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Host-pathogen interactions of Actinobacillus pleuropneumoniae with porcine lung and tracheal epithelial cellsLeishmania-induced inactivation of the macrophage transcription factor AP-1 is mediated by the parasite metalloprotease GP63.Impact of Leishmania mexicana infection on dendritic cell signaling and functionsImpact of neutrophil-secreted myeloid related proteins 8 and 14 (MRP 8/14) on leishmaniasis progression.Molecular mechanisms of cognitive impairment in iron deficiency: alterations in brain-derived neurotrophic factor and insulin-like growth factor expression and function in the central nervous system.Host cell signalling and leishmania mechanisms of evasion.Leishmania repression of host translation through mTOR cleavage is required for parasite survival and infection.In vitro characterization of the microglial inflammatory response to Streptococcus suis, an important emerging zoonotic agent of meningitis.Leishmania GP63 alters host signaling through cleavage-activated protein tyrosine phosphatases.A novel form of NF-kappaB is induced by Leishmania infection: involvement in macrophage gene expression.Effect of iron deficiency on the expression of insulin-like growth factor-II and its receptor in neuronal and glial cells.[Full blood count reference values in children of 8 to 12 years old residing at 2,760 m above sea level].Chronic Intake of Commercial Sweeteners Induces Changes in Feeding Behavior and Signaling Pathways Related to the Control of Appetite in BALB/c Mice.Leptin Signaling in the Control of Metabolism and Appetite: Lessons from Animal ModelsLeukocyte production of IFN-γ and TNF-α in 8- to 12-y-old children with low serum iron levelsChanges in nutrient and calorie intake, adipose mass, triglycerides and TNF-α concentrations after non-caloric sweetener intake: pilot study
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հետազոտող
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