containing the Staphylococcal Chromosome Cassette mec (SCCmec) Insertion Site | Q27675120 | ||
| Profile hidden Markov models | Q27860536 | ||
| Rapid evolution of virulence and drug resistance in the emerging zoonotic pathogen Streptococcus suis | Q28475752 | ||
| Integration and excision by the large serine recombinase phiRv1 integrase | Q28487617 | ||
| Regulation of a Bacillus subtilis mobile genetic element by intercellular signaling and the global DNA damage response | Q28769513 | ||
| The SOS response controls integron recombination. | Q29346620 | ||
| Prevalence of SOS-mediated control of integron integrase expression as an adaptive trait of chromosomal and mobile integrons. | Q29346731 | ||
| Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2) | Q29547307 | ||
| Accelerated Profile HMM Searches | Q29547576 | ||
| RNA-guided genetic silencing systems in bacteria and archaea | Q29614421 | ||
| Modular evolution of TnGBSs, a new family of integrative and conjugative elements associating insertion sequence transposition, plasmid replication, and conjugation for their spreading | Q30593485 | ||
| ICEA of Mycoplasma agalactiae: a new family of self-transmissible integrative elements that confers conjugative properties to the recipient strain | Q30657431 | ||
| The biphenyl- and 4-chlorobiphenyl-catabolic transposon Tn4371, a member of a new family of genomic islands related to IncP and Ti plasmids. | Q30816609 | ||
| Control of SXT integration and excision | Q30818840 | ||
| A 90-kilobase conjugative chromosomal element coding for biphenyl and salicylate catabolism in Pseudomonas putida KF715 | Q30846631 | ||
| Novel Tn4371-ICE like element in Ralstonia pickettii and genome mining for comparative elements | Q30920788 | ||
| Staphylococcal cassette chromosome mec (SCCmec) typing of methicillin-resistant Staphylococcus aureus strains isolated in 11 Asian countries: a proposal for a new nomenclature for SCCmec elements | Q33234536 | ||
| Control of phage Bxb1 excision by a novel recombination directionality factor | Q33244373 | ||
| Contribution of exogenous genetic elements to the group A Streptococcus metagenome | Q33295386 | ||
| The complete genome sequence of Yersinia pseudotuberculosis IP31758, the causative agent of Far East scarlet-like fever | Q33296886 | ||
| Klebsiella pneumoniae multiresistance plasmid pMET1: similarity with the Yersinia pestis plasmid pCRY and integrative conjugative elements | Q33324383 | ||
| The missing link: Bordetella petrii is endowed with both the metabolic versatility of environmental bacteria and virulence traits of pathogenic Bordetellae | Q33372924 | ||
| Atypical association of DDE transposition with conjugation specifies a new family of mobile elements. | Q33404415 | ||
| Genome evolution driven by host adaptations results in a more virulent and antimicrobial-resistant Streptococcus pneumoniae serotype 14 | Q33429266 | ||
| The defective prophage pool of Escherichia coli O157: prophage-prophage interactions potentiate horizontal transfer of virulence determinants | Q33438408 | ||
| Genomic island excisions in Bordetella petrii | Q33483715 | ||
| Integrative and sequence characteristics of a novel genetic element, ICE6013, in Staphylococcus aureus | Q33489278 | ||
| Analysis of the mobilization functions of the vancomycin resistance transposon Tn1549, a member of a new family of conjugative elements | Q33517437 | ||
| Mobile antibiotic resistance encoding elements promote their own diversity | Q33519503 | ||
| Comparative ICE genomics: insights into the evolution of the SXT/R391 family of ICEs | Q33521306 | ||
| Evolution in quantum leaps: multiple combinatorial transfers of HPI and other genetic modules in Enterobacteriaceae | Q33525055 | ||
| High-throughput genome sequencing of two Listeria monocytogenes clinical isolates during a large foodborne outbreak | Q33532309 | ||
| Characterization of a Bacteroides mobilizable transposon, NBU2, which carries a functional lincomycin resistance gene | Q33603130 | ||
| Whole genome analysis of a livestock-associated methicillin-resistant Staphylococcus aureus ST398 isolate from a case of human endocarditis | Q33603634 | ||
| Tight Regulation of the intS Gene of the KplE1 Prophage: A New Paradigm for Integrase Gene Regulation | Q33719522 | ||
| Genetic and structural analysis of the Bacteroides conjugative transposon CTn341. | Q33726833 | ||
| Conjugative DNA transfer induces the bacterial SOS response and promotes antibiotic resistance development through integron activation. | Q33727996 | ||
| The Salmonella genomic island 1 is specifically mobilized in trans by the IncA/C multidrug resistance plasmid family | Q33781122 | ||
| Complete genome sequence of a serotype 11A, ST62 Streptococcus pneumoniae invasive isolate | Q33809948 | ||
| Retrotransfer or gene capture: a feature of conjugative plasmids, with ecological and evolutionary significance | Q33812337 | ||
| Lateral gene transfer of streptococcal ICE element RD2 (region of difference 2) encoding secreted proteins | Q33860454 | ||
| Functional characterization of an alkaline exonuclease and single strand annealing protein from the SXT genetic element of Vibrio cholerae | Q33875807 | ||
| Avoiding self: two Tn7-encoded proteins mediate target immunity in Tn7 transposition | Q33887753 | ||
| Intra- and interspecies genomic transfer of the Enterococcus faecalis pathogenicity island. | Q33894601 | ||
| A cryptic 65-kilobase-pair transposonlike element isolated from Bacteroides uniformis has homology with Bacteroides conjugal tetracycline resistance elements | Q36159625 | ||
| The biology of restriction and anti-restriction | Q36175695 | ||
| Tn4399, a conjugal mobilizing transposon of Bacteroides fragilis | Q36179389 | ||
| Mobile genetic elements: the agents of open source evolution | Q36247081 | ||
| The region of a Bacteroides conjugal chromosomal tetracycline resistance element which is responsible for production of plasmidlike forms from unlinked chromosomal DNA might also be involved in transfer of the element | Q36254645 | ||
| Molecular and epidemiological evidence for spread of multiresistant methicillin-susceptible Staphylococcus aureus strains in hospitals | Q36313176 | ||
| The current ICE age: biology and evolution of SXT-related integrating conjugative elements. | Q36418823 | ||
| Characterization of integrative and conjugative element ICEKp1-associated genomic heterogeneity in a Klebsiella pneumoniae strain isolated from a primary liver abscess | Q36422212 | ||
| Sequence and functional analyses of Haemophilus spp. genomic islands | Q36482003 | ||
| Mechanisms of site-specific recombination. | Q36498339 | ||
| Genome characterization and population genetic structure of the zoonotic pathogen, Streptococcus canis | Q36521441 | ||
| Secondary chromosomal attachment site and tandem integration of the mobilizable Salmonella genomic island 1. | Q36544392 | ||
| Comparative analysis of mobilizable genomic islands | Q36559349 | ||
| Conjugative transfer and cis-mobilization of a genomic island by an integrative and conjugative element of Streptococcus agalactiae | Q36667414 | ||
| A genomic islet mediates flagellar phase variation in Escherichia coli strains carrying the flagellin-specifying locus flk. | Q36747391 | ||
| Bacterial group II introns: not just splicing | Q36765046 | ||
| Modular networks and cumulative impact of lateral transfer in prokaryote genome evolution | Q36775488 | ||
| The Whole-genome sequencing of the obligate intracellular bacterium Orientia tsutsugamushi revealed massive gene amplification during reductive genome evolution | Q36955974 | ||
| Tn7 elements: engendering diversity from chromosomes to episomes. | Q37037496 | ||
| Novel staphylococcal cassette chromosome mec type, tentatively designated type VIII, harboring class A mec and type 4 ccr gene complexes in a Canadian epidemic strain of methicillin-resistant Staphylococcus aureus | Q37071999 | ||
| Plasmid capture by the Bacillus thuringiensis conjugative plasmid pXO16. | Q37127797 | ||
| Actinomycete integrative and conjugative elements | Q37181824 | ||
| Genomic islands: tools of bacterial horizontal gene transfer and evolution | Q37248338 | ||
| Revised nomenclature for transposable genetic elements | Q37263470 | ||
| tISCpe8, an IS1595-family lincomycin resistance element located on a conjugative plasmid in Clostridium perfringens. | Q37365239 | ||
| Alternative interactions between the Tn7 transposase and the Tn7 target DNA binding protein regulate target immunity and transposition | Q37367632 | ||
| Comparative genomics reveal the mechanism of the parallel evolution of O157 and non-O157 enterohemorrhagic Escherichia coli | Q37394514 | ||
| Genetic structure and distribution of the colibactin genomic island among members of the family Enterobacteriaceae. | Q37410263 | ||
| Classification of staphylococcal cassette chromosome mec (SCCmec): guidelines for reporting novel SCCmec elements | Q37450667 | ||
| A modular master on the move: the Tn916 family of mobile genetic elements. | Q37493047 | ||
| Replication and conjugative mobilization of broad host-range IncQ plasmids | Q37493631 | ||
| Challenging a paradigm: the role of DNA homology in tyrosine recombinase reactions. | Q37504513 | ||
| Transferable antibiotic resistance elements in Haemophilus influenzae share a common evolutionary origin with a diverse family of syntenic genomic islands | Q37623029 | ||
| ICESluvan, a 94-kilobase mosaic integrative conjugative element conferring interspecies transfer of VanB-type glycopeptide resistance, a novel bacitracin resistance locus, and a toxin-antitoxin stabilization system. | Q42872099 | ||
| Nucleotide sequence and functional analysis of the tet (M)-carrying conjugative transposon Tn5251 of Streptococcus pneumoniae. | Q43058521 | ||
| Genomic and functional analysis of ICEPdaSpa1, a fish-pathogen-derived SXT-related integrating conjugative element that can mobilize a virulence plasmid. | Q43184083 | ||
| Analysis of a Bacteroides conjugative transposon using a novel "targeted capture" model system | Q43727479 | ||
| Analysis of the transcriptome of Legionella pneumophila hfq mutant reveals a new mobile genetic element. | Q44148902 | ||
| Two novel arginine catabolic mobile elements and staphylococcal chromosome cassette mec composite islands in community-acquired methicillin-resistant Staphylococcus aureus genotypes ST5-MRSA-V and ST5-MRSA-II. | Q44244004 | ||
| Transposon Tn7. cis-Acting sequences in transposition and transposition immunity | Q44700800 | ||
| Properties of polylysogens containing derepressed lambdaN- prophages. 3. A large number of intergrated lambda prophages | Q44789526 | ||
| Dichotomy in the evolution of pathogenicity island and bacteriophage encoded integrases from pathogenic Escherichia coli strains. | Q45085384 | ||
| Sphingobacterium sp. strain PM2-P1-29 harbours a functional tet(X) gene encoding for the degradation of tetracycline | Q46136624 | ||
| Initiation and termination of DNA transfer at F plasmid oriT. | Q46346774 | ||
| The highly dynamic CRISPR1 system of Streptococcus agalactiae controls the diversity of its mobilome. | Q46482246 | ||
| In vitro reconstitution of a single-stranded transposition mechanism of IS608. | Q46749573 | ||
| Genomic islands are dynamic, ancient integrative elements in bacterial evolution. | Q47623825 | ||
| Transposition of Tn4451 and Tn4453 involves a circular intermediate that forms a promoter for the large resolvase, TnpX. | Q47816165 | ||
| Monitoring genome evolution ex vivo: reversible chromosomal integration of a 106 kb plasmid at two tRNA(Lys) gene loci in sequential Pseudomonas aeruginosa airway isolates. | Q47824292 | ||
| Analysis of sequences flanking the vap regions of Dichelobacter nodosus: evidence for multiple integration events, a killer system, and a new genetic element | Q48054553 | ||
| A group II intron in a conjugative transposon from the gram-positive bacterium, Clostridium difficile | Q48059925 | ||
| Identification and characterization of a new conjugation/type IVA secretion system (trb/tra) of Legionella pneumophila Corby localized on two mobile genomic islands | Q48077439 | ||
| Mode and origin of replication of pSAM2, a conjugative integrating element of Streptomyces ambofaciens. | Q48095787 | ||
| Complete and variant forms of the 'gonococcal genetic island' in Neisseria meningitidis. | Q48108998 | ||
| Neisseria gonorrhoeae secretes chromosomal DNA via a novel type IV secretion system | Q48147768 | ||
| Evolution of genomic islands by deletion and tandem accretion by site-specific recombination: ICESt1-related elements from Streptococcus thermophilus | Q48195856 | ||
| Conjugal immunity of Streptomyces strains carrying the integrative element pSAM2 is due to the pif gene (pSAM2 immunity factor). | Q48258190 | ||
| The integrative element pSAM2 from Streptomyces: kinetics and mode of conjugal transfer | Q48336440 | ||
| The Salmonella genomic island 1 is an integrative mobilizable element. | Q50092650 | ||
| Shuttle transfer (or retrotransfer) of chromosomal markers mediated by plasmid pULB113. | Q50200850 | ||
| The new IS1595 family, its relation to IS1 and the frontier between insertion sequences and transposons. | Q51848539 | ||
| Development of an integrative vector for the expression of antisense RNA in Clostridium difficile. | Q53852733 | ||
| Growth-phase-dependent mobility of the lvh-encoding region in Legionella pneumophila strain Paris. | Q54568001 | ||
| Plasmids from freshwater environments capable of IncQ retrotransfer are diverse and include pQKH54, a new IncP-1 subgroup archetype. | Q54584426 | ||
| Retrotransfer of IncP plasmid R751 from Escherichia coli maxicells: evidence for the genetic sufficiency of self-transferable plasmids for bacterial conjugation. | Q54650772 | ||
| Intracellular excision and reintegration dynamics of the ICEclc genomic island of Pseudomonas knackmussii sp. strain B13 | Q56893600 | ||
| Tn4451 from Clostridium perfringens is a mobilizable transposon that encodes the functional Mob protein, TnpZ | Q58029354 | ||
| Heterogeneity of Tn5253-like composite elements in clinical Streptococcus pneumoniae isolates | Q34737570 | ||
| The arginine catabolic mobile element and staphylococcal chromosomal cassette mec linkage: convergence of virulence and resistance in the USA300 clone of methicillin-resistant Staphylococcus aureus | Q34808060 | ||
| Selective pressures to maintain attachment site specificity of integrative and conjugative elements | Q34845772 | ||
| Two distinct genetic elements are responsible for erm(TR)-mediated erythromycin resistance in tetracycline-susceptible and tetracycline-resistant strains of Streptococcus pyogenes | Q34933219 | ||
| Conjugative transposons: the tip of the iceberg. | Q34985996 | ||
| When phage, plasmids, and transposons collide: genomic islands, and conjugative- and mobilizable-transposons as a mosaic continuum | Q35013459 | ||
| The clostridial mobilisable transposons | Q35060037 | ||
| Insights on antibiotic resistance of Staphylococcus aureus from its whole genome: genomic island SCC. | Q35091151 | ||
| Antibiotic resistance conferred by a class I integron and SXT constin in Vibrio cholerae O1 strains isolated in Laos | Q35124484 | ||
| Detection of staphylococcal cassette chromosome mec type XI carrying highly divergent mecA, mecI, mecR1, blaZ, and ccr genes in human clinical isolates of clonal complex 130 methicillin-resistant Staphylococcus aureus | Q35139513 | ||
| The Gonococcal Genetic Island and Type IV Secretion in the Pathogenic Neisseria | Q35155296 | ||
| Genomic islands and the evolution of catabolic pathways in bacteria | Q35172595 | ||
| What traits are carried on mobile genetic elements, and why? | Q35246646 | ||
| Interstrain transfer of the large pathogenicity island (PAPI-1) of Pseudomonas aeruginosa | Q35544327 | ||
| Requirements for strand- and site-specific cleavage within the oriT region of Tn4399, a mobilizing transposon from Bacteroides fragilis | Q35587030 | ||
| The mobilization regions of two integrated Bacteroides elements, NBU1 and NBU2, have only a single mobilization protein and may be on a cassette | Q35589859 | ||
| A new type of conjugative transposon encodes resistance to sulfamethoxazole, trimethoprim, and streptomycin in Vibrio cholerae O139. | Q35609627 | ||
| Tn7 transposition as a probe of cis interactions between widely separated (190 kilobases apart) DNA sites in the Escherichia coli chromosome | Q35615633 | ||
| CTnscr94, a conjugative transposon found in enterobacteria | Q35621277 | ||
| Spontaneous staphylococcal cassette chromosome mec element excision in Staphylococcus aureus nasal carriers | Q35689101 | ||
| Genomic islands in pathogenic and environmental microorganisms | Q35752419 | ||
| Transposon Tn7 is widespread in diverse bacteria and forms genomic islands. | Q35759494 | ||
| Complete genome sequence of the prototype lactic acid bacterium Lactococcus lactis subsp. cremoris MG1363. | Q35759658 | ||
| Characterization of a small mobilizable transposon, MTnSag1, in Streptococcus agalactiae | Q35879324 | ||
| Prevalence and detailed mapping of the gonococcal genetic island in Neisseria meningitidis | Q35942819 | ||
| Retrotransfer in Escherichia coli conjugation: bidirectional exchange or de novo mating? | Q35966743 | ||
| Unexpected effect of a Bacteroides conjugative transposon, CTnDOT, on chromosomal gene expression in its bacterial host | Q35990796 | ||
| Lateral gene transfer between obligate intracellular bacteria: evidence from the Rickettsia massiliae genome | Q36098291 | ||
| Nucleotide sequence analysis of the termini and chromosomal locus involved in site-specific integration of the streptococcal conjugative transposon Tn5252. | Q36099736 | ||
| Characterization of the novel nisin-sucrose conjugative transposon Tn5276 and its insertion in Lactococcus lactis | Q36118343 | ||
| Characterization of a "mobilization cassette" in transposon Tn4399 from Bacteroides fragilis | Q36122099 | ||
| Excision, transfer, and integration of NBU1, a mobilizable site-selective insertion element | Q36123078 | ||
| Characterization of the mobilization region of a Bacteroides insertion element (NBU1) that is excised and transferred by Bacteroides conjugative transposons | Q36123086 | ||
| Towards a more accurate annotation of tyrosine-based site-specific recombinases in bacterial genomes | Q36150447 | ||
| Conjugative DNA metabolism in Gram-negative bacteria | Q37634129 | ||
| Novel non-mecA-containing staphylococcal chromosomal cassette composite island containing pbp4 and tagF genes in a commensal staphylococcal species: a possible reservoir for antibiotic resistance islands in Staphylococcus aureus | Q37734157 | ||
| Integrative and conjugative elements: mosaic mobile genetic elements enabling dynamic lateral gene flow. | Q37770056 | ||
| Integrons. | Q37779789 | ||
| Mobility of plasmids. | Q37784107 | ||
| Lateral genetic transfer and the construction of genetic exchange communities | Q37827559 | ||
| Tn916-like genetic elements: a diverse group of modular mobile elements conferring antibiotic resistance | Q37887044 | ||
| Combinatorial events of insertion sequences and ICE in Gram-negative bacteria | Q37897646 | ||
| Integrative mobile elements exploiting Xer recombination | Q38057830 | ||
| A phage protein that binds φC31 integrase to switch its directionality | Q38427999 | ||
| Mobilization of the incQ plasmid R300B with a chromosomal conjugation system in Salmonella enterica serovar typhi | Q38609060 | ||
| Structural comparison of three types of staphylococcal cassette chromosome mec integrated in the chromosome in methicillin-resistant Staphylococcus aureus | Q39477045 | ||
| Conjugative transposons and the dissemination of antibiotic resistance in streptococci | Q39505566 | ||
| Site-specific recombination with the chromosomal tRNA(Leu) gene by the large conjugative Haemophilus resistance plasmid | Q39651812 | ||
| Isolation and characterization of cLV25, a Bacteroides fragilis chromosomal transfer factor resembling multiple Bacteroides sp. mobilizable transposons | Q39678677 | ||
| Genomic and functional analyses of SXT, an integrating antibiotic resistance gene transfer element derived from Vibrio cholerae | Q39679833 | ||
| SGI2, a relative of Salmonella genomic island SGI1 with an independent origin. | Q39687304 | ||
| Differential regulation of two closely related integrative and conjugative elements from Streptococcus thermophilus. | Q39693385 | ||
| The streptomyces genome contains multiple pseudo-attB sites for the (phi)C31-encoded site-specific recombination system | Q39694905 | ||
| NikAB- or NikB-dependent intracellular recombination between tandemly repeated oriT sequences of plasmid R64 in plasmid or single-stranded phage vectors | Q39775222 | ||
| Regulation, integrase-dependent excision, and horizontal transfer of genomic islands in Legionella pneumophila | Q39797873 | ||
| DNA-damaging agents induce the RecA-independent homologous recombination functions of integrating conjugative elements of the SXT/R391 family | Q39799457 | ||
| Mechanism of retrotransfer in conjugation: prior transfer of the conjugative plasmid is required | Q39840515 | ||
| Homing of a group II intron from Lactococcus lactis subsp. lactis ML3. | Q39847386 | ||
| Composition, acquisition, and distribution of the Vi exopolysaccharide-encoding Salmonella enterica pathogenicity island SPI-7. | Q39853025 | ||
| Identification of a catabolic transposon, Tn4371, carrying biphenyl and 4-chlorobiphenyl degradation genes in Alcaligenes eutrophus A5. | Q39925494 | ||
| Identification of a circular intermediate in the transfer and transposition of Tn4555, a mobilizable transposon from Bacteroides spp. | Q39928223 | ||
| Conjugation-independent, site-specific recombination at the oriT of the IncW plasmid R388 mediated by TrwC. | Q39932074 | ||
| The presence of conjugative transposon Tn916 in the recipient strain does not impede transfer of a second copy of the element | Q39938842 | ||
| Tn5253, the pneumococcal omega (cat tet) BM6001 element, is a composite structure of two conjugative transposons, Tn5251 and Tn5252. | Q39939314 | ||
| Identification of Tn4451 and Tn4452, chloramphenicol resistance transposons from Clostridium perfringens | Q39956349 | ||
| Identification of a new insertion element, similar to gram-negative IS26, on the lactose plasmid of Streptococcus lactis ML3. | Q39963100 | ||
| Horizontally acquired genomic islands in the tubercle bacilli | Q40085600 | ||
| Pathogenicity islands and the evolution of microbes | Q33920183 | ||
| Site-specific mobilization of vinyl chloride respiration islands by a mechanism common in Dehalococcoides | Q33920363 | ||
| Molecular analysis of antibiotic resistance gene clusters in vibrio cholerae O139 and O1 SXT constins. | Q33983266 | ||
| Roles of CcrA and CcrB in excision and integration of staphylococcal cassette chromosome mec, a Staphylococcus aureus genomic island | Q33983355 | ||
| Characterization of a novel integrative element, ICESt1, in the lactic acid bacterium Streptococcus thermophilus | Q33987062 | ||
| Evidence for extensive resistance gene transfer among Bacteroides spp. and among Bacteroides and other genera in the human colon | Q33988772 | ||
| Characterization of the 13-kilobase ermF region of the Bacteroides conjugative transposon CTnDOT. | Q33990026 | ||
| Characterization of the ends and target sites of the novel conjugative transposon Tn5397 from Clostridium difficile: excision and circularization is mediated by the large resolvase, TndX. | Q33994284 | ||
| Integration and excision of a Bacteroides conjugative transposon, CTnDOT. | Q33994404 | ||
| Formation of chromosomal tandem arrays of the SXT element and R391, two conjugative chromosomally integrating elements that share an attachment site | Q33995532 | ||
| Complete nucleotide sequence of a 43-kilobase genomic island associated with the multidrug resistance region of Salmonella enterica serovar Typhimurium DT104 and its identification in phage type DT120 and serovar Agona | Q33996939 | ||
| Conserved target for group II intron insertion in relaxase genes of conjugative elements of gram-positive bacteria | Q33999519 | ||
| The repertoire of ICE in prokaryotes underscores the unity, diversity, and ubiquity of conjugation | Q34005318 | ||
| Genetic organisation, mobility and predicted functions of genes on integrated, mobile genetic elements in sequenced strains of Clostridium difficile. | Q34005408 | ||
| Bacteriophage genes that inactivate the CRISPR/Cas bacterial immune system. | Q34034778 | ||
| Genome organization of epidemic Acinetobacter baumannii strains | Q34045074 | ||
| Uncovering the prevalence and diversity of integrating conjugative elements in actinobacteria | Q34082912 | ||
| Widespread distribution of a tet W determinant among tetracycline-resistant isolates of the animal pathogen Arcanobacterium pyogenes | Q34107303 | ||
| The IncP island in the genome of Brucella suis 1330 was acquired by site-specific integration. | Q34111611 | ||
| Site-specific recombinase and integrase activities of a conjugative relaxase in recipient cells | Q34132259 | ||
| Bacterial plasmid partition machinery: a minimalist approach to survival | Q34239273 | ||
| Ecological fitness, genomic islands and bacterial pathogenicity. A Darwinian view of the evolution of microbes | Q34263261 | ||
| Phage integrases: biology and applications | Q34285284 | ||
| SOS response promotes horizontal dissemination of antibiotic resistance genes | Q34285480 | ||
| What makes the bacteriophage lambda Red system useful for genetic engineering: molecular mechanism and biological function | Q34303620 | ||
| Comparative sequence analysis of the symbiosis island of Mesorhizobium loti strain R7A. | Q34312033 | ||
| Amplification of the tetracycline resistance determinant of pAMalpha1 in Enterococcus faecalis requires a site-specific recombination event involving relaxase | Q34318344 | ||
| Molecular genetic analysis of ICEF, an integrative conjugal element that is present as a repetitive sequence in the chromosome of Mycoplasma fermentans PG18. | Q34321205 | ||
| Analysis of a Clostridium difficile PCR ribotype 078 100 kilobase island reveals the presence of a novel transposon, Tn6164 | Q34322185 | ||
| Shaping bacterial genomes with integrative and conjugative elements | Q34327965 | ||
| Horizontal gene transfer, genome innovation and evolution | Q34447824 | ||
| Characterization of a new CAMP factor carried by an integrative and conjugative element in Streptococcus agalactiae and spreading in Streptococci | Q34477545 | ||
| Mobile elements as a combination of functional modules. | Q34499476 | ||
| Genomic islands and the ecology and evolution of Prochlorococcus. | Q34504656 | ||
| The clc element of Pseudomonas sp. strain B13, a genomic island with various catabolic properties | Q34509988 | ||
| The CRISPRs, they are a-changin': how prokaryotes generate adaptive immunity | Q34645309 | ||
| A new integrative conjugative element occurs in Mycoplasma agalactiae as chromosomal and free circular forms | Q34697053 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | bacterial evolution | Q115395667 |
| P304 | page(s) | 720-760 | |
| P577 | publication date | 2014-01-27 | |
| P1433 | published in | FEMS Microbiology Reviews | Q15762226 |
| P1476 | title | Conjugative and mobilizable genomic islands in bacteria: evolution and diversity | |
| P478 | volume | 38 |
| Q46255535 | A DNA segment encoding the anticodon stem/loop of tRNA determines the specific recombination of integrative-conjugative elements in Acidithiobacillus species |
| Q37710403 | A Glimpse into the World of Integrative and Mobilizable Elements in Streptococci Reveals an Unexpected Diversity and Novel Families of Mobilization Proteins. |
| Q89995978 | A Yersinia ruckeri TIR Domain-Containing Protein (STIR-2) Mediates Immune Evasion by Targeting the MyD88 Adaptor |
| Q90694089 | A novel system of bacterial cell division arrest implicated in horizontal transmission of an integrative and conjugative element |
| Q35793792 | Adaptation in Toxic Environments: Arsenic Genomic Islands in the Bacterial Genus Thiomonas |
| Q51275252 | Aeromonas salmonicida subsp. salmonicida strains isolated from Chinese freshwater fish contain a novel genomic island and possible regional-specific mobile genetic elements profiles. |
| Q58697017 | An ancient family of mobile genomic islands introducing cephalosporinase and carbapenemase genes in Enterobacteriaceae |
| Q40896411 | An operon of three transcriptional regulators controls horizontal gene transfer of the integrative and conjugative element ICEclc in Pseudomonas knackmussii B13 |
| Q41363416 | Analysis of Streptococcus agalactiae pan-genome for prevalence, diversity and functionality of integrative and conjugative or mobilizable elements integrated in the tRNA(Lys CTT) gene |
| Q47769087 | Analysis of multiple haloarchaeal genomes suggests that the quinone-dependent respiratory nitric oxide reductase is an important source of nitrous oxide in hypersaline environments. |
| Q35883819 | Antibiotic Susceptibility Profiles of Dairy Leuconostoc, Analysis of the Genetic Basis of Atypical Resistances and Transfer of Genes In Vitro and in a Food Matrix |
| Q38608936 | Biological action in Read-Write genome evolution |
| Q64082357 | Biological and Structural Diversity of Type IV Secretion Systems |
| Q92351056 | Biphenyl/PCB Degrading bph Genes of Ten Bacterial Strains Isolated from Biphenyl-Contaminated Soil in Kitakyushu, Japan: Comparative and Dynamic Features as Integrative Conjugative Elements (ICEs) |
| Q39675245 | CRISPR-Cas Defense System and Potential Prophages in Cyanobacteria Associated with the Coral Black Band Disease |
| Q60043978 | Carbapenemases on the move: it’s good to be on ICEs |
| Q53789771 | Characterization of a genomic island harbouring a new vanD allele from Enterococcus faecium N15-508 isolated in Canada. |
| Q64068786 | Characterization of a relaxase belonging to the MOB family, a widespread family in Firmicutes mediating the transfer of ICEs |
| Q92282538 | Chromosomal Conjugative and Mobilizable Elements in Streptococcus suis: Major Actors in the Spreading of Antimicrobial Resistance and Bacteriocin Synthesis Genes |
| Q34611833 | Chromosomal transfers in mycoplasmas: when minimal genomes go mobile. |
| Q35328032 | Classification of prokaryotic genetic replicators: between selfishness and altruism |
| Q54231444 | ClustAGE: a tool for clustering and distribution analysis of bacterial accessory genomic elements. |
| Q92564790 | Comparative Genomics of Marine Sponge-Derived Streptomyces spp. Isolates SM17 and SM18 With Their Closest Terrestrial Relatives Provides Novel Insights Into Environmental Niche Adaptations and Secondary Metabolite Biosynthesis Potential |
| Q58546778 | Comparative genomics of the Komagataeibacter strains-Efficient bionanocellulose producers |
| Q91917473 | Comprehensive analysis of chromosomal mobile genetic elements in the gut microbiome reveals phylum-level niche-adaptive gene pools |
| Q26746938 | Computational methods for predicting genomic islands in microbial genomes |
| Q49408141 | Crosstalk between vertical and horizontal gene transfer: plasmid replication control by a conjugative relaxase |
| Q98882004 | Deciphering the mobility and bacterial hosts of antibiotic resistance genes under antibiotic selection pressure by metagenomic assembly and binning approaches |
| Q92881299 | Destabilization of the Tumor-Inducing Plasmid from an Octopine-Type Agrobacterium tumefaciens Lineage Drives a Large Deletion in the Co-resident At Megaplasmid |
| Q36644791 | Diversity and Evolution of the Tn5801-tet(M)-Like Integrative and Conjugative Elements among Enterococcus, Streptococcus, and Staphylococcus |
| Q46378972 | Diversity of Integrative and Conjugative Elements of Streptococcus salivarius and Their Intra- and Interspecies Transfer |
| Q37318052 | Evolution and Diversity of the Antimicrobial Resistance Associated Mobilome in Streptococcus suis: A Probable Mobile Genetic Elements Reservoir for Other Streptococci |
| Q46616134 | First identification of Tn916-like element in industrial strains of Lactobacillus vini that spread the tet-M resistance gene |
| Q57091716 | Genome Variation in the Model Halophilic Bacterium |
| Q38629272 | Genomic insights into the pathogenicity and environmental adaptability of Enterococcus hirae R17 isolated from pork offered for retail sale. |
| Q37739134 | Genomics Reveals a Unique Clone of Burkholderia cenocepacia Harboring an Actively Excising Novel Genomic Island. |
| Q38808071 | Genomics and the evolution of antibiotic resistance |
| Q37021832 | Highly variable individual donor cell fates characterize robust horizontal gene transfer of an integrative and conjugative element. |
| Q57618365 | Host range and genetic plasticity explain the co-existence of integrative and extrachromosomal mobile genetic elements |
| Q37023286 | ICESpy009, a Conjugative Genetic Element Carrying mef(E) in Streptococcus pyogenes |
| Q58587046 | ICEberg 2.0: an updated database of bacterial integrative and conjugative elements |
| Q90681057 | IS26-Mediated Genetic Rearrangements in Salmonella Genomic Island 1 of Proteus mirabilis |
| Q64056596 | Identification and Characterization of and Two Mobilization Genes Required for Conjugative Transfer of Genomic Island 1 |
| Q36324439 | Identification and analysis of genomic islands in Burkholderia cenocepacia AU 1054 with emphasis on pathogenicity islands. |
| Q41740772 | Identification and comparative analysis of a genomic island in Mycobacterium avium subsp. hominissuis |
| Q64081527 | Identification of Three Types of Integrative and Conjugative Elements in Elizabethkingia anophelis Strains Isolated from around the World |
| Q61445482 | Impact of Homologous Recombination on the Evolution of Prokaryotic Core Genomes |
| Q47287400 | Impact of cell surface molecules on conjugative transfer of the integrative and conjugative element ICESt3 of Streptococcus thermophilus. |
| Q30390741 | IncA/C Conjugative Plasmids Mobilize a New Family of Multidrug Resistance Islands in Clinical Vibrio cholerae Non-O1/Non-O139 Isolates from Haiti |
| Q37529766 | Integrative and Conjugative Elements (ICEs): What They Do and How They Work |
| Q41626922 | Integrative and conjugative elements and their hosts: composition, distribution and organization |
| Q36279479 | Interactions between closely related bacterial strains are revealed by deep transcriptome sequencing |
| Q90566341 | Jump ahead with a twist: DNA acrobatics drive transposition forward |
| Q42216560 | Klebsiella pneumoniae Asparagine tDNAs Are Integration Hotspots for Different Genomic Islands Encoding Microcin E492 Production Determinants and Other Putative Virulence Factors Present in Hypervirulent Strains |
| Q40515882 | Lateral gene transfer, bacterial genome evolution, and the Anthropocene |
| Q46246927 | Living Organisms Author Their Read-Write Genomes in Evolution |
| Q40867197 | Macrolide resistance gene erm(TR) and erm(TR)-carrying genetic elements in Streptococcus agalactiae: characterization of ICESagTR7, a new composite element containing IMESp2907. |
| Q40582007 | Methods for Determining Transfer of Mobile Genetic Elements in Clostridium difficile |
| Q39394653 | Mobile genetic elements in Neisseria gonorrhoeae: movement for change |
| Q40229412 | Mobilizable genomic islands, different strategies for the dissemination of multidrug resistance and other adaptive traits. |
| Q36240751 | Networking in microbes: conjugative elements and plasmids in the genus Alteromonas |
| Q36432032 | New Insights into the Classification and Integration Specificity of Streptococcus Integrative Conjugative Elements through Extensive Genome Exploration |
| Q26315280 | Nothing in Evolution Makes Sense Except in the Light of Genomics: Read-Write Genome Evolution as an Active Biological Process |
| Q51592249 | Novel chromosome-encoded erm(47) determinant responsible for constitutive MLSB resistance in Helcococcus kunzii. |
| Q49270548 | Phylogeographic diversity and mosaicism of the Helicobacter pylori tfs integrative and conjugative elements |
| Q49964207 | PlasFlow: predicting plasmid sequences in metagenomic data using genome signatures |
| Q58558160 | Prebiotics for Lactose Intolerance: Variability in Galacto-Oligosaccharide Utilization by Intestinal |
| Q40690041 | Prediction of Putative Resistance Islands in a Carbapenem-Resistant Acinetobacter baumannii Global Clone 2 Clinical Isolate |
| Q100958583 | Rapid growth inhibitory activity of a YafQ-family endonuclease toxin of the Helicobacter pylori tfs4 integrative and conjugative element |
| Q40984979 | Recombination between Streptococcus suis ICESsu32457 and Streptococcus agalactiae ICESa2603 yields a hybrid ICE transferable to Streptococcus pyogenes |
| Q41344454 | Resistance Genes and Genetic Elements Associated with Antibiotic Resistance in Clinical and Commensal Isolates of Streptococcus salivarius |
| Q26745983 | SXT/R391 Integrative and Conjugative Elements (ICEs) Encode a Novel 'Trap-Door' Strategy for Mobile Element Escape |
| Q92823684 | Salmonella Genomic Island 3 Is an Integrative and Conjugative Element and Contributes to Copper and Arsenic Tolerance of Salmonella enterica |
| Q36326607 | Salmonella genomic island 1 (SGI1) reshapes the mating apparatus of IncC conjugative plasmids to promote self-propagation. |
| Q36834448 | Sequence-Based Characterization of Tn5801-Like Genomic Islands in Tetracycline-Resistant Staphylococcus pseudintermedius and Other Gram-positive Bacteria from Humans and Animals |
| Q41643481 | Streptococcal group B integrative and mobilizable element IMESag-rpsI encodes a functional relaxase involved in its transfer |
| Q40121665 | Structural basis of a histidine-DNA nicking/joining mechanism for gene transfer and promiscuous spread of antibiotic resistance |
| Q55404079 | Surfaceome and Proteosurfaceome in Parietal Monoderm Bacteria: Focus on Protein Cell-Surface Display. |
| Q47135186 | The Different Faces of Rolling-Circle Replication and Its Multifunctional Initiator Proteins |
| Q51621347 | The ICEXTD of Azoarcus sp. CIB, an integrative and conjugative element with aerobic and anaerobic catabolic properties. |
| Q40931336 | The Landscape of Realized Homologous Recombination in Pathogenic Bacteria. |
| Q47161626 | The Obscure World of Integrative and Mobilizable Elements, Highly Widespread Elements that Pirate Bacterial Conjugative Systems. |
| Q35215425 | The dnd operon for DNA phosphorothioation modification system in Escherichia coli is located in diverse genomic islands |
| Q38498279 | The dualistic nature of integrative and conjugative elements |
| Q26782828 | The extended regulatory networks of SXT/R391 integrative and conjugative elements and IncA/C conjugative plasmids |
| Q38859993 | The hidden life of integrative and conjugative elements |
| Q54963115 | The lactose operon from Lactobacillus casei is involved in the transport and metabolism of the human milk oligosaccharide core-2 N-acetyllactosamine. |
| Q35361457 | The master activator of IncA/C conjugative plasmids stimulates genomic islands and multidrug resistance dissemination |
| Q36098194 | Thiomonas sp. CB2 is able to degrade urea and promote toxic metal precipitation in acid mine drainage waters supplemented with urea |
| Q35768051 | Transcriptional Analysis of the Conjugal Transfer Genes of Rickettsia bellii RML 369-C. |
| Q99237772 | Type IV Coupling Proteins as Potential Targets to Control the Dissemination of Antibiotic Resistance |
| Q50065182 | Unravelling the genome of a Pseudomonas aeruginosa isolate belonging to the high-risk clone ST235 reveals an integrative conjugative element housing a blaGES-6 carbapenemase |
Search more.