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Darwyn Kobasa

Researcher at St. Jude Children's Research Hospital

Publications -  6
Citations -  984

Darwyn Kobasa is an academic researcher from St. Jude Children's Research Hospital. The author has contributed to research in topics: Viral replication & Virus. The author has an hindex of 6, co-authored 6 publications receiving 947 citations.

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Balanced hemagglutinin and neuraminidase activities are critical for efficient replication of influenza a virus

TL;DR: The SD0 mutant of influenza virus A/WSN/33 (WSN), characterized by a 24-amino-acid deletion in the neuraminidase stalk, does not grow in embryonated chicken eggs because of defective NA function, demonstrating that balanced HA-NA functions are necessary for efficient influenza virus replication.
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Neuraminidase hemadsorption activity, conserved in avian influenza A viruses, does not influence viral replication in ducks.

TL;DR: Although conservation of NA hemadsorption activity among avian virus NAs suggests the maintenance of a required function of NA, loss of the activity does not preclude the replication of the virus in an avian host.
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DNA Vaccine Encoding Hemagglutinin Provides Protective Immunity against H5N1 Influenza Virus Infection in Mice

TL;DR: It is reported that a DNA vaccine encoding hemagglutinin from the index human influenza isolate A/HK/156/97 provides immunity against H5N1 infection of mice, and it is determined that unadapted H5n1 viruses are pathogenic in mice, which provides a well-defined mammalian system for immunological studies of lethal avian influenza virus infection.
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Amino Acid Residues Contributing to the Substrate Specificity of the Influenza A Virus Neuraminidase

TL;DR: This finding suggests that the adaptation of NA to different substrates occurs by a mechanism of amino acid substitutions that subtly alter the conformation of NA in and around the active site to facilitate the binding of different species of sialic acid.
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Strategies for inducing protection against avian influenza A virus subtypes with DNA vaccines

TL;DR: It is demonstrated that immunization with DNA encoding a type-specific gene may not be effective against either homologous or heterologous strains of virus, particularly if the challenge virus causes a highly lethal infection.