review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Daniel Yero | Q41047777 |
Isidre Gibert | Q41809594 | ||
Yamilé Lopez | Q55838391 | ||
P2093 | author name string | Juan M Pinos-Rodríguez | |
P2860 | cites work | Drosophila as a model host for Pseudomonas aeruginosa infection | Q24548933 |
Host-pathogen interactions made transparent with the zebrafish model | Q24604664 | ||
Immunostimulatory properties of the emerging pathogen Stenotrophomonas maltophilia | Q24672751 | ||
Recombinant bactericidal/permeability-increasing protein rBPI21 protects against pneumococcal disease | Q24678809 | ||
Measuring the lung function in the mouse: the challenge of size | Q24794879 | ||
Tuberculous granuloma formation is enhanced by a mycobacterium virulence determinant | Q24804152 | ||
Fit for consumption: zebrafish as a model for tuberculosis | Q26827390 | ||
Animal models for Francisella tularensis and Burkholderia species: scientific and regulatory gaps toward approval of antibiotics under the FDA Animal Rule | Q26859041 | ||
Stenotrophomonas maltophilia: an emerging global opportunistic pathogen | Q26995336 | ||
Development and validation of an automated high-throughput system for zebrafish in vivo screenings | Q27303272 | ||
Phosphorylation of the conserved transcription factor ATF-7 by PMK-1 p38 MAPK regulates innate immunity in Caenorhabditis elegans | Q27347875 | ||
Drosophila melanogaster as an animal model for the study of Pseudomonas aeruginosa biofilm infections in vivo | Q27348828 | ||
Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice | Q28255797 | ||
Low-dose aerosol infection model for testing drugs for efficacy against Mycobacterium tuberculosis | Q28379615 | ||
Murine model of pulmonary anthrax: kinetics of dissemination, histopathology, and mouse strain susceptibility | Q28383436 | ||
Culturable gut microbiota diversity in zebrafish | Q28468545 | ||
A mouse model of Streptococcus pneumoniae meningitis mimicking several features of human disease | Q43695063 | ||
Immune response in the skin of zebrafish, Danio rerio (Hamilton), against Staphylococcus chromogenes | Q43700849 | ||
Improved outcome of chronic Pseudomonas aeruginosa lung infection is associated with induction of a Th1-dominated cytokine response | Q43904318 | ||
Murine models of chronic Pseudomonas aeruginosa lung infection | Q44080662 | ||
Zebrafish (Danio rerio) as a screen for attenuation of Lancefield group C streptococci and a model for streptococcal pathogenesis | Q44094653 | ||
Neutrophil-induced lung protection and injury are dependent on the amount of Pseudomonas aeruginosa administered via airways in guinea pigs | Q44182484 | ||
Elastase activity in bronchoalveolar lavage fluid from oxygen-exposed, Pseudomonas-infected baboons | Q44231010 | ||
Changes in Caenorhabditis elegans life span and selective innate immune genes during Staphylococcus aureus infection | Q44401326 | ||
A mouse model for slowly progressive primary tuberculosis | Q44444232 | ||
Zebrafish-Mycobacterium marinum model for mycobacterial pathogenesis | Q44547546 | ||
Chronic Pseudomonas aeruginosa lung infection is more severe in Th2 responding BALB/c mice compared to Th1 responding C3H/HeN mice | Q44596439 | ||
Adult zebrafish model for pneumococcal pathogenesis | Q44636801 | ||
Mercaptoethylguanidine inhibits the inflammatory response in a murine model of chronic infection with Pseudomonas aeruginosa. | Q44857585 | ||
G551D CF mice display an abnormal host response and have impaired clearance of Pseudomonas lung disease | Q45145698 | ||
Immunological responses and protective immunity against tuberculosis conferred by vaccination of Balb/C mice with the attenuated Mycobacterium tuberculosis (phoP) SO2 strain. | Q46296027 | ||
Identification of host and pathogen factors involved in virulence using Caenorhabditis elegans | Q46443175 | ||
Susceptibility to severe Streptococcal sepsis: use of a large set of isogenic mouse lines to study genetic and environmental factors. | Q46673887 | ||
Streptococcus pneumoniae: proteomics of surface proteins for vaccine development | Q46885129 | ||
Immune response to postprimary tuberculosis in mice: Mycobacterium tuberculosis and Miycobacterium bovis bacille Calmette-Guérin induce equal protection | Q47223070 | ||
Experimental infection of mice with Staphylococcus aureus: evidence against alpha toxin and the terminal size of the bacterial population as determinants of lethality | Q47399095 | ||
Caenorhabditis elegans as a host model for community-associated methicillin-resistant Staphylococcus aureus | Q47760683 | ||
Fish-kill method questioned | Q47907190 | ||
Airway epithelial cell-pathogen interactions | Q47917528 | ||
Stenotrophomonas maltophilia strains from cystic fibrosis patients: genomic variability and molecular characterization of some virulence determinants | Q48062294 | ||
The role of flagellin versus motility in acute lung disease caused by Pseudomonas aeruginosa | Q48078797 | ||
A novel vertebrate model of Staphylococcus aureus infection reveals phagocyte-dependent resistance of zebrafish to non-host specialized pathogens. | Q51950759 | ||
Inducible Antibacterial Defence System in Drosophila | Q52478682 | ||
Burkholderia pseudomallei kills the nematode Caenorhabditis elegans using an endotoxin-mediated paralysis. | Q52543308 | ||
The development of the three Rs concept. | Q53643618 | ||
Long-lived C. elegans daf-2 mutants are resistant to bacterial pathogens. | Q53926483 | ||
Pneumococcal vaccines: an update on current strategies. | Q35776558 | ||
Ultra-low dose of Mycobacterium tuberculosis aerosol creates partial infection in mice | Q35785254 | ||
New models for the study of Mycobacterium-host interactions | Q35832065 | ||
A star with stripes: zebrafish as an infection model | Q35894129 | ||
Alternatives to the use of mammals for pain research | Q35920863 | ||
Widespread bronchogenic dissemination makes DBA/2 mice more susceptible than C57BL/6 mice to experimental aerosol infection with Mycobacterium tuberculosis | Q36044574 | ||
Pathogenicity of staphylococci: with special reference to the persitence of infection in mice | Q36051602 | ||
Current progress in tuberculosis vaccine development | Q36065379 | ||
Genomic copy number and expression variation within the C57BL/6J inbred mouse strain | Q36259308 | ||
Murine models of susceptibility to tuberculosis | Q36366387 | ||
Mouse models for the genetic study of tuberculosis susceptibility | Q36371782 | ||
Dormancy phenotype displayed by extracellular Mycobacterium tuberculosis within artificial granulomas in mice | Q36402431 | ||
A correlative analysis of epidemiologic and molecular characteristics of methicillin-resistant Staphylococcus aureus clones from diverse geographic locations with virulence measured by a Caenorhabditis elegans host model | Q36533368 | ||
The insect Galleria mellonella as a powerful infection model to investigate bacterial pathogenesis | Q36594846 | ||
Einstein Contained Aerosol Pulmonizer (ECAP): Improved Biosafety for Multi-Drug Resistant (MDR) and Extensively Drug Resistant (XDR) Mycobacterium tuberculosis Aerosol Infection Studies | Q36602068 | ||
Identification of innate immunity genes and pathways using a comparative genomics approach | Q36657572 | ||
Pathology of postprimary tuberculosis in humans and mice: contradiction of long-held beliefs | Q36763370 | ||
Pseudomonas aeruginosa biofilm formation in the cystic fibrosis airway | Q36889877 | ||
Pulmonary bacterial pathogens in cystic fibrosis patients and antibiotic therapy: a tool for the health workers | Q36980425 | ||
Interactions with microbial pathogens | Q37020414 | ||
Modeling inflammation in the zebrafish: how a fish can help us understand lung disease | Q37030673 | ||
Animal models of human pneumonia | Q37046353 | ||
Evolution of Pseudomonas aeruginosa type III secretion in cystic fibrosis: a paradigm of chronic infection | Q37067270 | ||
Comparative pathogenesis of Mycobacterium marinum and Mycobacterium tuberculosis | Q37094011 | ||
Depletion of phagocytes in the reticuloendothelial system causes increased inflammation and mortality in rabbits with Pseudomonas aeruginosa pneumonia | Q37100530 | ||
An evolutionarily conserved program of B-cell development and activation in zebrafish | Q37113110 | ||
Pseudomonas aeruginosa infection of zebrafish involves both host and pathogen determinants | Q37145061 | ||
Burkholderia pseudomallei suppresses Caenorhabditis elegans immunity by specific degradation of a GATA transcription factor | Q37173143 | ||
Role of cilia, mucus, and airway surface liquid in mucociliary dysfunction: lessons from mouse models | Q37179488 | ||
Pseudomonas aeruginosa killing of Caenorhabditis elegans used to identify P. aeruginosa virulence factors | Q37185887 | ||
What animal models teach humans about tuberculosis | Q37192066 | ||
Pseudomonas aeruginosa as a model microorganism for investigation of chemotactic behaviors in ecosystem. | Q37240227 | ||
Man and mouse TB: contradictions and solutions. | Q37250553 | ||
Animal models of ventilator-associated pneumonia | Q37360866 | ||
Susceptibility of Pseudomonas aeruginosa Biofilm to Alpha-Helical Peptides: D-enantiomer of LL-37 | Q35091629 | ||
Animal models of human respiratory syncytial virus disease | Q35159747 | ||
Experimental models of pulmonary infection | Q35169692 | ||
Adequate Th2-type response associates with restricted bacterial growth in latent mycobacterial infection of zebrafish | Q35195622 | ||
Bacterial superantigens | Q35203877 | ||
Mycobacterium marinum infection of adult zebrafish causes caseating granulomatous tuberculosis and is moderated by adaptive immunity | Q35217489 | ||
Interaction of pneumolysin-sufficient and -deficient isogenic variants of Streptococcus pneumoniae with human respiratory mucosa. | Q35383517 | ||
Endobronchial inflammation following Pseudomonas aeruginosa infection in resistant and susceptible strains of mice | Q35408151 | ||
Role of tumor necrosis factor alpha in innate resistance to mouse pulmonary infection with Pseudomonas aeruginosa | Q35433928 | ||
Short-course chemotherapy with TMC207 and rifapentine in a murine model of latent tuberculosis infection | Q35527885 | ||
The innate immune response to pneumococcal lung infection: the untold story. | Q35702813 | ||
Calcium signalling during cell interactions with bacterial pathogens | Q35749180 | ||
The Drosophila melanogaster host model | Q35773518 | ||
Murine model to study the invasion and survival of Mycobacterium tuberculosis in the central nervous system | Q28487245 | ||
Genome-wide identification of Pseudomonas aeruginosa virulence-related genes using a Caenorhabditis elegans infection model | Q28493168 | ||
Killing of Caenorhabditis elegans by Pseudomonas aeruginosa used to model mammalian bacterial pathogenesis | Q28776658 | ||
The host defense of Drosophila melanogaster | Q29617555 | ||
A conserved p38 MAP kinase pathway in Caenorhabditis elegans innate immunity | Q29617874 | ||
Use of animals in experimental research: an ethical dilemma? | Q30343672 | ||
From in vitro to in vivo Models of Bacterial Biofilm-Related Infections. | Q30424697 | ||
The worm has turned--microbial virulence modeled in Caenorhabditis elegans | Q30436071 | ||
Virulence of Staphylococcus aureus small colony variants in the Caenorhabditis elegans infection model | Q30439292 | ||
Staphylococcal biofilm exopolysaccharide protects against Caenorhabditis elegans immune defenses | Q30445078 | ||
The German Mouse Clinic: a platform for systemic phenotype analysis of mouse models. | Q30484053 | ||
Pseudomonas aeruginosa Type III secretion system interacts with phagocytes to modulate systemic infection of zebrafish embryos | Q30496444 | ||
The role of the granuloma in expansion and dissemination of early tuberculous infection | Q30502401 | ||
Evaluation of the pathogenesis and treatment of Mycobacterium marinum infection in zebrafish. | Q30571358 | ||
Intranasal application of S. epidermidis prevents colonization by methicillin-resistant Staphylococcus aureus in mice | Q31037497 | ||
Staphylococcus aureus virulence factors identified by using a high-throughput Caenorhabditis elegans-killing model | Q31142975 | ||
Immunization of mice with a Mycobacterium tuberculosis genomic expression library results in lower bacterial load in lungs after challenge with BCG. | Q33241558 | ||
Imaging macrophage chemotaxis in vivo: studies of microtubule function in zebrafish wound inflammation | Q33242045 | ||
Infection in a dish: high-throughput analyses of bacterial pathogenesis | Q33267048 | ||
A potential new pathway for Staphylococcus aureus dissemination: the silent survival of S. aureus phagocytosed by human monocyte-derived macrophages | Q33313866 | ||
Inactivation of the hmgA gene of Pseudomonas aeruginosa leads to pyomelanin hyperproduction, stress resistance and increased persistence in chronic lung infection | Q33424268 | ||
The origins and early days of the Three Rs concept | Q33493166 | ||
Impact of cigarette smoke exposure on innate immunity: a Caenorhabditis elegans model | Q33498516 | ||
A nasal epithelial receptor for Staphylococcus aureus WTA governs adhesion to epithelial cells and modulates nasal colonization | Q33553796 | ||
The Caenorhabditis elegans germ line regulates distinct signaling pathways to control lifespan and innate immunity | Q33581925 | ||
Two novel point mutations in clinical Staphylococcus aureus reduce linezolid susceptibility and switch on the stringent response to promote persistent infection | Q33604815 | ||
Drosophila melanogaster as a model host for the Burkholderia cepacia complex | Q33634104 | ||
Exploring zebrafish genomic, functional and phenotypic data using ZFIN | Q33690705 | ||
Mice fed lipid-encapsulated Mycobacterium bovis BCG are protected against aerosol challenge with Mycobacterium tuberculosis | Q33716157 | ||
Two different rpf clusters distributed among a population of Stenotrophomonas maltophilia clinical strains display differential diffusible signal factor production and virulence regulation | Q33743215 | ||
A chimeric influenza virus expressing an epitope of outer membrane protein F of Pseudomonas aeruginosa affords protection against challenge with P. aeruginosa in a murine model of chronic pulmonary infection | Q33760042 | ||
Macrophage and Galleria mellonella infection models reflect the virulence of naturally occurring isolates of B. pseudomallei, B. thailandensis and B. oklahomensis | Q33795181 | ||
Caenorhabditis elegans: a model genetic host to study Pseudomonas aeruginosa pathogenesis | Q33840568 | ||
Caenorhabditis elegans for the study of host-pathogen interactions | Q33856641 | ||
Role of excessive inflammatory response to Stenotrophomonas maltophilia lung infection in DBA/2 mice and implications for cystic fibrosis | Q33877139 | ||
Ca2+ signaling in airway epithelial cells facilitates leukocyte recruitment and transepithelial migration | Q37552431 | ||
Using in vivo zebrafish models to understand the biochemical basis of neutrophilic respiratory disease. | Q37554616 | ||
Mycobacterium marinum strains can be divided into two distinct types based on genetic diversity and virulence | Q37582846 | ||
The pathogenesis of acute pulmonary viral and bacterial infections: investigations in animal models | Q37613698 | ||
Preclinical models for pulmonary drug delivery | Q37620365 | ||
Anatomy, pathology, and physiology of the tracheobronchial tree: emphasis on the distal airways | Q37644683 | ||
The non-human primate model of tuberculosis | Q37652734 | ||
Mycobacteria manipulate macrophage recruitment through coordinated use of membrane lipids | Q37653944 | ||
Host-microbe interactions in the developing zebrafish | Q37691890 | ||
Microbial etiologies of hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia | Q37769547 | ||
Virulence on the fly: Drosophila melanogaster as a model genetic organism to decipher host-pathogen interactions | Q37848849 | ||
Chemokines in teleost fish species | Q37854137 | ||
Chemistry and the worm: Caenorhabditis elegans as a platform for integrating chemical and biological research | Q37866234 | ||
Zebrafish embryos and larvae: a new generation of disease models and drug screens. | Q37889217 | ||
Zebrafish embryos as an alternative to animal experiments--a commentary on the definition of the onset of protected life stages in animal welfare regulations | Q37897336 | ||
A review of murine models of latent tuberculosis infection | Q37926592 | ||
Infectious disease modeling and innate immune function in zebrafish embryos. | Q37939407 | ||
Of model hosts and man: using Caenorhabditis elegans, Drosophila melanogaster and Galleria mellonella as model hosts for infectious disease research | Q37962853 | ||
Immune system and immune responses in fish and their role in comparative immunity study: a model for higher organisms. | Q38035648 | ||
Myelopoiesis during zebrafish early development. | Q38047521 | ||
Hospital-acquired pneumonia and ventilator-associated pneumonia: recent advances in epidemiology and management | Q38092573 | ||
Infectious diseases in humanized mice | Q38126447 | ||
Enterococcus infection biology: lessons from invertebrate host models | Q38192499 | ||
The lack of a big picture in tuberculosis: the clinical point of view, the problems of experimental modeling and immunomodulation. The factors we should consider when designing novel treatment strategies | Q38193087 | ||
Mycobacterium marinum infection in Drosophila melanogaster for antimycobacterial activity assessment | Q38456839 | ||
No induction of antimicrobial resistance in Staphylococcus aureus and Listeria monocytogenes during continuous exposure to eugenol and citral. | Q38877750 | ||
Surveillance, control and management of infections in intensive care units in Southern Europe, Turkey and Iran--a prospective multicenter point prevalence study. | Q38994488 | ||
A novel zebrafish embryo xenotransplantation model to study primary human fibroblast motility in health and disease. | Q39392198 | ||
The virulence of Staphylococcus aureus correlates with strain genotype in a chicken embryo model but not a nematode model. | Q39541034 | ||
Establishment of multi-site infection model in zebrafish larvae for studying Staphylococcus aureus infectious disease | Q39545196 | ||
Diverse bacteria are pathogens of Caenorhabditis elegans | Q39655700 | ||
Drosophila melanogaster is a genetically tractable model host for Mycobacterium marinum | Q39755163 | ||
Role of phosphoglucomutase of Stenotrophomonas maltophilia in lipopolysaccharide biosynthesis, virulence, and antibiotic resistance | Q39755193 | ||
Role of coagulase in a murine model of hematogenous pulmonary infection induced by intravenous injection of Staphylococcus aureus enmeshed in agar beads | Q39827332 | ||
Increased susceptibility of RAG-2 SCID mice to dissemination of endodontic infections. | Q39830945 | ||
Identification and characterization of the transcription factors involved in T-cell development, t-bet, stat6 and foxp3, within the zebrafish, Danio rerio | Q39922677 | ||
Central roles for IL-2 and MCP-1 following intranasal exposure to SEB: a new mouse model | Q40046895 | ||
Morphological and immunohistochemical studies of the lungs and bronchus-associated lymphoid tissue in a rat model of chronic pulmonary infection with Pseudomonas aeruginosa | Q40150323 | ||
Experimental severe Pseudomonas aeruginosa pneumonia and antibiotic therapy in piglets receiving mechanical ventilation | Q40441932 | ||
Hydrogen peroxide-mediated killing of Caenorhabditis elegans: a common feature of different streptococcal species. | Q40470026 | ||
Cystic fibrosis pathogens activate Ca2+-dependent mitogen-activated protein kinase signaling pathways in airway epithelial cells | Q40817343 | ||
Insights into tuberculosis from the zebrafish model | Q41407201 | ||
A liquid-based method for the assessment of bacterial pathogenicity using the nematode Caenorhabditis elegans | Q41471775 | ||
Pathogenesis and host defense in pulmonary infections. | Q41637995 | ||
Distribution, clearance, and mortality of environmental pseudomonads in mice upon intranasal exposure | Q41880138 | ||
Galleria mellonella as an infection model for select agents | Q42001909 | ||
Synthetic epidermicin NI01 can protect Galleria mellonella larvae from infection with Staphylococcus aureus | Q42008325 | ||
A Streptococcus pneumoniae infection model in larvae of the wax moth Galleria mellonella | Q42013699 | ||
Wax moth larva (Galleria mellonella): an in vivo model for assessing the efficacy of antistaphylococcal agents. | Q42017051 | ||
Comparison of the regulation, metabolic functions, and roles in virulence of the glyceraldehyde-3-phosphate dehydrogenase homologues gapA and gapB in Staphylococcus aureus | Q42019553 | ||
Specific resistance to Pseudomonas aeruginosa infection in zebrafish is mediated by the cystic fibrosis transmembrane conductance regulator. | Q42043703 | ||
C. elegans detects pathogen-induced translational inhibition to activate immune signaling | Q42132857 | ||
Targeting and stimulation of the zebrafish (Danio rerio) innate immune system with LPS/dsRNA-loaded nanoliposomes. | Q42218098 | ||
Microbial aetiology of healthcare associated pneumonia in Spain: a prospective, multicentre, case-control study | Q42244046 | ||
Mice deficient in ficolin, a lectin complement pathway recognition molecule, are susceptible to Streptococcus pneumoniae infection | Q42286620 | ||
Mycobacterium marinum Erp is a virulence determinant required for cell wall integrity and intracellular survival | Q42408574 | ||
Models to study ancient host-pathogen interactions: lessons from Crete | Q42576216 | ||
Acute phase response in zebrafish upon Aeromonas salmonicida and Staphylococcus aureus infection: striking similarities and obvious differences with mammals | Q42683752 | ||
A lung segmental model of chronic Pseudomonas infection in sheep | Q43099699 | ||
Stenotrophomonas maltophilia: pathogenesis model using Caenorhabditis elegans | Q43457469 | ||
Pneumonia classification and healthcare-associated pneumonia: a new avenue or just a cul-de-sac? | Q43460571 | ||
Real-time visualization of mycobacterium-macrophage interactions leading to initiation of granuloma formation in zebrafish embryos | Q43464391 | ||
Defense of zebrafish embryos against Streptococcus pneumoniae infection is dependent on the phagocytic activity of leukocytes | Q43526326 | ||
Emergent immunoregulatory properties of combined glucocorticoid and anti-glucocorticoid steroids in a model of tuberculosis. | Q43589541 | ||
A simple model host for identifying Gram-positive virulence factors | Q33943933 | ||
Phenotypic and genotypic characterization of Stenotrophomonas maltophilia isolates from patients with cystic fibrosis: genome diversity, biofilm formation, and virulence. | Q33950924 | ||
Positive correlation between virulence of Pseudomonas aeruginosa mutants in mice and insects | Q33994325 | ||
Identification and characterization of a novel family of pneumococcal proteins that are protective against sepsis | Q34005995 | ||
Inhibition of cell surface export of group A streptococcal anchorless surface dehydrogenase affects bacterial adherence and antiphagocytic properties. | Q34033483 | ||
Host lung gene expression patterns predict infectious etiology in a mouse model of pneumonia | Q34036394 | ||
Ciprofloxacin in polyethylene glycol-coated liposomes: efficacy in rat models of acute or chronic Pseudomonas aeruginosa infection | Q34110906 | ||
Identification of dendritic antigen-presenting cells in the zebrafish. | Q34115751 | ||
Hydrogen peroxide-mediated killing of Caenorhabditis elegans by Streptococcus pyogenes | Q34130741 | ||
The potential for using protein vaccines to protect against otitis media caused by Streptococcus pneumoniae | Q34133049 | ||
Looking within the zebrafish to understand the tuberculous granuloma | Q34331528 | ||
Factors influencing the immune enhancement of intrapulmonary bactericidal mechanisms | Q34401592 | ||
Lung Bacterial Clearance in Murine Pneumococcal Pneumonia | Q34412153 | ||
Animal infection models and ethics -- the perfect infection model. | Q34413152 | ||
Mycobacterium marinum causes a latent infection that can be reactivated by gamma irradiation in adult zebrafish | Q34426515 | ||
Evolution of anaphylatoxins, their diversity and novel roles in innate immunity: insights from the study of fish complement | Q34444480 | ||
The ability of virulence factor expression by Pseudomonas aeruginosa to predict clinical disease in hospitalized patients | Q34478058 | ||
Assessment of virulence diversity of methicillin-resistant Staphylococcus aureus strains with a Drosophila melanogaster infection model | Q34486698 | ||
Mycobacterium bovis BCG substrains confer different levels of protection against Mycobacterium tuberculosis infection in a BALB/c model of progressive pulmonary tuberculosis. | Q34491796 | ||
Burkholderia thailandensis is virulent in Drosophila melanogaster | Q34499733 | ||
Identification of Pseudomonas aeruginosa phenazines that kill Caenorhabditis elegans | Q34539806 | ||
Passive administration of purified secretory IgA from human colostrum induces protection against Mycobacterium tuberculosis in a murine model of progressive pulmonary infection. | Q34607559 | ||
The functional ontogeny of the teleost gill: which comes first, gas or ion exchange? | Q34621709 | ||
The genetics of pathogen avoidance in Caenorhabditis elegans | Q34689601 | ||
Caenorhabditis elegans senses bacterial autoinducers | Q34718733 | ||
Immunology and zebrafish: spawning new models of human disease | Q34742171 | ||
Abundance of the Quorum-Sensing Factor Ax21 in Four Strains of Stenotrophomonas maltophilia Correlates with Mortality Rate in a New Zebrafish Model of Infection | Q34806726 | ||
Caenorhabditis elegans as a model host for Staphylococcus aureus pathogenesis | Q34855656 | ||
Refinement, reduction, and replacement of animal use for regulatory testing: current best scientific practices for the evaluation of safety and potency of biologicals | Q34975151 | ||
Evaluation of surrogate animal models of melioidosis | Q35028834 | ||
Mouse model of tuberculosis | Q35045094 | ||
Nasal immunity to staphylococcal toxic shock is controlled by the nasopharynx-associated lymphoid tissue | Q35066281 | ||
Tuberculous granuloma induction via interaction of a bacterial secreted protein with host epithelium | Q35076136 | ||
Quantitative and qualitative differences in bronchoalveolar inflammatory cells in Pseudomonas aeruginosa-resistant and -susceptible mice. | Q54106144 | ||
In vitro and in vivo T cell responses in mice during bronchopulmonary infection with mucoid Pseudomonas aeruginosa. | Q54185707 | ||
Mycobacterium tuberculosis strains with the Beijing genotype demonstrate variability in virulence associated with transmission. | Q54411828 | ||
Community-Acquired Pneumonia | Q56031753 | ||
An adult zebrafish model for preclinical tuberculosis vaccine development | Q60588213 | ||
Editorial | Q60787758 | ||
The natural history of Caenorhabditis elegans research | Q61950353 | ||
Induction of a protective response with an IgA monoclonal antibody against Mycobacterium tuberculosis 16kDa protein in a model of progressive pulmonary infection | Q63253484 | ||
Impaired ability of Cftr knockout mice to control lung infection with Pseudomonas aeruginosa. | Q64935300 | ||
Protection against mucoid Pseudomonas aeruginosa in rodent models of endobronchial infections | Q68347812 | ||
A mouse model of chronic pulmonary infection with Pseudomonas aeruginosa and Pseudomonas cepacia | Q68544977 | ||
Bacterial infection and acute lung injury in hamsters | Q69562867 | ||
Comparative characteristics of some experimental models of staphylococcus infection | Q70584456 | ||
Correlation between the kinetics of Th1, Th2 cells and pathology in a murine model of experimental pulmonary tuberculosis | Q71764410 | ||
Late results of long-term, intermittent chemotherapy of advanced, murine tuberculosis: Limits of the murine model | Q72242855 | ||
Exogenous rh-urokinase modifies inflammation and Pseudomonas aeruginosa infection in a rat chronic pulmonary infection model | Q72299727 | ||
Increased expression of Fas ligand on Mycobacterium tuberculosis infected macrophages: a potential novel mechanism of immune evasion by Mycobacterium tuberculosis? | Q73191991 | ||
Progress in applying the three Rs of Russell & Burch to the testing of biological products | Q73221489 | ||
IL-10 attenuates excessive inflammation in chronic Pseudomonas infection in mice | Q73251130 | ||
In situ expression of cytokines and cellular phenotypes in the lungs of mice with slowly progressive primary tuberculosis | Q73884399 | ||
Characterization of Burkholderia pseudomallei infection and identification of novel virulence factors using a Caenorhabditis elegans host system | Q74311679 | ||
Characterization of chronic bronchopulmonary Pseudomonas aeruginosa infection in resistant and susceptible inbred mouse strains | Q74665342 | ||
A mouse model for latent tuberculosis | Q74790339 | ||
A functional C5a anaphylatoxin receptor in a teleost species | Q75197429 | ||
Intranasal vaccination with a double mutant of staphylococcal enterotoxin C provides protection against Staphylococcus aureus infection | Q79336859 | ||
A panel of monoclonal antibodies recognizing the Staphylococcus epidermidis fibrinogen-binding MSCRAMM SdrG | Q79814485 | ||
[Impact of M. tuberculosis genotype on survival in mice with experimental tuberculosis] | Q80840344 | ||
Role of type 1 T helper cells in the resolution of acute Streptococcus pneumoniae sinusitis: a mouse model | Q81149580 | ||
Mouse and guinea pig models for testing new tuberculosis vaccines | Q81352721 | ||
Zebrafish and frog models of Mycobacterium marinum infection | Q81928376 | ||
Colonization and transmission of meticillin-susceptible and meticillin-resistant Staphylococcus aureus in a murine nasal colonization model | Q83402564 | ||
Intranasal exposure to staphylococcal enterotoxin B elicits an acute systemic inflammatory response | Q83834125 | ||
[Fundamental aspects on animal research as applied to experimental surgery] | Q83912028 | ||
Animal models of tuberculosis | Q84390170 | ||
Immunological parameters to define infection progression and therapy response in a well-defined tuberculosis model in mice | Q84703545 | ||
Are mouse models of human mycobacterial diseases relevant? Genetics says: 'yes!' | Q84899447 | ||
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 38 | |
P577 | publication date | 2015-02-04 | |
P1433 | published in | Frontiers in Microbiology | Q27723481 |
P1476 | title | Animals devoid of pulmonary system as infection models in the study of lung bacterial pathogens | |
P478 | volume | 6 |
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