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R Rott

Showing results (211-220 of 228) with videos related to

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The EMBO Journal|June 1, 1985
The receptor-destroying enzyme of influenza C virus is neuraminate-O-acetylesteraseG Herrler, R Rott, H D Klenk, et al.
Virology|July 1, 1993
Genomic organization of the structural proteins of borna disease virus revealed by a cDNA clone encoding the 38-kDa proteinJ M Pyper, J A Richt, L Brown, et al.
Journal of Virology|May 1, 1991
Site-specific mutagenesis identifies three cysteine residues in the cytoplasmic tail as acylation sites of influenza virus hemagglutininM Veit, E Kretzschmar, K Kuroda, et al.
Virology|February 1, 1989
Mutations at the cleavage site of the hemagglutinin after the pathogenicity of influenza virus A/chick/Penn/83 (H5N2)M Ohuchi, M Orlich, R Ohuchi, et al.
The EMBO Journal|December 20, 1984
Studies on the adaptation of influenza viruses to MDCK cellsR Rott, M Orlich, H D Klenk, et al.
Archives of Virology. Supplementum|January 1, 1993
Borna disease virus: nature of the etiologic agent and significance of infection in manJ A Richt, S Herzog, J Pyper, et al.
Virology|January 10, 1995
Induction of protection against Borna disease by inoculation with high-dose-attenuated Borna disease virusD Oldach, M C Zink, J M Pyper, et al.
Journal of Virology|April 1, 1989
Synthesis of biologically active influenza virus hemagglutinin in insect larvaeK Kuroda, A Gröner, K Frese, et al.
Virology|September 1, 1991
Pneumotropic revertants derived from a pantropic mutant, F1-R, of Sendai virusM Tashiro, I James, S Karri, et al.
The Journal of General Virology|November 1, 1991
Monoclonal antibodies differentiate between the haemagglutinating and the receptor-destroying activities of bovine coronavirusJ Storz, G Herrler, D R Snodgrass, et al.
Pageof 23

Showing results (211-220 of 228) with videos related to

Sort By:
Pageof 23
The EMBO Journal|June 1, 1985
The receptor-destroying enzyme of influenza C virus is neuraminate-O-acetylesteraseG Herrler, R Rott, H D Klenk, et al.
Virology|July 1, 1993
Genomic organization of the structural proteins of borna disease virus revealed by a cDNA clone encoding the 38-kDa proteinJ M Pyper, J A Richt, L Brown, et al.
Journal of Virology|May 1, 1991
Site-specific mutagenesis identifies three cysteine residues in the cytoplasmic tail as acylation sites of influenza virus hemagglutininM Veit, E Kretzschmar, K Kuroda, et al.
Virology|February 1, 1989
Mutations at the cleavage site of the hemagglutinin after the pathogenicity of influenza virus A/chick/Penn/83 (H5N2)M Ohuchi, M Orlich, R Ohuchi, et al.
The EMBO Journal|December 20, 1984
Studies on the adaptation of influenza viruses to MDCK cellsR Rott, M Orlich, H D Klenk, et al.
Archives of Virology. Supplementum|January 1, 1993
Borna disease virus: nature of the etiologic agent and significance of infection in manJ A Richt, S Herzog, J Pyper, et al.
Virology|January 10, 1995
Induction of protection against Borna disease by inoculation with high-dose-attenuated Borna disease virusD Oldach, M C Zink, J M Pyper, et al.
Journal of Virology|April 1, 1989
Synthesis of biologically active influenza virus hemagglutinin in insect larvaeK Kuroda, A Gröner, K Frese, et al.
Virology|September 1, 1991
Pneumotropic revertants derived from a pantropic mutant, F1-R, of Sendai virusM Tashiro, I James, S Karri, et al.
The Journal of General Virology|November 1, 1991
Monoclonal antibodies differentiate between the haemagglutinating and the receptor-destroying activities of bovine coronavirusJ Storz, G Herrler, D R Snodgrass, et al.
Pageof 23