scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1004946298 |
P356 | DOI | 10.1038/44593 |
P8608 | Fatcat ID | release_ptgpl7eu4raxzpaxfxq2ler6bi |
P698 | PubMed publication ID | 10548107 |
P50 | author | Ferric Fang | Q30098365 |
W. Tony Parks | Q43073471 | ||
P2093 | author name string | W Brown | |
A J Bäumler | |||
S Falkow | |||
M Le | |||
A Vazquez-Torres | |||
J Jones-Carson | |||
R Berggren | |||
R Valdivia | |||
P2860 | cites work | A novel suicide vector and its use in construction of insertion mutations: osmoregulation of outer membrane proteins and virulence determinants in Vibrio cholerae requires toxR | Q29615324 |
The lpf fimbrial operon mediates adhesion of Salmonella typhimurium to murine Peyer's patches | Q33616531 | ||
Cloning and molecular characterization of genes whose products allow Salmonella typhimurium to penetrate tissue culture cells | Q34298444 | ||
Ethanolamine utilization in Salmonella typhimurium: nucleotide sequence, protein expression, and mutational analysis of the cchA cchB eutE eutJ eutG eutH gene cluster | Q34319376 | ||
Synergistic effect of mutations in invA and lpfC on the ability of Salmonella typhimurium to cause murine typhoid. | Q35549256 | ||
Fur regulon of Salmonella typhimurium: identification of new iron-regulated genes. | Q35592292 | ||
Mutants of Salmonella typhimurium that cannot survive within the macrophage are avirulent | Q35617117 | ||
Salmonella typhimurium initiates murine infection by penetrating and destroying the specialized epithelial M cells of the Peyer's patches. | Q36363455 | ||
Bacterial genetics by flow cytometry: rapid isolation of Salmonella typhimurium acid-inducible promoters by differential fluorescence induction | Q36833896 | ||
Identification of a Salmonella typhimurium invasion locus by selection for hyperinvasive mutants | Q36864089 | ||
Listeria monocytogenes, but not Salmonella typhimurium, elicits a CD18-independent mechanism of neutrophil extravasation into the murine peritoneal cavity | Q40374484 | ||
Role of M cells in initial antigen uptake and in ulcer formation in the rabbit intestinal loop model of shigellosis | Q40426449 | ||
Non-invasive Salmonella typhimurium mutants are avirulent because of an inability to enter and destroy M cells of ileal Peyer's patches | Q40651358 | ||
The dissemination of Salmonella typhi, S. paratyphi A and S. paratyphi B through the organs of the white mouse by oral infection | Q40998019 | ||
Epithelial M cells: gateways for mucosal infection and immunization | Q41075139 | ||
Cloning of the YenI restriction endonuclease and methyltransferase from Yersinia enterocolitica serotype O8 and construction of a transformable R-M+ mutant | Q41501302 | ||
Ruffles induced by Salmonella and other stimuli direct macropinocytosis of bacteria | Q41502444 | ||
The invasion-associated type-III protein secretion system in Salmonella--a review | Q41532673 | ||
Contribution of CD11a/CD18, CD11b/CD18, ICAM-1 (CD54) and -2 (CD102) to human monocyte migration through endothelium and connective tissue fibroblast barriers | Q47915820 | ||
Amplification of an invA gene sequence of Salmonella typhimurium by polymerase chain reaction as a specific method of detection of Salmonella | Q50174322 | ||
Intestinal M Cells: A Pathway for Entry of Reovirus into the Host | Q72884912 | ||
P433 | issue | 6755 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 804-808 | |
P577 | publication date | 1999-10-01 | |
P1433 | published in | Nature | Q180445 |
P1476 | title | Extraintestinal dissemination of Salmonella by CD18-expressing phagocytes | |
P478 | volume | 401 |
Q37670529 | A Potential Role of Salmonella Infection in the Onset of Inflammatory Bowel Diseases |
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Q35146015 | A comprehensive study of the contribution of Salmonella enterica serovar Typhimurium SPI2 effectors to bacterial colonization, survival, and replication in typhoid fever, macrophage, and epithelial cell infection models |
Q50057697 | A dynamic view of the spread and intracellular distribution of Salmonella enterica |
Q33319574 | A model of Salmonella colitis with features of diarrhea in SLC11A1 wild-type mice |
Q30421834 | A naturally occurring single nucleotide polymorphism in the Salmonella SPI-2 type III effector srfH/sseI controls early extraintestinal dissemination |
Q37398323 | Absence of functional Hfe protects mice from invasive Salmonella enterica serovar Typhimurium infection via induction of lipocalin-2. |
Q36911506 | Absence of platelet endothelial cell adhesion molecule 1, PECAM-1/CD31, in vivo increases resistance to Salmonella enterica serovar Typhimurium in mice |
Q38909269 | Activation and Evasion of Inflammasomes by Yersinia |
Q30478868 | Activation of bone marrow-resident memory T cells by circulating, antigen-bearing dendritic cells |
Q39653766 | Adherence of Burkholderia pseudomallei cells to cultured human epithelial cell lines is regulated by growth temperature |
Q64238476 | Advances and Challenges in Understanding Cerebral Toxoplasmosis |
Q43198620 | After injection into the striatum, in vitro-differentiated microglia- and bone marrow-derived dendritic cells can leave the central nervous system via the blood stream. |
Q36483536 | Aggregation via the red, dry, and rough morphotype is not a virulence adaptation in Salmonella enterica serovar Typhimurium. |
Q47097934 | An Updated View on the Rck Invasin of Salmonella: Still Much to Discover. |
Q38896014 | Animal Models for Salmonellosis: Applications in Vaccine Research |
Q34469859 | Animal models of Salmonella infections: enteritis versus typhoid fever. |
Q35047221 | Animal models paving the way for clinical trials of attenuated Salmonella enterica serovar Typhi live oral vaccines and live vectors |
Q30784051 | Antigen-presenting cells and anti-Salmonella immunity |
Q36368785 | Antimicrobial actions of the NADPH phagocyte oxidase and inducible nitric oxide synthase in experimental salmonellosis. I. Effects on microbial killing by activated peritoneal macrophages in vitro |
Q38247207 | Apicomplexan infections in the gut. |
Q35809245 | Attenuated salmonella and Shigella as carriers for DNA vaccines |
Q90572987 | Autophagy Induction by a Small Molecule Inhibits Salmonella Survival in Macrophages and Mice |
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Q35848508 | CD11c- and CD11b-expressing mouse leukocytes transport single Toxoplasma gondii tachyzoites to the brain |
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Q30431794 | Caenorhabditis is a metazoan host for Legionella |
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Q28306024 | Cellular aspects of immunity to intracellular Salmonella enterica |
Q54764575 | Characteristics of claudin expression in follicle-associated epithelium of Peyer's patches: preferential localization of claudin-4 at the apex of the dome region. |
Q37863771 | Characterization of a porcine intestinal epithelial cell line for in vitro studies of microbial pathogenesis in swine |
Q35663955 | Chronic and acute infection of the gall bladder by Salmonella Typhi: understanding the carrier state |
Q34983834 | Chronic bacterial infections: living with unwanted guests |
Q33388431 | Chronic murine typhoid fever is a natural model of secondary hemophagocytic lymphohistiocytosis |
Q28347332 | Co-option of endocytic functions of cellular caveolae by pathogens |
Q54465090 | Colitogenic and non-colitogenic commensal bacteria differentially trigger DC maturation and Th cell polarization: an important role for IL-6. |
Q41892074 | Complement receptor 3 and Toll-like receptor 4 act sequentially in uptake and intracellular killing of unopsonized Salmonella enterica serovar Typhimurium by human neutrophils |
Q36313910 | Constitutive acid sphingomyelinase enhances early and late macrophage killing of Salmonella enterica serovar Typhimurium |
Q35164780 | Construction, characterization, and immunogenicity of an attenuated Salmonella enterica serovar typhimurium pgtE vaccine expressing fimbriae with integrated viral epitopes from the spiC promoter |
Q33410820 | Coordinated regulation of virulence during systemic infection of Salmonella enterica serovar Typhimurium |
Q89448413 | Critical Role for the Microbiota in CX3CR1+ Intestinal Mononuclear Phagocyte Regulation of Intestinal T Cell Responses |
Q98771929 | Culture-Dependent and Sequencing Methods Revealed the Absence of a Bacterial Community Residing in the Urine of Healthy Cats |
Q54239779 | Defective Phagocytic Properties of HIV-Infected Macrophages: How Might They Be Implicated in the Development of Invasive Salmonella Typhimurium? |
Q29619620 | Dendritic cells express tight junction proteins and penetrate gut epithelial monolayers to sample bacteria |
Q33989067 | Dendritic-cell trafficking to lymph nodes through lymphatic vessels |
Q39271503 | Detection of bacterial DNA in lymph nodes of Crohn's disease patients using high throughput sequencing. |
Q50079058 | Detection of pathogenic intestinal bacteria by Toll-like receptor 5 on intestinal CD11c+ lamina propria cells. |
Q35128104 | Development of acquired immunity to Salmonella |
Q33855197 | Development of protective immunity to Salmonella, a mucosal pathogen with a systemic agenda |
Q36277316 | Diarrhea and colitis in mice require the Salmonella pathogenicity island 2-encoded secretion function but not SifA or Spv effectors |
Q50088789 | Differential responses of macrophages to Salmonella enterica serovars Enteritidis and Typhimurium |
Q34127776 | Dissemination of Mycobacterium tuberculosis is influenced by host factors and precedes the initiation of T-cell immunity. |
Q37120272 | Energy Taxis toward Host-Derived Nitrate Supports a Salmonella Pathogenicity Island 1-Independent Mechanism of Invasion |
Q42127302 | Enhanced microscopic definition of Campylobacter jejuni 81-176 adherence to, invasion of, translocation across, and exocytosis from polarized human intestinal Caco-2 cells. |
Q60584774 | Enterobacteria and host resistance to infection |
Q35852370 | Entry and survival of Salmonella typhimurium in dendritic cells and presentation of recombinant antigens do not require macrophage-specific virulence factors |
Q21558786 | Evolution of Salmonella enterica virulence via point mutations in the fimbrial adhesin |
Q39655749 | Flavohemoglobin Hmp protects Salmonella enterica serovar typhimurium from nitric oxide-related killing by human macrophages. |
Q30925094 | Flow cytometric screening of cell-based libraries |
Q35178637 | Functions and effectors of the Salmonella pathogenicity island 2 type III secretion system |
Q37035982 | Gallbladder epithelium as a niche for chronic Salmonella carriage |
Q35134564 | Gastrointestinal disorders of the critically ill. Bacterial translocation in the gut. |
Q37747139 | Genetic and Dietary Iron Overload Differentially Affect the Course of Salmonella Typhimurium Infection |
Q36943767 | Genetics-squared: combining host and pathogen genetics in the analysis of innate immunity and bacterial virulence |
Q35765795 | Global analysis of Salmonella alternative sigma factor E on protein translation. |
Q27322348 | Granulocytes impose a tight bottleneck upon the gut luminal pathogen population during Salmonella typhimurium colitis |
Q28513033 | H2-M3 major histocompatibility complex class Ib-restricted CD8 T cells induced by Salmonella enterica serovar Typhimurium infection recognize proteins released by Salmonella serovar Typhimurium |
Q26997068 | Helicobacter and salmonella persistent infection strategies |
Q30479101 | Helicobacter pylori CagA induces AGS cell elongation through a cell retraction defect that is independent of Cdc42, Rac1, and Arp2/3. |
Q33358028 | High-throughput isolation and mapping of C. elegans mutants susceptible to pathogen infection |
Q35071133 | Histopathological analysis of Salmonella chronic carriage in the mouse hepatopancreatobiliary system |
Q35899292 | Host microarray analysis reveals a role for the Salmonella response regulator phoP in human macrophage cell death |
Q34440638 | Host-pathogen interaction in invasive Salmonellosis |
Q34600953 | Host-pathogen interactions: the seduction of molecular cross talk |
Q36583831 | How to outwit the enemy: dendritic cells face Salmonella |
Q34524241 | Human milk: a source of more life than we imagine |
Q37264606 | Identification of Salmonella enterica serovar Typhimurium genes regulated during biofilm formation on cholesterol gallstone surfaces |
Q34007106 | Identification of attenuated Yersinia pseudotuberculosis strains and characterization of an orogastric infection in BALB/c mice on day 5 postinfection by signature-tagged mutagenesis |
Q50110448 | Immune response to Salmonella: location, location, location? |
Q37528118 | Immune responses of TLR5(+) lamina propria dendritic cells in enterobacterial infection |
Q36977514 | Immune responses to commensal and environmental microbes |
Q37846872 | Immunity to salmonellosis |
Q46792678 | Immunological bases of increased susceptibility to invasive nontyphoidal Salmonella infection in children with malaria and anaemia. |
Q38832842 | Immunology, epidemiology and mathematical modelling towards a better understanding of invasive non-typhoidal Salmonella disease and rational vaccination approaches |
Q42011289 | Impact of delivery mode on the colostrum microbiota composition. |
Q33988694 | Improved expression systems for regulated expression in Salmonella infecting eukaryotic cells |
Q39522009 | In vivo activation of dendritic cells and T cells during Salmonella enterica serovar Typhimurium infection |
Q50079345 | In vivo, fliC expression by Salmonella enterica serovar Typhimurium is heterogeneous, regulated by ClpX, and anatomically restricted |
Q55512573 | Induction of Hypergammaglobulinemia and Autoantibodies by Salmonella Infection in MyD88-Deficient Mice. |
Q40773193 | Induction of specific CD8+ memory T cells and long lasting protection following immunization with Salmonella typhimurium expressing a lymphocytic choriomeningitis MHC class I-restricted epitope |
Q35661763 | Infection with Salmonella enterica Serovar Typhimurium Leads to Increased Proportions of F4/80+ Red Pulp Macrophages and Decreased Proportions of B and T Lymphocytes in the Spleen |
Q89611981 | Infection-based chemical screens uncover host-pathogen interactions |
Q64064814 | Infection-generated electric field in gut epithelium drives bidirectional migration of macrophages |
Q37153078 | Inflammation and oxidative stress in vertebrate host-parasite systems |
Q24620024 | Inhibition of the PtdIns(5) kinase PIKfyve disrupts intracellular replication of Salmonella |
Q34481840 | InlA promotes dissemination of Listeria monocytogenes to the mesenteric lymph nodes during food borne infection of mice |
Q37930865 | Innate immune control of Salmonella enterica serovar Typhimurium: mechanisms contributing to combating systemic Salmonella infection |
Q36019373 | Innate immune response to Salmonella typhimurium, a model enteric pathogen |
Q35134687 | Innate immunity and pathogen-host interaction |
Q55339472 | Integrin αDβ2 (CD11d/CD18) Modulates Leukocyte Accumulation, Pathogen Clearance, and Pyroptosis in Experimental Salmonella Typhimurium Infection. |
Q35130623 | Interaction of Yersinia enterocolitica with epithelial cells: invasin beyond invasion |
Q28081987 | Interactions of Salmonella with animals and plants |
Q39968051 | Interferon-gamma limits the availability of iron for intramacrophage Salmonella typhimurium. |
Q35130619 | Intestinal M cells and their role in bacterial infection |
Q27301176 | Intestinal colonization of IL-2 deficient mice with non-colitogenic B. vulgatus prevents DC maturation and T-cell polarization |
Q37647153 | Intestinal villous M cells: an antigen entry site in the mucosal epithelium |
Q37297067 | Intracellular Organisms as Placental Invaders |
Q37212318 | Intracellular microbes and haemophagocytosis |
Q50113387 | Intracellular replication of Salmonella typhimurium strains in specific subsets of splenic macrophages in vivo. |
Q34217562 | Intrauterine growth restriction is a direct consequence of localized maternal uropathogenic Escherichia coli cystitis |
Q36593956 | Intravaginal immunization of mice with recombinant Salmonella enterica serovar Typhimurium expressing human papillomavirus type 16 antigens as a potential route of vaccination against cervical cancer |
Q36984051 | Invasion and dissemination of Yersinia enterocolitica in the mouse infection model |
Q33598570 | Invasion genes are not required for Salmonella enterica serovar typhimurium to breach the intestinal epithelium: evidence that salmonella pathogenicity island 1 has alternative functions during infection |
Q24625439 | Invasion of the central nervous system by intracellular bacteria |
Q36339301 | Iron Regulatory Proteins Mediate Host Resistance to Salmonella Infection |
Q47644238 | Lactobacillus rhamnosus L34 Attenuates Gut Translocation-Induced Bacterial Sepsis in Murine Models of Leaky Gut. |
Q34102792 | Leukocyte-facilitated entry of intracellular pathogens into the central nervous system. |
Q36396704 | Lipocalin-2 ensures host defense against Salmonella Typhimurium by controlling macrophage iron homeostasis and immune response |
Q35689514 | Live attenuated Salmonella vaccines against Mycobacterium tuberculosis with antigen delivery via the type III secretion system |
Q39538602 | Living in stools is not as dumb as you think |
Q36736283 | Loss of Multicellular Behavior in Epidemic African Nontyphoidal Salmonella enterica Serovar Typhimurium ST313 Strain D23580. |
Q37450860 | Low-molecular-weight thiol-dependent antioxidant and antinitrosative defences in Salmonella pathogenesis |
Q39369936 | Lung B cells promote early pathogen dissemination and hasten death from inhalation anthrax |
Q91746238 | Maternal and Perinatal Factors Associated with the Human Milk Microbiome |
Q30374865 | Mechanisms of egg contamination by Salmonella Enteritidis. |
Q36155563 | Mechanisms of reovirus bloodstream dissemination |
Q40148415 | Mesenchymal Cell-Specific MyD88 Signaling Promotes Systemic Dissemination of Salmonella Typhimurium via Inflammatory Monocytes. |
Q40387427 | Mesenteric lymph nodes confine dendritic cell-mediated dissemination of Salmonella enterica serovar Typhimurium and limit systemic disease in mice |
Q37965684 | Microbes, intestinal inflammation and probiotics. |
Q73337324 | Microbial invasion across the intestinal epithelial barrier |
Q35867980 | Microbial programming of health and disease starts during fetal life. |
Q37013654 | Microbiota restricts trafficking of bacteria to mesenteric lymph nodes by CX(3)CR1(hi) cells |
Q26740646 | Models of intestinal infection by Salmonella enterica: introduction of a new neonate mouse model |
Q35074276 | Molecular basis of virulence in clinical isolates of Escherichia coli and Salmonella species from a tertiary hospital in the Eastern Cape, South Africa |
Q31079248 | Molecular insights into farm animal and zoonotic Salmonella infections |
Q28681765 | Mom knows best: the universality of maternal microbial transmission |
Q34065898 | Monocyte-mediated defense against microbial pathogens. |
Q36228955 | Monocytes give rise to mucosal, but not splenic, conventional dendritic cells |
Q30540134 | Motile invaded neutrophils in the small intestine of Toxoplasma gondii-infected mice reveal a potential mechanism for parasite spread |
Q33792879 | Mouse model of enteropathogenic Escherichia coli infection |
Q35783736 | Mouse model of oral infection with virulent type A Francisella tularensis |
Q37880344 | Mouse models to assess the efficacy of non-typhoidal Salmonella vaccines: revisiting the role of host innate susceptibility and routes of challenge |
Q36395663 | Multiplicity of Salmonella entry mechanisms, a new paradigm for Salmonella pathogenesis. |
Q37403782 | Mutations in the Salmonella enterica serovar Choleraesuis cAMP-receptor protein gene lead to functional defects in the SPI-1 Type III secretion system |
Q90249639 | Mycobacterium tuberculosis Dissemination Plays a Critical Role in Pathogenesis |
Q41639218 | Nanocapsules loaded with iron-saturated bovine lactoferrin have antimicrobial therapeutic potential and maintain calcium, zinc and iron metabolism |
Q37361936 | New insights into the roles of dendritic cells in intestinal immunity and tolerance |
Q42100653 | Nitric oxide and salmonella pathogenesis |
Q41780035 | Nod1 and Nod2 regulation of inflammation in the Salmonella colitis model |
Q26864351 | Non-genetic diversity shapes infectious capacity and host resistance |
Q35443593 | Non-typhoidal Salmonella Typhimurium ST313 isolates that cause bacteremia in humans stimulate less inflammasome activation than ST19 isolates associated with gastroenteritis |
Q27349004 | Nucleolar proteins suppress Caenorhabditis elegans innate immunity by inhibiting p53/CEP-1 |
Q35660952 | Oral Wild-Type Salmonella Typhi Challenge Induces Activation of Circulating Monocytes and Dendritic Cells in Individuals Who Develop Typhoid Disease |
Q35689551 | Oral infection with signature-tagged Listeria monocytogenes reveals organ-specific growth and dissemination routes in guinea pigs |
Q40832683 | Orally delivered siRNA targeting macrophage Map4k4 suppresses systemic inflammation |
Q37338949 | Origins and tissue-context-dependent fates of blood monocytes |
Q34134518 | Oxygen-dependent anti-Salmonella activity of macrophages |
Q31101613 | Pathogenicity of Salmonella enterica in Caenorhabditis elegans relies on disseminated oxidative stress in the infected host |
Q35889600 | Persistent bacterial infections: the interface of the pathogen and the host immune system |
Q35143668 | Persistent salmonellosis causes pancreatitis in a murine model of infection |
Q36483628 | Peyer's patches are required for intestinal immunoglobulin A responses to Salmonella spp. |
Q35034821 | Phylogenomic analysis identifies gene gains that define Salmonella enterica subspecies I. |
Q48320085 | Physiological Translocation of Lactic Acid Bacteria during Pregnancy Contributes to the Composition of the Milk Microbiota in Mice. |
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Q34257214 | Polyamines are required for virulence in Salmonella enterica serovar Typhimurium |
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Q33334033 | Presence of wild-type and attenuated Salmonella enterica strains in brain tissues following inoculation of mice by different routes |
Q34935646 | Pretreatment of mice with streptomycin provides a Salmonella enterica serovar Typhimurium colitis model that allows analysis of both pathogen and host |
Q42044118 | Probiotic Treatment Decreases the Number of CD14-Expressing Cells in Porcine Milk Which Correlates with Several Intestinal Immune Parameters in the Piglets |
Q35958581 | Probiotics in early life: a preventative and treatment approach |
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Q28087452 | Protective host immune responses to Salmonella infection |
Q64064522 | Proteomic Profiling during Infection Distinguishes the Intracellular Environment of Host Cells |
Q40338463 | Pseudogenization of the Secreted Effector Gene sseI Confers Rapid Systemic Dissemination of S. Typhimurium ST313 within Migratory Dendritic Cells. |
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Q35839664 | RNA-seq Brings New Insights to the Intra-Macrophage Transcriptome of Salmonella Typhimurium |
Q37111565 | RaoN, a small RNA encoded within Salmonella pathogenicity island-11, confers resistance to macrophage-induced stress |
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Q30486333 | Rapid dissemination of Francisella tularensis and the effect of route of infection |
Q35650847 | Regulation of phenotypic heterogeneity permits Salmonella evasion of the host caspase-1 inflammatory response |
Q50064747 | Resistance to antimicrobial peptides contributes to persistence of Salmonella typhimurium in the C. elegans intestine |
Q34110005 | Resolvase-in vivo expression technology analysis of the Salmonella enterica serovar Typhimurium PhoP and PmrA regulons in BALB/c mice |
Q41807359 | Role of Nod1 in mucosal dendritic cells during Salmonella pathogenicity island 1-independent Salmonella enterica serovar Typhimurium infection |
Q36227773 | Role of neutrophils in murine salmonellosis |
Q39526317 | Roles of hilC and hilD in regulation of hilA expression in Salmonella enterica serovar Typhimurium |
Q33755761 | Safety and immunogenicity of Salmonella typhimurium expressing C-terminal truncated human IL-2 in a murine model |
Q38727040 | Salmonella Co-opts Host Cell Chaperone-mediated Autophagy for Intracellular Growth |
Q92999225 | Salmonella enterica Effectors SifA, SpvB, SseF, SseJ, and SteA Contribute to Type III Secretion System 1-Independent Inflammation in a Streptomycin-Pretreated Mouse Model of Colitis |
Q90701291 | Salmonella enterica Requires Lipid Metabolism Genes To Replicate in Proinflammatory Macrophages and Mice |
Q42694341 | Salmonella enterica Serovar Typhimurium Strategies for Host Adaptation |
Q38444330 | Salmonella enterica serovar Enteritidis colonization of the chicken caecum requires the HilA regulatory protein |
Q24654040 | Salmonella enterica serovar Typhimurium can detect acyl homoserine lactone production by Yersinia enterocolitica in mice |
Q40507112 | Salmonella enterica serovar Typhimurium interaction with dendritic cells: impact of the sifA gene |
Q44896653 | Salmonella enterica serovar Typhimurium regulates intercellular junction proteins and facilitates transepithelial neutrophil and bacterial passage |
Q35550354 | Salmonella enterica serovar Typhimurium requires nonsterol precursors of the cholesterol biosynthetic pathway for intracellular proliferation |
Q41976795 | Salmonella enterica serovar enteritidis pathogenicity island 1 is not essential for but facilitates rapid systemic spread in chickens. |
Q26996526 | Salmonella enterica serovars Typhimurium and Typhi as model organisms: revealing paradigm of host-pathogen interactions |
Q36368780 | Salmonella exploits caspase-1 to colonize Peyer's patches in a murine typhoid model |
Q39442456 | Salmonella infection: Interplay between the bacteria and host immune system |
Q34469834 | Salmonella intracellular proliferation: where, when and how? |
Q33591947 | Salmonella pathogenicity island 1-independent induction of apoptosis in infected macrophages by Salmonella enterica serotype typhimurium |
Q24811102 | Salmonella pathogenicity island 2 is expressed prior to penetrating the intestine |
Q40764879 | Salmonella pathogenicity island 2-dependent macrophage death is mediated in part by the host cysteine protease caspase-1. |
Q50107502 | Salmonella pathogenicity island-2 and anticancer activity in mice |
Q34288964 | Salmonella pathogenicity islands encoding type III secretion systems |
Q35128691 | Salmonella typhimurium disseminates within its host by manipulating the motility of infected cells |
Q50116741 | Salmonella typhimurium induces apoptosis in human monocyte-derived macrophages |
Q50076195 | Salmonella typhimurium infection triggers dendritic cells and macrophages to adopt distinct migration patterns in vivo |
Q34469853 | Salmonella typhimurium outer membrane remodeling: role in resistance to host innate immunity |
Q36399044 | Salmonella typhimurium persists within macrophages in the mesenteric lymph nodes of chronically infected Nramp1+/+ mice and can be reactivated by IFNgamma neutralization |
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Q50078109 | Sensing by bacterial regulatory systems in host and non-host environments |
Q37392883 | Silica-antibiotic hybrid nanoparticles for targeting intracellular pathogens |
Q33876723 | Single-cell techniques using chromosomally tagged fluorescent bacteria to study Listeria monocytogenes infection processes |
Q36305784 | Slc11a1 limits intracellular growth of Salmonella enterica sv. Typhimurium by promoting macrophage immune effector functions and impairing bacterial iron acquisition. |
Q42799804 | Solitary intestinal lymphoid tissue provides a productive port of entry for Salmonella enterica serovar Typhimurium. |
Q37863249 | Spread of Salmonella enterica in the body during systemic infection: unravelling host and pathogen determinants |
Q39410321 | Studies on the effect of an Enterococcus faecium probiotic on T cell populations in peripheral blood and intestinal epithelium and on the susceptibility to Salmonella during a challenge infection with Salmonella Typhimurium in piglets |
Q40406172 | Survival of Salmonella enterica serovar Typhimurium within late endosomal-lysosomal compartments of B lymphocytes is associated with the inability to use the vacuolar alternative major histocompatibility complex class I antigen-processing pathway. |
Q35913406 | Systemic CD8 T-cell memory response to a Salmonella pathogenicity island 2 effector is restricted to Salmonella enterica encountered in the gastrointestinal mucosa |
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Q33295285 | Systemic translocation of Salmonella enterica serovar Dublin in cattle occurs predominantly via efferent lymphatics in a cell-free niche and requires type III secretion system 1 (T3SS-1) but not T3SS-2 |
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Q60960298 | The Prenatal Microbiome: A New Player for Human Health |
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