scholarly article | Q13442814 |
P2093 | author name string | James M Slauch | |
Alexander D Palmer | |||
P2860 | cites work | The global burden of nontyphoidal Salmonella gastroenteritis | Q50050617 |
A dynamic view of the spread and intracellular distribution of Salmonella enterica | Q50057697 | ||
Acid resistance variability among isolates of Salmonella enterica serovar Typhimurium DT104. | Q50087104 | ||
A recombinant Salmonella typhimurium vaccine strain is taken up and survives within murine Peyer's patch dendritic cells. | Q50117176 | ||
Salmonella induces macrophage death by caspase-1-dependent necrosis | Q50118912 | ||
Dendritic cells of the murine Peyer's patches colocalize with Salmonella typhimurium avirulent mutants in the subepithelial dome. | Q50136076 | ||
The genetic basis of microbial resistance to antimicrobial peptides | Q50136104 | ||
The acid tolerance response of Salmonella typhimurium provides protection against organic acids | Q50136930 | ||
Infective dose of Salmonella typhimurium in cheddar cheese | Q50205087 | ||
Pathology of salmonella colitis | Q50220542 | ||
Salmonella gastroenteritis in rhesus monkeys | Q50252329 | ||
Effect of motility and chemotaxis on the invasion of Salmonella typhimurium into HeLa cells. | Q50464677 | ||
The effect of an antibiotic on the susceptibility of the mouse's intestinal tract to Salmonella infection. | Q50509270 | ||
Effect of streptomycin on susceptibility of intestinal tract to experimental Salmonella infection | Q73544754 | ||
Oxidation of hydrogen sulfide and methanethiol to thiosulfate by rat tissues: a specialized function of the colonic mucosa | Q73965302 | ||
Intestinal microflora functions in laboratory mice claimed to harbor a "normal" intestinal microflora. Is the SPF concept running out of date? | Q84777287 | ||
What is type VI secretion doing in all those bugs? | Q24594338 | ||
Foodborne illness acquired in the United States--major pathogens | Q24603736 | ||
Salmonella takes control: effector-driven manipulation of the host | Q24648042 | ||
Global burden of invasive nontyphoidal Salmonella disease, 2010(1) | Q26828546 | ||
Systematic review: the use of proton pump inhibitors and increased susceptibility to enteric infection | Q26849521 | ||
The microbiota mediates pathogen clearance from the gut lumen after non-typhoidal Salmonella diarrhea | Q27313421 | ||
Hemophagocytic macrophages harbor Salmonella enterica during persistent infection | Q27319444 | ||
Salmonella uses energy taxis to benefit from intestinal inflammation | Q27335357 | ||
The cost of virulence: retarded growth of Salmonella Typhimurium cells expressing type III secretion system 1 | Q27349314 | ||
Identification of the major intestinal fatty acid transport protein | Q28145772 | ||
Divalent cation transport and susceptibility to infectious and autoimmune disease: continuation of the Ity/Lsh/Bcg/Nramp1/Slc11a1 gene story | Q28203008 | ||
Natural resistance to infection with intracellular parasites: molecular genetics identifies Nramp1 as the Bcg/Ity/Lsh locus | Q28509803 | ||
Salmonella enterica serovar Typhimurium periplasmic superoxide dismutase SodCI is a member of the PhoPQ regulon and is induced in macrophages | Q28766733 | ||
The effect of diet on the human gut microbiome: a metagenomic analysis in humanized gnotobiotic mice | Q29614457 | ||
Gut inflammation provides a respiratory electron acceptor for Salmonella | Q29615318 | ||
Dissemination of invasive Salmonella via bacterial-induced extrusion of mucosal epithelia. | Q30496997 | ||
Perturbation of the small intestine microbial ecology by streptomycin alters pathology in a Salmonella enterica serovar typhimurium murine model of infection | Q33443646 | ||
Like will to like: abundances of closely related species can predict susceptibility to intestinal colonization by pathogenic and commensal bacteria | Q33523015 | ||
The lpf fimbrial operon mediates adhesion of Salmonella typhimurium to murine Peyer's patches | Q33616531 | ||
A low pH-inducible, PhoPQ-dependent acid tolerance response protects Salmonella typhimurium against inorganic acid stress | Q33730040 | ||
Dose-response modeling of Salmonella using outbreak data | Q33734171 | ||
Of mice, calves, and men. Comparison of the mouse typhoid model with other Salmonella infections. | Q33830012 | ||
Mechanisms controlling pathogen colonization of the gut. | Q34147042 | ||
Noncanonical inflammasome activation of caspase-4/caspase-11 mediates epithelial defenses against enteric bacterial pathogens | Q34149021 | ||
Invasive non-typhoidal salmonella disease: an emerging and neglected tropical disease in Africa. | Q34275116 | ||
Breaking through the acid barrier: an orchestrated response to proton stress by enteric bacteria | Q34299106 | ||
Microbiota-mediated colonization resistance against intestinal pathogens | Q34324937 | ||
A national outbreak of Salmonella enteritidis infections from ice cream. The Investigation Team | Q34376406 | ||
Animal models of Salmonella infections: enteritis versus typhoid fever. | Q34469859 | ||
Pathology of the alimentary tract in Salmonella typhimurium food poisoning | Q34527310 | ||
Attribution of foodborne illnesses, hospitalizations, and deaths to food commodities by using outbreak data, United States, 1998-2008 | Q34691203 | ||
Quantitatively different, yet qualitatively alike: a meta-analysis of the mouse core gut microbiome with a view towards the human gut microbiome | Q34712628 | ||
How informative is the mouse for human gut microbiota research? | Q34818253 | ||
Pretreatment of mice with streptomycin provides a Salmonella enterica serovar Typhimurium colitis model that allows analysis of both pathogen and host | Q34935646 | ||
Integration of a complex regulatory cascade involving the SirA/BarA and Csr global regulatory systems that controls expression of the Salmonella SPI-1 and SPI-2 virulence regulons through HilD | Q35049823 | ||
Compounds Which Serve as the Sole Source of Carbon or Nitrogen for Salmonella typhimurium LT-2 | Q35157309 | ||
The role of gastric acid in preventing foodborne disease and how bacteria overcome acid conditions | Q35180934 | ||
Intestinal inflammation allows Salmonella to use ethanolamine to compete with the microbiota | Q35409022 | ||
Acidification of phagosomes containing Salmonella typhimurium in murine macrophages. | Q35506318 | ||
A Salmonella virulence factor activates the NOD1/NOD2 signaling pathway. | Q35614774 | ||
Nramp1 and Other Transporters Involved in Metal Withholding during Infection | Q35905314 | ||
Phage-mediated acquisition of a type III secreted effector protein boosts growth of salmonella by nitrate respiration | Q36029218 | ||
The phs gene and hydrogen sulfide production by Salmonella typhimurium | Q36236471 | ||
Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis. | Q36240466 | ||
The route of enteric infection in normal mice | Q36273394 | ||
Salmonella stimulate macrophage macropinocytosis and persist within spacious phagosomes. | Q36362706 | ||
Salmonella typhimurium initiates murine infection by penetrating and destroying the specialized epithelial M cells of the Peyer's patches. | Q36363455 | ||
Salmonella exploits caspase-1 to colonize Peyer's patches in a murine typhoid model | Q36368780 | ||
Salmonella typhimurium persists within macrophages in the mesenteric lymph nodes of chronically infected Nramp1+/+ mice and can be reactivated by IFNgamma neutralization | Q36399044 | ||
Intestinal Long-Chain Fatty Acids Act as a Direct Signal To Modulate Expression of the Salmonella Pathogenicity Island 1 Type III Secretion System | Q36577171 | ||
The intestinal fatty acid propionate inhibits Salmonella invasion through the post-translational control of HilD | Q36636799 | ||
Salmonella, the host and disease: a brief review | Q36673931 | ||
Infective disorders of the gastrointestinal tract | Q36699532 | ||
Formate acts as a diffusible signal to induce Salmonella invasion | Q36747272 | ||
Regulation of lipid A modifications by Salmonella typhimurium virulence genes phoP-phoQ. | Q36852656 | ||
Pyroptosis and host cell death responses during Salmonella infection | Q36917154 | ||
HilD-mediated transcriptional cross-talk between SPI-1 and SPI-2. | Q36936468 | ||
Salmonellae interplay with host cells | Q37008201 | ||
Effect of streptomycin administration on colonization resistance to Salmonella typhimurium in mice | Q37048358 | ||
The role of microbiota in infectious disease | Q37086530 | ||
Contribution of flagellin pattern recognition to intestinal inflammation during Salmonella enterica serotype typhimurium infection | Q37191428 | ||
Salmonella-containing vacuoles: directing traffic and nesting to grow. | Q37263303 | ||
Twin-arginine translocation system (tat) mutants of Salmonella are attenuated due to envelope defects, not respiratory defects | Q37265066 | ||
Salmonella typhimurium activates virulence gene transcription within acidified macrophage phagosomes | Q37265751 | ||
The PhoQ/PhoP regulatory network of Salmonella enterica | Q37269162 | ||
Salmonellae interactions with host processes. | Q37357805 | ||
Quantitative assessment of cytosolic Salmonella in epithelial cells. | Q37439277 | ||
Spatial segregation of virulence gene expression during acute enteric infection with Salmonella enterica serovar Typhimurium | Q37631507 | ||
Host-derived nitrate boosts growth of E. coli in the inflamed gut | Q37731297 | ||
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 | ||
Salmonella enterica: living a double life in epithelial cells. | Q38280748 | ||
Butyrate specifically down-regulates salmonella pathogenicity island 1 gene expression. | Q38317128 | ||
Inflammasomes of the intestinal epithelium | Q38545740 | ||
Salmonella and the Inflammasome: Battle for Intracellular Dominance | Q38909265 | ||
Analysis of the contribution of Salmonella pathogenicity islands 1 and 2 to enteric disease progression using a novel bovine ileal loop model and a murine model of infectious enterocolitis | Q39391975 | ||
Salmonella enterica serovars Typhimurium and Dublin can lyse macrophages by a mechanism distinct from apoptosis | Q39516604 | ||
NLRC4 expression in intestinal epithelial cells mediates protection against an enteric pathogen. | Q39606134 | ||
Integrating global regulatory input into the Salmonella pathogenicity island 1 type III secretion system | Q39694438 | ||
Lipid Digestion and Absorption | Q40148842 | ||
A review of human salmonellosis: I. Infective dose. | Q40251618 | ||
Genome-guided design of a defined mouse microbiota that confers colonization resistance against Salmonella enterica serovar Typhimurium | Q40442598 | ||
Histopathology of typhoid enteritis: morphologic and immunophenotypic findings | Q40631172 | ||
Intestinal short-chain fatty acids alter Salmonella typhimurium invasion gene expression and virulence through BarA/SirA. | Q40687509 | ||
Spatiotemporal analysis of acid adaptation-mediated Vibrio cholerae hyperinfectivity | Q40705279 | ||
A role for the PhoP/Q regulon in inhibition of fusion between lysosomes and Salmonella-containing vacuoles in macrophages. | Q40770373 | ||
Global transcriptome and mutagenic analyses of the acid tolerance response of Salmonella enterica serovar Typhimurium. | Q40991424 | ||
Roles for motility in bacterial–host interactions | Q41528040 | ||
Salmonella enterica serovar Typhimurium pathogenicity island 2 is necessary for complete virulence in a mouse model of infectious enterocolitis | Q41785768 | ||
The effect of an antibiotic on the susceptibility of the mouse's intestinal tract to Salmonella infection. | Q42015426 | ||
Cytopathogenic effect of Salmonella typhi GIFU 10007 on M cells of murine ileal Peyer's patches in ligated ileal loops: an ultrastructural study | Q42522319 | ||
Enhanced susceptibility to Salmonella infection in streptomycin-treated mice | Q43923685 | ||
The Salmonella pathogenicity island (SPI)-2 and SPI-1 type III secretion systems allow Salmonella serovar typhimurium to trigger colitis via MyD88-dependent and MyD88-independent mechanisms. | Q45232038 | ||
Aromatic-dependent "Salmonella sp." as live vaccine in mice and calves | Q45979424 | ||
Isolation of Salmonella typhi-murium from municipal water, Riverside, California, 1965 | Q46084968 | ||
Motility allows S. Typhimurium to benefit from the mucosal defence | Q46778188 | ||
Epithelium-intrinsic NAIP/NLRC4 inflammasome drives infected enterocyte expulsion to restrict Salmonella replication in the intestinal mucosa | Q46852337 | ||
Disparate impact of oxidative host defenses determines the fate of Salmonella during systemic infection in mice | Q46944630 | ||
PmrA-PmrB-regulated genes necessary for 4-aminoarabinose lipid A modification and polymyxin resistance | Q48038471 | ||
P433 | issue | 8 | |
P304 | page(s) | 1877-1892 | |
P577 | publication date | 2017-08-24 | |
P1433 | published in | Human and Ecological Risk Assessment: An International Journal | Q15759704 |
P1476 | title | Mechanisms of Salmonella pathogenesis in animal models | |
P478 | volume | 23 |
Q90591990 | Inhibition of invasive salmonella by orally administered IgA and IgG monoclonal antibodies |
Q91686490 | Pathogenicity island excision during an infection by Salmonella enterica serovar Enteritidis is required for crossing the intestinal epithelial barrier in mice to cause systemic infection |
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