scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1040351681 |
P356 | DOI | 10.1038/NATURE04616 |
P698 | PubMed publication ID | 16541065 |
P5875 | ResearchGate publication ID | 7237732 |
P50 | author | Thomas F. Meyer | Q2423758 |
P2093 | author name string | Matthias Mann | |
Matthias Selbach | |||
Daniel Becker | |||
Matthias Ballmaier | |||
Dirk Bumann | |||
Claudia Rollenhagen | |||
P2860 | cites work | Comparison of genome degradation in Paratyphi A and Typhi, human-restricted serovars of Salmonella enterica that cause typhoid | Q22122046 |
Complete genome sequence of Salmonella enterica serovar Typhimurium LT2 | Q22122369 | ||
Complete genome sequence of a multiple drug resistant Salmonella enterica serovar Typhi CT18 | Q22122370 | ||
From genetic footprinting to antimicrobial drug targets: examples in cofactor biosynthetic pathways | Q24539226 | ||
Comparative genomics of Salmonella enterica serovar Typhi strains Ty2 and CT18 | Q24554266 | ||
EcoCyc: a comprehensive database resource for Escherichia coli | Q24796847 | ||
Functional profiling of the Saccharomyces cerevisiae genome | Q27860544 | ||
Mass spectrometry-based proteomics | Q28182890 | ||
Typhoid and paratyphoid fever | Q28269252 | ||
The large-scale organization of metabolic networks | Q29547498 | ||
Genome-scale models of microbial cells: evaluating the consequences of constraints | Q29616789 | ||
A diarylquinoline drug active on the ATP synthase of Mycobacterium tuberculosis | Q29617342 | ||
Functional cartography of complex metabolic networks | Q30481006 | ||
Selection analyses of insertional mutants using subgenic-resolution arrays | Q30760746 | ||
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Large-scale identification of essential Salmonella genes by trapping lethal insertions | Q33199163 | ||
Metabolic functions of duplicate genes in Saccharomyces cerevisiae | Q33224556 | ||
Differences in gene content between Salmonella enterica serovar Enteritidis isolates and comparison to closely related serovars Gallinarum and Dublin. | Q34048325 | ||
Lipid biosynthesis as a target for antibacterial agents | Q34395560 | ||
Animal models of Salmonella infections: enteritis versus typhoid fever. | Q34469859 | ||
Salmonella enterica highly expressed genes are disease specific | Q34491811 | ||
Exploiting genomics, genetics and chemistry to combat antibiotic resistance. | Q35140829 | ||
Antibacterial research and development in the 21(st) Century--an industry perspective of the challenges | Q35903226 | ||
A millennium update on pediatric diarrheal illness in the developing world | Q36095978 | ||
Novel target sites in bacteria for overcoming antibiotic resistance | Q36159533 | ||
A mouse model for S. typhimurium-induced enterocolitis | Q36248020 | ||
Identification of Salmonella functions critical for bacterial cell division within eukaryotic cells | Q40445651 | ||
Unravelling the biology of macrophage infection by gene expression profiling of intracellular Salmonella enterica | Q43533379 | ||
Optimization of GFP levels for analyzing Salmonella gene expression during an infection | Q50109216 | ||
Recombinant avirulent Salmonella vaccine strains with stable maintenance and high level expression of cloned genes in vivo | Q50196578 | ||
P433 | issue | 7082 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 303-307 | |
P577 | publication date | 2006-03-01 | |
P1433 | published in | Nature | Q180445 |
P1476 | title | Robust Salmonella metabolism limits possibilities for new antimicrobials | |
P478 | volume | 440 |
Q37071956 | (15)N{(31)P} REDOR NMR studies of the binding of phosphonate reaction intermediate analogues to Saccharomyces cerevisiae lumazine synthase |
Q35940889 | A Comparison of the ATP Generating Pathways Used by S. Typhimurium to Fuel Replication within Human and Murine Macrophage and Epithelial Cell Lines |
Q34547091 | A community effort towards a knowledge-base and mathematical model of the human pathogen Salmonella Typhimurium LT2 |
Q37424840 | A link between gut community metabolism and pathogenesis: molecular hydrogen-stimulated glucarate catabolism aids Salmonella virulence |
Q35325775 | A metaproteomics approach to elucidate host and pathogen protein expression during catheter-associated urinary tract infections (CAUTIs). |
Q38668518 | A novel antimicrobial approach based on the inhibition of zinc uptake in Salmonella enterica. |
Q30974252 | A proteomic view of an important human pathogen--towards the quantification of the entire Staphylococcus aureus proteome |
Q35176370 | Absolute quantification of microbial proteomes at different states by directed mass spectrometry |
Q41042251 | Acidic pH sensing in the bacterial cytoplasm is required for Salmonella virulence |
Q40495826 | Alternative fluorescent labeling strategies for characterizing gram-positive pathogenic bacteria: Flow cytometry supported counting, sorting, and proteome analysis of Staphylococcus aureus retrieved from infected host cells |
Q34018578 | Amino acid recognition and gene regulation by riboswitches. |
Q37887170 | Antibiotic treatment of CF lung disease: from bench to bedside |
Q38049352 | Antibiotic-resistant bacteria: a challenge for the food industry. |
Q33301096 | Antimicrobial drug resistance of Salmonella enterica serovar typhi in asia and molecular mechanism of reduced susceptibility to the fluoroquinolones |
Q36757725 | Antimicrobial resistance and virulence: a successful or deleterious association in the bacterial world? |
Q59042634 | Application of Molecular Approaches for Understanding Foodborne Salmonella Establishment in Poultry Production |
Q94561463 | Aspartate semialdehyde dehydrogenase inhibition suppresses the growth of the pathogenic fungus Candida albicans |
Q33131299 | Assessing the Metabolic Diversity of Streptococcus from a Protein Domain Point of View |
Q38695278 | At the crossroads: communication of bacteria-containing vacuoles with host organelles. |
Q37899789 | Biochemistry of the non-mevalonate isoprenoid pathway |
Q91890032 | Blocks in Tricarboxylic Acid Cycle of Salmonella enterica Cause Global Perturbation of Carbon Storage, Motility, and Host-Pathogen Interaction |
Q42279950 | Both thiamine uptake and biosynthesis of thiamine precursors are required for intracellular replication of Listeria monocytogenes |
Q21089623 | Capnocytophaga canimorsus: a human pathogen feeding at the surface of epithelial cells and phagocytes |
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Q50537803 | Combined action of the type IV secretion effector proteins BepC and BepF promotes invasome formation of Bartonella henselae on endothelial and epithelial cells |
Q48171420 | Combined chemical genetics and data-driven bioinformatics approach identifies receptor tyrosine kinase inhibitors as host-directed antimicrobials |
Q34158566 | Complete proteome of a quinolone-resistant Salmonella Typhimurium phage type DT104B clinical strain |
Q27323145 | Comprehensive assignment of roles for Salmonella typhimurium genes in intestinal colonization of food-producing animals |
Q24649162 | Constraint-based analysis of metabolic capacity of Salmonella typhimurium during host-pathogen interaction |
Q28552763 | Core Proteomic Analysis of Unique Metabolic Pathways of Salmonella enterica for the Identification of Potential Drug Targets |
Q40567992 | Correlating Drug-Target Kinetics and In vivo Pharmacodynamics: Long Residence Time Inhibitors of the FabI Enoyl-ACP Reductase |
Q28252916 | Crystal structure of a type III pantothenate kinase: insight into the mechanism of an essential coenzyme A biosynthetic enzyme universally distributed in bacteria |
Q38261033 | Defining the metabolic requirements for the growth and colonization capacity of Campylobacter jejuni |
Q33874236 | Development of ELISAs for diagnosis of acute typhoid fever in Nigerian children. |
Q37143551 | Differential quantitative proteomics of Porphyromonas gingivalis by linear ion trap mass spectrometry: non-label methods comparison, q-values and LOWESS curve fitting |
Q47385425 | Distinguishing between metabolically active and dormant bacteria on paper. |
Q44480719 | Do targets limit antibiotic discovery? |
Q48220585 | Drugging tRNA aminoacylation. |
Q24285722 | Dual RNA-seq unveils noncoding RNA functions in host–pathogen interactions |
Q40046693 | During infection of epithelial cells Salmonella enterica serovar Typhimurium undergoes a time-dependent transcriptional adaptation that results in simultaneous expression of three type 3 secretion systems |
Q49587782 | Dysbiosis-Associated Change in Host Metabolism Generates Lactate to Support Salmonella Growth |
Q26774700 | Elucidating Host-Pathogen Interactions Based on Post-Translational Modifications Using Proteomics Approaches |
Q34240776 | Evolution of variation in presence and absence of genes in bacterial pathways |
Q34388303 | Extensive in vivo resilience of persistent Salmonella |
Q55397646 | Few Differences in Metabolic Network Use Found Between Salmonella enterica Colonization of Plants and Typhoidal Mice. |
Q21131360 | Fructose-asparagine is a primary nutrient during growth of Salmonella in the inflamed intestine |
Q89965574 | Functional Inhibition of Host Histone Deacetylases (HDACs) Enhances in vitro and in vivo Anti-mycobacterial Activity in Human Macrophages and in Zebrafish |
Q64980329 | Functional expansion of a TCA cycle operon mRNA by a 3' end-derived small RNA. |
Q37718885 | Functional single-cell analyses: flow cytometry and cell sorting of microbial populations and communities |
Q42111680 | Genetic determinants of resistance to fusidic acid among clinical bacteremia isolates of Staphylococcus aureus |
Q41871341 | Genetic screening for bacterial mutants in liquid growth media by fluorescence-activated cell sorting. |
Q34172679 | Genome scanning for conditionally essential genes in Salmonella enterica Serotype Typhimurium |
Q37256563 | Glucose and glycolysis are required for the successful infection of macrophages and mice by Salmonella enterica serovar typhimurium. |
Q34302315 | Glycerol supplementation enhances L. reuteri's protective effect against S. Typhimurium colonization in a 3-D model of colonic epithelium |
Q34286388 | High-throughput comparison of gene fitness among related bacteria |
Q33395856 | Histoplasma capsulatum proteome response to decreased iron availability |
Q34889881 | Host hydrogen rather than that produced by the pathogen is important for Salmonella enterica serovar Typhimurium virulence |
Q34305317 | Human genome-wide RNAi screen for host factors that modulate intracellular Salmonella growth |
Q38243324 | Identification of Protective Antigens for Vaccination against Systemic Salmonellosis |
Q30424877 | Identification of a common immune signature in murine and human systemic Salmonellosis |
Q50072446 | Identification of host-induced pathogen genes by differential fluorescence induction reporter systems |
Q33845728 | Identification of metabolic pathways essential for fitness of Salmonella Typhimurium in vivo |
Q36949434 | Identification of the genetic basis for clinical menadione-auxotrophic small-colony variant isolates of Staphylococcus aureus |
Q37719739 | Identifying potential therapeutic targets of methicillin-resistant Staphylococcus aureus through in vivo proteomic analysis |
Q34456080 | Immunity to intracellular Salmonella depends on surface-associated antigens |
Q34495624 | Immunological characterization of a gidA mutant strain of Salmonella for potential use in a live-attenuated vaccine |
Q36993458 | In vitro and in vivo validation of ligA and tarI as essential targets in Staphylococcus aureus |
Q33610279 | In vivo IFN-γ secretion by NK cells in response to Salmonella typhimurium requires NLRC4 inflammasomes |
Q39568172 | In vivo and in silico determination of essential genes of Campylobacter jejuni. |
Q30489356 | Inducing optimal substitution between antibiotics under open access to the resource of antibiotic susceptibility |
Q35109868 | Innate immune activation during Salmonella infection initiates extramedullary erythropoiesis and splenomegaly |
Q30480219 | Integrated network reconstruction, visualization and analysis using YANAsquare. |
Q33530403 | Integration of 'omics' data: does it lead to new insights into host-microbe interactions? |
Q31066785 | Integration of omics data: how well does it work for bacteria? |
Q35409022 | Intestinal inflammation allows Salmonella to use ethanolamine to compete with the microbiota |
Q38663493 | Intracellular Salmonella metabolism. |
Q27322699 | Intraspecies competition for niches in the distal gut dictate transmission during persistent Salmonella infection |
Q37897209 | Investigating pathogen biology at the level of the proteome |
Q33870965 | Isolation of F. novicida-Containing Phagosome from Infected Human Monocyte Derived Macrophages. |
Q39042382 | Labeling of the pathogenic bacterium Staphylococcus aureus with gold or ferric oxide-core nanoparticles highlights new capabilities for investigation of host-pathogen interactions |
Q34429033 | Live attenuated S. Typhimurium vaccine with improved safety in immuno-compromised mice |
Q38090511 | Lysine biosynthesis in microbes: relevance as drug target and prospects for β-lactam antibiotics production. |
Q26865681 | Mass spectrometry-based proteomic approaches to study pathogenic bacteria-host interactions |
Q30439892 | Mass spectrometry-based proteomics and its application to studies of Porphyromonas gingivalis invasion and pathogenicity |
Q33597003 | Mass spectrometry-based quantitative proteomic analysis of Salmonella enterica serovar Enteritidis protein expression upon exposure to hydrogen peroxide |
Q55448576 | Methionine biosynthesis and transport are functionally redundant for the growth and virulence of Salmonella Typhimurium. |
Q35804589 | Mlc regulation of Salmonella pathogenicity island I gene expression via hilE repression |
Q40460667 | Model-driven discovery of synergistic inhibitors against E. coli and S. enterica serovar Typhimurium targeting a novel synthetic lethal pair, aldA and prpC |
Q27306197 | Modification of Salmonella Typhimurium motility by the probiotic yeast strain Saccharomyces boulardii |
Q46248137 | Molecular evolution of an oligomeric biocatalyst functioning in lysine biosynthesis |
Q46778188 | Motility allows S. Typhimurium to benefit from the mucosal defence |
Q38325342 | Mycobacterial proteomics: analysis of expressed proteomes and post-translational modifications to identify candidate virulence factors |
Q35831206 | N-acetylglucosamine-6-phosphate deacetylase (NagA) of Listeria monocytogenes EGD, an essential enzyme for the metabolism and recycling of amino sugars. |
Q36596234 | NAD+ utilization in Pasteurellaceae: simplification of a complex pathway. |
Q26827940 | Network-based approaches in drug discovery and early development |
Q37329167 | New trends in pharmacogenomic strategies against resistance development in microbial infections |
Q35068795 | Non-essential genes form the hubs of genome scale protein function and environmental gene expression networks in Salmonella enterica serovar Typhimurium |
Q36358643 | Novel approaches to developing new antibiotics for bacterial infections |
Q34903245 | Novel classes of antibiotics or more of the same? |
Q40149893 | Novel targets for antibiotics in Staphylococcus aureus |
Q36239332 | O-Nucleoside, S-nucleoside, and N-nucleoside probes of lumazine synthase and riboflavin synthase |
Q42729379 | Orthogonal alkynyl amino acid reporter for selective labeling of bacterial proteomes during infection. |
Q34697874 | Parallel exploitation of diverse host nutrients enhances Salmonella virulence. |
Q34389664 | Polyfunctional CD4+ T cell responses to immunodominant epitopes correlate with disease activity of virulent Salmonella |
Q33745572 | Postgenomic strategies in antibacterial drug discovery. |
Q38452362 | Protein turnover analysis in Salmonella Typhimurium during infection by dynamic SILAC, Topograph, and quantitative proteomics |
Q47160568 | Proteogenomics in Aid of Host-Pathogen Interaction Studies: A Bacterial Perspective |
Q37895209 | Proteome analysis of host-pathogen interactions: Investigation of pathogen responses to the host cell environment |
Q34884343 | Proteomes of host cell membranes modified by intracellular activities of Salmonella enterica |
Q35745541 | Proteomic Analyses of Intracellular Salmonella enterica Serovar Typhimurium Reveal Extensive Bacterial Adaptations to Infected Host Epithelial Cells |
Q58572049 | Proteomic Profiling of During Host Infection Using Bio-Orthogonal Noncanonical Amino Acid Tagging (BONCAT) |
Q40222325 | Proteomic comparison between Salmonella Typhimurium and Salmonella Typhi |
Q37274847 | Proteomic investigation of the time course responses of RAW 264.7 macrophages to infection with Salmonella enterica |
Q64099626 | Proteomics of intracellular Salmonella enterica reveals roles of Salmonella pathogenicity island 2 in metabolism and antioxidant defense |
Q28080622 | Purification and proteomics of pathogen-modified vacuoles and membranes |
Q40198592 | Quantitative proteomic analysis of host epithelial cells infected by Salmonella enterica serovar Typhimurium. |
Q46859773 | Reactive oxygen species are the major antibacterials against Salmonella Typhimurium purine auxotrophs in the phagosome of RAW 264.7 cells |
Q30592724 | Reconciling a Salmonella enterica metabolic model with experimental data confirms that overexpression of the glyoxylate shunt can rescue a lethal ppc deletion mutant |
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Q33864950 | Staphylococcus aureus physiological growth limitations: insights from flux calculations built on proteomics and external metabolite data |
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