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Volumn 92, Issue 25, 1995, Pages 11563-11567
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Production of infectious human respiratory syncytial virus from cloned cDNA confirms an essential role for the transcription elongation factor from the 5′ proximal open reading frame of the M2 mRNA in gene expression and provides a capability for vaccine development
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Author keywords
Negative strand RNA virus; Paramyxovirus; Polymerase; Reverse genetics
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Indexed keywords
HUMAN RESPIRATORY SYNCYTIAL VIRUS;
PARAMYXOVIRIDAE;
RESPIRATORY SYNCYTIAL VIRUS;
RICE STRIPE VIRUS;
RNA VIRUSES;
SYNCYTIAL VIRUS;
MIRIDAE;
CAPSID PROTEIN;
COMPLEMENTARY DNA;
ELONGATION FACTOR;
MESSENGER RNA;
PHOSPHOPROTEIN;
TRANSCRIPTION FACTOR;
VIRUS PROTEIN;
VIRUS VACCINE;
ARTICLE;
GENE EXPRESSION;
HEP 2 CELL;
HUMAN;
HUMAN CELL;
MOLECULAR CLONING;
OPEN READING FRAME;
PLASMID;
PRIORITY JOURNAL;
RESPIRATORY SYNCYTIAL PNEUMOVIRUS;
VIRUS GENOME;
VIRUS INFECTION;
VIRUS NUCLEOCAPSID;
BASE SEQUENCE;
CLONING, MOLECULAR;
DNA, ANTISENSE;
DNA, COMPLEMENTARY;
GENE EXPRESSION REGULATION, VIRAL;
HN PROTEIN;
MOLECULAR SEQUENCE DATA;
OPEN READING FRAMES;
PLAQUE ASSAY;
RESPIRATORY SYNCYTIAL VIRUS, HUMAN;
RNA, MESSENGER;
RNA, VIRAL;
TRANSCRIPTION, GENETIC;
TRANSFECTION;
VACCINES, SYNTHETIC;
VIRAL ENVELOPE PROTEINS;
VIRAL PROTEINS;
VIRAL VACCINES;
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EID: 0029584042
PISSN: 00278424
EISSN: None
Source Type: Journal
DOI: 10.1073/pnas.92.25.11563 Document Type: Article |
Times cited : (377)
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References (21)
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