A critical threshold of meningococcal factor H binding protein expression is required for increased breadth of protective antibodies elicited by native outer membrane vesicle vaccines
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Outer membrane vesicles as platform vaccine technologyA Burkholderia pseudomallei outer membrane vesicle vaccine provides protection against lethal sepsis.The effect of human factor H on immunogenicity of meningococcal native outer membrane vesicle vaccines with over-expressed factor H binding protein.Mutant Native Outer Membrane Vesicles Combined with a Serogroup A Polysaccharide Conjugate Vaccine for Prevention of Meningococcal Epidemics in Africa.Immunogenicity of a meningococcal native outer membrane vesicle vaccine with attenuated endotoxin and over-expressed factor H binding protein in infant rhesus monkeys.A native outer membrane vesicle vaccine confers protection against meningococcal colonization in human CEACAM1 transgenic mice.Meningococcal factor H binding proteins in epidemic strains from Africa: implications for vaccine development.Importance of antibodies to lipopolysaccharide in natural and vaccine-induced serum bactericidal activity against Neisseria meningitidis group B.Global transcriptome analysis reveals small RNAs affecting Neisseria meningitidis bacteremia.Analysis of the bactericidal response to an experimental Neisseria meningitidis vesicle vaccineThe new multicomponent vaccine against meningococcal serogroup B, 4CMenB: immunological, functional and structural characterization of the antigens.The role of apolipoprotein N-acyl transferase, Lnt, in the lipidation of factor H binding protein of Neisseria meningitidis strain MC58 and its potential as a drug target.Impaired Immunogenicity of Meningococcal Neisserial Surface Protein A in Human Complement Factor H Transgenic Mice.The effect of iron availability on transcription of the Neisseria meningitidis fHbp gene varies among clonal complexes.Neisseria meningitidis B vaccines: recent advances and possible immunization policies.Neisseria meningitidis factor H-binding protein fHbp: a key virulence factor and vaccine antigen.HexR Controls Glucose-Responsive Genes and Central Carbon Metabolism in Neisseria meningitidis.Vaccines, reverse vaccinology, and bacterial pathogenesis.Gene variability and degree of expression of vaccine candidate factor H binding protein in clinical isolates of Neisseria meningitidis.
P2860
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P2860
A critical threshold of meningococcal factor H binding protein expression is required for increased breadth of protective antibodies elicited by native outer membrane vesicle vaccines
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
A critical threshold of mening ...... uter membrane vesicle vaccines
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A critical threshold of mening ...... uter membrane vesicle vaccines
@en
type
label
A critical threshold of mening ...... uter membrane vesicle vaccines
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A critical threshold of mening ...... uter membrane vesicle vaccines
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prefLabel
A critical threshold of mening ...... uter membrane vesicle vaccines
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A critical threshold of mening ...... uter membrane vesicle vaccines
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P2093
P2860
P356
P1476
A critical threshold of mening ...... uter membrane vesicle vaccines
@en
P2093
Dan M Granoff
Isabel Delany
Oliver Koeberling
P2860
P304
P356
10.1128/CVI.00542-10
P577
2011-03-02T00:00:00Z