Neuronal IFN signaling is dispensable for the establishment of HSV-1 latency

Virology

Volumn 497, Issue , 2016, Pages 323-327

  Rosato, Pamela C ^a,c   Katzenell, Sarah ^a   Pesola, Jean M ^b   North, Brian ^a   Coen, Donald M ^b   Leib, David A ^a  

^a DARTMOUTH MEDICAL SCHOOL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF MINNESOTA   (United States)

Author keywords

Herpes; Interferon; Latency; Neurons; Simplex

Indexed keywords

BETA INTERFERON; INTERFERON; LATENCY ASSOCIATED PEPTIDE; STAT1 PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL SURVIVAL; CENTRAL NERVOUS SYSTEM INFECTION; CONTROLLED STUDY; GANGLION; HERPES SIMPLEX; HERPES SIMPLEX VIRUS 1; MOUSE; NERVOUS TISSUE; NEUROPATHOLOGY; NONHUMAN; PRIORITY JOURNAL; SENSORY NERVE CELL; SIGNAL TRANSDUCTION; VIRUS GENOME; VIRUS LATENCY; VIRUS LOAD; VIRUS REACTIVATION; VIRUS VIRULENCE; ANIMAL; DEFICIENCY; DISEASE MODEL; KNOCKOUT MOUSE; METABOLISM; MORTALITY; NERVE CELL; PHYSIOLOGY; VIROLOGY; VIRUS REPLICATION;

ANIMALS; CELL SURVIVAL; DISEASE MODELS, ANIMAL; GANGLIA; HERPES SIMPLEX; HERPESVIRUS 1, HUMAN; INTERFERONS; MICE; MICE, KNOCKOUT; NEURONS; SIGNAL TRANSDUCTION; STAT1 TRANSCRIPTION FACTOR; VIRAL LOAD; VIRUS LATENCY; VIRUS REPLICATION;

EID: 84982957551     PISSN: 00426822     EISSN: 10960341     Source Type: Journal    
DOI: 10.1016/j.virol.2016.06.016     Document Type: Article

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