Примери за използване на Neutralizing antibody на Английски и техните преводи на Български
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The overall neutralizing antibody rate was 11/ 108 patients(10%).
Seroconversion rates and geometric mean titer for JEV neutralizing antibody at Day 70 n/ N.
This Ebola neutralizing antibody may be useful in vaccine development or as a passive prophylactic agent.
The potential clinical relevance of neutralizing antibody formation is not known.
A neutralizing antibody to CYP2C9 showed a minimal effect on cabozantinib metabolite formation(ie, a< 20% reduction).
Seroconversion rates andgeometric mean titer for anti-JEV neutralizing antibody at Day 56% with SCR.
Seroprotection rate(SPR) defined as neutralizing antibody titer≥1:10 and geometric mean titers(GMT) are presented in Table 11.
Investigations activated partial thromboplastin time prolonged, neutralizing antibody positive.
Positive responses in the neutralizing antibody(NAb) assay were detected in 1.0%, 1.6%, and 0.2% of patients on Kevzara 200 mg, Kevzara 150 mg, and placebo respectively.
There is no definitive correlation between the antibody titre and neutralizing antibody development.
Seroconversion rates andgeometric mean titer of JEV neutralizing antibody at Day 70 in the Intent-to-treat Population, for the entire study population and stratified by age.
Concomitant administration of IXIARO and inactivated hepatitis A vaccine was shown to be non-inferior to single vaccinations with regard to GMT of anti-JE virus neutralizing antibody and HAV antibody, and for seroconversion rates of both antibody types(Table 7).
Seroconversion rates andgeometric mean titer of anti JEV neutralizing antibody at Day 56 and seroconversion rates and geometric mean titer for HAV antibody at Day 28 in the Per Protocol Population.
After vaccination the rate of subjects with neutralizing antibody titres≥ 40, seroconversion rate and seroconversion factor as measured by microneutralisation assay(MN) in children aged 6 to 35 months.
Seroconversion rates andgeometric mean titer of JEV neutralizing antibody by vaccine dose and age group.
After vaccination, the rate of subjects with neutralizing antibody titers≥ 20, seroconversion rate and seroconversion factor, as measured by MN assay, in infants, children, and adolescents aged 6 months to 17 years were as follows.
We saw earlier that HlV is highly variable,that a broad neutralizing antibody latches on and disables multiple variations of the virus.
After vaccination the rate of subjects with neutralizing antibody titres≥ 40, seroconversion rate and seroconversion factor as measured by microneutralisation assay(MN) in children and adolescents aged 3 to 17 years were as follows.
Seroconversion rates, rates of subjects with at least 4-fold increase in JEV neutralizing antibody titers and Geometric Mean Titers at baseline, Day 56 and Month 7 stratified by age group.
During clinical development, neutralizing antibody titres for each serotype were measured with the plaque reduction neutralization test(PRNT) and presented as geometric mean titres(GMTs).
The first co-primary endpoint compared vaccinia-specific neutralizing antibody responses at the peak visits(Day 42 after first vaccination for Imvanex where the subjects received two doses according to the standard vaccination schedule and Day 28 for ACAM2000).
After vaccination, the rate of subjects with neutralizing antibody titers≥ 20, seroconversion rate and seroconversion factor, as measured by MN assay, in infants, children, and adolescents aged 6 months to 17 years were as follows.
After vaccination the rate of subjects with neutralizing antibody titres≥ 40, seroconversion rate and seroconversion factor as measured by microneutralisation assay(MN) in adults aged 18 to 59 years and in older subjects aged 60 years and above were as follows.
After primary vaccination the rate of subjects with neutralizing antibody titres> 20, seroconversion rate and seroconversion factor as measured by microneutralisation assay(MN) in adults aged 18 to 59 years and in elderly subjects aged 60 years and above were as follows.
Cabozantinib is a substrate for CYP3A4 metabolism in vitro, as a neutralizing antibody to CYP3A4 inhibited formation of metabolite XL184 N-oxide by> 80% in a NADPH-catalyzed human liver microsomal(HLM) incubation; in contrast, neutralizing antibodies to CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C19, CYP2D6 and CYP2E1 had no effect on cabozantinib metabolite formation.
Neutralizing antibodies were detected in 19 of 299 patients in CA204004.
Neutralizing antibodies were detected in 2 of 53 patients.
Neutralizing antibodies to immunomodulatory therapies in MS- part I.
Neutralizing antibodies(Inhibitors).