scholarly article | Q13442814 |
P50 | author | Arturo Casadevall | Q20807130 |
Liise-anne Pirofski | Q87765721 | ||
P2860 | cites work | Q and A: What is a pathogen? A question that begs the point | Q21245378 |
Potential Impact of Sexual Transmission on Ebola Virus Epidemiology: Sierra Leone as a Case Study | Q24288740 | ||
Antibiotics in early life alter the murine colonic microbiome and adiposity | Q24630877 | ||
Inherited resistance to HIV-1 conferred by an inactivating mutation in CC chemokine receptor 5: studies in populations with contrasting clinical phenotypes, defined racial background, and quantified risk | Q24654734 | ||
Midgut bacteria required for Bacillus thuringiensis insecticidal activity | Q24679507 | ||
Yersinia enterocolitica: the charisma continues | Q24683715 | ||
Dengue virus sero-cross-reactivity drives antibody-dependent enhancement of infection with zika virus | Q24737245 | ||
Human genetic basis of interindividual variability in the course of infection | Q26775894 | ||
Impact of climate change on human infectious diseases: Empirical evidence and human adaptation | Q26781889 | ||
The rise and fall of infectious disease in a warmer world | Q26970808 | ||
Prolonged shedding of Chikungunya virus in semen and urine: A new perspective for diagnosis and implications for transmission | Q27926247 | ||
How Relevant Is Sexual Transmission of Zika Virus? | Q27928047 | ||
Bat white-nose syndrome: an emerging fungal pathogen? | Q28299311 | ||
Susceptibility to Campylobacter infection is associated with the species composition of the human fecal microbiota | Q28394710 | ||
Recurrent Potent Human Neutralizing Antibodies to Zika Virus in Brazil and Mexico | Q30145646 | ||
Association between enteropathogens and malnutrition in children aged 6-23 mo in Bangladesh: a case-control study | Q30252712 | ||
Host-pathogen interactions: redefining the basic concepts of virulence and pathogenicity | Q33693878 | ||
MHC Ib molecule Qa-1 presents Mycobacterium tuberculosis peptide antigens to CD8+ T cells and contributes to protection against infection. | Q33699588 | ||
Susceptibility to Cryptococcal Meningoencephalitis Associated With Idiopathic CD4+ Lymphopenia and Secondary Germline or Acquired Defects | Q33772403 | ||
Host-pathogen interactions: basic concepts of microbial commensalism, colonization, infection, and disease | Q33925636 | ||
Genetic characterization of pathogenic Saccharomyces cerevisiae isolates. | Q33962722 | ||
Heterologous immunity between viruses | Q34051846 | ||
Defence responses of Arabidopsis thaliana to infection by Pseudomonas syringae are regulated by the circadian clock | Q34069647 | ||
Host-pathogen interactions: the attributes of virulence | Q34083331 | ||
Natural microbe-mediated refractoriness to Plasmodium infection in Anopheles gambiae | Q34133471 | ||
Microbiology: Ditch the term pathogen | Q34453606 | ||
The emerging world of the fungal microbiome | Q34727901 | ||
Vertebrate endothermy restricts most fungi as potential pathogens | Q35007892 | ||
Precision microbiome reconstitution restores bile acid mediated resistance to Clostridium difficile. | Q35163017 | ||
Viruses and the Microbiota | Q35216531 | ||
What is a host? Incorporating the microbiota into the damage-response framework | Q35409027 | ||
What is infectiveness and how is it involved in infection and immunity? | Q35607564 | ||
The damage-response framework of microbial pathogenesis | Q35709086 | ||
Differential interaction of dendritic cells with Rickettsia conorii: impact on host susceptibility to murine spotted fever rickettsiosis | Q35913371 | ||
SeXX Matters in Infectious Disease Pathogenesis | Q35927430 | ||
Thermal Restriction as an Antimicrobial Function of Fever | Q36009791 | ||
Candida albicans Pathogenesis: Fitting within the Host-Microbe Damage Response Framework | Q36080619 | ||
History and update on host defense against vaginal candidiasis | Q36677660 | ||
Major histocompatibility complex-conferred resistance to Theiler's virus-induced demyelinating disease is inherited as a dominant trait in B10 congenic mice | Q36793449 | ||
HIV, age, and the severity of hepatitis C virus-related liver disease: a cohort study | Q37003644 | ||
Saccharomyces cerevisiae pneumonia in a patient with acquired immune deficiency syndrome. | Q37177595 | ||
Serum metabolomics analysis of patients with chikungunya and dengue mono/co-infections reveals distinct metabolite signatures in the three disease conditions. | Q37414121 | ||
Diagnosis and classification of reactive arthritis | Q38177960 | ||
Defensive symbioses of animals with prokaryotic and eukaryotic microorganisms. | Q38428532 | ||
Saccharomyces cerevisiae vaginitis: transmission from yeast used in baking | Q38574088 | ||
Progression of hepatitis C in the haemophiliac population in Ireland, after 30 years of infection in the pre-DAA treatment era. | Q38655913 | ||
Obesity and infection: reciprocal causality | Q38672848 | ||
Sex differences in immune responses | Q38933353 | ||
Role of fever in disease | Q39226031 | ||
Histoplasmosis outbreak associated with the renovation of an old house - Quebec, Canada, 2013. | Q39281781 | ||
Intestinal microbiota promote enteric virus replication and systemic pathogenesis | Q39306213 | ||
Comorbidities and mortality among children hospitalized with diarrheal disease in an area of high prevalence of human immunodeficiency virus infection | Q39749819 | ||
From Original Antigenic Sin to the Universal Influenza Virus Vaccine | Q40059787 | ||
The circadian clock in immune cells controls the magnitude of Leishmania parasite infection. | Q40061584 | ||
The Pathogenic Potential of a Microbe | Q40311700 | ||
Histoplasmosis associated with exploring a bat-inhabited cave in Costa Rica, 1998-1999. | Q40535520 | ||
Perspective: hypothesis: serum IgG antibody is sufficient to confer protection against infectious diseases by inactivating the inoculum | Q40538332 | ||
Systemic inflammation and liver damage in HIV/hepatitis C virus coinfection. | Q40671632 | ||
Use of paraffin-embedded tissue for identification of Saccharomyces cerevisiae in a baker's lung nodule by fungal PCR and nucleotide sequencing | Q40938265 | ||
Genetic susceptibility to malaria and other infectious diseases: from the MHC to the whole genome | Q41018500 | ||
History of opportunistic infection in the immunocompromised host | Q41501502 | ||
Microbiota-activated PPAR-γ signaling inhibits dysbiotic Enterobacteriaceae expansion | Q42250704 | ||
Molecular epidemiology of Saccharomyces cerevisiae in an immunocompromised host unit | Q42675558 | ||
The microbiome revolution | Q42936861 | ||
Exposure to sublethal concentration of glyphosate or atrazine-based herbicides alters the phagocytic function and increases the susceptibility of silver catfish fingerlings (Rhamdia quelen) to Aeromonas hydrophila challenge. | Q42946346 | ||
Influence of hepatitis C virus genotypes and HIV infection on histological severity of chronic hepatitis C. The Hepatitis/HIV Spanish Study Group | Q42983830 | ||
Increased long-term mortality after an episode of community-acquired pneumonia--time to move beyond descriptive studies | Q44364579 | ||
Saccharomyces cerevisiae infection in a patient with acquired immunodeficiency syndrome. | Q45883121 | ||
Comparative pathogenesis of clinical and nonclinical isolates of Saccharomyces cerevisiae | Q46130009 | ||
What caused the epidemic of Pneumocystis pneumonia in European premature infants in the mid-20th century? | Q46942562 | ||
Recovery of little brown bats (Myotis lucifugus) from natural infection with Geomyces destructans, white-nose syndrome | Q47251558 | ||
Suppression of infection by famine and its activation by refeeding--a paradox? | Q47843257 | ||
Effect of road deicing salt on the susceptibility of amphibian embryos to infection by water molds | Q50615555 | ||
Collateral damage: rapid exposure-induced evolution of pesticide resistance leads to increased susceptibility to parasites. | Q51587298 | ||
Outbreak of hantavirus infection in the Four Corners region of the United States in the wake of the 1997-1998 El Nino-southern oscillation | Q56777006 | ||
Protein-calorie malnutrition. A host determinant for Pneumocystis carinii infection | Q67295926 | ||
Concurrent human and canine histoplasmosis from cutting decayed wood | Q68864623 | ||
The meaning of microbial exposure, infection, colonisation, and disease in clinical practice | Q78383830 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | immunology | Q101929 |
parasitology | Q180502 | ||
P577 | publication date | 2017-10-30 | |
P1433 | published in | Infection and Immunity | Q6029193 |
P1476 | title | What Is a Host? Attributes of Individual Susceptibility | |
P478 | volume | 86 |
Q89551956 | Antibiotic Delivery Strategies to Treat Skin Infections When Innate Antimicrobial Defense Fails |
Q64993874 | Benefits and Costs of Animal Virulence for Microbes. |
Q58615369 | Characterization of a signaling system in the oral commensal that mediates interspecies communication with the pathogen |
Q64911225 | Selection of Candida albicans trisomy during oropharyngeal infection results in a commensal-like phenotype. |
Q90400815 | Sequelae of Fetal Infection in a Non-human Primate Model of Listeriosis |
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