N-linked glycosylation facilitates sialic acid-independent attachment and entry of influenza A viruses into cells expressing DC-SIGN or L-SIGN

Journal of Virology

Volumn 85, Issue 6, 2011, Pages 2990-3000

  Londrigan, Sarah L ^a   Turville, Stuart G ^c   Tate, Michelle D ^a   Deng, Yi Mo ^b   Brooks, Andrew G ^a   Reading, Patrick C ^a,b  

^a UNIVERSITY OF MELBOURNE   (Australia)

^b VICTORIAN INFECTIOUS DISEASES REFERENCE LABORATORY   (Australia)

^c WESTMEAD HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ION; CD209 ANTIGEN; LECTIN; MANNAN; PROTEIN L SIGN; SIALIC ACID; SIALIDASE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL SURFACE; CHO CELL; CONTROLLED STUDY; INFECTION RESISTANCE; INFLUENZA VIRUS A H1N1; INFLUENZA VIRUS A H3N2; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN GLYCOSYLATION; VIRUS ATTACHMENT; VIRUS CELL INTERACTION; VIRUS ENTRY; VIRUS STRAIN;

ANIMALS; CALCIUM; CELL ADHESION MOLECULES; CHO CELLS; CRICETINAE; CRICETULUS; GLYCOSYLATION; INFLUENZA A VIRUS, H1N1 SUBTYPE; INFLUENZA A VIRUS, H3N2 SUBTYPE; LECTINS, C-TYPE; N-ACETYLNEURAMINIC ACID; RECEPTORS, CELL SURFACE; RECEPTORS, VIRUS; VIRUS INTERNALIZATION;

BACTERIA (MICROORGANISMS); CRICETULUS GRISEUS; INFLUENZA A VIRUS; MAMMALIA; ORTHOMYXOVIRIDAE;

EID: 79952410920     PISSN: 0022538X     EISSN: 10985514     Source Type: Journal    
DOI: 10.1128/JVI.01705-10     Document Type: Article

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