about
Clinical use of whole genome sequencing for Mycobacterium tuberculosisTranscriptional analysis of temporal gene expression in germinating Clostridium difficile 630 endosporesMycobacterium tuberculosis Is Resistant to Isoniazid at a Slow Growth Rate by Single Nucleotide Polymorphisms in katG Codon Ser315Identification of Plasmodium falciparum antigens by antigenic analysis of genomic and proteomic data.Development and application of the active surveillance of pathogens microarray to monitor bacterial gene flux.Deciphering the response of Mycobacterium smegmatis to nitrogen stress using bipartite active modules.Transcriptional analysis of in vivo Plasmodium yoelii liver stage gene expression.Genetic variation in spatio-temporal confined USA300 community-associated MRSA isolates: a shift from clonal dispersion to genetic evolution?Transcripts of developmentally regulated Plasmodium falciparum genes quantified by real-time RT-PCR.Immunogenicity and protective efficacy of a Plasmodium yoelii Hsp60 DNA vaccine in BALB/c mice.Comparative phylogenomics of the food-borne pathogen Campylobacter jejuni reveals genetic markers predictive of infection sourceEvolutionary genomics of Staphylococcus aureus reveals insights into the origin and molecular basis of ruminant host adaptation.Genome-level analyses of Mycobacterium bovis lineages reveal the role of SNPs and antisense transcription in differential gene expression.Clinical application of whole-genome sequencing to inform treatment for multidrug-resistant tuberculosis cases.The distribution of mobile genetic elements (MGEs) in MRSA CC398 is associated with both host and countryBμG@Sbase--a microbial gene expression and comparative genomic database.Genetic variation in Mycobacterium tuberculosis isolates from a London outbreak associated with isoniazid resistanceUse of whole-genome sequencing to distinguish relapse from reinfection in a completed tuberculosis clinical trialNovel antigen identification method for discovery of protective malaria antigens by rapid testing of DNA vaccines encoding exons from the parasite genome.BmuG@Sbase--a microarray database and analysis tool.Identification of Streptococcus suis Meningitis through Population-Based Surveillance, Togo, 2010-2014.High prevalence of antibiotic-resistant Mycoplasma genitalium in nongonococcal urethritis: the need for routine testing and the inadequacy of current treatment options.A two-component system that controls the expression of pneumococcal surface antigen A (PsaA) and regulates virulence and resistance to oxidative stress in Streptococcus pneumoniae.Posttranscriptional regulation of flagellin synthesis in Helicobacter pylori by the RpoN chaperone HP0958.Application of comparative phylogenomics to study the evolution of Yersinia enterocolitica and to identify genetic differences relating to pathogenicity.Within-host diversity of MRSA antimicrobial resistances.Design, validation, and application of a seven-strain Staphylococcus aureus PCR product microarray for comparative genomics.A computational strategy for the search of regulatory small RNAs in Actinobacillus pleuropneumoniae.XDR-TB transmission in London: Case management and contact tracing investigation assisted by early whole genome sequencing.Construction of a Yersinia pestis microarray.Whole-genome sequencing illuminates the evolution and spread of multidrug-resistant tuberculosis in Southwest Nigeria.Extensive horizontal gene transfer during Staphylococcus aureus co-colonization in vivo.Microarrays reveal that each of the ten dominant lineages of Staphylococcus aureus has a unique combination of surface-associated and regulatory genes.Genome sequencing and characterization of an extensively drug-resistant sequence type 111 serotype O12 hospital outbreak strain of Pseudomonas aeruginosa.Staphylococcus aureus temperate bacteriophage: carriage and horizontal gene transfer is lineage associatedGenomic variations define divergence of water/wildlife-associated Campylobacter jejuni niche specialists from common clonal complexes.Determining liver stage parasite burden by real time quantitative PCR as a method for evaluating pre-erythrocytic malaria vaccine efficacy.Quantitation of liver-stage parasites by automated TaqMan real-time PCR.Occupational Tuberculosis despite Minimal Nosocomial Contact in a Health Care Worker Undergoing Treatment with a Tumor Necrosis Factor Inhibitor.Identification of pathogen-specific genes through microarray analysis of pathogenic and commensal Neisseria species.
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description
hulumtues
@sq
researcher
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wetenschapper
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հետազոտող
@hy
name
Adam A Witney
@ast
Adam A Witney
@en
Adam A Witney
@es
Adam A Witney
@nl
type
label
Adam A Witney
@ast
Adam A Witney
@en
Adam A Witney
@es
Adam A Witney
@nl
prefLabel
Adam A Witney
@ast
Adam A Witney
@en
Adam A Witney
@es
Adam A Witney
@nl
P106
P21
P31
P496
0000-0003-4561-7170