fH-dependent complement evasion by disease-causing meningococcal strains with absent fHbp genes or frameshift mutations.
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How the Knowledge of Interactions between Meningococcus and the Human Immune System Has Been Used to Prepare Effective Neisseria meningitidis VaccinesInhibition of the alternative pathway of nonhuman infant complement by porin B2 contributes to virulence of Neisseria meningitidis in the infant rat modelBinding of complement factor H to PorB3 and NspA enhances resistance of Neisseria meningitidis to anti-factor H binding protein bactericidal activity.The Phosphocarrier Protein HPr Contributes to Meningococcal Survival during Infection.Factor H-dependent alternative pathway inhibition mediated by porin B contributes to virulence of Neisseria meningitidis.Neisseria meningitidis B vaccines: recent advances and possible immunization policies.Neisseria meningitidis factor H-binding protein fHbp: a key virulence factor and vaccine antigen.Neisseria meningitidis serogroup B bivalent factor H binding protein vaccine.
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P2860
fH-dependent complement evasion by disease-causing meningococcal strains with absent fHbp genes or frameshift mutations.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 17 June 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
fH-dependent complement evasio ...... genes or frameshift mutations.
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fH-dependent complement evasio ...... genes or frameshift mutations.
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type
label
fH-dependent complement evasio ...... genes or frameshift mutations.
@en
fH-dependent complement evasio ...... genes or frameshift mutations.
@nl
prefLabel
fH-dependent complement evasio ...... genes or frameshift mutations.
@en
fH-dependent complement evasio ...... genes or frameshift mutations.
@nl
P2860
P1433
P1476
fH-dependent complement evasio ...... genes or frameshift mutations
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P2093
Dan M Granoff
Serena Giuntini
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P304
P356
10.1016/J.VACCINE.2013.06.009
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P50
P577
2013-06-17T00:00:00Z