review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | C M Anjam Khan | Q79325676 |
P2093 | author name string | C. M. Anjam Khan | |
P2860 | cites work | Multilocus sequence typing as a replacement for serotyping in Salmonella enterica | Q21090489 |
Plants as alternative hosts for Salmonella | Q50427020 | ||
Bacteroides species produce Vibrio harveyi autoinducer 2-related molecules. | Q54465290 | ||
The core gut microbiome, energy balance and obesity | Q57012032 | ||
'Blooming' in the gut: how dysbiosis might contribute to pathogen evolution | Q63968591 | ||
Production of Shiga-like toxins by Escherichia coli O157:H7 can be influenced by the neuroendocrine hormone norepinephrine | Q71598028 | ||
Effect of lactulose on short-chain fatty acids and lactate production and on the growth of faecal flora, with special reference to Clostridium difficile | Q72998548 | ||
On coli antagonism, dysbacteria and coli therapy | Q78847779 | ||
DNA damage triggers genetic exchange in Helicobacter pylori | Q21090502 | ||
SdiA, an N-acylhomoserine lactone receptor, becomes active during the transit of Salmonella enterica through the gastrointestinal tract of turtles | Q21144271 | ||
The small regulatory RNA molecule MicA is involved in Salmonella enterica serovar Typhimurium biofilm formation | Q21263115 | ||
Genome sequencing reveals diversification of virulence factor content and possible host adaptation in distinct subpopulations of Salmonella enterica | Q21267180 | ||
A Genomic View of the Human-Bacteroides thetaiotaomicron Symbiosis | Q22065827 | ||
Prokaryotes: the unseen majority | Q22066200 | ||
Complete genome sequence of Salmonella enterica serovar Typhimurium LT2 | Q22122369 | ||
Complete genome sequence of a multiple drug resistant Salmonella enterica serovar Typhi CT18 | Q22122370 | ||
Microbial ecology of the gastrointestinal tract | Q22255628 | ||
Antimicrobials for treating symptomatic non-typhoidal Salmonella infection | Q24202903 | ||
Diversity of the human intestinal microbial flora | Q24544241 | ||
Linking long-term dietary patterns with gut microbial enterotypes | Q24609914 | ||
A human gut microbial gene catalogue established by metagenomic sequencing | Q24618931 | ||
Investigating the function of Rho family GTPases during Salmonella/host cell interactions | Q24649762 | ||
Salmonella enterica serovar Typhimurium can detect acyl homoserine lactone production by Yersinia enterocolitica in mice | Q24654040 | ||
Quorum sensing in Escherichia coli, Salmonella typhimurium, and Vibrio harveyi: a new family of genes responsible for autoinducer production | Q24672151 | ||
Bacteria-host communication: the language of hormones | Q24678649 | ||
Salmonella pathogenicity island 2 is expressed prior to penetrating the intestine | Q24811102 | ||
Salmonella effector proteins and host-cell responses | Q26825603 | ||
Interactions of Salmonella enterica with dendritic cells | Q26991988 | ||
Salmonella enterica serovars Typhimurium and Typhi as model organisms: revealing paradigm of host-pathogen interactions | Q26996526 | ||
Pathogen espionage: multiple bacterial adrenergic sensors eavesdrop on host communication systems | Q27003337 | ||
Control of pathogens and pathobionts by the gut microbiota | Q27013060 | ||
The microbiota mediates pathogen clearance from the gut lumen after non-typhoidal Salmonella diarrhea | Q27313421 | ||
Salmonella enterica serovar typhimurium exploits inflammation to compete with the intestinal microbiota | Q27334139 | ||
Salmonella uses energy taxis to benefit from intestinal inflammation | Q27335357 | ||
An obesity-associated gut microbiome with increased capacity for energy harvest | Q27860515 | ||
Host-bacterial mutualism in the human intestine | Q27861037 | ||
Protein delivery into eukaryotic cells by type III secretion machines | Q28276443 | ||
Salmonella Typhi sense host neuroendocrine stress hormones and release the toxin haemolysin E | Q28305602 | ||
SopB, a protein required for virulence of Salmonella dublin, is an inositol phosphate phosphatase | Q28369269 | ||
Specific responses of Salmonella enterica to tomato varieties and fruit ripeness identified by in vivo expression technology | Q28475358 | ||
The bacterial cytoskeleton modulates motility, type 3 secretion, and colonization in Salmonella | Q28480402 | ||
The Salmonella invasin SipB induces macrophage apoptosis by binding to caspase-1 | Q28512341 | ||
Inter-kingdom signaling: chemical language between bacteria and host | Q28833718 | ||
pH Sensing by Intracellular Salmonella Induces Effector Translocation | Q29037234 | ||
Bacterial community variation in human body habitats across space and time | Q29547432 | ||
Diet rapidly and reproducibly alters the human gut microbiome | Q29547454 | ||
The pervasive effects of an antibiotic on the human gut microbiota, as revealed by deep 16S rRNA sequencing | Q29615054 | ||
Gut inflammation provides a respiratory electron acceptor for Salmonella | Q29615318 | ||
Intracontinental spread of human invasive Salmonella Typhimurium pathovariants in sub-Saharan Africa | Q30421768 | ||
TLR signaling is required for Salmonella typhimurium virulence | Q30499020 | ||
Accuracy and quality assessment of 454 GS-FLX Titanium pyrosequencing. | Q30501204 | ||
Adrenaline modulates the global transcriptional profile of Salmonella revealing a role in the antimicrobial peptide and oxidative stress resistance responses | Q30848228 | ||
S. typhimurium encodes an activator of Rho GTPases that induces membrane ruffling and nuclear responses in host cells. | Q32060838 | ||
Signature-tagged mutagenesis: barcoding mutants for genome-wide screens | Q33265184 | ||
Eradication of Salmonella Typhimurium infection in a murine model of typhoid fever with the combination of probiotic Lactobacillus fermentum ME-3 and ofloxacin | Q33357682 | ||
Targeting QseC signaling and virulence for antibiotic development | Q33362330 | ||
Perturbation of the small intestine microbial ecology by streptomycin alters pathology in a Salmonella enterica serovar typhimurium murine model of infection | Q33443646 | ||
2D proteome analysis initiates new insights on the Salmonella Typhimurium LuxS protein | Q33503418 | ||
Comparative metagenomic analysis of plasmid encoded functions in the human gut microbiome | Q33525169 | ||
Distinguishable epidemics of multidrug-resistant Salmonella Typhimurium DT104 in different hosts | Q33575121 | ||
The bacterial signal indole increases epithelial-cell tight-junction resistance and attenuates indicators of inflammation | Q33591608 | ||
Modulation of the arginase pathway in the context of microbial pathogenesis: a metabolic enzyme moonlighting as an immune modulator | Q33619062 | ||
Dominant and diet-responsive groups of bacteria within the human colonic microbiota | Q33649520 | ||
IroN, a novel outer membrane siderophore receptor characteristic of Salmonella enterica | Q33726945 | ||
Evolution of host adaptation in Salmonella enterica | Q33764112 | ||
Comparison of Salmonella enterica serovar Typhimurium colitis in germfree mice and mice pretreated with streptomycin | Q33788040 | ||
Pathogenicity islands and the evolution of microbes | Q33920183 | ||
Epidemic salmonella typhimurium DT 104--a truly international multiresistant clone | Q33959619 | ||
Recombination and population structure in Salmonella enterica. | Q33987523 | ||
Salmonella typhimurium IroN and FepA proteins mediate uptake of enterobactin but differ in their specificity for other siderophores | Q33992252 | ||
Differences in attachment of Salmonella enterica serovars and Escherichia coli O157:H7 to alfalfa sprouts | Q34095662 | ||
Diverse virulence traits underlying different clinical outcomes of Salmonella infection | Q34206361 | ||
Innate immune response to Salmonella typhimurium, a model enteric pathogen | Q36019373 | ||
Phage-mediated acquisition of a type III secreted effector protein boosts growth of salmonella by nitrate respiration | Q36029218 | ||
Effects of indole on drug resistance and virulence of Salmonella enterica serovar Typhimurium revealed by genome-wide analyses. | Q36118186 | ||
A mouse model for S. typhimurium-induced enterocolitis | Q36248020 | ||
Colonization resistance of the digestive tract in conventional and antibiotic-treated mice | Q36252753 | ||
Salmonella typhimurium initiates murine infection by penetrating and destroying the specialized epithelial M cells of the Peyer's patches. | Q36363455 | ||
A composite bacteriophage alters colonization by an intestinal commensal bacterium. | Q36378467 | ||
Multiplicity of Salmonella entry mechanisms, a new paradigm for Salmonella pathogenesis. | Q36395663 | ||
How pathogenic bacteria evade mammalian sabotage in the battle for iron | Q36399419 | ||
Salmonella genomic island 1 (SGI1), variant SGI1-I, and new variant SGI1-O in proteus mirabilis clinical and food isolates from China. | Q36422613 | ||
Neutrophil influx during non-typhoidal salmonellosis: who is in the driver's seat? | Q36428605 | ||
Isolation of a temperate bacteriophage encoding the type III effector protein SopE from an epidemic Salmonella typhimurium strain | Q36437267 | ||
Fucose sensing regulates bacterial intestinal colonization | Q36456598 | ||
The clonal spread of multidrug-resistant non-typhi Salmonella serotypes | Q36484086 | ||
Are there acyl-homoserine lactones within mammalian intestines? | Q36558846 | ||
Quorum sensing by enteric pathogens | Q36667559 | ||
Evolutionary Genomics of Salmonella enterica Subspecies | Q36706268 | ||
Formate acts as a diffusible signal to induce Salmonella invasion | Q36747272 | ||
Escherichia coli Tryptophanase in the Enteric Environment | Q36774445 | ||
Modular networks and cumulative impact of lateral transfer in prokaryote genome evolution | Q36775488 | ||
The genome of Salmonella enterica serovar Typhi | Q36854781 | ||
Monoclonal secretory immunoglobulin A protects mice against oral challenge with the invasive pathogen Salmonella typhimurium | Q36944529 | ||
Streptomycin-induced inflammation enhances Escherichia coli gut colonization through nitrate respiration | Q36994397 | ||
Microbial endocrinology: how stress influences susceptibility to infection | Q37055720 | ||
Probiotic bacteria reduce salmonella typhimurium intestinal colonization by competing for iron | Q37118020 | ||
The long-term stability of the human gut microbiota | Q37217949 | ||
Coordinate regulation of glycan degradation and polysaccharide capsule biosynthesis by a prominent human gut symbiont | Q37258564 | ||
Malaria-associated L-arginine deficiency induces mast cell-associated disruption to intestinal barrier defenses against nontyphoidal Salmonella bacteremia | Q37264637 | ||
Arginine cools the inflamed gut. | Q37264641 | ||
Engagement of TLR signaling as adjuvant: towards smarter vaccine and beyond | Q37286716 | ||
Microbiota-liberated host sugars facilitate post-antibiotic expansion of enteric pathogens | Q37302434 | ||
Colonization outwith the colon: plants as an alternative environmental reservoir for human pathogenic enterobacteria | Q37348378 | ||
Lipocalin-2 resistance confers an advantage to Salmonella enterica serotype Typhimurium for growth and survival in the inflamed intestine | Q37401782 | ||
Molecular characterization and assembly of the needle complex of the Salmonella typhimurium type III protein secretion system | Q37434696 | ||
Enterohaemorrhagic Escherichia coli gains a competitive advantage by using ethanolamine as a nitrogen source in the bovine intestinal content | Q44511261 | ||
Lsr-mediated transport and processing of AI-2 in Salmonella typhimurium | Q44658473 | ||
Effect of Bifidobacterium longum ingestion on experimental salmonellosis in mice. | Q44928505 | ||
The structure of salmochelins: C-glucosylated enterobactins of Salmonella enterica | Q44983073 | ||
Microbiota-derived hydrogen fuels Salmonella typhimurium invasion of the gut ecosystem | Q45763464 | ||
Critical role of gut microbiota in the production of biologically active, free catecholamines in the gut lumen of mice. | Q46170383 | ||
A mixture containing galactooligosaccharide, produced by the enzymic activity of Bifidobacterium bifidum, reduces Salmonella enterica serovar Typhimurium infection in mice | Q46202314 | ||
Chemical synthesis of (S)-4,5-dihydroxy-2,3-pentanedione, a bacterial signal molecule precursor, and validation of its activity in Salmonella typhimurium. | Q46404123 | ||
Functions of the siderophore esterases IroD and IroE in iron-salmochelin utilization | Q46586809 | ||
Quorum sensing, communication and cross-kingdom signalling in the bacterial world. | Q46874295 | ||
3-O-deacylation of lipid A by PagL, a PhoP/PhoQ-regulated deacylase of Salmonella typhimurium, modulates signaling through Toll-like receptor 4. | Q47968723 | ||
Control of actin turnover by a salmonella invasion protein | Q48018016 | ||
Catecholamines increase conjugative gene transfer between enteric bacteria. | Q50042796 | ||
The S. Typhimurium effector SopE induces caspase-1 activation in stromal cells to initiate gut inflammation | Q50053617 | ||
SipA, SopA, SopB, SopD and SopE2 effector proteins of Salmonella enterica serovar Typhimurium are synthesized at late stages of infection in mice | Q50073002 | ||
Supplement 2002 (no. 46) to the Kauffmann-White scheme | Q50097498 | ||
Salmonella pathogenicity island 2-dependent evasion of the phagocyte NADPH oxidase | Q50122203 | ||
Inhibition of in vitro growth of enteropathogens by new Lactobacillus isolates of human intestinal origin | Q50133416 | ||
The origin and evolution of species differences in Escherichia coli and Salmonella typhimurium | Q50154091 | ||
Non-typhoidal salmonellosis: emerging problems | Q34254705 | ||
Type III secretion in Yersinia: injectisome or not? | Q34270387 | ||
Invasive non-typhoidal salmonella disease: an emerging and neglected tropical disease in Africa. | Q34275116 | ||
The languages of bacteria. | Q34284947 | ||
Honor thy gut symbionts redux | Q34295129 | ||
Cloning and molecular characterization of genes whose products allow Salmonella typhimurium to penetrate tissue culture cells | Q34298444 | ||
The Salmonella deubiquitinase SseL inhibits selective autophagy of cytosolic aggregates | Q34311564 | ||
Salmonella typhimurium recognizes a chemically distinct form of the bacterial quorum-sensing signal AI-2. | Q34345959 | ||
Identification of immunogenic Salmonella enterica serotype Typhi antigens expressed in chronic biliary carriers of S. Typhi in Kathmandu, Nepal | Q34363462 | ||
Salmonella interactions with host cells: type III secretion at work | Q34425135 | ||
Genetics and genomics in infectious disease susceptibility | Q34426106 | ||
Bile salt hydrolase activity in probiotics. | Q34432358 | ||
Host-pathogen interaction in invasive Salmonellosis | Q34440638 | ||
Chitin induces natural competence in Vibrio cholerae | Q34476987 | ||
SdiA sensing of acyl-homoserine lactones by enterohemorrhagic E. coli (EHEC) serotype O157:H7 in the bovine rumen | Q34664143 | ||
Salmochelins, siderophores of Salmonella enterica and uropathogenic Escherichia coli strains, are recognized by the outer membrane receptor IroN | Q34915244 | ||
Molecular pathogenesis of Salmonella enterica serotype typhimurium-induced diarrhea. | Q35032182 | ||
Bacterial quorum-sensing network architectures | Q35037002 | ||
Transcriptome analysis of genes controlled by luxS/autoinducer-2 in Salmonella enterica serovar Typhimurium | Q35093185 | ||
Intestinal inflammation allows Salmonella to use ethanolamine to compete with the microbiota | Q35409022 | ||
A secreted Salmonella protein induces a proinflammatory response in epithelial cells, which promotes neutrophil migration | Q35421297 | ||
Contribution of fimbrial operons to attachment to and invasion of epithelial cell lines by Salmonella typhimurium. | Q35493173 | ||
Role of the Salmonella pathogenicity island 1 effector proteins SipA, SopB, SopE, and SopE2 in Salmonella enterica subspecies 1 serovar Typhimurium colitis in streptomycin-pretreated mice | Q35549925 | ||
Pathology of Food-Borne Infectious Diseases of the Gastrointestinal Tract: An Update | Q35569366 | ||
Microbial endocrinology and infectious disease in the 21st century | Q35618732 | ||
The probiotic Escherichia coli strain Nissle 1917 (EcN) stops acute diarrhoea in infants and toddlers | Q35646959 | ||
Salmonella, the host and its microbiota | Q35693313 | ||
Gut inflammation can boost horizontal gene transfer between pathogenic and commensal Enterobacteriaceae | Q35709285 | ||
Zinc sequestration by the neutrophil protein calprotectin enhances Salmonella growth in the inflamed gut. | Q35841384 | ||
Evolution of pathogenicity islands of Salmonella enterica | Q35922677 | ||
The multifaceted roles of neutrophil gelatinase associated lipocalin (NGAL) in inflammation and cancer | Q35996059 | ||
Identification of a pathogenicity island required for Salmonella survival in host cells | Q37441337 | ||
Salmonella--the ultimate insider. Salmonella virulence factors that modulate intracellular survival. | Q37602205 | ||
So similar, yet so different: uncovering distinctive features in the genomes of Salmonella enterica serovars Typhimurium and Typhi. | Q37690405 | ||
Identification of a virulence locus encoding a second type III secretion system in Salmonella typhimurium | Q37698755 | ||
Role of intestinal mucins in innate host defense mechanisms against pathogens | Q37726707 | ||
Host-derived nitrate boosts growth of E. coli in the inflamed gut | Q37731297 | ||
Quorum sensing in bacterial virulence | Q37757803 | ||
Horizontal gene transfer amongst probiotic lactic acid bacteria and other intestinal microbiota: what are the possibilities? A review. | Q37824816 | ||
Metal sensing in Salmonella: implications for pathogenesis | Q37896785 | ||
Interkingdom crosstalk: host neuroendocrine stress hormones drive the hemolytic behavior of Salmonella typhi. | Q37901308 | ||
Salmonella persistence and transmission strategies | Q37964243 | ||
The streptomycin mouse model for Salmonella diarrhea: functional analysis of the microbiota, the pathogen's virulence factors, and the host's mucosal immune response | Q37968294 | ||
Functions of the Salmonella pathogenicity island 2 (SPI-2) type III secretion system effectors | Q37994160 | ||
The role of neutrophils during intestinal inflammation | Q38001546 | ||
Shedding light on Salmonella carriers | Q38010546 | ||
Mechanisms used by virulent Salmonella to impair dendritic cell function and evade adaptive immunity | Q38019049 | ||
New perspectives into bacterial DNA transfer to human cells | Q38022822 | ||
Salmonella T3SSs: successful mission of the secret(ion) agents. | Q38072180 | ||
Salmonella pathogenicity island 1(SPI-1) at work | Q38078232 | ||
Butyrate specifically down-regulates salmonella pathogenicity island 1 gene expression. | Q38317128 | ||
Structural diversity and specific distribution of O-glycans in normal human mucins along the intestinal tract | Q38336832 | ||
Bile-salt-mediated induction of antimicrobial and bile resistance in Salmonella typhimurium | Q38342630 | ||
Immunologic structures and functions of the gut. | Q38675604 | ||
Rck of Salmonella enterica, subspecies enterica serovar enteritidis, mediates zipper-like internalization. | Q39718726 | ||
Rapid disruption of epithelial barrier function by Salmonella typhimurium is associated with structural modification of intercellular junctions. | Q39821101 | ||
Role of acid tolerance response genes in Salmonella typhimurium virulence | Q40269189 | ||
Modulation of chloride secretory responses and barrier function of intestinal epithelial cells by the Salmonella effector protein SigD. | Q40549651 | ||
Simultaneous identification of bacterial virulence genes by negative selection. | Q40682435 | ||
Regulation of uptake and processing of the quorum-sensing autoinducer AI-2 in Escherichia coli | Q40731005 | ||
Precise estimation of the numbers of chronic carriers of Salmonella typhi in Santiago, Chile, an endemic area | Q40840867 | ||
Pathogenicity islands: bacterial evolution in quantum leaps | Q41245669 | ||
Extraintestinal dissemination of Salmonella by CD18-expressing phagocytes. | Q41481361 | ||
The function of the bacterial cytoskeleton in Salmonella pathogenesis. | Q41586920 | ||
LuxS affects flagellar phase variation independently of quorum sensing in Salmonella enterica serovar typhimurium | Q41911589 | ||
Signaling-mediated bacterial persister formation | Q41973955 | ||
AI-3 synthesis is not dependent on luxS in Escherichia coli | Q42066351 | ||
Heterologous expression of sahH reveals that biofilm formation is autoinducer-2-independent in Streptococcus sanguinis but is associated with an intact activated methionine cycle | Q42108971 | ||
Role of bile acids and metabolic activity of colonic bacteria in increased risk of colon cancer after cholecystectomy | Q42289405 | ||
Common and distinct structural features of Salmonella injectisome and flagellar basal body | Q42450071 | ||
Identification of a new iron regulated locus of Salmonella typhi | Q42648125 | ||
Direct nucleation and bundling of actin by the SipC protein of invasive Salmonella | Q42680869 | ||
Salmonella SPI1 effector SipA persists after entry and cooperates with a SPI2 effector to regulate phagosome maturation and intracellular replication | Q42756733 | ||
Genome-wide transposon mutagenesis identifies a role for host neuroendocrine stress hormones in regulating the expression of virulence genes in Salmonella. | Q42929336 | ||
A Rab32-dependent pathway contributes to Salmonella typhi host restriction | Q43114591 | ||
Production of AI-2 is mediated by the S-ribosylhomocystein lyase gene luxS in Bacteroides fragilis and Bacteroides vulgatus. | Q43759903 | ||
LuxS: its role in central metabolism and the in vitro synthesis of 4-hydroxy-5-methyl-3(2H)-furanone. | Q43946966 | ||
P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
P6216 | copyright status | copyrighted | Q50423863 |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 846049 | |
P577 | publication date | 2014-01-01 | |
P1433 | published in | International scholarly research notices | Q27726015 |
P1476 | title | The Dynamic Interactions between Salmonella and the Microbiota, within the Challenging Niche of the Gastrointestinal Tract | |
P478 | volume | 2014 |
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