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P50 | author | Claire Chewapreecha | Q56796221 |
Josephine M Bryant | Q56815996 | ||
Stephen D Bentley | Q87466237 | ||
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Citrobacter rodentium is an unstable pathogen showing evidence of significant genomic flux | Q21131422 | ||
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The CRISPRdb database and tools to display CRISPRs and to generate dictionaries of spacers and repeats | Q21284230 | ||
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Environments shape the nucleotide composition of genomes | Q24489465 | ||
Accelerated evolution and Muller's rachet in endosymbiotic bacteria | Q24568178 | ||
Evolutionary dynamics of Clostridium difficile over short and long time scales | Q24622076 | ||
Second-order selection for evolvability in a large Escherichia coli population | Q24635911 | ||
Nucleotide sequence of the iap gene, responsible for alkaline phosphatase isozyme conversion in Escherichia coli, and identification of the gene product | Q24679073 | ||
The genome sequence of Brucella pinnipedialis B2/94 sheds light on the evolutionary history of the genus Brucella | Q27496555 | ||
Comparative genomics of the bacterial genus Listeria: Genome evolution is characterized by limited gene acquisition and limited gene loss | Q27496585 | ||
Whole-genome random sequencing and assembly of Haemophilus influenzae Rd | Q27860765 | ||
Continuing evolution of Burkholderia mallei through genome reduction and large-scale rearrangements | Q28277593 | ||
Comparisons of dN/dS are time dependent for closely related bacterial genomes | Q28278192 | ||
The population dynamics and control of tuberculosis | Q28282446 | ||
Rapid evolution of virulence and drug resistance in the emerging zoonotic pathogen Streptococcus suis | Q28475752 | ||
Whole genome sequencing and complete genetic analysis reveals novel pathways to glycopeptide resistance in Staphylococcus aureus | Q28478770 | ||
Calibrating bacterial evolution | Q28776463 | ||
CRISPR/Cas, the immune system of bacteria and archaea | Q29614423 | ||
Evolution of MRSA during hospital transmission and intercontinental spread | Q29615141 | ||
Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patients | Q29615301 | ||
Rapid pneumococcal evolution in response to clinical interventions | Q29616646 | ||
CRISPR interference: RNA-directed adaptive immunity in bacteria and archaea | Q29617488 | ||
Evidence for time dependency of molecular rate estimates | Q29618705 | ||
Evidence for several waves of global transmission in the seventh cholera pandemic | Q30406370 | ||
Detection of recombination events in bacterial genomes from large population samples | Q30409108 | ||
Parallel bacterial evolution within multiple patients identifies candidate pathogenicity genes. | Q30426714 | ||
Genome assembly forensics: finding the elusive mis-assembly | Q30482123 | ||
Phylogenomic analysis of natural selection pressure in Streptococcus genomes | Q30833778 | ||
Phylogeographic reconstruction of a bacterial species with high levels of lateral gene transfer | Q30891438 | ||
Evidence that mutation is universally biased towards AT in bacteria | Q30989309 | ||
Evolution of competence and DNA uptake specificity in the Pasteurellaceae. | Q33260272 | ||
Bayesian modeling of recombination events in bacterial populations | Q33374425 | ||
Co-evolution of genomes and plasmids within Chlamydia trachomatis and the emergence in Sweden of a new variant strain | Q33449883 | ||
Tracking insertion mutants within libraries by deep sequencing and a genome-wide screen for Haemophilus genes required in the lung | Q33508764 | ||
Short-term signatures of evolutionary change in the Salmonella enterica serovar typhimurium 14028 genome | Q33586060 | ||
Evolutionary microbial genomics: insights into bacterial host adaptation | Q33592109 | ||
Identification, variation and transcription of pneumococcal repeat sequences | Q33824198 | ||
Assessing the benefits of using mate-pairs to resolve repeats in de novo short-read prokaryotic assemblies | Q33870636 | ||
Deletional bias and the evolution of bacterial genomes | Q33955011 | ||
Recombination and population structure in Salmonella enterica. | Q33987523 | ||
Simultaneous assay of every Salmonella Typhi gene using one million transposon mutants | Q34019749 | ||
Selection in coastal Synechococcus (cyanobacteria) populations evaluated from environmental metagenomes | Q34023328 | ||
The rate of synonymous substitution in enterobacterial genes is inversely related to codon usage bias | Q34049602 | ||
A universal TagModule collection for parallel genetic analysis of microorganisms | Q34058413 | ||
Gene decay in Shigella as an incipient stage of host-adaptation | Q34081810 | ||
The CRISPR system: small RNA-guided defense in bacteria and archaea | Q34096589 | ||
Diversity of CRISPR loci in Escherichia coli | Q34096997 | ||
Microbial minimalism: genome reduction in bacterial pathogens | Q34118332 | ||
The phage-related chromosomal islands of Gram-positive bacteria. | Q34126277 | ||
Behavior and target site selection of conjugative transposon Tn916 in two different strains of toxigenic Clostridium difficile | Q34135544 | ||
Comparative analysis of the genome sequences of Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica | Q34221221 | ||
A set of lacZ mutations in Escherichia coli that allow rapid detection of each of the six base substitutions | Q34290231 | ||
Bacterial virulence: can we draw the line? | Q34303616 | ||
Diversity and mobility of integrative and conjugative elements in bovine isolates of Streptococcus agalactiae, S. dysgalactiae subsp. dysgalactiae, and S. uberis | Q34432185 | ||
Genome-scale identification of resistance functions in Pseudomonas aeruginosa using Tn-seq | Q34504913 | ||
Heterogeneity of Tn5253-like composite elements in clinical Streptococcus pneumoniae isolates | Q34737570 | ||
Use of whole genome sequencing to estimate the mutation rate of Mycobacterium tuberculosis during latent infection | Q35006626 | ||
Flagellar phase variation in Salmonella enterica is mediated by a posttranscriptional control mechanism | Q35021032 | ||
Limitations of next-generation genome sequence assembly | Q35047159 | ||
Neutral mutations and neutral substitutions in bacterial genomes | Q35209355 | ||
Impact of small repeat sequences on bacterial genome evolution. | Q35253340 | ||
Targeted bacterial immunity buffers phage diversity | Q35274944 | ||
Whole-genome sequencing of rifampicin-resistant Mycobacterium tuberculosis strains identifies compensatory mutations in RNA polymerase genes. | Q35635595 | ||
Population structure in the Neisseria, and the biological significance of fuzzy species | Q35954300 | ||
A novel non-homologous recombination-mediated mechanism for Escherichia coli unilateral flagellar phase variation | Q36044816 | ||
Evolutionary paths to antibiotic resistance under dynamically sustained drug selection | Q36500996 | ||
The impact of the neisserial DNA uptake sequences on genome evolution and stability | Q36678612 | ||
Whole-genome mutational biases in bacteria | Q36976728 | ||
High frequency of hotspot mutations in core genes of Escherichia coli due to short-term positive selection. | Q37282428 | ||
Use of high throughput sequencing to observe genome dynamics at a single cell level | Q37469631 | ||
Rapidly evolving genes in pathogens: methods for detecting positive selection and examples among fungi, bacteria, viruses and protists | Q37482440 | ||
Genome flexibility in Neisseria meningitidis | Q37499451 | ||
Computational methods for discovering structural variation with next-generation sequencing | Q37618538 | ||
Genome structural variation discovery and genotyping | Q37848057 | ||
Antibiotic and antiseptic resistance genes are linked on a novel mobile genetic element: Tn6087. | Q38390674 | ||
Genetic diversity of Tn916-related transposons among drug-resistant Streptococcus pneumoniae isolates colonizing healthy children in Venezuela | Q38627345 | ||
Molecular mechanisms of tetracycline and macrolide resistance and emm characterization of Streptococcus pyogenes isolates in Tunisia | Q39080582 | ||
Transfer of TN916-like elements in microcosm dental plaques. | Q39478656 | ||
Natural transfer of conjugative transposon Tn916 between gram-positive and gram-negative bacteria | Q39938325 | ||
The competitive cost of antibiotic resistance in Mycobacterium tuberculosis | Q40311130 | ||
Tn2009, a Tn916-like element containing mef(E) in Streptococcus pneumoniae | Q40882823 | ||
Whole-Genome Sequencing of Sordaria macrospora Mutants Identifies Developmental Genes | Q41435196 | ||
Antagonistic coevolution accelerates molecular evolution | Q41813977 | ||
Population genomics of early events in the ecological differentiation of bacteria. | Q42136525 | ||
New functional identity for the DNA uptake sequence in transformation and its presence in transcriptional terminators | Q42845597 | ||
Diversity of the tetracycline resistance gene tet(M) and identification of Tn916- and Tn5801-like (Tn6014) transposons in Staphylococcus aureus from humans and animals | Q44803731 | ||
Molecular diversity and transferability of the tetracycline resistance gene tet(M), carried on Tn916-1545 family transposons, in enterococci from a total food chain. | Q46067992 | ||
Identification of Tn5397-like and Tn916-like transposons and diversity of the tetracycline resistance gene tet(M) in enterococci from humans, pigs and poultry | Q48094921 | ||
Hyper-recombination, diversity, and antibiotic resistance in pneumococcus. | Q51821002 | ||
Transcription profile of Thermus thermophilus CRISPR systems after phage infection. | Q52422306 | ||
Molecular evolution as predicted by natural selection. | Q53853033 | ||
Enterococcus faecalis from patients with chronic periodontitis: virulence and antimicrobial resistance traits and determinants | Q84325788 | ||
P433 | issue | 11 | |
P921 | main subject | bacterial evolution | Q115395667 |
P1104 | number of pages | 14 | |
P304 | page(s) | 1283-1296 | |
P577 | publication date | 2012-11-01 | |
P1433 | published in | Future Microbiology | Q15759961 |
P1476 | title | Developing insights into the mechanisms of evolution of bacterial pathogens from whole-genome sequences | |
P478 | volume | 7 |
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