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Integrated analysis of gene expression profiles reveals deregulation of the immune response genes during different phases of chronic hepatitis B infection is divided into different phases including immune tolerance (IT), immune clearance (or immune active [IA

A multiscale model suggests that a moderately weak inhibition of SARS-CoV-2 replication by type I IFN could accelerate the clearance of the virus could elicit a strong adaptive immune response which accelerates the clearance of the virus. Furthermore

Antiviral system of innate immunity: Covid-19 pathogenesis and treatment [АНТИВИРУСНАЯ СИСТЕМА ВРОЖДЕННОГО ИММУНИТЕТА: ПАТОГЕНЕЗ И ЛЕЧЕНИЕ COVID-19]Antiviral system of innate immunity includes two main components: the mitochondrial antiviral

Immunogenicity and protective efficacy of prime-boost immunization in mice vaccinated with live and inactivated influenza A (H5N1) vaccines was to compare immune response and protective efficacy of diverse prime-boost immunization protocols: 1) prime

Integrated analysis of gene expression profiles reveals deregulation of the immune response genes during different phases of chronic hepatitis B infection is divided into different phases including immune tolerance (IT), immune clearance (or immune active [IA

Immunological environment shifts during pregnancy may affect the risk of developing severe complications in COVID-19 patientsadaptive immunity

Mucociliary transport as a link between chronic rhinosinusitis and trace element dysbalance as certain forms of cancer. Alteration of mucociliary clearance frequently observed in the patients and plays

We should be prepared to smallpox re-emergence. The result of this decision is that the mankind lost the collective immunity not only to smallpox, but also

Correlation of T cell response and bacterial clearance in human volunteers challenged with Helicobacter pylori revealed by randomised controlled vaccination with Ty21a-based Salmonella vaccines for its control. Natural infection appears not to induce protective immunity. Thus, the feasibility of a

Prevention of Influenza A(H7N9) and Bacterial Infections in Mice Using Intranasal Immunization With Live Influenza Vaccine and the Group B Streptococcus Recombinant Polypeptides influenza infection followed by GBS burden. Mice were intranasally immunized using 107 50% egg infectious

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