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The infection generates economic losses in infected flocks (decrease in fertility, ban on trade).
As shown by previously published studies, LN activation during viral infection generates an [18F]-FDG signal that can be easily discerned from background activity [7, 18].
Summarizing recent data on the rate at which the treatment of influenza infection generates resistance de novo and on the transmission fitness of resistant virus, we discuss possible implications for the epidemiological spread of drug resistance in the context of an established population dynamic model.
Plasmodium falciparum infection generates pleiomorphic clinical outcomes, from asymptomatic to severe syndromes depending on transmission intensity, age of the individuals and on the immunity and the genetic background of the populations [2], [3], [4].
The co-infection of leprosy with tuberculosis is often the cause of death as M. leprae infection generates a compromised immune system, vulnerable to a subsequent M. tuberculosis infection that is still fatal in some parts of the world today.
They first increase because more infection generates a higher number of these cells.
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Although several reports have been published with these approaches, a high variability in parasite strains, host cells, mammal species, and times of infection generate a complex picture and few general conclusions.
C. burnetii infection generated more transcriptional changes in males than in females.
We observed significant amount of co localization of the WT viable Salmonella (green) and mCAT1 protein (red) after 4 h (Fig. 7C) and 12 h (Fig. 8C) of infection generating yellow colour.
Studies considered to report predominantly nonserious infection generated an RR of 1.05 (0.89, 1.24).
The model constructed to investigate the effect of the observed parameter values on the age of infection generated Fig. 5.
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