Results 271 to 280 of about 83,240 (318)

Hemagglutinin of vesicular stomatitis virus

Archiv f�r die gesamte Virusforschung, 1969
Hemagglutinin of vesicular stomatitis virus was prepared in suspension culture of BHK21/13 S cells maintained in a medium containing 0.4% bovine albumin and no serum. Optimal conditions for titration of VSV hemagglutinin included a low temperature, pH 5.8 and the use of goose erythrocytes.
P, Arstila, P, Halonen, A, Salmi
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The shape of vesicular stomatitis virus

Virology, 1976
Abstract Most vesicular stomatitis virus (VSV) particles in situ and in vitro after mild treatment appear bacilliform rather than bullet-shaped. However, the nucleocapsid is bullet-shaped. Budding begins with the hemisphere containing the rounded end of the nucleocapsid and finishes with the completion of the nonnucleocapsid-containing “terminal ...
J, Orenstein, L, Johnson, E, Shelton, R A, Lazzarini   +3 more
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Biophysical Studies of Vesicular Stomatitis Virus

Journal of Bacteriology, 1966
McCombs, Robert M.(Baylor University College of Medicine, Houston, Tex.),Matilda Benyesh-Melnick, and Jean P. Brunschwig. Biophysical studies of vesicular stomatitis virus: J. Bacteriol.91:803–812. 1966.—The infectivity and morphology of vesicular stomatitis virus (VSV) were studied after density gradient centrifugation in cesium chloride (CsCI ...
R M, McCombs, M B, Melnick, J P, Brunschwig   +2 more
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Interfering Component of Vesicular Stomatitis Virus

Nature, 1966
INTERFERENCE during the replication of vesicular stomatitis virus (VSV) was first described by Cooper and Bellett1, who suggested that the interfering activity which was present in viruses collected after several successive undiluted passages resulted from a transmissible component.
J, Crick, B, Cartwright, F, Brown
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Structural components of vesicular stomatitis virus

Virology, 1966
Abstract Fixed and unfixed suspensions of vesicular stomatitis virus (VSV) were examined by negative contrast techniques. The internal component of this virus showed two modes of release: (1) It was found free of the viral envelope as a large helical cylinder (500–550 A × 1600–2000 A) in various stages of disorganization.
R W, Simpson, R E, Hauser
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Superinfect on exclusion by vesicular stomatitis virus

Virology, 1983
The infection of baby hamster kidney (BHK21) cells by the Indiana strain of vesicular stomatitis virus (VSV) causes a rapid loss of the ability of the cells to be superinfected by VSV virions or defective-interfering particles. This exclusion phenomenon is at the level of virus penetration and requires viral gene expression and a functional VSV ...
P, Whitaker-Dowling, J S, Youngner, C C, Widnell, D K, Wilcox   +3 more
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Vesicular Stomatitis Virus Pseudotypes of Retroviruses

2003
Pseudotype viruses are phenotypically mixed virions containing the genome or nucleocapsid of one enveloped virus and the surface or envelope (env) glycoproteins of another. This chapter will concentrate on vesicular stomatitis virus (VSV) pseudotypes retaining the VSV nucleocapsid but with alternative env glycoproteins derived from retroviruses.
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Experimental vesicular stomatitis virus infection: Ultrastructural pathology

Experimental and Molecular Pathology, 1975
Abstract Vesicular stomatitis virus infection in mice and hamsters was rapidly lethal, but primary target organs and pathogenesis varied with the route of inoculation. Ultrastructural observations of brain tissue after intracerebral inoculation indicated widespread neuronal infection with viral maturation upon plasma membranes.
F A, Murphy, A K, Harrison, S P, Bauer
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Replication of vesicular stomatitis virus.

2012
The replication of the RNA genome of the rhabdovirus vesicular stomatitis virus (VSV) was studied in vivo and in vitro. The products of replication, (+) and (-) strand 42S RNA, were separated from the mRNA species in CsCI gradients, allowing the determination of the rates of 42S RNA synthesis throughout the infectious cycle. It was found that 42S RNA
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Control of vesicular stomatitis virus protein synthesis

Virology, 1976
Abstract The five structural polypeptides of vesicular stomatitis virus are synthesized in infected cells at nonequimolar rates which correspond to their relative amounts in the virus particle. These experiments are concerned with the mechanism(s) responsible for the relative rates of viral polypeptide synthesis.
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